about
Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear familySix novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesA mutation in APP protects against Alzheimer’s disease and age-related cognitive declineNew common variants affecting susceptibility to basal cell carcinomaRate of de novo mutations and the importance of father's age to disease riskA genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaMutations 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 obesityA rare variant in MYH6 is associated with high risk of sick sinus syndromeSequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionAssociation 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 aneurysmA 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.A variant in FTO shows association with melanoma risk not due to BMIThe BARD1 Cys557Ser variant and breast cancer risk in IcelandVariants conferring risk of atrial fibrillation on chromosome 4q25.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.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.Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.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 studiesMeta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Patrick Sulem
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Patrick Sulem
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Patrick Sulem
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Patrick Sulem
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Patrick Sulem
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type
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Patrick Sulem
@ast
Patrick Sulem
@en
Patrick Sulem
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Patrick Sulem
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Patrick Sulem
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prefLabel
Patrick Sulem
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Patrick Sulem
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Patrick Sulem
@es
Patrick Sulem
@nl
Patrick Sulem
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P106
P1960
7SUBeRMAAAAJ
P21
P31
P569
2000-01-01T00:00:00Z