No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees

por Allen-Brady, Kristina, Farnham, James M, Camp, Nicola J, Karlins, Eric, Ostrander, Elaine A, Cannon-Albright, Lisa A
Publicado 2009

Identifying, understanding, and correcting technical artifacts on the sex chromosomes in next-generation sequencing data

por Webster, Timothy H, Couse, Madeline, Grande, Bruno M, Karlins, Eric, Phung, Tanya N, Richmond, Phillip A, Whitford, Whitney, Wilson, Melissa A
Publicado 2019

A Copy Number Variant at the KITLG Locus Likely Confers Risk for Canine Squamous Cell Carcinoma of the Digit

por Karyadi, Danielle M., Karlins, Eric, Decker, Brennan, vonHoldt, Bridgett M., Carpintero-Ramirez, Gretchen, Parker, Heidi G., Wayne, Robert K., Ostrander, Elaine A.
Publicado 2013

Age-related DNA methylation in paired normal and tumour breast tissue in Chinese breast cancer patients

por Kiely, Maeve, Tse, Lap Ah, Koka, Hela, Wang, Difei, Lee, Priscilla, Wang, Feng, Wu, Cherry, Tsang, Koon Ho, Chan, Wing-Cheong, Law, Sze Hong, Zhang, Han, Karlins, Eric, Zhu, Bin, Hutchinson, Amy, Hicks, Belynda, Zhu, Bin, Yang, Xiaohong R.
Publicado 2020

Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor

por Decker, Brennan, Davis, Brian W., Rimbault, Maud, Long, Adrienne H., Karlins, Eric, Jagannathan, Vidhya, Reiman, Rebecca, Parker, Heidi G., Drögemüller, Cord, Corneveaux, Jason J., Chapman, Erica S., Trent, Jeffery M., Leeb, Tosso, Huentelman, Matthew J., Wayne, Robert K., Karyadi, Danielle M., Ostrander, Elaine A.
Publicado 2015

Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays

por Dagnall, Casey L., Morton, Lindsay M., Hicks, Belynda D., Li, Shengchao, Zhou, Weiyin, Karlins, Eric, Teshome, Kedest, Chowdhury, Salma, Lashley, Kerrie S., Sampson, Joshua N., Robison, Leslie L., Armstrong, Gregory T., Bhatia, Smita, Radloff, Gretchen A., Davies, Stella M., Tucker, Margaret A., Yeager, Meredith, Chanock, Stephen J.
Publicado 2018

Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susce...

por Karyadi, Danielle M., Geybels, Milan S., Karlins, Eric, Decker, Brennan, McIntosh, Laura, Hutchinson, Amy, Kolb, Suzanne, McDonnell, Shannon K., Hicks, Belynda, Middha, Sumit, FitzGerald, Liesel M., DeRycke, Melissa S., Yeager, Meredith, Schaid, Daniel J., Chanock, Stephen J., Thibodeau, Stephen N., Berndt, Sonja I., Stanford, Janet L., Ostrander, Elaine A.
Publicado 2016

Blood DNA methylation and breast cancer risk: a meta-analysis of four prospective cohort studies

por Bodelon, Clara, Ambatipudi, Srikant, Dugué, Pierre-Antoine, Johansson, Annelie, Sampson, Joshua N., Hicks, Belynda, Karlins, Eric, Hutchinson, Amy, Cuenin, Cyrille, Chajès, Veronique, Southey, Melissa C., Romieu, Isabelle, Giles, Graham G., English, Dallas, Polidoro, Silvia, Assumma, Manuela, Baglietto, Laura, Vineis, Paolo, Severi, Gianluca, Herceg, Zdenko, Flanagan, James M., Milne, Roger L., Garcia-Closas, Montserrat
Publicado 2019

Evaluating the Causal Link Between Malaria Infection and Endemic Burkitt Lymphoma in Northern Uganda: A Mendelian Randomization Study

por Legason, Ismail D., Pfeiffer, Ruth M., Udquim, Krizia-Ivana, Bergen, Andrew W., Gouveia, Mateus H., Kirimunda, Samuel, Otim, Isaac, Karlins, Eric, Kerchan, Patrick, Nabalende, Hadijah, Bayanjargal, Ariunaa, Emmanuel, Benjamin, Kagwa, Paul, Talisuna, Ambrose O., Bhatia, Kishor, Yeager, Meredith, Biggar, Robert J., Ayers, Leona W., Reynolds, Steven J., Goedert, James J., Ogwang, Martin D., Fraumeni, Joseph F., Prokunina-Olsson, Ludmila, Mbulaiteye, Sam M.
Publicado 2017

DNA methylation age in paired tumor and adjacent normal breast tissue in Chinese women with breast cancer

por Koka, Hela, Bodelon, Clara, Horvath, Steve, Lee, Priscilla Ming Yi, Wang, Difei, Song, Lei, Zhang, Tongwu, Hurson, Amber N., Guida, Jennifer Lyn, Zhu, Bin, Bailey-Whyte, Maeve, Wang, Feng, Wu, Cherry, Tsang, Koon Ho, Tsoi, Yee-Kei, Chan, W. C., Law, Sze Hong, Hung, Ray Ka Wai, Tse, Gary M., Yuen, Karen Ka-wan, Karlins, Eric, Jones, Kristine, Vogt, Aurelie, Zhu, Bin, Hutchinson, Amy, Hicks, Belynda, Garcia-Closas, Montserrat, Chanock, Stephen, Barnholtz-Sloan, Jill, Tse, Lap Ah, Yang, Xiaohong R.
Publicado 2023

Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity

por Beers, Breanna J., Similuk, Morgan N., Ghosh, Rajarshi, Seifert, Bryce A., Jamal, Leila, Kamen, Michael, Setzer, Michael R., Jodarski, Colleen, Duncan, Rylee, Hunt, Devin, Mixer, Madison, Cao, Wenjia, Bi, Weimin, Veltri, Daniel, Karlins, Eric, Zhang, Lingwen, Li, Zhiwen, Oler, Andrew J., Jevtich, Kathleen, Yu, Yunting, Hullfish, Haley, Bielekova, Bibiana, Frischmeyer-Guerrerio, Pamela, Dang Do, An, Huryn, Laryssa A., Olivier, Kenneth N., Su, Helen C., Lyons, Jonathan J., Zerbe, Christa S., Rao, V. Koneti, Keller, Michael D., Freeman, Alexandra F., Holland, Steven M., Franco, Luis M., Walkiewicz, Magdalena A., Yan, Jia
Publicado 2023

Immunogenetics associated with severe coccidioidomycosis

por Hsu, Amy P., Korzeniowska, Agnieszka, Aguilar, Cynthia C., Gu, Jingwen, Karlins, Eric, Oler, Andrew J., Chen, Gang, Reynoso, Glennys V., Davis, Joie, Chaput, Alexandria, Peng, Tao, Sun, Ling, Lack, Justin B., Bays, Derek J., Stewart, Ethan R., Waldman, Sarah E., Powell, Daniel A., Donovan, Fariba M., Desai, Jigar V., Pouladi, Nima, Long Priel, Debra A., Yamanaka, Daisuke, Rosenzweig, Sergio D., Niemela, Julie E., Stoddard, Jennifer, Freeman, Alexandra F., Zerbe, Christa S., Kuhns, Douglas B., Lussier, Yves A., Olivier, Kenneth N., Boucher, Richard C., Hickman, Heather D., Frelinger, Jeffrey, Fierer, Joshua, Shubitz, Lisa F., Leto, Thomas L., Thompson, George R., Galgiani, John N., Lionakis, Michail S., Holland, Steven M.
Publicado 2022

Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility

por Machiela, Mitchell J., Grünewald, Thomas G. P., Surdez, Didier, Reynaud, Stephanie, Mirabeau, Olivier, Karlins, Eric, Rubio, Rebeca Alba, Zaidi, Sakina, Grossetete-Lalami, Sandrine, Ballet, Stelly, Lapouble, Eve, Laurence, Valérie, Michon, Jean, Pierron, Gaelle, Kovar, Heinrich, Gaspar, Nathalie, Kontny, Udo, González-Neira, Anna, Picci, Piero, Alonso, Javier, Patino-Garcia, Ana, Corradini, Nadège, Bérard, Perrine Marec, Freedman, Neal D., Rothman, Nathaniel, Dagnall, Casey L., Burdett, Laurie, Jones, Kristine, Manning, Michelle, Wyatt, Kathleen, Zhou, Weiyin, Yeager, Meredith, Cox, David G., Hoover, Robert N., Khan, Javed, Armstrong, Gregory T., Leisenring, Wendy M., Bhatia, Smita, Robison, Leslie L., Kulozik, Andreas E., Kriebel, Jennifer, Meitinger, Thomas, Metzler, Markus, Hartmann, Wolfgang, Strauch, Konstantin, Kirchner, Thomas, Dirksen, Uta, Morton, Lindsay M., Mirabello, Lisa, Tucker, Margaret A., Tirode, Franck, Chanock, Stephen J., Delattre, Olivier
Publicado 2018

Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma

por Lin, Shu-Hong, Sampson, Joshua N., Grünewald, Thomas G. P., Surdez, Didier, Reynaud, Stephanie, Mirabeau, Olivier, Karlins, Eric, Rubio, Rebeca Alba, Zaidi, Sakina, Grossetête-Lalami, Sandrine, Ballet, Stelly, Lapouble, Eve, Laurence, Valérie, Michon, Jean, Pierron, Gaelle, Kovar, Heinrich, Kontny, Udo, González-Neira, Anna, Alonso, Javier, Patino-Garcia, Ana, Corradini, Nadège, Bérard, Perrine Marec, Miller, Jeremy, Freedman, Neal D., Rothman, Nathaniel, Carter, Brian D., Dagnall, Casey L., Burdett, Laurie, Jones, Kristine, Manning, Michelle, Wyatt, Kathleen, Zhou, Weiyin, Yeager, Meredith, Cox, David G., Hoover, Robert N., Khan, Javed, Armstrong, Gregory T., Leisenring, Wendy M., Bhatia, Smita, Robison, Leslie L., Kulozik, Andreas E., Kriebel, Jennifer, Meitinger, Thomas, Metzler, Markus, Krumbholz, Manuela, Hartmann, Wolfgang, Strauch, Konstantin, Kirchner, Thomas, Dirksen, Uta, Mirabello, Lisa, Tucker, Margaret A., Tirode, Franck, Morton, Lindsay M., Chanock, Stephen J., Delattre, Olivier, Machiela, Mitchell J.
Publicado 2020

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

por Machiela, Mitchell J., Zhou, Weiyin, Karlins, Eric, Sampson, Joshua N., Freedman, Neal D., Yang, Qi, Hicks, Belynda, Dagnall, Casey, Hautman, Christopher, Jacobs, Kevin B., Abnet, Christian C., Aldrich, Melinda C., Amos, Christopher, Amundadottir, Laufey T., Arslan, Alan A., Beane-Freeman, Laura E., Berndt, Sonja I., Black, Amanda, Blot, William J., Bock, Cathryn H., Bracci, Paige M., Brinton, Louise A., Bueno-de-Mesquita, H Bas, Burdett, Laurie, Buring, Julie E., Butler, Mary A., Canzian, Federico, Carreón, Tania, Chaffee, Kari G., Chang, I-Shou, Chatterjee, Nilanjan, Chen, Chu, Chen, Constance, Chen, Kexin, Chung, Charles C., Cook, Linda S., Crous Bou, Marta, Cullen, Michael, Davis, Faith G., De Vivo, Immaculata, Ding, Ti, Doherty, Jennifer, Duell, Eric J., Epstein, Caroline G., Fan, Jin-Hu, Figueroa, Jonine D., Fraumeni, Joseph F., Friedenreich, Christine M., Fuchs, Charles S., Gallinger, Steven, Gao, Yu-Tang, Gapstur, Susan M., Garcia-Closas, Montserrat, Gaudet, Mia M., Gaziano, J. Michael, Giles, Graham G., Gillanders, Elizabeth M., Giovannucci, Edward L., Goldin, Lynn, Goldstein, Alisa M., Haiman, Christopher A., Hallmans, Goran, Hankinson, Susan E., Harris, Curtis C., Henriksson, Roger, Holly, Elizabeth A., Hong, Yun-Chul, Hoover, Robert N., Hsiung, Chao A., Hu, Nan, Hu, Wei, Hunter, David J., Hutchinson, Amy, Jenab, Mazda, Johansen, Christoffer, Khaw, Kay-Tee, Kim, Hee Nam, Kim, Yeul Hong, Kim, Young Tae, Klein, Alison P., Klein, Robert, Koh, Woon-Puay, Kolonel, Laurence N., Kooperberg, Charles, Kraft, Peter, Krogh, Vittorio, Kurtz, Robert C., LaCroix, Andrea, Lan, Qing, Landi, Maria Teresa, Marchand, Loic Le, Li, Donghui, Liang, Xiaolin, Liao, Linda M., Lin, Dongxin, Liu, Jianjun, Lissowska, Jolanta, Lu, Lingeng, Magliocco, Anthony M., Malats, Nuria, Matsuo, Keitaro, McNeill, Lorna H., McWilliams, Robert R., Melin, Beatrice S., Mirabello, Lisa, Moore, Lee, Olson, Sara H., Orlow, Irene, Park, Jae Yong, Patiño-Garcia, Ana, Peplonska, Beata, Peters, Ulrike, Petersen, Gloria M., Pooler, Loreall, Prescott, Jennifer, Prokunina-Olsson, Ludmila, Purdue, Mark P., Qiao, You-Lin, Rajaraman, Preetha, Real, Francisco X., Riboli, Elio, Risch, Harvey A., Rodriguez-Santiago, Benjamin, Ruder, Avima M., Savage, Sharon A., Schumacher, Fredrick, Schwartz, Ann G., Schwartz, Kendra L., Seow, Adeline, Wendy Setiawan, Veronica, Severi, Gianluca, Shen, Hongbing, Sheng, Xin, Shin, Min-Ho, Shu, Xiao-Ou, Silverman, Debra T., Spitz, Margaret R., Stevens, Victoria L., Stolzenberg-Solomon, Rachael, Stram, Daniel, Tang, Ze-Zhong, Taylor, Philip R., Teras, Lauren R., Tobias, Geoffrey S., Van Den Berg, David, Visvanathan, Kala, Wacholder, Sholom, Wang, Jiu-Cun, Wang, Zhaoming, Wentzensen, Nicolas, Wheeler, William, White, Emily, Wiencke, John K., Wolpin, Brian M., Wong, Maria Pik, Wu, Chen, Wu, Tangchun, Wu, Xifeng, Wu, Yi-Long, Wunder, Jay S., Xia, Lucy, Yang, Hannah P., Yang, Pan-Chyr, Yu, Kai, Zanetti, Krista A., Zeleniuch-Jacquotte, Anne, Zheng, Wei, Zhou, Baosen, Ziegler, Regina G., Perez-Jurado, Luis A., Caporaso, Neil E., Rothman, Nathaniel, Tucker, Margaret, Dean, Michael C., Yeager, Meredith, Chanock, Stephen J.
Publicado 2016