Found: 27
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High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-53634-2
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- Publication type:
- Article
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-022-32936-3
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- Publication type:
- Article
Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-022-33626-w
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- Publication type:
- Article
Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32885-x
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- Publication type:
- Article
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 9, p. e129, doi. 10.1111/epi.13076
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- Publication type:
- Article
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Saccular Intracranial Aneurysms in Children When Both Parents Are Sporadic or Familial Carriers of Saccular Intracranial Aneurysms.
- Published in:
- Neuroepidemiology, 2019, v. 52, n. 1/2, p. 47, doi. 10.1159/000493856
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- Publication type:
- Article
Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer.
- Published in:
- 2021
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- Publication type:
- Correction Notice
The impact of non-additive genetic associations on age-related complex diseases.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21952-4
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- Publication type:
- Article
Diabetes is associated with familial idiopathic normal pressure hydrocephalus: a case–control comparison with family members.
- Published in:
- Fluids & Barriers of the CNS, 2020, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12987-020-00217-0
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- Publication type:
- Article
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.pgen.1007329
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- Publication type:
- Article
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11954-8
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- Publication type:
- Article
Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08262-y
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- Publication type:
- Article
TAFFEL: Independent Enrichment Analysis of gene sets.
- Published in:
- BMC Bioinformatics, 2011, v. 12, n. 1, p. 171, doi. 10.1186/1471-2105-12-171
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- Publication type:
- Article
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.
- Published in:
- JAMA Ophthalmology, 2023, v. 141, n. 2, p. 449, doi. 10.1001/jamaophthalmol.2023.0706
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- Publication type:
- Article
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.
- Published in:
- Nature Communications, 2016, v. 7, n. 9, p. 12869, doi. 10.1038/ncomms12869
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- Publication type:
- Article
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.
- Published in:
- Nature Communications, 2016, v. 7, n. 8, p. 12342, doi. 10.1038/ncomms12342
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- Publication type:
- Article
Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease.
- Published in:
- Frontiers in Neuroscience, 2023, p. 01, doi. 10.3389/fnins.2023.1123327
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- Publication type:
- Article
Increased Incidence of Aneurysmal Subarachnoid Hemorrhage on Sundays and Mondays in 1,862 Patients from Eastern Finland.
- Published in:
- Neuroepidemiology, 2011, v. 37, n. 3/4, p. 203, doi. 10.1159/000332055
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- Publication type:
- Article
High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 1, p. 1, doi. 10.1371/journal.pgen.1004134
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- Publication type:
- Article
Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 3, p. 1, doi. 10.1371/journal.pgen.1002563
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- Publication type:
- Article
LAVAA: a lightweight association viewer across ailments.
- Published in:
- Bioinformatics Advances, 2023, v. 3, n. 1, p. 1, doi. 10.1093/bioadv/vbad018
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- Publication type:
- Article
Secondary hypertension in patients with saccular intracranial aneurysm disease: A population based study.
- Published in:
- PLoS ONE, 2018, v. 13, n. 10, p. 1, doi. 10.1371/journal.pone.0206432
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- Publication type:
- Article
Type 2 Diabetes and Risk of Rupture of Saccular Intracranial Aneurysm in Eastern Finland.
- Published in:
- Diabetes Care, 2013, v. 36, n. 7, p. 2020, doi. 10.2337/dc12-1048
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- Publication type:
- Article
Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-022-04285-w
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- Publication type:
- Article
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-17718-z
- By:
- Publication type:
- Article
Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes.
- Published in:
- 2022
- By:
- Publication type:
- journal article