Genetics of schizophrenia in the South African Xhosa von Gulsuner, S, Stein, D J, Susser, E S, Sibeko, G, Pretorius, A, Walsh, T, Majara, L, Mndini, M M, Mqulwana, S G, Ntola, O A, Casadei, S, Ngqengelele, L L, Korchina, V, van der Merwe, C, Malan, M, Fader, K M, Feng, M, Willoughby, E, Muzny, D, Baldinger, A, Andrews, H F, Gur, R C, Gibbs, R A, Zingela, Z, Nagdee, M, Ramesar, R S, King, M-C, McClellan, J M

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BRCA1 and BRCA2 and the genetics of breast and ovarian cancer von Welcsh, P L, King, M C

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The effect of citalopram treatment on amyloid-β precursor protein processing and oxidative stress in human hNSC-derived neurons von Elsworthy, R. J., Crowe, J. A., King, M. C., Dunleavy, C., Fisher, E., Ludlam, A., Parri, H. R., Hill, E. J., Aldred, S.

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Tamoxifen and Breast Cancer Incidence Among Women With Inherited Mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Preventi... von King, Mary-Claire, Wieand, Sam, Hale, Kathryn, Lee, Ming, Walsh, Tom, Owens, Kelly, Tait, Jonathan, Ford, Leslie, Dunn, Barbara K, Costantino, Joseph, Wickerham, Lawrence, Wolmark, Norman, Fisher, Bernard

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Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X) von Basehore, M.J., Michaelson-Cohen, R., Levy-Lahad, E., Sismani, C., Bird, L.M., Friez, M.J., Walsh, T., Abidi, F., Holloway, L., Skinner, C., McGee, S., Alexandrou, A., Syrrou, M., Patsalis, P.C., Raymond, G., Wang, T., Schwartz, C.E., King, M.-C., Stevenson, R.E.

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Insights into the functions of BRCA1 and BRCA2 von Welcsh, Piri L, Owens, Kelly N, King, Mary-Claire

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Breast-Cancer Risk in Families with Mutations in PALB2 von Antoniou, Antonis C, Casadei, Silvia, Heikkinen, Tuomas, Barrowdale, Daniel, Pylkäs, Katri, Roberts, Jonathan, Lee, Andrew, Subramanian, Deepak, De Leeneer, Kim, Fostira, Florentia, Tomiak, Eva, Neuhausen, Susan L, Teo, Zhi L, Khan, Sofia, Aittomäki, Kristiina, Moilanen, Jukka S, Turnbull, Clare, Seal, Sheila, Mannermaa, Arto, Kallioniemi, Anne, Lindeman, Geoffrey J, Buys, Saundra S, Andrulis, Irene L, Radice, Paolo, Tondini, Carlo, Manoukian, Siranoush, Toland, Amanda E, Miron, Penelope, Weitzel, Jeffrey N, Domchek, Susan M, Poppe, Bruce, Claes, Kathleen B.M, Yannoukakos, Drakoulis, Concannon, Patrick, Bernstein, Jonine L, James, Paul A, Easton, Douglas F, Goldgar, David E, Hopper, John L, Rahman, Nazneen, Peterlongo, Paolo, Nevanlinna, Heli, King, Mary-Claire, Couch, Fergus J, Southey, Melissa C, Winqvist, Robert, Foulkes, William D, Tischkowitz, Marc

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Structure of a BRCA1-BARD1 heterodimeric RING-RING complex von Klevit, Rachel E, Brzovic, Peter S, Rajagopal, Ponni, Hoyt, David W, King, Mary-Claire

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A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss von Yariz, KO, Walsh, T, Akay, H, Duman, D, Akkaynak, AC, King, M-C, Tekin, M

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Population genetics of BRCA1 and BRCA2 von Szabo, C I, King, M C

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Frequency of Breast Cancer Attributable to BRCA1 in a Population-Based Series of American Women von Newman, Beth, Mu, Hua, Butler, Lesley M, Millikan, Robert C, Moorman, Patricia G, King, Mary-Claire

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Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanous von Lynch, Eric D., Lee, Ming K., Morrow, Jan E., Welcsh, Piri L., León, Pedro E., King, Mary-Claire

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Diagnostic per-lesion performance of a simulated gadoxetate disodium-enhanced abbreviated MRI protocol for hepatocellular carcinoma screening von Tillman, B.G., Gorman, J.D., Hru, J.M., Lee, M.H., King, M.C., Sirlin, C.B., Marks, R.M.

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The Founder Mutation MSH21906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population von Foulkes, W.D., Thiffault, I., Gruber, S.B., Horwitz, M., Hamel, N., Lee, C., Shia, J., Markowitz, A., Figer, A., Friedman, E., Farber, D., Greenwood, C. M.T., Bonner, J.D., Nafa, K., Walsh, T., Marcus, V., Tomsho, L., Gebert, J., Macrae, F.A., Gaff, C.L., Paillerets, B. Bressac-de, Gregersen, P.K., Weitzel, J.N., Gordon, P.H., MacNamara, E., King, M.-C., Hampel, H., de la Chapelle, A., Boyd, J., Offit, K., Rennert, G., Chong, G., Ellis, N.A.

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Growth retardation and tumour inhibition by BRCA1 von Holt, Jeffrey T, Thompson, Marilyn E, Szabo, Csilla, Robinson-Benion, Cheryl, Arteaga, Carlos L, King, Mary-Claire, Jensen, Roy A

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Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity von Zhang, Michael Y, Keel, Siobán B, Walsh, Tom, Lee, Ming K, Gulsuner, Suleyman, Watts, Amanda C, Pritchard, Colin C, Salipante, Stephen J, Jeng, Michael R, Hofmann, Inga, Williams, David A, Fleming, Mark D, Abkowitz, Janis L, King, Mary-Claire, Shimamura, Akiko

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Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans von Vahava, Oz, Morell, Robert, Lynch, Eric D., Weiss, Sigal, Kagan, Marjory E., Ahituv, Nadav, Morrow, Jan E., Lee, Ming K., Skvorak, Anne B., Morton, Cynthia C., Blumenfeld, Anat, Frydman, Moshe, Friedman, Thomas B., King, Mary-Claire, Avraham, Karen B.

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Effects of Total-Body Digital Photography on Cancer Worry in Patients With Atypical Mole Syndrome von Moye, Molly S, King, Sallyann M. C, Rice, Zakiya P, DeLong, Laura K, Seidler, Anne M, Veledar, Emir, Curiel-Lewandrowski, Clara, Chen, Suephy C

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Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1 von Smith, T M, Lee, M K, Szabo, C I, Jerome, N, McEuen, M, Taylor, M, Hood, L, King, M C

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Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families von Friedman, Lori S, Ostermeyer, Elizabeth A, Szabo, Csilla I, Dowd, Patrick, Lynch, Eric D, Rowell, Sarah E, King, Mary-Claire

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