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

The importance of intrafamilial cognitive phenotyping by the case of 22q11.2 deletion, 15q11.2 deletion, and families with inherited copy number variants of unknown significance

通过对22q11.2缺失、15q11.2缺失以及具有意义不明的遗传性拷贝数变异的家族进行研究,探讨家族内认知表型分析的重要性。

Pelgrims, Elise; Hannes, Laurens; Noens, Ilse; Peeters, Yoni; Peeters, Hilde; Fiksinski, Ania M; Heung, Tracy; Bassett, Anne S; Breckpot, Jeroen; Swillen, Ann

A comprehensive overview of neuropsychiatric symptoms in adolescents with 22q11.2 deletion syndrome

对患有 22q11.2 缺失综合征的青少年神经精神症状的全面概述

Selten, I; Blok, J; Boerma, T; Djelantik, A A A M J; Houben, M; Wijnen, F; Zinkstok, J; Vorstman, J A S; Fiksinski, A M

Multicenter retrospective study on effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndrome

一项多中心回顾性研究,探讨了选择性血清素再摄取抑制剂(SSRIs)在22q11.2缺失综合征中的疗效、报告的副作用和认知结果。

Latrèche, Caren; Mancini, Valentina; Dvojakovska, Marija; Kushan, Leila; Mchangama, Fatouma; Tair, Feryal; Cohen, Tal; Spapens, Jeltje; Reijn, Lieke; Díaz-Caneja, Covadonga M; Acheampong, Hayford; Troch, Lotte; Vergaelen, Elfi; Vogels, Annick; Swillen, Ann; Vingerhoets, Claudia; Boot, Erik; Arango, Celso; Velders, Fleur; Fiksinski, Ania; van Amelsvoort, Therese; Gothelf, Doron; Bearden, Carrie E; Chaumette, Boris; Schneider, Maude; Eliez, Stephan

Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

基于源形态测量法揭示22q11.2缺失综合征患者的脑结构模式异常

Ge, Ruiyang; Ching, Christopher R K; Bassett, Anne S; Kushan, Leila; Antshel, Kevin M; van Amelsvoort, Therese; Bakker, Geor; Butcher, Nancy J; Campbell, Linda E; Chow, Eva W C; Craig, Michael; Crossley, Nicolas A; Cunningham, Adam; Daly, Eileen; Doherty, Joanne L; Durdle, Courtney A; Emanuel, Beverly S; Fiksinski, Ania; Forsyth, Jennifer K; Fremont, Wanda; Goodrich-Hunsaker, Naomi J; Gudbrandsen, Maria; Gur, Raquel E; Jalbrzikowski, Maria; Kates, Wendy R; Lin, Amy; Linden, David E J; McCabe, Kathryn L; McDonald-McGinn, Donna; Moss, Hayley; Murphy, Declan G; Murphy, Kieran C; Owen, Michael J; Villalon-Reina, Julio E; Repetto, Gabriela M; Roalf, David R; Ruparel, Kosha; Schmitt, J Eric; Schuite-Koops, Sanne; Angkustsiri, Kathleen; Sun, Daqiang; Vajdi, Ariana; van den Bree, Marianne; Vorstman, Jacob; Thompson, Paul M; Vila-Rodriguez, Fidel; Bearden, Carrie E

A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome

以遗传学为先导的自闭症和精神分裂症谱系障碍研究:22q11.2缺失综合征

Fiksinski, Ania M; Hoftman, Gil D; Vorstman, Jacob A S; Bearden, Carrie E

A normative chart for cognitive development in a genetically selected population

基因选择人群认知发展规范图表

Fiksinski, Ania M; Bearden, Carrie E; Bassett, Anne S; Kahn, René S; Zinkstok, Janneke R; Hooper, Stephen R; Tempelaar, Wanda; McDonald-McGinn, Donna; Swillen, Ann; Emanuel, Beverly; Morrow, Bernice; Gur, Raquel; Chow, Eva; van den Bree, Marianne; Vermeesch, Joris; Warren, Stephen; Owen, Michael; van Amelsvoort, Therese; Eliez, Stephan; Gothelf, Doron; Arango, Celso; Kates, Wendy; Simon, Tony; Murphy, Kieran; Repetto, Gabriela; Suner, Damian Heine; Vicari, Stefano; Cubells, Joseph; Armando, Marco; Philip, Nicole; Campbell, Linda; Garcia-Minaur, Sixto; Schneider, Maude; Shashi, Vandana; Vorstman, Jacob; Breetvelt, Elemi J

Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome

对干血斑进行非靶向代谢分析揭示了22q11.2缺失综合征的代谢特征

Korteling, Dorinde; Boks, Marco P; Fiksinski, Ania M; van Hoek, Ilja N; Vorstman, Jacob A S; Verhoeven-Duif, Nanda M; Jans, Judith J M; Zinkstok, Janneke R

Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model

高风险遗传模型中家庭内部因素对维度神经行为特征的影响

Fiksinski, Ania M; Heung, Tracy; Corral, Maria; Breetvelt, Elemi J; Costain, Gregory; Marshall, Christian R; Kahn, Rene S; Vorstman, Jacob A S; Bassett, Anne S

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

以遗传学为先导的方法来剖析自闭症的异质性:自闭症风险拷贝数变异的表型比较

Chawner, Samuel J R A; Doherty, Joanne L; Anney, Richard J L; Antshel, Kevin M; Bearden, Carrie E; Bernier, Raphael; Chung, Wendy K; Clements, Caitlin C; Curran, Sarah R; Cuturilo, Goran; Fiksinski, Ania M; Gallagher, Louise; Goin-Kochel, Robin P; Gur, Raquel E; Hanson, Ellen; Jacquemont, Sebastien; Kates, Wendy R; Kushan, Leila; Maillard, Anne M; McDonald-McGinn, Donna M; Mihaljevic, Marina; Miller, Judith S; Moss, Hayley; Pejovic-Milovancevic, Milica; Schultz, Robert T; Green-Snyder, LeeAnne; Vorstman, Jacob A; Wenger, Tara L; Hall, Jeremy; Owen, Michael J; van den Bree, Marianne B M

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

22q11.2缺失存在时,精神分裂症风险的遗传因素

Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S; Heung, Tracy; Holleman, Aaron M; Johnston, H Richard; Monfeuga, Thomas; McDonald-McGinn, Donna M; Gur, Raquel E; Morrow, Bernice E; Swillen, Ann; Vorstman, Jacob A S; Bearden, Carrie E; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; Warren, Stephen T; Owen, Michael J; Chopra, Pankaj; Cutler, David J; Duncan, Richard; Kotlar, Alex V; Mulle, Jennifer G; Voss, Anna J; Zwick, Michael E; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih-Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold I; Tran, Oanh; Holmans, Peter; Pardinas, Antonio; Walters, James T R; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J; Costain, Gregory A; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A M J; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T Blaine; McGinn, Daniel E; Moss, Edward M; Sharkus, Robert J; Unolt, Marta; Zackai, Elaine H; Calkins, Monica E; Gallagher, Robert S; Gur, Ruben C; Tang, Sunny X; Fritsch, Rosemarie; Ornstein, Claudia; Repetto, Gabriela M; Breetvelt, Elemi; Duijff, Sasja N; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C; Prasad, Sarah E; Daly, Eileen M; Gudbrandsen, Maria; Murphy, Clodagh M; Murphy, Declan G; Buzzanca, Antonio; Fabio, Fabio Di; Digilio, Maria C; Pontillo, Maria; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F; Ousley, Opal Y; Carmel, Miri; Gothelf, Doron; Mekori-Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Weizman, Abraham; Kushan, Leila; Jalbrzikowski, Maria; Armando, Marco; Eliez, Stéphan; Sandini, Corrado; Schneider, Maude; Béna, Frédérique Sloan; Antshel, Kevin M; Fremont, Wanda; Kates, Wendy R; Belzeaux, Raoul; Busa, Tiffany; Philip, Nicole; Campbell, Linda E; McCabe, Kathryn L; Hooper, Stephen R; Schoch, Kelly; Shashi, Vandana; Simon, Tony J; Tassone, Flora; Arango, Celso; Fraguas, David; García-Miñaúr, Sixto; Morey-Canyelles, Jaume; Rosell, Jordi; Suñer, Damià H; Raventos-Simic, Jasna; Epstein, Michael P; Williams, Nigel M; Bassett, Anne S