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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Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations von Pickering, Diane L., Eudy, James D., Olney, Ann Haskins, Dave, Bhavana J., Golden, Denae, Stevens, Jadd, Sanger, Warren G.

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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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Frequency, variations, and prognostic implications of chromosome 14q32 deletions in chronic lymphocytic leukemia von Harris, Rachel A., Stevens, Jadd. M., Pickering, Diane L., Althof, Pamela A., Smith, Lynette M., Sanmann, Jennifer N., Dave, Bhavana J.

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BCL2 Translocation Defines a Unique Tumor Subset within the Germinal Center B-Cell-Like Diffuse Large B-Cell Lymphoma von Iqbal, Javeed, Sanger, Warren G., Horsman, Douglas E., Rosenwald, Andreas, Pickering, Diane L., Dave, Bhavana, Dave, Sandeep, Xiao, Li, Cao, Kajia, Zhu, Quiming, Sherman, Simon, Hans, Christine P., Weisenburger, Dennis D., Greiner, Timothy C., Gascoyne, Randy D., Ott, German, Müller-Hermelink, H. Konrad, Delabie, Jan, Braziel, Rita M., Jaffe, Elaine S., Campo, Elias, Lynch, James C., Connors, Joseph M., Vose, Julie M., Armitage, James O., Grogan, Thomas M., Staudt, Louis M., Chan, Wing C.

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Breast Cancer and Non-Hodgkin Lymphoma in a Young Male with Cowden Syndrome von Hagelstrom, Robert Tanner, Ford, James, Reiser, Gwendolyn M., Nelson, Marilu, Pickering, Diane L., Althof, Pamela A., Sanger, Warren G., Coccia, Peter F.

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The t(14;18) defines a unique subset of diffuse large B-cell lymphoma with a germinal center B-cell gene expression profile von Huang, James Z., Sanger, Warren G., Greiner, Timothy C., Staudt, Louis M., Weisenburger, Dennis D., Pickering, Diane L., Lynch, James C., Armitage, James O., Warnke, Roger A., Alizadeh, Ash A., Lossos, Izidore S., Levy, Ronald, Chan, Wing C.

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Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray von Sanmann, Jennifer N., Pickering, Diane L., Golden, Denae M., Stevens, Jadd M., Hempel, Thomas E., Althof, Pamela A., Wiggins, Michele L., Starr, Lois J., Davé, Bhavana J., Sanger, Warren G.

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Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: Patient report and review of 20qter duplications von Starr, Lois J., Truemper, Edward J., Pickering, Diane L., Sanger, Warren G., Olney, Ann Haskins

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Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome von Sanmann, Jennifer N., Bishay, Danielle L., Starr, Lois J., Bell, Carla A., Pickering, Diane L., Stevens, Jadd M., Kahler, Stephen G., Olney, Ann Haskins, Schaefer, G. Bradley, Sanger, Warren G.

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Microarray Detects Variation in Deletions of IGH (14q32) Gene Region in CLL von Utter, Rachel A, Pickering, Diane L, Stevens, Jadd M, Althof, Pamela A, Sanger, Warren G, Dave, Bhavana J

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Microarray Studies in Pediatric T-Cell Acute Lymphoblastic Leukemia/Lymphoma: A Report of Four Cases von Sanmann, Jennifer N, Pickering, Diane L, Stevens, Jadd M, Sanger, Warren G

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18q22.3 → 18q23 deletion syndrome and cleft palate von Eudy, James D., Pickering, Diane L., Lutz, Richard, Platt, Kristal, Dave, Bhavana J., Olney, Ann Haskins, Sanger, Warren G.

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Inherited 14q duplication and 21q deletion: A rare adjacent‐2 segregation in multiple family members von Dave, Bhavana J., Olney, Ann Haskins, Zaleski, Dianna H., Pickering, Diane L., Becker, Troy A., Chipman, Hope E., Sanger, Warren G.

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Rearrangements of Chromosome Band 1p36 in Non-Hodgkin’s Lymphoma von DAVE, B. J, HESS, M. M, PICKERING, D. L, ZALESKI, D. H, PFEIFER, A. L, WEISENBURGER, D. D, ARMITAGE, J. O, SANGER, W. G

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Breast Cancer and Non-Hodgkin Lymphoma in a Young Male with Cowden Syndrome: Male with Cowden Syndrome Presents with Lymphoma and Breast Cancer von Hagelstrom, Robert Tanner, Ford, James, Reiser, Gwendolyn M., Nelson, Marilu, Pickering, Diane L., Althof, Pamela A., Sanger, Warren G., Coccia, Peter F.

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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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18q22.3 RT 18q23 deletion syndrome and cleft palate von Eudy, James D, Pickering, Diane L, Lutz, Richard, Platt, Kristal, Dave, Bhavana J, Olney, Ann Haskins, Sanger, Warren G

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An evidence-based approach to establish the functional and clinical significance of CNVs 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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Deletion 1 7q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia von MORENO-DE-LUCA, Daniel, CONSORTIUM, Sgene, 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, MULLE, Jennifer G, SURTI, Urvashi, ARADHYA, Swaroop, PICKERING, Diane L, GOLDEN, Denae M, SANDER, Warren G, ASTON, Emily, BROTHMAN, Arthur R, GLIEM, Troy J, THORLAND, Erik C, ACKLEY, Todd, KAMINSKY, Erin B, IYER, Ram, SHUWEN HUANG, BARBER, John C, CROLLA, John A, WARREN, Stephen T, MARTIN, Christa L, LEDBETTER, David H, SANDERS, Stephan J, STAR, Gene, MYERS, Scott M, ADAM, Margaret P, PAKULA, Amy T, EISENHAUER, Nancy J

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