Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis

David R Booth; Robert N Heard; Graeme J Stewart; Mathew Cox; Rodney J Scott; Jeannette Lechner-Scott; An Goris; Rita Dobosi; Bénédicte Dubois; Janna Saarela; Virpi Leppä; Leena Peltonen; Tuula Pirttila; Isabelle Cournu-Rebeix; Bertrand Fontaine; Laura Bergamaschi; Sandra D'Alfonso; Maurizio Leone; Aslaug R Lorentzen; Hanne F Harbo; Elisabeth G Celius; Anne Spurkland; Jenny Link; Ingrid Kockum; Tomas Olsson; Jan Hillert; Maria Ban; Amie Baker; Anu Kemppinen; Stephen Sawcer; Alastair Compston; Neil P Robertson; Philip L De Jager; David A Hafler; Lisa F Barcellos; Adrian J Ivinson; Jacob L McCauley; Margaret A Pericak-Vance; Jorge R Oksenberg; Stephen L Hauser; David Sexton; Jonathan Haines

doi:10.1038/ng0610-469

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Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis

Journal article

Open access

Peer reviewed

Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis

David R Booth, Robert N Heard, Graeme J Stewart, Mathew Cox, Rodney J Scott, Jeannette Lechner-Scott, An Goris, Rita Dobosi, Bénédicte Dubois, Janna Saarela, …

Nature genetics, Vol.42(6), pp.469-470

2010-06

DOI: https://doi.org/10.1038/ng0610-469

PMCID: PMC3109873

PMID: 20502484

Abstract

Genetic Variation

Kinesin - genetics

Multiple Sclerosis - genetics

Genetic Predisposition to Disease

Humans

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https://doi.org/10.1038/ng0610-469View

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.203 Neuromuscular Disorders; 1.203.147 Multiple Sclerosis
Web Of Science research areas: Genetics & Heredity
ESI research areas: Molecular Biology & Genetics

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Source: InCites

Details

Title: Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis
Creators: David R Booth
Robert N Heard
Graeme J Stewart
Mathew Cox
Rodney J Scott
Jeannette Lechner-Scott
An Goris
Rita Dobosi
Bénédicte Dubois
Janna Saarela
Virpi Leppä
Leena Peltonen
Tuula Pirttila
Isabelle Cournu-Rebeix
Bertrand Fontaine
Laura Bergamaschi
Sandra D'Alfonso
Maurizio Leone
Aslaug R Lorentzen
Hanne F Harbo
Elisabeth G Celius
Anne Spurkland
Jenny Link
Ingrid Kockum
Tomas Olsson
Jan Hillert
Maria Ban
Amie Baker
Anu Kemppinen
Stephen Sawcer
Alastair Compston
Neil P Robertson
Philip L De Jager
David A Hafler
Lisa F Barcellos
Adrian J Ivinson
Jacob L McCauley
Margaret A Pericak-Vance
Jorge R Oksenberg
Stephen L Hauser
David Sexton
Jonathan Haines
Publication Details: Nature genetics, Vol.42(6), pp.469-470
Publisher: United States
Grant note: R01 NS049477-01A1 / NINDS NIH HHS R01 NS049477 / NINDS NIH HHS
Academic Unit: Miller School of Medicine; John P. Hussman Institute for Human Genomics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
Language: English
Resource Type: Journal article
PMID: 20502484
PMCID: PMC3109873
Record Identifier: 991031559656102976