Literature DB >> 15464261

The tau H2 haplotype is almost exclusively Caucasian in origin.

Whitney Evans1, Hon Chung Fung, John Steele, Johanna Eerola, Pentti Tienari, Alan Pittman, Rohan de Silva, Amanda Myers, Fabienne Wavrant-De Vrieze, Andrew Singleton, John Hardy.   

Abstract

We have assessed the distribution of the tau H1/H2 haplotype in the publicly available reference series of samples with representatives of most racial groups. This analysis shows that the H2 haplotype is probably exclusively Caucasian in origin and its marginal occurrence in other racial groups is likely to reflect admixture. We discuss this observation in terms of the origin of the H2 haplotype and the epidemiology of the tauopathies.

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Year:  2004        PMID: 15464261     DOI: 10.1016/j.neulet.2004.05.119

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  37 in total

1.  Secondary RNA structure and nucleotide specificity contribute to internal initiation mediated by the human tau 5' leader.

Authors:  Bethany L Veo; Leslie A Krushel
Journal:  RNA Biol       Date:  2012-09-20       Impact factor: 4.652

Review 2.  Genetic risk factors in Parkinson's disease.

Authors:  K J Billingsley; S Bandres-Ciga; S Saez-Atienzar; A B Singleton
Journal:  Cell Tissue Res       Date:  2018-03-13       Impact factor: 5.249

3.  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

4.  The distribution and most recent common ancestor of the 17q21 inversion in humans.

Authors:  Michael P Donnelly; Peristera Paschou; Elena Grigorenko; David Gurwitz; Syed Qasim Mehdi; Sylvester L B Kajuna; Csaba Barta; Selemani Kungulilo; N J Karoma; Ru-Band Lu; Olga V Zhukova; Jong-Jin Kim; David Comas; Marcello Siniscalco; Maria New; Peining Li; Hui Li; Vangelis G Manolopoulos; William C Speed; Haseena Rajeevan; Andrew J Pakstis; Judith R Kidd; Kenneth K Kidd
Journal:  Am J Hum Genet       Date:  2010-01-28       Impact factor: 11.025

Review 5.  The genetics of Parkinson's disease: progress and therapeutic implications.

Authors:  Andrew B Singleton; Matthew J Farrer; Vincenzo Bonifati
Journal:  Mov Disord       Date:  2013-01       Impact factor: 10.338

6.  Frontotemporal dementia in eight Chinese individuals.

Authors:  Steven Z Chao; Howard J Rosen; Virgina Azor; Hilary Ong; Marian M Tse; Ngan Betty Lai; Craig E Hou; William W Seeley; Bruce L Miller; Brandy R Matthews
Journal:  Neurocase       Date:  2012-06-14       Impact factor: 0.881

7.  Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.

Authors:  Michael G Heckman; Alexis Elbaz; Alexandra I Soto-Ortolaza; Daniel J Serie; Jan O Aasly; Grazia Annesi; Georg Auburger; Justin A Bacon; Magdalena Boczarska-Jedynak; Maria Bozi; Laura Brighina; Marie-Christine Chartier-Harlin; Efthimios Dardiotis; Alain Destée; Carlo Ferrarese; Alessandro Ferraris; Brian Fiske; Suzana Gispert; Georgios M Hadjigeorgiou; Nobutaka Hattori; John P A Ioannidis; Barbara Jasinska-Myga; Beom S Jeon; Yun Joong Kim; Christine Klein; Rejko Kruger; Elli Kyratzi; Chin-Hsien Lin; Katja Lohmann; Marie-Anne Loriot; Timothy Lynch; George D Mellick; Eugénie Mutez; Grzegorz Opala; Sung Sup Park; Simona Petrucci; Aldo Quattrone; Manu Sharma; Peter A Silburn; Young Ho Sohn; Leonidas Stefanis; Vera Tadic; Hiroyuki Tomiyama; Ryan J Uitti; Enza Maria Valente; Demetrios K Vassilatis; Carles Vilariño-Güell; Linda R White; Karin Wirdefeldt; Zbigniew K Wszolek; Ruey-Meei Wu; Georgia Xiromerisiou; Demetrius M Maraganore; Matthew J Farrer; Owen A Ross
Journal:  Neurobiol Aging       Date:  2013-08-17       Impact factor: 4.673

Review 8.  Functional MAPT haplotypes: bridging the gap between genotype and neuropathology.

Authors:  Tara M Caffrey; Richard Wade-Martins
Journal:  Neurobiol Dis       Date:  2007-05-05       Impact factor: 5.996

9.  Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland.

Authors:  Anna-Lotta Kaivorinne; Johanna Krüger; Katja Kuivaniemi; Hannu Tuominen; Virpi Moilanen; Kari Majamaa; Anne M Remes
Journal:  BMC Neurol       Date:  2008-12-17       Impact factor: 2.474

10.  Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease.

Authors:  Nikolaos Refenes; Juliane Bolbrinker; Georgios Tagaris; Antonio Orlacchio; Nikolaos Drakoulis; Reinhold Kreutz
Journal:  BMC Neurol       Date:  2009-06-28       Impact factor: 2.474

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