about
New common variants affecting susceptibility to basal cell carcinomaReplication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer ConsortiumA genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaThe Icelandic founder mutation BRCA2 999del5: analysis of expressionFlt3/Flk-2-ligand in synergy with thrombopoietin delays megakaryocyte development and increases the numbers of megakaryocyte progenitor cells in serum-free cultures initiated with CD34+ cellsMutations in BRIP1 confer high risk of ovarian cancerGenetic determinants of hair, eye and skin pigmentation in EuropeansMany sequence variants affecting diversity of adult human heightGene expression analysis of hematopoietic progenitor cells identifies Dlg7 as a potential stem cell geneGenome-wide association yields new sequence variants at seven loci that associate with measures of obesityA rare variant in MYH6 is associated with high risk of sick sinus syndromeAssociation of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer--a finding from Texas lung cancer genome-wide association studyCross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic AssociationsGermline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinomaA multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lociAssociation of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseasesRare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancerDiscovery 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 study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysmInfluence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controlsA genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.Common variants at 19p13 are associated with susceptibility to ovarian cancer.ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies.Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.A method for detecting long non-coding RNAs with tiled RNA expression microarrays.Sequence variant at 4q25 near PITX2 associates with appendicitis.Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studiesHypothetical and factual willingness to participate in biobank researchLarge-scale whole-genome sequencing of the Icelandic population.Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.Male-pattern baldness susceptibility locus at 20p11.Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma.
P50
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P50
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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Thorunn Rafnar
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P106
P21
P214
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P31
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