Copy number variations and clinical cytogenetic diagnosis of constitutional disorders von LEE, Charles, IAFRATE, A. John, BROTHMAN, Arthur R

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Prognostic value of an RNA expression signature derived from cell cycle proliferation genes in patients with prostate cancer: a retrospective study von Cuzick, Jack, Prof, Swanson, Gregory P, MD, Fisher, Gabrielle, PhD, Brothman, Arthur R, PhD, Berney, Daniel M, FRCPath, Reid, Julia E, MStat, Mesher, David, MSc, Speights, VO, MD, Stankiewicz, Elzbieta, MSc, Foster, Christopher S, MD, Møller, Henrik, MD, Scardino, Peter, MD, Warren, Jorja D, BA, Park, Jimmy, BS, Younus, Adib, BS, Flake, Darl D, MS, Wagner, Susanne, PhD, Gutin, Alexander, PhD, Lanchbury, Jerry S, PhD, Stone, Steven, PhD

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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities von Kaminsky, Erin B, Kaul, Vineith, Paschall, Justin, Church, Deanna M, Bunke, Brian, Kunig, Dawn, Moreno-De-Luca, Daniel, Moreno-De-Luca, Andres, Mulle, Jennifer G, Warren, Stephen T, Richard, Gabriele, Compton, John G, Fuller, Amy E, Gliem, Troy J, Huang, Shuwen, Collinson, Morag N, Beal, Sarah J, Ackley, Todd, Pickering, Diane L, Golden, Denae M, Aston, Emily, Whitby, Heidi, Shetty, Shashirekha, Rossi, Michael R, Rudd, M Katharine, South, Sarah T, Brothman, Arthur R, Sanger, Warren G, Iyer, Ramaswamy K, Crolla, John A, Thorland, Erik C, Aradhya, Swaroop, Ledbetter, David H, Martin, Christa L

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Genome-wide analysis reveals the unique stem cell identity of human amniocytes von Maguire, Colin T, Demarest, Bradley L, Hill, Jonathon T, Palmer, James D, Brothman, Arthur R, Yost, H Joseph, Condic, Maureen L

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Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH von Selzer, Rebecca R., Richmond, Todd A., Pofahl, Nathan J., Green, Roland D., Eis, Peggy S., Nair, Prakash, Brothman, Arthur R., Stallings, Raymond L.

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Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations von South, Sarah T, Whitby, Heidi, Battaglia, Agatino, Carey, John C, Brothman, Arthur R

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Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies von Miller, David T., Adam, Margaret P., Aradhya, Swaroop, Biesecker, Leslie G., Brothman, Arthur R., Carter, Nigel P., Church, Deanna M., Crolla, John A., Eichler, Evan E., Epstein, Charles J., Faucett, W. Andrew, Feuk, Lars, Friedman, Jan M., Hamosh, Ada, Jackson, Laird, Kaminsky, Erin B., Kok, Klaas, Krantz, Ian D., Kuhn, Robert M., Lee, Charles, Ostell, James M., Rosenberg, Carla, Scherer, Stephen W., Spinner, Nancy B., Stavropoulos, Dimitri J., Tepperberg, James H., Thorland, Erik C., Vermeesch, Joris R., Waggoner, Darrel J., Watson, Michael S., Martin, Christa Lese, Ledbetter, David H.

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Progression of metastatic human prostate cancer to androgen independence in immunodeficient SCID mice von Klein, Karen A, Reiter, Robert E, Redula, James, Moradi, Hamid, Zhu, Xaio Lin, Brothman, Arthur R, Lamb, Dolores J, Marcelli, Marco, Belldegrun, Arie, Witte, Owen N, Sawyers, Charles L

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Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia von Moreno-De-Luca, Daniel, Mulle, Jennifer G., Kaminsky, Erin B., Sanders, Stephan J., Myers, Scott M., Adam, Margaret P., Pakula, Amy T., Eisenhauer, Nancy J., Uhas, Kim, Weik, LuAnn, Guy, Lisa, Care, Melanie E., Morel, Chantal F., Boni, Charlotte, Salbert, Bonnie Anne, Chandrareddy, Ashadeep, Demmer, Laurie A., Chow, Eva W.C., Surti, Urvashi, Aradhya, Swaroop, Pickering, Diane L., Golden, Denae M., Sanger, Warren G., Aston, Emily, Brothman, Arthur R., Gliem, Troy J., Thorland, Erik C., Ackley, Todd, Iyer, Ram, Huang, Shuwen, Barber, John C., Crolla, John A., Warren, Stephen T., Martin, Christa L., Ledbetter, David H.

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Immortalization of normal human mammary epithelial cells in two steps by direct targeting of senescence barriers does not require gross genomic alterations von Garbe, James C, Vrba, Lukas, Sputova, Klara, Fuchs, Laura, Novak, Petr, Brothman, Arthur R, Jackson, Mark, Chin, Koei, LaBarge, Mark A, Watts, George, Futscher, Bernard W, Stampfer, Martha R

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Mutation of the MXI1 gene in prostate cancer von Eagle, Linette R, Yin, Xiaoying, Brothman, Arthur R, Williams, Briana J, Atkin, N.B, Prochownik, Edward V

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Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assay von Paxton, Christian N., Brothman, Arthur R., Geiersbach, Katherine B.

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Array Comparative Genomic Hybridization for Genetic Evaluation of Fetal Loss Between 10 and 20 Weeks of Gestation von Warren, Jennifer E., Turok, David K., Maxwell, Teresa M., Brothman, Arthur R., Silver, Robert M.

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Microarray analysis for constitutional cytogenetic abnormalities von Shaffer, Lisa G, Beaudet, Arthur L, Brothman, Arthur R, Hirsch, Betsy, Levy, Brynn, Martin, Christa Lese, Mascarello, James T, Rao, Kathleen W

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Paternal uniparental disomy of chromosome 14: Confirmation of a clinically‐recognizable phenotype von Stevenson, David A., Brothman, Arthur R., Chen, Zhong, Bayrak‐Toydemir, Pinar, Longo, Nicola

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Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories von Tsuchiya, Karen D, Shaffer, Lisa G, Aradhya, Swaroop, Gastier-Foster, Julie M, Patel, Ankita, Rudd, M Katharine, Biggerstaff, Julie Sanford, Sanger, Warren G, Schwartz, Stuart, Tepperberg, James H, Thorland, Erik C, Torchia, Beth A, Brothman, Arthur R

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How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delay von Saam, Jennifer, Gudgeon, Jim, Aston, Emily, Brothman, Arthur R.

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Natural History of Wolf-Hirschhorn Syndrome: Experience With 15 Cases von Battaglia, Agatino, Carey, John C, Cederholm, Peeches, Viskochil, David H, Brothman, Arthur R, Galasso, Cinzia

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Cytogenomic aberrations associated with prostate cancer von Gu, Guangyu, Brothman, Arthur R

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Co‐occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to... von South, Sarah T., Whitby, Heidi, Maxwell, Teresa, Aston, Emily, Brothman, Arthur R., Carey, John C.

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