Bharti Morar - Concepedia

Author

Bharti Morar

Harry Perkins Institute of Medical Research ORCID

Also Known As

B Morar, B. Morar, Bharti Morar, Bharti Morar (176448), V Pans

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Harry Perkins Institute of Medical Research The University of Western Australia Medical University of Sofia University of the Witwatersrand New Bulgarian University

About

Bharti Morar is an author at Harry Perkins Institute of Medical Research specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	18	1.6K
2	Language Studies	2	2	46
3	Education	1	1	206
4	Health Sciences	1	1	21
5	Natural Sciences	1	1	66

Bharti Morar

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time Lev A. Zhivotovsky, Peter A. Underhill, Cengiz Cinnioğlu, The American Journal of Human Genetics Linkage DisequilibriumMolecular EcologyEffective Mutation RateMedicineGenetics	2004	397
Origins and Divergence of the Roma (Gypsies) David Gresham, Bharti Morar, Peter A. Underhill, The American Journal of Human Genetics EthnicityEthnohistoryEducationAnthropologyCultural History	2001	206
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus Kenneth K. Kídd, Bharti Morar, Carmela M. Castiglione, Human Genetics Haplotype DeterminationLinkage DisequilibriumGenotype-phenotype AssociationMolecular EcologyDrd2 Locus	1998	203
Mutation History of the Roma/Gypsies Bharti Morar, David Gresham, Dora Angelicheva, The American Journal of Human Genetics MedicineGeneticsEvolutionary BiologyHuman OriginGenetic Variation	2004	165
Psychosis Susceptibility Gene ZNF804A and Cognitive Performance in Schizophrenia James Walters, Aiden Corvin, Michael J. Owen, Archives of General Psychiatry	2010	147
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome Raymonda Varon, Rebecca Gooding, Christina Steglich, Nature Genetics Partial DeficiencyOcular DiseaseOphthalmologyRna Polymerase IiGenetic Disorder	2003	142
A newly discovered founder population: the Roma/Gypsies Luba Kalaydjieva, Bharti Morar, Raphaëlle Chaix, BioEssays	2005	123
Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans Camille Humbert, Flora Silbermann, Bharti Morar, The American Journal of Human Genetics Integrin Alpha 8UrologyDevelopmental BiologyRenal FunctionMedicine	2014	100
Autosomal-Recessive Congenital Cerebellar Ataxia Is Caused by Mutations in Metabotropic Glutamate Receptor 1 Velina Guergueltcheva, Dimitar N. Azmanov, Dora Angelicheva, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsDegenerative DiseaseNeuroscience	2012	98
KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment Osvaldo P. Almeida, S.G. Schwab, Nicola T. Lautenschlager, Journal of Cellular and Molecular Medicine	2008	94

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