Varun Warrier
Varun Warrier
Autism Research Centre, University of Cambridge
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Cited by
Cited by
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
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
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
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
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 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
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
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
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
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), 1-9, 2018
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
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 variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome
A Di Napoli, V Warrier, S Baron-Cohen, B Chakrabarti
Molecular autism 6 (1), 1-7, 2015
Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome
J Durdiaková, V Warrier, S Baron-Cohen, B Chakrabarti
Molecular autism 5 (1), 1-5, 2014
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), 1-12, 2020
A pooled genome-wide association study of Asperger syndrome
V Warrier, B Chakrabarti, L Murphy, A Chan, I Craig, U Mallya, ...
PLoS One 10 (7), e0131202, 2015
CLN6 disease caused by the same mutation originating in Pakistan has varying pathology
R Guerreiro, JT Bras, M Vieira, V Warrier, S Agrawal, H Stewart, ...
european journal of paediatric neurology 17 (6), 657-660, 2013
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), 1-13, 2019
Integrated genetic and methylomic analyses identify shared biology between autism and autistic traits
A Massrali, H Brunel, E Hannon, C Wong, S Baron-Cohen, V Warrier
Molecular autism 10 (1), 1-14, 2019
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