检索结果 - McLean, Cory Y
- Showing 1 - 16 results of 16
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A Penile Spine/Vibrissa Enhancer Sequence Is Missing in Modern and Extinct Humans but Is Retained in Multiple Primates with Penile Spines and Sensory Vibrissae 由 Reno, Philip L., McLean, Cory Y., Hines, Jasmine E., Capellini, Terence D., Bejerano, Gill, Kingsley, David M.
出版 2013Text -
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A population-specific reference panel for improved genotype imputation in African Americans 由 O’Connell, Jared, Yun, Taedong, Moreno, Meghan, Li, Helen, Litterman, Nadia, Kolesnikov, Alexey, Noblin, Elizabeth, Chang, Pi-Chuan, Shastri, Anjali, Dorfman, Elizabeth H., Shringarpure, Suyash, Auton, Adam, Carroll, Andrew, McLean, Cory Y.
出版 2021Text -
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Human-specific loss of regulatory DNA and the evolution of human-specific traits 由 McLean, Cory Y., Reno, Philip L., Pollen, Alex A., Bassan, Abraham I., Capellini, Terence D., Guenther, Catherine, Indjeian, Vahan B., Lim, Xinhong, Menke, Douglas B., Schaar, Bruce T., Wenger, Aaron M., Bejerano, Gill, Kingsley, David M.
出版 2011Text -
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An open resource for accurately benchmarking small variant and reference calls 由 Zook, Justin M., McDaniel, Jennifer, Olson, Nathan D., Wagner, Justin, Parikh, Hemang, Heaton, Haynes, Irvine, Sean A., Trigg, Len, Truty, Rebecca, McLean, Cory Y., De La Vega, Francisco M., Xiao, Chunlin, Sherry, Stephen, Salit, Marc
出版 2019Text -
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Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology 由 Alipanahi, Babak, Hormozdiari, Farhad, Behsaz, Babak, Cosentino, Justin, McCaw, Zachary R., Schorsch, Emanuel, Sculley, D., Dorfman, Elizabeth H., Foster, Paul J., Peng, Lily H., Phene, Sonia, Hammel, Naama, Carroll, Andrew, Khawaja, Anthony P., McLean, Cory Y.
出版 2021Text -
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Mutational Analysis Reveals the Origin and Therapy-driven Evolution of Recurrent Glioma 由 Johnson, Brett E., Mazor, Tali, Hong, Chibo, Barnes, Michael, Aihara, Koki, McLean, Cory Y., Fouse, Shaun D., Yamamoto, Shogo, Ueda, Hiroki, Tatsuno, Kenji, Asthana, Saurabh, Jalbert, Llewellyn E., Nelson, Sarah J., Bollen, Andrew W., Gustafson, W. Clay, Charron, Elise, Weiss, William A., Smirnov, Ivan V., Song, Jun S., Olshen, Adam B., Cha, Soonmee, Zhao, Yongjun, Moore, Richard A., Mungall, Andrew J., Jones, Steven J.M., Hirst, Martin, Marra, Marco A., Saito, Nobuhito, Aburatani, Hiroyuki, Mukasa, Akitake, Berger, Mitchel S., Chang, Susan M., Taylor, Barry S., Costello, Joseph F.
出版 2013Text -
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Diagnosis of Parkinson’s disease on the basis of clinical–genetic classification: a population-based modelling study 由 Nalls, Mike A., McLean, Cory Y., Rick, Jacqueline, Eberly, Shirley, Hutten, Samantha J., Gwinn, Katrina, Sutherland, Margaret, Martinez, Maria, Heutink, Peter, Williams, Nigel, Hardy, John, Gasser, Thomas, Brice, Alexis, Price, T. Ryan, Nicolas, Aude, Keller, Margaux F., Molony, Cliona, Gibbs, J. Raphael, Chen-Plotkin, Alice, Suh, Eunran, Letson, Christopher, Fiandaca, Massimo S., Mapstone, Mark, Federoff, Howard J., Noyce, Alastair J, Morris, Huw, Van Deerlin, Vivianna M., Weintraub, Daniel, Zabetian, Cyrus, Hernandez, Dena G., Lesage, Suzanne, Mullins, Meghan, Conley, Emily Drabant, Northover, Carrie, Frasier, Mark, Marek, Ken, Day-Williams, Aaron G., Stone, David J., Ioannidis, John P. A., Singleton, Andrew B.
出版 2015Text -
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Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease 由 Lai, Dongbing, Alipanahi, Babak, Fontanillas, Pierre, Schwantes‐An, Tae‐Hwi, Aasly, Jan, Alcalay, Roy N., Beecham, Gary W., Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockman, Kathrin, Clark, Lorraine, Cookson, Mark, Das, Sayantan, Van Deerlin, Vivianna, Follett, Jordan, Farrer, Matthew J., Trinh, Joanne, Gasser, Thomas, Goldwurm, Stefano, Gustavsson, Emil, Klein, Christine, Lang, Anthony E., Langston, J. William, Latourelle, Jeanne, Lynch, Timothy, Marder, Karen, Marras, Connie, Martin, Eden R., McLean, Cory Y., Mejia‐Santana, Helen, Molho, Eric, Myers, Richard H., Nuytemans, Karen, Ozelius, Laurie, Payami, Haydeh, Raymond, Deborah, Rogaeva, Ekaterina, Rogers, Michael P., Ross, Owen A., Samii, Ali, Saunders‐Pullman, Rachel, Schüle, Birgitt, Schulte, Claudia, Scott, William K., Tanner, Caroline, Tolosa, Eduardo, Tomkins, James E., Vilas, Dolores, Trojanowski, John Q., Uitti, Ryan, Vance, Jeffery M., Visanji, Naomi P., Wszolek, Zbigniew K., Zabetian, Cyrus P., Mirelman, Anat, Giladi, Nir, Orr Urtreger, Avi, Cannon, Paul, Fiske, Brian, Foroud, Tatiana
出版 2021Text -
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Quantifying penetrance in a dominant disease gene using large population control cohorts 由 Minikel, Eric Vallabh, Vallabh, Sonia M., Lek, Monkol, Estrada, Karol, Samocha, Kaitlin E., Sathirapongsasuti, J. Fah, McLean, Cory Y., Tung, Joyce Y., Yu, Linda P.C., Gambetti, Pierluigi, Blevins, Janis, Zhang, Shulin, Cohen, Yvonne, Chen, Wei, Yamada, Masahito, Hamaguchi, Tsuyoshi, Sanjo, Nobuo, Mizusawa, Hidehiro, Nakamura, Yosikazu, Kitamoto, Tetsuyuki, Collins, Steven J., Boyd, Alison, Will, Robert G., Knight, Richard, Ponto, Claudia, Zerr, Inga, Kraus, Theo F.J., Eigenbrod, Sabina, Giese, Armin, Calero, Miguel, de Pedro-Cuesta, Jesús, Haïk, Stéphane, Laplanche, Jean-Louis, Bouaziz-Amar, Elodie, Brandel, Jean-Philippe, Capellari, Sabina, Parchi, Piero, Poleggi, Anna, Ladogana, Anna, O'Donnell-Luria, Anne H., Karczewski, Konrad J., Marshall, Jamie L., Boehnke, Michael, Laakso, Markku, Mohlke, Karen L., Kähler, Anna, Chambert, Kimberly, McCarroll, Steven, Sullivan, Patrick F., Hultman, Christina M., Purcell, Shaun M., Sklar, Pamela, van der Lee, Sven J., Rozemuller, Annemieke, Jansen, Casper, Hofman, Albert, Kraaij, Robert, van Rooij, Jeroen G.J., Ikram, M. Arfan, Uitterlinden, André G., van Duijn, Cornelia M., Daly, Mark J., MacArthur, Daniel G.
出版 2016Text