Author
Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
Mutual co-authors in cluster
3 papers
Recent·Most cited
Calwing Liao, Robert Ye, Julia Sealock, Toni A. Boltz, Franjo Ivankovic, Hilary K. Finucane, Daniel P. Howrigan, Yijia Christiana Liu, F. Kyle Satterstrom, Arsalan Hassan, Melkam Alemayehu Kebede, Stella Gichuru, Rehema M. Mwende, Charles R. J. C. Newton, Nastassja Koen, , Benjamin M. Neale
medRxiv · Oct 5, 2026 · PreprintGenetic & Genomic Medicine
Julia Sealock, Connor Dowd, Calwing Liao, Robert Ye, Daniel P. Howrigan, F. Kyle Satterstrom, Chiara Auwerx, Soyeon Kim, Cong Huai, Lin He, Melkam Alemayehu Kebede, Stella Gichuru, Rehema M. Mwende, Charles R. J. C. Newton, Nastassja Koen, , Akena Dickens
Ultra-rare damaging coding variants in 87,959 schizophrenia cases and 150,587 controls implicate 40 genes (16 exome-wide, 24 at 5% FDR), half overlapping autism, developmental delay or bipolar genes.
bioRxiv · Sep 21, 2026 · PreprintGenetics✦ In-depth digest
Nora I Strom, Zachary F Gerring, Marco Galimberti, Dongmei Yu, Matthew Halvorsen, Abdel Abdellaoui, Cristina Rodriguez‐Fontenla, Julia Sealock, Tim Bigdeli, Jonathan R Coleman, Behrang Mahjani, Jackson G Thorp, Katharina Bey, Christie L Burton, Jurjen J Luykx, , Bjarne K. A. Hansen
This study identifies 30 genome-wide significant loci for obsessive-compulsive disorder (OCD) using a large GWAS, linking risk to specific brain cell types and shared genetic risk with other psychiatric and non-psychiatric traits.
Research at the University of Copenhagen (University of Copenhagen) · Jan 1, 2025Peer-reviewedGenetic & Genomic Medicine