Resultados de Búsqueda por Autor

1

GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies por Stephanie M. Gogarten, Tushar Bhangale, Matthew P. Conomos, Cecelia Laurie, Caitlin McHugh, Ian Painter, Xiuwen Zheng, David R. Crosslin, David Levine, Thomas Lumley, Sarah C. Nelson, Kenneth Rice, Jess Shen, Rohit Swarnkar, Bruce S. Weir, Cathy C. Laurie

Publicado 2012

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2

Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program por Alyna Khan, Stephanie M. Gogarten, Caitlin McHugh, Adrienne M. Stilp, Tamar Sofer, Michael Bowers, Quenna Wong, L. Adrienne Cupples, Bertha Hidalgo, Andrew D. Johnson, Merry‐Lynn McDonald, Stephen T. McGarvey, Matthew R. Taylor, Stephanie M. Fullerton, Matthew P. Conomos, Sarah C. Nelson

Publicado 2022

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3

Genome‐Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry por Kimberly E. Taylor, Quenna Wong, David Levine, Caitlin McHugh, Cathy C. Laurie, Kimberly F. Doheny, Mi Y. Lam, Alan N. Baer, Stephen Challacombe, Héctor Lanfranchi, Morten Schiødt, Muthiah Srinivasan, Hisanori Umehara, Frederick B. Vivino, Yan Zhao, Stephen Shiboski, Troy E. Daniels, John S. Greenspan, Caroline H. Shiboski, Lindsey A. Criswell

Publicado 2017

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4

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association por Karl C. Desch, Ayse Bilge Ozel, David Siemieniak, Yossi Kalish, Jordan A. Shavit, Courtney D. Thornburg, Anjali Sharathkumar, Caitlin McHugh, Cathy C. Laurie, Andrew Crenshaw, Daniel B. Mirel, Yoonhee Kim, Cheryl D. Cropp, Anne M. Molloy, Peadar N. Kirke, Joan E. Bailey‐Wilson, Alexander F. Wilson, James L. Mills, John M. Scott, Lawrence C. Brody, Jun Z. Li, David Ginsburg

Publicado 2012

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5

Quality control and quality assurance in genotypic data for genome‐wide association studies por Cathy C. Laurie, Kimberly F. Doheny, Daniel B. Mirel, Elizabeth Pugh, Laura J. Bierut, Tushar Bhangale, Frederick J. Boehm, Neil E. Caporaso, Marilyn C. Cornelis, Howard J. Edenberg, Stacy Gabriel, Emily Harris, Frank B. Hu, Kevin B. Jacobs, Peter Kraft, Maria Teresa Landi, Thomas Lumley, Teri A. Manolio, Caitlin McHugh, Ian Painter, Justin Paschall, John P. Rice, Kenneth Rice, Xiuwen Zheng, Bruce S. Weir

Publicado 2010

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6

Identification of <i>HKDC1</i> and <i>BACE2</i> as Genes Influencing Glycemic Traits During Pregnancy Through Genome-Wide Association Studies por M. Geoffrey Hayes, Margrit Urbanek, Marie‐France Hivert, Loren L. Armstrong, Jean Morrison, Cong Guo, Lynn P. Lowe, Douglas A. Scheftner, Anna Pluzhnikov, David Levine, Caitlin McHugh, C. Ackerman, Luigi Bouchard, Diane Brisson, Brian T. Layden, Daniel B. Mirel, Kimberly F. Doheny, Marysa V. Leya, Rachel N. Lown-Hecht, Alan R. Dyer, Boyd E. Metzger, Timothy E. Reddy, Nancy J. Cox, William L. Lowe

Publicado 2013

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7

Genome-wide association study identifies novel loci predisposing to cutaneous melanoma† por Christopher I. Amos, Lie Wang, Jeffrey E. Lee, Hui Shen, Wei V. Chen, Shenying Fang, Roman Kosoy, Mingfeng Zhang, Abrar A. Qureshi, Selina Vattathil, Christopher W. Schacherer, Julie M. Gardner, Yuling Wang, D. Timothy Bishop, Jennifer H. Barrett, Stuart MacGregor, Nicholas K. Hayward, Nicholas G. Martin, David L. Duffy, Graham J. Mann, Anne Ε. Cust, John L. Hopper, Kevin M. Brown, Elizabeth A. Grimm, Yaji Xu, Younghun Han, Kaiyan Jing, Caitlin McHugh, Cathy C. Laurie, Kim Doheny, Elizabeth Pugh, Michael F. Seldin, Jiali Han, Qingyi Wei

Publicado 2011

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8

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos por Matthew P. Conomos, Cecelia Laurie, Adrienne M. Stilp, Stephanie M. Gogarten, Caitlin McHugh, Sarah C. Nelson, Tamar Sofer, Lindsay Fernández‐Rhodes, Anne E. Justice, Mariaelisa Graff, Kristin L. Young, Amanda A. Seyerle, Christy L. Avery, Kent D. Taylor, Jerome I. Rotter, Gregory A. Talavera, Martha L. Daviglus, Sylvia Wassertheil‐Smoller, Neil Schneiderman, Gerardo Heiss, Robert C. Kaplan, Nora Franceschini, Alex P. Reiner, John R. Shaffer, R. Graham Barr, Kathleen F. Kerr, Sharon R. Browning, Brian L. Browning, Bruce S. Weir, M. Larissa Avilés‐Santa, George Papanicolaou, Thomas Lumley, Adam A. Szpiro, Kari E. North, Kenneth Rice, Timothy A. Thornton, Cathy C. Laurie

Publicado 2016

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9

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans por 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

Publicado 2016

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10

Multiethnic genome-wide and HLA association study of total serum IgE level por Michelle Daya, Corey Cox, Nathalie Acevedo, Meher Preethi Boorgula, Monica Campbell, Sameer Chavan, Michael H. Cho, Gloria L. David, Priyadarshini Kachroo, Jessica Lasky‐Su, Xingnan Li, Caitlin McHugh, Dandi Qiao, Nicholas Rafaels, Lisa A. Beck, Eugene R. Bleecker, Luis Caraballo, L. Adrienne Cupples, Camila Alexandrina Figueiredo, Richard L. Gallo, Jon M. Hanifin, Nadia N. Hansel, Tissa Hata, Craig P. Hersh, Jennifer Knight‐Madden, Donald Y.M. Leung, Emma Guttman‐Yassky, Deborah A. Meyers, George O'connor, Carole Ober, Peck Y. Ong, Victor E. Ortega, Amy S. Paller, Nirupama Putcha, Robert M. Reed, Lynda C. Schneider, Edwin K. Silverman, Mark K. Slifka, Jonathan M. Spergel, Ramachandran S. Vasan, Karine A. Viaud‐Martinez, Harold Watson, Scott T. Weiss, Ingo Ruczinski, Terri H. Beaty, Rasika A. Mathias, Kathleen C. Barnes

Publicado 2021

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11

A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma por Shefali S. Verma, Harini V. Gudiseva, Venkata Ramana Murthy Chavali, Rebecca Salowe, Yuki Bradford, Lindsay Guare, Anastasia Lucas, David W. Collins, Vrathasha Vrathasha, Rohini Nair, Sonika Rathi, Bingxin Zhao, Jie He, Roy Lee, Selam Zenebe-Gete, Anita S. Bowman, Caitlin McHugh, Michael C. Zody, Maxwell Pistilli, Naira Khachatryan, Ebenezer Daniel, Windell Murphy, Jeffrey Henderer, Tyler G. Kinzy, Sudha K. Iyengar, Neal S. Peachey, Kent D. Taylor, Xiuqing Guo, Yii‐Der Ida Chen, Linda M. Zangwill, Christopher A. Girkin, Radha Ayyagari, Jeffrey M. Liebmann, Chimd M. Chuka-Okosa, Susan Williams, Stephen Akafo, Donald L. Budenz, Olusola Olawoye, Michèle Ramsay, Adeyinka Ashaye, Onoja Akpa, Tin Aung, Janey L. Wiggs, Ahmara G. Ross, Qi N. Cui, Victoria Addis, Amanda Lehman, Eydie Miller-Ellis, Prithvi S. Sankar, Scott M. Williams, Gui‐Shuang Ying, Jessica N. Cooke Bailey, Jerome I. Rotter, Robert N. Weinreb, Chiea Chuen Khor, Michael A. Hauser, Marylyn D. Ritchie, Joan M. O’Brien

Publicado 2024

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12

Detectable clonal mosaicism from birth to old age and its relationship to cancer por Cathy C. Laurie, Cecelia Laurie, Kenneth Rice, Kimberly F. Doheny, Leila R. Zelnick, Caitlin McHugh, Hua Ling, Kurt N. Hetrick, Elizabeth Pugh, Chris Amos, Qingyi Wei, Lie Wang, Jeffrey E. Lee, Kathleen C. Barnes, Nadia N. Hansel, Rasika A. Mathias, Denise Daley, Terri H. Beaty, Alan F. Scott, Ingo Ruczinski, Rob Scharpf, Laura J. Bierut, Sarah M. Hartz, Maria Teresa Landi, Neal D. Freedman, Lynn R. Goldin, David Ginsburg, Jun Li, Karl C. Desch, Sara S. Strom, William J. Blot, Lisa B. Signorello, Sue A. Ingles, Stephen J. Chanock, Sonja I. Berndt, Loı̈c Le Marchand, Brian E. Henderson, Kristine R. Monroe, John A. Heit, Mariza de Andrade, Sebastian M. Armasu, C Régnier, William L. Lowe, M. Geoffrey Hayes, Mary L. Marazita, Eleanor Feingold, Jeffrey C. Murray, Mads Melbye, Bjarke Feenstra, Jae H. Kang, Janey L. Wiggs, Gail P. Jarvik, Andrew McDavid, Venkatraman Seshan, Daniel B. Mirel, Andrew Crenshaw, Nataliya Sharopova, Anastasia L. Wise, Jess Shen, David R. Crosslin, David Levine, Xiuwen Zheng, Jenna Udren, Siiri Bennett, Sarah C. Nelson, Stephanie M. Gogarten, Matthew P. Conomos, Patrick J. Heagerty, Teri A. Manolio, Louis R. Pasquale, Christopher A. Haiman, Neil E. Caporaso, Bruce S. Weir

Publicado 2012

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13

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in adm... por Madeline H. Kowalski, Huijun Qian, Ziyi Hou, Jonathan D. Rosen, Amanda L. Tapia, Yue Shan, Deepti Jain, Maria Argos, Donna K. Arnett, Christy L. Avery, Kathleen C. Barnes, Lewis C. Becker, Stephanie A. Bien, Joshua C. Bis, John Blangero, Eric Boerwinkle, Donald W. Bowden, Steven Buyske, Jianwen Cai, Michael H. Cho, Seung Hoan Choi, Hélène Choquet, L. Adrienne Cupples, Mary Cushman, Michelle Daya, Paul S. de Vries, Patrick T. Ellinor, Nauder Faraday, Myriam Fornage, Stacey Gabriel, Santhi K. Ganesh, Misa Graff, Namrata Gupta, Jiang He, Susan R. Heckbert, Bertha Hidalgo, Chani J. Hodonsky, Marguerite R. Irvin, Andrew D. Johnson, Eric Jorgenson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Charles Kooperberg, Jessica Lasky‐Su, Ruth J. F. Loos, Steven A. Lubitz, Rasika A. Mathias, Caitlin McHugh, Courtney G. Montgomery, Jee‐Young Moon, Alanna C. Morrison, Colin N. A. Palmer, Nathan Pankratz, George Papanicolaou, Juan M. Peralta, Patricia A. Peyser, Stephen S. Rich, Jerome I. Rotter, Edwin K. Silverman, Jennifer A. Smith, Nicholas L. Smith, Kent D. Taylor, Timothy A. Thornton, Hemant K. Tiwari, Russell P. Tracy, Tao Wang, Scott T. Weiss, Lu‐Chen Weng, Kerri L. Wiggins, James G. Wilson, Lisa R. Yanek, Sebastian Zöllner, Kari E. North, Paul L. Auer, Laura M. Raffield, Alexander P. Reiner, Yun Li

Publicado 2019

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14

Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program por Yao Hu, Adrienne M. Stilp, Caitlin McHugh, Shuquan Rao, Deepti Jain, Xiuwen Zheng, John Lane, Sébastian Bellefon, Laura M. Raffield, Ming‐Huei Chen, Lisa R. Yanek, Marsha M. Wheeler, Yao Yao, Chunyan Ren, Jai Broome, Jee‐Young Moon, Paul S. de Vries, Brian D. Hobbs, Quan Sun, Praveen Surendran, Jennifer A. Brody, Thomas W. Blackwell, Hélène Choquet, Kathleen A. Ryan, Ravindranath Duggirala, Nancy L. Heard‐Costa, Zhe Wang, Nathalie Chami, Michael Preuß, Yuan‐I Min, Lynette Ekunwe, Leslie A. Lange, Mary Cushman, Nauder Faraday, Joanne E. Curran, Laura Almasy, Kousik Kundu, Albert V. Smith, Stacey Gabriel, Jerome I. Rotter, Myriam Fornage, Donald M. Lloyd‐Jones, Ramachandran S. Vasan, Nicholas L. Smith, Kari E. North, Eric Boerwinkle, Lewis C. Becker, Joshua P. Lewis, Gonçalo R. Abecasis, Lifang Hou, Jeffrey R. O’Connell, Alanna C. Morrison, Terri H. Beaty, Robert C. Kaplan, Adolfo Correa, John Blangero, Eric Jorgenson, Bruce M. Psaty, Charles Kooperberg, Russell T. Walton, Benjamin P. Kleinstiver, Hua Tang, Ruth J. F. Loos, Nicole Soranzo, Adam S. Butterworth, Debbie A. Nickerson, Stephen S. Rich, Braxton D. Mitchell, Andrew D. Johnson, Paul L. Auer, Yun Li, Rasika A. Mathias, Guillaume Lettre, Nathan Pankratz, Cathy C. Laurie, Cecelia Laurie, Daniel E. Bauer, Matthew P. Conomos, Alexander P. Reiner

Publicado 2021

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15

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data por Pierrick Wainschtein, Deepti Jain, Zhili Zheng, Stella Aslibekyan, Diane M. Becker, Wenjian Bi, Jennifer A. Brody, Jenna C. Carlson, Adolfo Correa, Margaret Mengmeng Du, Lindsay Fernández‐Rhodes, Kendra Ferrier, Misa Graff, Xiuqing Guo, Jiang He, Nancy L. Heard‐Costa, Heather M. Highland, Joel N. Hirschhorn, Candace M Howard-Claudio, Carmen R. Isasi, Rebecca D. Jackson, Jicai Jiang, Roby Joehanes, Anne E. Justice, Rita R. Kalyani, Sharon L. R. Kardia, Ethan M. Lange, Meryl S. LeBoff, Seunggeun Lee, Xihao Li, Zilin Li, Elise Lim, D. Y. Lin, Xihong Lin, Simin Liu, Yingchang Lu, JoAnn E. Manson, Lisa W. Martin, Caitlin McHugh, Julie Mikulla, Solomon K. Musani, Maggie Ng, Deborah A. Nickerson, Colin N. A. Palmer, James A. Perry, Ulrike Peters, Michael Preuß, Qibin Qi, Laura M. Raffield, Laura J. Rasmussen‐Torvik, Alex P. Reiner, Emily M. Russell, Colleen M. Sitlani, Jennifer A. Smith, Cassandra N. Spracklen, Tao Wang, Zhe Wang, Jennifer Wessel, Hanfei Xu, Mohammad Yaser, Sachiko Yoneyama, Kendra A. Young, Jingwen Zhang, Xinruo Zhang, Hufeng Zhou, Xiaofeng Zhu, Sebastian Zoellner, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell

Publicado 2022

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16

Novel genetic determinants of telomere length from a trans-ethnic analysis of 109,122 whole genome sequences in TOPMed por Margaret A. Taub, Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek, John Lane, Tyne W. Miller‐Fleming, Jennifer A. Brody, Caitlin McHugh, Deepti Jain, Stephanie M. Gogarten, Cecelia Laurie, Ali R. Keramati, Marios Arvanitis, Albert V. Smith, Ben Heavner, Lucas Barwick, Lewis C. Becker, Joshua C. Bis, John Blangero, Eugene R. Bleecker, Esteban G. Burchard, Juan C. Celedón, Yen Chang, Brian Custer, Dawood Darbar, Lisa de las Fuentes, Dawn L. DeMeo, Barry I. Freedman, Melanie E. Garrett, Mark T. Gladwin, Susan R. Heckbert, Bertha Hidalgo, Marguerite R. Irvin, Talat Islam, W. Craig Johnson, Stefan Kääb, Lenore Launer, Jiwon Lee, Simin Liu, Arden Moscati, Kari E. North, Patricia A. Peyser, Nicholas Rafaels, Laura M. Raffield, Christine E. Seidman, Daniel E. Weeks, Fayuan Wen, Marsha M. Wheeler, L. Keoki Williams, Ivana V. Yang, Wei Zhao, Stella Aslibekyan, Paul L. Auer, Donald W. Bowden, Brian E. Cade, Zhanghua Chen, Michael H. Cho, L Adrienne Cupples, Joanne E. Curran, Michelle Daya, Ranjan Deka, Celeste Eng, Tasha E. Fingerlin, Xiuqing Guo, Lifang Hou, Shih‐Jen Hwang, Jill M. Johnsen, Eimear E. Kenny, Albert M. Levin, Chunyu Liu, Ryan L. Minster, Take Naseri, Mehdi Nouraie, Muagututi‘a Sefuiva Reupena, Éster Cerdeira Sabino, Jennifer A. Smith, Nicholas L. Smith, Jessica Lasky‐Su, Taylor James G, Marilyn J. Telen, Hemant K. Tiwari, Russell P. Tracy, Marquitta J. White, Yingze Zhang, Kerri L. Wiggins, Scott T. Weiss, Ramachandran S. Vasan, Kent D. Taylor, Moritz F. Sinner, Edwin K. Silverman, M. Benjamin Shoemaker, Wayne H-H Sheu, Frank C. Sciurba, David A. Schwartz, Jerome I. Rotter, Daniel Roden, Susan Redline, Benjamin A. Raby

Publicado 2019

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Pré-impressão

17

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed por Margaret A. Taub, Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek, John Lane, Tyne W. Miller‐Fleming, Jennifer A. Brody, Laura M. Raffield, Caitlin McHugh, Deepti Jain, Stephanie M. Gogarten, Cecelia Laurie, Ali R. Keramati, Marios Arvanitis, Albert V. Smith, Ben Heavner, Lucas Barwick, Lewis C. Becker, Joshua C. Bis, John Blangero, Eugene R. Bleecker, Esteban G. Burchard, Juan C. Celedón, Yen Chang, Brian Custer, Dawood Darbar, Lisa de las Fuentes, Dawn L. DeMeo, Barry I. Freedman, Melanie E. Garrett, Mark T. Gladwin, Susan R. Heckbert, Bertha Hidalgo, Marguerite R. Irvin, Talat Islam, W. Craig Johnson, Stefan Kääb, Lenore Launer, Jiwon Lee, Simin Liu, Arden Moscati, Kari E. North, Patricia A. Peyser, Nicholas Rafaels, Christine E. Seidman, Daniel E. Weeks, Fayuan Wen, Marsha M. Wheeler, L. Keoki Williams, Ivana V. Yang, Wei Zhao, Stella Aslibekyan, Paul L. Auer, Donald W. Bowden, Brian E. Cade, Zhanghua Chen, Michael H. Cho, L. Adrienne Cupples, Joanne E. Curran, Michelle Daya, Ranjan Deka, Celeste Eng, Tasha E. Fingerlin, Xiuqing Guo, Lifang Hou, Shih‐Jen Hwang, Jill M. Johnsen, Eimear E. Kenny, Albert M. Levin, Chunyu Liu, Ryan L. Minster, Take Naseri, Mehdi Nouraie, Muagututi‘a Sefuiva Reupena, Éster Cerdeira Sabino, Jennifer A. Smith, Nicholas L. Smith, Jessica Lasky‐Su, James G. Taylor, Marilyn J. Telen, Hemant K. Tiwari, Russell P. Tracy, Marquitta J. White, Yingze Zhang, Kerri L. Wiggins, Scott T. Weiss, Ramachandran S. Vasan, Kent D. Taylor, Moritz F. Sinner, Edwin K. Silverman, M. Benjamin Shoemaker, Wayne H.-H. Sheu, Frank C. Sciurba, David A. Schwartz, Jerome I. Rotter, Daniel Roden, Susan Redline, Benjamin A. Raby

Publicado 2022

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18

Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification por Paul S. de Vries, Matthew P. Conomos, Kuldeep Singh, Christopher Nicholson, Deepti Jain, Natalie R. Hasbani, Wanlin Jiang, Sujin Lee, Christian L. Lino Cardenas, Sharon M. Lutz, Doris Wong, Xiuqing Guo, Jie Yao, Erica P. Young, Catherine Tcheandjieu, Austin T. Hilliard, Joshua C. Bis, Lawrence F. Bielak, Michael R. Brown, Shaila Musharoff, Shoa L. Clarke, James G. Terry, Colin N. A. Palmer, Lisa R. Yanek, Huichun Xu, Nancy L. Heard‐Costa, Jennifer Wessel, Margaret Sunitha Selvaraj, Rebecca Li, Xiao Sun, Adam W. Turner, Adrienne M. Stilp, Alyna Khan, Anne B. Newman, Asif Rasheed, Barry I. Freedman, Brian G. Kral, Caitlin McHugh, Chani J. Hodonsky, Danish Saleheen, David M. Herrington, David R. Jacobs, Deborah A. Nickerson, Eric Boerwinkle, Fei Fei Wang, Gerardo Heiss, Goo Jun, Gregory L. Kinney, Haakon H. Sigurslid, HarshaVardhan Doddapaneni, Ira M. Hall, Isabela M Benseñor, Jai Broome, James D. Crapo, James G. Wilson, Jennifer A. Smith, John Blangero, Jose D. Vargas, José Verdezoto Mosquera, Joshua D. Smith, Karine A. Viaud‐Martinez, Kathleen A. Ryan, Kendra A. Young, Kent D. Taylor, Leslie A. Lange, Leslie Emery, Márcio Sommer Bittencourt, Matthew J. Budoff, May E. Montasser, Miao Yu, Michael C. Mahaney, Mohammed Mahamdeh, Myriam Fornage, Nora Franceschini, Paulo A. Lotufo, Pradeep Natarajan, Quenna Wong, Rasika A. Mathias, Richard A. Gibbs, Ron Do, Roxana Mehran, Russell P. Tracy, Ryan W. Kim, Sarah C. Nelson, Scott M. Damrauer, Sharon L. R. Kardia, Stephen S. Rich, Valentı́n Fuster, Valerio Napolioni, Wei Zhao, Wenjie Tian, Xianyong Yin, Yuan‐I Min, Alisa K. Manning, Gina M. Peloso, Tanika N. Kelly, Christopher J. O’Donnell, Alanna C. Morrison, Joanne E. Curran, Warren M. Zapol

Publicado 2023

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19

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele por Xinruo Zhang, Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu, Zhe Wang, Kendra Ferrier, Geetha Chittoor, Navya Shilpa Josyula, Mariah Meyer, Shreyash Gupta, Xihao Li, Zilin Li, Matthew Allison, Diane M. Becker, Lawrence F. Bielak, Joshua C. Bis, Meher Preethi Boorgula, Donald W. Bowden, Jai Broome, Erin Buth, Christopher S. Carlson, Kyong–Mi Chang, Sameer Chavan, Yen‐Feng Chiu, Lee‐Ming Chuang, Matthew P. Conomos, Dawn L. DeMeo, Mengmeng Du, Ravindranath Duggirala, Celeste Eng, Alison E. Fohner, Barry I. Freedman, Melanie E. Garrett, Xiuqing Guo, Chris Haiman, Ben Heavner, Bertha Hidalgo, James E. Hixson, Yuk‐Lam Ho, Brian D. Hobbs, Donglei Hu, Qin Hui, Chii‐Min Hwu, Rebecca D. Jackson, Deepti Jain, Rita R. Kalyani, Sharon L.R. Kardia, Tanika N. Kelly, Ethan M. Lange, Michael A. LeNoir, Changwei Li, Loı̈c Le Marchand, Merry‐Lynn McDonald, Caitlin McHugh, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Christopher J O'Donnell, Nicholette D. Allred, James S. Pankow, James A. Perry, Ulrike Peters, Michael Preuß, D. C. Rao, Elizabeth A. Regan, Sefuiva M Reupena, Dan M. Roden, José Rodríguez‐Santana, Colleen M. Sitlani, Jennifer A. Smith, Hemant K. Tiwari, Ramachandran S. Vasan, Zeyuan Wang, Daniel E. Weeks, Jennifer Wessel, Kerri L. Wiggins, Lynne R. Wilkens, Peter W.F. Wilson, Lisa R. Yanek, Zachary T. Yoneda, Wei Zhao, Sebastian Zöllner, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes, John Blangero, Eric Boerwinkle, Esteban G. Burchard, April P. Carson, Daniel I. Chasman, Yii‐Der Ida Chen, Joanne E. Curran, Myriam Fornage, Victor R. Gordeuk, Jiang He, Susan R. Heckbert, Lifang Hou, Marguerite R. Irvin

Publicado 2025

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