Literature DB >> 16163730

A newly discovered founder population: the Roma/Gypsies.

Luba Kalaydjieva1, Bharti Morar, Raphaelle Chaix, Hua Tang.   

Abstract

The Gypsies (a misnomer, derived from an early legend about Egyptian origins) defy the conventional definition of a population: they have no nation-state, speak different languages, belong to many religions and comprise a mosaic of socially and culturally divergent groups separated by strict rules of endogamy. Referred to as "the invisible minority", the Gypsies have for centuries been ignored by Western medicine, and their genetic heritage has only recently attracted attention. Common origins from a small group of ancestors characterise the 8-10 million European Gypsies as an unusual trans-national founder population, whose exodus from India played the role of a profound demographic bottleneck. Social and economic pressures within Europe led to gradual fragmentation, generating multiple genetically differentiated subisolates. The string of population bottlenecks and founder effects have shaped a unique genetic profile, whose potential for genetic research can be met only by study designs that acknowledge cultural tradition and self-identity. (c) 2005 Wiley Periodicals, Inc.

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Year:  2005        PMID: 16163730     DOI: 10.1002/bies.20287

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  27 in total

1.  Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.

Authors:  Dana Gabrikova; Martin Mistrik; Jarmila Bernasovska; Alexandra Bozikova; Regina Behulova; Iveta Tothova; Sona Macekova
Journal:  J Appl Genet       Date:  2013-08-31       Impact factor: 3.240

2.  ANO10 c.1150_1151del is a founder mutation causing autosomal recessive cerebellar ataxia in Roma/Gypsies.

Authors:  Teodora Chamova; Laura Florez; Velina Guergueltcheva; Margarita Raycheva; Radka Kaneva; Hanns Lochmüller; Luba Kalaydjieva; Ivailo Tournev
Journal:  J Neurol       Date:  2011-10-19       Impact factor: 4.849

3.  Carrier rates of four single-gene disorders in Croatian Bayash Roma.

Authors:  Ana Barešić; Marijana Peričić Salihović
Journal:  Genet Test Mol Biomarkers       Date:  2013-11-04

4.  A Roma founder BIN1 mutation causes a novel phenotype of centronuclear myopathy with rigid spine.

Authors:  Macarena Cabrera-Serrano; Fabiola Mavillard; Valerie Biancalana; Eloy Rivas; Bharti Morar; Aurelio Hernández-Laín; Montse Olive; Nuria Muelas; Eduardo Khan; Alejandra Carvajal; Pablo Quiroga; Jordi Diaz-Manera; Mark Davis; Rainiero Ávila; Cristina Domínguez; Norma Beatriz Romero; Juan J Vílchez; David Comas; Nigel G Laing; Jocelyn Laporte; Luba Kalaydjieva; Carmen Paradas
Journal:  Neurology       Date:  2018-06-27       Impact factor: 9.910

5.  A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q.

Authors:  Kunka Kamenarova; Sylvia Cherninkova; Margarita Romero Durán; DeQuincy Prescott; Maria Lourdes Valdés Sánchez; Vanio Mitev; Ivo Kremensky; Radka Kaneva; Shomi S Bhattacharya; Ivailo Tournev; Christina Chakarova
Journal:  Eur J Hum Genet       Date:  2012-08-29       Impact factor: 4.246

Review 6.  High prevalence of CYP2C19*2 allele in Roma samples: study on Roma and Hungarian population samples with review of the literature.

Authors:  Csilla Sipeky; Agnes Weber; Melinda Szabo; Bela I Melegh; Ingrid Janicsek; Greta Tarlos; Istvan Szabo; Katalin Sumegi; Bela Melegh
Journal:  Mol Biol Rep       Date:  2013-05-05       Impact factor: 2.316

7.  Tau haplotypes support the Asian ancestry of the Roma population settled in the Basque Country.

Authors:  Miguel A Alfonso-Sánchez; Ibone Espinosa; Luis Gómez-Pérez; Alaitz Poveda; Esther Rebato; Jose A Peña
Journal:  Heredity (Edinb)       Date:  2017-12-11       Impact factor: 3.821

8.  Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.

Authors:  Lenka Slachtova; Ondrej Seda; Jana Behunova; Martin Mistrik; Pavel Martasek
Journal:  Eur J Hum Genet       Date:  2015-09-09       Impact factor: 4.246

9.  Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.

Authors:  Velina Guergueltcheva; Dimitar N Azmanov; Dora Angelicheva; Katherine R Smith; Teodora Chamova; Laura Florez; Michael Bynevelt; Thai Nguyen; Sylvia Cherninkova; Veneta Bojinova; Ara Kaprelyan; Lyudmila Angelova; Bharti Morar; David Chandler; Radka Kaneva; Melanie Bahlo; Ivailo Tournev; Luba Kalaydjieva
Journal:  Am J Hum Genet       Date:  2012-08-16       Impact factor: 11.025

10.  A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR).

Authors:  Janina Hantke; David Chandler; Rosalind King; Ronald J A Wanders; Dora Angelicheva; Ivailo Tournev; Elyshia McNamara; Marcel Kwa; Velina Guergueltcheva; Radka Kaneva; Frank Baas; Luba Kalaydjieva
Journal:  Eur J Hum Genet       Date:  2009-06-17       Impact factor: 4.246

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