![]() Online ahead of print.PMID: 36747475Ĭausal relationships between migraine and microstructural white matter: a Mendelian randomization study. Genetic variants associated with syncope implicate neural and autonomic processes.Įur Heart J. Schlaikjær Hartwig T, Ambye L, Gruhn JR, Petersen JF, Wrønding T, et al. eCollection 2023.PMID: 36926036 Free PMC article.Ĭell-free fetal DNA for genetic evaluation in Copenhagen Pregnancy Loss Study (COPL): a prospective cohort study. Online ahead of print.PMID: 36931692įour missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.įront Endocrinol (Lausanne). ![]() Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect.Īnn Rheum Dis. Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.Īnn Rheum Dis. Preprint.PMID: 37034649 Free PMC article. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Epub 2023 Apr 3.PMID: 37012456 Free PMC article.Ĭartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank Resource.Īrthritis Rheumatol. Genetic effects on the timing of parturition and links to fetal birth weight. Online ahead of print.PMID: 37210288ĭanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals.īMC Genom Data. Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights.Įur Urol. doi: 10.1093/eurheartj/ehad142.PMID: 37038246 Free PMC article.ĭeep integrative models for large-scale human genomics. PMID: 37326842ĭyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. Genome-wide investigation of persistence to treatment with methotrexate in early rheumatoid arthritis. Migraine, chronic kidney disease and kidney function: observational and genetic analyses. PMID: 37334623ĭeficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. ![]() ![]() Multi-polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives.Īm J Med Genet B Neuropsychiatr Genet. Sequence variants affecting the genome-wide rate of germline microsatellite mutations. Sequence variants affecting voice pitch in humans. PMID: 37414856 Free PMC article.Ĭluster headache genome-wide association study and meta-analysis identifies eight loci and implicates smoking as causal risk factor.Īnn Neurol. Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study.Ĭommun Med (Lond). Polygenic risk prediction: why and when out-of-sample prediction R 2 can exceed SNP-based heritability. PMID: 37449562 Free article.ĭepression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland. PMID: 37430141 Free PMC article.īone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.Ĭommun Biol. Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.Ĭommun Biol. International Headache Genetics Consortium. PMID: 37414752 Free PMC article.Ī causal effects of gut microbiota in the development of migraine. PMID: 37379836Ĭharacterizing the evolution and phenotypic impact of ampliconic Y chromosome regions. Polygenic risk prediction: why and when out-of-sample prediction R 2 can exceed SNP-based heritability.Īm J Hum Genet. International Multiple Sclerosis Genetics Consortium MultipleMS Consortium. Locus for severity implicates CNS resilience in progression of multiple sclerosis. The Association of Alcohol Consumption with Glaucoma and Related Traits: Findings from the UK Biobank.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |