Hasil Pencarian - David R Crosslin

Perbaiki Hasil
  1. 1
    Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL[S]

    Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL[S] oleh Daniel S. Kim, Amber A. Burt, David R. Crosslin, Peggy D. Robertson, Jane E. Ranchalis, Edward J. Boyko, Deborah A. Nickerson, Clement E. Furlong, Gail P. Jarvik

    Diterbitkan 2013-02-01
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  2. 2
    Copy Number Variation Analysis in the Context of Electronic Medical Records & Large-Scale Genomics Consortium Efforts

    Copy Number Variation Analysis in the Context of Electronic Medical Records & Large-Scale Genomics Consortium Efforts oleh John J Connolly, Joseph T Glessner, Joseph T Glessner, Berta eAlmoguera, David R Crosslin, Gail P Jarvik, Patrick eSleiman, Patrick eSleiman, Hakon eHakonarson, Hakon eHakonarson

    Diterbitkan 2014-03-01
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  3. 3
    Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach

    Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach oleh Neha A. Sathe, Su Xian, F. Linzee Mabrey, David R. Crosslin, Sean D. Mooney, Eric D. Morrell, Kevin Lybarger, Meliha Yetisgen, Gail P. Jarvik, Pavan K. Bhatraju, Mark M. Wurfel

    Diterbitkan 2023-08-01
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  4. 4
    eMERGEing progress in genomics---the first seven years

    eMERGEing progress in genomics---the first seven years oleh Dana C. Crawford, Dana C. Crawford, David R. Crosslin, David R. Crosslin, Gerard eTromp, Iftikhar J. Kullo, Helena eKuivaniemi, M. Geoffrey Hayes, Joshua C. Denny, Joshua C. Denny, William Scott Bush, William Scott Bush, Jonathan L. Haines, Jonathan L. Haines, Dan M. Roden, Dan M. Roden, Catherine Anne McCarty, Gail P. Jarvik, Gail P. Jarvik, Marylyn D. Ritchie, Marylyn D. Ritchie

    Diterbitkan 2014-06-01
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  5. 5
    Confirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancer.

    Confirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancer. oleh Ursula M Schick, Andrew McDavid, Paul K Crane, Noah Weston, Kelly Ehrlich, Katherine M Newton, Robert Wallace, Ebony Bookman, Tabitha Harrison, Aaron Aragaki, David R Crosslin, Sophia S Wang, Alex P Reiner, Rebecca D Jackson, Ulrike Peters, Eric B Larson, Gail P Jarvik, Christopher S Carlson

    Diterbitkan 2013-01-01
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  6. 6
    Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project[S]

    Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project[S] oleh Daniel Seung Kim, David R. Crosslin, Paul L. Auer, Stephanie M. Suzuki, Judit Marsillach, Amber A. Burt, Adam S. Gordon, James F. Meschia, Mike A. Nalls, Bradford B. Worrall, W.T. Longstreth, Jr., Rebecca F. Gottesman, Clement E. Furlong, Ulrike Peters, Stephen S. Rich, Deborah A. Nickerson, Gail P. Jarvik

    Diterbitkan 2014-06-01
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  7. 7
    GATA2 is associated with familial early-onset coronary artery disease.

    GATA2 is associated with familial early-onset coronary artery disease. oleh Jessica J Connelly, Tianyuan Wang, Julie E Cox, Carol Haynes, Liyong Wang, Svati H Shah, David R Crosslin, A Brent Hale, Sarah Nelson, David C Crossman, Christopher B Granger, Jonathan L Haines, Christopher J H Jones, Jeffery M Vance, Pascal J Goldschmidt-Clermont, William E Kraus, Elizabeth R Hauser, Simon G Gregory

    Diterbitkan 2006-08-01
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  8. 8
    Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

    Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience oleh Kathleen D. Muenzen, Laura M. Amendola, Tia L. Kauffman, Kathleen F. Mittendorf, Jeannette T. Bensen, Flavia Chen, Richard Green, Bradford C. Powell, Mark Kvale, Frank Angelo, Laura Farnan, Stephanie M. Fullerton, Jill O. Robinson, Tianran Li, Priyanka Murali, James M.J. Lawlor, Jeffrey Ou, Lucia A. Hindorff, Gail P. Jarvik, David R. Crosslin

    Diterbitkan 2022-07-01
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  9. 9
    Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort

    Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort oleh Elisabeth A. Rosenthal, David R. Crosslin, Adam S. Gordon, David S. Carrell, Ian B. Stanaway, Eric B. Larson, Jane Grafton, Wei-Qi Wei, Joshua C. Denny, Qi-Ping Feng, Amy S. Shah, Amy C. Sturm, Marylyn D. Ritchie, Jennifer A. Pacheco, Hakon Hakonarson, Laura J. Rasmussen-Torvik, John J. Connolly, Xiao Fan, Maya Safarova, Iftikhar J. Kullo, Gail P. Jarvik

    Diterbitkan 2021-01-01
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  10. 10
    Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.

    Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis. oleh Svati H Shah, Neil J Freedman, Lisheng Zhang, David R Crosslin, David H Stone, Carol Haynes, Jessica Johnson, Sarah Nelson, Liyong Wang, Jessica J Connelly, Michael Muehlbauer, Geoffrey S Ginsburg, David C Crossman, Christopher J H Jones, Jeffery Vance, Michael H Sketch, Christopher B Granger, Christopher B Newgard, Simon G Gregory, Pascal J Goldschmidt-Clermont, William E Kraus, Elizabeth R Hauser

    Diterbitkan 2009-01-01
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  11. 11
    Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data.

    Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. oleh Jonathan D Mosley, Sara L Van Driest, Emma K Larkin, Peter E Weeke, John S Witte, Quinn S Wells, Jason H Karnes, Yan Guo, Lisa Bastarache, Lana M Olson, Catherine A McCarty, Jennifer A Pacheco, Gail P Jarvik, David S Carrell, Eric B Larson, David R Crosslin, Iftikhar J Kullo, Gerard Tromp, Helena Kuivaniemi, David J Carey, Marylyn D Ritchie, Josh C Denny, Dan M Roden

    Diterbitkan 2013-01-01
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  12. 12
    Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

    Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection oleh Kathleen Ferar, Taryn O. Hall, Dana C. Crawford, Robb Rowley, Benjamin A. Satterfield, Rongling Li, Loren Gragert, Elizabeth W. Karlson, Mariza de Andrade, Iftikhar J. Kullo, Catherine A. McCarty, Abel Kho, M. Geoffrey Hayes, Marylyn D. Ritchie, Paul K. Crane, Daniel B. Mirel, Christopher Carlson, John J. Connolly, Hakon Hakonarson, Andrew T. Crenshaw, David Carrell, Yuan Luo, Ozan Dikilitas, Joshua C. Denny, Gail P. Jarvik, David R. Crosslin

    Diterbitkan 2023-11-01
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  13. 13
    Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

    Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection oleh Kathleen Ferar, Taryn O. Hall, Dana C. Crawford, Robb Rowley, Benjamin A. Satterfield, Rongling Li, Loren Gragert, Elizabeth W. Karlson, Mariza de Andrade, Iftikhar J. Kullo, Catherine A. McCarty, Abel Kho, M. Geoffrey Hayes, Marylyn D. Ritchie, Paul K. Crane, Daniel B. Mirel, Christopher Carlson, John J. Connolly, Hakon Hakonarson, Andrew T. Crenshaw, David Carrell, Yuan Luo, Ozan Dikilitas, Joshua C. Denny, Gail P. Jarvik, David R. Crosslin

    Diterbitkan 2023-10-01
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  14. 14
    Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.

    Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. oleh Jennifer R Malinowski, Joshua C Denny, Suzette J Bielinski, Melissa A Basford, Yuki Bradford, Peggy L Peissig, David Carrell, David R Crosslin, Jyotishman Pathak, Luke Rasmussen, Jennifer Pacheco, Abel Kho, Katherine M Newton, Rongling Li, Iftikhar J Kullo, Christopher G Chute, Rex L Chisholm, Gail P Jarvik, Eric B Larson, Catherine A McCarty, Daniel R Masys, Dan M Roden, Mariza de Andrade, Marylyn D Ritchie, Dana C Crawford

    Diterbitkan 2014-01-01
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  15. 15
    GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network

    GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network oleh Bahram Namjou, Todd Lingren, Yongbo Huang, Sreeja Parameswaran, Beth L. Cobb, Ian B. Stanaway, John J. Connolly, Frank D. Mentch, Barbara Benoit, Xinnan Niu, Wei-Qi Wei, Robert J. Carroll, Jennifer A. Pacheco, Isaac T. W. Harley, Senad Divanovic, David S. Carrell, Eric B. Larson, David J. Carey, Shefali Verma, Marylyn D. Ritchie, Ali G. Gharavi, Shawn Murphy, Marc S. Williams, David R. Crosslin, Gail P. Jarvik, Iftikhar J. Kullo, Hakon Hakonarson, Rongling Li, The eMERGE Network, Stavra A. Xanthakos, John B. Harley

    Diterbitkan 2019-07-01
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  16. 16
    Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.

    Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. oleh Andrew McDavid, Paul K Crane, Katherine M Newton, David R Crosslin, Wayne McCormick, Noah Weston, Kelly Ehrlich, Eugene Hart, Robert Harrison, Walter A Kukull, Carla Rottscheit, Peggy Peissig, Elisha Stefanski, Catherine A McCarty, Rebecca Lynn Zuvich, Marylyn D Ritchie, Jonathan L Haines, Joshua C Denny, Gerard D Schellenberg, Mariza de Andrade, Iftikhar Kullo, Rongling Li, Daniel Mirel, Andrew Crenshaw, James D Bowen, Ge Li, Debby Tsuang, Susan McCurry, Linda Teri, Eric B Larson, Gail P Jarvik, Chris S Carlson

    Diterbitkan 2013-01-01
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  17. 17
    Medical records-based chronic kidney disease phenotype for clinical care and “big data” observational and genetic studies

    Medical records-based chronic kidney disease phenotype for clinical care and “big data” observational and genetic studies oleh Ning Shang, Atlas Khan, Fernanda Polubriaginof, Francesca Zanoni, Karla Mehl, David Fasel, Paul E. Drawz, Robert J. Carrol, Joshua C. Denny, Matthew A. Hathcock, Adelaide M. Arruda-Olson, Peggy L. Peissig, Richard A. Dart, Murray H. Brilliant, Eric B. Larson, David S. Carrell, Sarah Pendergrass, Shefali Setia Verma, Marylyn D. Ritchie, Barbara Benoit, Vivian S. Gainer, Elizabeth W. Karlson, Adam S. Gordon, Gail P. Jarvik, Ian B. Stanaway, David R. Crosslin, Sumit Mohan, Iuliana Ionita-Laza, Nicholas P. Tatonetti, Ali G. Gharavi, George Hripcsak, Chunhua Weng, Krzysztof Kiryluk

    Diterbitkan 2021-04-01
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  18. 18
    A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers

    A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers oleh Jonathan D. Mosley, QiPing Feng, Quinn S. Wells, Sara L. Van Driest, Christian M. Shaffer, Todd L. Edwards, Lisa Bastarache, Wei-Qi Wei, Lea K. Davis, Catherine A. McCarty, Will Thompson, Christopher G. Chute, Gail P. Jarvik, Adam S. Gordon, Melody R. Palmer, David R. Crosslin, Eric B. Larson, David S. Carrell, Iftikhar J. Kullo, Jennifer A. Pacheco, Peggy L. Peissig, Murray H. Brilliant, James G. Linneman, Bahram Namjou, Marc S. Williams, Marylyn D. Ritchie, Kenneth M. Borthwick, Shefali S. Verma, Jason H. Karnes, Scott T. Weiss, Thomas J. Wang, C. Michael Stein, Josh C. Denny, Dan M. Roden

    Diterbitkan 2018-08-01
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  19. 19
    Phenome Wide Association Studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

    Phenome Wide Association Studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index oleh Robert Michael Cronin, Julie R Field, Yuki eBradford, Christian M Shaffer, Robert J Carroll, Jonathan D Mosley, Lisa eBastarache, Todd L Edwards, Scott J Hebbring, Simon eLin, Lucia A Hindorff, Paul K Crane, Sarah ePendergrass, Marylyn D Ritchie, Dana C Crawford, Jyotishman ePathak, Suzette eBielinski, David S Carrell, David R Crosslin, David H Ledbetter, David J Carey, Gerard eTromp, Marc S Williams, Eric B Larson, Gail P Jarvik, Peggy L Peissig, Murray H Brilliant, Catherine Anne McCarty, Christopher G Chute, Iftikhar J Kullo, Erwin eBottinger, Rex eChisholm, Maureen E Smith, Dan M Roden, Joshua C Denny

    Diterbitkan 2014-08-01
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  20. 20
    Genome-wide association study of susceptibility to hospitalised respiratory infections [version 2; peer review: 1 approved, 2 approved with reservations]

    Genome-wide association study of susceptibility to hospitalised respiratory infections [version 2; peer review: 1 approved, 2 approved with reservations] oleh Sina A. Gharib, Louise V. Wain, Tõnu Esko, Gail P. Jarvik, Scott Hebbring, Eric B. Larson, Sarah H. Landis, Ruth J.F. Loos, Jiangyuan Liu, Caroline Hayward, Arden Moscati, Yuan Luo, Bahram Namjou, Hana Mullerova, Marjo-Riitta Järvelin, Jennifer K. Quint, Eeva Sliz, Marylyn D. Ritchie, Laurent Thomas, Ian B. Stanaway, Kristian Hveem, David Michalovich, Ian P. Hall, James F. Wilson, Jing Chen, Alexander T. Williams, Martin D. Tobin, Joanna C. Betts, Hardeep Naghra-van Gijzel, Richard Packer, Edith M. Hessel, Astrid J. Yeo, Nicola F. Reeve, Bjørn Olav Åsvold, Erik Abner, Archie Campbell, Traci M. Bartz, Juha Auvinen, Catherine John, Ben Brumpton, Yuki Bradford, Su Chu, David J. Porteous, Nick Shrine, Michael H. Cho, QiPing Feng, David R. Crosslin

    Diterbitkan 2023-11-01
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