Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) wor... by Chun, Kathy, Wenger, Gail D., Chaubey, Alka, Dash, D.P., Kanagal-Shamanna, Rashmi, Kantarci, Sibel, Kolhe, Ravindra, Van Dyke, Daniel L., Wang, Lu, Wolff, Daynna J., Miron, Patricia M.

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Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays by Auer, Herbert, Newsom, David L, Nowak, Norma J, McHugh, Kirk M, Singh, Sunita, Yu, Chack-Yung, Yang, Yan, Wenger, Gail D, Gastier-Foster, Julie M, Kornacker, Karl

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CGC Working Group Recommendations for CLL: Utility of Molecular Technologies Such as Microarrays and NGS for Routine Diagnostic Use by Miron, Patricia M, Wenger, Gail D, Chaubey, Alka

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Somatostatin receptor gene expression in neuroblastoma by Albers, Anne R, O’Dorisio, M.Sue, Balster, Douglas A, Caprara, Moonkyung, Gosh, Pradip, Chen, Feng, Hoeger, Carl, Rivier, Jean, Wenger, Gail D, O’Dorisio, Thomas M, Qualman, Stephen J

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Atypical X-chromosome inactivation in an X;1 translocation patient demonstrating Xq28 functional disomy by Cottrell, Catherine E., Sommer, Annemarie, Wenger, Gail D., Bullard, Steven, Busch, Tamara, Krahn, Katherine Nash, Lidral, Andrew C., Gastier-Foster, Julie M.

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Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia by Tsao, Chang Y., Wenger, Gail D., Bartholomew, Dennis W.

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18 - CGC Working Group Recommendations for CLL: Utility of Molecular Technologies Such as Microarrays and NGS for Routine Diagnostic Use by Miron, Patricia M., Wenger, Gail D., Chaubey, Alka

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Vasoactive Intestinal Peptide. Messenger in a Neuroimmune Axis by WENGER, GAIL D., O'DORISIO, M. SUE, GOETZL, EDWARD J.

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Vasoactive Intestinal Peptide. Messenger in a Neuroimmune Axisa by WENGER, GAIL D., O'DORISIO, M. SUE, GOETZL, EDWARD J.

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Use of Electron Microscopy and Other Special Techniques in the Investigation of Suspected Specimen Contamination by Zuppan, Craig W., Weeks, Douglas A., Wenger, Gail D., Alvarez, Ofelia A., Mierau, Gary W.

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Viscometric and Spectrophotometric Measurements of Hemoglobin S Polymerization Kinetics by Wenger, Gail D., Balcerzak, Stanley P.

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A Multicenter Investigation with D-FISH BCR/ABL1 Probes by Dewald, Gordon, Stallard, Richard, Alsaadi, A., Arnold, Susan, Blough, Ruthann, Ceperich, Tina M., Elejalde, B.Rafael, Fink, James, Higgins, James V., Higgins, Rodney R., Hoeltge, Gerald A., Hsu, Wei-Tong, Johnson, Eric B., Kronberger, Diane, McCorquodale, D.James, Meisner, Lorraine F., Micale, Mark A., Oseth, LeAnn, Payne, Janet S., Schwartz, Stuart, Sheldon, Susan, Sophian, Ardis, Storto, Patrick, Van Tuinen, Peter, Wenger, Gail D., Wiktor, Ann, Willis, Leslie A., Yung, Jar-Fee, Zenger-Hain, Julie

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2012 American College of Rheumatology guidelines for management of gout. Part 1: Systematic nonpharmacologic and pharmacologic therapeutic approaches to hyperuricemia by Khanna, Dinesh, Fitzgerald, John D., Khanna, Puja P., Bae, Sangmee, Singh, Manjit K., Neogi, Tuhina, Pillinger, Michael H., Merill, Joan, Lee, Susan, Prakash, Shraddha, Kaldas, Marian, Gogia, Maneesh, Perez‐Ruiz, Fernando, Taylor, Will, Lioté, Frédéric, Choi, Hyon, Singh, Jasvinder A., Dalbeth, Nicola, Kaplan, Sanford, Niyyar, Vandana, Jones, Danielle, Yarows, Steven A., Roessler, Blake, Kerr, Gail, King, Charles, Levy, Gerald, Furst, Daniel E., Edwards, N. Lawrence, Mandell, Brian, Schumacher, H. Ralph, Robbins, Mark, Wenger, Neil, Terkeltaub, Robert

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Ischemia and No Obstructive Coronary Artery Disease (INOCA): Developing Evidence-Based Therapies and Research Agenda for the Next Decade by Bairey Merz, C Noel, Pepine, Carl J, Walsh, Mary Norine, Fleg, Jerome L, Camici, Paolo G, Chilian, William M, Clayton, Janine Austin, Cooper, Lawton S, Crea, Filippo, Di Carli, Marcelo, Douglas, Pamela S, Galis, Zorina S, Gurbel, Paul, Handberg, Eileen M, Hasan, Ahmed, Hill, Joseph A, Hochman, Judith S, Iturriaga, Erin, Kirby, Ruth, Levine, Glenn N, Libby, Peter, Lima, Joao, Mehta, Puja, Desvigne-Nickens, Patrice, Olive, Michelle, Pearson, Gail D, Quyyumi, Arshed A, Reynolds, Harmony, Robinson, British, Sopko, George, Taqueti, Viviany, Wei, Janet, Wenger, Nanette

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2012 American College of Rheumatology guidelines for management of gout. Part 2: Therapy and antiinflammatory prophylaxis of acute gouty arthritis by Khanna, Dinesh, Khanna, Puja P., Fitzgerald, John D., Singh, Manjit K., Bae, Sangmee, Neogi, Tuhina, Pillinger, Michael H., Merill, Joan, Lee, Susan, Prakash, Shraddha, Kaldas, Marian, Gogia, Maneesh, Perez‐Ruiz, Fernando, Taylor, Will, Lioté, Frédéric, Choi, Hyon, Singh, Jasvinder A., Dalbeth, Nicola, Kaplan, Sanford, Niyyar, Vandana, Jones, Danielle, Yarows, Steven A., Roessler, Blake, Kerr, Gail, King, Charles, Levy, Gerald, Furst, Daniel E., Edwards, N. Lawrence, Mandell, Brian, Schumacher, H. Ralph, Robbins, Mark, Wenger, Neil, Terkeltaub, Robert

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Reanalysis of RNA sequencing data ends diagnostic odyssey and expands the phenotypic spectrum of congenital titinopathy by McNamee, Lucy, Huang, Alden, Wang, Lee‐kai, Buckley, Anne F., Adams, David R., Afzali, Ben, Allworth, Aimee, Alvey, Justin, Andrews, Ashley, Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Borja, Nicholas, Briere, Lauren C., Callaway, Kaitlin, Chanprasert, Sirisak, Coggins, Matthew, Craigen, William J., Cuddapah, Vishnu, Darr, Kahlen, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Karasozen, Yigit, Ketkar, Shamika, Kilich, Gonench, Klee, Eric, Kohler, Jennefer N., Korrick, Susan, Kravets, Elijah, Lalani, Seema R., Latchman, Kumarie, LeBlanc, Kimberly, Liu, Pengfei, Longo, Nicola, MacRae, Calum A., Maghiro, AudreyStephannie, Mahoney, Rachel, Malicdan, May Christine V., Martin, Beth A., Miller, Danny, Moretti, Paolo, Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant by Gulsevin, Alican, Hamid, Rizwan, Neumann, Serena, Phillips, John A., Adams, David R., Afzali, Ben, Andrews, Ashley, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Borja, Nicholas, Butte, Manish J., Byrd, William E., Callaway, Kaitlin, Carvalho, George, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Cogan, Joy D., Coggins, Matthew, Corner, Brian, Dipple, Katrina, Doherty, Daniel, Douglas, Jessica, Emrick, Lisa T., Eng, Christine M., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Hing, Anne, Horike‐Pyne, Martha, Huang, Alden, Huang, Yan, Kaitryn, Emerald, Kanca, Oguz, Kohler, Jennefer N., Krakow, Deborah, Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., Liu, Pengfei, Longo, Nicola, Mahoney, Rachel, Marth, Gabor, McCray, Alexa T., Might, Matthew, Miller, Danny, Moretti, Paolo, Mulvihill, John J., Mulvihill, Lindsay, Neumann, Serena, Novacic, Donna, Orengo, James P., Pace, Laura, Pak, Stephen, Parker, Neil H., Pinto e Vairo, Filippo, Posey, Jennifer E., Potocki, Lorraine, Rader, Daniel J., Rosenfeld, Jill A., Ruzhnikov, Maura, Sampson, Jacinda B., Schoch, Kelly, Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Skelton, Tammi, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sutton, Shirley, Sweetser, David A., Tabor, Holly K., Tan, Queenie, Tan, Amelia L. M., Tifft, Cynthia J., Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wood, Heidi, Worley, Kim

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Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome by Pujol‐Giménez, Jonai, Miller, Danny E., Allworth, Aimee, Chanprasert, Sirisak, Folta, Andrew B., Hing, Anne, Horike‐Pyne, Martha, Leppig, Kathleen A., Parhin, Azma, Rosenthal, Elisabeth A., Schwarze, Ulrike, Strohbehn, Samuel, Sybert, Virginia P., Timms, Andrew, Wener, Mark, Bamshad, Michael J., Bacus, Tamara J., Blue, Elizabeth E., Brower, Katherine, Sánchez, Diana Cornejo, Gomeztagle‐Burgess, Katherine, Hurless, Jameson R., Shively, Kathryn M., Weiss, Jeffrey M., Wheeler, Marsha M., Adam, Margaret, Alvey, Justin, Amendola, Laura, Andrews, Ashley, Ashley, Euan A., Barbouth, Deborah, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Bivona, Stephanie, Blue, Elizabeth, Bonner, Devon, Byers, Peter, Cassini, Thomas, Chang, Ta Chen Peter, Chanprasert, Sirisak, Clark, Gary D., Cole, F. Sessions, Corona, Rosario, Crouse, Andrew B., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Emrick, Lisa T., Fisher, Paul G., Gahl, William A., Hadley, Don, Hahn, Sihoun, High, Frances, Hing, Anne, Hisama, Fuki M., Horike‐Pyne, Martha, Hutchison, Sarah, Izumi, Kosuke, Kohane, Isaac S., Kohler, Jennefer N., Lalani, Seema R., Lam, Byron, Lanpher, Brendan C., Lewis, Richard A., Liu, Xue Zhong, Maduro, Valerie V., Manolio, Teri A., McCauley, Jacob, McCray, Alexa T., Mefford, Heather, Moretti, Paolo, Nickerson, Deborah, Nieves‐Rodriguez, Shirley, Orengo, James P., Pak, Stephen, Papp, Jeanette C., Parker, Neil H., Phillips, John A., Rao, Deepak A., Raskind, Wendy, Renteria, Genecee, Rosenfeld, Jill A., Saporta, Mario, Schaechter, Judy, Scott, Daryl A., Sisco, Kathy, Spillmann, Rebecca C., Sullivan, Jennifer A., Tabor, Holly K., Tifft, Cynthia J., Ungar, Rachel A., Walker, Melissa, Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Wener, Mark, Yamamoto, Shinya, Dipple, Katrina M., Stergachis, Andrew B.

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Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy by Donkervoort, Sandra, Mohassel, Payam, Brull, Astrid, Mozaffar, Tahseen, Dyment, David A., Pajusalu, Sander, Hurth, Kyle, McWalter, Kirsty, Warman‐Chardon, Jodi, Crunk, Amy, Foley, A. Reghan, Allworth, Aimee, Andrews, Ashley, Bacino, Carlos A., Bademci, Guney, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Beggs, Alan H., Berry, Gerard T., Bivona, Stephanie, Blue, Elizabeth, Brown, Gabrielle, Butte, Manish J., Cassini, Thomas, Chao, Hsiao‐Tuan, Chinn, Ivan, Cogan, Joy D., Coggins, Matthew, Corona, Rosario, Crouse, Andrew B., Dai, Hongzheng, Davis, Joie, Douine, Emilie D., Emrick, Lisa T., Fu, Jiayu, Hamid, Rizwan, High, Frances, Hing, Anne, Hisama, Fuki M., Horike‐Pyne, Martha, Huang, Yan, Hutchison, Sarah, Kilich, Gonench, Kobren, Shilpa N., Krakow, Deborah, Krasnewich, Donna M., Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., Liu, Pengfei, Longo, Nicola, Maduro, Valerie V., Manolio, Teri A., Mao, Rong, Marom, Ronit, Martin, Beth A., Martin, Martin G., Marwaha, Shruti, McConkie‐Rosell, Allyn, McGee, Elisabeth, Miller, Danny, Mirzaa, Ghayda, Nakano‐Okuno, Mariko, Nelson, Stanley F., Nieves‐Rodriguez, Shirley, Pallais, J. Carl, Petcharet, Leoyklang, Phillips, John A., Quinlan, Aaron, Rosenfeld, Jill A., Sabaii, Marla, Scott, Daryl A., Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Sisco, Kathy, Solomon, Ben, Sullivan, Kathleen, Sutton, Shirley, Tan, Queenie K.‐G., Amelia, L. M. Tan, Taylor, Herman, Tekin, Mustafa, Toro, Camilo, Ungar, Rachel A., Vanderver, Adeline, Walker, Melissa, Wang, Lee‐kai, Wangler, Michael F., Wegner, Daniel, Wener, Mark, Westerfield, Monte, Whitlock, Jordan, Wolfe, Lynne A., Worley, Kim, Yamamoto, Shinya, Zhang, Zhe, Mammen, Andrew L., O'Donnell‐Luria, Anne

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Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism by Rebelo, Adriana P., Jeanne, Médéric, Danzi, Matt C., Tekin, Mustafa, Acosta, Maria T., Andrews, Ashley, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Butte, Manish J., Byrd, William E., Cassini, Thomas, Chao, Hsiao‐Tuan, Coakley, Terra R., Cobban, Laurel A., Cole, F. Sessions, Colley, Heather A., Corner, Brian, Dai, Hongzheng, Davis, Joie, Delgado, Margaret, Douine, Emilie D., Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Fisher, Paul G., Fogel, Brent L., Fu, Jiayu, Glass, Ian, Gropman, Andrea, Halley, Meghan C., Hassey, Kelly, Hayes, Nichole, Horike‐Pyne, Martha, Huang, Alden, Izumi, Kosuke, Jean‐Marie, Orpa, Jobanputra, Vaidehi, Ketkar, Shamika, Kohler, Jennefer N., Kravets, Elijah, Lalani, Seema R., Latchman, Kumarie, LeBlanc, Kimberly, Lewis, Richard A., Liu, Pengfei, Loo, Sandra K., MacRae, Calum A., Maghiro, AudreyStephannie C., Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Marth, Gabor, Martínez‐Agosto, Julian A., McConkie‐Rosell, Allyn, Morava, Eva, Moretti, Paolo, Morimoto, Marie, Neumann, Serena, Novacic, Donna, Oglesbee, Devin, Papp, Jeanette C., Petcharet, Leoyklang, Posey, Jennifer E., Potocki, Lorraine, Rao, Deepak A., Raskind, Wendy, Rosenfeld, Jill A., Sabaii, Marla, Scott, Daryl A., Shashi, Vandana, Shin, Jimann, Silverman, Edwin K., Sisco, Kathy, Smith, Edward C., Smith, Carson A., Smith, Kevin S., Solomon, Ben, Stergachis, Andrew, Sullivan, Kathleen, Tabor, Holly K., Tan, Queenie K.‐G., Thorson, Willa, Viskochil, Dave, Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wenger, Tara, Westerfield, Monte, Worley, Kim

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