Cynthia Forster‐Gibson

Author

Also Known As

C Forster-Gibson, C J Forster-Gibson, C. Forster-Gibson, C. J. Forster-gibson, C.J. Forster-Gibson, Cynthia Forster-Gibson, Cynthia Forster‐Gibson, Cynthia J Forster-Gibson, Cynthia J. Forster-Gibson, Cynthia J. Forster‐Gibson

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Queen's University University of British Columbia Child and Family Research Institute University of Manitoba New York State Office for People With Developmental Disabilities

About

Cynthia Forster‐Gibson is an author at Queen's University specializing in medicine, genetics, and autism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	557
2	Engineering	1	1	62
3	Natural Sciences	1	1	226
4	Social Sciences	1	1	113
5	Biochemistry	1	1	226

Cynthia Forster‐Gibson

Publications

952

Citations

H-Index

Page 1

	Year	Citations
Temperature-dependent cytosol-to-nucleus translocation of the Ah receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin in continuous cell culture lines. Allan B. Okey, Greg Bondy, Michelle E. Mason, Journal of Biological Chemistry Molecular PharmacologySignal TransductionBiochemistryNatural SciencesBiochemical Genetics	1980	226
Face–brain asymmetry in autism spectrum disorders Peter Hammond, Cynthia Forster‐Gibson, Albert E. Chudley, Molecular Psychiatry Brain DevelopmentDevelopmental Cognitive NeuroscienceFace–brain AsymmetrySyndromic AutismAutism	2008	113
Consensus guidelines for primary health care of adults with developmental disabilities. William F. Sullivan, John Heng, Donna Cameron, PubMed	2006	100
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders Xudong Liu, Natalia Novosedlik, Ami Wang, European Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologySyndromic AutismGenetic DisorderGenetics	2008	92
Autism severity is associated with child and maternal MAOA genotypes IL Cohen, X Liu, M. E. Suzanne Lewis, Clinical Genetics	2010	73
Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders Patrick Malenfant, Xudong Liu, Melissa L. Hudson, Journal of Autism and Developmental Disorders Autism Spectrum DisordersSyndromic AutismGenetic DisorderPsychiatric GeneticsPathology	2011	70
Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions Jill A. Rosenfeld, John A. Crolla, Susan Tomkins, American Journal of Medical Genetics Part A EngineeringCytogeneticsGeneticsCausative GenesMolecular Genetics	2010	62
Multilocus analysis of the fragile X syndrome W. Ted Brown, Amy C. Gross, Catherine B. Chan, Human Genetics Down SyndromeMendelian DisorderGenetic DisorderGeneticsFragile X Spectrum	1988	59
Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. Lois M. Mulligan, Mark Phillips, Cynthia Forster‐Gibson, PubMed	1985	51
2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders Xudong Liu, Patrick Malenfant, Chelsea Reesor, European Journal of Human Genetics Autism Spectrum DisordersSyndromic AutismGeneticsPathogenesisGenetic Disorder	2011	38

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