Rezultati pretrage - Deepti Jain
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Effective thrombolysis without marked plasminemia after bolus intravenous administration of vampire bat salivary plasminogen activator in rabbits. od Stephen J. Gardell, Denise Ramjit, Inez I. Stabilito, Tsuneo Fujita, Joseph J. Lynch, G C Cuca, Deepti Jain, S P Wang, J S Tung, G E Mark
Izdano 1991Artigo -
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Occupancy by key transcription factors is a more accurate predictor of enhancer activity than histone modifications or chromatin accessibility od Nergiz Doğan, Wei-Sheng Wu, Christapher S. Morrissey, Kuan-Bei Chen, Aaron J. Stonestrom, Maria Long, Cheryl A. Keller, Yong Cheng, Deepti Jain, Axel Visel, L Pennacchio, Mitchell J. Weiss, Gerd A. Blobel, Ross C. Hardison
Izdano 2015Artigo -
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Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos od Deepti Jain, Chani J. Hodonsky, Ursula M. Schick, Jean Morrison, Sharon Minnerath, Lisa Brown, Claudia Schurmann, Yongmei Liu, Paul L. Auer, Cecelia Laurie, Kent D. Taylor, Brian L. Browning, George Papanicolaou, Sharon R. Browning, Ruth J. F. Loos, Kari E. North, Bharat Thyagarajan, Cathy C. Laurie, Timothy A. Thornton, Tamar Sofer, Alexander P. Reiner
Izdano 2017Artigo -
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GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos od Anne E. Sanders, Deepti Jain, Tamar Sofer, Kathleen F. Kerr, Cathy C. Laurie, John R. Shaffer, Mary L. Marazita, Linda M. Kaste, Gary D. Slade, Roger B. Fillingim, Richard Ohrbach, William Maixner, Thomas Kocher, Olaf Bernhardt, Alexander Teumer, Christian Schwahn, Kirsi Sipilä, Raija Lähdesmäki, Minna Männikkö, Paula Pesonen, Marjo‐Riitta Järvelin, Célia Marisa Rizzatti‐Barbosa, Carolina B. Meloto, Margarete Ribeiro-Dasilva, Luda Diatchenko, Priscila de Oliveira Serrano, Shad B. Smith
Izdano 2017Revisão -
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Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease od Laura M. Raffield, Jacob C. Ulirsch, Rakhi P. Naik, Samuel Lessard, Robert E. Handsaker, Deepti Jain, Hyun Min Kang, Nathan Pankratz, Paul L. Auer, Erik L. Bao, Joshua D. Smith, Leslie A. Lange, Ethan M. Lange, Yun Li, Timothy A. Thornton, Bessie A. Young, Gonçalo R. Abecasis, Cathy C. Laurie, Deborah A. Nickerson, Steven A. McCarroll, Adolfo Correa, James G. Wilson, Guillaume Lettre, Vijay G. Sankaran, Alex P. Reiner
Izdano 2018Artigo -
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Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos od Chani J. Hodonsky, Deepti Jain, Ursula M. Schick, Jean Morrison, Lisa Brown, Caitlin P. McHugh, Claudia Schurmann, Diane D. Chen, Yong Mei Liu, Paul L. Auer, Cecilia A. Laurie, Kent D. Taylor, Brian L. Browning, Yun Li, George Papanicolaou, Jerome I. Rotter, Ryo Kurita, Yukio Nakamura, Sharon R. Browning, Ruth J. F. Loos, Kari E. North, Cathy C. Laurie, Timothy A. Thornton, Nathan Pankratz, Daniel E. Bauer, Tamar Sofer, Alex P. Reiner
Izdano 2017Artigo -
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Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans od Ursula M. Schick, Deepti Jain, Chani J. Hodonsky, Jean Morrison, James P. Davis, Lisa Brown, Tamar Sofer, Matthew P. Conomos, Claudia Schurmann, Caitlin McHugh, Sarah C. Nelson, Swarooparani Vadlamudi, Adrienne M. Stilp, Anna Plantinga, Leslie J. Baier, Stephanie A. Bien, Stephanie M. Gogarten, Cecelia Laurie, Kent D. Taylor, Yongmei Liu, Paul L. Auer, Nora Franceschini, Adam A. Szpiro, Kenneth Rice, Kathleen F. Kerr, Jerome I. Rotter, Robert L. Hanson, George Papanicolaou, Stephen S. Rich, Ruth J. F. Loos, Brian L. Browning, Sharon R. Browning, Bruce S. Weir, Cathy C. Laurie, Karen L. Mohlke, Kari E. North, Timothy A. Thornton, Alex P. Reiner
Izdano 2016Artigo -
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Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males od Shad B. Smith, Marc Parisien, Eric Bair, Inna Belfer, Anne‐Julie Chabot‐Doré, Pavel Gris, Samar Khoury, Shannon Tansley, Yelizaveta Torosyan, Dmitri V. Zaykin, Olaf Bernhardt, Priscila de Oliveira Serrano, Richard H. Gracely, Deepti Jain, Marjo‐Riitta Järvelin, Linda M. Kaste, Kathleen F. Kerr, Thomas Kocher, Raija Lähdesmäki, Nadia Laniado, Cathy C. Laurie, Cecelia Laurie, Minna Männikkö, Carolina B. Meloto, Andrea G. Nackley, Sarah C. Nelson, Paula Pesonen, Margarete Ribeiro-Dasilva, Célia Marisa Rizzatti‐Barbosa, Anne E. Sanders, Christian Schwahn, Kirsi Sipilä, Tamar Sofer, Alexander Teumer, Jeffrey S. Mogil, Roger B. Fillingim, Joel D. Greenspan, Richard Ohrbach, Gary D. Slade, William Maixner, Luda Diatchenko
Izdano 2018Revisão -
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Recovery of trait heritability from whole genome sequence data od Pierrick Wainschtein, Deepti Jain, Loïc Yengo, Zhili Zheng, L. Adrienne Cupples, Aladdin H. Shadyab, Barbara McKnight, Benjamin M. Shoemaker, Braxton D. Mitchell, Bruce M. Psaty, Charles Kooperberg, Dan M. Roden, Dawood Darbar, Donna K. Arnett, Elizabeth A. Regan, Eric Boerwinkle, Jerome I. Rotter, Matthew Allison, Merry‐Lynn McDonald, Mina K. Chung, Nicholas L. Smith, Patrick T. Ellinor, Ramachandran S. Vasan, Rasika A. Mathias, Stephen S. Rich, Susan R. Heckbert, Susan Redline, Xiuqing Guo, Y-D Ida Chen, Yongmei Liu, Mariza de Andrade, Lisa R. Yanek, Christine M. Albert, Ryan D. Hernandez, Stephen T. McGarvey, Kari E. North, Leslie A. Lange, Bruce S. Weir, Cathy C. Laurie, Jian Yang, Peter M. Visscher
Izdano 2019Artigo -
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Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program od Chloé Sarnowski, Aaron Leong, Laura M. Raffield, Peitao Wu, Paul S. de Vries, Daniel DiCorpo, Xiuqing Guo, Huichun Xu, Yongmei Liu, Xiuwen Zheng, Yao Hu, Jennifer A. Brody, Mark O. Goodarzi, Bertha Hidalgo, Heather M. Highland, Deepti Jain, Yongmei Liu, Rakhi P. Naik, Jeffrey R. O’Connell, James A. Perry, Bianca Porneala, Elizabeth Selvin, Jennifer Wessel, Bruce M. Psaty, Joanne E. Curran, Juan M. Peralta, John Blangero, Charles Kooperberg, Rasika A. Mathias, Andrew D. Johnson, Alexander P. Reiner, Braxton D. Mitchell, L. Adrienne Cupples, Ramachandran S. Vasan, Adolfo Correa, Alanna C. Morrison, Eric Boerwinkle, Jerome I. Rotter, Stephen S. Rich, Alisa K. Manning, Josée Dupuis, James B. Meigs
Izdano 2019Artigo -
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Association of clonal hematopoiesis with chronic obstructive pulmonary disease od Peter G. Miller, Dandi Qiao, Joselyn Rojas, Michael C. Honigberg, Adam S. Sperling, Christopher J. Gibson, Alexander G. Bick, Abhishek Niroula, Marie McConkey, Brittany Sandoval, Brian C. Miller, Weiwei Shi, Kaushik Viswanathan, Matthew Leventhal, Lillian Werner, Matthew Moll, Brian E. Cade, R. Graham Barr, Adolfo Correa, L. Adrienne Cupples, Sina A. Gharib, Deepti Jain, Stephanie M. Gogarten, Leslie A. Lange, Stephanie J. London, Ani Manichaikul, George O'connor, Elizabeth C. Oelsner, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Ramachandran S. Vasan, Bing Yu, Lynette M. Sholl, Donna Neuberg, Siddhartha Jaiswal, Bruce D. Levy, Caroline A. Owen, Pradeep Natarajan, Edwin K. Silverman, Peter van Galen, Yohannes Tesfaigzi, Michael H. Cho, Benjamin L. Ebert
Izdano 2021Artigo -
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Recovery of trait heritability from whole genome sequence data od Pierrick Wainschtein, Deepti Jain, Zhili Zheng, L. Adrienne Cupples, Aladdin H. Shadyab, Barbara McKnight, Benjamin M. Shoemaker, Braxton D. Mitchell, Bruce M. Psaty, Charles Kooperberg, Yongmei Liu, Christine M. Albert, Dan M. Roden, Daniel I. Chasman, Dawood Darbar, Donald M. Lloyd‐Jones, Donna K. Arnett, Elizabeth A. Regan, Eric Boerwinkle, Jerome I. Rotter, Jeffrey R. O’Connell, Lisa R. Yanek, Mariza de Andrade, Matthew Allison, Merry‐Lynn McDonald, Mina K. Chung, Myriam Fornage, Nathalie Chami, Nicholas L. Smith, Patrick T. Ellinor, Ramachandran S. Vasan, Rasika A. Mathias, Ruth J. F. Loos, Stephen S. Rich, Steven A. Lubitz, Susan R. Heckbert, Susan Redline, Xiuqing Guo, Yii-DerIda Chen, Cecelia Laurie, Ryan D. Hernandez, Stephen T. McGarvey, Michael E. Goddard, Cathy C. Laurie, Kari E. North, Leslie A. Lange, Bruce S. Weir, Loïc Yengo, Jian Yang, Peter M. Visscher
Izdano 2019Pré-impressão
Alati za pretragu:
Povezani predmeti
Biology
Genetics
Gene
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Computational biology
Medicine
Genetic association
Genome
Internal medicine
Computer science
Bioinformatics
Minor allele frequency
Programming language
Quantitative trait locus
Transcription factor
Allele
Allele frequency
Cell biology
Endocrinology
Linkage disequilibrium
Trait
Genotyping
Immunology
Imputation (statistics)
Missing data
Chromatin
Disease
Environmental health