A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia
Trittmann, Jennifer K., Gastier-Foster, Julie M., Zmuda, Erik J., Frick, Jessica, Rogers, Lynette K., Vieland, Veronica J., Chicoine, Louis G., Nelin, Leif D.
Published in Acta Paediatrica (01.04.2016)
Published in Acta Paediatrica (01.04.2016)
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Examination of AVPR1a as an autism susceptibility gene
WASSINK, T. H, PIVEN, J, VIELAND, V. J, PIETILA, J, GOEDKEN, R. J, FOLSTEIN, S. E, SHEFFIELD, V. C
Published in Molecular psychiatry (01.10.2004)
Published in Molecular psychiatry (01.10.2004)
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Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasia
Trittmann, JK, Nelin, LD, Zmuda, EJ, Gastier-Foster, JM, Chen, B, Backes, CH, Frick, J, Vaynshtok, P, Vieland, VJ, Klebanoff, MA
Published in Acta Paediatrica (01.10.2014)
Published in Acta Paediatrica (01.10.2014)
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Journal Article
A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21
Bartlett, Christopher W., Flax, Judy F., Logue, Mark W., Vieland, Veronica J., Bassett, Anne S., Tallal, Paula, Brzustowicz, Linda M.
Published in American journal of human genetics (01.07.2002)
Published in American journal of human genetics (01.07.2002)
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Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes
Woodbury-Smith, Marc, Paterson, Andrew D., Thiruvahindrapduram, Bhooma, Lionel, Anath C., Marshall, Christian R., Merico, Daniele, Fernandez, Bridget A., Duku, Eric, Sutcliffe, James S., O’Conner, Irene, Chrysler, Christina, Thompson, Ann, Kellam, Barbara, Tammimies, Kristiina, Walker, Susan, Yuen, Ryan K. C., Uddin, Mohammed, Howe, Jennifer L., Parlier, Morgan, Whitten, Kathy, Szatmari, Peter, Vieland, Veronica J., Piven, Joseph, Scherer, Stephen W.
Published in Human genetics (01.02.2015)
Published in Human genetics (01.02.2015)
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Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene
Wassink, Thomas H., Piven, Joseph, Vieland, Veronica J., Jenkins, Laura, Frantz, Rebecca, Bartlett, Christopher W., Goedken, Rhinda, Childress, Deb, Spence, M. Anne, Smith, Moyra, Sheffield, Val C.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2005)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2005)
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Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7
Logue, Mark W., Vieland, Veronica J., Goedken, Rhinda J., Crowe, Raymond R.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.08.2003)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (15.08.2003)
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Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment
Bartlett, Christopher W., Flax, Judy F., Logue, Mark W., Smith, Brett J., Vieland, Veronica J., Tallal, Paula, Brzustowicz, Linda M.
Published in Human heredity (01.01.2004)
Published in Human heredity (01.01.2004)
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Journal Article
Evaluation of FOXP2 as an autism susceptibility gene
Wassink, Thomas H, Piven, Joseph, Vieland, Veronica J, Pietila, Jennifer, Goedken, Rhinda J, Folstein, Susan E, Sheffield, Val C
Published in American journal of medical genetics (08.07.2002)
Published in American journal of medical genetics (08.07.2002)
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Journal Article
The Emperor’s New Methods
Spence, M. Anne, Greenberg, David A., Hodge, Susan E., Vieland, Veronica J.
Published in American journal of human genetics (01.05.2003)
Published in American journal of human genetics (01.05.2003)
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