Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing by Reuter, Chloe M., Kohler, Jennefer N., Bonner, Devon, Zastrow, Diane, Fernandez, Liliana, Dries, Annika, Marwaha, Shruti, Davidson, Jean, Brokamp, Elly, Herzog, Matthew, Hong, Joyce, Macnamara, Ellen, Rosenfeld, Jill A., Schoch, Kelly, Spillmann, Rebecca, Loscalzo, Joseph, Krier, Joel, Stoler, Joan, Sweetser, David, Palmer, Christina G.S., Phillips, John A., Shashi, Vandana, Adams, David A., Yang, Yaping, Ashley, Euan A., Fisher, Paul G., Mulvihill, John J., Bernstein, Jonathan A., Wheeler, Matthew T.

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Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision by Baldridge, Dustin, Wangler, Michael F, Bowman, Angela N, Yamamoto, Shinya, Schedl, Tim, Pak, Stephen C, Postlethwait, John H, Shin, Jimann, Solnica-Krezel, Lilianna, Bellen, Hugo J, Westerfield, Monte

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Bi-allelic variants in INTS11 are associated with a complex neurological disorder by Tepe, Burak, Cogne, Benjamin, Neil, Jennifer E., Walsh, Christopher A., Magal, Nurit, Drasinover, Valerie, Schwab, Tanya, Schmitz, Chris, Clark, Karl, Blanc, Pierre, Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bayrak-Toydemir, Pinar, Beck, Anita, Behrens, Edward, Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Boyd, Brenna, Briere, Lauren C., Brown, Gabrielle, Byers, Peter, Byrd, William E., Carey, John, Clark, Gary D., Coakley, Terra R., Colley, Heather A., Craigen, William J., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Deardorff, Matthew, Dipple, Katrina, Doherty, Daniel, Doss, Argenia L., Emrick, Lisa T., Fernandez, Liliana, Forghani, Irman, Glass, Ian, Gochuico, Bernadette, Golden-Grant, Katie, Goldrich, Madison P., Gutierrez, Irma, Hamid, Rizwan, Hayes, Nichole, Hom, Jason, Horike-Pyne, Martha, Isasi, Rosario, Jarvik, Jeffrey, Jobanputra, Vaidehi, Karaviti, Lefkothea, Kiley, Dana, Kobren, Shilpa N., Krasnewich, Donna M., LeBlanc, Kimberly, Levitt, Roy, Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Mao, Rong, Maravilla, Kenneth, Marom, Ronit, Martin, Martin G., Martínez-Agosto, Julian A., Merritt, J. Lawrence, Morava, Eva, Newman, John H., Nickerson, Deborah, Novacic, Donna, Oglesbee, Devin, Pace, Laura, Palmer, Christina GS, Papp, Jeanette C., Rao, Deepak A., Renteria, Genecee, Reuter, Chloe M., Robertson, Amy K., Rosenfeld, Jill A., Rossignol, Francis, Ruzhnikov, Maura, Scott, C. Ron, Shin, Jimann, Sinsheimer, Janet S., Sullivan, Jennifer A., Sun, Angela, Tabor, Holly K., Telischi, Fred, Toro, Camilo, Tucker, Brianna M., Urv, Tiina K., Vogel, Tiphanie P., Walker, Melissa, Wangler, Michael F., Perry, Katherine Wesseling, Westerfield, Monte, Wolfe, Lynne A., Worley, Kim, Xiao, Changrui, Zuchner, Stephan

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Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling by Johnson, Brett V., Alexander, Suzy, Vega, Michelle Sanchez, Domingo, Deepti, Oh, Tracey, Lines, Matthew, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Billette de Villemeur, Thierry, Koolen, David A., Sa, Joaquim, Santiago-Fernández, Olaya, Fernández-Jaén, Alberto, Goldstein, Amy, Madan-Khetarpal, Suneeta, Sullivan, Jennifer A., Bacino, Carlos A., Baker, Eva, Bellen, Hugo J., Bernstein, Jonathan A., Bick, David P., Butte, Manish J., Davids, Mariska, Davidson, Jean M., Dayal, Jyoti G., Dhar, Shweta U., Douine, Emilie D., Draper, David D., Emrick, Lisa T., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Forghani, Irman, Friedman, Noah D., Gahl, William A., Godfrey, Rena A., Hanchard, Neil A., Jiang, Yong-hui, Karaviti, Lefkothea, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lanpher, Brendan C., LeBlanc, Kimberly, Lee, Brendan H., Liu, Xue Zhong, Marwaha, Shruti, McCauley, Jacob, Morimoto, Marie, Nath, Avi, Nelson, Stan F., Newman, John H., Oglesbee, Devin, Orengo, James P., Pak, Stephen, Parker, Neil H., Phillips, John A., Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Sampson, Jacinda B., Schedl, Timothy, Shakachite, Lisa, Sharma, Prashant, Signer, Rebecca, Silverman, Edwin K., Sinsheimer, Janet S., Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Vogel, Tiphanie P., Wahl, Colleen E., Walsh, Chris A., Wang, Lee-kai, Wangler, Michael F., Worthey, Elizabeth A., Yu, Guoyun, Zastrow, Diane B., Zhao, Chunli, Gahl, William, Sullivan, Jennifer A., Barnett, Sarah S., Perry, M. Scott, Schuette, Jane L., Smith, Laurie D., Rosenfeld, Jill A., Bhoj, Elizabeth, Kaplan, Paige, Oegema, Renske, Armstrong, Martin, Lin, Angela E., Hollander, Nicolette den, Hoffer, Mariëtte J.V., Mosher, Theresa Mihalic, Tezcan, Kamer, Penzes, Peter, Piper, Michael

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Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era by Macnamara, Ellen F., Schoch, Kelly, Kelley, Emily G., Fieg, Elizabeth, Brokamp, Elly, Signer, Rebecca, LeBlanc, Kimberly, McConkie‐Rosell, Allyn, Palmer, Christina G.S.

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The genome empowerment scale: An assessment of parental empowerment in families with undiagnosed disease by McConkie‐Rosell, Allyn, Schoch, Kelly, Sullivan, Jennifer, Cope, Heidi, Spillmann, Rebecca, Palmer, Christina G.S., Pena, Loren, Jiang, Yong‐Hui, Daniels, Nicole, Walley, Nicole, Tan, Khoon G., Hooper, Stephen R., Shashi, Vandana

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EFEMP1 haploinsufficiency causes a Marfan‐like hereditary connective tissue disorder by Forghani, Irman, Adam, Margaret, Azamian, Mahshid S., Baker, Eva, Baldridge, Dustin, Bale, Jim, Beck, Anita, Berg‐Rood, Beverly, Berry, Gerard T., Bican, Anna, Boyd, Brenna, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Byers, Peter, Carey, John, Chang, Ta Chen Peter, Cogan, Joy D., Colley, Heather A., D'Souza, Precilla, Dasari, Surendra, Dell'Angelica, Esteban C., Duncan, Laura, Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Esteves, Cecilia, Fernandez, Liliana, Fieg, Elizabeth L., Forghani, Irman, Gochuico, Bernadette, Grajewski, Alana, Hahn, Sihoun, Hamid, Rizwan, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Jamal, Fariha, Jayadev, Suman, Kohler, Jennefer N., Krakow, Deborah, Kravets, Elijah, Koziura, Mary, Lam, Byron, Lam, Christina, Lanza, Ian R., LeBlanc, Kimberly, Lee, Brendan H., Lee, Hane, Levitt, Roy, Liu, Pengfei, Maas, Richard L., Macnamara, Ellen F., Maduro, Valerie V., Majcherska, Marta M., Manolio, Teri A., Marth, Gabor, Martínez‐Agosto, Julian A., Marwaha, Shruti, McCauley, Jacob, McConkie‐Rosell, Allyn, McGee, Elisabeth, Might, Matthew, Mirzaa, Ghayda, Moretti, Paolo M., Mosbrook‐Davis, Deborah, Murdock, David R., Nieves‐Rodriguez, Shirley, Parker, Neil H., Phillips, John A., Power, Bradley, Pusey, Barbara N., Quinlan, Aaron, Raskind, Wendy, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Shin, Jimann, Silverman, Edwin K., Sinsheimer, Janet S., Solem, Emily, Stoler, Joan M., Sun, Angela, Tabor, Holly K., Tan, Amelia L. M., Telischi, Fred, Tifft, Cynthia J., Toro, Camilo, Tucker, Brianna M., Vogel, Tiphanie P., Wambach, Jennifer, Wang, Lee‐kai, Wegner, Daniel, Wenger, Tara, Westerfield, Monte, Wolfe, Lynne A., Zein, Wadih, Zuchner, Stephan

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VarSight: prioritizing clinically reported variants with binary classification algorithms by Holt, James M, Wilk, Brandon, Birch, Camille L, Brown, Donna M, Gajapathy, Manavalan, Moss, Alexander C, Sosonkina, Nadiya, Wilk, Melissa A, Anderson, Julie A, Harris, Jeremy M, Kelly, Jacob M, Shaterferdosian, Fariba, Uno-Antonison, Angelina E, Weborg, Arthur, Worthey, Elizabeth A

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Using a social marketing framework to evaluate recruitment of a prospective study of genetic counseling and testing for the deaf community by Kobayashi, Yoko, Boudreault, Patrick, Hill, Karin, Sinsheimer, Janet S, Palmer, Christina G S

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Assessing Deaf Awareness Training: Knowledge and Attitudes of Recent Genetic Counseling Graduates by Nagakura, Honey, Schneider, Gretchen, Morris, James, Lafferty, Katherine A., Palmer, Christina G. S.

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Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation by Kelley, Emily G., Boyd, Brenna M., Acosta, Maria T, Adams, David R, Amendola, Laura, Andrews, Ashley, Baker, Eva, Bale, Jim, Beggs, Alan H, Behrens, Edward, Bejerano, Gill, Bennet, Jimmy, Berry, Gerard T, Blue, Elizabeth, Bonnenmann, Carsten, Bonner, Devon, Brokamp, Elly, Brown, Gabrielle, Burrage, Lindsay C, Carrasquillo, Olveen, Chao, Hsiao‐Tuan, Sessions Cole, F, Cooper, Cynthia M, Crouse, Andrew B, Dai, Hongzheng, Davis, Joie, Dayal, Jyoti G, Deardorff, Matthew, Dhar, Shweta U, Doherty, Daniel, Duncan, Laura, Eckstein, David J, Emrick, Lisa T, Eng, Christine M, Esteves, Cecilia, Falk, Marni, Fisher, Paul G, Fogel, Brent L, Forghani, Irman, Fresard, Laure, Gahl, William A, Glass, Ian, Godfrey, Rena A, Golden‐Grant, Katie, Goldrich, Madison P, Groden, Catherine A, Gutierrez, Irma, Hahn, Sihoun, Hayes, Nichole, Hing, Anne, Isasi, Rosario, Karaviti, Lefkothea, Kiley, Dana, Kobren, Shilpa N, Kohler, Jennefer N, Krasnewich, Donna M, Krier, Joel B, Latham, Lea, Lee, Hane, Liu, Xue Zhong, Maas, Richard L, Mak, Bryan C, Maclidan, May Christine V., Martínez‐Agosto, Julian A, McGee, Elisabeth, Might, Matthew, Moretti, Paolo M, Nicholas, Sarah K, Novacic, Donna, Pace, Laura, Papp, Jeanette C, Phillips, John A, Posey, Jennifer E, Potocki, Lorraine, Quinlan, Aaron, Rao, Deepak A, Rives, Lynette, Rosenfeld, Jill A, Smith, Edward C, Spillmann, Rebecca C, Stoler, Joan M, Sybert, Virginia, Tekin, Mustafa, Thorson, Willa, Thurm, Audrey, Toro, Camilo, Tucker, Brianna M, Vanderver, Adeline, Velinder, Matt, Vogel, Tiphanie P, Wallace, Stephanie, Walley, Nicole M, Walker, Melissa, Wambach, Jennifer, Wan, Jijun, Wangler, Michael F, Wener, Mark, Wenger, Tara, Yang, John, Yousef, Muhammad

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Effect of Pre-test Genetic Counseling for Deaf Adults on Knowledge of Genetic Testing by Baldwin, Erin E., Boudreault, Patrick, Fox, Michelle, Sinsheimer, Janet S., Palmer, Christina G. S.

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Deaf Genetic Testing and Psychological Well-Being in Deaf Adults by Palmer, Christina G. S., Boudreault, Patrick, Baldwin, Erin E., Fox, Michelle, Deignan, Joshua L., Kobayashi, Yoko, Sininger, Yvonne, Grody, Wayne, Sinsheimer, Janet S.

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Evidence for Maternal-Fetal Genotype Incompatibility as a Risk Factor for Schizophrenia by Palmer, Christina G. S.

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Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy by Bhatia, Aashim, Mobley, Bret C., Koziura, Mary E., Phillips, John, Moore, Steven A., Alvey, Justin, Ashley, Euan A., Balasubramanyam, Ashok, Barbouth, Deborah, Beggs, Alan H., Bejerano, Gill, Berry, Gerard T., Bican, Anna, Birch, Camille L., Bonnenmann, Carsten, Botto, Lorenzo, Brokamp, Elly, Brown, Donna M., Chang, Ta Chen Peter, Chao, Hsiao-Tuan, Clark, Gary D., Cobban, Laurel A., Cogan, Joy D., Cope, Heidi, Craigen, William J., Davids, Mariska, Dell'Angelica, Esteban C., Dorrani, Naghmeh, Eckstein, David J., Emrick, Lisa T., Fogel, Brent L., Godfrey, Rena A., Hamid, Rizwan, High, Frances, Holm, Ingrid A., Jamal, Fariha, Johnston, Jean M., Karaviti, Lefkothea, Kelley, Emily G., Kiley, Dana, Koeller, David M., Kohler, Jennefer N., Korrick, Susan, Koziura, Mary, Krier, Joel B., Kyle, Jennifer E., Lam, Byron, Lanpher, Brendan C., Lazar, Jozef, Lee, Brendan H., Levy, Shawn E., Lewis, Richard A., Liu, Xue Zhong, Loo, Sandra K., MacRae, Calum A., Manolio, Teri A., Markello, Thomas C., Marth, Gabor, May, Thomas, McCauley, Jacob, McConkie-Rosell, Allyn, McCormack, Colleen E., Morava-Kozicz, Eva, Morimoto, Marie, Mulvihill, John J., Nelson, Stan F., Newberry, J. Scott, Newman, John H., Orengo, James P., Phillips, John A., Quinlan, Aaron, Renteria, Genecee, Robertson, Amy K., Sampson, Jacinda B., Saporta, Mario, Schaechter, Judy, Shakachite, Lisa, Sharma, Prashant, Shashi, Vandana, Shin, Jimann, Signer, Rebecca, Silverman, Edwin K., Sinsheimer, Janet S., Smith, Kevin S., Telischi, Fred, Tifft, Cynthia J., Toro, Camilo, Urv, Tiina K., Velinder, Matt, Walley, Nicole M., Wangler, Michael F., Ward, Patricia A., Waters, Katrina M., Webb-Robertson, Bobbie-Jo M., Wheeler, Matthew T., Yang, John, Yoon, Amanda J., Yu, Guoyun, Zastrow, Diane B., Zhao, Chunli

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Examining the Relationship Between Genetic Counselors’ Attitudes Toward Deaf People and the Genetic Counseling Session by Enns, Emily E., Boudreault, Patrick, Palmer, Christina G. S.

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Publishing a Master’s Thesis: A Guide for Novice Authors by Resta, Robert G., McCarthy Veach, Patricia, Charles, Sarah, Vogel, Kristen, Blase, Terri, Palmer, Christina G. S.

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Ethnic Differences in Parental Perceptions of Genetic Testing for Deaf Infants by Palmer, Christina G. S., Martinez, Ariadna, Fox, Michelle, Sininger, Yvonne, Grody, Wayne W., Schimmenti, Lisa A.

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Psychiatric Disorders in Clinical Genetics II: Individualizing Recurrence Risks by Austin, Jehannine C., Palmer, Christina G. S., Rosen-Sheidley, Beth, Veach, Patricia McCarthy, Gettig, Elizabeth, Peay, Holly L.

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Sharing GJB2/GJB6 Genetic Test Information with Family Members by Blase, Terri, Martinez, Ariadna, Grody, Wayne W., Schimmenti, Lisa, Palmer, Christina G. S.

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