Sara B. Estruch

机构：Max Planck Institute for Psycholinguistics · ORCID：0000-0001-7474-6735

发表论文 30 篇 · 总被引 660 次 · h-index 11

代表论文

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription (2016 · The American Journal of Human Genetics · 被引 165)
De novo TBR1 mutations in sporadic autism disrupt protein functions (2014 · Nature Communications · 被引 121)
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders (2018 · Human Molecular Genetics · 被引 67)
The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers (2016 · Scientific Reports · 被引 45)
Functional characterization of TBR1 variants in neurodevelopmental disorder (2018 · Scientific Reports · 被引 37)
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder (2016 · Journal of Neurodevelopmental Disorders · 被引 27)