An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Werling, Donna M., Brand, Harrison, An, Joon-Yong, Stone, Matthew R., Zhu, Lingxue, Glessner, Joseph T., Collins, Ryan L., Dong, Shan, Layer, Ryan M., Markenscoff-Papadimitriou, Eirene, Farrell, Andrew, Schwartz, Grace B., Wang, Harold Z., Currall, Benjamin B., Zhao, Xuefang, Dea, Jeanselle, Duhn, Clif, Erdman, Carolyn A., Gilson, Michael C., Yadav, Rachita, Handsaker, Robert E., Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey D., Nowakowski, Tomasz J., Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Walker, Michael F., Waterman, Matthew J., He, Xin, Kriegstein, Arnold R., Rubenstein, John L., Sestan, Nenad, McCarroll, Steven A., Neale, Benjamin M., Coon, Hilary, Willsey, A. Jeremy, Buxbaum, Joseph D., Daly, Mark J., State, Matthew W., Quinlan, Aaron R., Marth, Gabor T., Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael E., Sanders, Stephan J.
Published in Nature genetics (26.04.2018)
Published in Nature genetics (26.04.2018)
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Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
An, Joon-Yong, Lin, Kevin, Zhu, Lingxue, Werling, Donna M, Dong, Shan, Brand, Harrison, Wang, Harold Z, Zhao, Xuefang, Schwartz, Grace B, Collins, Ryan L, Currall, Benjamin B, Dastmalchi, Claudia, Dea, Jeanselle, Duhn, Clif, Gilson, Michael C, Klei, Lambertus, Liang, Lindsay, Markenscoff-Papadimitriou, Eirene, Pochareddy, Sirisha, Ahituv, Nadav, Buxbaum, Joseph D, Coon, Hilary, Daly, Mark J, Kim, Young Shin, Marth, Gabor T, Neale, Benjamin M, Quinlan, Aaron R, Rubenstein, John L, Sestan, Nenad, State, Matthew W, Willsey, A Jeremy, Talkowski, Michael E, Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J
Published in Science (American Association for the Advancement of Science) (14.12.2018)
Published in Science (American Association for the Advancement of Science) (14.12.2018)
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Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies
Lowther, Chelsea, Valkanas, Elise, Giordano, Jessica L., Wang, Harold Z., Currall, Benjamin B., O’Keefe, Kathryn, Pierce-Hoffman, Emma, Kurtas, Nehir E., Whelan, Christopher W., Hao, Stephanie P., Weisburd, Ben, Jalili, Vahid, Fu, Jack, Wong, Isaac, Collins, Ryan L., Zhao, Xuefang, Austin-Tse, Christina A., Evangelista, Emily, Lemire, Gabrielle, Aggarwal, Vimla S., Lucente, Diane, Gauthier, Laura D., Tolonen, Charlotte, Sahakian, Nareh, Stevens, Christine, An, Joon-Yong, Dong, Shan, Norton, Mary E., MacKenzie, Tippi C., Devlin, Bernie, Gilmore, Kelly, Powell, Bradford C., Brandt, Alicia, Vetrini, Francesco, DiVito, Michelle, Sanders, Stephan J., MacArthur, Daniel G., Hodge, Jennelle C., O'Donnell-Luria, Anne, Rehm, Heidi L., Vora, Neeta L., Levy, Brynn, Brand, Harrison, Wapner, Ronald J., Talkowski, Michael E.
Published in American journal of human genetics (07.09.2023)
Published in American journal of human genetics (07.09.2023)
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Functional annotation of rare structural variation in the human brain
Han, Lide, Zhao, Xuefang, Benton, Mary Lauren, Perumal, Thaneer, Collins, Ryan L., Hoffman, Gabriel E., Johnson, Jessica S., Sloofman, Laura, Wang, Harold Z., Stone, Matthew R., Brennand, Kristen J., Brand, Harrison, Sieberts, Solveig K., Marenco, Stefano, Peters, Mette A., Lipska, Barbara K., Roussos, Panos, Capra, John A., Talkowski, Michael, Ruderfer, Douglas M.
Published in Nature communications (12.06.2020)
Published in Nature communications (12.06.2020)
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Potential involvement of the interleukin-18 pathway in schizophrenia
Xu, Yong, Yue, Weihua, Shugart, Yin Yao, Yuan, Jianmin, Wang, Guoqiang, Wang, Harold Z, Lehrman, Benjamin, Zhang, Fuquan, Zhang, Dai
Published in Journal of psychiatric research (01.03.2016)
Published in Journal of psychiatric research (01.03.2016)
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Family-based tests applied to extended pedigrees identify rare variants related to hypertension
Xu, Mengyuan, Wang, Harold Z, Guo, Wei, Qin, Haide, Shugart, Yin Y
Published in BMC proceedings (17.06.2014)
Published in BMC proceedings (17.06.2014)
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New insights into the genetic mechanism of IQ in autism spectrum disorders
Wang, Harold Z, Qin, Hai-De, Guo, Wei, Samuels, Jack, Shugart, Yin Yao
Published in Frontiers in genetics (2013)
Published in Frontiers in genetics (2013)
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Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families
Werling, Donna M, Brand, Harrison, Joon-Yong, An, Stone, Matthew R, Glessner, Joseph T, Zhu, Lingxue, Collins, Ryan L, Dong, Shan, Layer, Ryan M, Markenscoff-Papadimitriou, Eiriene-Chloe, Farrell, Andrew, Schwartz, Grace B, Currall, Benjamin B, Jeanselle Dea, Duhn, Clif, Erdman, Carolyn, Gilson, Michael, Handsaker, Robert E, Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey D, Nowakowski, Tomasz J, Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Walker, Michael F, Wang, Harold Z, Waterman, Mathew J, He, Xin, Kriegstein, Arnold R, Rubenstein, John L, Sestan, Nenad, Mccarroll, Steven A, Neale, Ben M, Coon, Hilary, Willsey, A Jeremy, Buxbaum, Joseph D, Daly, Mark J, State, Matthew W, Quinlan, Aaron, Marth, Gabor T, Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael E, Sanders, Stephan J
Published in bioRxiv (13.04.2017)
Published in bioRxiv (13.04.2017)
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Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies
Lowther, Chelsea, Valkanas, Elise, Giordano, Jessica L, Wang, Harold Z, Currall, Benjamin B, O'keefe, Kathryn, Pierce-Hoffman, Emma, Kurtas, Nehir E, Whelan, Christopher W, Hao, Stephanie P, Weisburd, Ben W, Jalili, Vahid, Fu, Jack, Wong, Isaac, Collins, Ryan L, Zhao, Xuefang, Austin-Tse, Christina A, Evangelista, Emily, Lemire, Gabrielle, Aggarwal, Vimla, Lucente, Diane, Gauthier, Laura D, Tolonen, Charlotte, Sahakian, Nareh, Stevens, Christine, Joon-Yong, An, Dong, Shan, Norton, Mary E, Mackenzie, Tippi, Devlin, Bernie, Gilmore, Kelly, Powell, Bradford, Brandt, Alicia, Vetrini, Francesco, Divito, Michelle, Sanders, Stephan J, Macarthur, Daniel G, Hodge, Jennelle C, O'donnell-Luria, Anne, Rehm, Heidi, Vora, Neeta, Levy, Brynn, Brand, Harrison, Wapner, Ronald, Talkowski, Michael E
Published in bioRxiv (23.09.2022)
Published in bioRxiv (23.09.2022)
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