A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronar...

by Wilson Alexander F, Ruczinski Ingo, Hererra-Galeano J Enrique, Mantese VJ, Yanek Lisa R, Sung Heejong, Kim Yoonhee, Mathias Rasika A, Faraday Nauder, Becker Lewis C, Becker Diane M
Published 2010-06-01

A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q

by Togias Alkis, Malveaux Floyd J, Dunston Georgia M, Furbert-Harris Paulette, Pugh Elizabeth W, Wilson Alexander F, Goldstein Janet L, Gao Peisong, Mathias Rasika A, Barnes Kathleen C, Beaty Terri H, Huang Shau-Ku
Published 2006-06-01

The impact of <it>FADS </it>genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans

by Rudock Megan E, Freedman Barry I, Yanek Lisa R, Case Douglas, Ivester Priscilla, Ziegler Julie T, Suktitipat Bhoom, Vaidya Dhananjay, Kubala Meghan, Hugenschmidt Christina E, Torgerson Dara G, Ruczinski Ingo, Sergeant Susan, Mathias Rasika A, Barnes Kathleen C, Langefeld Carl D, Becker Lewis C, Bowden Donald W, Becker Diane M, Chilton Floyd H
Published 2011-05-01

Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.

by Daya, Michelle, Rafaels, Nicholas, Brunetti, Tonya M, Chavan, Sameer, Levin, Albert M, Shetty, Aniket, Gignoux, Christopher R, Boorgula, Meher Preethi, Wojcik, Genevieve, Campbell, Monica, Vergara, Candelaria, Torgerson, Dara G, Ortega, Victor E, Doumatey, Ayo, Johnston, Henry Richard, Acevedo, Nathalie, Araujo, Maria Ilma, Avila, Pedro C, Belbin, Gillian, Bleecker, Eugene, Bustamante, Carlos, Caraballo, Luis, Cruz, Alvaro, Dunston, Georgia M, Eng, Celeste, Faruque, Mezbah U, Ferguson, Trevor S, Figueiredo, Camila, Ford, Jean G, Gan, Weiniu, Gourraud, Pierre-Antoine, Hansel, Nadia N, Hernandez, Ryan D, Herrera-Paz, Edwin Francisco, Jiménez, Silvia, Kenny, Eimear E, Knight-Madden, Jennifer, Kumar, Rajesh, Lange, Leslie A, Lange, Ethan M, Lizee, Antoine, Maul, Pissamai, Maul, Trevor, Mayorga, Alvaro, Meyers, Deborah, Nicolae, Dan L, O'Connor, Timothy D, Oliveira, Ricardo Riccio, Olopade, Christopher O, Olopade, Olufunmilayo, Qin, Zhaohui S, Rotimi, Charles, Vince, Nicolas, Watson, Harold, Wilks, Rainford J, Wilson, James G, Salzberg, Steven, Ober, Carole, Burchard, Esteban G, Williams, L Keoki, Beaty, Terri H, Taub, Margaret A, Ruczinski, Ingo, Mathias, Rasika A, Barnes, Kathleen C, CAAPA
Published 2019

On the Analysis of Genome-Wide Association Studies in Family-Based Designs: A Universal, Robust Analysis Approach and an Application to Four Genome-Wide Association Studies

by Won, Sungho, Wilk, Jemma B, Mathias, Rasika A., O'Donnell, Christopher Joseph, Silverman, Edwin Kepner, Barnes, Kathleen, O'Connor, George T., Weiss, Scott Tillman, Lange, Christoph
Published 2011

Sensitive Detection of Chromosomal Segments of Distinct Ancestry in Admixed Populations

by Price, Alkes, Tandon, Arti, Patterson, Nick, Barnes, Kathleen C., Rafaels, Nicholas, Ruczinski, Ingo, Beaty, Terri H., Mathias, Rasika, Reich, David Emil, Myers, Simon
Published 2011

Genomic integrity of human induced pluripotent stem cells across nine studies in the NHLBI NextGen program.

by Kanchan, Kanika, Iyer, Kruthika, Yanek, Lisa R, Carcamo-Orive, Ivan, Taub, Margaret A, Malley, Claire, Baldwin, Kristin, Becker, Lewis C, Broeckel, Ulrich, Cheng, Linzhao, Cowan, Chad, D'Antonio, Matteo, Frazer, Kelly A, Quertermous, Thomas, Mostoslavsky, Gustavo, Murphy, George, Rabinovitch, Marlene, Rader, Daniel J, Steinberg, Martin H, Topol, Eric, Yang, Wenli, Knowles, Joshua W, Jaquish, Cashell E, Ruczinski, Ingo, Mathias, Rasika A
Published 2020

Host methylation predicts SARS-CoV-2 infection and clinical outcome.

by Konigsberg, Iain R, Barnes, Bret, Campbell, Monica, Davidson, Elizabeth, Zhen, Yingfei, Pallisard, Olivia, Boorgula, Meher Preethi, Cox, Corey, Nandy, Debmalya, Seal, Souvik, Crooks, Kristy, Sticca, Evan, Harrison, Genelle F, Hopkinson, Andrew, Vest, Alexis, Arnold, Cosby G, Kahn, Michael G, Kao, David P, Peterson, Brett R, Wicks, Stephen J, Ghosh, Debashis, Horvath, Steve, Zhou, Wanding, Mathias, Rasika A, Norman, Paul J, Porecha, Rishi, Yang, Ivana V, Gignoux, Christopher R, Monte, Andrew A, Taye, Alem, Barnes, Kathleen C
Published 2021

Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma

by Igartua, Catherine, Myers, Rachel A., Mathias, Rasika A., Pino-Yanes, Maria, Eng, Celeste, Graves, Penelope E., Levin, Albert M., Del-Rio-Navarro, Blanca E., Jackson, Daniel J., Livne, Oren E., Rafaels, Nicholas, Edlund, Christopher K., Yang, James J., Huntsman, Scott, Salam, Muhammad T., Romieu, Isabelle, Mourad, Raphael, Gern, James E., Lemanske, Robert F., Wyss, Annah, Hoppin, Jane A., Barnes, Kathleen C., Burchard, Esteban G., Gauderman, W. James, Martinez, Fernando D., Raby, Benjamin A., Weiss, Scott T., Williams, L. Keoki, London, Stephanie J., Gilliland, Frank D., Nicolae, Dan L., Ober, Carole
Published 2015

Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.

by Daya, Michelle, Rafaels, Nicholas, Brunetti, Tonya M, Chavan, Sameer, Levin, Albert M, Shetty, Aniket, Gignoux, Christopher R, Boorgula, Meher Preethi, Wojcik, Genevieve, Campbell, Monica, Vergara, Candelaria, Torgerson, Dara G, Ortega, Victor E, Doumatey, Ayo, Johnston, Henry Richard, Acevedo, Nathalie, Araujo, Maria Ilma, Avila, Pedro C, Belbin, Gillian, Bleecker, Eugene, Bustamante, Carlos, Caraballo, Luis, Cruz, Alvaro, Dunston, Georgia M, Eng, Celeste, Faruque, Mezbah U, Ferguson, Trevor S, Figueiredo, Camila, Ford, Jean G, Gan, Weiniu, Gourraud, Pierre-Antoine, Hansel, Nadia N, Hernandez, Ryan D, Herrera-Paz, Edwin Francisco, Jiménez, Silvia, Kenny, Eimear E, Knight-Madden, Jennifer, Kumar, Rajesh, Lange, Leslie A, Lange, Ethan M, Lizee, Antoine, Maul, Pissamai, Maul, Trevor, Mayorga, Alvaro, Meyers, Deborah, Nicolae, Dan L, O'Connor, Timothy D, Oliveira, Ricardo Riccio, Olopade, Christopher O, Olopade, Olufunmilayo, Qin, Zhaohui S, Rotimi, Charles, Vince, Nicolas, Watson, Harold, Wilks, Rainford J, Wilson, James G, Salzberg, Steven, Ober, Carole, Burchard, Esteban G, Williams, L Keoki, Beaty, Terri H, Taub, Margaret A, Ruczinski, Ingo, Mathias, Rasika A, Barnes, Kathleen C, CAAPA
Published 2019

De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.

by Kessler, Michael, Loesch, Douglas, Perry, James, Heard-Costa, Nancy, Taliun, Daniel, Cade, Brian, Wang, Heming, Daya, Michelle, Ziniti, John, Datta, Soma, Celedón, Juan, Soto-Quiros, Manuel, Avila, Lydiana, Weiss, Scott, Barnes, Kathleen, Redline, Susan, Vasan, Ramachandran, Johnson, Andrew, Mathias, Rasika, Hernandez, Ryan, Wilson, James, Nickerson, Deborah, Abecasis, Goncalo, Browning, Sharon, Zöllner, Sebastian, OConnell, Jeffrey, Mitchell, Braxton, OConnor, Timothy
Published 2020

Surfactant protein D is a causal risk factor for COPD: results of Mendelian randomisation.

by Obeidat, Ma'en, Li, Xuan, Burgess, Stephen, Zhou, Guohai, Fishbane, Nick, Hansel, Nadia N, Bossé, Yohan, Joubert, Philippe, Hao, Ke, Nickle, David C, van den Berge, Maarten, Timens, Wim, Cho, Michael H, Hobbs, Brian D, de Jong, Kim, Boezen, Marike, Hung, Rayjean J, Rafaels, Nicholas, Mathias, Rasika, Ruczinski, Ingo, Beaty, Terri H, Barnes, Kathleen C, Paré, Peter D, Sin, Don D, International COPD Genetics Consortium, Lung eQTL Consortium, Lung Health Study
Published 2018

TSLP Polymorphisms are Associated with Asthma in a Sex-Specific Fashion

by Hunninghake, Gary, Soto-Quirós, Manuel E., Avila, Lydiana, Kim, Hong P., Lasky‐Su, Jessica A., Rafaels, Nicholas, Ruczinski, Ingo, Beaty, Terry H., Mathias, Rasika A., Barnes, Kathleen C., Wilk, Jemma B., O’Connor, George T., Gauderman, W. James, Vora, Hita, Baurley, James W., Gilliland, Frank, Liang, Catherine, Sylvia, Jody, Klanderman, Barbara, Sharma, Sunita, Himes, Blanca E., Bossley, Cara J., Israel, Elliot, Raby, Benjamin, Bush, Andrew, Choi, Augustine M.K., Weiss, Scott, Celedón, Juan C.
Published 2021

A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.

by van der Lee, Sven J, Knol, Maria J, Chauhan, Ganesh, Satizabal, Claudia L, Smith, Albert Vernon, Hofer, Edith, Bis, Joshua C, Hibar, Derrek P, Hilal, Saima, van den Akker, Erik B, Arfanakis, Konstantinos, Bernard, Manon, Yanek, Lisa R, Amin, Najaf, Crivello, Fabrice, Cheung, Josh W, Harris, Tamara B, Saba, Yasaman, Lopez, Oscar L, Li, Shuo, van der Grond, Jeroen, Yu, Lei, Paus, Tomas, Roshchupkin, Gennady V, Amouyel, Philippe, Jahanshad, Neda, Taylor, Kent D, Yang, Qiong, Mathias, Rasika A, Boehringer, Stefan, Mazoyer, Bernard, Rice, Ken, Cheng, Ching Yu, Maillard, Pauline, van Heemst, Diana, Wong, Tien Yin, Niessen, Wiro J, Beiser, Alexa S, Beekman, Marian, Zhao, Wanting, Nyquist, Paul A, Chen, Christopher, Launer, Lenore J, Psaty, Bruce M, Ikram, M Kamran, Vernooij, Meike W, Schmidt, Helena, Pausova, Zdenka, Becker, Diane M, De Jager, Philip L, Thompson, Paul M, van Duijn, Cornelia M, Bennett, David A, Slagboom, P Eline, Schmidt, Reinhold, Longstreth, WT, Ikram, M Arfan, Seshadri, Sudha, Debette, Stéphanie, Gudnason, Vilmundur, Adams, Hieab HH, DeCarli, Charles
Published 2019

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.

by Kraja, Aldi T, Vaidya, Dhananjay, Pankow, James S, Goodarzi, Mark O, Assimes, Themistocles L, Kullo, Iftikhar J, Sovio, Ulla, Mathias, Rasika A, Sun, Yan V, Franceschini, Nora, Absher, Devin, Li, Guo, Zhang, Qunyuan, Feitosa, Mary F, Glazer, Nicole L, Haritunians, Talin, Hartikainen, Anna-Liisa, Knowles, Joshua W, North, Kari E, Iribarren, Carlos, Kral, Brian, Yanek, Lisa, O'Reilly, Paul F, McCarthy, Mark I, Jaquish, Cashell, Couper, David J, Chakravarti, Aravinda, Psaty, Bruce M, Becker, Lewis C, Province, Michael A, Boerwinkle, Eric, Quertermous, Thomas, Palotie, Leena, Jarvelin, Marjo-Riitta, Becker, Diane M, Kardia, Sharon LR, Rotter, Jerome I, Chen, Yii-Der Ida, Borecki, Ingrid B
Published 2011

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.

by Huffman, Jennifer E, de Vries, Paul S, Morrison, Alanna C, Sabater-Lleal, Maria, Kacprowski, Tim, Auer, Paul L, Brody, Jennifer A, Chasman, Daniel I, Chen, Ming-Huei, Guo, Xiuqing, Lin, Li-An, Marioni, Riccardo E, Müller-Nurasyid, Martina, Yanek, Lisa R, Pankratz, Nathan, Grove, Megan L, de Maat, Moniek PM, Cushman, Mary, Wiggins, Kerri L, Qi, Lihong, Sennblad, Bengt, Harris, Sarah E, Polasek, Ozren, Riess, Helene, Rivadeneira, Fernando, Rose, Lynda M, Goel, Anuj, Taylor, Kent D, Teumer, Alexander, Uitterlinden, André G, Vaidya, Dhananjay, Yao, Jie, Tang, Weihong, Levy, Daniel, Waldenberger, Melanie, Becker, Diane M, Folsom, Aaron R, Giulianini, Franco, Greinacher, Andreas, Hofman, Albert, Huang, Chiang-Ching, Kooperberg, Charles, Silveira, Angela, Starr, John M, Strauch, Konstantin, Strawbridge, Rona J, Wright, Alan F, McKnight, Barbara, Franco, Oscar H, Zakai, Neil, Mathias, Rasika A, Psaty, Bruce M, Ridker, Paul M, Tofler, Geoffrey H, Völker, Uwe, Watkins, Hugh, Fornage, Myriam, Hamsten, Anders, Deary, Ian J, Boerwinkle, Eric, Koenig, Wolfgang, Rotter, Jerome I, Hayward, Caroline, Dehghan, Abbas, Reiner, Alex P, O'Donnell, Christopher J, Smith, Nicholas L
Published 2015

Detectable Clonal Mosaicism from Birth to Old Age and its Relationship to Cancer

by Laurie, Cathy C., Laurie, Cecelia A., Doheny, Kimberly F., Zelnick, Leila R., McHugh, Caitlin P., Ling, Hua, Hetrick, Kurt N., Amos, Chris, Wei, Qingyi, Wang, Li-e, Hansel, Nadia N., Mathias, Rasika, Daley, Denise, Beaty, Terri H., Scott, Alan F., Ruczinski, Ingo, Scharpf, Rob B., Bierut, Laura J., Hartz, Sarah M., Landi, Maria Teresa, Freedman, Neal D., Goldin, Lynn R., Ginsburg, David, Desch, Karl C., Strom, Sara S., Blot, William J., Ingles, Sue A., Chanock, Stephen J., Berndt, Sonja I., Le Marchand, Loic, Monroe, Kristine R, Heit, John A., de Andrade, Mariza, Armasu, Sebastian M., Regnier, Cynthia, Lowe, William L., Marazita, Mary L., Feingold, Eleanor, Murray, Jeffrey C., Melbye, Mads, Feenstra, Bjarke, Jarvik, Gail P., McDavid, Andrew N., Seshan, Venkatraman E., Mirel, Daniel B., Crenshaw, Andrew, Sharopova, Nataliya, Wise, Anastasia, Shen, Jess, Crosslin, David R., Zheng, Xiuwen, Udren, Jenna I, Bennett, Siiri, Gogarten, Stephanie M., Conomos, Matthew P., Heagerty, Patrick, Manolio, Teri, Haiman, Christopher A., Caporaso, Neil, Weir, Bruce S., Rice, Kenneth, Kang, Jae Hee, Pugh, Elizabeth W., Lee, Jeffrey E., Barnes, Kathleen C., Li, Jun, Signorello, Lisa B, Henderson, Brian E., Hayes, M. Geoffrey, Wiggs, Janey Lee, Levine, David M., Nelson, Sarah C., Pasquale, Louis
Published 2013

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program.

by DiCorpo, Daniel, Gaynor, Sheila M, Russell, Emily M, Westerman, Kenneth E, Raffield, Laura M, Majarian, Timothy D, Wu, Peitao, Sarnowski, Chloé, Highland, Heather M, Jackson, Anne, Hasbani, Natalie R, de Vries, Paul S, Brody, Jennifer A, Hidalgo, Bertha, Guo, Xiuqing, Perry, James A, O'Connell, Jeffrey R, Lent, Samantha, Montasser, May E, Cade, Brian E, Jain, Deepti, Wang, Heming, D'Oliveira Albanus, Ricardo, Varshney, Arushi, Yanek, Lisa R, Lange, Leslie, Palmer, Nicholette D, Almeida, Marcio, Peralta, Juan M, Aslibekyan, Stella, Baldridge, Abigail S, Bertoni, Alain G, Bielak, Lawrence F, Chen, Chung-Shiuan, Chen, Yii-Der Ida, Choi, Won Jung, Goodarzi, Mark O, Floyd, James S, Irvin, Marguerite R, Kalyani, Rita R, Kelly, Tanika N, Lee, Seonwook, Liu, Ching-Ti, Loesch, Douglas, Manson, JoAnn E, Minster, Ryan L, Naseri, Take, Pankow, James S, Rasmussen-Torvik, Laura J, Reiner, Alexander P, Reupena, Muagututi'a Sefuiva, Selvin, Elizabeth, Smith, Jennifer A, Weeks, Daniel E, Xu, Huichun, Yao, Jie, Zhao, Wei, Parker, Stephen, Alonso, Alvaro, Arnett, Donna K, Blangero, John, Boerwinkle, Eric, Correa, Adolfo, Cupples, L Adrienne, Curran, Joanne E, Duggirala, Ravindranath, He, Jiang, Heckbert, Susan R, Kardia, Sharon LR, Kim, Ryan W, Kooperberg, Charles, Liu, Simin, Mathias, Rasika A, McGarvey, Stephen T, Mitchell, Braxton D, Morrison, Alanna C, Peyser, Patricia A, Psaty, Bruce M, Redline, Susan, Shuldiner, Alan R, Taylor, Kent D, Vasan, Ramachandran S, Viaud-Martinez, Karine A, Florez, Jose C, Wilson, James G, Sladek, Robert, Rich, Stephen S, Rotter, Jerome I, Lin, Xihong, Dupuis, Josée, Meigs, James B, Wessel, Jennifer, Manning, Alisa K
Published 2022

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.

by Nielsen, Jonas B, Rom, Oren, Surakka, Ida, Graham, Sarah E, Zhou, Wei, Roychowdhury, Tanmoy, Fritsche, Lars G, Gagliano Taliun, Sarah A, Sidore, Carlo, Liu, Yuhao, Gabrielsen, Maiken E, Skogholt, Anne Heidi, Wolford, Brooke, Overton, William, Zhao, Ying, Chen, Jin, Zhang, He, Hornsby, Whitney E, Acheampong, Akua, Grooms, Austen, Schaefer, Amanda, Zajac, Gregory JM, Villacorta, Luis, Zhang, Jifeng, Brumpton, Ben, Løset, Mari, Rai, Vivek, Lundegaard, Pia R, Olesen, Morten S, Taylor, Kent D, Palmer, Nicholette D, Chen, Yii-Der, Choi, Seung H, Lubitz, Steven A, Ellinor, Patrick T, Barnes, Kathleen C, Daya, Michelle, Rafaels, Nicholas, Weiss, Scott T, Lasky-Su, Jessica, Tracy, Russell P, Vasan, Ramachandran S, Cupples, L Adrienne, Mathias, Rasika A, Yanek, Lisa R, Becker, Lewis C, Peyser, Patricia A, Bielak, Lawrence F, Smith, Jennifer A, Aslibekyan, Stella, Hidalgo, Bertha A, Arnett, Donna K, Irvin, Marguerite R, Wilson, James G, Musani, Solomon K, Correa, Adolfo, Rich, Stephen S, Guo, Xiuqing, Rotter, Jerome I, Konkle, Barbara A, Johnsen, Jill M, Ashley-Koch, Allison E, Telen, Marilyn J, Sheehan, Vivien A, Blangero, John, Curran, Joanne E, Peralta, Juan M, Montgomery, Courtney, Sheu, Wayne H-H, Chung, Ren-Hua, Schwander, Karen, Nouraie, Seyed M, Gordeuk, Victor R, Zhang, Yingze, Kooperberg, Charles, Reiner, Alexander P, Jackson, Rebecca D, Bleecker, Eugene R, Meyers, Deborah A, Li, Xingnan, Das, Sayantan, Yu, Ketian, LeFaive, Jonathon, Smith, Albert, Blackwell, Tom, Taliun, Daniel, Zollner, Sebastian, Forer, Lukas, Schoenherr, Sebastian, Fuchsberger, Christian, Pandit, Anita, Zawistowski, Matthew, Kheterpal, Sachin, Brummett, Chad M, Natarajan, Pradeep, Schlessinger, David, Lee, Seunggeun, Kang, Hyun Min, Cucca, Francesco, Holmen, Oddgeir L
Published 2020

Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis

by Bunyavanich, Supinda, Schadt, Eric E, Himes, Blanca E, Lasky-Su, Jessica, Qiu, Weiliang, Lazarus, Ross, Ziniti, John P, Cohain, Ariella, Linderman, Michael, Torgerson, Dara G, Eng, Celeste S, Pino-Yanes, Maria, Padhukasahasram, Badri, Yang, James J, Mathias, Rasika A, Beaty, Terri H, Li, Xingnan, Graves, Penelope, Romieu, Isabelle, Navarro, Blanca del Rio, Salam, M Towhid, Vora, Hita, Nicolae, Dan L, Ober, Carole, Martinez, Fernando D, Bleecker, Eugene R, Meyers, Deborah A, Gauderman, W James, Gilliland, Frank, Burchard, Esteban G, Barnes, Kathleen C, Williams, L Keoki, London, Stephanie J, Zhang, Bin, Raby, Benjamin A, Weiss, Scott T
Published 2014