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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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HPA axis in major depression: cortisol, clinical symptomatology and genetic variation predict cognition
Keller, J, Gomez, R, Williams, G, Lembke, A, Lazzeroni, L, Murphy, G M, Schatzberg, A F
Published in Molecular psychiatry (01.04.2017)
Published in Molecular psychiatry (01.04.2017)
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Analysis of protein-coding genetic variation in 60,706 humans
Lek, Monkol, Karczewski, Konrad J., Minikel, Eric V., Samocha, Kaitlin E., Banks, Eric, Fennell, Timothy, O’Donnell-Luria, Anne H., Ware, James S., Hill, Andrew J., Cummings, Beryl B., Tukiainen, Taru, Birnbaum, Daniel P., Kosmicki, Jack A., Duncan, Laramie E., Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N., Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I., Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M., Poplin, Ryan, Rivas, Manuel A., Ruano-Rubio, Valentin, Rose, Samuel A., Ruderfer, Douglas M., Shakir, Khalid, Stenson, Peter D., Stevens, Christine, Thomas, Brett P., Tiao, Grace, Tusie-Luna, Maria T., Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M., Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C., Gabriel, Stacey B., Getz, Gad, Glatt, Stephen J., Hultman, Christina M., Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I., McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M., Palotie, Aarno, Purcell, Shaun M., Saleheen, Danish, Scharf, Jeremiah M., Sklar, Pamela, Sullivan, Patrick F., Tuomilehto, Jaakko, Tsuang, Ming T., Watkins, Hugh C., Wilson, James G., Daly, Mark J., MacArthur, Daniel G.
Published in Nature (London) (18.08.2016)
Published in Nature (London) (18.08.2016)
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Common genetic variation in GLP1R and insulin secretion in response to exogenous GLP-1 in nondiabetic subjects: a pilot study
Sathananthan, Airani, Man, Chiara Dalla, Micheletto, Francesco, Zinsmeister, Alan R, Camilleri, Michael, Giesler, Paula D, Laugen, Jeanette M, Toffolo, Gianna, Rizza, Robert A, Cobelli, Claudio, Vella, Adrian
Published in Diabetes care (01.09.2010)
Published in Diabetes care (01.09.2010)
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Genetic variation in catechol‐O‐methyltransferase is associated with individual differences in conditioned pain modulation in healthy subjects
Korczeniewska, Olga A., Kuo, Fengshen, Huang, Ching‐Yu, Nasri‐Heir, Cibele, Khan, Junad, Benoliel, Rafael, Hirschberg, Craig, Eliav, Eli, Diehl, Scott R.
Published in The journal of gene medicine (01.11.2021)
Published in The journal of gene medicine (01.11.2021)
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Genetic Variation in KCNQ1 Associates With Fasting Glucose and β-Cell Function: A Study of 3,734 Subjects Comprising Three Ethnicities Living in Singapore
TAN, Jonathan T, NURBAYA, Siti, GARDENER, Daphne, YE, Sandra, TAI, E. Shyong, NG, Daniel P. K
Published in Diabetes (New York, N.Y.) (01.06.2009)
Published in Diabetes (New York, N.Y.) (01.06.2009)
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Effect of CES1 genetic variation on enalapril steady‐state pharmacokinetics and pharmacodynamics in healthy subjects
Her, Lucy H., Wang, Xinwen, Shi, Jian, Choi, Hee Jae, Jung, Sun Min, Smith, Logan S., Wu, Audrey H., Bleske, Barry E., Zhu, Hao‐Jie
Published in British journal of clinical pharmacology (01.12.2021)
Published in British journal of clinical pharmacology (01.12.2021)
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Common genetic variation influencing human white matter microstructure
Zhao, Bingxin, Li, Tengfei, Yang, Yue, Wang, Xifeng, Luo, Tianyou, Shan, Yue, Zhu, Ziliang, Xiong, Di, Hauberg, Mads E., Bendl, Jaroslav, Fullard, John F., Roussos, Panagiotis, Li, Yun, Stein, Jason L., Zhu, Hongtu
Published in Science (American Association for the Advancement of Science) (18.06.2021)
Published in Science (American Association for the Advancement of Science) (18.06.2021)
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A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts
Lindström, Sara, Loomis, Stephanie, Turman, Constance, Huang, Hongyan, Huang, Jinyan, Aschard, Hugues, Chan, Andrew T., Choi, Hyon, Cornelis, Marilyn, Curhan, Gary, De Vivo, Immaculata, Eliassen, A. Heather, Fuchs, Charles, Gaziano, Michael, Hankinson, Susan E., Hu, Frank, Jensen, Majken, Kang, Jae H., Kabrhel, Christopher, Liang, Liming, Pasquale, Louis R., Rimm, Eric, Stampfer, Meir J., Tamimi, Rulla M., Tworoger, Shelley S., Wiggs, Janey L., Hunter, David J., Kraft, Peter
Published in PloS one (16.03.2017)
Published in PloS one (16.03.2017)
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Genetic variation in a human odorant receptor alters odour perception
Keller, Andreas, Zhuang, Hanyi, Chi, Qiuyi, Vosshall, Leslie B., Matsunami, Hiroaki
Published in Nature (27.09.2007)
Published in Nature (27.09.2007)
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Genetic variation in PNPLA3 (adiponutrin) confers sensitivity to weight loss-induced decrease in liver fat in humans
Sevastianova, Ksenia, Kotronen, Anna, Gastaldelli, Amalia, Perttilä, Julia, Hakkarainen, Antti, Lundbom, Jesper, Suojanen, Laura, Orho-Melander, Marju, Lundbom, Nina, Ferrannini, Eleuterio, Rissanen, Aila, Olkkonen, Vesa M, Yki-Järvinen, Hannele
Published in The American journal of clinical nutrition (01.07.2011)
Published in The American journal of clinical nutrition (01.07.2011)
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An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
Petrovski, Slavé, Todd, Jamie L., Durheim, Michael T., Wang, Quanli, Chien, Jason W., Kelly, Fran L., Frankel, Courtney, Mebane, Caroline M., Ren, Zhong, Bridgers, Joshua, Urban, Thomas J., Malone, Colin D., Finlen Copeland, Ashley, Brinkley, Christie, Allen, Andrew S., O’Riordan, Thomas, McHutchison, John G., Palmer, Scott M., Goldstein, David B.
Published in American journal of respiratory and critical care medicine (01.07.2017)
Published in American journal of respiratory and critical care medicine (01.07.2017)
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How Natural Genetic Variation Shapes Behavior
Niepoth, Natalie, Bendesky, Andres
Published in Annual review of genomics and human genetics (31.08.2020)
Published in Annual review of genomics and human genetics (31.08.2020)
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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
Scott, Eric M, Halees, Anason, Itan, Yuval, Spencer, Emily G, He, Yupeng, Azab, Mostafa Abdellateef, Gabriel, Stacey B, Belkadi, Aziz, Boisson, Bertrand, Abel, Laurent, Clark, Andrew G, Alkuraya, Fowzan S, Casanova, Jean-Laurent, Gleeson, Joseph G
Published in Nature genetics (01.09.2016)
Published in Nature genetics (01.09.2016)
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Model of genetic variation in human social networks
Fowler, James H, Dawes, Christopher T, Christakis, Nicholas A
Published in Proceedings of the National Academy of Sciences - PNAS (10.02.2009)
Published in Proceedings of the National Academy of Sciences - PNAS (10.02.2009)
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Genetic variation in taste perception: does it have a role in healthy eating?
Feeney, E., O'Brien, S., Scannell, A., Markey, A., Gibney, E. R.
Published in Proceedings of the Nutrition Society (01.02.2011)
Published in Proceedings of the Nutrition Society (01.02.2011)
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DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits
Oliva, Meritxell, Demanelis, Kathryn, Lu, Yihao, Chernoff, Meytal, Jasmine, Farzana, Ahsan, Habibul, Kibriya, Muhammad G., Chen, Lin S., Pierce, Brandon L.
Published in Nature genetics (01.01.2023)
Published in Nature genetics (01.01.2023)
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Evolution via somatic genetic variation in modular species
Reusch, Thorsten B.H., Baums, Iliana B., Werner, Benjamin
Published in Trends in ecology & evolution (Amsterdam) (01.12.2021)
Published in Trends in ecology & evolution (Amsterdam) (01.12.2021)
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Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy
Refaat, Marwan M., Lubitz, Steven A., Makino, Seiko, Islam, Zahid, Frangiskakis, J. Michael, Mehdi, Haider, Gutmann, Rebecca, Zhang, Michael L., Bloom, Heather L., MacRae, Calum A., Dudley, Samuel C., Shalaby, Alaa A., Weiss, Raul, McNamara, Dennis M., London, Barry, Ellinor, Patrick T.
Published in Heart rhythm (01.03.2012)
Published in Heart rhythm (01.03.2012)
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