Varun Warrier

Employment

• University of Cambridge

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (14)

• Genetic contribution to 'theory of mind' in adolescence
  Scientific Reports 2018 DOI: 10.1038/s41598-018-21737-8
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• Genome-wide analyses of self-reported empathy: Correlations with autism, schizophrenia, and anorexia nervosa
  Varun Warrier, Roberto Toro, Bhismadev Chakrabarti +6 more
  Translational Psychiatry 2018 DOI: 10.1038/s41398-017-0082-6
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• Genome-wide meta-analysis of cognitive empathy: Heritability, and correlates with sex, neuropsychiatric conditions and cognition
  Varun Warrier, Katrina L. Grasby, Florina Uzefovsky +15 more
  Molecular Psychiatry 2018 DOI: 10.1038/mp.2017.122
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• Synaptic and transcriptionally downregulated genes are associated with cortical thickness differences in autism
  Molecular Psychiatry 2018 DOI: 10.1038/s41380-018-0023-7
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• A comprehensive meta-analysis of common genetic variants in autism spectrum conditions
  Molecular Autism 2015 DOI: 10.1186/s13229-015-0041-0
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• A pooled genome-wide association study of asperger syndrome
  Varun Warrier, Bhismadev Chakrabarti, Laura C. Murphy +10 more
  PLoS ONE 2015 DOI: 10.1371/journal.pone.0131202
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• Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome
  Agnese Di Napoli, Varun Warrier, Simon Baron‐Cohen +1 more
  Molecular Autism 2015 DOI: 10.1186/s13229-015-0009-0
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• 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
  Simon Baron‐Cohen, Laura C. Murphy, Bhismadev Chakrabarti +9 more
  PLoS ONE 2014 DOI: 10.1371/journal.pone.0096374
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• Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome
  Molecular Autism 2014 DOI: 10.1186/2040-2392-5-48
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• STX1A and Asperger syndrome: A replication study
  Molecular Autism 2014 DOI: 10.1186/2040-2392-5-14
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• Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome
  Jaroslava Durdiaková, Varun Warrier, Simon Baron‐Cohen +1 more
  Molecular Autism 2014 DOI: 10.1186/2040-2392-5-25
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• CLN6 disease caused by the same mutation originating in Pakistan has varying pathology
  European Journal of Paediatric Neurology 2013 DOI: 10.1016/j.ejpn.2013.04.011
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• Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses
  Biochimica et Biophysica Acta - Molecular Basis of Disease 2013 DOI: 10.1016/j.bbadis.2013.03.017
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• Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism
  Varun Warrier, Simon Baron‐Cohen, Bhismadev Chakrabarti
  Molecular Autism 2013 DOI: 10.1186/2040-2392-4-48
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