Cindy Hudson

School of the Art Institute of Chicago — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

6h-index1.0kcitations8works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(3), Genomics and Rare Diseases(2), Congenital heart defects research(2), Virus-based gene therapy research(1), Cellular transport and secretion(1)

Publications8 total

Phenotypic spectrum of <i>GABRA1</i>
Neurology·2016· 137 citedOpen Access
Issue Information
Human Mutation·2016Open Access
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update
Human Mutation·2015· 71 citedOpen Access
Mutations in <i>SPECC1L</i>, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome
Journal of Medical Genetics·2014· 48 citedOpen Access
Confirmation of 6q21–6q22.1 deletion in Acro‐cardio‐facial syndrome and further delineation of this contiguous gene deletion syndrome
American Journal of Medical Genetics Part A·2014· 48 citedOpen Access
Table of Contents, Volume 155, Number 4, April 2011
American Journal of Medical Genetics Part A·2011Open Access
Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C
American Journal of Medical Genetics Part A·2011· 68 citedOpen Access
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Nature Genetics·2010· 669 citedOpen Access

Frequent Co-authors

John P. Johnson(5), Elaine H. Zackai(4), William B. Dobyns(4), Karen W. Gripp(4), Judith Allanson(3), Margaret Harr(3), Alasdair G. W. Hunter(3), Raoul Heller(3), Donna M. McDonald‐McGinn(2), Matthew A. Deardorff(2), Abdallah F. Elias(2), Lijia Huang(2), Megan R. Vanstone(2), Taila Hartley(2), Matthew Osmond(2), Nick Barrowman(2), Katrina M. Dipple(2), Jane Estrella(2), Hanna Faghfoury(2), Francine Pinheiro Favaro(2)