A Predictive Metabolic Signature for the Transition From Gestational Diabetes Mellitus to Type 2 Diabetes von Allalou, Amina, Nalla, Amarnadh, Prentice, Kacey J, Liu, Ying, Zhang, Ming, Dai, Feihan F, Ning, Xian, Osborne, Lucy R, Cox, Brian J, Gunderson, Erica P, Wheeler, Michael B

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Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23 von Strong, Emma, Butcher, Darci T., Singhania, Rajat, Mervis, Carolyn B., Morris, Colleen A., De Carvalho, Daniel, Weksberg, Rosanna, Osborne, Lucy R.

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Duplication of GTF2I Results in Separation Anxiety in Mice and Humans von Mervis, Carolyn B., Dida, Joana, Lam, Emily, Crawford-Zelli, Nicole A., Young, Edwin J., Henderson, Danielle R., Onay, Tuncer, Morris, Colleen A., Woodruff-Borden, Janet, Yeomans, John, Osborne, Lucy R.

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First Mouse Model for Combined Osteogenesis Imperfecta and Ehlers‐Danlos Syndrome von Chen, Frieda, Guo, Ruolin, Itoh, Shousaku, Moreno, Luisa, Rosenthal, Esther, Zappitelli, Tanya, Zirngibl, Ralph A, Flenniken, Ann, Cole, William, Grynpas, Marc, Osborne, Lucy R, Vogel, Wolfgang, Adamson, Lee, Rossant, Janet, Aubin, Jane E

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Global analysis of gene expression in the developing brain of Gtf2ird1 knockout mice von O'Leary, Jennifer, Osborne, Lucy R

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Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype von Qaiser, Farah, Yin, Yue, Mervis, Carolyn B, Morris, Colleen A, Klein-Tasman, Bonita P, Tam, Elaine, Osborne, Lucy R, Yuen, Ryan K C

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Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome von Liu, Delong, Billington, Jr, Charles J, Raja, Neelam, Wong, Zoe C, Levin, Mark D, Resch, Wulfgang, Alba, Camille, Hupalo, Daniel N, Biamino, Elisa, Bedeschi, Maria Francesca, Digilio, Maria Cristina, Squeo, Gabriella Maria, Villa, Roberta, Parrish, Pheobe C R, Knutsen, Russell H, Osgood, Sharon, Freeman, Joy A, Dalgard, Clifton L, Merla, Giuseppe, Pober, Barbara R, Mervis, Carolyn B, Roberts, Amy E, Morris, Colleen A, Osborne, Lucy R, Kozel, Beth A

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DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy number von Strong, Emma, Mervis, Carolyn B., Tam, Elaine, Morris, Colleen A., Klein-Tasman, Bonita P., Velleman, Shelley L., Osborne, Lucy R.

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7q11.23 deletion and duplication von Osborne, Lucy R, Mervis, Carolyn B

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Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia von Feuk, Lars, Kalervo, Aino, Lipsanen-Nyman, Marita, Skaug, Jennifer, Nakabayashi, Kazuhiko, Finucane, Brenda, Hartung, Danielle, Innes, Micheil, Kerem, Batsheva, Nowaczyk, Małgorzata J., Rivlin, Joseph, Roberts, Wendy, Senman, Lili, Summers, Anne, Szatmari, Peter, Wong, Virginia, Vincent, John B., Zeesman, Susan, Osborne, Lucy R., Cardy, Janis Oram, Kere, Juha, Scherer, Stephen W., Hannula-Jouppi, Katariina

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Williams syndrome von Kozel, Beth A., Barak, Boaz, Kim, Chong Ae, Mervis, Carolyn B., Osborne, Lucy R., Porter, Melanie, Pober, Barbara R.

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Essential Role of Fkbp6 in Male Fertility and Homologous Chromosome Pairing in Meiosis von Crackower, Michael A., Kolas, Nadine K., Noguchi, Junko, Sarao, Renu, Kikuchi, Kazuhiro, Kaneko, Hiroyuki, Kobayashi, Eiji, Kawai, Yasuhiro, Kozieradzki, Ivona, Landers, Rushin, Mo, Rong, Hui, Chi-Chung, Nieves, Edward, Cohen, Paula E., Osborne, Lucy R., Wada, Teiji, Kunieda, Tetsuo, Moens, Peter B., Penninger, Josef M.

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Rearrangements of the Williams–Beuren syndrome locus: molecular basis and implications for speech and language development von Osborne, Lucy R., Mervis, Carolyn B.

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Enu mutagenesis identifies a novel platelet phenotype in a loss-of-function Jak2 allele von Anderson, Nicole M, Javadi, Mojib, Berndl, Elizabeth, Berberovic, Zorana, Bailey, Monica L, Huang, Kai, Flenniken, Ann M, Osborne, Lucy R, Adamson, S Lee, Rossant, Janet, Carter-Su, Christin, Wang, Chen, McNagny, Kelly M, Paulson, Robert F, Minden, Mark D, Stanford, William L, Barber, Dwayne L

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Transgenic Mouse Overexpressing Syntaxin-1A as a Diabetes Model von LAM, Patrick P. L, LEUNG, Yuk-Man, SHEU, Laura, ELLIS, James, TSUSHIMA, Robert G, OSBORNE, Lucy R, GAISANO, Herbert Y

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A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis von Hughes, Michael R, Anderson, Nicole, Maltby, Steven, Wong, Justin, Berberovic, Zorana, Birkenmeier, Connie S, Haddon, D. James, Garcha, Kamal, Flenniken, Ann, Osborne, Lucy R, Adamson, S. Lee, Rossant, Janet, Peters, Luanne L, Minden, Mark D, Paulson, Robert F, Wang, Chen, Barber, Dwayne L, McNagny, Kelly M, Stanford, William L

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7q11.23 Duplication syndrome: Physical characteristics and natural history von Morris, Colleen A., Mervis, Carolyn B., Paciorkowski, Alex P., Abdul-Rahman, Omar, Dugan, Sarah L., Rope, Alan F., Bader, Patricia, Hendon, Laura G., Velleman, Shelley L., Klein-Tasman, Bonita P., Osborne, Lucy R.

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Spatial gene expression analysis of neuroanatomical differences in mouse models von Fernandes, Darren J., Ellegood, Jacob, Askalan, Rand, Blakely, Randy D., Dicicco-Bloom, Emanuel, Egan, Sean E., Osborne, Lucy R., Powell, Craig M., Raznahan, Armin, Robins, Diane M., Salter, Michael W., Sengar, Ameet S., Veenstra-VanderWeele, Jeremy, Henkelman, R.M., Lerch, Jason P.

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Caveat mTOR: aberrant signaling disrupts corticogenesis von Osborne, Lucy R

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Children with 7q11.23 duplication syndrome: Psychological characteristics von Mervis, Carolyn B., Klein-Tasman, Bonita P., Huffman, Myra J., Velleman, Shelley L., Pitts, C. Holley, Henderson, Danielle R., Woodruff-Borden, Janet, Morris, Colleen A., Osborne, Lucy R.

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