Результати пошуку - Cox, Hannah C
- Показ 1 - 14 результатів із 14
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Whole-genome haplotyping approaches and genomic medicine за авторством Glusman, Gustavo, Cox, Hannah C, Roach, Jared C
Опубліковано 2014Текст -
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Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate за авторством Cox, Hannah C., Lea, Rod A., Bellis, Claire, Carless, Melanie, Dyer, Tom, Blangero, John, Griffiths, Lyn R.
Опубліковано 2011Текст -
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A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next‐generation sequencing hereditary pan‐cancer panel are acquired somatically за авторством Coffee, Bradford, Cox, Hannah C., Bernhisel, Ryan, Manley, Susan, Bowles, Karla, Roa, Benjamin B., Mancini‐DiNardo, Debora
Опубліковано 2019Текст -
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Family history of breast cancer in men with non-BRCA male breast cancer: implications for cancer risk counseling за авторством Calip, Gregory S., Kidd, John, Bernhisel, Ryan, Cox, Hannah C., Saam, Jennifer, Rauscher, Garth H., Lancaster, Johnathan M., Hoskins, Kent F.
Опубліковано 2020Текст -
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Principal Component and Linkage Analysis of Cardiovascular Risk Traits in the Norfolk Isolate за авторством Cox, Hannah C., Bellis, Claire, Lea, Rod A., Quinlan, Sharon, Hughes, Roger, Dyer, Thomas, Charlesworth, Jac, Blangero, John, Griffiths, Lyn R.
Опубліковано 2009Текст -
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Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing за авторством Mersch, Jacqueline, Brown, Nichole, Pirzadeh-Miller, Sara, Mundt, Erin, Cox, Hannah C., Brown, Krystal, Aston, Melissa, Esterling, Lisa, Manley, Susan, Ross, Theodora
Опубліковано 2018Текст -
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Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing за авторством Slavin, Thomas P., Coffee, Bradford, Bernhisel, Ryan, Logan, Jennifer, Cox, Hannah C., Marcucci, Guido, Weitzel, Jeffrey, Neuhausen, Susan L., Mancini-DiNardo, Debora
Опубліковано 2019Текст -
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HERITABILITY AND GENOME-WIDE LINKAGE ANALYSIS OF MIGRAINE IN THE GENETIC ISOLATE OF NORFOLK ISLAND за авторством Cox, Hannah C, Lea, Rod A, Bellis, Claire, Nyholt, Dale R, Dyer, Thomas D, Haupt, Larisa M., Charlesworth, Jac, Matovinovic, Elizabeth, Blangero, John, Griffiths, Lyn R
Опубліковано 2011Текст -
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A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility за авторством Cox, Hannah C., Lea, Rod A., Bellis, Claire, Carless, Melanie, Dyer, Thomas D., Curran, Joanne, Charlesworth, Jac, Macgregor, Stuart, Nyholt, Dale, Chasman, Daniel, Ridker, Paul M., Schürks, Markus, Blangero, John, Griffiths, Lyn R.
Опубліковано 2012Текст -
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Origin of the PSEN1 E280A mutation causing early–onset Alzheimer’s disease за авторством Lalli, Matthew A., Cox, Hannah C., Arcila, Mary L., Cadavid, Liliana, Moreno, Sonia, Garcia, Gloria, Madrigal, Lucia, Reiman, Eric M., Arcos–Burgos, Mauricio, Bedoya, Gabriel, Brunkow, Mary E., Glusman, Gustavo, Roach, Jared C., Hood, Leroy, Kosik, Kenneth S., Lopera, Francisco
Опубліковано 2013Текст -
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An X Chromosome Association Scan of the Norfolk Island Genetic Isolate Provides Evidence for a Novel Migraine Susceptibility Locus at Xq12 за авторством Maher, Bridget H., Lea, Rod A., Benton, Miles, Cox, Hannah C., Bellis, Claire, Carless, Melanie, Dyer, Thomas D., Curran, Joanne, Charlesworth, Jac C., Buring, Julie E., Kurth, Tobias, Chasman, Daniel I., Ridker, Paul M., Schürks, Markus, Blangero, John, Griffiths, Lyn R.
Опубліковано 2012Текст -
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Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes за авторством Kerr, Iain D., Cox, Hannah C., Moyes, Kelsey, Evans, Brent, Burdett, Brianna C., van Kan, Aric, McElroy, Heather, Vail, Paris J., Brown, Krystal L., Sumampong, Dechie B., Monteferrante, Nicholas J., Hardman, Kennedy L., Theisen, Aaron, Mundt, Erin, Wenstrup, Richard J., Eggington, Julie M.
Опубліковано 2017Текст -
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An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge за авторством Brownstein, Catherine A, Beggs, Alan H, Homer, Nils, Merriman, Barry, Yu, Timothy W, Flannery, Katherine C, DeChene, Elizabeth T, Towne, Meghan C, Savage, Sarah K, Price, Emily N, Holm, Ingrid A, Luquette, Lovelace J, Lyon, Elaine, Majzoub, Joseph, Neupert, Peter, McCallie Jr, David, Szolovits, Peter, Willard, Huntington F, Mendelsohn, Nancy J, Temme, Renee, Finkel, Richard S, Yum, Sabrina W, Medne, Livija, Sunyaev, Shamil R, Adzhubey, Ivan, Cassa, Christopher A, de Bakker, Paul IW, Duzkale, Hatice, Dworzyński, Piotr, Fairbrother, William, Francioli, Laurent, Funke, Birgit H, Giovanni, Monica A, Handsaker, Robert E, Lage, Kasper, Lebo, Matthew S, Lek, Monkol, Leshchiner, Ignaty, MacArthur, Daniel G, McLaughlin, Heather M, Murray, Michael F, Pers, Tune H, Polak, Paz P, Raychaudhuri, Soumya, Rehm, Heidi L, Soemedi, Rachel, Stitziel, Nathan O, Vestecka, Sara, Supper, Jochen, Gugenmus, Claudia, Klocke, Bernward, Hahn, Alexander, Schubach, Max, Menzel, Mortiz, Biskup, Saskia, Freisinger, Peter, Deng, Mario, Braun, Martin, Perner, Sven, Smith, Richard JH, Andorf, Janeen L, Huang, Jian, Ryckman, Kelli, Sheffield, Val C, Stone, Edwin M, Bair, Thomas, Black-Ziegelbein, E Ann, Braun, Terry A, Darbro, Benjamin, DeLuca, Adam P, Kolbe, Diana L, Scheetz, Todd E, Shearer, Aiden E, Sompallae, Rama, Wang, Kai, Bassuk, Alexander G, Edens, Erik, Mathews, Katherine, Moore, Steven A, Shchelochkov, Oleg A, Trapane, Pamela, Bossler, Aaron, Campbell, Colleen A, Heusel, Jonathan W, Kwitek, Anne, Maga, Tara, Panzer, Karin, Wassink, Thomas, Van Daele, Douglas, Azaiez, Hela, Booth, Kevin, Meyer, Nic, Segal, Michael M, Williams, Marc S, Tromp, Gerard, White, Peter, Corsmeier, Donald, Fitzgerald-Butt, Sara, Herman, Gail, Lamb-Thrush, Devon, McBride, Kim L, Newsom, David, Pierson, Christopher R, Rakowsky, Alexander T, Maver, Aleš, Lovrečić, Luca, Palandačić, Anja, Peterlin, Borut, Torkamani, Ali, Wedell, Anna, Huss, Mikael, Alexeyenko, Andrey, Lindvall, Jessica M, Magnusson, Måns, Nilsson, Daniel, Stranneheim, Henrik, Taylan, Fulya, Gilissen, Christian, Hoischen, Alexander, van Bon, Bregje, Yntema, Helger, Nelen, Marcel, Zhang, Weidong, Sager, Jason, Zhang, Lu, Blair, Kathryn, Kural, Deniz, Cariaso, Michael, Lennon, Greg G, Javed, Asif, Agrawal, Saloni, Ng, Pauline C, Sandhu, Komal S, Krishna, Shuba, Veeramachaneni, Vamsi, Isakov, Ofer, Halperin, Eran, Friedman, Eitan, Shomron, Noam, Glusman, Gustavo, Roach, Jared C, Caballero, Juan, Cox, Hannah C, Mauldin, Denise, Ament, Seth A, Rowen, Lee, Richards, Daniel R, Lucas, F Anthony San, Gonzalez-Garay, Manuel L, Caskey, C Thomas, Bai, Yu, Huang, Ying, Fang, Fang, Zhang, Yan, Wang, Zhengyuan, Barrera, Jorge, Garcia-Lobo, Juan M, González-Lamuño, Domingo, Llorca, Javier, Rodriguez, Maria C, Varela, Ignacio, Reese, Martin G, De La Vega, Francisco M, Kiruluta, Edward, Cargill, Michele, Hart, Reece K, Sorenson, Jon M, Lyon, Gholson J, Stevenson, David A, Bray, Bruce E, Moore, Barry M, Eilbeck, Karen, Yandell, Mark, Zhao, Hongyu, Hou, Lin, Chen, Xiaowei, Yan, Xiting, Chen, Mengjie, Li, Cong, Yang, Can, Gunel, Murat, Li, Peining, Kong, Yong, Alexander, Austin C, Albertyn, Zayed I, Boycott, Kym M, Bulman, Dennis E, Gordon, Paul MK, Innes, A Micheil, Knoppers, Bartha M, Majewski, Jacek, Marshall, Christian R, Parboosingh, Jillian S, Sawyer, Sarah L, Samuels, Mark E, Schwartzentruber, Jeremy, Kohane, Isaac S, Margulies, David M
Опубліковано 2014Текст