List of works - Adalbjorg Jonasdottir

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma

scientific article

A sequence variant on 17q21 is associated with age at onset and severity of asthma

scientific article

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

scientific article published on 28 October 2012

Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

scientific article published on 3 February 2016

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

scientific article

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

scientific article published on 12 September 2010

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

scientific journal article

HLA class II sequence variants influence tuberculosis risk in populations of European ancestry

scientific article published on February 2016

Identification of a large set of rare complete human knockouts

scientific article

Large recurrent microdeletions associated with schizophrenia

scientific article

Multi-nucleotide de novo Mutations in Humans

scientific article

Mutations in BRIP1 confer high risk of ovarian cancer

scientific article

Parental origin of sequence variants associated with complex diseases

scientific article published on December 2009

Rare mutations associating with serum creatinine and chronic kidney disease

scientific article

Rate of de novo mutations and the importance of father's age to disease risk

scientific article

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

scientific article

The rate of meiotic gene conversion varies by sex and age.

scientific article published on 19 September 2016

Variants conferring risk of atrial fibrillation on chromosome 4q25.

scientific article

List of works by Adalbjorg Jonasdottir

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma

A sequence variant on 17q21 is associated with age at onset and severity of asthma

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

HLA class II sequence variants influence tuberculosis risk in populations of European ancestry

Identification of a large set of rare complete human knockouts

Large recurrent microdeletions associated with schizophrenia

Multi-nucleotide de novo Mutations in Humans

Mutations in BRIP1 confer high risk of ovarian cancer

Parental origin of sequence variants associated with complex diseases

Rare mutations associating with serum creatinine and chronic kidney disease

Rate of de novo mutations and the importance of father's age to disease risk

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption

The rate of meiotic gene conversion varies by sex and age.

Variants conferring risk of atrial fibrillation on chromosome 4q25.