Bharti Morar
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The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time
LA Zhivotovsky, PA Underhill, C Cinnioğlu, M Kayser, B Morar, T Kivisild, ...
The American Journal of Human Genetics 74 (1), 50-61, 2004
Origins and divergence of the Roma (gypsies)
D Gresham, B Morar, PA Underhill, G Passarino, AA Lin, C Wise, ...
The American Journal of Human Genetics 69 (6), 1314-1331, 2001
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus
KK Kidd, B Morar, CM Castiglione, H Zhao, AJ Pakstis, WC Speed, ...
Human genetics 103, 211-227, 1998
Mutation history of the roma/gypsies
B Morar, D Gresham, D Angelicheva, I Tournev, R Gooding, ...
The American Journal of Human Genetics 75 (4), 596-609, 2004
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome
R Varon, R Gooding, C Steglich, L Marns, H Tang, D Angelicheva, ...
Nature genetics 35 (2), 185-189, 2003
Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia
JTR Walters, A Corvin, MJ Owen, H Williams, M Dragovic, EM Quinn, ...
Archives of general psychiatry 67 (7), 692-700, 2010
A newly discovered founder population: the Roma/Gypsies
L Kalaydjieva, B Morar, R Chaix, H Tang
Bioessays 27 (10), 1084-1094, 2005
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1
V Guergueltcheva, DN Azmanov, D Angelicheva, KR Smith, T Chamova, ...
The American Journal of Human Genetics 91 (3), 553-564, 2012
KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment
OP Almeida, SG Schwab, NT Lautenschlager, B Morar, KR Greenop, ...
Journal of cellular and molecular medicine 12 (5a), 1672-1676, 2008
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans
C Humbert, F Silbermann, B Morar, M Parisot, M Zarhrate, C Masson, ...
The American Journal of Human Genetics 94 (2), 288-294, 2014
Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition
B Morar, M Dragović, FAV Waters, D Chandler, L Kalaydjieva, ...
Molecular psychiatry 16 (8), 860-866, 2011
LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population
DN Azmanov, S Dimitrova, L Florez, S Cherninkova, D Draganov, B Morar, ...
European journal of human genetics 19 (3), 326-333, 2011
Genetic substructure in South African Bantu‐speakers: evidence from autosomal DNA and Y‐chromosome studies
AB Lane, H Soodyall, S Arndt, ME Ratshikhopha, E Jonker, C Freeman, ...
American Journal of Physical Anthropology: The Official Publication of the …, 2002
Deleterious GRM1 mutations in schizophrenia
MA Ayoub, D Angelicheva, D Vile, D Chandler, B Morar, JA Cavanaugh, ...
PLoS One 7 (3), e32849, 2012
Mutation screening of the N‐myc downstream‐regulated gene 1 (NDRG1) in patients with Charcot‐Marie‐Tooth Disease
M Hunter, R Bernard, E Freitas, A Boyer, B Morar, IJ Martins, I Tournev, ...
Human mutation 22 (2), 129-135, 2003
Transcriptome-wide effects of a POLR3A gene mutation in patients with an unusual phenotype of striatal involvement
DN Azmanov, SJ Siira, T Chamova, A Kaprelyan, V Guergueltcheva, ...
Human molecular genetics 25 (19), 4302-4314, 2016
Y-chromosomal evidence for a strong reduction in male population size of Yakuts
B Pakendorf, B Morar, LA Tarskaia, M Kayser, H Soodyall, A Rodewald, ...
Human genetics 110, 198-200, 2002
Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia
A Jablensky, B Morar, S Wiltshire, K Carter, M Dragovic, JC Badcock, ...
Genes, brain and behavior 10 (4), 410-417, 2011
UFM1 founder mutation in the Roma population causes recessive variant of H-ABC
EMC Hamilton, E Bertini, L Kalaydjieva, B Morar, D Dojčáková, J Liu, ...
Neurology 89 (17), 1821-1828, 2017
A standard protocol for single nucleotide primer extension in the human genome using matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry
CA Wise, M Paris, B Morar, W Wang, L Kalaydjieva, AH Bittles
Rapid Communications in Mass Spectrometry 17 (11), 1195-1202, 2003
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