Varun Warrier
Varun Warrier
Zweryfikowany adres z medschl.cam.ac.uk
Cytowane przez
Cytowane przez
Testing the Empathizing–Systemizing theory of sex differences and the Extreme Male Brain theory of autism in half a million people
DM Greenberg, V Warrier, C Allison, S Baron-Cohen
Proceedings of the National Academy of Sciences 115 (48), 12152-12157, 2018
Elevated rates of autism, other neurodevelopmental and psychiatric diagnoses, and autistic traits in transgender and gender-diverse individuals
V Warrier, DM Greenberg, E Weir, C Buckingham, P Smith, MC Lai, ...
Nature communications 11 (1), 3959, 2020
Brain charts for the human lifespan
RAI Bethlehem, J Seidlitz, SR White, JW Vogel, KM Anderson, ...
Nature 604 (7906), 525-533, 2022
Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition
V Warrier, KL Grasby, F Uzefovsky, R Toro, P Smith, B Chakrabarti, ...
Molecular psychiatry 23 (6), 1402-1409, 2018
Synaptic and transcriptionally downregulated genes are associated with cortical thickness differences in autism
R Romero-Garcia, V Warrier, ET Bullmore, S Baron-Cohen, ...
Molecular psychiatry 24 (7), 1053-1064, 2019
Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses
V Warrier, M Vieira, SE Mole
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1832 (11 …, 2013
Genomewide analyses of empathy and systemizing: heritability and correlates with sex, education, and psychiatric risk
V Warrier, R Toro, B Chakrabarti, N Litterman, D Hinds, T Bourgeron, ...
bioRxiv 44, 50682, 2016
Social and non-social autism symptoms and trait domains are genetically dissociable
V Warrier, R Toro, H Won, CS Leblond, F Cliquet, R Delorme, W De Witte, ...
Communications biology 2 (1), 1-13, 2019
Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome
A Di Napoli, V Warrier, S Baron-Cohen, B Chakrabarti
Molecular autism 5 (1), 1-7, 2014
Gene–environment correlations and causal effects of childhood maltreatment on physical and mental health: a genetically informed approach
V Warrier, ASF Kwong, M Luo, S Dalvie, J Croft, HM Sallis, J Baldwin, ...
The Lancet Psychiatry 8 (5), 373-386, 2021
Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism
V Warrier, S Baron-Cohen, B Chakrabarti
Molecular autism 4 (1), 1-11, 2013
A comprehensive meta-analysis of common genetic variants in autism spectrum conditions
V Warrier, V Chee, P Smith, B Chakrabarti, S Baron-Cohen
Molecular autism 6 (1), 1-11, 2015
Large-scale associations between the leukocyte transcriptome and BOLD responses to speech differ in autism early language outcome subtypes
MV Lombardo, T Pramparo, V Gazestani, V Warrier, RAI Bethlehem, ...
Nature neuroscience 21 (12), 1680-1688, 2018
Genetic contribution to ‘theory of mind’in adolescence
V Warrier, S Baron-Cohen
Scientific reports 8 (1), 3465, 2018
A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study
S Baron-Cohen, L Murphy, B Chakrabarti, I Craig, U Mallya, S Lakatošová, ...
PloS one 9 (5), e96374, 2014
Childhood trauma, life-time self-harm, and suicidal behaviour and ideation are associated with polygenic scores for autism
V Warrier, S Baron-Cohen
Molecular psychiatry 26 (5), 1670-1684, 2021
The oxytocin receptor gene predicts brain activity during an emotion recognition task in autism
F Uzefovsky, RAI Bethlehem, S Shamay-Tsoory, A Ruigrok, R Holt, ...
Molecular autism 10, 1-13, 2019
Increased prevalence of non-communicable physical health conditions among autistic adults
E Weir, C Allison, V Warrier, S Baron-Cohen
Autism 25 (3), 681-694, 2021
Genetic contributions to autism spectrum disorder
A Havdahl, M Niarchou, A Starnawska, M Uddin, C van der Merwe, ...
Psychological medicine 51 (13), 2260-2273, 2021
STX1A and Asperger syndrome: a replication study
J Durdiaková, V Warrier, S Banerjee-Basu, S Baron-Cohen, B Chakrabarti
Molecular Autism 5 (1), 1-4, 2014
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