about
Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear familyA mutation in APP protects against Alzheimer’s disease and age-related cognitive declineNew common variants affecting susceptibility to basal cell carcinomaNeuregulin 1 and susceptibility to schizophrenia.Hundreds of variants clustered in genomic loci and biological pathways affect human heightRate of de novo mutations and the importance of father's age to disease riskLarge recurrent microdeletions associated with schizophreniaNationwide study on hypertrophic cardiomyopathy in Iceland: evidence of a MYBPC3 founder mutationMutations in BRIP1 confer high risk of ovarian cancerGenetic determinants of hair, eye and skin pigmentation in EuropeansLarge-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairMany sequence variants affecting diversity of adult human heightGenome-wide association yields new sequence variants at seven loci that associate with measures of obesityNew sequence variants associated with bone mineral densityA rare variant in MYH6 is associated with high risk of sick sinus syndromeSequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionEuropean bone mineral density loci are also associated with BMD in East-Asian populationsGermline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinomaAssociation of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseasesDiscovery of common variants associated with low TSH levels and thyroid cancer riskSequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityCommon sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancerGenome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumptionA high-resolution recombination map of the human genomeGenetics of gene expression and its effect on diseaseA common inversion under selection in EuropeansA common variant on chromosome 9p21 affects the risk of myocardial infarctionAllegro, a new computer program for multipoint linkage analysisA common biological basis of obesity and nicotine addiction15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.Variants conferring risk of atrial fibrillation on chromosome 4q25.ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.Addictions and their familiality in Iceland.Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies.Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) geneAncestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.Loss-of-function mutations in SLC30A8 protect against type 2 diabetesSequence variant at 4q25 near PITX2 associates with appendicitis.Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
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description
hulumtues
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onderzoeker
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researcher
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հետազոտող
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name
Daniel F Gudbjartsson
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Daniel F Gudbjartsson
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Daniel F Gudbjartsson
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Daniel F Gudbjartsson
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Daniel Gudbjartsson
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type
label
Daniel F Gudbjartsson
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Daniel F Gudbjartsson
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Daniel F Gudbjartsson
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Daniel F Gudbjartsson
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Daniel Gudbjartsson
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Daniel Gudbjartsson
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Gudbjartsson DF
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Daniel F Gudbjartsson
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Daniel F Gudbjartsson
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Daniel F Gudbjartsson
@nl
Daniel F Gudbjartsson
@sl
Daniel Gudbjartsson
@fr
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P244
P106
P108
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0000 0000 4091 1766
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no2001050652
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0000-0002-5222-9857
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P7859
lccn-no2001050652