Search Results - "Genetic association study"

Association of Clinicopathological Factors With MMP13 (rs2252070) Gene Polymorphism in Swedish Patients With Colorectal Cancer

Authors: van Nguyen, Song Shamoun, Levar Landerholm, Kalle et al.

Source: In Vivo. 38(4):1775-1782

Subject Terms: clinical parameters, colorectal cancer, MMP13, SNP, Adult, Aged, 80 and over, Alleles, Biomarkers, Tumor, Carcinoembryonic Antigen, Colorectal Neoplasms, Female, Genetic Association Studies, Genetic Predisposition to Disease, Genotype, Humans, Kaplan-Meier Estimate, Male, Matrix Metalloproteinase 13, Middle Aged, Neoplasm Staging, Polymorphism, Single Nucleotide, Prognosis, Sweden, collagenase 3, MMP13 protein, human, tumor marker, allele, antigen blood level, Article, cancer patient, cancer prevention, cancer specific survival, clinical feature, colorectal adenocarcinoma, controlled study, DNA polymorphism, follow up, genetic association, genotyping, histopathology, human tissue, long term survival, lymph node, lymph vessel metastasis, major clinical study, perineural invasion, polymerase chain reaction, single nucleotide polymorphism, Swedish citizen, tumor differentiation, tumor volume, very elderly, blood, cancer staging, colorectal tumor, epidemiology, genetic association study, genetic predisposition, genetics, Kaplan Meier method, mortality, pathology

File Description: print

Access URL: https://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-65694
https://doi.org/10.21873/invivo.13628

A novel combination of genomic loci in ITGB2, COL5A1 and VEGFA associated with anterior cruciate ligament rupture susceptibility: insights From Australian, Polish, Swedish, And South African Cohorts

Authors: Dlamini, Senanile B. Saunders, Colleen J. Cieszczyk, Paweł et al.

Source: Biology of Sport. 43:3-20

Subject Terms: Biomedical knowledge graph, Genetic association study, Cell signalling, Extracellular Matrix Organization pathway, Integrin protein complex, medicinsk genetik, Medical Genetics

File Description: print

Access URL: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-246051

HLA-DRB1*15:01 is associated with a reduced likelihood of longevity in northern European men

Authors: Nicolás Mendoza-Mejía Daniel Kolbe Onur Özer et al.

Source: Genome Medicine, Vol 17, Iss 1, Pp 1-13 (2025)

Subject Terms: Human leukocyte antigen, Longevity, Genetic association study, Ageing, Immunogenetics, Medicine, Genetics, QH426-470

File Description: electronic resource

Relation: https://doaj.org/toc/1756-994X

Access URL: https://doaj.org/article/3cee53e2bb1d424a938ea925aa632947

Association between TG Genetic Polymorphisms and Thyroid Diseases

Authors: Gaeun KIM Eun-Jung KIM

Source: Korean Journal of Clinical Laboratory Science, Vol 57, Iss 1, Pp 66-75 (2025)

Subject Terms: Medicine (General), R5-920, genetic association study, polymorphism, single nucleotide, thyroglobulin, thyroid diseases

Access URL: https://doaj.org/article/ad60acb3589744fdad91f8b94651c31c

Rare MTNR1B variants causing diminished MT2 signalling associate with elevated HbA1c levels but not with type 2 diabetes

Authors: Kimmie V. Sørensen Johanne M. Justesen Lars Ängquist et al.

Source: Diabetologia
Sørensen, K V, Justesen, J M, Ängquist, L, Bork-Jensen, J, Hartmann, B, Jørgensen, N R, Rungby, J, Sørensen, H T, Vaag, A, Nielsen, J S, Holst, J J, Pedersen, O, Linneberg, A, Hansen, T & Grarup, N 2025, ' Rare MTNR1B variants causing diminished MT2 signalling associate with elevated HbA 1c levels but not with type 2 diabetes ', Diabetologia, vol. 68, pp. 1016–1030 . https://doi.org/10.1007/s00125-025-06381-y
Sørensen, K V, Justesen, J M, Ängquist, L, Bork-Jensen, J, Hartmann, B, Jørgensen, N R, Rungby, J, Sørensen, H T, Vaag, A, Nielsen, J S, Holst, J J, Pedersen, O, Linneberg, A, Hansen, T & Grarup, N 2025, 'Rare MTNR1B variants causing diminished MT2 signalling associate with elevated HbA 1c levels but not with type 2 diabetes', Diabetologia, vol. 68, no. 5, pp. 1016-1030. https://doi.org/10.1007/s00125-025-06381-y

Subject Terms: Male, Type 2/genetics, Adult, Genotype, Melatonin receptor type 2, Glycated Hemoglobin/metabolism, rs10830963, Article, Diabetes Mellitus, Humans, HbA, Polymorphism, Aged, Genetic association study, Melatonin, Blood Glucose/metabolism, MTNR1B, MT2, Type 2 diabetes, Single Nucleotide, Middle Aged, Cross-Sectional Studies, Phenotype, Case-Control Studies, Signal Transduction/genetics, Female, Recall-by-genotype investigation, MT2/genetics, Variants impairing receptor function, Receptor

File Description: application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/40064676
https://curis.ku.dk/ws/files/448096096/Rare_MTNR1B_variants.pdf
http://www.scopus.com/inward/record.url?scp=86000730121&partnerID=8YFLogxK
https://pure.au.dk/portal/en/publications/9bc98620-986e-4b9b-bc40-a8760ba1dfa2
https://doi.org/10.1007/s00125-025-06381-y

Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits

Authors: Nora Scherer Daniel Fässler Oleg Borisov et al.

Source: Nat Genet
Nature Genetics

Subject Terms: Exome/genetics, Male, ddc:610, Heterozygote, 610 Medizin, Metabolome/genetics, Genetic Variation, Metabolism, Inborn Errors/genetics, Epidemiology, Genetic association study, Genetics research, Metabolomics, Population genetics, Sulfate Transporters/genetics, Article, Phenotype, Sulfate Transporters, Exome Sequencing, Metabolome, Metabolomics, Humans, Metabolomics/methods, Exome, Female, Metabolism, Inborn Errors

File Description: application/pdf; pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/39747595
https://epub.uni-regensburg.de/76564/

PatientMatcher: A customizable Python-based open-source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network

Authors: Rasi, Chiara Nilsson, Daniel Magnusson, Måns et al.

Source: Human Mutation. 43(6):708-716

Subject Terms: gene discovery, genomic API, Matchmaker Exchange, matchmaking, rare disease, algorithm, Article, data availability, data integration, e-mail, equipment design, genomic medicine, genotype, human, open source software, patient coding, patient information, undiagnosed disease, genetic association study, genetic predisposition, genetics, information dissemination, procedures, software, Genetic Association Studies, Genetic Predisposition to Disease, Humans, Rare Diseases, Undiagnosed Diseases

File Description: print

Access URL: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-321868
https://doi.org/10.1002/humu.24358

Carboxyl ester lipase hybrid 1 (CEL-HYB1) haplotypes confer varying risk for chronic pancreatitis.

Authors: Berke, Gergő Sándor, Máté Xiao, Xunjun et al.

Source: Scientific Reports. 14(1)

Subject Terms: Endoplasmic reticulum stress, Genetic association study, Lipase, Misfolding, Pancreatitis, Humans, Haplotypes, Pancreatitis, Chronic, Genetic Predisposition to Disease, Male, Female, Hungary, Lipase, Endoplasmic Reticulum Stress, Case-Control Studies, Pseudogenes, Middle Aged, Poland, Adult, Alleles, Germany

File Description: application/pdf

Access URL: https://escholarship.org/uc/item/4dn7x0g2
https://escholarship.org/content/qt4dn7x0g2/qt4dn7x0g2.pdf

Angiotensin-converting Enzyme Insertion/Deletion Polymorphism Distribution in the North Indian Population of Jammu and Kashmir and Its Positive Correlation with Male Infertility: A Case Control Study

Authors: Sonali Bhan Manisha Bhagat Shreya Sopori et al.

Source: Journal of Human Reproductive Sciences, Vol 18, Iss 3, Pp 166-173 (2025)

Subject Terms: angiotensin converting enzyme insertion/deletion polymorphism, asthenoteratozoospermia, case–control study, genetic association study, idiopathy, male infertility, teratozoospermia, Gynecology and obstetrics, RG1-991

File Description: electronic resource

Relation: https://journals.lww.com/10.4103/jhrs.jhrs_79_25; https://doaj.org/toc/0974-1208; https://doaj.org/toc/1998-4766

Access URL: https://doaj.org/article/ed0f1776ed53422e9a61d2ab96251a77

Genotype and transcript processing of the tumour necrosis factor receptor TNFRSF1A in epithelial cells: implications for survival in cystic fibrosisResearch in context

Authors: Alexander Uden Inga Dunsche Sabina Janciauskiene et al.

Source: EBioMedicine, Vol 118, Iss, Pp 105848-(2025)

Subject Terms: Medicine (General), R5-920, TNFRSF1A, Alternative transcript, Patient survival, Medicine, Tumour necrosis factor receptor, Cystic fibrosis, Genetic association study

Access URL: https://doaj.org/article/369245248bfd492e82e5818a6b2d6790

Maternal genetic risk factors for spontaneous preterm birth: A systematic review and meta‐analysis

Authors: Tea Mladenić Anita Barišić Nina Pereza et al.

Source: International Journal of Gynecology & Obstetrics. 169:458-473

Subject Terms: 0301 basic medicine, 03 medical and health sciences, 0302 clinical medicine, genetic association study, spontaneous preterm birth, preterm birth, premature birth, gene, exome sequencing, genome‐wide association study

Access URL: https://pubmed.ncbi.nlm.nih.gov/39620886

The Swedish bipolar collection (SWEBIC)

Authors: Mikael Landén Erik Joas Alina Karanti et al.

Source: International Journal of Bipolar Disorders, Vol 13, Iss 1, Pp 1-11 (2025)

Subject Terms: Bipolar disorder, Cohort study, Registry, Genetic association study, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurophysiology and neuropsychology, QP351-495

File Description: electronic resource

Relation: https://doaj.org/toc/2194-7511

Access URL: https://doaj.org/article/4d13c60b16fc4f19b573012871a01a00

Systems genetics uncovers associations among host amylase locus, gut microbiome, and metabolic traits in mice

Authors: Qijun Zhang Evan R. Hutchison Calvin Pan et al.

Source: Microbiome, Vol 13, Iss 1, Pp 1-14 (2025)

Subject Terms: Systems genetics, Gut microbiome, Genetic association study, Metagenomics, Hybrid mouse diversity panel, Microbial ecology, QR100-130

File Description: electronic resource

Relation: https://doaj.org/toc/2049-2618

Access URL: https://doaj.org/article/bf9039b19dc14edd8f3e0185793f7fdc

Association between LRRK2 gene polymorphisms and Parkinson’s disease progression in a Chinese Han population

Authors: Zhaoting Zhang Lei Geng Jiuxin Gao et al.

Source: Frontiers in Genetics, Vol 16 (2025)

Subject Terms: Parkinson’s disease risk, LRRK2 polymorphisms, disease progression, disease severity, genetic association study, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2025.1662348/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/cb5230ace8c34835b0f9c7df0921a060

HLA variation associated with peanut allergy and anaphylaxis among non-Hispanic Black individuals

Authors: Baojun Wu, PhD Mao Yang, MS Donglei Hu, PhD et al.

Source: Journal of Allergy and Clinical Immunology: Global, Vol 4, Iss 3, Pp 100485- (2025)

Subject Terms: Peanut hypersensitivity, food hypersensitivity, anaphylaxis, genetic association study, HLA antigens, MHC, Immunologic diseases. Allergy, RC581-607

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2772829325000864; https://doaj.org/toc/2772-8293

Access URL: https://doaj.org/article/e5a3a2e5ed2140c498bfc73816d03862

Risk of chronic pancreatitis in carriers of the c.180C>T (p.Gly60=) CTRC variant: case-control studies and meta-analysis.

Authors: Berke, Gergő Beer, Sebastian Gede, Noémi et al.

Source: Pancreatology. 23(5)

Subject Terms: Chymotrypsin, Genetic association study, Meta-Analysis, Pancreatitis, Humans, Trypsin, Pancreatitis, Chronic, Chymotrypsin, Case-Control Studies, Genetic Predisposition to Disease, Mutation

File Description: application/pdf

Access URL: https://escholarship.org/uc/item/6080m1hm
https://escholarship.org/content/qt6080m1hm/qt6080m1hm.pdf

Associations between common genetic variants and income provide insights about the socioeconomic health gradient

Authors: Hyeokmoon Kweon Casper A.P. Burik Yuchen Ning et al.

Contributors: Hyeokmoon Kweon Casper A.P. Burik Yuchen Ning et al.

Source: Nat Hum Behav
Nature human behaviour, vol. 9, no. 4, pp. 794-805
Kweon, H, Burik, C A P, Ning, Y, Ahlskog, R, Xia, C, Abner, E, Bao, Y, Bhatta, L, Faquih, T O, de Feijter, M, Fisher, P, Gelemanović, A, Giannelis, A, Hottenga, J-J, Khalili, B, Lee, Y, Li-Gao, R, Masso, J, Myhre, R, Palviainen, T, Rietveld, C A, Teumer, A, Verweij, R M, Willoughby, E A, Agerbo, E, Bergmann, S, Boomsma, D I, Børglum, A D, Brumpton, B M, Davies, N M, Esko, T, Gordon, S D, Homuth, G, Ikram, M A, Johannesson, M, Kaprio, J, Kidd, M P, Kutalik, Z, Kwong, A S F, Lee, J J, Luik, A I, Magnus, P, Marques-Vidal, P, Martin, N G, Mook-Kanamori, D O, Mortensen, P B, Oskarsson, S, Pedersen, E M, Polašek, O & Rosendaal, F R 2025, 'Associations between common genetic variants and income provide insights about the socio-economic health gradient', Nature Human Behaviour, vol. 9, no. 4, 12681, pp. 794-805. https://doi.org/10.1038/s41562-024-02080-7

Subject Terms: Resource, Adult, Male, Multifactorial Inheritance, Economics, Humans, Genome-Wide Association Study, Income/statistics & numerical data, Female, Middle Aged, Health Status Disparities, Educational Status, Socioeconomic Factors, Social Class, Genetic Variation, White People/genetics, Mental Health, Polymorphism, Single Nucleotide, United-states, Social Sciences, Genome-wide association studies, Article, Medical Genetics and Genomics, Education, Heritability, SDG 3 - Good Health and Well-being, Genetics, Psychology, Mortality, Polymorphism, Determinants, Genetic association study, Genome-wide association, Folkhälsovetenskap, global hälsa och socialmedicin, Single Nucleotide, Metaanalysis, Biological Sciences, Public Health, Global Health and Social Medicine, Medicinsk genetik och genomik, Inequality, Earnings, Genetics, developmental biology, physiology, Income

File Description: pdf; application/pdf; text

Access URL: https://pubmed.ncbi.nlm.nih.gov/39875632
https://pure.eur.nl/en/publications/b331f0c9-d196-40bd-8b23-da24659c6b0a
https://doi.org/10.1038/s41562-024-02080-7
https://research.vu.nl/en/publications/b6e70e0d-930b-43e7-84ce-81ad28740c99
https://doi.org/10.1038/s41562-024-02080-7
https://hdl.handle.net/1871.1/b6e70e0d-930b-43e7-84ce-81ad28740c99
https://hdl.handle.net/11370/becc8ef0-a18b-4218-bc06-0d4bb86187f1
https://research.rug.nl/en/publications/becc8ef0-a18b-4218-bc06-0d4bb86187f1
https://doi.org/10.1038/s41562-024-02080-7
http://hdl.handle.net/10138/599863
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_1386C6C6562F0
https://serval.unil.ch/notice/serval:BIB_1386C6C6562F
https://serval.unil.ch/resource/serval:BIB_1386C6C6562F.P001/REF.pdf
https://hdl.handle.net/1887/4214846
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-557472

Genetic predisposition to nephropathy and associated cardiovascular disease in people with type 1 diabetes: role of the angiotensinI-converting enzyme (ACE), and beyond; a narrative review

Authors: Kamel Mohammedi Michel Marre François Alhenc-Gelas

Source: Cardiovascular Diabetology, Vol 23, Iss 1, Pp 1-10 (2024)

Subject Terms: Type 1 diabetes mellitus, Diabetic nephropathy, Cardiovascular disease, Genetics, Genetic association study, ACE, Diseases of the circulatory (Cardiovascular) system, RC666-701

File Description: electronic resource

Relation: https://doaj.org/toc/1475-2840

Access URL: https://doaj.org/article/ac9e18f9dbc4465aaa6d682148ff3edf

Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

Authors: Robin N. Beaumont Christopher Flatley Marc Vaudel et al.

Contributors: Robin N. Beaumont Christopher Flatley Marc Vaudel et al.

Source: Nat Genet
NATURE GENETICS
r-FISABIO. Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Beaumont, R N, Flatley, C, Vaudel, M, Wu, X, Chen, J, Moen, G-H, Skotte, L, Helgeland, Ø, Solé-Navais, P, Banasik, K, Albiñana, C, Ronkainen, J, Fadista, J, Stinson, S E, Trajanoska, K, Wang, C A, Westergaard, D, Srinivasan, S, Sánchez-Soriano, C, Bilbao, J R, Allard, C, Groleau, M, Kuulasmaa, T, Leirer, D J, White, F, Jacques, P-É, Cheng, H, Hao, K, Andreassen, O A, Åsvold, B O, Atalay, M, Bhatta, L, Bouchard, L, Brumpton, B M, Brunak, S, Bybjerg-Grauholm, J, Ebbing, C, Elliott, P, Engelbrechtsen, L, Erikstrup, C, Estarlich, M, Franks, S, Gaillard, R, Geller, F, Grove, J, Hougaard, D M, Kajantie, E, Morgen, C S, Nohr, E A, Nyegaard, M, Palmer, C N A, Pedersen, O B, Early Growth Genetics (EGG) Consortium, Rivadeneira, F, Sebert, S, Shields, B M, Stoltenberg, C, Surakka, I, Thørner, L W, Ullum, H, Vaarasmaki, M, Vilhjalmsson, B J, Willer, C J, Lakka, T A, Gybel-Brask, D, Bustamante, M, Hansen, T, Pearson, E R, Reynolds, R M, Ostrowski, S R, Pennell, C E, Jaddoe, V W V, Felix, J F, Hattersley, A T, Melbye, M, Lawlor, D A, Hveem, K, Werge, T, Nielsen, H S, Magnus, P, Evans, D M, Jacobsson, B, Järvelin, M-R, Zhang, G, Hivert, M-F, Johansson, S, Freathy, R M, Feenstra, B & Njølstad, P R 2023, 'Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth', Nature Genetics, vol. 55, no. 11, pp. 1807-1819. https://doi.org/10.1038/s41588-023-01520-w
Beaumont, R N, Flatley, C, Vaudel, M, Wu, X, Chen, J, Moen, G H, Skotte, L, Helgeland, Ø, Solé-Navais, P, Banasik, K, Albiñana, C, Ronkainen, J, Fadista, J, Stinson, S E, Trajanoska, K, Wang, C A, Westergaard, D, Srinivasan, S, Sánchez-Soriano, C, Bilbao, J R, Allard, C, Groleau, M, Kuulasmaa, T, Leirer, D J, White, F, Jacques, P É, Cheng, H, Hao, K, Andreassen, O A, Åsvold, B O, Atalay, M, Bhatta, L, Bouchard, L, Brumpton, B M, Brunak, S, Bybjerg-Grauholm, J, Ebbing, C, Elliott, P, Engelbrechtsen, L, Erikstrup, C, Estarlich, M, Franks, S, Gaillard, R, Geller, F, Grove, J, Hougaard, D, Kajantie, E, Morgen, C S, Nohr, E A, Nyegaard, M, Palmer, C N A, Pedersen, O B, The Early Growth Genetics (EGG) Consortium, Rivadeneira, F, Sebert, S P, Shields, B, Stoltenberg, C, Surakka, I, Thørner, L W, Ullum, H, Vaarasmaki, M, Vilhjalmsson, B J, Willer, C J, Lakka, T A, Gybel-Brask, D, Bustamante, M, Hansen, T, Pearson, E R, Reynolds, R, Ostrowski, S R, Pennell, C E, Jaddoe, V W V, F. Felix, J, Hattersley, A T, Melbye, M, Lawlor, D A, Hveem, K, Werge, T, Nielsen, H S, Magnus, P, Evans, D, Jacobsson, B, Järvelin, M-R, Zhang, G, Hivert, M-F, Johansson, S E, Freathy, R M, Feenstra, B & Njølstad, P R 2023, 'Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth', Nature Genetics, vol. 55, no. 11, pp. 1807-1819. https://doi.org/10.1038/s41588-023-01520-w
Beaumont, R N, Flatley, C, Vaudel, M, Wu, X, Lawlor, D A, Chen, J, Moen, G-H, Skotte, L, Helgeland, Ø, Navais, P S, Banasik, K, Albiñana, C, Roinkainen, J, Fadista, J, Stinson, S, Trajanoska, K, Wang, C A, Westergaard, D, Srinivasan, S, Sánchez-Soriano, C, Ramon Bilbao, J, Allard, C, Groleau, M, Kuulasmaa, T, Leirer, D, White, F, Jacques, P-É, Cheng, H, Hao, K, Andreassen, O A, Åsvold, B O, Atalay, M, Bhatta, L, Bouchard, L, Brumpton, B M, Brunak, S, Bybjerg-Grauholm, J, Ebbing, C, Elliott, P, Engelbrechtsen, L, Erikstrup, C, Estarlich, M, Franks, S, Gaillard, R, Geller, F, Grove, J, Hougaard, D M, Kajantie, E, Morgen, C S, Nohr, E A, Nyegaard, M, Palmer, C, Birger Pedersen, O, Rivadeneira, F, Sebert, S P, Shields, B M, Stoltenberg, C, Surakka, I, Wegner Thørner, L, Ullum, H, Vaarasmaki, M & Vilhjalmsson, B 2023, ' Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth ', Nature Genetics, vol. 55, pp. 1807–1819 . https://doi.org/10.1038/s41588-023-01520-w
Beaumont, R N, Flatley, C, Vaudel, M, Wu, X, Chen, J, Moen, G H, Skotte, L, Helgeland, Ø, Solé-Navais, P, Banasik, K, Albiñana, C, Ronkainen, J, Fadista, J, Stinson, S E, Trajanoska, K, Wang, C A, Westergaard, D, Srinivasan, S, Sánchez-Soriano, C, Bilbao, J R, Allard, C, Groleau, M, Kuulasmaa, T, Leirer, D J, White, F, Jacques, P É, Cheng, H, Hao, K, Andreassen, O A, Åsvold, B O, Atalay, M, Bhatta, L, Bouchard, L, Brumpton, B M, Brunak, S, Bybjerg-Grauholm, J, Ebbing, C, Elliott, P, Engelbrechtsen, L, Erikstrup, C, Estarlich, M, Franks, S, Gaillard, R, Geller, F, Grove, J, Hougaard, D M, Kajantie, E, Morgen, C S, Nohr, E A, Nyegaard, M, Palmer, C N A, Pedersen, O B, Rivadeneira, F, Sebert, S, Shields, B M, Stoltenberg, C, Surakka, I, Thørner, L W, Ullum, H, Vaarasmaki, M, Vilhjalmsson, B J, Willer, C J, Lakka, T A, Gybel-Brask, D, Bustamante, M, Hansen, T, Pearson, E R, Reynolds, R M, Ostrowski, S R, Pennell, C E, Jaddoe, V W V, Felix, J F, Hattersley, A T, Melbye, M, Lawlor, D A, Hveem, K, Werge, T, Nielsen, H S, Magnus, P, Evans, D M, Jacobsson, B, Järvelin, M R, Zhang, G, Hivert, M F, Johansson, S, Freathy, R M, Feenstra, B & Njølstad, P R 2023, ' Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth ', Nature Genetics, vol. 55, no. 11, pp. 1807-1819 . https://doi.org/10.1038/s41588-023-01520-w
Nature Genetics

Subject Terms: Male, 2. Zero hunger, name=Genetics, Placenta, Birth Weight/genetics, Fetal Development/genetics, Article, 3. Good health, Fetal Development, SDG 3 - Good Health and Well-being, 5. Gender equality, Genetics, developmental biology, physiology, Pregnancy, Genetics research, Placenta/metabolism, Humans, Birth Weight, Insulin, Female, Genetic association study, Genome-Wide Association Study

File Description: application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/37798380
https://fisabio.portalinvestigacion.com/publicaciones/15719
https://fisabio.portalinvestigacion.com/publicaciones/16312
https://vbn.aau.dk/da/publications/9b60e609-9298-4cba-9cb4-263fa35899a7
https://vbn.aau.dk/ws/files/579866926/s41588-023-01520-w.pdf
https://doi.org/10.1038/s41588-023-01520-w
http://www.scopus.com/inward/record.url?scp=85173791824&partnerID=8YFLogxK
https://pure.eur.nl/en/publications/297fbb1e-6664-4929-9824-35d34dc8fc54
https://doi.org/10.1038/s41588-023-01520-w
http://hdl.handle.net/10852/105934
https://doi.org/10.1038/s41588-023-01520-w
http://hdl.handle.net/10044/1/108593
http://hdl.handle.net/10138/572424
https://pure.au.dk/ws/files/371287864/s41588-023-01520-w.pdf
https://research-information.bris.ac.uk/ws/files/381631870/64936_3_merged_1692965386.pdf
https://hdl.handle.net/1983/74cad765-97e5-4108-b6a0-6b305dd0c109
https://curis.ku.dk/ws/files/375629764/s41588_023_01520_w_2_.pdf
https://portal.findresearcher.sdu.dk/da/publications/8b4eccc1-7638-46f0-8f34-975e01d634e1
https://doi.org/10.1038/s41588-023-01520-w
https://pure.au.dk/ws/files/371287864/s41588-023-01520-w.pdf
https://doi.org/10.1038/s41588-023-01520-w
https://pure.au.dk/portal/en/publications/29f049c8-bbaa-4089-806d-66fa74a1cc94
http://www.scopus.com/inward/record.url?scp=85173791824&partnerID=8YFLogxK

The Association of the COL27A1 rs946053 and TNC rs2104772s with Tendinopathies: A Case–Control Study in High-Level Croatian Athletes

Authors: Goran Vrgoč Saša Janković Damir Knjaz et al.

Source: Genes. 16:935

Subject Terms: sport injury, collagen 27 alpha1, Achilles tendinopathy, genetic association study, tenascin C, single-nucleotide polymorphism (SNP), soft tissue injury (STI)