Excited to share our latest manuscript in @NatureGenet! Utilizing high-resolution genetic data imputed with a population-matched reference panel, we uncovered causal genetic variants for a wide range of human traits over 200K participants from Japan (1/20)
https://t.co/gYThPqMe59
Check out our latest findings on X-inactivation in iPSCs now out in Genome Biology https://t.co/SWpIukchnB A great collaboration with Dr Olli Pietiläinen and a cool demonstration of the many complexities of the X chromosome 😎
Extremely excited to share our work on #V2F method SCAVENGE for the disease/trait relevant causal cell type/state identification using single-cell epigenomic data https://t.co/rD9vl71LNE out now in @NatureBiotech. The R package can be found https://t.co/snBR3Fqi4o.
Our UK Biobank mito-phewas is finally out! Great collaborative work. Congrats to @DoingYonova, Dr. Jo Howson, @auroradevea et al. Exciting times ahead for mitochondrial genomics! @cam_mito
https://t.co/e6tm8h5GA5
Excited to share this preprint from the lab led by my talented postdoc Jaakko T. Leinonen (not on Twitter) where we used both UK Biobank and FinnGen data to comprehensively profile the role of testosterone in human health and disease. Thread 👇https://t.co/hbvKa1K71W
Our paper (led by Pyry Helkkula & Ida Surakka) on lipid associated pLoFs and their impact on cardiometabolic risk is now out. Leading the pack is 80-times Finnish enriched PTV in ANGPTL8 gene. @PLOSGenetics@CoECDG@FinnGen_FI@FIMM_UH
https://t.co/PdnvgDWDco
In our new paper we do in-depth follow-up of Alzheimer’s disease GWAS: integrating fine-mapping, colocalization, gene network analyses, and single-cell gene expression to prioritise risk genes. This figure would have better represented the work.
With FINEMAP, we identified >27,000 distinct signals in >5,000 regions across the 35 traits, of which >2,500 signals were fine-mapped to a single variant. We also trained sparse polygenic risk score (PRS) models with Lasso L1- penalized regression using the snpnet package. (4/n)
our hemorrhoids GWAS preprint is out, almost 1 M people studied! 1st time the genetic architecture of this trait is investigated, we detect 102 loci that point to smooth muscle, epithelial and connective tissue dysfunction
with @an_franke and many others
https://t.co/ocAQICR9xJ
Here we go. The PGC Schizophrenia GWAS (phase 3) paper in preprint. A massive group effort and thanks to participants and researchers internationally. Also special mention to SCHEMA colleagues and the papers bear reading alongside each other. https://t.co/dxl7O94U9S
You have a GWAS SNP.
Great.
Now, what's the causal gene?
Really excited to share this preprint with coauthors Vince Forgetta and Lai Jiang, @BrentRichards19 , @markmccarthyoxf , @Greenwood_LDI and others
https://t.co/wNnDFwum8X