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

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

精神疾病的全基因组测序:WGSPD联盟

Sanders, Stephan J; Neale, Benjamin M; Huang, Hailiang; Werling, Donna M; An, Joon-Yong; Dong, Shan; Abecasis, Goncalo; Arguello, P Alexander; Blangero, John; Boehnke, Michael; Daly, Mark J; Eggan, Kevin; Geschwind, Daniel H; Glahn, David C; Goldstein, David B; Gur, Raquel E; Handsaker, Robert E; McCarroll, Steven A; Ophoff, Roel A; Palotie, Aarno; Pato, Carlos N; Sabatti, Chiara; State, Matthew W; Willsey, A Jeremy; Hyman, Steven E; Addington, Anjene M; Lehner, Thomas; Freimer, Nelson B

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.

16p11.2 微缺失和微重复对整体转录谱的影响

Kusenda Mary, Vacic Vladimir, Malhotra Dheeraj, Rodgers Linda, Pavon Kevin, Meth Jennifer, Kumar Ravinesh A, Christian Susan L, Peeters Hilde, Cho Shawn S, Addington Anjene, Rapoport Judith L, Sebat Jonathan

Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls

儿茶酚-O-甲基转移酶 (COMT) val158met 多态性与儿童期起病精神分裂症患者、其非精神病性兄弟姐妹以及健康对照组的青少年皮质发育的关系

Raznahan, Armin; Greenstein, Deanna; Lee, Yohan; Long, Robert; Clasen, Liv; Gochman, Pete; Addington, Anjene; Giedd, Jay N; Rapoport, Judith L; Gogtay, Nitin

Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data

通过对已发表的全基因组关联研究(GWAS)数据进行数量性状和亚表型关联分析,揭示了新的自闭症亚型依赖性遗传变异。

Hu, Valerie W; Addington, Anjene; Hyman, Alexander

Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence

纵向研究性别和雄激素信号对青春期人类皮层成熟动态的影响

Raznahan, Armin; Lee, Yohan; Stidd, Reva; Long, Robert; Greenstein, Dede; Clasen, Liv; Addington, Anjene; Gogtay, Nitin; Rapoport, Judith L; Giedd, Jay N

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

SYNGAP1基因突变与常染色体非综合征型智力低下有关

Hamdan, Fadi F; Gauthier, Julie; Spiegelman, Dan; Noreau, Anne; Yang, Yan; Pellerin, Stéphanie; Dobrzeniecka, Sylvia; Côté, Mélanie; Perreau-Linck, Elizabeth; Carmant, Lionel; D'Anjou, Guy; Fombonne, Eric; Addington, Anjene M; Rapoport, Judith L; Delisi, Lynn E; Krebs, Marie-Odile; Mouaffak, Faycal; Joober, Ridha; Mottron, Laurent; Drapeau, Pierre; Marineau, Claude; Lafrenière, Ronald G; Lacaille, Jean Claude; Rouleau, Guy A; Michaud, Jacques L

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

自闭症谱系障碍与儿童期起病的精神分裂症:重新审视二者关系中的临床和生物学因素

Rapoport, Judith; Chavez, Alex; Greenstein, Deanna; Addington, Anjene; Gogtay, Nitin