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Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.

author

Janna Saarela

1966 -

Seppo Meri

Aarno Palotie

Mark Joseph Daly

David A. Hafler

Leena Peltonen-Palotie

1952 - 2010

Philip L De Jager

Hanne F Harbo

published in: Human Molecular Genetics

date of publication: 2009-02-16

main subject: rare disease

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Mohsen Khademi, Janna Saarela, Ingrid Kockum, Hanne F Harbo, Elisabeth Gulowsen Celius, Tomas Olsson, Ellen Iacobaeus, Frida Lundmark Hedman, Annette B Oturai, Lars P. Ryder, Kristina Duvefelt
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Immunoglobulins and complement factor C4 in adult rhinosinusitis

Mikko Seppänen, Hanna Jarva, Seppo Meri
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Henrik Brønnum-Hansen
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Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis

Tommy Olsson
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Julian Maller, Mark Joseph Daly
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Evaluating whole genome amplification via multiply-primed rolling circle amplification for SNP genotyping of samples with low DNA yield.

Kari Kuulasmaa, Janna Saarela, Markus Perola, Veikko Salomaa, Leena Peltonen-Palotie, Kaisa Silander, Pekka Ellonen, Kati Komulainen, Mervi Alanne
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Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12

Janna Saarela, Eric M. Sobel, Leena Peltonen-Palotie
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Article - wd:Q37154268

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