检索结果 - Cecelia Laurie

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  1. 1
    Mapping epistatic quantitative trait loci

    Mapping epistatic quantitative trait loci 由 Cecelia Laurie, Shengchu Wang, L. A. Carlini‐Garcia, Zhao‐Bang Zeng

    出版 2014
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  2. 2
    Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays

    Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays 由 Sarah C. Nelson, Kimberly F. Doheny, Elizabeth Pugh, Jane Romm, Hua Ling, Cecelia Laurie, Sharon R. Browning, Bruce S. Weir, Cathy C. Laurie

    出版 2013
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  3. 3
    GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies

    GWASTools: an R/Bioconductor package for quality control and analysis of genome-wide association studies 由 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

    出版 2012
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  4. 4
    Premature Menopause, Clonal Hematopoiesis, and Coronary Artery Disease in Postmenopausal Women

    Premature Menopause, Clonal Hematopoiesis, and Coronary Artery Disease in Postmenopausal Women 由 Michael C. Honigberg, Seyedeh M. Zekavat, Abhishek Niroula, Gabriel K. Griffin, Alexander G. Bick, James P. Pirruccello, Tetsushi Nakao, Eric A. Whitsel, Leslie V. Farland, Cecelia Laurie, Charles Kooperberg, JoAnn E. Manson, Stacey Gabriel, Peter Libby, Alexander P. Reiner, Benjamin L. Ebert, Pradeep Natarajan

    出版 2020
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  5. 5
    A fully adjusted two‐stage procedure for rank‐normalization in genetic association studies

    A fully adjusted two‐stage procedure for rank‐normalization in genetic association studies 由 Tamar Sofer, Xiuwen Zheng, Stephanie M. Gogarten, Cecelia Laurie, Kelsey Grinde, John R. Shaffer, Dmitry Shungin, Jeffrey R. O’Connell, Ramon A. Durazo‐Arvizo, Laura M. Raffield, Leslie A. Lange, Solomon K. Musani, Ramachandran S. Vasan, L. Adrienne Cupples, Alexander P. Reiner, Cathy C. Laurie, Kenneth Rice

    出版 2019
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  6. 6
    Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos

    Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos 由 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

    出版 2017
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  7. 7
    D-Dimer in African Americans

    D-Dimer in African Americans 由 Laura M. Raffield, Neil A. Zakai, Qing Duan, Cecelia Laurie, Joshua D. Smith, Marguerite R. Irvin, Margaret F. Doyle, Rakhi P. Naik, Ci Song, Ani Manichaikul, Yongmei Liu, Peter Durda, Jerome I. Rotter, Nancy S. Jenny, Stephen S. Rich, James G. Wilson, Andrew D. Johnson, Adolfo Correa, Yun Li, Deborah A. Nickerson, Kenneth Rice, Ethan M. Lange, Mary Cushman, Leslie A. Lange, Alex P. Reiner

    出版 2017
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  8. 8
    Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

    Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology 由 John R. Shaffer, Ekaterina Orlova, Myoung Keun Lee, Elizabeth J. Leslie, Zachary D. Raffensperger, Carrie L. Heike, Michael L. Cunningham, Jacqueline T. Hecht, Chung How Kau, Nichole Nidey, Lina M. Moreno, George L. Wehby, Jeffrey C. Murray, Cecelia Laurie, Cathy C. Laurie, Joanne B. Cole, Tracey M. Ferrara, Stephanie A. Santorico, Ophir D. Klein, Washington Mio, Eleanor Feingold, Benedikt Hallgrímsson, Richard A. Spritz, Mary L. Marazita, Seth M. Weinberg

    出版 2016
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  9. 9
    Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

    Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos 由 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

    出版 2016
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  10. 10
    Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans

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

    出版 2016
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  11. 11
    Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males

    Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males 由 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

    出版 2018
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  12. 12
    Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

    Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21 由 Craig C. Teerlink, Daniel Leongamornlert, Tokhir Dadaev, Alun Thomas, James M. Farnham, Robert A. Stephenson, Shaun M. Riska, Shannon K. McDonnell, Daniel J. Schaid, William J. Catàlona, S. Lilly Zheng, Kathleen A. Cooney, Anna M. Ray, Kimberly A. Zuhlke, Ethan M. Lange, Graham G. Giles, Melissa C. Southey, Liesel M. FitzGerald, Antje E. Rinckleb, Manuel Luedeke, Christiane Maier, Janet L. Stanford, Elaine A. Ostrander, Elina Kaikkonen, Csilla Sipeky, Teuvo L.J. Tammela, Johanna Schleutker, Kathleen E. Wiley, Sarah D. Isaacs, Patrick C. Walsh, William B. Isaacs, Jianfeng Xu, Géraldine Cancel‐Tassin, Olivier Cussenot, Diptasri Mandal, Cecelia Laurie, Cathy C. Laurie, Stephen N. Thibodeau, Rosalind A. Eeles, Zsofia Kote‐Jarai, Lisa Cannon‐Albright

    出版 2016
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  13. 13
    Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

    Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation 由 Seung Hoan Choi, Lu‐Chen Weng, Carolina Roselli, Honghuang Lin, Christopher M. Haggerty, M. Benjamin Shoemaker, John Barnard, Dan E. Arking, Daniel I. Chasman, Christine M. Albert, Mark Chaffin, Nathan R. Tucker, Jonathan D. Smith, Namrata Gupta, Stacey Gabriel, Lauren Margolin, Marisa A. Shea, Christian M. Shaffer, Zachary T. Yoneda, Eric Boerwinkle, Nicholas L. Smith, Edwin K. Silverman, Susan Redline, Ramachandran S. Vasan, Esteban G. Burchard, Stephanie M. Gogarten, Cecelia Laurie, Thomas W. Blackwell, Gonçalo R. Abecasis, David J. Carey, Brandon K. Fornwalt, Diane T. Smelser, Aris Baras, Frederick E. Dewey, Cashell E. Jaquish, George Papanicolaou, Nona Sotoodehnia, David R. Van Wagoner, Bruce M. Psaty, Sekar Kathiresan, Dawood Darbar, Álvaro Alonso, Susan R. Heckbert, Mina K. Chung, Dan M. Roden, Emelia J. Benjamin, Michael F. Murray, Kathryn L. Lunetta, Steven A. Lubitz, Patrick T. Ellinor

    出版 2018
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  14. 14
    Recovery of trait heritability from whole genome sequence data

    Recovery of trait heritability from whole genome sequence data 由 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

    出版 2019
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  15. 15
    A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13

    A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 由 Elizabeth J. Leslie, Jenna C. Carlson, John R. Shaffer, Eleanor Feingold, George L. Wehby, Cecelia Laurie, Deepti Jain, Cathy C. Laurie, Kimberly F. Doheny, Toby McHenry, Judith Resick, Carla Sanchez, Jennifer Jacobs, Beth Emanuele, Alexandre R. Vieira, Katherine Neiswanger, Andrew C. Lidral, Luz Consuelo Valencia‐Ramirez, Ana María López-Palacio, Dora Rivera Valencia, Mauricio Arcos‐Burgos, Andrew E. Czeizel, L. Leigh Field, Carmencita D. Padilla, Cristina Maria, Frederic W.‐B. Deleyiannis, Kaare Christensen, Ronald G. Munger, Rolv T. Lie, Allen J. Wilcox, Paul A. Romitti, Eduardo E. Castilla, Juan C. Mereb, Fernando A. Poletta, Iêda M. Orioli, Flávia Martinez de Carvalho, Jacqueline T. Hecht, Susan H. Blanton, Carmen J. Buxó, Azeez Butali, Peter Mossey, Wasiu Lanre Adeyemo, Olutayo James, Ramat Oyebunmi Braimah, Babatunde S. Aregbesola, Mekonen Eshete, Fikre Abate, Mine Koruyucu, Figen Seymen, Lian Ma, Javier Salamanca, Seth M. Weinberg, Lina M. Moreno, Jeffrey C. Murray, Mary L. Marazita

    出版 2016
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  16. 16
    A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

    A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 由 Elizabeth J. Leslie, Huan Liu, Jenna C. Carlson, John R. Shaffer, Eleanor Feingold, George L. Wehby, Cecelia Laurie, Deepti Jain, Cathy C. Laurie, Kimberly F. Doheny, Toby McHenry, Judith Resick, Carla Sanchez, Jennifer Jacobs, Beth Emanuele, Alexandre R. Vieira, Katherine Neiswanger, Jennifer Standley, Andrew E. Czeizel, Frederic W.‐B. Deleyiannis, Kaare Christensen, Ronald G. Munger, Rolv T. Lie, Allen J. Wilcox, Paul A. Romitti, L. Leigh Field, Carmencita D. Padilla, Eva Maria C. Cutiongco–de la Paz, Andrew C. Lidral, Luz Consuelo Valencia‐Ramirez, Ana María López-Palacio, Dora Rivera Valencia, Mauricio Arcos‐Burgos, Eduardo E. Castilla, Juan C. Mereb, Fernando A. Poletta, Iêda M. Orioli, Flávia Martinez de Carvalho, Jacqueline T. Hecht, Susan H. Blanton, Carmen J. Buxó, Azeez Butali, Peter Mossey, Wasiu Lanre Adeyemo, Olutayo James, Ramat Oyebunmi Braimah, Babatunde S. Aregbesola, Mekonen Eshete, Milliard Deribew, Mine Koruyucu, Figen Seymen, Lian Ma, Javier Salamanca, Seth M. Weinberg, Lina M. Moreno, Robert A. Cornell, Jeffrey C. Murray, Mary L. Marazita

    出版 2016
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  17. 17
    Genomic analyses in African populations identify novel risk loci for cleft palate

    Genomic analyses in African populations identify novel risk loci for cleft palate 由 Azeez Butali, Peter Mossey, Wasiu Lanre Adeyemo, Mekonen Eshete, Lord J. J. Gowans, Tamara Busch, Deepti Jain, Wenjie Yu, Huan Liu, Cecelia Laurie, Cathy C. Laurie, Sarah C. Nelson, Mary Li, Pedro A. Sanchez‐Lara, William P. Magee, Kathleen Magee, Allyn Auslander, Frederick Brindopke, Denise M. Kay, Michele Caggana, Paul A. Romitti, James L. Mills, Rosemary Audu, Chika Onwuamah, G.O. Oseni, Arwa Owais, Olutayo James, Peter B Olaitan, Babatunde S. Aregbesola, Ramat Oyebunmi Braimah, Fadekemi Olufunmilayo Oginni, Ayodeji O. Oladele, S.A. Bello, Jennifer Rhodes, Rita Shiang, Peter Donkor, Solomon Obiri‐Yeboah, Fareed K. N. Arthur, Peter Twumasi, Pius Agbenorku, Gyikua Plange‐Rhule, Alexander Acheampong Oti, Olugbenga M. Ogunlewe, Afisu A. Oladega, Adegbayi Adeola Adekunle, Olufemi Erinoso, Olawale Adamson, Abosede A Elufowoju, Oluwanifemi I Ayelomi, Taiye Hailu, Abiye Hailu, Yohannes Demissie, Miliard Derebew, Steve Eliason, Miguel Romero-Bustillous, Cynthia Lo, James O. Park, S. Desai, Muiawa Mohammed, Firke Abate, LO Abdur-Rahman, Deepti Anand, Irfan Saadi, Abimibola Victoria Oladugba, Salil A. Lachke, Brad A. Amendt, Charles N. Rotimi, Mary L. Marazita, Robert A. Cornell, Jeffrey C. Murray, Adebowale Adeyemo

    出版 2018
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  18. 18
    Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

    Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants 由 Xutong Zhao, Dandi Qiao, Chaojie Yang, Silva Kasela, Wonji Kim, Yanlin Ma, Nick Shrine, Chiara Batini, Tamar Sofer, Sarah A. Gagliano Taliun, Phuwanat Sakornsakolpat, Pallavi Balte, Dmitry Prokopenko, Bing Yu, Leslie A. Lange, Josée Dupuis, Brian E. Cade, Jiwon Lee, Sina A. Gharib, Michelle Daya, Cecelia Laurie, Ingo Ruczinski, L. Adrienne Cupples, Laura R. Loehr, Traci M. Bartz, Alanna C. Morrison, Bruce M. Psaty, Ramachandran S. Vasan, James G. Wilson, Kent D. Taylor, Peter Durda, W. Craig Johnson, Elaine Cornell, Xiuqing Guo, Yongmei Liu, Russell P. Tracy, Kristin Ardlie, François Aguet, David J. Vandenberg, George Papanicolaou, Jerome I. Rotter, Kathleen C. Barnes, Deepti Jain, Deborah A. Nickerson, Donna M. Muzny, Ginger Metcalf, HarshaVardhan Doddapaneni, Shannon Dugan‐Perez, Namrata Gupta, Stacey Gabriel, Stephen S. Rich, George O'connor, Susan Redline, Robert M. Reed, Cathy C. Laurie, Martha L. Daviglus, Liana K. Preudhomme, Kristin M. Burkart, Robert C. Kaplan, Louise V. Wain, Martin D. Tobin, Stephanie J. London, Tuuli Lappalainen, Elizabeth C. Oelsner, Gonçalo R. Abecasis, Edwin K. Silverman, R. Graham Barr, Michael H. Cho, Ani Manichaikul

    出版 2020
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  19. 19
    Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants

    Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants 由 Kruthika Iyer, Shoa L. Clarke, Rodrigo Guarischi‐Sousa, Ketrin Gjoni, Adam S. Heath, Erica P. Young, Nathan O. Stitziel, Cecelia Laurie, Jai Broome, Alyna Khan, Joshua P. Lewis, Huichun Xu, May E. Montasser, Kellan E. Ashley, Natalie R. Hasbani, Eric Boerwinkle, Alanna C. Morrison, Nathalie Chami, Ron Do, Ghislain Rocheleau, Donald M. Lloyd‐Jones, Rozenn N. Lemaître, Joshua C. Bis, James S. Floyd, Gregory L. Kinney, Donald W. Bowden, Nicholette D. Allred, Emelia J. Benjamin, Matthew Nayor, Lisa R. Yanek, Brian G. Kral, Lewis C. Becker, Sharon L. R. Kardia, Jennifer A. Smith, Lawrence F. Bielak, Arnita F. Norwood, Yuan‐I Min, April P. Carson, Wendy S. Post, Stephen S. Rich, David M. Herrington, Xiuqing Guo, Kent D. Taylor, JoAnn E. Manson, Nora Franceschini, Katherine S. Pollard, Braxton D. Mitchell, Ruth J. F. Loos, Myriam Fornage, Lifang Hou, Bruce M. Psaty, Kendra A. Young, Elizabeth A. Regan, Barry I. Freedman, Ramachandran S. Vasan, Daniel Levy, Rasika A. Mathias, Patricia A. Peyser, Laura M. Raffield, Charles Kooperberg, Alex P. Reiner, Jerome I. Rotter, Goo Jun, Paul S. de Vries, Themistocles L. Assimes

    出版 2025
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  20. 20
    Detectable clonal mosaicism from birth to old age and its relationship to cancer

    Detectable clonal mosaicism from birth to old age and its relationship to cancer 由 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

    出版 2012
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