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Publications by Helgi Jónsson

Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3

American Journal of Human Genetics

English

Related publications

Matrilin-3 Mutations That Cause Chondrodysplasias Interfere With Protein Trafficking While a Mutation Associated With Hand Osteoarthritis Does Not

Journal of Medical Genetics

English

Spondylo-Epi-Metaphyseal Dysplasia (SEMD) Matrilin 3 Type: Homozygote Matrilin 3 Mutation in a Novel Form of SEMD

Journal of Medical Genetics

English

A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder

American Journal of Human Genetics

English

A Genomewide Linkage Scan for Quantitative-Trait Loci for Obesity Phenotypes

American Journal of Human Genetics

English

Genomewide Scan for Real-Word Reading Subphenotypes of Dyslexia: Novel Chromosome 13 Locus and Genetic Complexity

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics

Molecular Neuroscience

English

Spondyloepimetaphyseal Dysplasia, Matrilin-3 Type

English

Expanded Genomewide Scan Implicates a Novel Locus at 3q28 Among Caribbean Hispanics With Familial Alzheimer Disease

Archives of Neurology

English

New Guidelines for Hand Osteoarthritis

English

A Genomewide Scan for Attention-Deficit/Hyperactivity Disorder in an Extended Sample: Suggestive Linkage on 17p11

American Journal of Human Genetics

English