Velo-cardio-facial syndrome: 30 Years of study von Shprintzen, Robert J.

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Adaptive living skills, sleep problems, and mental health disorders in adults with 22q11.21 deletion syndrome von Leader, Geraldine, Curtin, Andrea, Shprintzen, Robert J., Whelan, Sally, Coyne, Rory, Mannion, Arlene

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An examination of adaptive behavior and functional outcomes in adults with 22q11.2 deletion syndrome: A parental perspective von Curtin, Andrea, Mannion, Arlene, Shprintzen, Robert J., Whelan, Sally, Coyne, Rory, Leader, Geraldine

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Defining the Clinical Spectrum of Deletion 22q11.2 von Robin, Nathaniel H., Shprintzen, Robert J.

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Autistic Spectrum Disorders in Velo-Cardio Facial Syndrome (22q11.2 Deletion) von Antshel, Kevin M, Aneja, Alka, Strunge, Leslie, Peebles, Jena, Fremont, Wanda P, Stallone, Kimberly, AbdulSabur, Nuria, Higgins, Anne Marie, Shprintzen, Robert J, Kates, Wendy R

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Cognitive and Psychiatric Predictors to Psychosis in Velocardiofacial Syndrome: A 3-Year Follow-Up Study von Antshel, Kevin M., Ph.D, Shprintzen, Robert, Ph.D, Fremont, Wanda, M.D, Higgins, Anne Marie, N.P, Faraone, Stephen V., Ph.D, Kates, Wendy R., Ph.D

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“Retrofitting” established genetic disorders and diseases through big data and phenomics von Graf, William D., Shprintzen, Robert J.

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Velopharyngeal insufficiency: diagnosis and management von Shprintzen, Robert J, Marrinan, Eileen

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Neuroanatomic Predictors to Prodromal Psychosis in Velocardiofacial Syndrome (22q11.2 Deletion Syndrome): A Longitudinal Study von Kates, Wendy R, Antshel, Kevin M, Faraone, Stephen V, Fremont, Wanda P, Higgins, Anne Marie, Shprintzen, Robert J, Botti, Jo-Anna, Kelchner, Lauren, McCarthy, Christopher

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4.19 TREATMENT OF VELO-CARDIO-FACIAL SYNDROME-RELATED PSYCHOSIS WITH METYROSINE von Faedda, Gianni L., MD, Graf, William, MD, Shprintzen, Robert, D Phil

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Catatonia in an adolescent with velo-cardio-facial syndrome von Faedda, Gianni L., Wachtel, Lee E., Higgins, Anne Marie, Shprintzen, Robert J.

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Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes von Radoeva, Petya D, Coman, Ioana L, Salazar, Cynthia A, Gentile, Karen L, Higgins, Anne Marie, Middleton, Frank A, Antshel, Kevin M, Fremont, Wanda, Shprintzen, Robert J, Morrow, Bernice E, Kates, Wendy R

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Genomic disorders on chromosome 22 von Yu, Shihui, Graf, William D, Shprintzen, Robert J

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Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings von Radoeva, Petya D, Coman, Ioana L, Antshel, Kevin M, Fremont, Wanda, McCarthy, Christopher S, Kotkar, Ashwini, Wang, Dongliang, Shprintzen, Robert J, Kates, Wendy R

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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes von Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jarlbrzkowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria, van den Bree, Marianne, Owen, Michael J., Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S., Morrow, Bernice E.

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Mapping Cortical Morphology in Youth With Velocardiofacial (22q11.2 Deletion) Syndrome von Kates, Wendy R., Ph.D, Bansal, Ravi, Ph.D, Fremont, Wanda, M.D, Antshel, Kevin M., Ph.D, Hao, Xuejun, Ph.D, Higgins, Anne Marie, N.P, Liu, Jun, Ph.D, Shprintzen, Robert J., Ph.D, Peterson, Bradley S., M.D

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Cortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: A longitudinal study von Kunwar, Arun, Ramanathan, Seethalakshmi, Nelson, Joshua, Antshel, Kevin M, Fremont, Wanda, Higgins, Anne Marie, Shprintzen, Robert J, Kates, Wendy R

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The Longitudinal Course of Attention Deficit/Hyperactivity Disorder in Velo-Cardio-Facial Syndrome von Antshel, Kevin M., PhD, Hendricks, Kaitlin, MS, Shprintzen, Robert, PhD, Fremont, Wanda, MD, Higgins, Anne Marie, NP, Faraone, Stephen V., PhD, Kates, Wendy R., PhD

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The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI s... von Coman, Ioana L., Gnirke, Matthew H., Middleton, Frank A., Antshel, Kevin M., Fremont, Wanda, Higgins, Anne Marie, Shprintzen, Robert J., Kates, Wendy R.

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A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome) von Kates, Wendy R., Antshel, Kevin M., AbdulSabur, Nuria, Colgan, Deirdre, Funke, Birgit, Fremont, Wanda, Higgins, Anne Marie, Kucherlapati, Raju, Shprintzen, Robert J.

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