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Irritable bowel syndrome 2018 GWAS: European ancestry

  • Read more about Irritable bowel syndrome 2018 GWAS: European ancestry

Summary statistics are available for download from the GWAS Catalog.

Publications

Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome.
Bonfiglio F, et al.
Gastroenterology. 2018 Jul;155(1):168-179. doi: 10.1053/j.gastro.2018.03.064.
PMID: 29626450

Amyotrophic lateral sclerosis 2018 GWAS: European ancestry

  • Read more about Amyotrophic lateral sclerosis 2018 GWAS: European ancestry

Summary statistics are available for download from the GWAS Catalog.

Publications

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Nicolas A, et al.
Neuron. 2018 Mar 21;97(6):1268-1283.e6. doi: 10.1016/j.neuron.2018.02.027.
PMID: 29566793

SUGAR-MGH 2023 sulfonylurea and metformin response GWAS: trans-ancestry

  • Read more about SUGAR-MGH 2023 sulfonylurea and metformin response GWAS: trans-ancestry

Download summary statistics | README | Additional information

Varicose veins 2023 GWAS: European ancestry

  • Read more about Varicose veins 2023 GWAS: European ancestry

Summary statistics are available for download from the GWAS Catalog.

Publications

Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.
Helkkula P, et al.
Commun Biol. 2023 Jan 18;6(1):71. doi: 10.1038/s42003-022-04285-w.
PMID: 36653477

Polycystic ovary syndrome 2018 GWAS: European ancestry

  • Read more about Polycystic ovary syndrome 2018 GWAS: European ancestry

Summary statistics are available for download from the GWAS Catalog.

Publications

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
Day F, et al.
PLoS Genet. 2018 Dec 19;14(12):e1007813.
PMID: 30566500

Primary open-angle glaucoma 2018 GWAS: trans-ancestry

  • Read more about Primary open-angle glaucoma 2018 GWAS: trans-ancestry

Summary statistics are available for download from the GWAS Catalog.

Publications

A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.
Choquet H, et al.
Nat Commun. 2018 Jun 11;9(1):2278. doi: 10.1038/s41467-018-04555-4.
PMID: 29891935

Intrahepatic cholestasis of pregnancy 2022 GWAS: European ancestry

  • Read more about Intrahepatic cholestasis of pregnancy 2022 GWAS: European ancestry

Summary statistics are available for download from the GWAS Catalog.

Publications

GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements.
Dixon PH, Levine AP, Cebola I, et al.
Nat Commun. 2022 Aug 17;13(1):4840. doi: 10.1038/s41467-022-29931-z.
PMID: 35977952

SiGN and ISGC 2016 stroke GWAS: African ancestry

  • Read more about SiGN and ISGC 2016 stroke GWAS: African ancestry

Download summary statistics

Publications

Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
NINDS Stroke Genetics Network (SiGN); International Stroke Genetics Consortium (ISGC).
Lancet Neurol. 2016 Feb;15(2):174-184. doi: 10.1016/S1474-4422(15)00338-5.
PMID: 26708676

SiGN and ISGC 2016 stroke GWAS: Hispanic ancestry

  • Read more about SiGN and ISGC 2016 stroke GWAS: Hispanic ancestry

Download summary statistics

Publications

Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
NINDS Stroke Genetics Network (SiGN); International Stroke Genetics Consortium (ISGC).
Lancet Neurol. 2016 Feb;15(2):174-184. doi: 10.1016/S1474-4422(15)00338-5.
PMID: 26708676

SiGN and ISGC 2016 stroke GWAS: European ancestry

  • Read more about SiGN and ISGC 2016 stroke GWAS: European ancestry

Download summary statistics

Publications

Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
NINDS Stroke Genetics Network (SiGN); International Stroke Genetics Consortium (ISGC).
Lancet Neurol. 2016 Feb;15(2):174-184. doi: 10.1016/S1474-4422(15)00338-5.
PMID: 26708676

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