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

Sex differences in orienting to pictures with and without humans: evidence from the cardiac evoked response (ECR) and the cortical long latency parietal positivity (LPP)

对有人物和无人物图片的定向反应存在性别差异:来自心脏诱发反应 (ECR) 和皮层长潜伏期顶叶正波 (LPP) 的证据

Althaus, Monika; Groen, Yvonne; van der Schaft, Lutske; Minderaa, Ruud B; Tucha, Oliver; Mulder, Lambertus J M; Wijers, Albertus A

Parental rearing and psychopathology in mothers of adolescents with and without borderline personality symptoms

父母教养方式与青少年母亲的精神病理学:有边缘型人格症状和无边缘型人格症状的青少年的母亲

Schuppert, H Marieke; Albers, Casper J; Minderaa, Ruud B; Emmelkamp, Paul Mg; Nauta, Maaike H

Standardized ADOS scores: measuring severity of autism spectrum disorders in a Dutch sample

标准化ADOS评分:衡量荷兰样本中自闭症谱系障碍的严重程度

de Bildt, Annelies; Oosterling, Iris J; van Lang, Natasja D J; Sytema, Sjoerd; Minderaa, Ruud B; van Engeland, Herman; Roos, Sascha; Buitelaar, Jan K; van der Gaag, Rutger-Jan; de Jonge, Maretha V

Diagnosing autism spectrum disorders in adults: the use of Autism Diagnostic Observation Schedule (ADOS) module 4

成人自闭症谱系障碍的诊断:自闭症诊断观察量表(ADOS)模块4的应用

Bastiaansen, Jojanneke A; Meffert, Harma; Hein, Simone; Huizinga, Petra; Ketelaars, Cees; Pijnenborg, Marieke; Bartels, Arnold; Minderaa, Ruud; Keysers, Christian; de Bildt, Annelies

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

高密度SNP关联研究和AUTS1和AUTS5基因座拷贝数变异分析表明IMMP2L-DOCK4基因区域与自闭症易感性有关。

Maestrini, E; Pagnamenta, A T; Lamb, J A; Bacchelli, E; Sykes, N H; Sousa, I; Toma, C; Barnby, G; Butler, H; Winchester, L; Scerri, T S; Minopoli, F; Reichert, J; Cai, G; Buxbaum, J D; Korvatska, O; Schellenberg, G D; Dawson, G; de Bildt, A; Minderaa, R B; Mulder, E J; Morris, A P; Bailey, A J; Monaco, A P

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach

利用全基因组QTL连锁分析方法鉴定注意力缺陷/多动障碍和自闭症谱系障碍重叠的基因位点

Nijmeijer, Judith S; Arias-Vásquez, Alejandro; Rommelse, Nanda N J; Altink, Marieke E; Anney, Richard J L; Asherson, Philip; Banaschewski, Tobias; Buschgens, Cathelijne J M; Fliers, Ellen A; Gill, Michael; Minderaa, Ruud B; Poustka, Luise; Sergeant, Joseph A; Buitelaar, Jan K; Franke, Barbara; Ebstein, Richard P; Miranda, Ana; Mulas, Fernando; Oades, Robert D; Roeyers, Herbert; Rothenberger, Aribert; Sonuga-Barke, Edmund J S; Steinhausen, Hans-Christoph; Faraone, Stephen V; Hartman, Catharina A; Hoekstra, Pieter J

Perinatal risk factors interacting with catechol O-methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD

围产期危险因素与儿茶酚O-甲基转移酶和血清素转运蛋白基因相互作用,可预测患有注意力缺陷多动障碍(ADHD)儿童的自闭症谱系障碍(ASD)症状。

Nijmeijer, Judith S; Hartman, Catharina A; Rommelse, Nanda N J; Altink, Marieke E; Buschgens, Cathelijne J M; Fliers, Ellen A; Franke, Barbara; Minderaa, Ruud B; Ormel, Johan; Sergeant, Joseph A; Verhulst, Frank C; Buitelaar, Jan K; Hoekstra, Pieter J

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry

富含亮氨酸重复序列基因的多态性与欧洲血统人群的自闭症谱系障碍易感性相关。

Sousa, Inês; Clark, Taane G; Holt, Richard; Pagnamenta, Alistair T; Mulder, Erik J; Minderaa, Ruud B; Bailey, Anthony J; Battaglia, Agatino; Klauck, Sabine M; Poustka, Fritz; Monaco, Anthony P

Risperidone-induced weight gain in referred children with autism spectrum disorders is associated with a common polymorphism in the 5-hydroxytryptamine 2C receptor gene

利培酮引起的自闭症谱系障碍患儿体重增加与5-羟色胺2C受体基因的常见多态性相关。

Hoekstra, Pieter J; Troost, Pieter W; Lahuis, Bertine E; Mulder, Hans; Mulder, Erik J; Franke, Barbara; Buitelaar, Jan K; Anderson, George M; Scahill, Lawrence; Minderaa, Ruud B

Prevalence of treated autism spectrum disorders in Aruba

阿鲁巴接受治疗的自闭症谱系障碍患病率

van Balkom, Ingrid D C; Bresnahan, Michaeline; Vogtländer, Marrit F; van Hoeken, Daphne; Minderaa, Ruud B; Susser, Ezra; Hoek, Hans W