Ancestry-specific recent effective population size in the Americas

por Browning, Sharon R., Browning, Brian L., Daviglus, Martha L., Durazo-Arvizu, Ramon A., Schneiderman, Neil, Kaplan, Robert C., Laurie, Cathy C.
Publicado 2018

Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays

por Nelson, Sarah C., Doheny, Kimberly F., Pugh, Elizabeth W., Romm, Jane M., Ling, Hua, Laurie, Cecelia A., Browning, Sharon R., Weir, Bruce S., Laurie, Cathy C.
Publicado 2013

Linkage Disequilibrium in Wild Mice

por Laurie, Cathy C, Nickerson, Deborah A, Anderson, Amy D, Weir, Bruce S, Livingston, Robert J, Dean, Matthew D, Smith, Kimberly L, Schadt, Eric E, Nachman, Michael W
Publicado 2007

Local Ancestry Inference in a Large US-Based Hispanic/Latino Study: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

por Browning, Sharon R., Grinde, Kelsey, Plantinga, Anna, Gogarten, Stephanie M., Stilp, Adrienne M., Kaplan, Robert C., Avilés-Santa, M. Larissa, Browning, Brian L., Laurie, Cathy C.
Publicado 2016

Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN)

por Mitchell, Braxton D., Fornage, Myriam, McArdle, Patrick F., Cheng, Yu-Ching, Pulit, Sara L., Wong, Quenna, Dave, Tushar, Williams, Stephen R., Corriveau, Roderick, Gwinn, Katrina, Doheny, Kimberly, Laurie, Cathy C., Rich, Stephen S., de Bakker, Paul I. W.
Publicado 2014

Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos

por Sofer, Tamar, Emery, Leslie, Jain, Deepti, Ellis, Alicia M., Laurie, Cathy C., Allison, Matthew A., Lee, Jiwon, Kurniansyah, Nuzulul, Kerr, Kathleen F., González, Hector M., Tarraf, Wassim, Criqui, Michael H., Lange, Leslie A., Palmas, Walter R., Franceschini, Nora, Wassel, Christina L.
Publicado 2019

Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial

por Keene, Keith L., Chen, Wei-Min, Chen, Fang, Williams, Stephen R., Elkhatib, Stacey D., Hsu, Fang-Chi, Mychaleckyj, Josyf C., Doheny, Kimberly F., Pugh, Elizabeth W., Ling, Hua, Laurie, Cathy C., Gogarten, Stephanie M., Madden, Ebony B., Worrall, Bradford B., Sale, Michele M.
Publicado 2014

Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

por Hidalgo, Bertha A., Sofer, Tamar, Qi, Qibin, Schneiderman, Neil, Chen, Y.-D. Ida, Kaplan, Robert C., Avilés-Santa, M. Larissa, North, Kari E., Arnett, Donna K., Szpiro, Adam, Cai, Jianwen, Yu, Bing, Boerwinkle, Eric, Papanicolaou, George, Laurie, Cathy C., Rotter, Jerome I., Stilp, Adrienne M.
Publicado 2019

Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

por Qi, Qibin, Stilp, Adrienne M., Sofer, Tamar, Moon, Jee-Young, Hidalgo, Bertha, Szpiro, Adam A., Wang, Tao, Ng, Maggie C.Y., Guo, Xiuqing, Chen, Yii-Der Ida, Taylor, Kent D., Aviles-Santa, M. Larissa, Papanicolaou, George, Pankow, James S., Schneiderman, Neil, Laurie, Cathy C., Rotter, Jerome I., Kaplan, Robert C.
Publicado 2017

Complex patterns of direct and indirect association between the transcription Factor-7 like 2 gene, body mass index and type 2 diabetes diagnosis in adulthood in the Hispanic Commu...

por Fernández-Rhodes, Lindsay, Howard, Annie Green, Graff, Mariaelisa, Isasi, Carmen R., Highland, Heather M., Young, Kristin L., Parra, Esteban, Below, Jennifer E., Qi, Qibin, Kaplan, Robert C., Justice, Anne E., Papanicolaou, George, Laurie, Cathy C., Grant, Struan F. A., Haiman, Christopher, Loos, Ruth J. F., North, Kari E.
Publicado 2018

Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos

por Jian, Xueqiu, Sofer, Tamar, Tarraf, Wassim, Bressler, Jan, Faul, Jessica D., Zhao, Wei, Ratliff, Scott M., Lamar, Melissa, Launer, Lenore J., Laurie, Cathy C., Schneiderman, Neil, Weir, David R., Wright, Clinton B., Yaffe, Kristine, Zeng, Donglin, DeCarli, Charles, Mosley, Thomas H., Smith, Jennifer A., González, Hector M., Fornage, Myriam
Publicado 2020

Genome-wide association Scan of dental caries in the permanent dentition

por Wang, Xiaojing, Shaffer, John R, Zeng, Zhen, Begum, Ferdouse, Vieira, Alexandre R, Noel, Jacqueline, Anjomshoaa, Ida, Cuenco, Karen T, Lee, Myoung-Keun, Beck, James, Boerwinkle, Eric, Cornelis, Marilyn C, Hu, Frank B, Crosslin, David R, Laurie, Cathy C, Nelson, Sarah C, Doheny, Kimberly F, Pugh, Elizabeth W, Polk, Deborah E, Weyant, Robert J, Crout, Richard, McNeil, Daniel W, Weeks, Daniel E, Feingold, Eleanor, Marazita, Mary L
Publicado 2012

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

por Shaffer, John R., Orlova, Ekaterina, Lee, Myoung Keun, Leslie, Elizabeth J., Raffensperger, Zachary D., Heike, Carrie L., Cunningham, Michael L., Hecht, Jacqueline T., Kau, Chung How, Nidey, Nichole L., Moreno, Lina M., Wehby, George L., Murray, Jeffrey C., Laurie, Cecelia A., Laurie, Cathy C., Cole, Joanne, Ferrara, Tracey, Santorico, Stephanie, Klein, Ophir, Mio, Washington, Feingold, Eleanor, Hallgrimsson, Benedikt, Spritz, Richard A., Marazita, Mary L., Weinberg, Seth M.
Publicado 2016

Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma

por Wang, Zhaoxi, Wei, Yongyue, Zhang, Ruyang, Su, Li, Gogarten, Stephanie M., Liu, Geoffrey, Brennan, Paul, Field, John K., McKay, James D., Lissowska, Jolanta, Swiatkowska, Beata, Janout, Vladimir, Bolca, Ciprian, Kontic, Milica, Scelo, Ghislaine, Zaridze, David, Laurie, Cathy C., Doheny, Kimberly F., Pugh, Elizabeth K., Marosy, Beth A., Hetrick, Kurt N., Xiao, Xiangjun, Pikielny, Claudio, Hung, Rayjean J., Amos, Christopher I., Lin, Xihong, Christiani, David C.
Publicado 2018

GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals

por Méndez-Giráldez, Raúl, Gogarten, Stephanie M., Below, Jennifer E., Yao, Jie, Seyerle, Amanda A., Highland, Heather M., Kooperberg, Charles, Soliman, Elsayed Z., Rotter, Jerome I., Kerr, Kathleen F., Ryckman, Kelli K., Taylor, Kent D., Petty, Lauren E., Shah, Sanjiv J., Conomos, Matthew P., Sotoodehnia, Nona, Cheng, Susan, Heckbert, Susan R., Sofer, Tamar, Guo, Xiuqing, Whitsel, Eric A., Lin, Henry J., Hanis, Craig L., Laurie, Cathy C., Avery, Christy L.
Publicado 2017

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease

por Raffield, Laura M., Ulirsch, Jacob C., Naik, Rakhi P., Lessard, Samuel, Handsaker, Robert E., Jain, Deepti, Kang, Hyun M., Pankratz, Nathan, Auer, Paul L., Bao, Erik L., Smith, Joshua D., Lange, Leslie A., Lange, Ethan M., Li, Yun, Thornton, Timothy A., Young, Bessie A., Abecasis, Goncalo R., Laurie, Cathy C., Nickerson, Deborah A., McCarroll, Steven A., Correa, Adolfo, Wilson, James G., Lettre, Guillaume, Sankaran, Vijay G., Reiner, Alex P.
Publicado 2018

Genome-Wide Association Analysis of Ischemic Stroke in Young Adults

por Cheng, Yu-Ching, O’Connell, Jeffrey R., Cole, John W., Stine, O. Colin, Dueker, Nicole, McArdle, Patrick F., Sparks, Mary J., Shen, Jess, Laurie, Cathy C., Nelson, Sarah, Doheny, Kimberly F., Ling, Hua, Pugh, Elizabeth W., Brott, Thomas G., Brown, Robert D., Meschia, James F., Nalls, Michael, Rich, Stephen S., Worrall, Bradford, Anderson, Christopher D., Biffi, Alessandro, Cortellini, Lynelle, Furie, Karen L., Rost, Natalia S., Rosand, Jonathan, Manolio, Teri A., Kittner, Steven J., Mitchell, Braxton D.
Publicado 2011

Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos

por Hodonsky, Chani J., Jain, Deepti, Schick, Ursula M., Morrison, Jean V., Brown, Lisa, McHugh, Caitlin P., Schurmann, Claudia, Chen, Diane D., Liu, Yong Mei, Auer, Paul L., Laurie, Cecilia A., Taylor, Kent D., Browning, Brian L., Li, Yun, Papanicolaou, George, Rotter, Jerome I., Kurita, Ryo, Nakamura, Yukio, Browning, Sharon R., Loos, Ruth J. F., North, Kari E., Laurie, Cathy C., Thornton, Timothy A., Pankratz, Nathan, Bauer, Daniel E., Sofer, Tamar, Reiner, Alex P.
Publicado 2017

Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts

por Oseni, Ganiyu O., Jain, Deepti, Mossey, Peter A., Busch, Tamara D., Gowans, Lord J.J., Eshete, Mekonen A., Adeyemo, Wasiu L., Laurie, Cecelia A., Laurie, Cathy C., Owais, Arwa, Olaitan, Peter B., Aregbesola, Babatunde S., Oginni, Fadekemi O., Bello, Saidu A., Donkor, Peter, Audu, Rosemary, Onwuamah, Chika, Obiri‐Yeboah, Solomon, Plange‐Rhule, Gyikua, Ogunlewe, Olugbenga M., James, Olutayo, Halilu, Taiye, Abate, Firke, Abdur‐Rahman, Lukman O., Oladugba, Abimbola V., Marazita, Mary L., Murray, Jeffrey C., Adeyemo, Adebowale A., Butali, Azeez
Publicado 2018

GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations

por Swenson, Brenton R., Louie, Tin, Lin, Henry J., Méndez-Giráldez, Raúl, Below, Jennifer E., Laurie, Cathy C., Kerr, Kathleen F., Highland, Heather, Thornton, Timothy A., Ryckman, Kelli K., Kooperberg, Charles, Soliman, Elsayed Z., Seyerle, Amanda A., Guo, Xiuqing, Taylor, Kent D., Yao, Jie, Heckbert, Susan R., Darbar, Dawood, Petty, Lauren E., McKnight, Barbara, Cheng, Susan, Bello, Natalie A., Whitsel, Eric A., Hanis, Craig L., Nalls, Mike A., Evans, Daniel S., Rotter, Jerome I., Sofer, Tamar, Avery, Christy L., Sotoodehnia, Nona
Publicado 2019