Genetics of height and risk of atrial fibrillation: A Mendelian randomization study
Levin, Michael G, Judy, Renae, Gill, Dipender, Vujkovic, Marijana, Verma, Shefali S, Bradford, Yuki, Ritchie, Marylyn D, Hyman, Matthew C, Nazarian, Saman, Rader, Daniel J, Voight, Benjamin F, Damrauer, Scott M
Published in PLoS medicine (08.10.2020)
Published in PLoS medicine (08.10.2020)
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A Genome-First Approach to Estimate Prevalence of Germline Pathogenic Variants and Risk of Pancreatic Cancer in Select Cancer Susceptibility Genes
Astiazaran-Symonds, Esteban, Kim, Jung, Haley, Jeremy S, Kim, Sun Young, Rao, H Shanker, Genetics Center, Regeneron, Carey, David J, Stewart, Douglas R, Goldstein, Alisa M
Published in Cancers (02.07.2022)
Published in Cancers (02.07.2022)
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Germline POT1 variants can predispose to myeloid and lymphoid neoplasms
Lim, Tristan L, Lieberman, David B, Davis, Adam R, Loren, Alison W, Hausler, Ryan, Bigdeli, Ashkan, Li, Yimei, Powers, Jacquelyn, Raper, Anna, Regeneron Genetics Center, Carty, Shannon A, Nathanson, Katherine L, Bagg, Adam, Hexner, Elizabeth O, Maxwell, Kara N, Morrissette, Jennifer J D, Babushok, Daria V
Published in Leukemia (01.01.2022)
Published in Leukemia (01.01.2022)
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Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort
Hui, Daniel, Mehrabi, Shadi, Quimby, Alexandra E, Chen, Tingfang, Chen, Sixing, Park, Joseph, Li, Binglan, Ruckenstein, Michael J, Rader, Daniel J, Ritchie, Marylyn D, Brant, Jason A, Epstein, Douglas J, Mathieson, Iain
Published in PLoS genetics (19.01.2023)
Published in PLoS genetics (19.01.2023)
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Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals
Gao, Chuan, Marcketta, Anthony, Backman, Joshua D., O'Dushlaine, Colm, Staples, Jeffrey, Ferreira, Manuel Allen Revez, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Mirshahi, Tooraj, Regeneron Genetics Center, Geisinger Regeneron Discovehr Collaboration, Baras, Aris, Abecasis, Gonçalo, Shuldiner, Alan R., Van Hout, Cristopher V., McCarthy, Shane
Published in Genetic epidemiology (01.09.2021)
Published in Genetic epidemiology (01.09.2021)
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Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies
Cavazos, Taylor B, Kachuri, Linda, Graff, Rebecca E, Nierenberg, Jovia L, Thai, Khanh K, Alexeeff, Stacey, Van Den Eeden, Stephen, Corley, Douglas A, Kushi, Lawrence H, Hoffmann, Thomas J, Ziv, Elad, Habel, Laurel A, Jorgenson, Eric, Sakoda, Lori C, Witte, John S
Published in BMC medicine (06.10.2022)
Published in BMC medicine (06.10.2022)
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Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank
Park, Joseph, MacLean, Matthew T., Lucas, Anastasia M., Torigian, Drew A., Schneider, Carolin V., Cherlin, Tess, Xiao, Brenda, Miller, Jason E., Bradford, Yuki, Judy, Renae L., Verma, Anurag, Damrauer, Scott M., Ritchie, Marylyn D., Witschey, Walter R., Rader, Daniel J.
Published in Cell reports. Medicine (20.12.2022)
Published in Cell reports. Medicine (20.12.2022)
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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Shah, Sonia, Roselli, Carolina, Lin, Honghuang, Fatemifar, Ghazaleh, Hedman, Åsa K, Morley, Michael P, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Ärnlöv, Johan, Backman, Joshua D, Biggs, Mary L, Bloom, Heather L, Brown, Michael R, Buckbinder, Leonard, Chasman, Daniel I, Chen, Xing, Chen, Xu, Chung, Jonathan, Chutkow, William, Delgado, Graciela E, Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C, Dunn, Michael E, Felix, Stephan B, Finan, Chris, Ghanbari, Mohsen, Ghasemi, Sahar, Giedraitis, Vilmantas, Giulianini, Franco, Gottdiener, John S, Gross, Stefan, Guðbjartsson, Daníel F, van der Harst, Pim, Hyde, Craig L, Ingelsson, Erik, Jukema, J Wouter, Khaw, Kay-Tee, Kleber, Marcus E, Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, London, Barry, Lovering, Ruth C, Luan, Jian'an, Magnusson, Patrik, Mahajan, Anubha, Melander, Olle, Mordi, Ify R, Morgan, Thomas, Morris, Andrew D, Morris, Andrew P, Morrison, Alanna C, Nagle, Michael W, Niessner, Alexander, O'Donoghue, Michelle L, Owens, Anjali T, Palmer, Colin N A, Parry, Helen M, Portilla-Fernandez, Eliana, Psaty, Bruce M, Rice, Kenneth M, Ridker, Paul M, Romaine, Simon P R, Salo, Perttu, Salomaa, Veikko, Smith, Nicholas L, Stender, Steen, Stott, David J, Svensson, Per, Taylor, Kent D, Teumer, Alexander, Thorgeirsson, Guðmundur, Thorsteinsdottir, Unnur, Tyl, Benoit, Uitterlinden, Andre G, Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A, Wang, Xiaosong, Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L, Xing, Heming, Yerges-Armstrong, Laura M, Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, Samani, Nilesh J, Malarstig, Anders, Asselbergs, Folkert W, Kuchenbaecker, Karoline, Lang, Chim C, Stefansson, Kari, Smith, J Gustav, Swerdlow, Daniel I, Lumbers, R Thomas
Published in Nature communications (2020)
Published in Nature communications (2020)
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Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
Horowitz, Julie E, Kosmicki, Jack A, Damask, Amy, Sharma, Deepika, Roberts, Genevieve H L, Justice, Anne E, Banerjee, Nilanjana, Coignet, Marie V, Yadav, Ashish, Leader, Joseph B, Marcketta, Anthony, Park, Danny S, Lanche, Rouel, Maxwell, Evan, Knight, Spencer C, Bai, Xiaodong, Guturu, Harendra, Sun, Dylan, Baltzell, Asher, Kury, Fabricio S P, Backman, Joshua D, Girshick, Ahna R, O'Dushlaine, Colm, McCurdy, Shannon R, Partha, Raghavendran, Mansfield, Adam J, Turissini, David A, Li, Alexander H, Zhang, Miao, Mbatchou, Joelle, Watanabe, Kyoko, Gurski, Lauren, McCarthy, Shane E, Kang, Hyun M, Dobbyn, Lee, Stahl, Eli, Verma, Anurag, Sirugo, Giorgio, Ritchie, Marylyn D, Jones, Marcus, Balasubramanian, Suganthi, Siminovitch, Katherine, Salerno, William J, Shuldiner, Alan R, Rader, Daniel J, Mirshahi, Tooraj, Locke, Adam E, Marchini, Jonathan, Overton, John D, Carey, David J, Habegger, Lukas, Cantor, Michael N, Rand, Kristin A, Hong, Eurie L, Reid, Jeffrey G, Ball, Catherine A, Baras, Aris, Abecasis, Gonçalo R, Ferreira, Manuel A R
Published in Nature genetics (01.04.2022)
Published in Nature genetics (01.04.2022)
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Polygenic risk scores for mood disorders predict future strokes in women: a Mendelian randomization study
Goncalves, I, Borne, Y, Edsfeldt, A, Wang, Y, Pan, M, Regeneron Genetics Center, Mellander, O, Engstrom, G, Sun, J
Published in European heart journal (03.10.2022)
Published in European heart journal (03.10.2022)
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Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
Mansour Aly, Dina, Dwivedi, Om Prakash, Prasad, Rashmi B, Käräjämäki, Annemari, Hjort, Rebecka, Thangam, Manonanthini, Åkerlund, Mikael, Mahajan, Anubha, Udler, Miriam S, Florez, Jose C, McCarthy, Mark I, Brosnan, Julia, Melander, Olle, Carlsson, Sofia, Hansson, Ola, Tuomi, Tiinamaija, Groop, Leif, Ahlqvist, Emma
Published in Nature genetics (01.11.2021)
Published in Nature genetics (01.11.2021)
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Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
Jurgens, Sean J, Choi, Seung Hoan, Morrill, Valerie N, Chaffin, Mark, Pirruccello, James P, Halford, Jennifer L, Weng, Lu-Chen, Nauffal, Victor, Roselli, Carolina, Hall, Amelia W, Oetjens, Matthew T, Lagerman, Braxton, vanMaanen, David P, Aragam, Krishna G, Lunetta, Kathryn L, Haggerty, Christopher M, Lubitz, Steven A, Ellinor, Patrick T
Published in Nature genetics (01.03.2022)
Published in Nature genetics (01.03.2022)
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47. EXOME-WIDE ASSOCIATION STUDY IN ∼750,000 INDIVIDUALS IDENTIFIES CHRNB2 AS A POTENTIAL DRUG TARGET FOR SMOKING
Rajagopal, Veera, Sharma, Deepika, Kessler, Michael, Jorgenson, Eric, Cantor, Michael, Regeneron Genetics Center, DiscovEHR Collaboration, Baras, Aris, Coppola, Giovanni
Published in European neuropsychopharmacology (01.10.2022)
Published in European neuropsychopharmacology (01.10.2022)
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Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
Yu Chen, Hao, Dina, Christian, Small, Aeron M, Shaffer, Christian M, Levinson, Rebecca T, Helgadóttir, Anna, Capoulade, Romain, Munter, Hans Markus, Martinsson, Andreas, Cairns, Benjamin J, Trudsø, Linea C, Hoekstra, Mary, Burr, Hannah A, Marsh, Thomas W, Damrauer, Scott M, Dufresne, Line, Le Scouarnec, Solena, Messika-Zeitoun, David, Ranatunga, Dilrini K, Whitmer, Rachel A, Bonnefond, Amélie, Sveinbjornsson, Garðar, Daníelsen, Ragnar, Arnar, David O, Thorgeirsson, Gudmundur, Thorsteinsdottir, Unnur, Gudbjartsson, Daníel F, Hólm, Hilma, Ghouse, Jonas, Olesen, Morten Salling, Christensen, Alex H, Mikkelsen, Susan, Jacobsen, Rikke Louise, Dowsett, Joseph, Pedersen, Ole Birger Vesterager, Erikstrup, Christian, Ostrowski, Sisse R, O’Donnell, Christopher J, Budoff, Matthew J, Gudnason, Vilmundur, Post, Wendy S, Rotter, Jerome I, Lathrop, Mark, Bundgaard, Henning, Johansson, Bengt, Ljungberg, Johan, Näslund, Ulf, Le Tourneau, Thierry, Smith, J Gustav, Wells, Quinn S, Söderberg, Stefan, Stefánsson, Kári, Schott, Jean-Jacques, Rader, Daniel J, Clarke, Robert, Engert, James C, Thanassoulis, George
Published in European heart journal (01.06.2023)
Published in European heart journal (01.06.2023)
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Thrombomodulin (THBD) gene variants and thrombotic risk in a population‐based cohort study
Manderstedt, Eric, Halldén, Christer, Lind‐Halldén, Christina, Elf, Johan, Svensson, Peter J., Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A., Zöller, Bengt
Published in Journal of thrombosis and haemostasis (01.04.2022)
Published in Journal of thrombosis and haemostasis (01.04.2022)
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Association of Inherited Mutations in DNA Repair Genes with Localized Prostate Cancer
Lee, Daniel J., Hausler, Ryan, Le, Anh N., Kelly, Gregory, Powers, Jacquelyn, Ding, James, Feld, Emily, Desai, Heena, Morrison, Casey, Doucette, Abigail, Gabriel, Peter, Genetics Center, Regeneron, Judy, Renae L., Weaver, Joellen, Kember, Rachel, Damrauer, Scott M., Rader, Daniel J., Domchek, Susan M., Narayan, Vivek, Schwartz, Lauren E., Maxwell, Kara N.
Published in European urology (01.06.2022)
Published in European urology (01.06.2022)
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Prediction of Kv11.1 potassium channel PAS-domain variants trafficking via machine learning
Immadisetty, Kalyan, Fang, Xuan, Ramon, Geraldine San, Hartle, Cassandra M., McCoy, Thomas P., Center, Regeneron Genetics, Mirshahi, Tooraj, Delisle, Brian P., Kekenes-Huskey, Peter M.
Published in Journal of molecular and cellular cardiology (01.07.2023)
Published in Journal of molecular and cellular cardiology (01.07.2023)
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