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Bharti Morar

Research Profile

Living Beings

Gypsies

Phenomena

Founder Effect

Physiology

Genes & Molecular Sequences

Anatomy

Chromosomes, Human, Y

Disorders

Occupations

Genetics, Population

Concepts & Ideas

Procedures

Chemicals & Drugs

Receptors, Metabotropic Glutamate

Activities & Behaviors

Schizophrenic Psychology

Co-author Network

Publications

TOP 3
Assen Jablensky; S MacGregor; A McRae; Bharti Morar; D W Morris; M Phillips; Oliver Rackham; Kim Rasmussen; A Usheva; P L Verbrugghe; C S Weickert; Boian Alexandrov; Osvaldo P Almeida; Dora Angelicheva; D N Azmanov; Johanna Badcock; A R Bishop; E Bramon-Bosch; Kim Carter; David Chandler; M Cooper; Aiden Corvin; Mark Nicholas Cruickshank; Gary Donohoe; Milan Dragovic; Aleksandra Filipovska; Leon Flicker; M Gill; Luba Kalaydjieva
Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.
Velina Guergueltcheva; RAdka Kaneva; Ara Kaprelyan; Bharti Morar; Thai Nguyen; Katherine R Smith; Ivailo Tournev; Dora Angelicheva; Lyudmila Angelova; Dimitar N Azmanov; Melanie Bahlo; Veneta Bojinova; Michael Bynevelt; Teodora Chamova; David Chandler; Sylvia Cherninkova; Laura Florez; Luba Kalaydjieva
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.
Phebe Verbrugghe; Steven Wiltshire; Grant Montgomery; Bharti Morar; Muhammad F M Razif; Osvaldo P Almeida; Johanna Badcock; Sonja Bouwer; Vaughan Carr; Kim Carter; David Chandler; Matthew Cooper; Milan Dragovic; Leon Flicker; Anjali K Henders; Assen Jablensky; Luba Kalaydjieva
Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia.

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All Publications

2012: Assen Jablensky; S MacGregor; A McRae; Bharti Morar; D W Morris; M Phillips; Oliver Rackham; Kim Rasmussen; A Usheva; P L Verbrugghe; C S Weickert; Boian Alexandrov; Osvaldo P Almeida; Dora Angelicheva; D N Azmanov; Johanna Badcock; A R Bishop; E Bramon-Bosch; Kim Carter; David Chandler; M Cooper; Aiden Corvin; Mark Nicholas Cruickshank; Gary Donohoe; Milan Dragovic; Aleksandra Filipovska; Leon Flicker; M Gill; Luba Kalaydjieva
Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.
Molecular psychiatry 2012;17(12):1328-39.
2012: Velina Guergueltcheva; RAdka Kaneva; Ara Kaprelyan; Bharti Morar; Thai Nguyen; Katherine R Smith; Ivailo Tournev; Dora Angelicheva; Lyudmila Angelova; Dimitar N Azmanov; Melanie Bahlo; Veneta Bojinova; Michael Bynevelt; Teodora Chamova; David Chandler; Sylvia Cherninkova; Laura Florez; Luba Kalaydjieva
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.
American journal of human genetics 2012;91(3):553-64.
2012: Phebe Verbrugghe; Steven Wiltshire; Grant Montgomery; Bharti Morar; Muhammad F M Razif; Osvaldo P Almeida; Johanna Badcock; Sonja Bouwer; Vaughan Carr; Kim Carter; David Chandler; Matthew Cooper; Milan Dragovic; Leon Flicker; Anjali K Henders; Assen Jablensky; Luba Kalaydjieva
Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012;159B(4):392-404.
2012: Mohammed Akli Ayoub; Juleen A Cavanaugh; David Chandler; Assen Jablensky; Bharti Morar; Kevin D G Pfleger; David Vile; Peter M Visscher; Dora Angelicheva; Luba Kalaydjieva
Deleterious GRM1 mutations in schizophrenia.
PloS one 2012;7(3):e32849.
2011: Bharti Morar; Melania Radionova; Ingrid E Scheffer; Ivailo Tournev; Sashka Zhelyazkova; Dora Angelicheva; Dimitar N Azmanov; Velina Guergueltcheva; Luba Kalaydjieva; RAdka Kaneva; Josemir W. Sander
A novel GEFS+ locus on 12p13.33 in a large Roma family.
Epilepsy research 2011;97(1-2):198-207.
2011: Dimitar N Azmanov; Luba Kalaydjieva; RAdka Kaneva; Bharti Morar; Melania Radionova; Ivailo Tournev; Sashka Zhelyazkova; Dora Zlatareva; Dora Angelicheva; Josemir W. Sander
Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3.
Epilepsy research 2011;96(1-2):101-8.
2011: Bharti Morar; Flavie A V Waters; David Chandler; M Dragović; Luba Kalaydjieva; Assen Jablensky
Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition.
Molecular psychiatry 2011;16(8):860-6.
2011: Assen Jablensky; Bharti Morar; K Peters; S Wiltshire; Johanna Badcock; Kim Carter; David Chandler; Milan Dragovic; Luba Kalaydjieva
Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia.
Genes, brain, and behavior 2011;10(4):410-7.
2011: Dimitar N Azmanov; Stanislava Dimitrova; Laura Florez; Sylvia Cherninkova; Dragomir Draganov; Bharti Morar; Rosmawati Saat; Manel Juan; Juan I Arostegui; Sriparna Ganguly; Himla Soodyall; Subhabrata Chakrabarti; Harish Padh; Miguel A López-Nevot; Violeta Chernodrinska; Botio Anguelov; Partha Majumder; Lyudmila Angelova; RAdka Kaneva; David A Mackey; Ivailo Tournev; Luba Kalaydjieva
LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population.
European journal of human genetics : EJHG 2011;19(3):326-33.
2009: Dora Angelicheva; Ivailo Tournev; Velina Guergueltcheva; Violeta Mihaylova; Dimitar N Azmanov; Bharti Morar; Melania Radionova; Shelagh J Smith; Dora Zlatareva; John M Stevens; RAdka Kaneva; Veneta Bojinova; Kim Carter; Matthew Brown; Assen Jablensky; Luba Kalaydjieva; Josemir W Sander
Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32.
Epilepsia 2009;50(7):1679-88.
2007: Bharti Morar; Sibylle G Schwab; Margot Albus; Wolfgang Maier; Bernard Lerer; Dieter B Wildenauer
Evaluation of association of SNPs in the TNF alpha gene region with schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(3):318-24.
2005: Luba Kalaydjieva; Bharti Morar; Raphaëlle Chaix; Hua Tang
A newly discovered founder population: the Roma/Gypsies.
BioEssays : news and reviews in molecular, cellular and developmental biology 2005;27(10):1084-94.
2004: Bharti Morar; David Gresham; Dora Angelicheva; Ivailo Tournev; Rebecca Gooding; Velina Guergueltcheva; Carolin Schmidt; Angela Abicht; Hanns Lochmuller; Attila Tordai; Lajos Kalmár; Melinda Nagy; Veronika Karcagi; Marc Jeanpierre; Agnes Herczegfalvi; David Beeson; Viswanathan Venkataraman; Kim Warwick Carter; Jeff Reeve; Rosario de Pablo; Vaidutis Kucinskas; Luba Kalaydjieva
Mutation history of the roma/gypsies.
American journal of human genetics 2004;75(4):596-609.
2004: Raphaëlle Chaix; Frédéric Austerlitz; Bharti Morar; Luba Kalaydjieva; Evelyne Heyer
Vlax Roma history: what do coalescent-based methods tell us?
European journal of human genetics : EJHG 2004;12(4):285-92.
2004: Lev Zhivotovsky; Peter A Underhill; Cengiz Cinnioğlu; Manfred Kayser; Bharti Morar; Toomas Kivisild; Rosaria Scozzari; Fulvio Cruciani; Giovanni Destro-Bisol; Gabriella Spedini; Geoffrey K Chambers; Rene J Herrera; Kiau Kiun Yong; David Gresham; Ivailo Tournev; marcel salathe; Luba Kalaydjieva
The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time.
American journal of human genetics 2004;74(1):50-61.
2003: Raymonda Varon; Rebecca Gooding; Christina Steglich; Lorna Marns; Hua Tang; Dora Angelicheva; Kiau Kiun Yong; Petra Ambrugger; Anke Reinhold; Bharti Morar; Frank Baas; Marcel Kwa; Ivailo Tournev; Velina Guerguelcheva; Ivo Kremensky; Hanns Lochmüller; Andrea Müllner-Eidenböck; Luciano Merlini; Luitgard Neumann; Joachim Bürger; Maggie Walter; Kathryn Swoboda; PK Thomas; Arpad von Moers; Neil Risch; Luba Kalaydjieva
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome.
Nature genetics 2003;35(2):185-9.
2003: Himla Soodyall; Almut Nebel; Bharti Morar; Trefor Jenkins
Genealogy and genes: tracing the founding fathers of Tristan da Cunha.
European journal of human genetics : EJHG 2003;11(9):705-9.
2003: Michael Hunter; Rafaëlle Bernard; Elizabeth M Freitas; Amandine Boyer; Bharti Morar; Ian J Martins; Ivailo Tournev; Albena Jordanova; Velina Guergelcheva; Boryana Ishpekova; Ivo Kremensky; Garth Nicholson; Beate Schlotter; Hanns Lochmüller; Thomas Voit; Jaume Colomer; PK Thomas; Nicolas Levy; Luba Kalaydjieva
Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease.
Human mutation 2003;22(2):129-35.
2003: Cheryl A Wise; Maxime Paris; Bharti Morar; Wei Wang; Luba Kalaydjieva; Alan H Bittles
A standard protocol for single nucleotide primer extension in the human genome using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
Rapid communications in mass spectrometry : RCM 2003;17(11):1195-202.
2002: A B Lane; Himla Soodyall; S Arndt; M E Ratshikhopha; E Jonker; C Freeman; L Young; Bharti Morar; L Toffie
Genetic substructure in South African Bantu-speakers: evidence from autosomal DNA and Y-chromosome studies.
American journal of physical anthropology 2002;119(2):175-85.
2002: Brigitte Pakendorf; Bharti Morar; Larissa A Tarskaia; Manfred Kayser; Himla Soodyall; Alexander Rodewald; Mark Stoneking
Y-chromosomal evidence for a strong reduction in male population size of Yakuts.
Human genetics 2002;110(2):198-200.
2001: David Gresham; Bharti Morar; Peter A Underhill; Giuseppe Passarino; Alice A Lin; Cheryl A Wise; Dora Angelicheva; Francesc Calafell; Peter J Oefner; P Shen; Ivailo Tournev; Rosario de Pablo; V Kuĉinskas; Anna Perez-Lezaun; E Marushiakova; V Popov; Luba Kalaydjieva
Origins and divergence of the Roma (gypsies).
American journal of human genetics 2001;69(6):1314-31.
1998: Kenneth K Kidd; Bharti Morar; CM Castiglione; H Zhao; Andrew J Pakstis; William C Speed; Batsheva Bonne-Tamir; Ru-Band Lu; David Goldman; C Lee; Y S Nam; David K Grandy; T Jenkins; Judith R Kidd
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus.
Human genetics 1998;103(2):211-27.