日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes

注意力缺陷多动障碍的遗传结构及其与其他精神疾病和认知相关表型的重叠

Ribasés, M; Mitjans, M; Hartman, C A; Soler Artigas, M; Demontis, D; Larsson, H; Ramos-Quiroga, J A; Kuntsi, J; Faraone, S V; Børglum, A D; Reif, A; Franke, B; Cormand, B

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM

基于4,408,646名同胞和半同胞的家庭数据以及333,748例病例和对照的遗传数据,探讨八种精神疾病的遗传影响——更正

Pettersson, E; Lichtenstein, P; Larsson, H; Song, J; Agrawal, A; Børglum, A D; Bulik, C M; Daly, M J; Davis, L K; Demontis, D; Edenberg, H J; Grove, J; Gelernter, J; Neale, B M; Pardiñas, A F; Stahl, E; Walters, J T R; Walters, R; Sullivan, P F; Posthuma, D; Polderman, T J C

Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

对来自孤立人群的个体进行全外显子组测序,发现罕见风险变异与双相情感障碍有关。

Lescai, F; Als, T D; Li, Q; Nyegaard, M; Andorsdottir, G; Biskopstø, M; Hedemand, A; Fiorentino, A; O'Brien, N; Jarram, A; Liang, J; Grove, J; Pallesen, J; Eickhardt, E; Mattheisen, M; Bolund, L; Demontis, D; Wang, A G; McQuillin, A; Mors, O; Wang, J; Børglum, A D

CACNA1C hypermethylation is associated with bipolar disorder

CACNA1C 高甲基化与双相情感障碍相关

Starnawska, A; Demontis, D; Pen, A; Hedemand, A; Nielsen, A L; Staunstrup, N H; Grove, J; Als, T D; Jarram, A; O'Brien, N L; Mors, O; McQuillin, A; Børglum, A D; Nyegaard, M

Increased serum levels of sortilin are associated with depression and correlated with BDNF and VEGF.

血清中 sortilin 水平升高与抑郁症相关,并且与 BDNF 和 VEGF 相关

Buttenschøn H N, Demontis D, Kaas M, Elfving B, Mølgaard S, Gustafsen C, Kaerlev L, Petersen C M, Børglum A D, Mors O, Glerup S

Common variant at 16p11.2 conferring risk of psychosis

16p11.2 上的常见变异会增加患精神病的风险

Steinberg, S; de Jong, S; Mattheisen, M; Costas, J; Demontis, D; Jamain, S; Pietiläinen, O P H; Lin, K; Papiol, S; Huttenlocher, J; Sigurdsson, E; Vassos, E; Giegling, I; Breuer, R; Fraser, G; Walker, N; Melle, I; Djurovic, S; Agartz, I; Tuulio-Henriksson, A; Suvisaari, J; Lönnqvist, J; Paunio, T; Olsen, L; Hansen, T; Ingason, A; Pirinen, M; Strengman, E; Hougaard, D M; Orntoft, T; Didriksen, M; Hollegaard, M V; Nordentoft, M; Abramova, L; Kaleda, V; Arrojo, M; Sanjuán, J; Arango, C; Etain, B; Bellivier, F; Méary, A; Schürhoff, F; Szoke, A; Ribolsi, M; Magni, V; Siracusano, A; Sperling, S; Rossner, M; Christiansen, C; Kiemeney, L A; Franke, B; van den Berg, L H; Veldink, J; Curran, S; Bolton, P; Poot, M; Staal, W; Rehnstrom, K; Kilpinen, H; Freitag, C M; Meyer, J; Magnusson, P; Saemundsen, E; Martsenkovsky, I; Bikshaieva, I; Martsenkovska, I; Vashchenko, O; Raleva, M; Paketchieva, K; Stefanovski, B; Durmishi, N; Pejovic Milovancevic, M; Lecic Tosevski, D; Silagadze, T; Naneishvili, N; Mikeladze, N; Surguladze, S; Vincent, J B; Farmer, A; Mitchell, P B; Wright, A; Schofield, P R; Fullerton, J M; Montgomery, G W; Martin, N G; Rubino, I A; van Winkel, R; Kenis, G; De Hert, M; Réthelyi, J M; Bitter, I; Terenius, L; Jönsson, E G; Bakker, S; van Os, J; Jablensky, A; Leboyer, M; Bramon, E; Powell, J; Murray, R; Corvin, A; Gill, M; Morris, D; O'Neill, F A; Kendler, K; Riley, B; Craddock, N; Owen, M J; O'Donovan, M C; Thorsteinsdottir, U; Kong, A; Ehrenreich, H; Carracedo, A; Golimbet, V; Andreassen, O A; Børglum, A D; Mors, O; Mortensen, P B; Werge, T; Ophoff, R A; Nöthen, M M; Rietschel, M; Cichon, S; Ruggeri, M; Tosato, S; Palotie, A; St Clair, D; Rujescu, D; Collier, D A; Stefansson, H; Stefansson, K