about
Rate of de novo mutations and the importance of father's age to disease riskLarge recurrent microdeletions associated with schizophreniaMutations in BRIP1 confer high risk of ovarian cancerGenome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysmVariants conferring risk of atrial fibrillation on chromosome 4q25.Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.A sequence variant on 17q21 is associated with age at onset and severity of asthma.Identification of a large set of rare complete human knockouts.Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumptionRare mutations associating with serum creatinine and chronic kidney disease.Common variants near CAV1 and CAV2 are associated with primary open-angle glaucomaMulti-nucleotide de novo Mutations in Humans.A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.Parental origin of sequence variants associated with complex diseasesHLA class II sequence variants influence tuberculosis risk in populations of European ancestry.The rate of meiotic gene conversion varies by sex and age.
P50
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P50
description
onderzoeker
@nl
name
Adalbjorg Jonasdottir
@ast
Adalbjorg Jonasdottir
@en
Adalbjorg Jonasdottir
@es
type
label
Adalbjorg Jonasdottir
@ast
Adalbjorg Jonasdottir
@en
Adalbjorg Jonasdottir
@es
prefLabel
Adalbjorg Jonasdottir
@ast
Adalbjorg Jonasdottir
@en
Adalbjorg Jonasdottir
@es
P106
P21
P214
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