Search Results - "Multifactorial Inheritance/genetics"
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1
Authors: et al.
Contributors: et al.
Source: 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-zSubject Terms: 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
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Access URL: 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 -
2
Authors: et al.
Contributors: et al.
Source: Nat Genet
Nature genetics, vol. 57, no. 7, pp. 1620-1627Subject Terms: Cardiovascular outcomes, Biomedicine, Propensity score, Genetics, developmental biology, physiology, Humans, Multifactorial Inheritance/genetics, Randomized Controlled Trials as Topic/methods, Mendelian Randomization Analysis/methods, Research Design, Computer Simulation, Empagliflozin, Warfarin, Mortality, Article, Causal inference
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Authors: et al.
Contributors: et al.
Source: The Biobank Japan Project, Regeneron Genetics Center & DBDS Genomic Consortium 2025, 'Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases', Nature Genetics, vol. 57, no. 3, 11303, pp. 539-547. https://doi.org/10.1038/s41588-024-02072-3
Subject Terms: Male, Multifactorial Inheritance, Chromatin/genetics, Myocytes, Cardiac/metabolism, Polymorphism, Single Nucleotide, Chromatin, Risk Factors, Atrial Fibrillation, Journal Article, Atrial Fibrillation/genetics, Humans, Genetic Predisposition to Disease, Myocytes, Cardiac, Female, Multifactorial Inheritance/genetics, Meta-Analysis, Genome-Wide Association Study
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Access URL: https://pubmed.ncbi.nlm.nih.gov/40050429
https://pure.eur.nl/en/publications/237b7043-3634-44ac-9b90-75088f7db236
https://doi.org/10.1038/s41588-024-02072-3
https://research.rug.nl/en/publications/53d9b249-f19d-4049-bd7a-bb75a8906c5c
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https://doi.org/10.1038/s41588-024-02072-3
https://cris.maastrichtuniversity.nl/en/publications/46250563-cacb-4c39-8fda-522c20ad2948
https://doi.org/10.1038/s41588-024-02072-3
https://dspace.library.uu.nl/handle/1874/461036
https://pure.amsterdamumc.nl/en/publications/a48166d2-0768-4e4f-a706-b41e5cefaded
https://doi.org/10.1038/s41588-024-02072-3
https://hdl.handle.net/2108/417467
https://doi.org/10.1038/s41588-024-02072-3
https://pure.au.dk/portal/en/publications/bec4a97c-1b69-4103-95c8-405c1de3c10f
http://www.scopus.com/inward/record.url?scp=105001208957&partnerID=8YFLogxK
https://doi.org/10.1038/s41588-024-02072-3 -
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Authors: et al.
Source: Nature
Stæger, F F, Andersen, M K, Li, Z, Hjerresen, J P, He, S, Santander, C G, Jensen, R T, Rex, K F, Thuesen, A C B, Hanghøj, K, Seiding, I H, Jørsboe, E, Stinson, S E, Rasmussen, M S, Balboa, R F, Larsen, C V L, Bjerregaard, P, Schubert, M, Meisner, J, Linneberg, A, Grarup, N, Zeggini, E, Nielsen, R, Jørgensen, M E, Hansen, T, Moltke, I & Albrechtsen, A 2025, 'Genetic architecture in Greenland is shaped by demography, structure and selection', Nature, vol. 639, no. 8054, 6668, pp. 404-410. https://doi.org/10.1038/s41586-024-08516-4
Stæger, F F, Andersen, M K, Li, Z, Hjerresen, J P, He, S, Santander, C G, Jensen, R T, Rex, K F, Thuesen, A C B, Hanghøj, K, Seiding, I H, Jørsboe, E, Stinson, S E, Rasmussen, M S, Balboa, R F, Larsen, C V L, Bjerregaard, P, Schubert, M, Meisner, J, Linneberg, A, Grarup, N, Zeggini, E, Nielsen, R, Jørgensen, M E, Hansen, T, Moltke, I & Albrechtsen, A 2025, ' Genetic architecture in Greenland is shaped by demography, structure and selection ', Nature, vol. 639, no. 8054, pp. 404–410 . https://doi.org/10.1038/s41586-024-08516-4
Nature, vol 639, iss 8054Subject Terms: Male, Multifactorial Inheritance, General Science & Technology, Population, Greenland, White, Inuit/genetics, Europe/ethnology, Article, White People, Genetic, Health Sciences, Genetics, Humans, Genetic Testing, Selection, Genetic, Selection, Multifactorial Inheritance/genetics, Demography, Genome, Human/genetics, Genome, Human, Arctic Regions, Human Genome, Genetic Drift, Biological Sciences, Health Disparities, Europe, Genetics, Population, Phenotype, Inuit, Genome, Human/genetics, Female, Generic health relevance, Human, White People/genetics, Genome-Wide Association Study
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Access URL: https://pubmed.ncbi.nlm.nih.gov/39939757
https://vbn.aau.dk/da/publications/8e5db065-84da-4b88-b22a-cf9c490fe6b9
https://vbn.aau.dk/ws/files/772565726/St_ger_et_al._2025_._Genetic_architecture_in_Greenland_is_shaped_by_demography_structure_and_selection.pdf
https://doi.org/10.1038/s41586-024-08516-4
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https://ora.ox.ac.uk/objects/uuid:732a2cfa-00c1-485d-ad9c-3514a7f1a920
https://doi.org/10.1038/s41586-024-08516-4
https://curis.ku.dk/ws/files/431871695/s41586_024_08516_4.pdf
https://portal.findresearcher.sdu.dk/da/publications/86f7e323-ba90-498d-97b1-9d08838cdf98
https://doi.org/10.1038/s41586-024-08516-4
https://escholarship.org/uc/item/4x0163gq
https://escholarship.org/content/qt4x0163gq/qt4x0163gq.pdf -
5
Authors: et al.
Source: Mol Psychiatry
Molecular psychiatry 29, 3151-3159 (2024). doi:10.1038/s41380-024-02577-7
Molecular PsychiatrySubject Terms: Male, Adult, 0301 basic medicine, Multifactorial Inheritance, Female [MeSH], Multifactorial Inheritance/genetics [MeSH], 59/57, Adult [MeSH], Humans [MeSH], Nerve Net/physiopathology [MeSH], Depressive Disorder, Major/metabolism [MeSH], Depressive Disorder, Major/genetics [MeSH], Middle Aged [MeSH], Processing Speed [MeSH], 692/699/476/1414, Article, Brain/physiopathology [MeSH], Depressive Disorder, Major/physiopathology [MeSH], Male [MeSH], Nerve Net/metabolism [MeSH], Nerve Net/diagnostic imaging [MeSH], Brain/metabolism [MeSH], Magnetic Resonance Imaging/methods [MeSH], Tumor Necrosis Factor-alpha/metabolism [MeSH], 631/378, article, Neuropsychological Tests [MeSH], Neuropsychological Tests, Magnetic Resonance Imaging/methods, Nerve Net/metabolism, 03 medical and health sciences, 0302 clinical medicine, Brain/metabolism, Humans, Multifactorial Inheritance/genetics, Processing Speed, Tumor Necrosis Factor-alpha/metabolism, Depressive Disorder, Depressive Disorder, Major, Tumor Necrosis Factor-alpha, Brain, Major/genetics, Middle Aged, Magnetic Resonance Imaging, Female, Nerve Net
Access URL: https://pubmed.ncbi.nlm.nih.gov/38693319
https://research.vu.nl/en/publications/3ca947ed-9539-4dfc-bc88-7e6616c75d05
https://doi.org/10.1038/s41380-024-02577-7
https://hdl.handle.net/1871.1/3ca947ed-9539-4dfc-bc88-7e6616c75d05
https://juser.fz-juelich.de/record/1026976
https://repository.publisso.de/resource/frl:6521043 -
6
Authors: et al.
Contributors: et al.
Source: medRxiv
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Nature genetics 56(11), 2333-2344 (2024). doi:10.1038/s41588-024-01951-z
Nature Genetics, 56, 11, pp. 2333-2344
Nature Genetics, vol 56, iss 11Subject Terms: Male, Organ Size/genetics, Multifactorial Inheritance, Biological Psychology, 270 Language and Computation in Neural Systems, Human Genetics - Radboud University Medical Center - DCMN, genetics [Attention Deficit Disorder with Hyperactivity], Medical and Health Sciences, Psychiatry - Radboud University Medical Center - DCMN, pathology [Brain], genetics [Parkinson Disease], Psychology, 2.1 Biological and endogenous factors, Parkinson Disease/genetics, genetics [Multifactorial Inheritance], methods [Genomics], 220 Statistical Imaging Neuroscience, Cognitive Neuroscience - Radboud University Medical Center - DCMN, Brain, Parkinson Disease, Pharmacology and Pharmaceutical Sciences, Single Nucleotide, Organ Size, Genomics, Biological Sciences, Middle Aged, Mental Illness, Bioinformatics and computational biology, Mental Health, Neurological, Mental health, Female, [SHS] Humanities and Social Sciences, Attention Deficit Disorder with Hyperactivity/genetics, White People/genetics, Biotechnology, Adult, Agricultural biotechnology, genetics [White People], Polymorphism, Single Nucleotide, 150 000 MR Techniques in Brain Function, Article, White People, ddc:570, Journal Article, Genetics, Humans, Brain/pathology, Genetic Predisposition to Disease, Polymorphism, Multifactorial Inheritance/genetics, Biomedical and Clinical Sciences, genetics [Organ Size], Human Genome, Neurosciences, pathology [Attention Deficit Disorder with Hyperactivity], Genomics/methods, Brain Disorders, pathology [Parkinson Disease], Good Health and Well Being, [SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie, Attention Deficit Disorder with Hyperactivity, name=Bristol Population Health Science Institute, Developmental Biology, Genome-Wide Association Study
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Access URL: https://pubmed.ncbi.nlm.nih.gov/39433889
https://pubmed.ncbi.nlm.nih.gov/39371125
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https://doi.org/10.1038/s41588-024-01951-z
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https://juser.fz-juelich.de/record/1032350
https://hdl.handle.net/11391/1589699
https://doi.org/10.1038/s41588-024-01951-z
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https://doi.org/10.1038/s41588-024-01951-z
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https://escholarship.org/uc/item/9bp1077g -
7
Authors: et al.
Source: Mol Psychiatry
Molecular psychiatry 30(2), 497-505 (2025). doi:10.1038/s41380-024-02688-1Subject Terms: Male, Adult, 0301 basic medicine, 0303 health sciences, Resilience, Psychological, Middle Aged, methods [Genome-Wide Association Study], Article, ddc, 3. Good health, Female [MeSH], Multifactorial Inheritance/genetics [MeSH], 631/208, Personality/genetics [MeSH], Resilience, Psychological [MeSH], Adult [MeSH], Humans [MeSH], Mental Health [MeSH], Middle Aged [MeSH], 692/699/476, Polymorphism, Single Nucleotide/genetics [MeSH], Cohort Studies [MeSH], 631/477, Genome-Wide Association Study/methods [MeSH], Male [MeSH], 45/43, Germany [MeSH], article, Cohort Studies, 03 medical and health sciences, Mental Health, Germany, genetics [Polymorphism, Single Nucleotide], Humans, genetics [Personality], Female, ddc:610, genetics [Multifactorial Inheritance]
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/39112778
https://cris.maastrichtuniversity.nl/en/publications/6705496c-b5a2-468c-a0ae-f49f18427510
https://doi.org/10.1038/s41380-024-02688-1
https://pub.dzne.de/record/276147
https://repository.publisso.de/resource/frl:6503734
https://mediatum.ub.tum.de/doc/1769787/document.pdf -
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Authors: et al.
Source: Nature Genetics. 56:838-845
Subject Terms: 0301 basic medicine, Multifactorial Inheritance, 0303 health sciences, Quantitative Trait Loci, Chromosome Mapping, Single Nucleotide, Polymorphism, Single Nucleotide, Autoimmune Diseases, 3. Good health, 03 medical and health sciences, Case-Control Studies, Autoimmune Diseases/genetics, Humans, Genetic Predisposition to Disease, Polymorphism, Multifactorial Inheritance/genetics, Alleles, Genome-Wide Association Study
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Access URL: https://pubmed.ncbi.nlm.nih.gov/38741015
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9
Authors: et al.
Contributors: et al.
Source: Nat Genet
Nature genetics, vol. 56, no. 5, pp. 778-791
Keaton, J M, Kamali, Z, Xie, T, Vaez, A, Williams, A, Goleva, S B, Ani, A, Evangelou, E, Hellwege, J N, Yengo, L, Young, W J, Traylor, M, Giri, A, Zheng, Z, Zeng, J, Chasman, D I, Morris, A P, Caulfield, M J, Hwang, S J, Kooner, J S, Conen, D, Attia, J R, Morrison, A C, Loos, R J F, Kristiansson, K, Schmidt, R, Hicks, A A, Pramstaller, P P, Nelson, C P, Samani, N J, Risch, L, Gyllensten, U, Melander, O, Riese, H, Wilson, J F, Campbell, H, Rich, S S, Psaty, B M, Lu, Y, Rotter, J I, Guo, X, Rice, K M, Vollenweider, P, Sundström, J, Langenberg, C, Tobin, M D, Giedraitis, V, Luan, J, Tuomilehto, J, Sun, Y V, Million Veteran Program, LifeLines Cohort Study, CHARGE Consortium & ICBP Consortium 2024, ' Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits ', Nature Genetics, vol. 56, no. 5, pp. 778-791 . https://doi.org/10.1038/s41588-024-01714-w
Nature Genetics, vol 56, iss 5Subject Terms: genomic studies, Male, Multifactorial Inheritance, Medical Sciences, hypertension, Bioinformatics, name=Genetics, CHARGE consortium, Blood Pressure, Humans, Genome-Wide Association Study, Multifactorial Inheritance/genetics, Blood Pressure/genetics, White People/genetics, Polymorphism, Single Nucleotide, Hypertension/genetics, Genetic Predisposition to Disease, Risk Factors, Female, Genetic Risk Score, White People, Article, Biomedical Informatics, Medical Genetics and Genomics, Lifelines Cohort Study, Genetics, Medical Specialties, Medicine and Health Sciences, Polymorphism, 10. No inequality, metagenomics, Polygenic Risk Score, Genome-wide Association study, Million Veteran Program, Life Sciences, Genetics and Genomics, Blood pressure, Single Nucleotide, predictive models, Medicinsk genetik och genomik, 3. Good health, Oncology, Hypertension, ICBP Consortium, Hypertension, Metagenomics, Medical Genetics
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Access URL: https://pubmed.ncbi.nlm.nih.gov/38689001
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https://hdl.handle.net/11368/3079899
https://hdl.handle.net/20.500.14243/515188
https://doi.org/10.1038/s41588-024-01714-w
https://hdl.handle.net/11388/346609
https://doi.org/10.1038/s41588-024-01714-w
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http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-546354 -
10
Authors: et al.
Source: Nat Genet
Ghouse, J, Sveinbjörnsson, G, Vujkovic, M, Seidelin, A-S, Gellert-Kristensen, H, Ahlberg, G, Tragante, V, Rand, S A, Brancale, J, Vilarinho, S, Lundegaard, P R, Sørensen, E, Erikstrup, C, Bruun, M T, Jensen, B A, Brunak, S, Banasik, K, Ullum, H, DBDS Genomic Consortium, Verweij, N, Lotta, L, Baras, A, Regeneron Genetics Center, Mirshahi, T, Carey, D J, Geisinger-Regeneron DiscovEHR Collaboration, VA Million Veteran Program, Kaplan, D E, Lynch, J, Morgan, T, Schwantes-An, T-H, Dochtermann, D R, Pyarajan, S, Tsao, P S, Estonian Biobank Research Team, Laisk, T, Mägi, R, Kozlitina, J, Tybjærg-Hansen, A, Jones, D, Knowlton, K U, Nadauld, L, Ferkingstad, E, Björnsson, E S, Ulfarsson, M O, Sturluson, Á, Sulem, P, Pedersen, O B, Ostrowski, S R, Gudbjartsson, D F, Stefansson, K, Olesen, M S, Chang, K-M, Holm, H, Bundgaard, H & Stender, S 2024, 'Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis', Nature Genetics, vol. 56, no. 5, pp. 827-837. https://doi.org/10.1038/s41588-024-01720-y
Ghouse, J, Sveinbjörnsson, G, Vujkovic, M, Seidelin, A-S, Gellert-Kristensen, H, Ahlberg, G, Tragante, V, Rand, S A, Brancale, J, Vilarinho, S, Lundegaard, P R, Sørensen, E, Erikstrup, C, Bruun, M T, Jensen, B A, Brunak, S, Banasik, K, Ullum, H, Verweij, N, Lotta, L, Baras, A, Mirshahi, T, Carey, D J, Kaplan, D E, Lynch, J, Morgan, T, Schwantes-An, T-H, Dochtermann, D R, Pyarajan, S, Tsao, P S, Laisk, T, Mägi, R, Kozlitina, J, Tybjærg-Hansen, A, Jones, D, Knowlton, K U, Nadauld, L, Ferkingstad, E, Björnsson, E S, Ulfarsson, M O, Sturluson, Á, Sulem, P, Pedersen, O B, Ostrowski, S R, Gudbjartsson, D F, Stefansson, K, Olesen, M S, Chang, K-M, Bundgaard, H, Stender, S & DBDS Genomic Consortium 2024, ' Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis ', Nature Genetics, vol. 56, pp. 827–837 . https://doi.org/10.1038/s41588-024-01720-y
Nature Genetics, vol 56, iss 5
Ghouse, J, Sveinbjörnsson, G, Vujkovic, M, Seidelin, A S, Gellert-Kristensen, H, Ahlberg, G, Tragante, V, Rand, S A, Brancale, J, Vilarinho, S, Lundegaard, P R, Sørensen, E, Erikstrup, C, Bruun, M T, Jensen, B A, Brunak, S, Banasik, K, Ullum, H, Verweij, N, Lotta, L, Baras, A, Mirshahi, T, Carey, D J, Kaplan, D E, Lynch, J, Morgan, T, Schwantes-An, T H, Dochtermann, D R, Pyarajan, S, Tsao, P S, Laisk, T, Mägi, R, Kozlitina, J, Tybjærg-Hansen, A, Jones, D, Knowlton, K U, Nadauld, L, Ferkingstad, E, Björnsson, E S, Ulfarsson, M O, Sturluson, Á, Sulem, P, Pedersen, O B, Ostrowski, S R, Gudbjartsson, D F, Stefansson, K, Olesen, M S, Chang, K M, Holm, H, Bundgaard, H, Stender, S, DBDS Genomic Consortium, Regeneron Genetics Center, Geisinger-Regeneron DiscovEHR Collaboration, VA Million Veteran Program & Estonian Biobank Research Team 2024, 'Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis', Nature Genetics, vol. 56, no. 5, pp. 827-837. https://doi.org/10.1038/s41588-024-01720-ySubject Terms: gamma-Glutamyltransferase/genetics, Liver Cirrhosis, Male, Multifactorial Inheritance, Carcinoma, Hepatocellular, Polymorphism, Single Nucleotide, Article, Cohort Studies, Liver Cirrhosis/genetics, Risk Factors, Humans, Genetic Predisposition to Disease, Polymorphism, Alanine Transaminase/blood, Membrane Proteins/genetics, Liver Neoplasms/genetics, Multifactorial Inheritance/genetics, Carcinoma, Carcinoma, Hepatocellular/genetics, Liver Neoplasms, Membrane Proteins, Genetic Variation, Hepatocellular, Alanine Transaminase, Single Nucleotide, Lipase, gamma-Glutamyltransferase, 3. Good health, Case-Control Studies, Female, Hepatocellular/genetics, Lipase/genetics, Genome-Wide Association Study
File Description: application/pdf
Access URL: https://pubmed.ncbi.nlm.nih.gov/38632349
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https://doi.org/10.1038/s41588-024-01720-y
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11
Authors: et al.
Contributors: et al.
Source: Nature
Repisalud
Instituto de Salud Carlos III (ISCIII)
Suzuki, K, Hatzikotoulas, K, Southam, L, Taylor, H J, Yin, X, Lorenz, K M, Mandla, R, Huerta-Chagoya, A, Melloni, G E M, Kanoni, S, Rayner, N W, Bocher, O, Arruda, A L, Sonehara, K, Namba, S, Lee, S S K, Preuss, M H, Petty, L E, Schroeder, P, Vanderwerff, B, Kals, M, Bragg, F, Lin, K, Guo, X, Zhang, W, Yao, J, Kim, Y J, Graff, M, Takeuchi, F, Nano, J, Lamri, A, Nakatochi, M, Moon, S, Scott, R A, Cook, J P, Lee, J-J, Pan, I, Taliun, D, Parra, E J, Chai, J-F, Bielak, L F, Tabara, Y, Hai, Y, Thorleifsson, G, Grarup, N, Sofer, T, Wuttke, M, Sarnowski, C, Gieger, C, Nousome, D, Trompet, S, Kwak, S-H, Long, J, Sun, M, Tong, L, Chen, W-M, Nongmaithem, S S, Noordam, R, Lim, V J Y, Tam, C H T, Joo, Y Y, Chen, C-H, Raffield, L M, Prins, B P, Nicolas, A, Yanek, L R, Chen, G, Brody, J A, Kabagambe, E, An, P, Xiang, A H, Choi, H S, Cade, B E, Tan, J, Broadaway, K A, Williamson, A, Kamali, Z, Cui, J, Thangam, M, Adair, L S, Adeyemo, A, Aguilar-Salinas, C A, Ahluwalia, T S, Anand, S S, Bertoni, A, Bork-Jensen, J, Brandslund, I, Buchanan, T A, Burant, C F, Butterworth, A S, 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, Danesh, J, 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, Franco, O H, Frayling, T M, Freedman, B I, Genter, P, Gerstein, H C, Giedraitis, V, González-Villalpando, C, González-Villalpando, M E, Gordon-Larsen, P, Gross, M, Guare, L A, Hackinger, S, Hakaste, L, Han, S, Hattersley, A T, Herder, C, Horikoshi, M, 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, T, Kamanu, F K, 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, Kronenberg, F, Kuusisto, J, Läll, K, Lange, L A, Lee, K M, 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, Lynch, J A, Lyssenko, V, Maeda, S, Mamakou, V, Mansuri, S R, Matsuda, K, Meitinger, T, Melander, O, Metspalu, A, Mo, H, Morris, A D, Moura, F A, Nadler, J L, Nalls, M A, Nayak, U, Ntalla, I, Okada, Y, Orozco, L, Patel, S R, Patil, S, Pei, P, Pereira, M A, Peters, A, Pirie, F J, Polikowsky, H G, Porneala, B, Prasad, G, Rasmussen-Torvik, L J, Reiner, A P, Roden, M, Rohde, R, Roll, K, Sabanayagam, C, Sandow, K, Sankareswaran, A, Sattar, N, Schönherr, S, Shahriar, M, Shen, B, Shi, J, Shin, D M, Shojima, N, Smith, J A, So, W Y, Stančáková, A, Steinthorsdottir, V, Stilp, A M, Strauch, K, Taylor, K D, Thorand, B, Thorsteinsdottir, U, Tomlinson, B, Tran, T C, Tsai, F-J, Tuomilehto, J, Tusie-Luna, T, Udler, M S, Valladares-Salgado, A, van Dam, R M, van Klinken, J B, Varma, R, Wacher-Rodarte, N, Wheeler, E, Wickremasinghe, A R, van Dijk, K W, Witte, D R, Yajnik, C S, Yamamoto, K, Yamamoto, K, Yoon, K, Yu, C, Yuan, J-M, Yusuf, S, Zawistowski, M, Zhang, L, Zheng, W, Raffel, L J, Igase, M, Ipp, E, Redline, S, Cho, Y S, Lind, L, Province, M A, Fornage, M, Hanis, C L, Ingelsson, E, Zonderman, A B, Psaty, B M, Wang, Y-X, Rotimi, C N, Becker, D M, Matsuda, F, Liu, Y, Yokota, M, Kardia, S L R, Peyser, P A, Pankow, J S, Engert, J C, Bonnefond, A, Froguel, P, Wilson, J G, Sheu, W H H, Wu, J-Y, Hayes, M G, Ma, R C W, Wong, T-Y, Mook-Kanamori, D O, Tuomi, T, 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, Chen, Y-D I, Rich, S S, McKean-Cowdin, R, Grallert, H, Cheng, C-Y, Ghanbari, M, Tai, E-S, Dupuis, J, Kato, N, Laakso, M, Köttgen, A, Koh, W-P, Bowden, D W, Palmer, C N A, Kooner, J S, Kooperberg, C, Liu, S, North, K E, Saleheen, D, Hansen, T, Pedersen, O, Wareham, N J, Lee, J, Kim, B-J, Millwood, I Y, Walters, R G, Stefansson, K, Ahlqvist, E, Goodarzi, M O, Mohlke, K L, Langenberg, C, Haiman, C A, Loos, R J F, Florez, J C, Rader, D J, Ritchie, M D, Zöllner, S, Mägi, R, Marston, N A, Ruff, C T, van Heel, D A, Finer, S, Denny, J C, Yamauchi, T, Kadowaki, T, Chambers, J C, Ng, M C Y, Sim, X, Below, J E, Tsao, P S, Chang, K-M, McCarthy, M I, Meigs, J B, Mahajan, A, Spracklen, C N, Mercader, J M, Boehnke, M, Rotter, J I, Vujkovic, M, Voight, B F, Morris, A P, Zeggini, E & VA Million Veteran Program 2024, 'Genetic drivers of heterogeneity in type 2 diabetes pathophysiology', Nature, vol. 627, no. 8003, pp. 347-357. https://doi.org/10.1038/s41586-024-07019-6
Suzuki, K, Hatzikotoulas, K, Southam, L, Taylor, H J, Yin, X, Lorenz, K M, Mandla, R, Huerta-Chagoya, A, Melloni, G E M, Kanoni, S, Rayner, N W, Bocher, O, Arruda, A L, Sonehara, K, Namba, S, Lee, S S K, Preuss, M H, Petty, L E, Schroeder, P, Vanderwerff, B, Kals, M, Bragg, F, Lin, K, Guo, X, Zhang, W, Yao, J, Kim, Y J, Graff, M, Takeuchi, F, Nano, J, Lamri, A, Nakatochi, M, Moon, S, Scott, R A, Cook, J P, Lee, J-J, Pan, I, Taliun, D, Parra, E J, Grarup, N, Chen, W-M, Bork-Jensen, J, Islam, M T, Jørgensen, T, Linneberg, A, Witte, D R, Lind, L, Hansen, T, Pedersen, O, Loos, R J F & VA Million Veteran Program 2024, ' Genetic drivers of heterogeneity in type 2 diabetes pathophysiology ', Nature, vol. 627, no. 8003, pp. 347-357 . https://doi.org/10.1038/s41586-024-07019-6
VA Million Veteran Program, AMED GRIFIN Diabetes Initiative Japan, BioBank Japan Project, Penn Medicine BioBank, Regeneron Genetics Center, Genes & Health Research Team, eMERGE Consortium, International Consortium of Blood Pressure (ICBP), Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC), Suzuki, K, Morris, A P & al, E 2024, 'Genetic drivers of heterogeneity in type 2 diabetes pathophysiology', Nature: international weekly journal of science. https://doi.org/10.1038/s41586-024-07019-6
Nature: New biology, vol 627, iss 8003
VA Million Veteran Program 2024, 'Genetic drivers of heterogeneity in type 2 diabetes pathophysiology', Nature, vol. 627, no. 8003, pp. 347-357. https://doi.org/10.1038/s41586-024-07019-6Subject Terms: Epigenomics, Multifactorial Inheritance, Diseases, Coronary Artery Disease, Medical Genetics and Genomics, Endocrinology, Medical Specialties, Medicine and Health Sciences, Adipocytes, Diabetic Nephropathies, Chromatin/genetics, Genetic Predisposition to Disease/genetics, Diabetes, Life Sciences, Medicinsk genetik och genomik, Chromatin, [SDV] Life Sciences [q-bio], Endokrinologi och diabetes, VA Million Veteran Program, Disease Progression, Diabetes Mellitus, Type 2/genetics, Type 2/classification, Public Health, Islets of Langerhans/metabolism, Single-Cell Analysis, Type 2, Coronary Artery Disease/complications, Enteroendocrine Cells, Endocrinology and Diabetes, Endothelial Cells/metabolism, Endocrine System Diseases, Polymorphism, Single Nucleotide, Article, Islets of Langerhans, Peripheral Arterial Disease, Diabetes Mellitus, Humans, Genetic Predisposition to Disease, Multifactorial Inheritance/genetics, Diabetic Nephropathies/complications, ICTS (Institute of Clinical and Translational Sciences), Endothelial Cells, Genetics and Genomics, and Metabolism, Diabetes Mellitus, Type 2, Adipocytes/metabolism, Peripheral Arterial Disease/complications, Diabetes Mellitus, Type 2/classification, Genome-Wide Association Study
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12
Authors: et al.
Contributors: et al.
Source: Human Molecular Genetics. 34:711-725
Subject Terms: Male, Adult, Back Pain/genetics, Multifactorial Inheritance, Genetics & genetic processes, Polymorphism, Single Nucleotide, Génétique & processus génétiques, Genetics, shared genetic background, Humans, Genetic Predisposition to Disease, Multifactorial Inheritance/genetics, Molecular Biology, low back pain, Genetics (clinical), genome-wide association study, Middle Aged, Life sciences, 3. Good health, subphenotyping, Phenotype, Back Pain, polygenic risk score, Sciences du vivant, Chronic Pain/genetics, Female, Chronic Pain, Genetic Background, Genome-Wide Association Study
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13
Authors: et al.
Contributors: et al.
Source: Nature
Irving-Pease, E K, Refoyo-Martínez, A, Barrie, W, Ingason, A, Pearson, A, Fischer, A, Sjögren, K-G, Halgren, A S, Macleod, R, Demeter, F, Henriksen, R A, Vimala, T, McColl, H, Vaughn, A H, Speidel, L, Stern, A J, Scorrano, G, Ramsøe, A, Schork, A J, Rosengren, A, Zhao, L, Kristiansen, K, Iversen, A K N, Fugger, L, Sudmant, P H, Lawson, D J, Durbin, R, Korneliussen, T, Werge, T, Allentoft, M E, Sikora, M, Nielsen, R, Racimo, F & Willerslev, E 2024, ' The selection landscape and genetic legacy of ancient Eurasians ', Nature, vol. 625, no. 7994, pp. 312-320 . https://doi.org/10.1038/s41586-023-06705-1
Nature, vol 625, iss 7994
Irving-Pease, E K, Refoyo-Martínez, A, Barrie, W, Ingason, A, Pearson, A, Fischer, A, Sjögren, K G, Halgren, A S, Macleod, R, Demeter, F, Henriksen, R A, Vimala, T, McColl, H, Vaughn, A H, Speidel, L, Stern, A J, Scorrano, G, Ramsøe, A, Schork, A J, Rosengren, A, Zhao, L, Kristiansen, K, Iversen, A K N, Fugger, L, Sudmant, P H, Lawson, D J, Durbin, R, Korneliussen, T, Werge, T, Allentoft, M E, Sikora, M, Nielsen, R, Racimo, F & Willerslev, E 2024, 'The selection landscape and genetic legacy of ancient Eurasians', Nature, vol. 625, no. 7994, pp. 312-320. https://doi.org/10.1038/s41586-023-06705-1Subject Terms: History, Multifactorial Inheritance, European People, Population genetics, Diabetes Mellitus/genetics, Historical Studies, History, Ancient, 2. Zero hunger, Asia/ethnology, Human/genetics, Genome, Farmers, Settore BIOS-03/B - Antropologia, Agriculture, Genomics, Multigene Family/genetics, Biological Sciences, Europe, Phenotype, Archaeology, Multigene Family, Agriculture/history, Genetic Loci/genetics, Human, UK Biobank, Asia, General Science & Technology, Human Migration, Settore BIO/08, Europe/ethnology, Evolutionary genetics, Article, Ancient, Genetic, Farmers/history, Alzheimer Disease, evolution, Genetics, Diabetes Mellitus, Hunting, Humans, Genetic Predisposition to Disease, Selection, Genetic, Heritage and Archaeology, Multifactorial Inheritance/genetics, Selection, Alleles, Alzheimer Disease/genetics, Hunting/history, Asian, Asian/genetics, Genome, Human, Molecular, 15. Life on land, Human Society, Affect, Good Health and Well Being, Genetic Loci, Anthropology, European People/genetics, 2.4 Surveillance and distribution
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https://www.repository.cam.ac.uk/handle/1810/363366
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https://doi.org/10.1038/s41586-023-06705-1 -
14
Authors: et al.
Source: Human Molecular Genetics, 34 (8), 711 - 725 (2025-04-06)
Subject Terms: genome-wide association study, low back pain, polygenic risk score, shared genetic background, subphenotyping, Humans, Female, Male, Multifactorial Inheritance/genetics, Genome-Wide Association Study, Middle Aged, Phenotype, Polymorphism, Single Nucleotide, Adult, Back Pain/genetics, Chronic Pain/genetics, Genetic Predisposition to Disease, Genetic Background, Back Pain, Chronic Pain, Multifactorial Inheritance, Molecular Biology, Genetics, Genetics (clinical), Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques
Relation: https://academic.oup.com/hmg/article-pdf/34/8/711/61738796/ddae195.pdf; urn:issn:0964-6906; urn:issn:1460-2083
Access URL: https://orbi.uliege.be/handle/2268/335059
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15
Authors: et al.
Source: LaBianca, S, Brikell, I, Helenius, D, Loughnan, R, Mefford, J, Palmer, C E, Walker, R, Gådin, J R, Krebs, M, Appadurai, V, Vaez, M, Agerbo, E, Pedersen, M G, Børglum, A D, Hougaard, D M, Mors, O, Nordentoft, M, Mortensen, P B, Kendler, K S, Jernigan, T L, Geschwind, D H, Ingason, A, Dahl, A W, Zaitlen, N, Dalsgaard, S, Werge, T M & Schork, A J 2024, ' Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder ', Nature Genetics, vol. 56, no. 2, pp. 234-244 . https://doi.org/10.1038/s41588-023-01593-7
Nature Genetics, vol 56, iss 2
LaBianca, S, Brikell, I, Helenius, D, Loughnan, R, Mefford, J, Palmer, C E, Walker, R, Gådin, J R, Krebs, M, Appadurai, V, Vaez, M, Agerbo, E, Pedersen, M G, Børglum, A D, Hougaard, D M, Mors, O, Nordentoft, M, Mortensen, P B, Kendler, K S, Jernigan, T L, Geschwind, D H, Ingason, A, Dahl, A W, Zaitlen, N, Dalsgaard, S, Werge, T M & Schork, A J 2024, 'Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder', Nature Genetics, vol. 56, no. 2, pp. 234-244. https://doi.org/10.1038/s41588-023-01593-7Subject Terms: Multifactorial Inheritance, Autism Spectrum Disorder, Intellectual and Developmental Disabilities (IDD), Autism, Agricultural biotechnology, Medical and Health Sciences, Clinical Research, 2.3 Psychological, Behavioral and Social Science, Genetics, 2.1 Biological and endogenous factors, Humans, Multifactorial Inheritance/genetics, Pediatric, Prevention, Human Genome, Biological Sciences, Mental Illness, Attention Deficit Hyperactivity Disorder (ADHD), Bioinformatics and computational biology, 3. Good health, Brain Disorders, Autism Spectrum Disorder/genetics, Mental Health, Good Health and Well Being, Attention Deficit Disorder with Hyperactivity, Mental health, social and economic factors, Attention Deficit Disorder with Hyperactivity/genetics, Developmental Biology
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https://doi.org/10.1038/s41588-023-01593-7 -
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Authors:
Source: J Hum Genet
Subject Terms: 0301 basic medicine, Multifactorial Inheritance, Population, Polymorphism, Single Nucleotide, Article, Quantitative Trait, 03 medical and health sciences, Quantitative Trait, Heritable, Genetic, Models, Genetics, Humans, Computer Simulation, Polymorphism, Selection, Genetic, Multifactorial Inheritance/genetics, Heritable, Selection, 0303 health sciences, Models, Genetic, Single Nucleotide, Genetics, Population, Phenotype, Genome-Wide Association Study/methods, Genome-Wide Association Study
Access URL: https://pubmed.ncbi.nlm.nih.gov/38589509
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Authors: et al.
Contributors: et al.
Source: Nat Genet
Nature genetics 57(7), 1598-1610 (2025). doi:10.1038/s41588-025-02227-w
Nature genetics, vol. 57, no. 7, pp. 1598-1610
EADB, Leonard, H L, Yokoyama, J S, Nalls, M A, Miyashita, A, Hara, N, Ozaki, K, Niida, S, Williams, J, Masullo, C, Amouyel, P, Preux, P-M, Mbelesso, P, Bandzouzi, B, Saykin, A, Jessen, F, Kehoe, P G, van Duijn, C, Ben Salem, N, Frikke-Schmidt, R, Cherni, L, Greicius, M D, Tsolaki, M, Sanchez-Juan, P, Silva, M A R, Porter, T, Laws, S M, Sleegers, K, Ingelsson, M, Dartigues, J F, Seshadri, S, Rossi, G, Morelli, L, Hiltunen, M, Sims, R, van der Flier, W M, Andreassen, O A, Arboleda, H, Cruchaga, C, Escott-Price, V, Qvist Thomassen, J, Ruiz, A, Lee, K H, Ikeuchi, T, Ramirez, A, Gim, J, Logue, M W, Lambert, J C, Nordestgaard, B & Tybjærg-Hansen, A 2025, ' Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populations ', Nature Genetics, vol. 57, no. 7, pp. 1598-1610 . https://doi.org/10.1038/s41588-025-02227-w
In Review
medRxivSubject Terms: Male, Multifactorial Inheritance, Letter, 3001 Agricultural biotechnology, epidemiology [Alzheimer Disease], genetics [White People], genetics [Alzheimer Disease], Alzheimer's disease, genetics, Polymorphism, Single Nucleotide, White People, 3105 Genetics, Medical Genetics and Genomics, EADB, Apolipoproteins E, Alzheimer Disease, Risk Factors, ddc:570, Humans, Genetic Predisposition to Disease, Alzheimer Disease/genetics, Alzheimer Disease/epidemiology, Alzheimer Disease/cerebrospinal fluid, Multifactorial Inheritance/genetics, White People/genetics, Genome-Wide Association Study, Europe/epidemiology, Apolipoproteins E/genetics, Female, Aged, Biomarkers/cerebrospinal fluid, Genetic Risk Score, genetics [Multifactorial Inheritance], 11 Medical and Health Sciences, Genetics & Heredity, Science & Technology, ASSOCIATION, epidemiology [Europe], 06 Biological Sciences, Medicinsk genetik och genomik, 3. Good health, Europe, cerebrospinal fluid [Alzheimer Disease], cerebrospinal fluid [Biomarkers], 3102 Bioinformatics and computational biology, genetics [Apolipoproteins E], Life Sciences & Biomedicine, Biomarkers, Developmental Biology
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Authors: et al.
Contributors: et al.
Source: Nielsen, T T, Bali, P, Grove, J, Mohr-Jensen, C, Werge, T, Dalsgaard, S, Børglum, A D, Sonuga-Barke, E, Minnis, H, Demontis, D & Autism Spectrum Working Group of the Psychiatric Genomics Consortium 2025, 'Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses', JAMA Psychiatry, vol. 82, no. 8, e0243639, pp. 790-800. https://doi.org/10.1001/jamapsychiatry.2025.0828
Nielsen, T T, Bali, P, Grove, J, Mohr-Jensen, C, Werge, T, Dalsgaard, S, Børglum, A D, Sonuga-Barke, E, Minnis, H, Corfield, E C, Tbartz van Elst, L, Mattheisen, M, de Wit, M M, Uddin, M J, Anney, R J L, Scherer, S W, Bourgeron, T, Polderman, T J C, Autism Spectrum Working Group of the Psychiatric Genomics Consortium & Demontis, D 2025, 'Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses', JAMA Psychiatry. https://doi.org/10.1001/jamapsychiatry.2025.0828Subject Terms: Male, Adult, Mental Disorders/genetics, Schizophrenia/genetics, Adolescent, Bipolar Disorder/genetics, [SCCO.NEUR] Cognitive science/Neuroscience, Young Adult, Child Abuse/statistics & numerical data, Risk Factors, Case-Control Studies, Humans, Educational Status, Female, Genetic Predisposition to Disease, Adult Survivors of Child Abuse/psychology, Child, Attention Deficit Disorder with Hyperactivity/genetics, Multifactorial Inheritance/genetics, Substance-Related Disorders/genetics, Genome-Wide Association Study
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https://doi.org/10.1001/jamapsychiatry.2025.0828
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https://doi.org/10.1001/jamapsychiatry.2025.0828
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https://doi.org/10.1001/jamapsychiatry.2025.0828
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https://doi.org/10.1001/jamapsychiatry.2025.0828
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https://doi.org/10.1001/jamapsychiatry.2025.0828 -
19
Authors: et al.
Source: Shrestha, M, Bai, Z, Gholipourshahraki, T, Hjelholt, A J, Hu, S, Kjolby, M, Rohde, P D & Sørensen, P 2025, 'Enhanced genetic fine mapping accuracy with Bayesian Linear Regression models in diverse genetic architectures', PLOS Genetics, vol. 21, no. 7, e1011783, pp. e1011783. https://doi.org/10.1371/journal.pgen.1011783
Shrestha, M, Bai, Z, Gholipourshahraki, T, Hjelholt, A J, Hu, S, Kjolby, M, Rohde, P D & Sørensen, P 2025, 'Enhanced genetic fine mapping accuracy with Bayesian Linear Regression models in diverse genetic architectures', PLOS Genetics, vol. 21, no. 7, e1011783. https://doi.org/10.1371/journal.pgen.1011783Subject Terms: Phenotype, Models, Genetic, Genome-Wide Association Study/methods, Linear Models, Humans, Bayes Theorem, Computer Simulation, Chromosome Mapping/methods, Polymorphism, Single Nucleotide/genetics, Quantitative Trait Loci/genetics, Multifactorial Inheritance/genetics
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20
Authors: et al.
Source: Antonatos, C, Budu-Aggrey, A, Pontikas, A, Akritidis, A, Pasmatzi, E, Tsiogka, A, Gregoriou, S, Grafanaki, K, Paternoster, L & Vasilopoulos, Y 2025, 'Polygenic transcriptome risk scores enhance predictive accuracy in atopic dermatitis', Journal of Translational Medicine, vol. 23, no. 1, 575. https://doi.org/10.1186/s12967-025-06570-8
Subject Terms: Humans, Dermatitis, Atopic/genetics, Transcriptome/genetics, Multifactorial Inheritance/genetics, Genetic Predisposition to Disease, Risk Factors, Female, Male, Middle Aged, Adult
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