Rita M. Cantor - Concepedia

Author

Rita M. Cantor

Also Known As

Bene, Judit, Bevra H. Hahn, Cantor, Rita M, Cook, Edwin H., Dragan M Svrakic, Elisabeth B Binder, Hu, Xinli, Mazziotta, John C., Murphy, Kieran C., N B Freimer

166

Publications

38.4K

Citations

H-Index

146

Concepts

All Affiliations

University of California, Los Angeles Icahn School of Medicine at Mount Sinai University of California, San Francisco Stanford University Center for Autism and Related Disorders

About

Rita M. Cantor is an author at University of California, Los Angeles specializing in medicine, genetics, and autism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Arts	1	1	54
2	Education	1	1	68
3	Engineering	1	1	1.5K
4	Health Sciences	1	1	103
5	Humanities	1	1	68

Rita M. Cantor

Publications

23.2K

Citations

H-Index

Page 1

	Year	Citations
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Transcriptomic analysis of autistic brain reveals convergent molecular pathology Irina Voineagu, Xinchen Wang, Patrick G. Johnston, Nature Molecular NeuroscienceSyndromic AutismAutismSocial SciencesNeuroscience	2011	1.9K
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci Stephan Sanders, Xin He, A. Jeremy Willsey, Neuron Genome-wide Association StudySyndromic AutismGeneticsRisk LociMolecular Biology	2015	1.5K
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores Bjarni J. Vilhjálmsson, Jian Yang, Hilary K. Finucane, The American Journal of Human Genetics Linkage DisequilibriumEngineeringPolygenic RiskRisk ManagementPolygenic Risk Scores	2015	1.5K
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Neuron Neurodevelopmental DisordersWilliams Syndrome RegionSyndromic AutismGenetic DisorderGenetics	2011	1.3K
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects Christian R. Marshall, Daniel P. Howrigan, Daniele Merico, Nature Genetics PsychiatryGeneticsPsychiatric GeneticsGenetic EpidemiologyCopy Number Variants	2016	1.1K
Common genetic variants on 5p14.1 associate with autism spectrum disorders Kai Wang, Haitao Zhang, Deqiong Ma, Nature Neurodevelopmental DisordersSyndromic AutismGenetic DisorderGeneticsPsychiatric Genetics	2009	968
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene Maricela Alarcón, Brett S. Abrahams, Jennifer Stone, The American Journal of Human Genetics Autism-susceptibility GeneSyndromic AutismNatural SciencesGeneticsPsychiatric Genetics	2008	819
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes Douglas M. Ruderfer, Stephan Ripke, Andrew McQuillin, Cell PsychiatryPsychotic DisorderGeneticsSchizophreniaSocial Sciences	2018	797

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