Items where authors include "Hakonarson, H."

Article

Papadopoulou, A. orcid.org/0000-0003-3158-7951, Litkowski, E.M., Graff, M. orcid.org/0000-0001-6380-1735 et al. (36 more authors) (2025) Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height. npj Genomic Medicine, 10 (1). 14. ISSN 2056-7944

Kentistou, K.A. orcid.org/0000-0002-5816-664X, Kaisinger, L.R. orcid.org/0000-0002-0849-3191, Stankovic, S. orcid.org/0000-0002-6602-1379 et al. (220 more authors) (2024) Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (7). pp. 1397-1411. ISSN 1061-4036

Kousathanas, A. orcid.org/0000-0001-6265-6521, Pairo-Castineira, E. orcid.org/0000-0002-2423-3090, Rawlik, K. orcid.org/0000-0002-0010-370X et al. (2377 more authors) (2022) Whole-genome sequencing reveals host factors underlying critical COVID-19. Nature, 607. pp. 97-103. ISSN 0028-0836

Lill, C.M., Rengmark, A., Pihlstrøm, L. et al. (49 more authors) (2015) The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease. Alzheimer's and Dementia, 11 (12). pp. 1407-1416. ISSN 1552-5260

Van Deerlin, V.M., Sleiman, P.M.A., Martinez-Lage, M. et al. (97 more authors) (2010) Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions. Nature Genetics, 42 (3). pp. 234-239. ISSN 1061-4036,