Summary statistics are available for download from the GWAS Catalog.
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease.
Duperron MG, et al.
Nat Med. 2023 Apr;29(4):950-962. doi: 10.1038/s41591-023-02268-w. Epub 2023 Apr 17.
PMID: 37069360
Summary statistics are available for download from the GWAS Catalog.
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease.
Duperron MG, et al.
Nat Med. 2023 Apr;29(4):950-962. doi: 10.1038/s41591-023-02268-w. Epub 2023 Apr 17.
PMID: 37069360
Summary statistics are available for download from the GWAS Catalog.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Debiec H, et al.
J Am Soc Nephrol. 2018 Jul;29(7):2000-2013. doi: 10.1681/ASN.2017111185. Epub 2018 Jun 14.
PMID: 29903748
Summary statistics are available for download from the GWAS Catalog.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Debiec H, et al.
J Am Soc Nephrol. 2018 Jul;29(7):2000-2013. doi: 10.1681/ASN.2017111185. Epub 2018 Jun 14.
PMID: 29903748
Summary statistics are available for download from the GWAS Catalog.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Debiec H, et al.
J Am Soc Nephrol. 2018 Jul;29(7):2000-2013. doi: 10.1681/ASN.2017111185. Epub 2018 Jun 14.
PMID: 29903748
Summary statistics are available for download from the GWAS Catalog.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Debiec H, et al.
J Am Soc Nephrol. 2018 Jul;29(7):2000-2013. doi: 10.1681/ASN.2017111185. Epub 2018 Jun 14.
PMID: 29903748
Summary statistics are available for download from the authors.
A whole-genome reference panel of 14,393 individuals for East Asian populations accelerates discovery of rare functional variants.
Choi J, et al.
Sci Adv. 2023 Aug 9;9(32):eadg6319. doi: 10.1126/sciadv.adg6319. Epub 2023 Aug 9.
PMID: 37556544
Summary statistics are available for download from the GWAS Catalog.
Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring.
Campos AI, et al.
Sleep. 2023 Mar 9;46(3):zsac308. doi: 10.1093/sleep/zsac308.
PMID: 36525587
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
Blauwendraat C, et al.
Mov Disord. 2019 Jun;34(6):866-875. doi: 10.1002/mds.27659. Epub 2019 Apr 7.
PMID: 30957308
Summary statistics are available for download from the authors.
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia.
Palmer DS, et al.
Nat Genet. 2022 May;54(5):541-547. doi: 10.1038/s41588-022-01034-x. Epub 2022 Apr 11.
PMID: 35410376