1
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A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.
|
Nat Genet
|
2010
|
8.48
|
2
|
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
|
Nat Genet
|
2012
|
4.13
|
3
|
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
|
Am J Hum Genet
|
2008
|
2.16
|
4
|
Meta-analysis of genome-wide studies of psoriasis susceptibility reveals linkage to chromosomes 6p21 and 4q28-q31 in Caucasian and Chinese Hans population.
|
J Invest Dermatol
|
2004
|
1.87
|
5
|
Stress and well-being among parents of children with rare diseases: a prospective intervention study.
|
J Adv Nurs
|
2006
|
1.41
|
6
|
Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patients.
|
Genet Test
|
2003
|
1.27
|
7
|
Identification of a psoriasis susceptibility candidate gene by linkage disequilibrium mapping with a localized single nucleotide polymorphism map.
|
Genomics
|
2002
|
1.12
|
8
|
Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms.
|
Am J Med Genet B Neuropsychiatr Genet
|
2008
|
1.04
|
9
|
Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families.
|
Exp Dermatol
|
2008
|
0.93
|
10
|
Effects on airways of short-term exposure to two kinds of wood smoke in a chamber study of healthy humans.
|
Inhal Toxicol
|
2012
|
0.92
|
11
|
Centrosomal localization of the psoriasis candidate gene product, CCHCR1, supports a role in cytoskeletal organization.
|
PLoS One
|
2012
|
0.91
|
12
|
Surfactant protein A and albumin in particles in exhaled air.
|
Respir Med
|
2011
|
0.90
|
13
|
Analysis of chromosome 5q31-32 and psoriasis: confirmation of a susceptibility locus but no association with SNPs within SLC22A4 and SLC22A5.
|
J Invest Dermatol
|
2006
|
0.88
|
14
|
Collecting a set of psoriasis family material through a patient organisation; clinical characterisation and presence of additional disorders.
|
BMC Dermatol
|
2005
|
0.83
|
15
|
Depression in Myotonic Dystrophy type 1: clinical and neuronal correlates.
|
Behav Brain Funct
|
2010
|
0.83
|
16
|
UBE2A deficiency syndrome: a report of two unrelated cases with large Xq24 deletions encompassing UBE2A gene.
|
Am J Med Genet A
|
2014
|
0.79
|
17
|
Analysis of 6 genetic loci for disease susceptibility in psoriatic arthritis.
|
J Rheumatol
|
2004
|
0.75
|