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Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28167-1
- By:
- Publication type:
- Article
Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33076-4
- By:
- Publication type:
- Article
Genetic architecture of band neutrophil fraction in Iceland.
- Published in:
- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03462-1
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- Publication type:
- Article
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02224-9
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- Publication type:
- Article
Comparing migraine with and without aura to healthy controls using RNA sequencing.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28167-1
- By:
- Publication type:
- Article
Functional dissection of inherited non-coding variation influencing multiple myeloma risk.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27666-x
- By:
- Publication type:
- Article
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Sequence variants affecting the genome-wide rate of germline microsatellite mutations.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39547-6
- By:
- Publication type:
- Article
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38951-2
- By:
- Publication type:
- Article
Genetic insight into sick sinus syndrome.
- Published in:
- European Heart Journal, 2021, v. 42, n. 20, p. 1959, doi. 10.1093/eurheartj/ehaa1108
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- Publication type:
- Article
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09860-0
- By:
- Publication type:
- Article
Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07460-y
- By:
- Publication type:
- Article
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06920-9
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- Publication type:
- Article
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-020-01575-z
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- Publication type:
- Article
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.
- Published in:
- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0921-5
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- Publication type:
- Article
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.
- Published in:
- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0857-9
- By:
- Publication type:
- Article
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 15789, doi. 10.1038/ncomms15789
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- Publication type:
- Article
A genome-wide association study yields five novel thyroid cancer risk loci.
- Published in:
- Nature Communications, 2017, v. 8, n. 2, p. 14517, doi. 10.1038/ncomms14517
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- Publication type:
- Article
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.
- Published in:
- Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
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- Publication type:
- Article
Thirty novel sequence variants impacting human intracranial volume.
- Published in:
- Brain Communications, 2022, v. 4, n. 6, p. 1, doi. 10.1093/braincomms/fcac271
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- Publication type:
- Article
Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Germline variants at SOHLH2 influence multiple myeloma risk.
- Published in:
- Blood Cancer Journal, 2021, v. 11, n. 4, p. 1, doi. 10.1038/s41408-021-00468-6
- By:
- Publication type:
- Article
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation.
- Published in:
- Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0068-9
- By:
- 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
- By:
- Publication type:
- Article
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-05079-4
- By:
- Publication type:
- Article
Deciphering the genetics and mechanisms of predisposition to multiple myeloma.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50932-7
- By:
- Publication type:
- Article
HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2.
- Published in:
- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03893-w
- By:
- Publication type:
- Article
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-14144-8
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- Publication type:
- Article