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Familial Risk of Lung Carcinoma in the Icelandic Population.
- Published in:
- JAMA: Journal of the American Medical Association, 2004, v. 292, n. 24, p. 2977, doi. 10.1001/jama.292.24.2977
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- Article
Rare mutations associating with serum creatinine and chronic kidney disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 25, p. 6935, doi. 10.1093/hmg/ddu399
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- Publication type:
- Article
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
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- Human Molecular Genetics, 2014, v. 23, n. 11, p. 3045, doi. 10.1093/hmg/ddt671
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- Article
Rare mutations associating with serum creatinine and chronic kidney disease.
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- Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu399
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- Publication type:
- Article
Sequence variants at CYP1A1–CYP1A2 and AHR associate with coffee consumption.
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- Human Molecular Genetics, 2011, v. 20, n. 10, p. 2071, doi. 10.1093/hmg/ddr086
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- Article
Reproductive fitness and genetic risk of psychiatric disorders in the general population.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/ncomms15833
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- Article
A genome-wide association study yields five novel thyroid cancer risk loci.
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- Nature Communications, 2017, v. 8, n. 2, p. 14517, doi. 10.1038/ncomms14517
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- Publication type:
- Article
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma.
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- Nature Communications, 2016, v. 7, n. 7, p. 12050, doi. 10.1038/ncomms12050
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- Article
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.
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- Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
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- Article
Common and rare variants associated with kidney stones and biochemical traits.
- Published in:
- Nature Communications, 2015, v. 6, n. 8, p. 7975, doi. 10.1038/ncomms8975
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- Article
A common variant at 8q24.21 is associated with renal cell cancer.
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- Nature Communications, 2013, v. 4, n. 11, p. 2776, doi. 10.1038/ncomms3776
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- Article
Comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics".
- Published in:
- Science Translational Medicine, 2021, v. 13, n. 622, p. 1, doi. 10.1126/scitranslmed.abe8497
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- Article
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA.
- Published in:
- 2017
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- Case Study
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.
- Published in:
- 2017
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- Publication type:
- Case Study
Rate of de novo mutations and the importance of father's age to disease risk.
- Published in:
- Nature, 2012, v. 488, n. 7412, p. 471, doi. 10.1038/nature11396
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- Article
Fine-scale recombination rate differences between sexes, populations and individuals.
- Published in:
- Nature, 2010, v. 467, n. 7319, p. 1099, doi. 10.1038/nature09525
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- Article
Variants conferring risk of atrial fibrillation on chromosome 4q25.
- Published in:
- Nature, 2007, v. 448, n. 7151, p. 353, doi. 10.1038/nature06007
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- Publication type:
- Article
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin.
- Published in:
- Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0053-3
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- Publication type:
- Article
Predicting the presence of coronary plaques featuring high-risk characteristics using polygenic risk scores and targeted proteomics in patients with suspected coronary artery disease.
- Published in:
- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01313-8
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- Article
A sequence variant on 17q21 is associated with age at onset and severity of asthma.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 8, p. 902, doi. 10.1038/ejhg.2010.38
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- Publication type:
- Article
Inheritance of human longevity in Iceland.
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- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 743, doi. 10.1038/sj.ejhg.5200527
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- Publication type:
- Article
Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis.
- Published in:
- British Journal of Cancer, 2023, v. 129, n. 7, p. 1142, doi. 10.1038/s41416-023-02374-z
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- Publication type:
- Article
Loss-of-function variants in ATM confer risk of gastric cancer.
- Published in:
- Nature Genetics, 2015, v. 47, n. 8, p. 906, doi. 10.1038/ng.3342
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- Article
Identification of a large set of rare complete human knockouts.
- Published in:
- Nature Genetics, 2015, v. 47, n. 5, p. 448, doi. 10.1038/ng.3243
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- Publication type:
- Article
Large-scale whole-genome sequencing of the Icelandic population.
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- Nature Genetics, 2015, v. 47, n. 5, p. 435, doi. 10.1038/ng.3247
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- Publication type:
- Article
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
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- Nature Genetics, 2014, v. 46, n. 8, p. 826, doi. 10.1038/ng.3014
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- Publication type:
- Article
Common and low-frequency variants associated with genome-wide recombination rate.
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- Nature Genetics, 2014, v. 46, n. 1, p. 11, doi. 10.1038/ng.2833
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- Publication type:
- Article
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.
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- Nature Genetics, 2013, v. 45, n. 11, p. 1371, doi. 10.1038/ng.2740
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- Publication type:
- Article
A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.
- Published in:
- Nature Genetics, 2012, v. 44, n. 12, p. 1326, doi. 10.1038/ng.2437
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- Publication type:
- Article
Discovery of common variants associated with low TSH levels and thyroid cancer risk.
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- Nature Genetics, 2012, v. 44, n. 3, p. 319, doi. 10.1038/ng.1046
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- Publication type:
- Article
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.
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- Nature Genetics, 2012, v. 44, n. 3, p. 260, doi. 10.1038/ng.1051
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- Publication type:
- Article
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.
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- Nature Genetics, 2011, v. 43, n. 11, p. 1098, doi. 10.1038/ng.926
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- Publication type:
- Article
Identification of low-frequency variants associated with gout and serum uric acid levels.
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- Nature Genetics, 2011, v. 43, n. 11, p. 1127, doi. 10.1038/ng.972
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- Publication type:
- Article
Mutations in BRIP1 confer high risk of ovarian cancer.
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- Nature Genetics, 2011, v. 43, n. 11, p. 1104, doi. 10.1038/ng.955
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- Publication type:
- Article
A rare variant in MYH6 is associated with high risk of sick sinus syndrome.
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- Nature Genetics, 2011, v. 43, n. 4, p. 316, doi. 10.1038/ng.781
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- Publication type:
- Article
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
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- Nature Genetics, 2010, v. 42, n. 12, p. 1077, doi. 10.1038/ng.714
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- Article
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.
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- Nature Genetics, 2010, v. 42, n. 5, p. 415, doi. 10.1038/ng.558
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- Publication type:
- Article
Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior.
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- Nature Genetics, 2010, v. 42, n. 5, p. 448, doi. 10.1038/ng.573
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- Article
Several common variants modulate heart rate, PR interval and QRS duration.
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- Nature Genetics, 2010, v. 42, n. 2, p. 117, doi. 10.1038/ng.511
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- Publication type:
- Article
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.
- Published in:
- Nature Genetics, 2009, v. 41, n. 10, p. 1122, doi. 10.1038/ng.448
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- Article
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
- Published in:
- Nature Genetics, 2009, v. 41, n. 8, p. 876, doi. 10.1038/ng.417
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- Article
New common variants affecting susceptibility to basal cell carcinoma.
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- Nature Genetics, 2009, v. 41, n. 8, p. 909, doi. 10.1038/ng.412
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- Article
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.
- Published in:
- Nature Genetics, 2009, v. 41, n. 8, p. 926, doi. 10.1038/ng.404
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- Publication type:
- Article
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.
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- Nature Genetics, 2009, v. 41, n. 6, p. 734, doi. 10.1038/ng.383
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- Article
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
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- Nature Genetics, 2009, v. 41, n. 4, p. 460, doi. 10.1038/ng.339
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- Article
New sequence variants associated with bone mineral density.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 15, doi. 10.1038/ng.284
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- Publication type:
- Article
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 18, doi. 10.1038/ng.274
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- Publication type:
- Article
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.
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- Nature Genetics, 2008, v. 40, n. 11, p. 1313, doi. 10.1038/ng.234
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- Publication type:
- Article
Detection of sharing by descent, long-range phasing and haplotype imputation.
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- Nature Genetics, 2008, v. 40, n. 9, p. 1068, doi. 10.1038/ng.216
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- Article
Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
- Published in:
- 2008
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- Publication type:
- Correction notice