Genomic screen and follow-up analysis for autistic disorder
Shao, Yujun, Wolpert, Chantelle M, Raiford, Kimberly L, Menold, Marisa M, Donnelly, Shannon L, Ravan, Sarah A, Bass, Meredyth P, McClain, Cate, von Wendt, Lennart, Vance, Jeffery M, Abramson, Ruth H, Wright, Harry H, Ashley-Koch, Allison, Gilbert, John R, DeLong, Robert G, Cuccaro, Michael L, Pericak-Vance, Margaret A
Published in American journal of medical genetics (08.01.2002)
Published in American journal of medical genetics (08.01.2002)
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Accelerated head growth in early development of individuals with autism
Dementieva, Yulia A., Vance, Danica D., Donnelly, Shannon L., Elston, Leigh A., Wolpert, Chantelle M., Ravan, Sarah A., DeLong, G. Robert, Abramson, Ruth K., Wright, Harry H., Cuccaro, Michael L.
Published in Pediatric neurology (01.02.2005)
Published in Pediatric neurology (01.02.2005)
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Identification of MeCP2 mutations in a series of females with autistic disorder
Carney, Regina M., Wolpert, Chantelle M., Ravan, Sarah A., Shahbazian, Mona, Ashley-Koch, Allison, Cuccaro, Michael L., Vance, Jeffery M., Pericak-Vance, Margaret A.
Published in Pediatric neurology (01.03.2003)
Published in Pediatric neurology (01.03.2003)
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Factor analysis of restricted and repetitive behaviors in Autism using the Autism Diagnostic interview-R
CUCCARO, Michael L, YUJAN SHAO, PERICAK-VANCE, Margaret A, GRUBBER, Janet, SLIFER, Michael, WOLPERT, Chantelle M, DONNELLY, Shannon L, ABRAMSON, Ruth K, RAVAN, Sarah A, WRIGHT, Harry H, DELONG, G. Robert
Published in Child psychiatry and human development (01.09.2003)
Published in Child psychiatry and human development (01.09.2003)
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Phenotypic Homogeneity Provides Increased Support for Linkage on Chromosome 2 in Autistic Disorder
Shao, Yujun, Raiford, Kimberly L., Wolpert, Chantelle M., Cope, Heidi A., Ravan, Sarah A., Ashley-Koch, Allison A., Abramson, Ruth K., Wright, Harry H., DeLong, Robert G., Gilbert, John R., Cuccaro, Michael L., Pericak-Vance, Margaret A.
Published in American journal of human genetics (01.04.2002)
Published in American journal of human genetics (01.04.2002)
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Harnessing the Power of the Pedigree
Wolpert, Chantelle M., Speer, Marcy C.
Published in Journal of midwifery & women's health (01.05.2005)
Published in Journal of midwifery & women's health (01.05.2005)
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Journal Article
No association between the WNT2 gene and autistic disorder
McCoy, Pinky A, Shao, Yujun, Wolpert, Chantelle M, Donnelly, Shannon L, Ashley-Koch, Allison, Abel, Heidi L, Ravan, Sarah A, Abramson, Ruth K, Wright, Harry H, DeLong, G Robert, Cuccaro, Michael L, Gilbert, John R, Pericak-Vance, Margaret A
Published in American journal of medical genetics (08.01.2002)
Published in American journal of medical genetics (08.01.2002)
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Behavioral Comparisons in Autistic Individuals from Multiplex and Singleton Families
Cuccaro, Michael L, Shao, Yujun, Bass, Meredyth P, Abramson, Ruth K, Ravan, Sarah A, Wright, Harry H, Wolpert, Chantelle M, Donnelly, Shannon L, Pericak-Vance, Margaret A
Published in Journal of autism and developmental disorders (01.02.2003)
Published in Journal of autism and developmental disorders (01.02.2003)
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Speaking the Language of Genetics: A Primer
Wolpert, Chantelle M., Singer, Margaret L., Speer, Marcy C.
Published in Journal of midwifery & women's health (01.05.2005)
Published in Journal of midwifery & women's health (01.05.2005)
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Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
ASHLEY-KOCH, Allison, BONNER, Erin R, MARCHUK, Douglas A, BOUSTANY, Rose-Mary N, VANCE, Jeffery M, SCOTT, William K, PERICAK-VANCE, Margaret A, GASKELL, P. Craig, WEST, Sandra G, TIM, Richard, WOLPERT, Chantelle M, JONES, Rodney, FARRELL, Carolyn D, NANCE, Martha, SVENSON, Ingrid K
Published in Neurogenetics (01.03.2001)
Published in Neurogenetics (01.03.2001)
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Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder
Menold, M M, Shao, Y, Wolpert, C M, Donnelly, S L, Raiford, K L, Martin, E R, Ravan, S A, Abramson, R K, Wright, H H, Delong, G R, Cuccaro, M L, Pericak-Vance, M A, Gilbert, J R
Published in Journal of neurogenetics (2001)
Published in Journal of neurogenetics (2001)
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Three probands with autistic disorder and isodicentric chromosome 15
Wolpert, C M, Menold, M M, Bass, M P, Qumsiyeh, M B, Donnelly, S L, Ravan, S A, Vance, J M, Gilbert, J R, Abramson, R K, Wright, H H, Cuccaro, M L, Pericak-Vance, M A
Published in American journal of medical genetics (12.06.2000)
Published in American journal of medical genetics (12.06.2000)
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A genetic hypothesis for Chiari I malformation with or without syringomyelia
Speer, M C, George, T M, Enterline, D S, Franklin, A, Wolpert, C M, Milhorat, T H
Published in Neurosurgical focus (15.03.2000)
Published in Neurosurgical focus (15.03.2000)
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Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome
Donnelly, S L, Wolpert, C M, Menold, M M, Bass, M P, Gilbert, J R, Cuccaro, M L, Delong, G R, Pericak-Vance, M A
Published in American journal of medical genetics (12.06.2000)
Published in American journal of medical genetics (12.06.2000)
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Genetic studies in autistic disorder and chromosome 15
BASS, M. P, MENOLD, M. M, GILBERT, J. R, CUCCARO, M. L, DELONG, G. R, PERICAK-VANCE, M. A, WOLPERT, C. M, DONNELLY, S. L, RAVAN, S. A, HAUSER, E. R, MADDOX, L. O, VANCE, J. M, ABRAMSON, R. K, WRIGHT, H. H
Published in Neurogenetics (01.03.2000)
Published in Neurogenetics (01.03.2000)
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Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia
Scott, W K, Gaskell, P C, Lennon, F, Wolpert, C M, Menold, M M, Aylsworth, A S, Warner, C, Farrell, C D, Boustany, R M, Albright, S G, Boyd, E, Kingston, H M, Cumming, W J, Vance, J M, Pericak-Vance, M A
Published in Neurogenetics (01.11.1997)
Published in Neurogenetics (01.11.1997)
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