Výsledky vyhľadávania - "Fuchsberger, C."

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Autori: Smit RAJ Wade KH Hui Q a ďalší

Prispievatelia: Smit RAJ Wade KH Hui Q a ďalší

Zdroj: 23andMe Research Team 2025, 'Polygenic prediction of body mass index and obesity through the life course and across ancestries', Nature Medicine, vol. 31, no. 9, pp. 3151-3168. https://doi.org/10.1038/s41591-025-03827-z
Smit, R A J, Wade, K H, Hui, Q, Arias, J D, Yin, X, Christiansen, M R, Yengo, L, Preuss, M H, Nakabuye, M, Rocheleau, G, Graham, S E, Buchanan, V L, Chittoor, G, Graff, M, Guindo-Martínez, M, Lu, Y, Marouli, E, Sakaue, S, Spracklen, C N, Vedantam, S, Wilson, E P, Chen, S-H, Ferreira, T, Ji, Y, Karaderi, T, Lüll, K, Machado, M, Malden, D E, Medina-Gomez, C, Moore, A, Rüeger, S, Akiyama, M, Allison, M A, Alvarez, M, Andersen, M K, Appadurai, V, Arbeeva, L, Bartell, E, Cañadas-Garre, M, Li, X, Nelson, C P, Smyth, L J, Sun, L, Wang, Z, Cole, J W, Cooper, R S, Kee, F, McKnight, A J, Weir, D R, Wilson, P W F & 23andMe Research Team 2025, 'Polygenic prediction of body mass index and obesity through the life course and across ancestries', Nature Medicine. https://doi.org/10.1038/s41591-025-03827-z
23andMe Research Team 2025, ' Polygenic prediction of body mass index and obesity through the life course and across ancestries ', Nature Medicine, vol. 31, no. 9, pp. 3151-3168 . https://doi.org/10.1038/s41591-025-03827-z

Predmety: Adult, Male, Understanding Society Scientific Group, Multifactorial Inheritance, Adolescent, Obesity/genetics, body mass index, 23andMe Research Team, White People, Body Mass Index, Young Adult, Polygenic score, Racial Groups/genetics, DiscovEHR (DiscovEHR and MyCode Community Health Initiative), PRACTICAL Consortium, Humans, Genetic Predisposition to Disease, name=SDG 3 - Good Health and Well-being, Obesity, Child, Multifactorial Inheritance/genetics, Polygenic scores body mass index, Adiposity, eMERGE (Electronic Medical Records and Genomics Network), Racial Groups, Middle Aged, GPC-UGR, Adiposity/genetics, Child, Preschool, VA Million Veteran Program, Female, White People/genetics

Popis súboru: ELETTRONICO; application/pdf; application/zip; text/xml

Prístupová URL adresa: https://hdl.handle.net/11368/3114138
https://www.nature.com/articles/s41591-025-03827-z
https://hdl.handle.net/1871.1/f1cbb1a3-1b84-4784-a426-405af1fee45e
https://research.vu.nl/en/publications/f1cbb1a3-1b84-4784-a426-405af1fee45e
https://doi.org/10.1038/s41591-025-03827-z
https://research.rug.nl/en/publications/e9e305b4-e4e2-49e5-8913-9ee6becbc545
https://hdl.handle.net/11370/e9e305b4-e4e2-49e5-8913-9ee6becbc545
https://doi.org/10.1038/s41591-025-03827-z
https://www.nature.com/articles/s41591-025-03827-z
https://doi.org/10.1038/s41591-025-03827-z
https://pure.amsterdamumc.nl/en/publications/9ea056f1-f4e5-439d-8d54-4e112d504c80
https://doi.org/10.1038/s41591-025-03827-z
https://hdl.handle.net/11388/367573
https://doi.org/10.1038/s41591-025-03827-z
https://pure.qub.ac.uk/en/publications/c00dd1f6-fbfd-4fb5-893d-9b8db0783578
https://curis.ku.dk/ws/files/499174807/s41591-025-03827-z.pdf
https://hdl.handle.net/11368/3114138
https://pubmed.ncbi.nlm.nih.gov/40691366/
https://www.repository.cam.ac.uk/handle/1810/389554
https://doi.org/10.1038/s41591-025-03827-z
https://www.repository.cam.ac.uk/handle/1810/389594
https://doi.org/10.1038/s41591-025-03827-z

Associations of autozygosity with a broad range of human phenotypes

Autori: Clark, D.W. Okada, Y. Moore, K.H.S. a ďalší

Predmety: Consanguinity, Genetic association study, Genetic markers, Inbreeding, Inbreeding depression

Dostupnosť: http://hdl.handle.net/10454/18210

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Autori: Smit, R.A.J. Wade, K.H. Hui, Q. a ďalší

Prístupová URL adresa: https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/324490

Systematic assessment of COVID-19 host genetics using whole genome sequencing data

Autori: Schmidt, A Casadei, N Brand, F a ďalší

Relation: https://doi.org/10.1371/journal.ppat.1012786

Dostupnosť: https://doi.org/10.1371/journal.ppat.1012786
https://ora.ox.ac.uk/objects/uuid:8de339a4-9652-4e38-988f-1de904cbdeec

Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

Autori: Huffman JE Nicolas J Hahn J a ďalší

Prispievatelia: Huffman JE Nicolas J Hahn J a ďalší

Zdroj: Huffman, J E, Nicolas, J, Hahn, J, Heath, A S, Raffield, L M, Yanek, L R, Brody, J A, Thibord, F, Almasy, L, Bartz, T M, Bielak, L F, Bowler, R P, Carrasquilla, G D, Chasman, D I, Chen, M-H, Emmert, D B, Ghanbari, M, Haessle, J, Hottenga, J-J, Kleber, M E, Le, N-Q, Lee, J, Howard, T, Beswick, A, Harris, S E, Smith, J A, Wilson, P, Ben-Shlomo, Y & Wilson, J F & Johnson, A D 2024, 'Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles', Blood. https://doi.org/10.1101/2023.06.07.23291095, https://doi.org/10.1182/blood.2023022596

Predmety: Male, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Polymorphism, Single Nucleotide, genetic study, lipids, Gene Frequency, Humans, Fibrinogen -- genetics, Polymorphism, thrombotic disease, Whole Genome Sequencing, Fibrinogen, Fibrinogen -- metabolism, Single Nucleotide, inflammatory disease, 3. Good health, [SDV] Life Sciences [q-bio], Liver, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Liver -- metabolism, Female, fibrinogen, blood cells, Genome-Wide Association Study

Popis súboru: application/pdf; application/octet-stream; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/37398003
https://pubmed.ncbi.nlm.nih.gov/39226462
https://hdl.handle.net/1871.1/7d7d8a5c-fd9c-4399-9a04-0c1ac1cc6d4a
https://doi.org/10.1182/blood.2023022596
https://research.vu.nl/en/publications/7d7d8a5c-fd9c-4399-9a04-0c1ac1cc6d4a
https://hdl.handle.net/20.500.14243/454816
https://doi.org/10.1182/blood.2023022596
https://research-information.bris.ac.uk/ws/files/413242797/TOPMed_CHARGE.Fibrinogen.Supplemental_Data.Revision2.pdf
https://hdl.handle.net/1983/bc1f1161-65a9-432f-ae22-c97c4e9ddad1

A saturated map of common genetic variants associated with human height

Autori: Yengo, L. Vedantam, S. Marouli, E. a ďalší

Prispievatelia: Yengo, L. Vedantam, S. Marouli, E. a ďalší

Zdroj: Nature
NATURE
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Nature 610 (2022): 704–712. doi:10.1038/s41586-022-05275-y
info:cnr-pdr/source/autori:Loïc Yengo # 1, Sailaja Vedantam # 2 3, Eirini Marouli # 4, Julia Sidorenko 5, Eric Bartell 2 3 6, Saori Sakaue 3 7 8 9, Marielisa Graff 10, Anders U Eliasen 11 12, Yunxuan Jiang 13, Sridharan Raghavan 14 15, Jenkai Miao 2 3, Joshua D Arias 16, Sarah E Graham 17, Ronen E Mukamel 3 18 19, Cassandra N Spracklen 20 21, Xianyong Yin 22, Shyh-Huei Chen 23, Teresa Ferreira 24, Heather H Highland 10, Yingjie Ji 25, Tugce Karaderi 26 27, Kuang Lin 28, Kreete Lüll 29, Deborah E Malden 28, Carolina Medina-Gomez 30, Moara Machado 16, Amy Moore 31, Sina Rüeger 32 33, Xueling Sim 34, Scott Vrieze 35, Tarunveer S Ahluwalia 36 37, Masato Akiyama 7 38, Matthew A Allison 39, Marcus Alvarez 40, Mette K Andersen 41, Alireza Ani 42 43, Vivek Appadurai 44, Liubov Arbeeva 45, Seema Bhaskar 46, Lawrence F Bielak 47, Sailalitha Bollepalli 48, Lori L Bonnycastle 49, Jette Bork-Jensen 41, Jonathan P Bradfield 50 51, Yuki Bradford 52, Peter S Braund 53 54, Jennifer A Brody 55, Kristoffer S Burgdorf 56 57, Brian E Cade 6 58, Hui Cai 59, Qiuyin Cai 59, Archie Campbell 60, Marisa Cañadas-Garre 61, Eulalia Catamo 62, Jin-Fang Chai 34, Xiaoran Chai 63 64, Li-Ching Chang 65, Yi-Cheng Chang 65 66 67, Chien-Hsiun Chen 65, Alessandra Chesi 68 69, Seung Hoan Choi 70, Ren-Hua Chung 71, Massimiliano Cocca 62, Maria Pina Concas 62, Christian Couture 72, Gabriel Cuellar-Partida 13 73, Rebecca Danning 74, E Warwick Daw 75, Frauke Degenhard 76, Graciela E Delgado 77, Alessandro Delitala 78, Ayse Demirkan 79 80, Xuan Deng 81, Poornima Devineni 82, Alexander Dietl 83 84, Maria Dimitriou 85, Latchezar Dimitrov 86, Rajkumar Dorajoo 87 88, Arif B Ekici 89, Jorgen E Engmann 90, Zammy Fairhurst-Hunter 28, Aliki-Eleni Farmaki 85, Jessica D Faul 91, Juan-Carlos Fernandez-Lopez 92, Lukas Forer 93, Margherita Francescatto 94, Sandra Freitag-Wolf 95, Christian Fuchsberger 96, Tessel E Galesloot 97, Yan Gao 98, Zishan Gao 99 100 101, Frank Geller 102, Olga Giannakopoulou 4, Franco Giulianini 74, Anette P Gjesing 41, Anuj Goel 27 103, Scott D Gordon 104, Mathias Gorski 83, Jakob Grove 105 106 107, Xiuqing Guo 108, Stefan Gustafsson 109, Jeffrey Haessler 110, Thomas F Hansen 44 57 111, Aki S Havulinna 48 112, Simon J Haworth 113 114, Jing He 59, Nancy Heard-Costa 115 116, Prashantha Hebbar 117, George Hindy 3 118, Yuk-Lam A Ho 119, Edith Hofer 120 121, Elizabeth Holliday 122, Katrin Horn 123 124, Whitney E Hornsby 17, Jouke-Jan Hottenga 125, Hongyan Huang 126, Jie Huang 127 128, Alicia Huerta-Chagoya 129 130 131, Jennifer E Huffman 119, Yi-Jen Hung 132, Shaofeng Huo 133, Mi Yeong Hwang 134, Hiroyuki Iha 135, Daisuke D Ikeda 135, Masato Isono 136, Anne U Jackson 22, Susanne Jäger 137 138, Iris E Jansen 139 140, Ingegerd Johansson 141 142, Jost B Jonas 143 144 145 146, Anna Jonsson 41, Torben Jørgensen 147 148, Ioanna-Panagiota Kalafati 85, Masahiro Kanai 3 7 8, Stavroula Kanoni 4, Line L Kårhus 147, Anuradhani Kasturiratne 149, Tomohiro Katsuya 150, Takahisa Kawaguchi 151, Rachel L Kember 152, Katherine A Kentistou 153 154, Han-Na Kim 155 156, Young Jin Kim 134, Marcus E Kleber 77 157, Maria J Knol 79, Azra Kurbasic 158, Marie Lauzon 108, Phuong Le 159 160, Rodney Lea 161, Jong-Young Lee 162, Hampton L Leonard 163 164 165, Shengchao A Li 16 166, Xiaohui Li 108, Xiaoyin Li 167 168, Jingjing Liang 167, Honghuang Lin 169, Shih-Yi Lin 170, Jun Liu 28 79, Xueping Liu 102, Ken Sin Lo 171, Jirong Long 59, Laura Lores-Motta 172, Jian'an Luan 173, Valeriya Lyssenko 174 175, Leo-Pekka Lyytikäinen 176 177 178, Anubha Mahajan 27 179, Vasiliki Mamakou 180, Massimo Mangino 181 182, Ani Manichaikul 183, Jonathan Marten 184, Manuel Mattheisen 105 185 186, Laven Mavarani 187, Aaron F McDaid 32 33, Karina Meidtner 137 138, Tori L Melendez 17, Josep M Mercader 19 129 188 189, Yuri Milaneschi 190, Jason E Miller 191 192, Iona Y Millwood 28 193, Pashupati P Mishra 176 177, Ruth E Mitchell 113 194, Line T Møllehave 147, Anna Morgan 62, Soeren Mucha 195, Matthias Munz 195, Masahiro Nakatochi 196, Christopher P Nelson 53 54, Maria Nethander 197 198, Chu Won Nho 199, Aneta A Nielsen 200, Ilja M Nolte 42, Suraj S Nongmaithem 46 201, Raymond Noordam 202, Ioanna Ntalla 4, Teresa Nutile 203, Anita Pandit 22, Paraskevi Christofidou 181, Katri Pärna 29 42, Marc Pauper 172, Eva R B Petersen 204, Liselotte V Petersen 106 205, Niina Pitkänen 206 207, Ozren Pola?ek 208 209, Alaitz Poveda 158, Michael H Preuss 210 211, Saiju Pyarajan 6 58 82, Laura M Raffield 20, Hiromi Rakugi 150, Julia Ramirez 4 212 213, Asif Rasheed 214, Dennis Raven 215, Nigel W Rayner 27 201 216 217, Carlos Riveros 218 219, Rebecca Rohde 10, Daniela Ruggiero 203 220, Sanni E Ruotsalainen 48, Kathleen A Ryan 221 222, Maria Sabater-Lleal 223 224, Richa Saxena 3 189, Markus Scholz 123 124, Anoop Sendamarai 82, Botong Shen 225, Jingchunzi Shi 13, Jae Hun Shin 226, Carlo Sidore 227, Colleen M Sitlani 55, Roderick C Slieker 228 229 230, Roelof A J Smit 210 231, Albert V Smith 47 232, Jennifer A Smith 47 91, Laura J Smyth 61, Lorraine Southam 216 233, Valgerdur Steinthorsdottir 234, Liang Sun 133, Fumihiko Takeuchi 136, Divya Sri Priyanka Tallapragada 46 235, Kent D Taylor 108, Bamidele O Tayo 236, Catherine Tcheandjieu 237 238, Natalie Terzikhan 79, Paola Tesolin 94, Alexander Teumer 239 240, Elizabeth Theusch 241, Deborah J Thompson 242 243, Gudmar Thorleifsson 234, Paul R H J Timmers 153 184, Stella Trompet 202 244, Constance Turman 126, Simona Vaccargiu 227, Sander W van der Laan 245, Peter J van der Most 42, Jan B van Klinken 246 247 248, Jessica van Setten 249, Shefali S Verma 68, Niek Verweij 250, Yogasudha Veturi 52, Carol A Wang 218 219, Chaolong Wang 87 251, Lihua Wang 75, Zhe Wang 210, Helen R Warren 4 252, Wen Bin Wei 253, Ananda R Wickremasinghe 149, Matthias Wielscher 254 255, Kerri L Wiggins 55, Bendik S Winsvold 256 257, Andrew Wong 258, Yang Wu 5, Matthias Wuttke 259 260, Rui Xia 261, Tian Xie 42, Ken Yamamoto 262, Jingyun Yang 263 264, Jie Yao 108, Hannah Young 35, Noha A Yousri 265 266, Lei Yu 263 264, Lingyao Zeng 267, Weihua Zhang 268 269, Xinyuan Zhang 52, Jing-Hua Zhao 270, Wei Zhao 47, Wei Zhou 3 271 272 273, Martina E Zimmermann 83, Magdalena Zoledziewska 227, Linda S Adair 274 275, Hieab H H Adams 276 277 278, Carlos A Aguilar-Salinas 279 280, Fahd Al-Mulla 117, Donna K Arnett 281, Folkert W Asselbergs 249 282 283, Bjørn Olav Åsvold 284 285 286, John Attia 122, Bernhard Banas 287, Stefania Bandinelli 288, David A Bennett 263 264, Tobias Bergler 287, Dwaipayan Bharadwaj 289, Ginevra Biino 290, Hans Bisgaard 11, Eric Boerwinkle 291, Carsten A Böger 287 292 293, Klaus Bønnelykke 11, Dorret I Boomsma 125, Anders D Børglum 105 106 294 295, Judith B Borja 296 297, Claude Bouchard 298, Donald W Bowden 86 299, Ivan Brandslund 300 301, Ben Brumpton 284 302, Julie E Buring 6 74, Mark J Caulfield 4 252, John C Chambers 268 269 303 304, Giriraj R Chandak 46 305, Stephen J Chanock 16, Nish Chaturvedi 258, Yii-Der Ida Chen 108, Zhengming Chen 28 193, Ching-Yu Cheng 63 306, Ingrid E Christophersen 307 308, Marina Ciullo 203 220, John W Cole 309 310, Francis S Collins 49, Richard S Cooper 236, Miguel Cruz 311, Francesco Cucca 227 312, L Adrienne Cupples 81 116, Michael J Cutler 313, Scott M Damrauer 52 314 315, Thomas M Dantoft 147, Gert J de Borst 316, Lisette C P G M de Groot 317, Philip L De Jager 3 318, Dominique P V de Kleijn 316, H Janaka de Silva 149, George V Dedoussis 85, Anneke I den Hollander 172, Shufa Du 274 275, Douglas F Easton 242 319, Petra J M Elders 320, A Heather Eliassen 58 126 321, Patrick T Ellinor 70 322 323, Sölve Elmståhl 324, Jeanette Erdmann 195, Michele K Evans 225, Diane Fatkin 325 326 327, Bjarke Feenstra 102, Mary F Feitosa 75, Luigi Ferrucci 328, Ian Ford 329, Myriam Fornage 261 330, Andre Franke 76, Paul W Franks 158 321 331, Barry I Freedman 332, Paolo Gasparini 62 94, Christian Gieger 100 138, Giorgia Girotto 62 94, Michael E Goddard 333 334, Yvonne M Golightly 10 45 335 336, Clicerio Gonzalez-Villalpando 337, Penny Gordon-Larsen 274 275, Harald Grallert 100 138, Struan F A Grant 50 338 339 340, Niels Grarup 41, Lyn Griffiths 161, Vilmundur Gudnason 232 341, Christopher Haiman 342, Hakon Hakonarson 50 338 343 344, Torben Hansen 41, Catharina A Hartman 215, Andrew T Hattersley 345, Caroline Hayward 184, Susan R Heckbert 346, Chew-Kiat Heng 347 348, Christian Hengstenberg 349, Alex W Hewitt 350 351 352, Haretsugu Hishigaki 135, Carel B Hoyng 172, Paul L Huang 6 323 353, Wei Huang 354, Steven C Hunt 265 355, Kristian Hveem 284 285, Elina Hyppönen 356 357, William G Iacono 35, Sahoko Ichihara 358, M Arfan Ikram 79, Carmen R Isasi 359, Rebecca D Jackson 360, Marjo-Riitta Jarvelin 254 361 362 363, Zi-Bing Jin 146 364, Karl-Heinz Jöckel 187, Peter K Joshi 154, Pekka Jousilahti 112, J Wouter Jukema 244 365 366, Mika Kähönen 367 368, Yoichiro Kamatani 7 369, Kui Dong Kang 370, Jaakko Kaprio 48, Sharon L R Kardia 47, Fredrik Karpe 217 371, Norihiro Kato 136, Frank Kee 61, Thorsten Kessler 267 372, Amit V Khera 3 189, Chiea Chuen Khor 87, Lambertus A L M Kiemeney 97 373, Bong-Jo Kim 134, Eung Kweon Kim 374 375, Hyung-Lae Kim 376, Paulus Kirchhof 377 378 379 380, Mika Kivimaki 381, Woon-Puay Koh 382, Heikki A Koistinen 112 383 384, Genovefa D Kolovou 385, Jaspal S Kooner 268 304 386 387, Charles Kooperberg 110, Anna Köttgen 259, Peter Kovacs 388, Adriaan Kraaijeveld 249, Peter Kraft 126, Ronald M Krauss 241, Meena Kumari 389, Zoltan Kutalik 32 33, Markku Laakso 390, Leslie A Lange 391, Claudia Langenberg 173 392, Lenore J Launer 225, Loic Le Marchand 393, Hyejin Lee 394, Nanette R Lee 296, Terho Lehtimäki 176 177, Huaixing Li 133, Liming Li 395 396, Wolfgang Lieb 397, Xu Lin 133 398, Lars Lind 109, Allan Linneberg 147 399, Ching-Ti Liu 81, Jianjun Liu 87, Markus Loeffler 123 124, Barry London 400, Steven A Lubitz 70 322 323, Stephen J Lye 401, David A Mackey 350 352, Reedik Mägi 29, Patrik K E Magnusson 402, Gregory M Marcus 403, Pedro Marques Vidal 404 405, Nicholas G Martin 104, Winfried März 77 406 407, Fumihiko Matsuda 151, Robert W McGarrah 408 409, Matt McGue 35, Amy Jayne McKnight 61, Sarah E Medland 410, Dan Mellström 197 411, Andres Metspalu 29, Braxton D Mitchell 221 222 412, Paul Mitchell 413, Dennis O Mook-Kanamori 231 414, Andrew D Morris 415, Lorelei A Mucci 126, Patricia B Munroe 4 252, Mike A Nalls 163 164 165, Saman Nazarian 416, Amanda E Nelson 45 417, Matt J Neville 217 371, Christopher Newton-Cheh 189 323, Christopher S Nielsen 418 419, Markus M Nöthen 420, Claes Ohlsson 197 421, Albertine J Oldehinkel 215, Lorena Orozco 422, Katja Pahkala 206 207 423, Päivi Pajukanta 40 424, Colin N A Palmer 425, Esteban J Parra 160, Cristian Pattaro 96, Oluf Pedersen 41, Craig E Pennell 218 219, Brenda W J H Penninx 190, Louis Perusse 72 426, Annette Peters 101 138 427, Patricia A Peyser 47, David J Porteous 60, Danielle Posthuma 139, Chris Power 428, Peter P Pramstaller 96, Michael A Province 75, Qibin Qi 359, Jia Qu 364, Daniel J Rader 52 429, Olli T Raitakari 206 207 430, Sarju Ralhan 431, Loukianos S Rallidis 432, Dabeeru C Rao 433, Susan Redline 6 58, Dermot F Reilly 434, Alexander P Reiner 110 435, Sang Youl Rhee 436, Paul M Ridker 6 74, Michiel Rienstra 250, Samuli Ripatti 3 48 437, Marylyn D Ritchie 52, Dan M Roden 438, Frits R Rosendaal 231, Jerome I Rotter 108, Igor Rudan 153, Femke Rutters 439, Charumathi Sabanayagam 63 306, Danish Saleheen 214 440, Veikko Salomaa 112, Nilesh J Samani 53 54, Dharambir K Sanghera 441 442 443 444, Naveed Sattar 445, Börge Schmidt 187, Helena Schmidt 446, Reinhold Schmidt 120, Matthias B Schulze 137 138 447, Heribert Schunkert 448, Laura J Scott 22, Rodney J Scott 449, Peter Sever 387, Eric J Shiroma 225, M Benjamin Shoemaker 450, Xiao-Ou Shu 59, Eleanor M Simonsick 328, Mario Sims 98, Jai Rup Singh 451, Andrew B Singleton 163, Moritz F Sinner 372 452, J Gustav Smith 453 454 455, Harold Snieder 42, Tim D Spector 181, Meir J Stampfer 58 126 321, Klaus J Stark 83, David P Strachan 456, Leen M 't Hart 228 229 230 457, Yasuharu Tabara 151, Hua Tang 458, Jean-Claude Tardif 171 459, Thangavel A Thanaraj 117, Nicholas J Timpson 113 194, Anke Tönjes 388, Angelo Tremblay 72 426, Tiinamaija Tuomi 48 175 460 461, Jaakko Tuomilehto 112 462 463, Maria-Teresa Tusié-Luna 464 465, Andre G Uitterlinden 30, Rob M van Dam 34 466 467, Pim van der Harst 249 250, Nathalie Van der Velde 30 468, Cornelia M van Duijn 28 79, Natasja M van Schoor 469, Veronique Vitart 184, Uwe Völker 240 470, Peter Vollenweider 404 405, Henry Völzke 239 240, Niels H Wacher-Rodarte 471, Mark Walker 472, Ya Xing Wang 146, Nicholas J Wareham 173, Richard M Watanabe 473 474 475, Hugh Watkins 27 103, David R Weir 91, Thomas M Werge 44 399 476, Elisabeth Widen 48, Lynne R Wilkens 393, Gonneke Willemsen 125, Walter C Willett 126 321, James F Wilson 153 184, Tien-Yin Wong 63 306, Jeong-Taek Woo 436, Alan F Wright 184, Jer-Yuarn Wu 65 477, Huichun Xu 221 222, Chittaranjan S Yajnik 478, Mitsuhiro Yokota 479, Jian-Min Yuan 480 481, Eleftheria Zeggini 216 233 482, Babette S Zemel 52 69 340 343, Wei Zheng 59, Xiaofeng Zhu 167, Joseph M Zmuda 481, Alan B Zonderman 225, John-Anker Zwart 256 483 ; 23andMe Research Team; VA Million Veteran Program; DiscovEHR (DiscovEHR and MyCode Community Health Initiative); eMERGE (Electronic Medical Records and Genomics Network); Lifelines Cohort Study; PRACTICAL Consortium; Understanding Society Scientific Group; Daniel I Chasman 6 74, Yoon Shin Cho 226, Iris M Heid 83, Mark I McCarthy 27 217 484, Maggie C Y Ng 86 485, Christopher J O'Donnell 6 58 486, Fernando Rivadeneira 30, Unnur Thorsteinsdottir 234 341, Yan V Sun 487 488, E Shyong Tai 34 466, Michael Boehnke 22, Panos Deloukas 4 489, Anne E Justice 10 490, Cecilia M Lindgren 3 24 27, Ruth J F Loos 41 210 211 491, Karen L Mohlke 20, Kari E North 10, Kari Stefansson 234 341, Robin G Walters 28 193, Thomas W Winkler 83, Kristin L Young 10, Po-Ru Loh 3 18 19, Jian Yang 5 492 493, Tõnu Esko 29, Themistocles L Assimes 237 238, Adam Auton 13, Goncalo R Abecasis 22, Cristen J Willer 17 271 494, Adam E Locke 495, Sonja I Berndt 16, Guillaume Lettre 171 459, Timothy M Frayling 25, Yukinori Okada 496 497 498 499 500 501, Andrew R Wood 502, Peter M Visscher 503, Joel N Hirschhorn 504 505 506/titolo:A saturated map of common genetic variants associated with human height/doi:10.1038%2Fs41586-022-05275-y/rivista:Nature/anno:2022/pagina_da:704/pagina_a:712/intervallo_pagine:704–712/volume:610
eMERGE (Electronic Medical Records and Genomics Network), The PRACTICAL consortium, Lifelines Cohort Study, 23andMe Research team, Understanding Society Scientific group, VA Million Veteran Program & DiscovEHR (DiscovEHR and MyCode Community Health Initiative) 2022, 'A saturated map of common genetic variants associated with human height', Nature, vol. 610, pp. 704-712. https://doi.org/10.1038/s41586-022-05275-y
23andMe Research Team, VA Million Veteran Program, DiscovEHR (DiscovEHR and MyCode Community Health Initiative), eMERGE (Electronic Medical Records and Genomics Network), Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
Nature, 610, 7933, pp. 704-712
Nature, vol. 610, no. 7933, pp. 704-712
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Andersen, M K, Grove, J, Hansen, T F, Jørgensen, T, Mattheisen, M, Petersen, L V, Wang, Z, Børglum, A D, Dantoft, T M, Grarup, N, Hansen, T, Huang, W, Nielsen, C S, Pedersen, O, Ng, M C Y, Sun, Y V, Winkler, T W, Yang, J, 23andMe Research Team, VA Million Vet Program, DiscovEHR Collaboration, eMERGE Consortium, Lifelines Cohort Study, The PRACTICAL Consortium & Understanding Society Scientific Group 2022, 'A saturated map of common genetic variants associated with human height', Nature, vol. 610, no. 7933, pp. 704–712. https://doi.org/10.1038/s41586-022-05275-y
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lüll, K, Malden, D E, Medina-Gomez, C, Machado, M, Moore, A, Rüeger, S, Sim, X, Vrieze, S, Ahluwalia, T S, Akiyama, M, Allison, M A, Alvarez, M, Andersen, M K, Ani, A, Appadurai, V, Arbeeva, L, Cai, H, Cañadas-Garre, M, Li, X, Nelson, C P, Smyth, L J, Sun, L, Wang, Z, Cole, J W, Cooper, R S, Kee, F, McKnight, A J, Weir, D R & 23andMe Research Team 2022, 'A saturated map of common genetic variants associated with human height', Nature. https://doi.org/10.1038/s41586-022-05275-y
Yengo, L, Vedantam, S, Marouli, E, Sidorenko, J, Bartell, E, Sakaue, S, Graff, M, Eliasen, A U, Jiang, Y, Raghavan, S, Miao, J, Arias, J D, Graham, S E, Mukamel, R E, Spracklen, C N, Yin, X, Chen, S-H, Ferreira, T, Highland, H H, Ji, Y, Karaderi, T, Lin, K, Lull, K, Malden, D E, Andersen, M K, Appadurai, V, Bork-Jensen, J, Burgdorf, K S, Hansen, T F, Jonsson, A, Jorgensen, T, Liu, J, Mollehave, L T, Smit, R A J, Zhao, J-H, Bisgaard, H, Bonnelykke, K, Dantoft, T M, Grarup, N, Hansen, T, Jackson, R D, Karpe, F, Kovacs, P, Lind, L, Linneberg, A, Pedersen, O, Werge, T M, Sun, Y, Loos, R J F, Winkler, T W, 23andMe Res Team, VA Million Vet Program, DiscovEHR DiscovEHR MyCode Communi, eEMERGE Elect Med Records Genomics, LifeLines Cohort Study, PRACTICAL consortium & Understanding Soc Sci Grp 2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, pp. 704–712 . https://doi.org/10.1038/s41586-022-05275-y
2022, ' A saturated map of common genetic variants associated with human height ', Nature, vol. 610, no. 7933, pp. 704-712 . https://doi.org/10.1038/s41586-022-05275-y
Nature 610, 704–712 (2022)

Predmety: genetic association, Epidemiology, multi-ancestry, 45/43, heritability, Quantitative trait, Linkage Disequilibrium, Medical Genetics and Genomics, human experiment, IMPUTATION, GWAS, genetics, 10. No inequality, Radboudumc 4: lnfectious Diseases and Global Health RIMLS: Radboud Institute for Molecular Life Sciences, Human/genetics, Body Height/genetics, HERITABILITY, SCORES, Radboudumc 12: Sensory disorders DCMN: Donders Center for Medical Neuroscience, adult, allele, 631/208/721, common single-nucleotide polymorphisms (SNPs), ddc, 3. Good health, Science & Technology - Other Topics, Molecular and Laser Physics, genes, dimorphism, blood, lipid, Single Nucleotide/genetics, Human, Gene Frequency / genetics, Haplotypes/genetics, 631/208/205/2138, single-nucleotide polymorphisms (SNPs), Article, eMERGE, Lifelines Cohort Study, RESOURCE, Health Sciences, REVEALS, Genetics, Humans, genomic regions, human, GENOME-WIDE ASSOCIATION, Polymorphism, genome, DiscovEHR, Science & Technology, eMERGE (Electronic Medical Records and Genomics Network), ancestry, genetic variants, ta3121, major clinical study, gene linkage disequilibrium, human height, Urology - Radboud University Medical Center, Genetic markers, Haplotypes / genetics, genetic, Europe / ethnology, height, Medizin, Genome-wide association studies, Human / genetics, RARE, Gene Frequency, single nucleotide polymorphism, genetic variability, Medicine and Health Sciences, PRACTICAL Consortium, 2. Zero hunger, ddc:610, ARCHITECTURE, Genome, article, Chromosome Mapping, Single Nucleotide, Biological Sciences, Polymorphism, Single Nucleotide/genetics, Medicinsk genetik och genomik, sample size, Multidisciplinary Sciences, haplotype map, Europe, female, Phenotype, Gene Frequency/genetics, VA Million Veteran Program, Body Height* / genetics, Medical Genetics, Ophthalmology - Radboud University Medical Center, Health Evidence - Radboud University Medical Center, SNPs, genetic variant, Understanding Society Scientific Group, Linkage Disequilibrium / genetics, General Science & Technology, effect size, Radboudumc 15: Urological cancers RIHS: Radboud Institute for Health Sciences, gene frequency, saturated map, 23andMe Research Team, Polymorphism, Single Nucleotide, Europe/ethnology, male, UK BIOBANK, Life Science, DiscovEHR (DiscovEHR and MyCode Community Health Initiative), Linkage Disequilibrium/genetics, gene, 631/208/480, Medicinsk genetik, genome-wide association study, Height, Genome, Human, Spectroscopy of Cold Molecules, Human Genome, Quantitative traits, Genome, Human/genetics, Genome-Wide Association Study, Sample Size, prediction, Single Nucleotide* / genetics, Body Height, Haplotypes, Institut für Ernährungswissenschaft, Height GWAS, 3111 Biomedicine

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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Autori: Mahajan, A. Spracklen, C.N. Zhang, W. a ďalší

Prispievatelia: Mahajan, A. Spracklen, C.N. Zhang, W. a ďalší

Zdroj: Nat Genet
Mahajan, A, Spracklen, C N, Zhang, W, Ng, M C Y, Petty, L E, Kitajima, H, Yu, G Z, Rüeger, S, Speidel, L, Kim, Y J, Horikoshi, M, Mercader, J M, Taliun, D, Moon, S, Kwak, S-H, Robertson, N R, Rayner, N W, Loh, M, Kim, B-J, Chiou, J, Miguel-Escalada, I, Della Briotta Parolo, P, Lin, K, Bragg, F, Preuss, M H, Takeuchi, F, Nano, J, Guo, X, Lamri, A, Nakatochi, M, Scott, R A, Lee, J-J, Huerta-Chagoya, A, Graff, M, Chai, J-F, Parra, E J, Yao, J, Bielak, L F, Tabara, Y, Hai, Y, Steinthorsdottir, V, Cook, J P, Kals, M, Grarup, N, Schmidt, E M, Pan, I, Sofer, T, Wuttke, M, Sarnowski, C, Gieger, C, Nousome, D, Trompet, S, Long, J, Sun, M, Tong, L, Chen, W-M, Ahmad, M, Noordam, R, Lim, V J Y, Tam, C H T, Joo, Y Y, Chen, C-H, Raffield, L M, Lecoeur, C, Prins, B P, Nicolas, A, Yanek, L R, Chen, G, Jensen, R A, Tajuddin, S, Kabagambe, E K, An, P, Xiang, A H, Choi, H S, Cade, B E, Tan, J, Flanagan, J, Abaitua, F, Adair, L S, Adeyemo, A, Aguilar-Salinas, C A, Akiyama, M, Anand, S S, Bertoni, A, Bian, Z, Bork-Jensen, J, Brandslund, I, Brody, J A, Brummett, C M, Buchanan, T A, Canouil, M, Chan, J C N, Chang, L-C, Chee, M-L, Chen, J, Chen, S-H, Chen, Y-T, Chen, Z, Chuang, L-M, Cushman, M, Das, S K, de Silva, H J, Dedoussis, G, Dimitrov, L, Doumatey, A P, Du, S, Duan, Q, Eckardt, K-U, Emery, L S, Evans, D S, Evans, M K, Fischer, K, Floyd, J S, Ford, I, Fornage, M, Franco, O H, Frayling, T M, Freedman, B I, Fuchsberger, C, Genter, P, Gerstein, H C, Giedraitis, V, González-Villalpando, C, González-Villalpando, M E, Goodarzi, M O, Gordon-Larsen, P, Gorkin, D, Gross, M, Guo, Y, Hackinger, S, Han, S, Hattersley, A T, Herder, C, Howard, A-G, Hsueh, W, Huang, M, Huang, W, Hung, Y-J, Hwang, M Y, Hwu, C-M, Ichihara, S, Ikram, M A, Ingelsson, M, Islam, M T, Isono, M, Jang, H-M, Jasmine, F, Jiang, G, Jonas, J B, Jørgensen, M E, Jørgensen, T, Kamatani, Y, Kandeel, F R, Kasturiratne, A, Katsuya, T, Kaur, V, Kawaguchi, T, Keaton, J M, Kho, A N, Khor, C-C, Kibriya, M G, Kim, D-H, Kohara, K, Kriebel, J, Kronenberg, F, Kuusisto, J, Läll, K, Lange, L A, Lee, M-S, Lee, N R, Leong, A, Li, L, Li, Y, Li-Gao, R, Ligthart, S, Lindgren, C M, Linneberg, A, Liu, C-T, Liu, J, Locke, A E, Louie, T, Luan, J, Luk, A O, Luo, X, Lv, J, Lyssenko, V, Mamakou, V, Mani, K R, Meitinger, T, Metspalu, A, Morris, A D, Nadkarni, G N, Nadler, J L, Nalls, M A, Nayak, U, Nongmaithem, S S, Ntalla, I, Okada, Y, Orozco, L, Patel, S R, Pereira, M A, Peters, A, Pirie, F J, Porneala, B, Prasad, G, Preissl, S, Rasmussen-Torvik, L J, Reiner, A P, Roden, M, Rohde, R, Roll, K, Sabanayagam, C, Sander, M, Sandow, K, Sattar, N, Schönherr, S, Schurmann, C, Shahriar, M, Shi, J, Shin, D M, Shriner, D, Smith, J A, So, W Y, Stančáková, A, Stilp, A M, Strauch, K, Suzuki, K, Takahashi, A, Taylor, K D, Thorand, B, Thorleifsson, G, Thorsteinsdottir, U, Tomlinson, B, Torres, J M, Tsai, F-J, Tuomilehto, J, Tusie-Luna, T, Udler, M S, Valladares-Salgado, A, van Dam, R M, van Klinken, J B, Varma, R, Vujkovic, M, Wacher-Rodarte, N, Wheeler, E, Whitsel, E A, Wickremasinghe, A R, van Dijk, K W, Witte, D R, Yajnik, C S, Yamamoto, K, Yamauchi, T, Yengo, L, Yoon, K, Yu, C, Yuan, J-M, Yusuf, S, Zhang, L, Zheng, W, Raffel, L J, Igase, M, Ipp, E, Redline, S, Cho, Y S, Lind, L, Province, M A, Hanis, C L, Peyser, P A, Ingelsson, E, Zonderman, A B, Psaty, B M, Wang, Y-X, Rotimi, C N, Becker, D M, Matsuda, F, Liu, Y, Zeggini, E, Yokota, M, Rich, S S, Kooperberg, C, Pankow, J S, Engert, J C, Chen, Y-D I, Froguel, P, Wilson, J G, Sheu, W H H, Kardia, S L R, Wu, J-Y, Hayes, M G, Ma, R C W, Wong, T-Y, Groop, L, Mook-Kanamori, D O, Chandak, G R, Collins, F S, Bharadwaj, D, Paré, G, Sale, M M, Ahsan, H, Motala, A A, Shu, X-O, Park, K-S, Jukema, J W, Cruz, M, McKean-Cowdin, R, Grallert, H, Cheng, C-Y, Bottinger, E P, Dehghan, A, Tai, E-S, Dupuis, J, Kato, N, Laakso, M, Köttgen, A, Koh, W-P, Palmer, C N A, Liu, S, Abecasis, G, Kooner, J S, Loos, R J F, North, K E, Haiman, C A, Florez, J C, Saleheen, D, Hansen, T, Pedersen, O, Mägi, R, Langenberg, C, Wareham, N J, Maeda, S, Kadowaki, T, Lee, J, Millwood, I Y, Walters, R G, Stefansson, K, Myers, S R, Ferrer, J, Gaulton, K J, Meigs, J B, Mohlke, K L, Gloyn, A L, Bowden, D W, Below, J E, Chambers, J C, Sim, X, Boehnke, M, Rotter, J I, McCarthy, M I, Morris, A P, FinnGen & eMERGE Consortium 2022, 'Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation', Nature Genetics, vol. 54, no. 5, pp. 560-572. https://doi.org/10.1038/s41588-022-01058-3
Mahajan, A, Spracklen, C N, Zhang, W, Ng, M C Y, Petty, L E, Kitajima, H, Yu, G Z, Rüeger, S, Speidel, L, Kim, Y J, Horikoshi, M, Mercader, J M, Taliun, D, Moon, S, Kwak, S-H, Robertson, N R, Rayner, N W, Loh, M, Kim, B-J, Chiou, J, Miguel-Escalada, I, Della Briotta Parolo, P, Lin, K, Bragg, F, Preuss, M H, Takeuchi, F, Nano, J, Guo, X, Lamri, A, Nakatochi, M, Scott, R A, Lee, J-J, Huerta-Chagoya, A, Graff, M, Chai, J-F, Parra, E J, Yao, J, Bielak, L F, Grarup, N, Chen, W-M, Bork-Jensen, J, Islam, M T, Jørgensen, M E, Jørgensen, T, Linneberg, A, Witte, D R, Lind, L, Loos, R J F, Hansen, T, Pedersen, O & FinnGen 2022, ' Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation ', Nature Genetics, vol. 54, no. 5, pp. 560-572 . https://doi.org/10.1038/s41588-022-01058-3
2022, ' Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation ', Nature Genetics, vol. 54, no. 5, pp. 560-572 . https://doi.org/10.1038/s41588-022-01058-3
Nat. Genet. 54, 560-572 (2022)
Mahajan, A, Spracklen, C N, Zhang, W, Ng, M C Y, Petty, L E, Kitajima, H, Yu, G Z, Rüeger, S, Speidel, L, Kim, Y J, Horikoshi, M, Mercader, J M, Taliun, D, Moon, S, Kwak, S, Robertson, N R, Rayner, N W, Loh, M, Kim, B, Chiou, J, Miguel-escalada, I, Della Briotta Parolo, P, Lin, K, Bragg, F, Preuss, M H, Takeuchi, F, Nano, J, Guo, X, Lamri, A, Nakatochi, M, Scott, R A, Lee, J, Huerta-chagoya, A, Graff, M, Chai, J, Parra, E J, Yao, J, Bielak, L F, Tabara, Y, Hai, Y, Steinthorsdottir, V, Cook, J P, Kals, M, Grarup, N, Schmidt, E M, Pan, I, Sofer, T, Wuttke, M, Sarnowski, C, Gieger, C, Nousome, D, Trompet, S, Long, J, Sun, M, Tong, L, Chen, W, Ahmad, M, Noordam, R, Lim, V J Y, Tam, C H T, Joo, Y Y, Chen, C, Raffield, L M, Lecoeur, C, Prins, B P, Nicolas, A, Yanek, L R, Chen, G, Jensen, R A, Tajuddin, S, Kabagambe, E K, An, P, Xiang, A H, Choi, H S, Cade, B E, Tan, J, Flanagan, J, Abaitua, F, Adair, L S, Adeyemo, A, Aguilar-salinas, C A, Akiyama, M, Anand, S S, Bertoni, A, Bian, Z, Bork-jensen, J, Brandslund, I, Brody, J A, Brummett, C M, Buchanan, T A, Canouil, M, Chan, J C N, Chang, L, Chee, M, Chen, J, Chen, S, Chen, Y, Chen, Z, Chuang, L, Cushman, M, Das, S K, De Silva, H J, Dedoussis, G, Dimitrov, L, Doumatey, A P, Du, S, Duan, Q, Eckardt, K, Emery, L S, Evans, D S, Evans, M K, Fischer, K, Floyd, J S, Ford, I, Fornage, M, Franco, O H, Frayling, T M, Freedman, B I, Fuchsberger, C, Genter, P, Gerstein, H C, Giedraitis, V, González-villalpando, C, González-villalpando, M E, Goodarzi, M O, Gordon-larsen, P, Gorkin, D, Gross, M, Guo, Y, Hackinger, S, Han, S, Hattersley, A T, Herder, C, Howard, A, Hsueh, W, Huang, M, Huang, W, Hung, Y, Hwang, M Y, Hwu, C, Ichihara, S, Ikram, M A, Ingelsson, M, Islam, M T, Isono, M, Jang, H, Jasmine, F, Jiang, G, Jonas, J B, Jørgensen, M E, Jørgensen, T, Kamatani, Y, Kandeel, F R, Kasturiratne, A, Katsuya, T, Kaur, V, Kawaguchi, T, Keaton, J M, Kho, A N, Khor, C, Kibriya, M G, Kim, D, Kohara, K, Kriebel, J, Kronenberg, F, Kuusisto, J, Läll, K, Lange, L A, Lee, M, Lee, N R, Leong, A, Li, L, Li, Y, Li-gao, R, Ligthart, S, Lindgren, C M, Linneberg, A, Liu, C, Liu, J, Locke, A E, Louie, T, Luan, J, Luk, A O, Luo, X, Lv, J, Lyssenko, V, Mamakou, V, Mani, K R, Meitinger, T, Metspalu, A, Morris, A D, Nadkarni, G N, Nadler, J L, Nalls, M A, Nayak, U, Nongmaithem, S S, Ntalla, I, Okada, Y, Orozco, L, Patel, S R, Pereira, M A, Peters, A, Pirie, F J, Porneala, B, Prasad, G, Preissl, S, Rasmussen-torvik, L J, Reiner, A P, Roden, M, Rohde, R, Roll, K, Sabanayagam, C, Sander, M, Sandow, K, Sattar, N, Schönherr, S, Schurmann, C, Shahriar, M, Shi, J, Shin, D M, Shriner, D, Smith, J A, So, W Y, Stančáková, A, Stilp, A M, Strauch, K, Suzuki, K, Takahashi, A, Taylor, K D, Thorand, B, Thorleifsson, G, Thorsteinsdottir, U, Tomlinson, B, Torres, J M, Tsai, F, Tuomilehto, J, Tusie-luna, T, Udler, M S, Valladares-salgado, A, Van Dam, R M, Van Klinken, J B, Varma, R, Vujkovic, M, Wacher-rodarte, N, Wheeler, E, Whitsel, E A, Wickremasinghe, A R, Van Dijk, K W, Witte, D R, Yajnik, C S, Yamamoto, K, Yamauchi, T, Yengo, L, Yoon, K, Yu, C, Yuan, J, Yusuf, S, Zhang, L, Zheng, W, Rüeger, S, Della Briotta Parolo, P, Joo, Y Y, Hayes, M G, Raffel, L J, Igase, M, Ipp, E, Redline, S, Cho, Y S, Lind, L, Province, M A, Hanis, C L, Peyser, P A, Ingelsson, E, Zonderman, A B, Psaty, B M, Wang, Y, Rotimi, C N, Becker, D M, Matsuda, F, Liu, Y, Zeggini, E, Yokota, M, Rich, S S, Kooperberg, C, Pankow, J S, Engert, J C, Chen, Y I, Froguel, P, Wilson, J G, Sheu, W H H, Kardia, S L R, Wu, J, Hayes, M G, Ma, R C W, Wong, T, Groop, L, Mook-kanamori, D O, Chandak, G R, Collins, F S, Bharadwaj, D, Paré, G, Sale, M M, Ahsan, H, Motala, A A, Shu, X, Park, K, Jukema, J W, Cruz, M, Mckean-cowdin, R, Grallert, H, Cheng, C, Bottinger, E P, Dehghan, A, Tai, E, Dupuis, J, Kato, N, Laakso, M, Köttgen, A, Koh, W, Palmer, C N A, Liu, S, Abecasis, G, Kooner, J S, Loos, R J F, North, K E, Haiman, C A, Florez, J C, Saleheen, D, Hansen, T, Pedersen, O, Mägi, R, Langenberg, C, Wareham, N J, Maeda, S, Kadowaki, T, Lee, J, Millwood, I Y, Walters, R G, Stefansson, K, Myers, S R, Ferrer, J, Gaulton, K J, Meigs, J B, Mohlke, K L, Gloyn, A L, Bowden, D W, Below, J E, Chambers, J C, Sim, X, Boehnke, M, Rotter, J I, Mccarthy, M I & Morris, A P 2022, 'Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation', Nature Genetics, vol. 54, no. 5, pp. 560-572. https://doi.org/10.1038/s41588-022-01058-3
Nature Genetics, vol 54, iss 5
Mahajan, A, Spracklen, C N, Zhang, W, Ng, M C Y, Petty, L E, Kitajima, H, Yu, G Z, Rüeger, S, Speidel, L, Kim, Y J, Horikoshi, M, Mercader, J M, Taliun, D, Moon, S, Kwak, S H, Robertson, N R, Rayner, N W, Loh, M, Kim, B J, Chiou, J, Miguel-Escalada, I, della Briotta Parolo, P, Lin, K, Bragg, F, Preuss, M H, Takeuchi, F, Nano, J, Guo, X, Lamri, A, Nakatochi, M, Scott, R A, Lee, J J, Huerta-Chagoya, A, Graff, M, Chai, J F, Parra, E J, Yao, J, Bielak, L F, Tabara, Y, Grarup, N, Chen, W M, Jensen, R A, Chen, J, Huang, W, Jørgensen, M E, Jørgensen, T, Witte, D R, Zhang, L, Hansen, T, Pedersen, O, FinnGen & eMERGE Consortium 2022, 'Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation', Nature Genetics, vol. 54, no. 5, pp. 560-572. https://doi.org/10.1038/s41588-022-01058-3

Predmety: 0301 basic medicine, name=Genetics, Hasso-Plattner-Institut für Digital Engineering gGmbH, eMERGE Consortium, Medical and Health Sciences, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Risk Factors, Genetics, Diabetes Mellitus, Ethnicity, Humans, Genetic Predisposition to Disease, Polymorphism, Type 2/epidemiology, Metabolic and endocrine, ddc:610, 0303 health sciences, Diabetes, Human Genome, Single Nucleotide, Biological Sciences, Polymorphism, Single Nucleotide/genetics, R1, 3. Good health, FinnGen, [SDV] Life Sciences [q-bio], Diabetes Mellitus, Type 2/epidemiology, Diabetes Mellitus, Type 2, Single Nucleotide/genetics, Type 2, Developmental Biology, Genome-Wide Association Study

Popis súboru: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/35551307
https://eprints.gla.ac.uk/271636/1/271636.pdf
https://hdl.handle.net/1887/3479795
https://pure.amsterdamumc.nl/en/publications/9f15452f-a5dd-480c-babc-ac5f9b81c476
https://doi.org/10.1038/s41588-022-01058-3
https://pergamos.lib.uoa.gr/uoa/dl/object/3346931
https://curis.ku.dk/ws/files/362320626/Multi_ancestry_genetic_study_of_type_2_diabetes_highlights_the_power_of_diverse_populations_for_discovery_and_translation.pdf
https://hdl.handle.net/20.500.11820/9676888f-1f60-44ff-8c62-09196c2c8dee
https://www.pure.ed.ac.uk/ws/files/266903807/Multi_ancestry_genetic_study_of_type_2_diabetes_highlights_the_power_of_diverse_populations_for_discovery_and_translation.pdf
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=65002
https://discovery-pp.ucl.ac.uk/id/eprint/10155438/
https://escholarship.org/uc/item/59z0821f
https://pure.au.dk/portal/en/publications/04d034b2-c833-41e4-8665-f9fb146b8f52
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Autori: Sterenborg, R.B.T.M. Steinbrenner, I. Li, Yong a ďalší

Prístupová URL adresa: https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/304858

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

Autori: Ramdas, S. Judd, J. Graham, S. E. a ďalší

Zdroj: American Journal of Human Genetics. 109(8):1366-1387

Predmety: Genetics and Genomics, Genetik och genomik, integrative analysis, wide association, 3d genome, variants, cholesterol, annotation, obesity, common, loci, expression, Genetics & Heredity

Prístupová URL adresa: https://gup.ub.gu.se/publication/318991

Genome-Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125 393 Participants.

Autori: Young, WJ van der Most, PJ Bartz, TM a ďalší

Predmety: ECG intervals, calcium, gene‐lifestyle interaction, genome‐wide association study, ventricular repolarization, Humans, Action Potentials, Arrhythmias, Cardiac, Electrocardiography, Genetic Predisposition to Disease, Genome-Wide Association Study, Heart Rate, Polymorphism, Single Nucleotide, Risk Factors, Time Factors

Popis súboru: e034760 - ?

Relation: J Am Heart Assoc; https://qmro.qmul.ac.uk/xmlui/handle/123456789/99885

Dostupnosť: https://qmro.qmul.ac.uk/xmlui/handle/123456789/99885
https://doi.org/10.1161/JAHA.123.034760

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications.

Autori: Sterenborg, RBTM Steinbrenner, I Li, Y a ďalší

Predmety: Humans, Thyroid Gland, Thyroxine, Genome-Wide Association Study, Triiodothyronine, Thyrotropin

Popis súboru: 888 - ?

Relation: Nat Commun; https://qmro.qmul.ac.uk/xmlui/handle/123456789/95973

Dostupnosť: https://qmro.qmul.ac.uk/xmlui/handle/123456789/95973
https://doi.org/10.1038/s41467-024-44701-9

Association of mitochondrial DNA copy number with metabolic syndrome and type 2 diabetes in 14 176 individuals

Autori: Fazzini, F. Lamina, C. Raftopoulou, A. a ďalší

Zdroj: J Intern Med

Predmety: Male, Metabolic Syndrome, 0301 basic medicine, ddc:610, 0303 health sciences, DNA Copy Number Variations, chronic kidney disease, diabetes, metabolic syndrome, mitochondrial DNA copy number, 610 Medizin, Original Articles, Middle Aged, DNA, Mitochondrial, Body Mass Index, 3. Good health, 03 medical and health sciences, Cross-Sectional Studies, Diabetes Mellitus, Type 2, Humans, Female, Prospective Studies, Waist Circumference, Triglycerides, Aged

Popis súboru: application/pdf

Prístupová URL adresa: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/joim.13242
https://pubmed.ncbi.nlm.nih.gov/33453124
https://www.ncbi.nlm.nih.gov/pubmed/33453124
https://pubmed.ncbi.nlm.nih.gov/33453124/
https://onlinelibrary.wiley.com/doi/10.1111/joim.13242
https://epub.uni-regensburg.de/45894/

Antithrombin, protein C, and protein S: genome and transcriptome-wide association studies identify 7 novel loci regulating plasma levels

Autori: Ji, Y.K. Temprano-Sagrera, G. Holle, L.A. a ďalší

Predmety: antithrombin, genome-wide association study, genotype, anticoagulant, hemostasis, protein C, protein S

Popis súboru: application/pdf

Prístupová URL adresa: https://hdl.handle.net/1887/3722085

The power of genetic diversity in genome-wide association studies of lipids (vol 600, pg 675, 2021)

Autori: Graham, SE Clarke, SL Wu, K-HH a ďalší

Popis súboru: application/pdf

Prístupová URL adresa: https://hdl.handle.net/1887/3720827

A catalog of genetic loci associated with kidney function from analyses of a million individuals

Autori: Wuttke M Li Y Li M a ďalší

Prispievatelia: Wuttke M Li Y Li M a ďalší

Zdroj: Nature genetics
51 (2019): 957–972. doi:10.1038/s41588-019-0407-x
info:cnr-pdr/source/autori:Wuttke, Matthias; Li, Yong; Li, Man; Sieber, Karsten B.; Feitosa, Mary F.; Gorski, Mathias; Tin, Adrienne; Wang, Lihua; Chu, Audrey Y.; Hoppmann, Anselm; Kirsten, Holger; Giri, Ayush; Chai, Jin-Fang; Sveinbjornsson, Gardar; Tayo, Bamidele O.; Nutile, Teresa; Fuchsberger, Christian; Marten, Jonathan; Cocca, Massimiliano; Ghasemi, Sahar; Xu, Yizhe; Horn, Katrin; Noce, Damia; Van der Most, Peter J.; Sedaghat, Sanaz; Yu, Zhi; Akiyama, Masato; Afaq, Saima; Ahluwalia, Tarunveer S.; Almgren, Peter; Amin, Najaf; Arnlov, Johan; Bakker, Stephan J. L.; Bansal, Nisha; Baptista, Daniela; Bergmann, Sven; Biggs, Mary L.; Biino, Ginevra; Boehnke, Michael; Boerwinkle, Eric; Boissel, Mathilde; Bottinger, Erwin P.; Boutin, Thibaud S.; Brenner, Hermann; Brumat, Marco; Burkhardt, Ralph; Butterworth, Adam S.; Campana, Eric; Campbell, Archie; Campbell, Harry; Canouil, Mickael; Carroll, Robert J.; Catamo, Eulalia; Chambers, John C.; Chee, Miao-Ling; Chee, Miao-Li; Chen, Xu; Cheng, Ching-Yu; Cheng, Yurong; Christensen, Kaare; Cifkova, Renata; Ciullo, Marina; Concas, Maria Pina; Cook, James P.; Coresh, Josef; Corre, Tanguy; Sala, Cinzia Felicita; Cusi, Daniele; Danesh, John; Daw, E. Warwick; De Borst, Martin H.; De Grandi, Alessandro; De Mutsert, Renee; De Vries, Aiko P. J.; Degenhardt, Frauke; Delgado, Graciela; Demirkan, Ayse; Di Angelantonio, Emanuele; Dittrich, Katalin; Divers, Jasmin; Dorajoo, Rajkumar; Eckardt, Kai-Uwe; Ehret, Georg; Elliott, Paul; Endlich, Karlhans; Evans, Michele K.; Felix, Janine F.; Foo, Valencia Hui Xian; Franco, Oscar H.; Franke, Andre; Freedman, Barry I.; Freitag-Wolf, Sandra; Friedlander, Yechiel; Froguel, Philippe; Gansevoort, Ron T.; Gao, He; Gasparini, Paolo; Gaziano, J. Michael; Giedraitis, Vilmantas; Gieger, Christian; Girotto, Giorgia; Giulianini, Franco; Gogele, Martin; Gordon, Scott D.; Gudbjartsson, Daniel F.; Gudnason, Vilmundur; Haller, Toomas; Hamet, Pavel; Harris, Tamara B.; Hartman, Catharina A.; Hayward, Caroline; Hellwege, Jacklyn N.; Heng, Chew-Kiat; Hicks, Andrew A.; Hofer, Edith; Huang, Wei; Hutri-Kahonen, Nina; Hwang, Shih-Jen; Ikram, M. Arfan; Indridason, Olafur S.; Ingelsson, Erik; Ising, Marcus; Jaddoe, Vincent W. V.; Jakobsdottir, Johanna; Jonas, Jost B.; Joshi, Peter K.; Josyula, Navya Shilpa; Jung, Bettina; Kahonen, Mika; Kamatani, Yoichiro; Kammerer, Candace M.; Kanai, Masahiro; Kastarinen, Mika; Kerr, Shona M.; Khor, Chiea-Chuen; Kiess, Wieland; Kleber, Marcus E.; Koenig, Wolfgang; Kooner, Jaspal S.; Korner, Antje; Kovacs, Peter; Kraja, Aldi T.; Krajcoviechova, Alena; Kramer, Holly; Kramer, Bernhard K.; Kronenberg, Florian; Kubo, Michiaki; Kuhnel, Brigitte; Kuokkanen, Mikko; Kuusisto, Johanna; La Bianca, Martina; Laakso, Markku; Lange, Leslie A.; Langefeld, Carl D.; Lee, Jeannette Jen-Mai; Lehne, Benjamin; Lehtimaki, Terho; Lieb, Wolfgang; Lim, Su-Chi; Lind, Lars; Lindgren, Cecilia M.; Liu, Jun; Liu, Jianjun; Loeffler, Markus; Loos, Ruth J. F.; Lucae, Susanne; Lukas, Mary Ann; Lyytikainen, Leo-Pekka; Magi, Reedik; Magnusson, Patrik K. E.; Mahajan, Anubha; Martin, Nicholas G.; Martins, Jade; Marz, Winfried; Mascalzoni, Deborah; Matsuda, Koichi; Meisinger, Christa; Meitinger, Thomas; Melander, Olle; Metspalu, Andres; Mikaelsdottir, Evgenia K.; Milaneschi, Yuri; Miliku, Kozeta; Mishra, Pashupati P.; Program, V. A. Million Veteran; Mohlke, Karen L.; Mononen, Nina; Montgomery, Grant W.; Mook-Kanamori, Dennis O.; Mychaleckyj, Josyf C.; Nadkarni, Girish N.; Nalls, Mike A.; Nauck, Matthias; Nikus, Kjell; Ning, Boting; Nolte, Ilja M.; Noordam, Raymond; O'Connell, Jeffrey; O'Donoghue, Michelle L.; Olafsson, Isleifur; Oldehinkel, Albertine J.; Orho-Melander, Marju; Ouwehand, Willem H.; Padmanabhan, Sandosh; Palmer, Nicholette D.; Palsson, Runolfur; Penninx, Brenda W. J. H.; Perls, Thomas; Perola, Markus; Pirastu, Mario; Pirastu, Nicola; Pistis, Giorgio; Podgornaia, Anna I.; Polasek, Ozren; Ponte, Belen; Porteous, David J.; Poulain, Tanja; Pramstaller, Peter P.; Preuss, Michael H.; Prins, Bram P.; Province, Michael A.; Rabelink, Ton J.; Raffield, Laura M.; Raitakari, Olli T.; Reilly, Dermot F.; Rettig, Rainer; Rheinberger, Myriam; Rice, Kenneth M.; Ridker, Paul M.; Rivadeneira, Fernando; Rizzi, Federica; Roberts, David J.; Robino, Antonietta; Rossing, Peter; Rudan, Igor; Rueedi, Rico; Ruggiero, Daniela; Ryan, Kathleen A.; Saba, Yasaman; Sabanayagam, Charumathi; Salomaa, Veikko; Salvi, Erika; Saum, Kai-Uwe; Schmidt, Helena; Schmidt, Reinhold; Ben Schottker; Schulz, Christina-Alexandra; Schupf, Nicole; Shaffer, Christian M.; Shi, Yuan; Smith, Albert V.; Smith, Blair H.; Soranzo, Nicole; Spracklen, Cassandra N.; Strauch, Konstantin; Stringham, Heather M.; Stumvoll, Michael; Svensson, Per O.; Szymczak, Silke; Tai, E-Shyong; Tajuddin, Salman M.; Tan, Nicholas Y. Q.; Taylor, Kent D.; Teren, Andrej; Tham, Yih-Chung; Thiery, Joachim; Thio, Chris H. L.; Thomsen, Hauke; Thorleifsson, Gudmar; Toniolo, Daniela; Tonjes, Anke; Tremblay, Johanne; Tzoulaki, Ioanna; Uitterlinden, Andre G.; Vaccargiu, Simona; Van Dam, Rob M.; Van der Harst, Pim; Van Duijn, Cornelia M.; Edward, Digna R. Velez; Verweij, Niek; Vogelezang, Suzanne; Volker, Uwe; Vollenweider, Peter; Waeber, Gerard; Waldenberger, Melanie; Wallentin, Lars; Wang, Ya Xing; Wang, Chaolong; Waterworth, Dawn M.; Bin Wei, Wen; White, Harvey; Whitfield, John B.; Wild, Sarah H.; Wilson, James F.; Wojczynski, Mary K.; Wong, Charlene; Wong, Tien-Yin; Xu, Liang; Yang, Qiong; Yasuda, Masayuki; Yerges-Armstrong, Laura M.; Zhang, Weihua; Zonderman, Alan B.; Rotter, Jerome I.; Bochud, Murielle; Psaty, Bruce M.; Vitart, Veronique; Wilson, James G.; Dehghan, Abbas; Parsa, Afshin; Chasman, Daniel I.; Ho, Kevin; Morris, Andrew P.; Devuyst, Olivier; Akilesh, Shreeram; Pendergrass, Sarah A.; Sim, Xueling; Boger, Carsten A.; Okada, Yukinori; Edwards, Todd L.; Snieder, Harold; Stefansson, Kari; Hung, Adriana M.; Heid, Iris M.; Scholz, Markus; Teumer, Alexander; Kottgen, Anna; Pattaro, Cristian/titolo:A catalog of genetic loci associated with kidney function from analyses of a million individuals/doi:10.1038%2Fs41588-019-0407-x/rivista:Nature genetics (Print)/anno:2019/pagina_da:957/pagina_a:972/intervallo_pagine:957–972/volume:51
Wuttke, M, Li, Y, Li, M, Sieber, K B, Feitosa, M F, Gorski, M, Tin, A, Wang, L, Chu, A Y, Hoppmann, A, Kirsten, H, Giri, A, Chai, J-F, Sveinbjornsson, G, Tayo, B O, Nutile, T, Fuchsberger, C, Marten, J, Cocca, M, Ghasemi, S, Xu, Y, Horn, K, Noce, D, van der Most, P J, Sedaghat, S, Yu, Z, Akiyama, M, Afaq, S, Ahluwalia, T S, Almgren, P, Amin, N, Ärnlöv, J, Bakker, S J L, Bansal, N, Baptista, D, Bergmann, S, Biggs, M L, Biino, G, Boehnke, M, Boerwinkle, E, Boissel, M, Bottinger, E P, Boutin, T S, Brenner, H, Brumat, M, Burkhardt, R, Butterworth, A S, Campana, E, Milaneschi, Y, Penninx, B W J H, Köttgen, A, Pattaro, C, Lifelines Cohort Study & V. A. Million Veteran Program 2019, 'A catalog of genetic loci associated with kidney function from analyses of a million individuals', Nature Genetics, vol. 51, no. 6, pp. 957-972. https://doi.org/10.1038/s41588-019-0407-x
Nature Genetics, Vol. 51, No 6 (2019) pp. 957-972
Wuttke, M, Li, Y, Li, M, Sieber, K B, Feitosa, M F, Gorski, M, Tin, A, Wang, L, Chu, A Y, Hoppmann, A, Kirsten, H, Giri, A, Chai, J F, Sveinbjornsson, G, Tayo, B O, Nutile, T, Fuchsberger, C, Marten, J, Cocca, M, Ghasemi, S, Xu, Y, Horn, K, Noce, D, van der Most, P J, Sedaghat, S, Yu, Z, Akiyama, M, Afaq, S, Ahluwalia, T S, Almgren, P, Amin, N, Ärnlöv, J, Bakker, S J L, Bansal, N, Baptista, D, Bergmann, S, Biggs, M L, Biino, G, Boehnke, M, Boerwinkle, E, Boissel, M, Bottinger, E P, Boutin, T S, Brenner, H, Brumat, M, Burkhardt, R, Butterworth, A S, Campana, E, Christensen, K, Lifelines Cohort Study & V. A. Million Veteran Program 2019, ' A catalog of genetic loci associated with kidney function from analyses of a million individuals ', Nature Genetics, vol. 51, no. 6, pp. 957-972 . https://doi.org/10.1038/s41588-019-0407-x
Wuttke, M, Li, Y, Li, M, Sieber, K B, Feitosa, M F, Gorski, M, Tin, A, Wang, L, Chu, A Y, Hoppmann, A, Kirsten, H, Giri, A, Chai, J F, Sveinbjornsson, G, Tayo, B O, Nutile, T, Fuchsberger, C, Marten, J, Cocca, M, Ghasemi, S, Xu, Y, Horn, K, Noce, D, van der Most, P J, Sedaghat, S, Yu, Z, Akiyama, M, Afaq, S, Ahluwalia, T S, Almgren, P, Amin, N, Ärnlöv, J, Bakker, S J L, Bansal, N, Baptista, D, Bergmann, S, Biggs, M L, Biino, G, Boehnke, M, Boerwinkle, E, Boissel, M, Bottinger, E P, Boutin, T, Brenner, H, Brumat, M, Campbell, A, Campbell, H, Hayward, C, Joshi, P K, Kerr, S, Lim, S-C, Lind, L, Lindgren, C M, Liu, J, Liu, J, Loeffler, M, Loos, R J F, Lucae, S, Lukas, M A, Lyytikäinen, L-P, Mägi, R, Magnusson, P K E, Mahajan, A, Martin, N G, Martins, J, März, W, Mascalzoni, D, Matsuda, K, Meisinger, C, Meitinger, T, Melander, O, Metspalu, A, Mikaelsdottir, E K, Milaneschi, Y, Miliku, K, Mishra, P P, Mohlke, K L, Montgomery, G W, Mychaleckyj, J C, Nadkarni, G N, Nalls, M A, Nauck, M, Nikus, K, Ning, B, Nolte, I M, Noordam, R, O’Connell, J R, O'Donoghue, M L, Olafsson, I, Oldehinkel, A J, Orho-Melander, M, Ouwehand, W H, Padmanabhan, S, Palmer, N D, Palsson, R, Penninx, B W J H, Perls, T, Perola, M, Pirastu, M, Pirastu, N, Pistis, G, Podgornaia, A I, Polasek, O, Ponte, B, Porteous, D J, Poulain, T, Pramstaller, P P, Preuss, M H, Prins, B P, Province, M A, Rabelink, T J, Raffield, L M, Raitakari, O T, Reilly, D F, Rettig, R, Rheinberger, M, Rice, K M, Ridker, P M, Rivadeneira, F, Rizzi, F, Roberts, D J, Robino, A, Rossing, P, Rudan, I, Rueedi, R, Ruggiero, D, Ryan, K A, Saba, Y, Sabanayagam, C, Salomaa, V, Salvi, E, Saum, K-U, Schmidt, H, Schmidt, R, Schöttker, B, Schulz, C-A, Schupf, N, Shaffer, C M, Shi, Y, Smith, A V, Smith, B H, Soranzo, N, Spracklen, C N, Strauch, K, Stringham, H M, Stumvoll, M, Svensson, P O, Szymczak, S, Tai, E-S, Tajuddin, S M, Tan, N Y Q, Taylor, K D, Teren, A, Tham, Y-C, Thiery, J, Thio, C H L, Thomsen, H, Thorleifsson, G, Toniolo, D, Tönjes, A, Tremblay, J, Tzoulaki, I, Uitterlinden, A G, Vaccargiu, S, van Dam, R M, van der Harst, P, van Duijn, C M, Velez Edwards, D R, Verweij, N, Vogelezang, S, Völker, U, Vollenweider, P, Waeber, G, Waldenberger, M, Wallentin, L, Wang, Y X, Wang, C, Waterworth, D M, Wei, W B, White, H, Whitfield, J B, Wild, S H, Wilson, J F, Wojczynski, M K, Wong, C, Wong, T-Y, Xu, L, Yang, Q, Yasuda, M, Yerges-Armstrong, L M, Zhang, W, Zonderman, A B, Rotter, J I, Bochud, M, Psaty, B M, Vitart, V, Wilson, J G, Dehghan, A, Parsa, A, Chasman, D I, Ho, K, Morris, A P, Devuyst, O, Akilesh, S, Pendergrass, S A, Sim, X, Böger, C A, Okada, Y, Edwards, T L, Snieder, H, Stefansson, K, Hung, A M, Heid, I M, Scholz, M & Teumer, A & Köttgen, A & Pattaro, C 2019, ' A catalog of genetic loci associated with kidney function from analyses of a million individuals ', Nature Genetics, vol. 51, no. 6, pp. 957-972 . https://doi.org/10.1038/s41588-019-0407-x
LifeLines Cohort Study 2019, 'A catalog of genetic loci associated with kidney function from analyses of a million individuals', Nature Genetics, vol. 51, no. 6, pp. 957-972. https://doi.org/10.1038/s41588-019-0407-x
Lifelines Cohort Study & V. A. Million Veteran Program 2019, ' A catalog of genetic loci associated with kidney function from analyses of a million individuals ', Nature Genetics, vol. 51, no. 6, pp. 957-972 . https://doi.org/10.1038/s41588-019-0407-x
Nature Genetics

Predmety: EMC MM-04-54-08-A, 0301 basic medicine, catalog, ddc:000, Inheritance Patterns, Hasso-Plattner-Institut für Digital Engineering GmbH, Kidney Function Tests, DISEASE, 10052 Institute of Physiology, Uromodulin/urine, Disease, Renal Insufficiency, kidney function, 11 Medical and Health Sciences, ddc:616, Genetics & Heredity, 0303 health sciences, Genome-wide association, HERITABILITY, GENOME-WIDE ASSOCIATION, COMMON VARIANTS, RENAL-FUNCTION, TRANS-EQTLS, METAANALYSIS, TRANSPORTER, CLASSIFICATION, INTEGRATION, Nierenfunktion, Chromosome Mapping, Single Nucleotide, 3. Good health, [SDV] Life Sciences [q-bio], Phenotype, Common variants, Renal function, Trans-EQTLS, Metaanalysis, Heritability, Transporter, Life Sciences & Biomedicine, Glomerular Filtration Rate, Metaanalysi, name=Genetics, European Continental Ancestry Group, Quantitative Trait Loci, 610 Medicine & health, Common variant, Polymorphism, Single Nucleotide, V. A. Million Veteran Program, White People, Chronic/genetics, Quantitative Trait, 03 medical and health sciences, Quantitative Trait, Heritable, 1311 Genetics, Lifelines Cohort Study, Uromodulin, Genetics, Humans, Genetic Predisposition to Disease, Polymorphism, Renal Insufficiency, Chronic, Heritable, Genetic Association Studies, Science & Technology, association, genetic loci, 06 Biological Sciences, ta3121, Renal Insufficiency, Chronic/genetics/physiopathology/urine, Genetic Association Studies/methods, 570 Life sciences, biology, Developmental Biology, Genome-Wide Association Study

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https://www.research.ed.ac.uk/en/publications/a-catalog-of-genetic-loci-associated-with-kidney-function-from-an
https://mdanderson.elsevierpure.com/en/publications/a-catalog-of-genetic-loci-associated-with-kidney-function-from-an
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https://hdl.handle.net/20.500.11820/d9d3a633-5b02-49dc-9b40-4c2cc3adaff9
https://pure.manchester.ac.uk/ws/files/114540768/eGFR_CKDGen_R4_manuscript_REV3_20190304_final.docx
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https://hal.science/hal-04535875v1
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https://www.repository.cam.ac.uk/handle/1810/292676
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Author Correction: The power of genetic diversity in genome-wide association studies of lipids (Nature, (2021), 600, 7890, (675-679), 10.1038/s41586-021-04064-3)

Autori: Graham, S.E. Clarke, S.L. Wu, K.-H.H. Kanoni, S. Zajac, G.J.M. Ramdas, S. Surakka, I. Ntalla, I. Vedantam, S. Winkler, T.W. Locke, A.E. Marouli, E. Hwang, M.Y. Han, S. Narita, A. Choudhury, A. Bentley, A.R. Ekoru, K. Verma, A. Trivedi, B. Martin, H.C. Hunt, K.A. Hui, Q. Klarin, D. Zhu, X. Thorleifsson, G. Helgadottir, A. Gudbjartsson, D.F. Holm, H. Olafsson, I. Akiyama, M. Sakaue, S. Terao, C. Kanai, M. Zhou, W. Brumpton, B.M. Rasheed, H. Ruotsalainen, S.E. Havulinna, A.S. Veturi, Y. Feng, Q.P. Rosenthal, E.A. Lingren, T. Pacheco, J.A. Pendergrass, S.A. Haessler, J. Giulianini, F. Bradford, Y. Miller, J.E. Campbell, A. Lin, K. Millwood, I.Y. Hindy, G. Rasheed, A. Faul, J.D. Zhao, W. Weir, D.R. Turman, C. Huang, H. Graff, M. Mahajan, A. Brown, M.R. Zhang, W. Yu, K. Schmidt, E.M. Pandit, A. Gustafsson, S. Yin, X. Luan, J. Zhao, J.-H. Matsuda, F. Jang, H.-M. Yoon, K. Medina-Gomez, C. Pitsillides, A. Hottenga, J.J. Willemsen, G. Wood, A.R. Ji, Y. Gao, Z. Haworth, S. Mitchell, R.E. Chai, J.F. Aadahl, M. Yao, J. Manichaikul, A. Warren, H.R. Ramirez, J. Bork-Jensen, J. Kårhus, L.L. Goel, A. Sabater-Lleal, M. Noordam, R. Sidore, C. Fiorillo, E. McDaid, A.F. Marques-Vidal, P. Wielscher, M. Trompet, S. Sattar, N. Møllehave, L.T. Thuesen, B.H. Munz, M. Zeng, L. Huang, J. Yang, B. Poveda, A. Kurbasic, A. Lamina, C. Forer, L. Scholz, M. Galesloot, T.E. Bradfield, J.P. Daw, E.W. Zmuda, J.M. Mitchell, J.S. Fuchsberger, C. Christensen, H. Brody, J.A. Feitosa, M.F. Wojczynski, M.K. Preuss, M. Mangino, M. Christofidou, P. Verweij, N. Benjamins, J.W. Engmann, J. Kember, R.L. Slieker, R.C. Lo, K.S. Zilhao, N.R. Le, P. Kleber, M.E. Delgado, G.E. Huo, S. Ikeda, D.D. Iha, H. Yang, J. Liu, J. Leonard, H.L. Marten, J. Schmidt, B. Arendt, M. Smyth, L.J. Cañadas-Garre, M. Wang, C. Nakatochi, M. Wong, A. Hutri-Kähönen, N. Sim, X. Xia, R. Huerta-Chagoya, A. Fernandez-Lopez, J.C. Lyssenko, V. Ahmed, M. Jackson, A.U. Yousri, N.A. Irvin, M.R. Oldmeadow, C. Kim, H.-N. Ryu, S. Timmers, P.R.H.J. Arbeeva, L. Dorajoo, R. Lange, L.A. Chai, X. Prasad, G. Lorés-Motta, L. Pauper, M. Long, J. Li, X. Theusch, E. Takeuchi, F. Spracklen, C.N. Loukola, A. Bollepalli, S. Warner, S.C. Wang, Y.X. Wei, W.B. Nutile, T. Ruggiero, D. Sung, Y.J. Hung, Y.-J. Chen, S. Liu, F. Yang, J. Kentistou, K.A. Gorski, M. Brumat, M. Meidtner, K. Bielak, L.F. Smith, J.A. Hebbar, P. Farmaki, A.-E. Hofer, E. Lin, M. Xue, C. Zhang, J. Concas, M.P. Vaccargiu, S. van der Most, P.J. Pitkänen, N. Cade, B.E. Lee, J. van der Laan, S.W. Chitrala, K.N. Weiss, S. Zimmermann, M.E. Lee, J.Y. Choi, H.S. Nethander, M. Freitag-Wolf, S. Southam, L. Rayner, N.W. Wang, C.A. Lin, S.-Y. Wang, J.-S. Couture, C. Lyytikäinen, L.-P. Nikus, K. Cuellar-Partida, G. Vestergaard, H. Hildalgo, B. Giannakopoulou, O. Cai, Q. Obura, M.O. van Setten, J. Li, X. Schwander, K. Terzikhan, N. Shin, J.H. Jackson, R.D. Reiner, A.P. Martin, L.W. Chen, Z. Li, L. Highland, H.M. Young, K.L. Kawaguchi, T. Thiery, J. Bis, J.C. Nadkarni, G.N. Launer, L.J. Li, H. Nalls, M.A. Raitakari, O.T. Ichihara, S. Wild, S.H. Nelson, C.P. Campbell, H. Jäger, S. Nabika, T. Al-Mulla, F. Niinikoski, H. Braund, P.S. Kolcic, I. Kovacs, P. Giardoglou, T. Katsuya, T. Bhatti, K.F. de Kleijn, D. de Borst, G.J. Kim, E.K. Adams, H.H.H. Ikram, M.A. Zhu, X. Asselbergs, F.W. Kraaijeveld, A.O. Beulens, J.W.J. Shu, X.-O. Rallidis, L.S. Pedersen, O. Hansen, T. Mitchell, P. Hewitt, A.W. Kähönen, M. Pérusse, L. Bouchard, C. Tönjes, A. Chen, Y.-D.I. Pennell, C.E. Mori, T.A. Lieb, W. Franke, A. Ohlsson, C. Mellström, D. Cho, Y.S. Lee, H. Yuan, J.-M. Koh, W.-P. Rhee, S.Y. Woo, J.-T. Heid, I.M. Stark, K.J. Völzke, H. Homuth, G. Evans, M.K. Zonderman, A.B. Polasek, O. Pasterkamp, G. Hoefer, I.E. Redline, S. Pahkala, K. Oldehinkel, A.J. Snieder, H. Biino, G. Schmidt, R. Schmidt, H. Chen, Y.E. Bandinelli, S. Dedoussis, G. Thanaraj, T.A. Kardia, S.L.R. Kato, N. Schulze, M.B. Girotto, G. Jung, B. Böger, C.A. Joshi, P.K. Bennett, D.A. De Jager, P.L. Lu, X. Mamakou, V. Brown, M. Caulfield, M.J. Munroe, P.B. Guo, X. Ciullo, M. Jonas, J.B. Samani, N.J. Kaprio, J. Pajukanta, P. Adair, L.S. Bechayda, S.A. de Silva, H.J. Wickremasinghe, A.R. Krauss, R.M. Wu, J.-Y. Zheng, W. den Hollander, A.I. Bharadwaj, D. Correa, A. Wilson, J.G. Lind, L. Heng, C.-K. Nelson, A.E. Golightly, Y.M. Wilson, J.F. Penninx, B. Kim, H.-L. Attia, J. Scott, R.J. Rao, D.C. Arnett, D.K. Hunt, S.C. Walker, M. Koistinen, H.A. Chandak, G.R. Yajnik, C.S. Mercader, J.M. Tusié-Luna, T. Aguilar-Salinas, C.A. Villalpando, C.G. Orozco, L. Fornage, M. Tai, E.S. van Dam, R.M. Lehtimäki, T. Chaturvedi, N. Yokota, M. Liu, J. Reilly, D.F. McKnight, A.J. Kee, F. Jöckel, K.-H. McCarthy, M.I. Palmer, C.N.A. Vitart, V. Hayward, C. Simonsick, E. van Duijn, C.M. Lu, F. Qu, J. Hishigaki, H. Lin, X. März, W. Parra, E.J. Cruz, M. Gudnason, V. Tardif, J.-C. Lettre, G. ’t Hart, L.M. Elders, P.J.M. Damrauer, S.M. Kumari, M. Kivimaki, M. van der Harst, P. Spector, T.D. Loos, R.J.F. Province, M.A. Psaty, B.M. Brandslund, I. Pramstaller, P.P. Christensen, K. Ripatti, S. Widén, E. Hakonarson, H. Grant, S.F.A. Kiemeney, L.A.L.M. de Graaf, J. Loeffler, M. Kronenberg, F. Gu, D. Erdmann, J. Schunkert, H. Franks, P.W. Linneberg, A. Jukema, J.W. Khera, A.V. Männikkö, M. Jarvelin, M.-R. Kutalik, Z. Cucca, F. Mook-Kanamori, D.O. van Dijk, K.W. Watkins, H. Strachan, D.P. Grarup, N. Sever, P. Poulter, N. Rotter, J.I. Dantoft, T.M. Karpe, F. Neville, M.J. Timpson, N.J. Cheng, C.-Y. Wong, T.-Y. Khor, C.C. Sabanayagam, C. Peters, A. Gieger, C. Hattersley, A.T. Pedersen, N.L. Magnusson, P.K.E. Boomsma, D.I. de Geus, E.J.C. Cupples, L.A. van Meurs, J.B.J. Ghanbari, M. Gordon-Larsen, P. Huang, W. Kim, Y.J. Tabara, Y. Wareham, N.J. Langenberg, C. Zeggini, E. Kuusisto, J. Laakso, M. Ingelsson, E. Abecasis, G. Chambers, J.C. Kooner, J.S. de Vries, P.S. Morrison, A.C. North, K.E. Daviglus, M. Kraft, P. Martin, N.G. Whitfield, J.B. Abbas, S. Saleheen, D. Walters, R.G. Holmes, M.V. Black, C. Smith, B.H. Justice, A.E. Baras, A. Buring, J.E. Ridker, P.M. Chasman, D.I. Kooperberg, C. Wei, W.-Q. Jarvik, G.P. Namjou, B. Hayes, M.G. Ritchie, M.D. Jousilahti, P. Salomaa, V. Hveem, K. Åsvold, B.O. Kubo, M. Kamatani, Y. Okada, Y. Murakami, Y. Thorsteinsdottir, U. Stefansson, K. Ho, Y.-L. Lynch, J.A. Rader, D.J. Tsao, P.S. Chang, K.-M. Cho, K. O’Donnell, C.J. Gaziano, J.M. Wilson, P. Rotimi, C.N. Hazelhurst, S. Ramsay, M. Trembath, R.C. van Heel, D.A. Tamiya, G. Yamamoto, M. Kim, B.-J. Mohlke, K.L. Frayling, T.M. Hirschhorn, J.N. Kathiresan, S. Boehnke, M. Natarajan, P. Peloso, G.M. Brown, C.D. Morris, A.P. Assimes, T.L. Deloukas, P. Sun, Y.V. Willer, C.J. VA Million Veteran Program Global Lipids Genetics Consortium

Predmety: 3. Good health

Prístupová URL adresa: https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3342972

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease

Autori: Young, W. J. Haessler, J. Benjamins, J. W. a ďalší

Popis súboru: application/pdf

Relation: info:eu-repo/grantAgreement/EC/H2020/786833/EU/GENetics and the Electrocardiogram for predicting Scd rISk/GENESIS; This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 786833-GENESIS; info:eu-repo/grantAgreement/EC/H2020/860974/EU/Personalized Therapies for Atrial Fibrillation. A Translational Approach/PersonalizeAF; This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 860974-PersonalizeAF; info:eu-repo/grantAgreement/EC/H2020/965286/EU/Machine Learning Artificial Intelligence Early Detection Stroke Atrial Fibrillation/MAESTRIA; This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No H2020 965286-MAESTRIA; http://zaguan.unizar.es/record/125982

Dostupnosť: http://zaguan.unizar.es/record/125982
https://doi.org/10.1038/s41467-023-36997-w

Genetic determinants of complement activation in the general population.

Autori: Noce, D Foco, L Orth-Höller, D a ďalší

Predmety: C7, CHRIS study, CP: Genomics, CP: Immunology, Cooperative Health Research in South Tyrol study, MBL2, Mendelian randomization, alternative pathway, classical pathway, complement system, genome-wide association study, lectin pathway, Humans, Complement Activation, Complement System Proteins, Lectins, Haplotypes, Mannose-Binding Lectin

Popis súboru: 113611 - ?

Relation: Cell Rep; https://qmro.qmul.ac.uk/xmlui/handle/123456789/103681

Dostupnosť: https://qmro.qmul.ac.uk/xmlui/handle/123456789/103681
https://doi.org/10.1016/j.celrep.2023.113611

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Autori: Young W. J. Lahrouchi N. Isaacs A. a ďalší

Prispievatelia: Young W. J. Lahrouchi N. Isaacs A. a ďalší

Predmety: Death, Sudden, Cardiac, Genetic Testing, Human, Male, Arrhythmias, Electrocardiography

Relation: info:eu-repo/semantics/altIdentifier/pmid/36050321; info:eu-repo/semantics/altIdentifier/wos/WOS:000848744900005; volume:13; issue:1; firstpage:5144; journal:NATURE COMMUNICATIONS; https://hdl.handle.net/11577/3455564

Dostupnosť: https://hdl.handle.net/11577/3455564
https://doi.org/10.1038/s41467-022-32821-z

Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.

Autori: Teumer, A. Tin, A. Sorice, R. a ďalší

Prispievatelia: Teumer, A. Tin, A. Sorice, R. a ďalší

Popis súboru: application/pdf

Relation: Diabetes; https://iris.unil.ch/handle/iris/274797; serval:BIB_F3223C4A8D96; 000370961000032

Dostupnosť: https://iris.unil.ch/handle/iris/274797
https://doi.org/10.2337/db15-1313