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Genetic Variance in Heparan Sulfation Is Associated With Salt Sensitivity
Oppelaar, Jetta J., Ferwerda, Bart, Romman, Mohamed A., Sahebdin, Ghazalah N., Zwinderman, Aeilko H., Galenkamp, Henrike, Boekholdt, S. Matthijs, van den Born, Bert-Jan H., Olde Engberink, Rik H.G., Vogt, Liffert
Published in Hypertension (Dallas, Tex. 1979) (01.10.2024)
Published in Hypertension (Dallas, Tex. 1979) (01.10.2024)
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Genetic variance in human disease – modelling the future of genomic medicine
Lek, Monkol, Hmeljak, Julija, Hooper, Kirsty M.
Published in Disease models & mechanisms (01.06.2022)
Published in Disease models & mechanisms (01.06.2022)
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Abstract 72: Genetic variance in heparan sulfation is associated with salt-sensitivity: a gene-environment analysis in EPIC-Norfolk, UK biobank, and HELIUS
Oppelaar, Jetta, Romman, Mohamed, Sahebdin, Ghazalah, Zwinderman, Aeilko, Galenkamp, Henrike, Boekholdt, S, Van den Born, Bert-Jan, Olde Engberink, Rik, Vogt, Liffert
Published in Hypertension (Dallas, Tex. 1979) (01.09.2024)
Published in Hypertension (Dallas, Tex. 1979) (01.09.2024)
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Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia
Hysi, Pirro G., Choquet, Hélène, Khawaja, Anthony P., Wojciechowski, Robert, Tedja, Milly S., Yin, Jie, Simcoe, Mark J., Patasova, Karina, Mahroo, Omar A., Thai, Khanh K., Cumberland, Phillippa M., Melles, Ronald B., Verhoeven, Virginie J. M., Vitart, Veronique, Segre, Ayellet, Stone, Richard A., Wareham, Nick, Hewitt, Alex W., Mackey, David A., Klaver, Caroline C. W., MacGregor, Stuart, Khaw, Peng T., Foster, Paul J., Guggenheim, Jeremy A., Rahi, Jugnoo S., Jorgenson, Eric, Hammond, Christopher J.
Published in Nature genetics (01.04.2020)
Published in Nature genetics (01.04.2020)
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An Erythroid Enhancer of BCL11A Subject to Genetic Variation Determines Fetal Hemoglobin Level
Bauer, Daniel E., Kamran, Sophia C., Lessard, Samuel, Xu, Jian, Fujiwara, Yuko, Lin, Carrie, Shao, Zhen, Canver, Matthew C., Smith, Elenoe C., Pinello, Luca, Sabo, Peter J., Vierstra, Jeff, Voit, Richard A., Yuan, Guo-Cheng, Porteus, Matthew H., Stamatoyannopoulos, John A., Lettre, Guillaume, Orkin, Stuart H.
Published in Science (American Association for the Advancement of Science) (11.10.2013)
Published in Science (American Association for the Advancement of Science) (11.10.2013)
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Murine genetic variance in muscarinic cholinergic receptor antagonism of sucrose and saccharin solution intakes in three inbred mouse strains
Bourie, Faye, Olsson, Kerstin, Iskhakov, Ben, Buras, Agata, Fazilov, Gabriela, Shenouda, Merna, Zhezherya, Julia, Bodnar, Richard J.
Published in Pharmacology, biochemistry and behavior (01.12.2017)
Published in Pharmacology, biochemistry and behavior (01.12.2017)
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Genome-wide analyses of behavioural traits are subject to bias by misreports and longitudinal changes
Xue, Angli, Jiang, Longda, Zhu, Zhihong, Wray, Naomi R., Visscher, Peter M., Zeng, Jian, Yang, Jian
Published in Nature communications (12.01.2021)
Published in Nature communications (12.01.2021)
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Sex-specific additive genetic variances and correlations for fitness in a song sparrow (Melospiza melodia) population subject to natural immigration and inbreeding
Wolak, Matthew E., Arcese, Peter, Keller, Lukas F., Nietlisbach, Pirmin, Reid, Jane M.
Published in Evolution (01.10.2018)
Published in Evolution (01.10.2018)
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Genetic variance of transforming growth factor β2 gene in conotruncal heart defects
Chen, Yu, Zhang, Rui, Xie, Jun, Li, Yajiao, Shi, Shaoqing, Qian, Hong, Yan, Zhiguo, Rao, Li
Published in Biomarkers (19.05.2017)
Published in Biomarkers (19.05.2017)
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Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects
van Eijk, Kristel R, de Jong, Simone, Boks, Marco PM, Langeveld, Terry, Colas, Fabrice, Veldink, Jan H, de Kovel, Carolien GF, Janson, Esther, Strengman, Eric, Langfelder, Peter, Kahn, René S, van den Berg, Leonard H, Horvath, Steve, Ophoff, Roel A
Published in BMC genomics (17.11.2012)
Published in BMC genomics (17.11.2012)
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Possible Association Between OPRM1 Genetic Variance at the 118 Locus and Alcohol Dependence in a Large Treatment Sample: Relationship to Alcohol Dependence Symptoms
Koller, Gabriele, Zill, Peter, Rujescu, Dan, Ridinger, Monika, Pogarell, Oliver, Fehr, Christoph, Wodarz, Norbert, Bondy, Brigitta, Soyka, Michael, Preuss, Ulrich W.
Published in Alcoholism, clinical and experimental research (01.07.2012)
Published in Alcoholism, clinical and experimental research (01.07.2012)
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Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID-19
López-Rodríguez, Rosario, Del Pozo-Valero, Marta, Corton, Marta, Minguez, Pablo, Ruiz-Hornillos, Javier, Pérez-Tomás, María Elena, Barreda-Sánchez, María, Mancebo, Esther, Villaverde, Cristina, Núñez-Moreno, Gonzalo, Romero, Raquel, Paz-Artal, Estela, Guillén-Navarro, Encarna, Almoguera, Berta, Ayuso, Carmen
Published in Scientific reports (20.06.2022)
Published in Scientific reports (20.06.2022)
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Prevalence and prognosis of genetically proven familial hypercholesterolemia in subjects with coronary artery disease and reduced ejection fraction
Lee, Wen-Jane, Chuang, Han-Ni, Hsiao, Tzu-Hung, Lee, Wen-Lieng, Wu, Jen-Pey, Sheu, Wayne H.-H., Liang, Kae-Woei
Published in Scientific reports (07.10.2023)
Published in Scientific reports (07.10.2023)
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