Literature DB >> 12080390

Linkage disequilibrium and demographic history of the isolated population of the Faroe Islands.

Tove H Jorgensen1, Birte Degn, August G Wang, Maria Vang, Hugh Gurling, Gursharan Kalsi, Andrew McQuillin, Torben A Kruse, Ole Mors, Henrik Ewald.   

Abstract

The isolated population of the Faroe Islands has a history of recent expansion after being limited to a small size for centuries. Such an isolated population may be ideal for linkage disequilibrium mapping of disease genes if linkage disequilibrium (LD) extends over large regions. Analyses of 18 markers on 12q24.3, spanning a region of 4.3 Mb (16 cM), revealed extensive LD in the Faroese population. Maximum LD was found between marker pairs separated by more than 3.8 Mb. The same region had a maximum LD of only 1.2 and 1.4 Mb respectively in two outbred Danish and British populations analysed here for comparison. The analyses of gene diversity excess at 15 unlinked microsatellite markers did not reveal any sign of a severe bottleneck to have occurred within approximately 1200 years' history of the Faroese population. The extensive LD in this population may, therefore, have arisen primarily by random genetic drift. The implications for future gene mapping studies are discussed.

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Year:  2002        PMID: 12080390     DOI: 10.1038/sj.ejhg.5200816

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  9 in total

1.  The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers.

Authors:  Tove H Jorgensen; Henriette N Buttenschön; August G Wang; Thomas D Als; Anders D Børglum; Henrik Ewald
Journal:  Hum Genet       Date:  2004-04-09       Impact factor: 4.132

2.  A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene.

Authors:  Noomi Gregersen; Hans A Dahl; Henriette N Buttenschøn; Mette Nyegaard; Anne Hedemand; Thomas D Als; August G Wang; Sofus Joensen; David Pd Woldbye; Pernille Koefoed; Ann S Kristensen; Torben A Kruse; Anders D Børglum; Ole Mors
Journal:  Eur J Hum Genet       Date:  2011-08-03       Impact factor: 4.246

3.  Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands.

Authors:  Jan Rasmussen; Olav W Nielsen; Nils Janzen; Morten Duno; Hannes Gislason; Lars Køber; Ulrike Steuerwald; Allan M Lund
Journal:  J Inherit Metab Dis       Date:  2013-05-08       Impact factor: 4.982

4.  Primary Carnitine Deficiency: Is Foetal Development Affected and Can Newborn Screening Be Improved?

Authors:  Jan Rasmussen; David M Hougaard; Noreen Sandhu; Katrine Fjællegaard; Poula R Petersen; Ulrike Steuerwald; Allan M Lund
Journal:  JIMD Rep       Date:  2017-01-20

5.  Is L-Carnitine Supplementation Beneficial in 3-Methylcrotonyl-CoA Carboxylase Deficiency?

Authors:  Jákup Andreas Thomsen; Allan Meldgaard Lund; Jess Have Olesen; Magni Mohr; Jan Rasmussen
Journal:  JIMD Rep       Date:  2015-03-03

6.  Performance of Expanded Newborn Screening in Norway Supported by Post-Analytical Bioinformatics Tools and Rapid Second-Tier DNA Analyses.

Authors:  Trine Tangeraas; Ingjerd Sæves; Claus Klingenberg; Jens Jørgensen; Erle Kristensen; Gunnþórunn Gunnarsdottir; Eirik Vangsøy Hansen; Janne Strand; Emma Lundman; Sacha Ferdinandusse; Cathrin Lytomt Salvador; Berit Woldseth; Yngve T Bliksrud; Carlos Sagredo; Øyvind E Olsen; Mona C Berge; Anette Kjoshagen Trømborg; Anders Ziegler; Jin Hui Zhang; Linda Karlsen Sørgjerd; Mari Ytre-Arne; Silje Hogner; Siv M Løvoll; Mette R Kløvstad Olavsen; Dionne Navarrete; Hege J Gaup; Rina Lilje; Rolf H Zetterström; Asbjørg Stray-Pedersen; Terje Rootwelt; Piero Rinaldo; Alexander D Rowe; Rolf D Pettersen
Journal:  Int J Neonatal Screen       Date:  2020-06-27

7.  Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy.

Authors:  E Ostergaard; M Batbayli; M Duno; K Vilhelmsen; T Rosenberg
Journal:  J Med Genet       Date:  2010-08-30       Impact factor: 6.318

8.  Theory of the effects of population structure and sampling on patterns of linkage disequilibrium applied to genomic data from humans.

Authors:  John Wakeley; Sabin Lessard
Journal:  Genetics       Date:  2003-07       Impact factor: 4.562

9.  Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder.

Authors:  F Lescai; T D Als; Q Li; M Nyegaard; G Andorsdottir; M Biskopstø; A Hedemand; A Fiorentino; N O'Brien; A Jarram; J Liang; J Grove; J Pallesen; E Eickhardt; M Mattheisen; L Bolund; D Demontis; A G Wang; A McQuillin; O Mors; J Wang; A D Børglum
Journal:  Transl Psychiatry       Date:  2017-02-14       Impact factor: 6.222

  9 in total

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