Rare coding variation implicates thirteen genes in bipolar disorder across 232,536 individuals from global populations.
Author / Organization: Liao C, Ye R, Sealock JM, Boltz T, Ivankovic F, Finucane H, Howrigan D, Liu YC, Satterstrom FK, Hassan A, Alemayehu M, Gichuru S, Mwende RM, Newton CRJC, Koen N, Zingela Z, Diaz-Zuluaga AM, Ramirez-Diaz AM, Reus VI, Teshiba T, Palotie A, Hämäläinen E, Pietiläinen O, Lind PA, Siskind DJ, Hickie IB, Morales-Cedillo P, Jiménez-Pavón J, Sanabrais-Jiménez MA, Sotelo-Ramírez CE, Hahn E, Nguyen VP, Karlson E, Chang CE, Chen HC, Alda M, Landén M, Smoller JW, Craddock N, Vawter MP, Curtis D, McQuillin A, Kahn RS, Ophoff RA, Vreeker A, Hultman C, Sullivan PF, Talkowski ME, Blackwood DH, McIntosh A, Pulver AE, Cohen B, Adolfsson R, Reif A, Goes F, Yolken R, Corvin AP, Morris DW, BIPEX Collection Scientists, Cerrato F, Chapman SB, Cusick C, Guo Z, Olivares AM, Rouleau GA, Viswanath B, Kuo PH, Nguyen VT, Ta TMT, Camarena B, Pato CN, Pato MT, Medland SE, Freimer N, Olde Loohuis L, Lopez-Jaramillo C, Stroud R, Atwoli L, Dickens A, Koenen KC, Kariuki SM, Teferra S, Stein DJ, Ayub M, Knowles JA, Daly MJ, Huang H, Neale BM
| File Format | PDF (Portable Document Format) |
|---|---|
| Publication Year | 2026 |
| Source Host |
PubMed Central
(pmc.ncbi.nlm.nih.gov)
|
| License / Terms | Open Access / Creative Commons |
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