Literature DB >> 3904447

History and relevance of the Hutterite population for genetic studies.

J A Hostetler.   

Abstract

The social and cultural origins of the Hutterian Brethren, the most inbred population in North America, are described along with the characteristics that make the group useful for genetic studies. The Hutterites represent a closed population, with high levels of fertility and consanguinity. The group maintains a stable residence pattern and keeps extensive genealogic records. The uniform pattern of communal living, the existence of endogamous subgroups within the population, and an orderly design for colony fission facilitates comparisons rarely found in other accessible populations. This inbred population is useful for detecting new recessively inherited diseases, for advancing our knowledge of the effect of inbreeding, and for analyzing human chromosomal variation. Selected demographic and genetic studies are cited.

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Year:  1985        PMID: 3904447     DOI: 10.1002/ajmg.1320220303

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  19 in total

1.  CFTR mutations and reproductive outcomes in a population isolate.

Authors:  Irene Gallego Romero; Carole Ober
Journal:  Hum Genet       Date:  2007-09-28       Impact factor: 4.132

2.  Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes.

Authors:  Irene Pichler; Christian Fuchsberger; Christa Platzer; Minal Calişkan; Fabio Marroni; Peter P Pramstaller; Carole Ober
Journal:  Eur J Hum Genet       Date:  2009-10-21       Impact factor: 4.246

3.  Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification.

Authors:  Kym M Boycott; Shauna Flavelle; Alexandre Bureau; Hannah C Glass; T Mary Fujiwara; Elaine Wirrell; Krista Davey; Albert E Chudley; James N Scott; D Ross McLeod; Jillian S Parboosingh
Journal:  Am J Hum Genet       Date:  2005-07-22       Impact factor: 11.025

4.  Genetic analysis of HLA in the U.S. Schmiedenleut Hutterites.

Authors:  D D Kostyu; C L Ober; D V Dawson; M Ghanayem; S Elias; A O Martin
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

Review 5.  Linkage disequilibrium as a gene-mapping tool.

Authors:  L B Jorde
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

6.  Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.

Authors:  Nina Bögershausen; Nassim Shahrzad; Jessica X Chong; Jürgen-Christoph von Kleist-Retzow; Daniela Stanga; Yun Li; Francois P Bernier; Catrina M Loucks; Radu Wirth; Eric G Puffenberger; Robert A Hegele; Julia Schreml; Gabriel Lapointe; Katharina Keupp; Christopher L Brett; Rebecca Anderson; Andreas Hahn; A Micheil Innes; Oksana Suchowersky; Marilyn B Mets; Gudrun Nürnberg; D Ross McLeod; Holger Thiele; Darrel Waggoner; Janine Altmüller; Kym M Boycott; Benedikt Schoser; Peter Nürnberg; Carole Ober; Raoul Heller; Jillian S Parboosingh; Bernd Wollnik; Michael Sacher; Ryan E Lamont
Journal:  Am J Hum Genet       Date:  2013-07-03       Impact factor: 11.025

7.  Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition.

Authors:  K M Davey; J S Parboosingh; D R McLeod; A Chan; R Casey; P Ferreira; F F Snyder; P J Bridge; F P Bernier
Journal:  J Med Genet       Date:  2005-07-31       Impact factor: 6.318

8.  Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite population.

Authors:  J Zielenski; T M Fujiwara; D Markiewicz; A J Paradis; A I Anacleto; B Richards; R H Schwartz; K W Klinger; L C Tsui; K Morgan
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

9.  Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans.

Authors:  Emma E Thompson; Ying Sun; Dan Nicolae; Carole Ober
Journal:  Genet Epidemiol       Date:  2010-02       Impact factor: 2.135

10.  Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.

Authors:  Kym M Boycott; Chandree L Beaulieu; Kristin D Kernohan; Ola H Gebril; Aziz Mhanni; Albert E Chudley; David Redl; Wen Qin; Sarah Hampson; Sébastien Küry; Martine Tetreault; Erik G Puffenberger; James N Scott; Stéphane Bezieau; André Reis; Steffen Uebe; Johannes Schumacher; Robert A Hegele; D Ross McLeod; Marina Gálvez-Peralta; Jacek Majewski; Vincent T Ramaekers; Daniel W Nebert; A Micheil Innes; Jillian S Parboosingh; Rami Abou Jamra
Journal:  Am J Hum Genet       Date:  2015-12-03       Impact factor: 11.025

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