Impact of genetic counseling and Connexin-26 and Connexin-30 testing on deaf identity and comprehension of genetic test results in a sample of deaf adults: a prospective, longitudi... von Palmer, Christina G S, Boudreault, Patrick, Baldwin, Erin E, Sinsheimer, Janet S

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Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing von Miller, Christine E., Krautscheid, Patti, Baldwin, Erin E., Tvrdik, Tatiana, Openshaw, Amanda S., Hart, Kim, LaGrave, Danielle

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Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability von Andersen, Erica F., Baldwin, Erin E., Ellingwood, Sara, Smith, Rosemarie, Lamb, Allen N.

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Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature von Herriges, John C., Arch, Ellen M., Burgio, Pamela A., Baldwin, Erin E., LaGrave, Danielle, Lamb, Allen N., Toydemir, Reha M.

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Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy von Wong, Lee‐Jun C., Brunetti‐Pierri, Nicola, Zhang, Qing, Yazigi, Nada, Bove, Kevin E., Dahms, Beverly B., Puchowicz, Michelle A., Gonzalez‐Gomez, Ignacio, Schmitt, Eric S., Truong, Cavatina K., Hoppel, Charles L., Chou, Ping‐Chieh, Wang, Jing, Baldwin, Erin E., Adams, Darius, Leslie, Nancy, Boles, Richard G., Kerr, Douglas S., Craigen, William J.

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Combined Cyclic Vomiting and Kearns-Sayre Syndromes von Boles, Richard G., MD, Baldwin, Erin E., MS, Prezant, Toni R., PhD

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L1CAM whole gene deletion in a child with L1 syndrome von Chidsey, Brandalyn A., Baldwin, Erin E., Toydemir, Reha, Ahles, Lauren, Hanson, Heather, Stevenson, David A.

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Transient Leukoencephalopathy Associated With X-Linked Charcot-Marie-Tooth Disease von Rosser, Tena, Muir, Jason, Panigrahy, Ashok, Baldwin, Erin E., Boles, Richard G.

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Clinical Utility of Chromosomal Microarray Analysis of DNA from Buccal Cells: Detection of Mosaicism in Three Patients von Sdano, Mallory R., Vanzo, Rena J., Martin, Megan M., Baldwin, Erin E., South, Sarah T., Rope, Alan F., Allen, William P., Kearney, Hutton

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Effect of Pre-test Genetic Counseling for Deaf Adults on Knowledge of Genetic Testing von 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 von 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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B-Acute lymphoblastic leukemia and cystinuria in a patient with duplication 22q11.21 detected by chromosomal microarray analysis von Chang, Vivian Y., Quintero-Rivera, Fabiola, Baldwin, Erin E., Woo, Kathy, Martinez-Agosto, Julian A., Fu, Cecilia, Gomperts, Brigitte N.

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Deaf Adults' Reasons for Genetic Testing Depend on Cultural Affiliation: Results From a Prospective, Longitudinal Genetic Counseling and Testing Study von Boudreault, Patrick, Baldwin, Erin E., Fox, Michelle, Dutton, Loriel, Tullis, LeeElle, Linden, Joyce, Kobayashi, Yoko, Zhou, Jin, Sinsheimer, Janet S., Sininger, Yvonne, Grody, Wayne W., Palmer, Christina G. S.

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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome von Chen, Yuyang, Kim, Hyung Chul, Ljungdahl, Alicia, Stenton, Sarah L., Lord, Jenny, Lemire, Gabrielle, Martin-Geary, Alexandra C., Ganesh, Vijay S., Ma, Jialan, Ellingford, Jamie M., Delage, Erwan, D’Souza, Elston N., Dong, Shan, Adams, David R., Allan, Kirsten, Bakshi, Madhura, Baldwin, Erin E., Berger, Seth I., Brown, Natasha J., Burrage, Lindsay C., Chapman, Kimberly, Coman, David J., Compton, Alison G., Cunningham, Chloe A., D’Souza, Precilla, Danecek, Petr, Délot, Emmanuèle C., Dias, Kerith-Rae, Elias, Ellen R., Elmslie, Frances, Evans, Care-Anne, Ezell, Kimberly, Fraser, Jamie L., Gallacher, Lyndon, Genetti, Casie A., Grant, Christina L., Haack, Tobias, Higgs, Jenny E., Hinch, Anjali G., Hurles, Matthew E., Kuechler, Alma, Lecoquierre, François, Fevre, Anna Le, Leventer, Richard J., Liebelt, Jan E., Lindsay, Sarah, Lockhart, Paul J., Ma, Alan S., Macnamara, Ellen F., Mendez, Hector R., Metcalfe, Kay, Montgomery, Stephen B., Moosajee, Mariya, Nassogne, Marie-Cécile, Neumann, Serena, O’Donoghue, Michael, O’Leary, Melanie, Palmer, Elizabeth E., Pattani, Nikhil, Pitsava, Georgia, Pysar, Ryan, Rehm, Heidi L., Reuter, Chloe M., Revencu, Nicole, Riess, Angelika, Rodan, Lance, Roscioli, Tony, Rosenfeld, Jill A., Sachdev, Rani, Shaw-Smith, Charles J., Simons, Cas, Sisodiya, Sanjay M., Snell, Penny, St Clair, Laura, Stewart, Helen S., Tan, Natalie B., Temple, Suzanna E. L., Thorburn, David R., Tifft, Cynthia J., VanNoy, Grace E., Vilain, Eric, Viskochil, David H., Wedd, Laura, Wheeler, Matthew T., White, Susan M., Wojcik, Monica, Wolfe, Lynne A., Wolfenson, Zoe, Wright, Caroline F., Xiao, Changrui, Zocche, David, Rubenstein, John L., Markenscoff-Papadimitriou, Eirene, Fica, Sebastian M., Baralle, Diana, Depienne, Christel, MacArthur, Daniel G., Sanders, Stephan J., O’Donnell-Luria, Anne, Whiffin, Nicola

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51 A common mtDNA control region polymorphism 16519T is associated with migraine without aura and cyclic vomiting von Zaki, Essam A., Freilinger, Tobias, Klopstock, Thomas, Heisner, Katherine R.U., Baldwin, Erin E., Adams, Kathleen, Dichgans, Martin, Boles, Richard G.

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Characterization of the rumen microbiota of pre-ruminant calves using metagenomic tools von Li, Robert W., Connor, Erin E., Li, Congjun, Baldwin, VI, Ransom L., Sparks, Michael E.

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Hospitalizations and Deaths Associated with EVALI von Werner, Angela K, Koumans, Emilia H, Chatham-Stephens, Kevin, Salvatore, Phillip P, Armatas, Christina, Byers, Paul, Clark, Charles R, Ghinai, Isaac, Holzbauer, Stacy M, Navarette, Kristen A, Danielson, Melissa L, Ellington, Sascha, Moritz, Erin D, Petersen, Emily E, Kiernan, Emily A, Baldwin, Grant T, Briss, Peter, Jones, Christopher M, King, Brian A, Krishnasamy, Vikram, Rose, Dale A, Reagan-Steiner, Sarah

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Functional annotation of the cattle genome through systematic discovery and characterization of chromatin states and butyrate-induced variations von Fang, Lingzhao, Liu, Shuli, Liu, Mei, Kang, Xiaolong, Lin, Shudai, Li, Bingjie, Connor, Erin E, Baldwin, 6th, Ransom L, Tenesa, Albert, Ma, Li, Liu, George E, Li, Cong-Jun

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Haemopedia RNA-seq: a database of gene expression during haematopoiesis in mice and humans von Choi, Jarny, Baldwin, Tracey M, Wong, Mae, Bolden, Jessica E, Fairfax, Kirsten A, Lucas, Erin C, Cole, Rebecca, Biben, Christine, Morgan, Clare, Ramsay, Kerry A, Ng, Ashley P, Kauppi, Maria, Corcoran, Lynn M, Shi, Wei, Wilson, Nick, Wilson, Michael J, Alexander, Warren S, Hilton, Douglas J, de Graaf, Carolyn A

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Comparative whole genome DNA methylation profiling across cattle tissues reveals global and tissue-specific methylation patterns von Zhou, Yang, Liu, Shuli, Hu, Yan, Fang, Lingzhao, Gao, Yahui, Xia, Han, Schroeder, Steven G, Rosen, Benjamin D, Connor, Erin E, Li, Cong-Jun, Baldwin, Ransom L, Cole, John B, Van Tassell, Curtis P, Yang, Liguo, Ma, Li, Liu, George E

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