Resultados da pesquisa - Adam E. Locke

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  1. 1
    Validity of Self-Reported Sunscreen Use by Parents, Children, and Lifeguards

    Validity of Self-Reported Sunscreen Use by Parents, Children, and Lifeguards Por Karen Glanz, Frances McCarty, Eric J. Nehl, David L. O’Riordan, Peter Gies, Łucja Bundy, Adam E. Locke, Dawn M. Hall

    Publicado em 2008
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  2. 2
    An Excess of Deleterious Variants in VEGF-A Pathway Genes in Down-Syndrome-Associated Atrioventricular Septal Defects

    An Excess of Deleterious Variants in VEGF-A Pathway Genes in Down-Syndrome-Associated Atrioventricular Septal Defects Por 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

    Publicado em 2012
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  3. 3
    Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project

    Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project Por 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

    Publicado em 2008
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  4. 4
    Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome

    Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome Por 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

    Publicado em 2010
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  5. 5
    Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: A report from the National Down Syndrome Project

    Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: A report from the National Down Syndrome Project Por 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

    Publicado em 2011
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  6. 6
    Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

    Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study Por 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

    Publicado em 2017
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  7. 7
    Next-generation genotype imputation service and methods

    Next-generation genotype imputation service and methods Por 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

    Publicado em 2016
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  8. 8
    Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution

    Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution Por 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

    Publicado em 2019
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  9. 9
    Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity

    Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity Por 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

    Publicado em 2015
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  10. 10
    Quality control and conduct of genome-wide association meta-analyses

    Quality control and conduct of genome-wide association meta-analyses Por 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

    Publicado em 2014
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  11. 11
    Exome Sequencing of Familial Bipolar Disorder

    Exome Sequencing of Familial Bipolar Disorder Por 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

    Publicado em 2016
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  12. 12
    Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits

    Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits Por 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

    Publicado em 2019
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  13. 13
    Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

    Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans Por 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

    Publicado em 2018
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  14. 14
    Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

    Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk Por 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

    Publicado em 2022
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  15. 15
    Interaction between the <i>FTO</i> gene, body mass index and depression: meta-analysis of 13701 individuals

    Interaction between the <i>FTO</i> gene, body mass index and depression: meta-analysis of 13701 individuals Por 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

    Publicado em 2017
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  16. 16
    Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

    Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci Por 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

    Publicado em 2022
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  17. 17
    Exome sequencing and analysis of 454,787 UK Biobank participants

    Exome sequencing and analysis of 454,787 UK Biobank participants Por 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

    Publicado em 2021
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  18. 18
    Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk

    Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk Por 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

    Publicado em 2015
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  19. 19
    Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

    Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum Por 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

    Publicado em 2018
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  20. 20
    Exome sequencing of Finnish isolates enhances rare-variant association power

    Exome sequencing of Finnish isolates enhances rare-variant association power Por 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

    Publicado em 2019
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