Zobrazeno 1 - 10
of 124
pro vyhledávání: '"M. Anne Spence"'
Autor:
M. Anne Spence, S Yee, Terry J. Hassold, Sarah Ennis, John A. Crolla, D. C. Rao, Bronya J.B. Keats, Stephanie L. Sherman, Aravinda Chakravarti, Robert C. Elston, Neil Risch
Publikováno v:
The American Journal of Human Genetics. 102:1011-1017
Autor:
M. Anne Spence, Veronica J. Vieland
Publikováno v:
Wiley StatsRef: Statistics Reference Online. :1-8
Autor:
Mariella Simon, Moyra Smith, Richard H. Haas, J. Jay Gargus, Gail E. Reiner, Katherine Osann, M. Anne Spence, Pamela Flodman, Douglas C. Wallace, Kimberley Verrell, Robert K. Naviaux
Publikováno v:
Smith, Moyra; Flodman, Pamela L.; Gargus, John J.; Simon, Mariella T; Verrell, Kimberley; Haas, Richard; et al.(2012). Mitochondrial and Ion Channel Gene Alterations in Autism. Biochimica et biophysica acta, 1817(10), 1796-1802. UC Irvine: Institute for Clinical and Translational Science. Retrieved from: http://www.escholarship.org/uc/item/4wh2p4kb
To evaluate the potential importance in autistic subjects of copy number variants (CNVs) that alter genes of relevance to bioenergetics, ionic metabolism, and synaptic function, we conducted a detailed microarray analysis of 69 autism probands and 35
Autor:
Agnes R. Ly, Maryam M. Abdullah, Kathryn Osann, Wendy A. Goldberg, Angela F. Lukowski, Kara L. Thorsen, M. Anne Spence, Nicole L. Matthews
Publikováno v:
Developmental Science. 15:25-34
A deficit in theory of mind (ToM), or the ability to infer the mental states of others, has been implicated as one of the major characteristics of Autism Spectrum Disorder (ASD); however, little attention has been devoted to possible differences in T
Autor:
Nathan D. Wong, M. Anne Spence, Julius M. Gardin, Renee L. Bess, Sharon K. Sklar, Zuhair Allebban, Harrihar A. Pershadsingh
Publikováno v:
Metabolism. 59:1551-1555
Metabolic syndrome (MetS) is associated with increased risk for cardiovascular disease (CVD). Mexican Americans (MA) exhibit increases in CVD risk factors compared with non-Hispanic whites (NHW), but few data exist comparing the relation of MetS to s
Autor:
J. Bronwyn Bateman, Julielani T. Ngo, M. Anne Spence, Victoria K. Cortessis, Robert S. Sparkes
Publikováno v:
Clinical Genetics. 34:43-47
We have identified a family affected with X-linked recessive Norrie disease, in which a recombinational event occurred between the disease locus and the DXS7 locus identified by the probe L1.28. The addition of our family brings the total of publishe
Autor:
Kathryn Osann, William M. McMahon, Andrew Pickles, Sally J. Rogers, Geraldine Dawson, Eric Hollander, Marian Sigman, Patricia M. Rodier, Susan L. Hyman, Alice S. Carter, Helen Tager-Flusberg, Pamela Flodman, Robert M. Joseph, M. Anne Spence, Catherine Lord, Fred R. Volkmar, Rebecca Landa, Joseph D. Buxbaum, Susan Hepburn, Katherine Gotham, Susan Risi
Publikováno v:
Journal of the American Academy of Child & Adolescent Psychiatry. 47:642-651
Objective: To replicate the factor structure and predictive validity of revised Autism Diagnostic Observation Schedule algorithms in an independent dataset ( N = 1,282). Method: Algorithm revisions were replicated using data from children ages 18 mon
Publikováno v:
Journal of Autism and Developmental Disorders. 38:1136-1146
The current study examined consistency between parental reports on early language development and behaviors in non-language domains and observer-coded videotapes of young children with and without autism spectrum disorder (ASD) and autistic regressio
Publikováno v:
Journal of Autism and Developmental Disorders. 38:1047-1058
The present study examines whether children display different frequencies of behaviors at birthday party as compared to non-birthday party settings, and elucidates in which setting behavior is more predictive of later child functioning. Behavior in b
Autor:
Susan E. Hodge, M. Anne Spence
Publikováno v:
Journal of genetic counseling. 9(3)
An ongoing problem in the genetics clinic is the calculation of inbreeding coefficients and recurrence risks for complex pedigrees, particularly when multiple “loops” are present. Although the Human Genome Project promises information about more