Lehtonen J, Hakonen AH, Hassinen A, Lurås SI, Kaustio M, Glumoff V, Hinrichsen F, Li W, Sulonen AM, Wickman S, Almusa H, Polso M, Palomäki M, Kivirikko S, Avela K, Heiskanen K, Pietiäinen V, Aittomäki K, Saarela J (2025) Genome sequencing reveals CCDC88A variants in malformations of cortical development and immune dysfunction Hum Mol Genet (in press) DOI 10.1093/hmg/ddaf081, PubMed 40401444 Strom NI, Gerring ZF, Galimberti M, Yu D, Halvorsen MW, Abdellaoui A, Rodriguez-Fontenla C, Sealock JM, Bigdeli T, Coleman JR, Mahjani B, Thorp JG, Bey K, Burton CL, Luykx JJ, Zai G, Alemany S, Andre C, Askland KD, Bäckman J, Banaj N, Barlassina C, Nissen JB, Bienvenu OJ, Black D et al. (2025) Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder Nat Genet (in press) DOI 10.1038/s41588-025-02189-z, PubMed 40360802 Icick R, Shadrin A, Holen B, Karadag N, Parker N, O'Connell KS, Frei O, Bahrami S, Høegh MC, Lagerberg TV, Cheng W, Seibert TM, Djurovic S, Dale AM, Zhou H, Edenberg HJ, Gelernter J, Smeland OB, Hindley G, Andreassen OA (2025) Identification of risk variants and cross-disorder pleiotropy through multi-ancestry genome-wide analysis of alcohol use disorder Nat Ment Health, 3 (2), 253-265 DOI 10.1038/s44220-024-00353-8, PubMed 40322774 More publications