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Lista de obras de Kate Baker

Annual research review: Rare genotypes and childhood psychopathology--uncovering diverse developmental mechanisms of ADHD risk

artículo científico

Assessing the landscape of STXBP1-related disorders in 534 individuals

artículo científico publicado en 2022

COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome

artículo científico publicado en 2005

Childhood intellectual disability and parents' mental health: integrating social, psychological and genetic influences

scientific article published on 11 March 2020

Chromosomal microarray analysis-a routine clinical genetic test for patients with schizophrenia

artículo científico publicado en 2014

Cognitive training enhances intrinsic brain connectivity in childhood

artículo científico publicado en 2015

Electrophysiological measures of resting state functional connectivity and their relationship with working memory capacity in childhood.

artículo científico publicado en 2015

Epilepsy, cognitive deficits and neuroanatomy in males with ZDHHC9 mutations.

artículo científico publicado en 2015

Functional network dynamics in a neurodevelopmental disorder of known genetic origin

artículo científico publicado en 2019

Genetic investigation for adults with intellectual disability: opportunities and challenges

artículo científico

Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling

artículo científico publicado en 2015

Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome? ⬇️

artículo científico publicado el 1 de abril de 2012

Making sense of cilia in disease: the human ciliopathies.

artículo científico publicado en 2009

Neocortical and hippocampal volume loss in a human ciliopathy: A quantitative MRI study in Bardet-Biedl syndrome

scientific article published on 17 November 2010

Neuroanatomy in adolescents and young adults with 22q11 deletion syndrome: comparison to an IQ-matched group.

artículo científico publicado en 2010

Protein structure and phenotypic analysis of pathogenic and population missense variants in STXBP1.

artículo científico publicado en 2017

Psychopathology and cognitive performance in individuals with membrane-associated guanylate kinase mutations: a functional network phenotyping study

artículo científico publicado en 2015

STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics

artículo científico publicado en 2019

Structural brain abnormalities in a single gene disorder associated with epilepsy, language impairment and intellectual disability.

scientific article published on 04 August 2016

The Neurodevelopmental Spectrum of Synaptic Vesicle Cycling Disorders

artículo científico publicado en 2020

Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times

artículo científico publicado en 2014

Training Working Memory in Childhood Enhances Coupling between Frontoparietal Control Network and Task-Related Regions

artículo científico publicado en 2016

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