Sharmila Banerjee‐Basu

Author

National Human Genome Research Institute ORCID

Also Known As

Banerjee-Basu, Sharmila, S Banerjee-Basu, S. Banerjee-Basu, S. Banerjee‐Basu, Sharmila Banerjee-Basu, Sharmila Banerjee‐Basu

Publications

3.9K

Citations

H-Index

Concepts

All Affiliations

National Human Genome Research Institute National Institutes of Health MindSpec Ben-Gurion University of the Negev Johns Hopkins University

About

Sharmila Banerjee‐Basu is an author at National Human Genome Research Institute specializing in medicine, genetics, and systems biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	19	2.4K
2	Natural Sciences	5	5	247
3	Engineering	3	3	421
4	Public Health	2	2	473
5	Social Sciences	2	2	312

Sharmila Banerjee‐Basu

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs) Brett S. Abrahams, Dan E. Arking, Heather C. Mefford, Molecular Autism	2013	895
AutDB: a gene reference resource for autism research Saumyendra N. Basu, Ravi Kollu, Sharmila Banerjee‐Basu Nucleic Acids Research Autism Spectrum DisordersGeneticsGenetic EpidemiologyDisease Gene IdentificationBioinformatics Database	2008	417
SFARI Gene: an evolving database for the autism research community Sharmila Banerjee‐Basu, Alan Packer Disease Models & Mechanisms Autism Research InitiativeFunctional GenomicsDevelopmental BiologyPsychiatryEngineering	2010	357
MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability Steven M. Lipkin, Victoria Wang, Russell F. Jacoby, Nature Genetics Genome InstabilityGenetic DisorderGeneticsMolecular GeneticsMammalian Microsatellite Instability	2000	327
Genes related to sex steroids, neural growth, and social–emotional behavior are associated with autistic traits, empathy, and Asperger syndrome Bhismadev Chakrabarti, Frank Dudbridge, Lindsey Kent, Autism Research Brain DevelopmentGeneticsAffective NeuroscienceNeuroendocrinologyPsychology	2009	291
Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome Deborah L. Stone, Anne Slavotinek, Gerard G. Bouffard, Nature Genetics Genetic DisorderPutative ChaperoninGeneticsPathogenesisProtein Genetics	2000	201
Molecular evolution of the homeodomain family of transcription factors Sharmila Banerjee‐Basu Nucleic Acids Research GeneticsMolecular GeneticsGenomicsPhylogenetic AnalysisHomeodomain Family	2001	182
Chicken homeobox gene prox 1 related toDrosophila prospero is expressed in the developing lens and retina Stanislav I. Tomarev, Olof Sundin, Sharmila Banerjee‐Basu, Developmental Dynamics	1996	140
Loss-of-Function Mutations in Growth Differentiation Factor-1 (GDF1) Are Associated with Congenital Heart Defects in Humans Jayaprakash D. Karkera, J.S. Lee, Erich Roessler, The American Journal of Human Genetics Heart FailureDevelopmental BiologyCardiac ReprogrammingGeneticsLoss-of-function Mutations	2007	137
Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1 Ramsey A. Saleem, Sharmila Banerjee‐Basu, Fred B. Berry, The American Journal of Human Genetics GeneticsMolecular BiologyGenetic MechanismMolecular GeneticsDisease Gene Identification	2001	119

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