檢索結果 - Adam E. Locke
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An Excess of Deleterious Variants in VEGF-A Pathway Genes in Down-Syndrome-Associated Atrioventricular Septal Defects 由 C. Ackerman, Adam E. Locke, Eleanor Feingold, Benjamin Reshey, Karina España, Janita Thusberg, Sean D. Mooney, Lora Jh Bean, Kenneth J. Dooley, L. Clifford, Roger H. Reeves, Stephanie L. Sherman, Cheryl L. Maslen
出版 2012Artigo -
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Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project 由 Sallie B. Freeman, Lora Bean, Emily G. Allen, Stuart W. Tinker, Adam E. Locke, Charlotte M. Druschel, Charlotte A. Hobbs, Paul A. Romitti, Marjorie H. Royle, Claudine P. Torfs, Kenneth J. Dooley, Stephanie L. Sherman
出版 2008Artigo -
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Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome 由 Adam E. Locke, Kenneth J. Dooley, Stuart W. Tinker, Soo Yeon Cheong, Eleanor Feingold, Emily G. Allen, Sallie B. Freeman, Claudine P. Torfs, L. Clifford, Michael P. Epstein, Michael C. Wu, Xihong Lin, George Capone, Stephanie L. Sherman, Lora Jh Bean
出版 2010Artigo -
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Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: A report from the National Down Syndrome Project 由 Lora Jh Bean, Emily G. Allen, Stuart W. Tinker, NaTasha D. Hollis, Adam E. Locke, Charlotte M. Druschel, Charlotte A. Hobbs, Leslie A. O’Leary, Paul A. Romitti, Marjorie H. Royle, Claudine P. Torfs, Kenneth J. Dooley, Sallie B. Freeman, Stephanie L. Sherman
出版 2011Artigo -
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Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study 由 James P. Davis, Jeroen R. Huyghe, Adam E. Locke, Anne Jackson, Xueling Sim, Heather M. Stringham, Tanya M. Teslovich, Ryan Welch, Christian Fuchsberger, Narisu Narisu, Peter S. Chines, Antti J. Kangas, Pasi Soininen, Mika Ala‐Korpela, Johanna Kuusisto, Francis S. Collins, Markku Laakso, Michael Boehnke, Karen L. Mohlke
出版 2017Artigo -
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Next-generation genotype imputation service and methods 由 Sayantan Das, Lukas Forer, Sebastian Schönherr, Carlo Sidore, Adam E. Locke, Alan Kwong, Scott Vrieze, Emily Y. Chew, Shawn Levy, Matt McGue, David Schlessinger, Dwight Stambolian, Po‐Ru Loh, William G. Iacono, Anand Swaroop, Laura J. Scott, Francesco Cucca, Florian Kronenberg, Michael Boehnke, Gonçalo R. Abecasis, Christian Fuchsberger
出版 2016Artigo -
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Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution 由 Ying Wu, K. Alaine Broadaway, Chelsea K. Raulerson, Laura J. Scott, Calvin Pan, Arthur Ko, Aiqing He, Charles Tilford, Christian Fuchsberger, Adam E. Locke, Heather M. Stringham, Anne Jackson, Narisu Narisu, Johanna Kuusisto, Päivi Pajukanta, Francis S. Collins, Michael Boehnke, Markku Laakso, Aldons J. Lusis, Mete Civelek, Karen L. Mohlke
出版 2019Artigo -
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Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity 由 Sara Hägg, Andrea Ganna, Sander W. van der Laan, Tõnu Esko, Tune H. Pers, Adam E. Locke, Sonja I. Berndt, Anne E. Justice, Bratati Kahali, Marten A. Siemelink, Gerard Pasterkamp, David P. Strachan, Elizabeth K. Speliotes, Kari E. North, Ruth J. F. Loos, Joel N. Hirschhorn, Yudi Pawitan, Erik Ingelsson
出版 2015Revisão -
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Quality control and conduct of genome-wide association meta-analyses 由 Thomas W Winkler, Felix R. Day, Damien C. Croteau‐Chonka, Andrew R. Wood, Adam E. Locke, Reedik Mägi, Teresa Ferreira, Tove Fall, Mariaelisa Graff, Anne E. Justice, Jian’an Luan, Stefan Gustafsson, Joshua C. Randall, Sailaja Vedantam, Tsegaselassie Workalemahu, Tuomas O. Kilpeläinen, André Scherag, Tõnu Esko, Zoltán Kutalik, Iris M. Heid, Ruth J. F. Loos
出版 2014Artigo -
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Exome Sequencing of Familial Bipolar Disorder 由 Fernando S. Goes, Mehdi Pirooznia, Jennifer Parla, Melissa Kramer, Elena Ghiban, Senem Mavruk, Yun-Ching Chen, Eric T. Monson, Virginia L. Willour, Rachel Karchin, Matthew Flickinger, Adam E. Locke, Shawn Levy, Laura J. Scott, Michael Boehnke, Eli Stahl, Jennifer L. Moran, Christina M. Hultman, Mikael Landén, Shaun Purcell, Pamela Sklar, Peter P. Zandi, W. Richard McCombie, James B. Potash
出版 2016Revisão -
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Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits 由 Chelsea K. Raulerson, Arthur Ko, John Kidd, Kevin W. Currin, Sarah M. Brotman, Maren E. Cannon, Ying Wu, Cassandra N. Spracklen, Anne Jackson, Heather M. Stringham, Ryan Welch, Christian Fuchsberger, Adam E. Locke, Narisu Narisu, Aldons J. Lusis, Mete Civelek, Terrence S. Furey, Johanna Kuusisto, Francis S. Collins, Michael Boehnke, Laura J. Scott, D. Y. Lin, Michael I. Love, Markku Laakso, Päivi Pajukanta, Karen L. Mohlke
出版 2019Artigo -
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Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans 由 Jedidiah Carlson, Adam E. Locke, Matthew Flickinger, Matthew Zawistowski, Shawn Levy, R Myers, Michael Boehnke, Hyun Min Kang, Laura J. Scott, Jun Z. Li, Sebastian Zöllner, Devin Absher, Huda Akil, Gerome Breen, Margit Burmeister, Sarah Cohen‐Woods, William G. Iacono, James A. Knowles, Lisa N. Legrand, Qing Lu, Matthew McGue, Melvin G. McInnis, Carlos N. Pato, Michele T. Pato, Margarita Rivera, Janet L. Sobell, John B. Vincent, Stanley J. Watson
出版 2018Artigo -
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Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk 由 Xianyong Yin, Debraj Bose, Annie Kwon, Sarah C. Hanks, Anne Jackson, Heather M. Stringham, Ryan Welch, Anniina Oravilahti, Lilian Fernandes Silva, Adam E. Locke, Christian Fuchsberger, Susan K. Service, Michael R. Erdos, Lori L. Bonnycastle, Johanna Kuusisto, Nathan O. Stitziel, Ira M. Hall, Jean Morrison, Samuli Ripatti, Aarno Palotie, Nelson B. Freimer, Francis S. Collins, Karen L. Mohlke, Laura J. Scott, Eric B. Fauman, Charles Burant, Michael Boehnke, Markku Laakso, Xiaoquan Wen
出版 2022Artigo -
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Interaction between the <i>FTO</i> gene, body mass index and depression: meta-analysis of 13701 individuals 由 Margarita Rivera, Adam E. Locke, Tanguy Corre, Darina Czamara, Christiane Wolf, Ana Ching-López, Yuri Milaneschi, Stefan Kloiber, Sarah Cohen‐Woods, James Rucker, Katherine J. Aitchison, Sven Bergmann, Dorret I. Boomsma, Nick Craddock, Michael Gill, Herta Flor, Jouke‐Jan Hottenga, Ania Korszun, Zoltán Kutalik, Susanne Lucae, Wolfgang Maier, Ole Mors, Bertram Müller‐Myhsok, Michael J. Owen, Brenda W.J.H. Penninx, Martin Preisig, John P. Rice, Marcella Rietschel, Federica Tozzi, Rudolf Uher, Péter Vollenweider, Gérard Waeber, Gonneke Willemsen, Ian Craig, Anne Farmer, Cathryn M. Lewis, Gerome Breen, Peter McGuffin
出版 2017Revisão -
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Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci 由 Xianyong Yin, Lap Sum Chan, Debraj Bose, Anne Jackson, Peter VandeHaar, Adam E. Locke, Christian Fuchsberger, Heather M. Stringham, Ryan Welch, Ketian Yu, Lilian Fernandes Silva, Susan K. Service, Daiwei Zhang, Emily C. Hector, Erica P. Young, Liron Ganel, Indraniel Das, Haley Abel, Michael R. Erdos, Lori L. Bonnycastle, Johanna Kuusisto, Nathan O. Stitziel, Ira M. Hall, Gregory R. Wagner, Jian Kang, Jean Morrison, Charles Burant, Francis S. Collins, Samuli Ripatti, Aarno Palotie, Nelson B. Freimer, Karen L. Mohlke, Laura J. Scott, Xiaoquan Wen, Eric B. Fauman, Markku Laakso, Michael Boehnke
出版 2022Artigo -
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Exome sequencing and analysis of 454,787 UK Biobank participants 由 Joshua Backman, Alexander Li, Anthony Marcketta, Dylan Sun, Joelle Mbatchou, Michael D. Kessler, Christian Benner, Daren Liu, Adam E. Locke, Suganthi Balasubramanian, Ashish Yadav, Nilanjana Banerjee, Christopher E. Gillies, Amy Damask, Simon Liu, Xiaodong Bai, Alicia Hawes, Evan K. Maxwell, Lauren Gurski, Kyoko Watanabe, Jack A. Kosmicki, Veera M. Rajagopal, Jason Mighty, Marcus B. Jones, Lyndon J. Mitnaul, Eli A. Stahl, Giovanni Coppola, Eric Jorgenson, Lukas Habegger, William Salerno, Alan R. Shuldiner, Luca A. Lotta, John D. Overton, Michael Cantor, Jeffrey G. Reid, George D. Yancopoulos, Hyun Min Kang, Jonathan Marchini, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira
出版 2021Artigo -
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Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk 由 Aaron P. Thrift, Jian Gong, Ulrike Peters, Jenny Chang‐Claude, Anja Rudolph, Martha L. Slattery, Andrew T. Chan, Adam E. Locke, Bratati Kahali, Anne E. Justice, Tune H. Pers, Steven Gallinger, Richard B. Hayes, John A. Baron, Bette J. Caan, Shuji Ogino, Sonja I. Berndt, Stephen J. Chanock, Graham Casey, Robert W. Haile, Mengmeng Du, Tabitha A. Harrison, Mark Thornquist, David Duggan, Loı̈c Le Marchand, Noralane M. Lindor, Daniela Seminara, Mingyang Song, Kana Wu, Stephen N. Thibodeau, Michelle Cotterchio, Aung Ko Win, Mark A. Jenkins, John L. Hopper, Cornelia M. Ulrich, John D. Potter, Polly A. Newcomb, Michael Hoffmeister, Hermann Brenner, Emily White, Li Hsu, Peter T. Campbell
出版 2015Artigo -
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Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum 由 Andrea Ganna, F. Kyle Satterstrom, Seyedeh M. Zekavat, Indraniel Das, Mitja Kurki, Tracy Air, Jessica Alföldi, Alicia R. Martin, Aki S. Havulinna, Andrea Byrnes, Wesley K. Thompson, Philip Nielsen, Konrad J. Karczewski, Elmo Saarentaus, Manuel A. Rivas, Namrata Gupta, Olli Pietiläinen, Connor A. Emdin, Francesco Lescai, Jonas Bybjerg‐Grauholm, Jason Flannick, Josep M. Mercader, Miriam S. Udler, Markku Laakso, Veikko Salomaa, Christina M. Hultman, Samuli Ripatti, Eija Hämäläinen, Jukka S. Moilanen, Jarmo Körkkö, Outi Kuismin, Merete Nordentoft, David M. Hougaard, Ole Mors, Thomas Werge, Preben Bo Mortensen, Daniel G. MacArthur, Mark J. Daly, Patrick F. Sullivan, Adam E. Locke, Aarno Palotie, Anders D. Børglum, Sekar Kathiresan, Benjamin M. Neale
出版 2018Artigo -
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Exome sequencing of Finnish isolates enhances rare-variant association power 由 Adam E. Locke, Karyn Meltz Steinberg, Charleston W. K. Chiang, Susan K. Service, Aki S. Havulinna, Laurel Stell, Matti Pirinen, Haley Abel, Colby Chiang, Robert S. Fulton, Anne Jackson, Chul Joo Kang, Krishna Kanchi, Daniel C. Koboldt, David E. Larson, Joanne O. Nelson, Thomas J. Nicholas, Arto Pietilä, Vasily Ramensky, Debashree Ray, Laura J. Scott, Heather M. Stringham, Jagadish Vangipurapu, Ryan Welch, Pranav Yajnik, Xianyong Yin, Johan G. Eriksson, Mika Ala‐Korpela, Marjo‐Riitta Järvelin, Minna Männikkö, Hannele Laivuori, Susan K. Dutcher, Nathan O. Stitziel, Richard K. Wilson, Ira M. Hall, Chiara Sabatti, Aarno Palotie, Veikko Salomaa, Markku Laakso, Samuli Ripatti, Michael Boehnke, Nelson B. Freimer
出版 2019Artigo
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Biology
Genetics
Gene
Medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Internal medicine
Computational biology
Endocrinology
Genetic association
Exome
Exome sequencing
Allele
Genome
Mutation
Phenotype
Allele frequency
Disease
Environmental health
Evolutionary biology
Body mass index
Computer science
Population
Quantitative trait locus
Bioinformatics
Diabetes mellitus
Minor allele frequency
Type 2 diabetes
Adipose tissue