ZCCHC8 , the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation von Gable, Dustin L, Gaysinskaya, Valeriya, Atik, Christine C, Talbot, Jr, C Conover, Kang, Byunghak, Stanley, Susan E, Pugh, Elizabeth W, Amat-Codina, Nuria, Schenk, Kara M, Arcasoy, Murat O, Brayton, Cory, Florea, Liliana, Armanios, Mary

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Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients von Zhou, Yi-Hui, Gallins, Paul J, Pace, Rhonda G, Dang, Hong, Aksit, Melis A, Blue, Elizabeth E, Buckingham, Kati J, Collaco, Joseph M, Faino, Anna V, Gordon, William W, Hetrick, Kurt N, Ling, Hua, Liu, Weifang, Onchiri, Frankline M, Pagel, Kymberleigh, Pugh, Elizabeth W, Raraigh, Karen S, Rosenfeld, Margaret, Sun, Quan, Wen, Jia, Li, Yun, Corvol, Harriet, Strug, Lisa J, Bamshad, Michael J, Blackman, Scott M, Cutting, Garry R, Gibson, Ronald L, O'Neal, Wanda K, Wright, Fred A, Knowles, Michael R

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Genetic modifiers of body mass index in individuals with cystic fibrosis von Ling, Hua, Raraigh, Karen S., Pugh, Elizabeth W., Aksit, Melis A., Zhang, Peng, Pace, Rhonda G., Faino, Anna V., Bamshad, Michael J., Gibson, Ronald L., O’Neal, Wanda, Knowles, Michael R., Blackman, Scott M., Cutting, Garry R., Aksit, Melis A., Bamshad, Michael J., Blackman, Scott M., Blue, Elizabeth, Buckingham, Kati, Chong, Jessica X., Collaco, J. Michael, Cutting, Garry R., Dang, Hong, Eastman, Alice, Faino, Anna, Gallins, Paul J., Gibson, Ronald, Godwin, Beth, Gordon, William W., Hetrick, Kurt, Huang, Le, Knowles, Michael R., Lam, Anh-Thu N., Ling, Hua, Liu, Weifang, Li, Yun, Onchiri, Frankline, O'Neal, Wanda K., Pace, Rhonda G., Pagel, Kymberleigh, Porter, Mark, Pugh, Elizabeth, Raraigh, Karen S., Mikeasky, Rebekah, Rosenfeld, Margaret, Rosen, Jonathan, Stilp, Adrienne, Stonebraker, Jaclyn R., Sun, Quan, Wen, Jia, Wright, Fred A., Yang, Yingxi, Zhang, Peng, Zhou, Yi-Hui

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease von Pankratz, Nathan, Wilk, Jemma B, Latourelle, Jeanne C, DeStefano, Anita L, Halter, Cheryl, Pugh, Elizabeth W, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Foroud, Tatiana, Myers, Richard H

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Genome partitioning of genetic variation for complex traits using common SNPs von Yang, Jian, Manolio, Teri A, Pasquale, Louis R, Boerwinkle, Eric, Caporaso, Neil, Cunningham, Julie M, de Andrade, Mariza, Feenstra, Bjarke, Feingold, Eleanor, Hayes, M Geoffrey, Hill, William G, Landi, Maria Teresa, Alonso, Alvaro, Lettre, Guillaume, Lin, Peng, Ling, Hua, Lowe, William, Mathias, Rasika A, Melbye, Mads, Pugh, Elizabeth, Cornelis, Marilyn C, Weir, Bruce S, Goddard, Michael E, Visscher, Peter M

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

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Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndrome von Moreno, Carolina Araujo, Sobreira, Nara, Pugh, Elizabeth, Zhang, Peng, Steel, Gary, Torres, Fábio Rossi, Cavalcanti, Denise Pontes

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Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients von Sun, Quan, Liu, Weifang, Rosen, Jonathan D., Huang, Le, Pace, Rhonda G., Dang, Hong, Gallins, Paul J., Blue, Elizabeth E., Ling, Hua, Corvol, Harriet, Strug, Lisa J., Bamshad, Michael J., Gibson, Ronald L., Pugh, Elizabeth W., Blackman, Scott M., Cutting, Garry R., O'Neal, Wanda K., Zhou, Yi-Hui, Wright, Fred A., Knowles, Michael R., Wen, Jia, Li, Yun

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Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics von Jurgens, Julie, Ling, Hua, Hetrick, Kurt, Pugh, Elizabeth, Schiettecatte, Francois, Doheny, Kimberly, Hamosh, Ada, Avramopoulos, Dimitri, Valle, David, Sobreira, Nara

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Common variants in the GDF5-UQCC region are associated with variation in human height von Abecasis, Gonçalo R, Mohlke, Karen L, Sanna, Serena, Jackson, Anne U, Nagaraja, Ramaiah, Willer, Cristen J, Chen, Wei-Min, Bonnycastle, Lori L, Shen, Haiqing, Timpson, Nicholas, Lettre, Guillaume, Usala, Gianluca, Chines, Peter S, Stringham, Heather M, Scott, Laura J, Dei, Mariano, Lai, Sandra, Albai, Giuseppe, Crisponi, Laura, Naitza, Silvia, Doheny, Kimberly F, Pugh, Elizabeth W, Ben-Shlomo, Yoav, Ebrahim, Shah, Lawlor, Debbie A, Bergman, Richard N, Watanabe, Richard M, Uda, Manuela, Tuomilehto, Jaakko, Coresh, Josef, Hirschhorn, Joel N, Shuldiner, Alan R, Schlessinger, David, Collins, Francis S, Smith, George Davey, Boerwinkle, Eric, Cao, Antonio, Boehnke, Michael

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Preparation and use of varied natural tools for extractive foraging by bonobos (Pan Paniscus) von Roffman, Itai, Savage-Rumbaugh, Sue, Rubert-Pugh, Elizabeth, Stadler, André, Ronen, Avraham, Nevo, Eviatar

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Imputation and quality control steps for combining multiple genome-wide datasets von Verma, Shefali S, de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P, Kottyan, Leah C, Burt, Amber, Bradford, Yuki, Armstrong, Gretta D, Derr, Kimberly, Crawford, Dana C, Haines, Jonathan L, Li, Rongling, Crosslin, David, Ritchie, Marylyn D

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DNA Identifications after the 9/11 World Trade Center Attack von Biesecker, Leslie G., Bailey-Wilson, Joan E., Ballantyne, Jack, Baum, Howard, Bieber, Frederick R., Brenner, Charles, Budowle, Bruce, Butler, John M., Carmody, George, Conneally, P. Michael, Duceman, Barry, Eisenberg, Arthur, Forman, Lisa, Kidd, Kenneth K., Leclair, Benoît, Niezgoda, Steven, Parsons, Thomas J., Pugh, Elizabeth, Shaler, Robert, Sherry, Stephen T., Sozer, Amanda, Walsh, Anne

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

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Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate von Beaty, Terri H., Ruczinski, Ingo, Murray, Jeffrey C., Marazita, Mary L., Munger, Ronald G., Hetmanski, Jacqueline B., Murray, Tanda, Redett, Richard J., Fallin, M. Daniele, Liang, Kung Yee, Wu, Tao, Patel, Poorav J., Jin, Sheng‐Chih, Zhang, Tian Xiao, Schwender, Holger, Wu‐Chou, Yah Huei, Chen, Philip K., Chong, Samuel S., Cheah, Felicia, Yeow, Vincent, Ye, Xiaoqian, Wang, Hong, Huang, Shangzhi, Jabs, Ethylin W., Shi, Bing, Wilcox, Allen J., Lie, Rolv T., Jee, Sun Ha, Christensen, Kaare, Doheny, Kimberley F., Pugh, Elizabeth W., Ling, Hua, Scott, Alan F.

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A genome-wide association study on African-ancestry populations for asthma von Mathias, Rasika A., ScD, Grant, Audrey V., PhD, Rafaels, Nicholas, MS, Hand, Tracey, MS, Gao, Li, MD, PhD, Vergara, Candelaria, MSc, Tsai, Yuhjung J., MD, Yang, Mao, MS, Campbell, Monica, BS, Foster, Cassandra, Gao, Peisong, MD, PhD, Togias, A., MD, Hansel, Nadia N., MD, MPH, Diette, Gregory, MD, Adkinson, N. Franklin, MD, Liu, Mark C., MD, Faruque, Mezbah, MD, PhD, Dunston, Georgia M., PhD, Watson, Harold R., MD, Bracken, Michael B., PhD, Hoh, Josephine, PhD, Maul, Pissamai, RN, Maul, Trevor, RN, Jedlicka, Anne E., MS, Murray, Tanda, MS, Hetmanski, Jacqueline B., MS, Ashworth, Roxann, MHS, Ongaco, Chrissie M., BS, Hetrick, Kurt N., MS, Doheny, Kimberly F., PhD, Pugh, Elizabeth W., PhD, MPH, Rotimi, Charles N., PhD, Ford, Jean, MD, Eng, Celeste, BS, Burchard, Esteban G., MD, Sleiman, Patrick M.A., PhD, Hakonarson, Hakon, MD, PhD, Forno, Erick, MD, Raby, Benjamin A., MD, Weiss, Scott T., MD, Scott, Alan F., PhD, Kabesch, Michael, MD, Liang, Liming, MS, Abecasis, Gonçalo, PhD, Moffatt, Miriam F., PhD, Cookson, William O.C., MD, Ruczinski, Ingo, PhD, Beaty, Terri H., PhD, Barnes, Kathleen C., PhD

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Identification of candidate regions for familial idiopathic scoliosis von MILLER, Nancy H, JUSTICE, Cristina M, MAROSY, Beth, DOHENY, Kimberly F, PUGH, Elizabeth, JUN ZHANG, DIETZ, Harry C, WILSON, Alexander F

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Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes von Gaulton, Kyle J, Willer, Cristen J, Li, Yun, Scott, Laura J, Conneely, Karen N, Jackson, Anne U, Duren, William L, Chines, Peter S, Narisu, Narisu, Bonnycastle, Lori L, Luo, Jingchun, Tong, Maurine, Sprau, Andrew G, Pugh, Elizabeth W, Doheny, Kimberly F, Valle, Timo T, Abecasis, Gonçalo R, Tuomilehto, Jaakko, Bergman, Richard N, Collins, Francis S, Boehnke, Michael, Mohlke, Karen L

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Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion von Huyghe, Jeroen R, Jackson, Anne U, Fogarty, Marie P, Buchkovich, Martin L, Stančáková, Alena, Stringham, Heather M, Sim, Xueling, Yang, Lingyao, Fuchsberger, Christian, Cederberg, Henna, Chines, Peter S, Teslovich, Tanya M, Romm, Jane M, Ling, Hua, McMullen, Ivy, Ingersoll, Roxann, Pugh, Elizabeth W, Doheny, Kimberly F, Neale, Benjamin M, Daly, Mark J, Kuusisto, Johanna, Scott, Laura J, Kang, Hyun Min, Collins, Francis S, Abecasis, Gonçalo R, Watanabe, Richard M, Boehnke, Michael, Laakso, Markku, Mohlke, Karen L

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The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions von Cornelis, Marilyn C., Agrawal, Arpana, Cole, John W., Hansel, Nadia N., Barnes, Kathleen C., Beaty, Terri H., Bennett, Siiri N., Bierut, Laura J., Boerwinkle, Eric, Doheny, Kimberly F., Feenstra, Bjarke, Feingold, Eleanor, Fornage, Myriam, Haiman, Christopher A., Harris, Emily L., Hayes, M. Geoffrey, Heit, John A., Hu, Frank B., Kang, Jae H., Laurie, Cathy C., Ling, Hua, Manolio, Teri A., Marazita, Mary L., Mathias, Rasika A., Mirel, Daniel B., Paschall, Justin, Pasquale, Louis R., Pugh, Elizabeth W., Rice, John P., Udren, Jenna, van Dam, Rob M., Wang, Xiaojing, Wiggs, Janey L., Williams, Kayleen, Yu, Kai

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