Literature DB >> 11704928

Origins and divergence of the Roma (gypsies).

D Gresham1, B Morar, P A Underhill, G Passarino, A A Lin, C Wise, D Angelicheva, F Calafell, P J Oefner, P Shen, I Tournev, R de Pablo, V Kuĉinskas, A Perez-Lezaun, E Marushiakova, V Popov, L Kalaydjieva.   

Abstract

The identification of a growing number of novel Mendelian disorders and private mutations in the Roma (Gypsies) points to their unique genetic heritage. Linguistic evidence suggests that they are of diverse Indian origins. Their social structure within Europe resembles that of the jatis of India, where the endogamous group, often defined by profession, is the primary unit. Genetic studies have reported dramatic differences in the frequencies of mutations and neutral polymorphisms in different Romani populations. However, these studies have not resolved ambiguities regarding the origins and relatedness of Romani populations. In this study, we examine the genetic structure of 14 well-defined Romani populations. Y-chromosome and mtDNA markers of different mutability were analyzed in a total of 275 individuals. Asian Y-chromosome haplogroup VI-68, defined by a mutation at the M82 locus, was present in all 14 populations and accounted for 44.8% of Romani Y chromosomes. Asian mtDNA-haplogroup M was also identified in all Romani populations and accounted for 26.5% of female lineages in the sample. Limited diversity within these two haplogroups, measured by the variation at eight short-tandem-repeat loci for the Y chromosome, and sequencing of the HVS1 for the mtDNA are consistent with a small group of founders splitting from a single ethnic population in the Indian subcontinent. Principal-components analysis and analysis of molecular variance indicate that genetic structure in extant endogamous Romani populations has been shaped by genetic drift and differential admixture and correlates with the migrational history of the Roma in Europe. By contrast, social organization and professional group divisions appear to be the product of a more recent restitution of the caste system of India.

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Year:  2001        PMID: 11704928      PMCID: PMC1235543          DOI: 10.1086/324681

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  44 in total

1.  Hypervariable sites in the mtDNA control region are mutational hotspots.

Authors:  M Stoneking
Journal:  Am J Hum Genet       Date:  2000-08-30       Impact factor: 11.025

2.  N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.

Authors:  L Kalaydjieva; D Gresham; R Gooding; L Heather; F Baas; R de Jonge; K Blechschmidt; D Angelicheva; D Chandler; P Worsley; A Rosenthal; R H King; P K Thomas
Journal:  Am J Hum Genet       Date:  2000-05-30       Impact factor: 11.025

3.  From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and Turks.

Authors:  F Calafell; P Underhill; A Tolun; D Angelicheva; L Kalaydjieva
Journal:  Ann Hum Genet       Date:  1996-01       Impact factor: 1.670

4.  Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24.

Authors:  L Kalaydjieva; J Hallmayer; D Chandler; A Savov; A Nikolova; D Angelicheva; R H King; B Ishpekova; K Honeyman; F Calafell; A Shmarov; J Petrova; I Turnev; A Hristova; M Moskov; S Stancheva; I Petkova; A H Bittles; V Georgieva; L Middleton; P K Thomas
Journal:  Nat Genet       Date:  1996-10       Impact factor: 38.330

5.  Evaluation of Y-chromosomal STRs: a multicenter study.

Authors:  M Kayser; A Caglià; D Corach; N Fretwell; C Gehrig; G Graziosi; F Heidorn; S Herrmann; B Herzog; M Hidding; K Honda; M Jobling; M Krawczak; K Leim; S Meuser; E Meyer; W Oesterreich; A Pandya; W Parson; G Penacino; A Perez-Lezaun; A Piccinini; M Prinz; C Schmitt; L Roewer
Journal:  Int J Legal Med       Date:  1997       Impact factor: 2.686

6.  A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.

Authors:  A Abicht; R Stucka; V Karcagi; A Herczegfalvi; R Horváth; W Mortier; U Schara; V Ramaekers; W Jost; J Brunner; G Janssen; U Seidel; B Schlotter; W Müller-Felber; D Pongratz; R Rüdel; H Lochmüller
Journal:  Neurology       Date:  1999-10-22       Impact factor: 9.910

7.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

8.  Peripheral nerve abnormalities in the congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome.

Authors:  I Tournev; R H King; J Workman; M Nourallah; J R Muddle; L Kalaydjieva; K Romanski; P K Thomas
Journal:  Acta Neuropathol       Date:  1999-08       Impact factor: 17.088

9.  Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees.

Authors:  E Heyer; J Puymirat; P Dieltjes; E Bakker; P de Knijff
Journal:  Hum Mol Genet       Date:  1997-05       Impact factor: 6.150

10.  A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies).

Authors:  L Kalaydjieva; A Perez-Lezaun; D Angelicheva; S Onengut; D Dye; N U Bosshard; A Jordanova; A Savov; P Yanakiev; I Kremensky; B Radeva; J Hallmayer; A Markov; V Nedkova; I Tournev; L Aneva; R Gitzelmann
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

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  59 in total

1.  SNPSTRs: empirically derived, rapidly typed, autosomal haplotypes for inference of population history and mutational processes.

Authors:  Joanna L Mountain; Alec Knight; Matthew Jobin; Christopher Gignoux; Adam Miller; Alice A Lin; Peter A Underhill
Journal:  Genome Res       Date:  2002-11       Impact factor: 9.043

2.  No evidence of association between 118A>G OPRM1 polymorphism and heroin dependence in a large Bulgarian case-control sample.

Authors:  Momchil A Nikolov; Olga Beltcheva; Antoaneta Galabova; Anna Ljubenova; Elena Jankova; Galin Gergov; Atanas A Russev; Michael T Lynskey; Elliot C Nelson; Eleonora Nesheva; Dorita Krasteva; Philip Lazarov; Vanio I Mitev; Ivo M Kremensky; Radka P Kaneva; Alexandre A Todorov
Journal:  Drug Alcohol Depend       Date:  2011-01-31       Impact factor: 4.492

3.  The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time.

Authors:  Lev A 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; Marcus W Feldman; Luba Kalaydjieva
Journal:  Am J Hum Genet       Date:  2003-12-19       Impact factor: 11.025

4.  Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal data.

Authors:  Stephen Wooding; Christopher Ostler; B V Ravi Prasad; W Scott Watkins; Sandy Sung; Mike Bamshad; Lynn B Jorde
Journal:  Hum Genet       Date:  2004-07-01       Impact factor: 4.132

5.  Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans.

Authors:  Bo Wen; Xuanhua Xie; Song Gao; Hui Li; Hong Shi; Xiufeng Song; Tingzhi Qian; Chunjie Xiao; Jianzhong Jin; Bing Su; Daru Lu; Ranajit Chakraborty; Li Jin
Journal:  Am J Hum Genet       Date:  2004-03-24       Impact factor: 11.025

6.  On the Etruscan mitochondrial DNA contribution to modern humans.

Authors:  Boris A Malyarchuk; Igor B Rogozin
Journal:  Am J Hum Genet       Date:  2004-11       Impact factor: 11.025

Review 7.  Prospects for admixture mapping of complex traits.

Authors:  Paul M McKeigue
Journal:  Am J Hum Genet       Date:  2004-11-11       Impact factor: 11.025

Review 8.  The impact of recent events on human genetic diversity.

Authors:  Mark A Jobling
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2012-03-19       Impact factor: 6.237

9.  Y-STR variation in Albanian populations: implications on the match probabilities and the genetic legacy of the minority claiming an Egyptian descent.

Authors:  Gianmarco Ferri; Sergio Tofanelli; Milena Alù; Luca Taglioli; Erjon Radheshi; Beatrice Corradini; Giorgio Paoli; Cristian Capelli; Giovanni Beduschi
Journal:  Int J Legal Med       Date:  2010-03-18       Impact factor: 2.686

10.  Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans.

Authors:  Camille Humbert; Flora Silbermann; Bharti Morar; Mélanie Parisot; Mohammed Zarhrate; Cécile Masson; Frédéric Tores; Patricia Blanchet; Marie-José Perez; Yuliya Petrov; Philippe Khau Van Kien; Joelle Roume; Brigitte Leroy; Olivier Gribouval; Luba Kalaydjieva; Laurence Heidet; Rémi Salomon; Corinne Antignac; Alexandre Benmerah; Sophie Saunier; Cécile Jeanpierre
Journal:  Am J Hum Genet       Date:  2014-01-16       Impact factor: 11.025

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