| 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 | 534 | 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 | 312 | 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 | 240 | 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 | 195 | 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 | 191 | 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 | 176 | 2010 |
| A newly discovered founder population: the Roma/Gypsies L Kalaydjieva, B Morar, R Chaix, H Tang Bioessays 27 (10), 1084-1094, 2005 | 132 | 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 | 106 | 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 | 104 | 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 | 103 | 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 | 83 | 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 | 80 | 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 | 79 | 2002 |
| Deleterious GRM1 mutations in schizophrenia MA Ayoub, D Angelicheva, D Vile, D Chandler, B Morar, JA Cavanaugh, ... PLoS One 7 (3), e32849, 2012 | 74 | 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 | 66 | 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 | 59 | 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 | 59 | 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 | 55 | 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 | 51 | 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 | 48 | 2003 |
