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

Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia

自闭症谱系障碍和精神分裂症中N-甲基-D-天冬氨酸谷氨酸受体的罕见突变

Tarabeux, J; Kebir, O; Gauthier, J; Hamdan, F F; Xiong, L; Piton, A; Spiegelman, D; Henrion, É; Millet, B; Fathalli, F; Joober, R; Rapoport, J L; DeLisi, L E; Fombonne, É; Mottron, L; Forget-Dubois, N; Boivin, M; Michaud, J L; Drapeau, P; Lafrenière, R G; Rouleau, G A; Krebs, M-O

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

自闭症谱系障碍和精神分裂症中 NRXN2 和 NRXN1 的截断突变

Gauthier, Julie; Siddiqui, Tabrez J; Huashan, Peng; Yokomaku, Daisaku; Hamdan, Fadi F; Champagne, Nathalie; Lapointe, Mathieu; Spiegelman, Dan; Noreau, Anne; Lafrenière, Ronald G; Fathalli, Ferid; Joober, Ridha; Krebs, Marie-Odile; DeLisi, Lynn E; Mottron, Laurent; Fombonne, Eric; Michaud, Jacques L; Drapeau, Pierre; Carbonetto, Salvatore; Craig, Ann Marie; Rouleau, Guy A

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

在确诊为精神分裂症的患者中,编码突触支架蛋白 SHANK3 的基因存在新生突变

Gauthier, Julie; Champagne, Nathalie; Lafrenière, Ronald G; Xiong, Lan; Spiegelman, Dan; Brustein, Edna; Lapointe, Mathieu; Peng, Huashan; Côté, Mélanie; Noreau, Anne; Hamdan, Fadi F; Addington, Anjené M; Rapoport, Judith L; Delisi, Lynn E; Krebs, Marie-Odile; Joober, Ridha; Fathalli, Ferid; Mouaffak, Fayçal; Haghighi, Ali P; Néri, Christian; Dubé, Marie-Pierre; Samuels, Mark E; Marineau, Claude; Stone, Eric A; Awadalla, Philip; Barker, Philip A; Carbonetto, Salvatore; Drapeau, Pierre; Rouleau, Guy A

Association study of the trinucleotide repeat polymorphism within SMARCA2 and schizophrenia

SMARCA2基因内三核苷酸重复序列多态性与精神分裂症的关联研究

Sengupta, Sarojini; Xiong, Lan; Fathalli, Ferid; Benkelfat, Chawki; Tabbane, Karim; Danics, Zoltan; Labelle, Alain; Lal, Samarthji; Krebs, Marie-Odile; Rouleau, Guy; Joober, Ridha