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Items: 22


Social and non-social autism symptoms and trait domains are genetically dissociable.

Warrier V, Toro R, Won H, Leblond CS, Cliquet F, Delorme R, De Witte W, Bralten J, Chakrabarti B, Børglum AD, Grove J, Poelmans G, Hinds DA, Bourgeron T, Baron-Cohen S.

Commun Biol. 2019 Sep 3;2:328. doi: 10.1038/s42003-019-0558-4. eCollection 2019.


Integrated genetic and methylomic analyses identify shared biology between autism and autistic traits.

Massrali A, Brunel H, Hannon E, Wong C; iPSYCH-MINERvA Epigenetics Group, Baron-Cohen S, Warrier V.

Mol Autism. 2019 Jul 17;10:31. doi: 10.1186/s13229-019-0279-z. eCollection 2019.


Reply to Perrykkad and Hohwy: When big data are the answer.

Greenberg DM, Warrier V, Allison C, Baron-Cohen S.

Proc Natl Acad Sci U S A. 2019 Jul 9;116(28):13740-13741. doi: 10.1073/pnas.1903773116. Epub 2019 Jul 3. No abstract available.


Mapping genotype to phenotype in neurodevelopmental copy number variants.

Warrier V, Baron-Cohen S.

Lancet Psychiatry. 2019 Jun;6(6):455-456. doi: 10.1016/S2215-0366(19)30163-4. Epub 2019 May 2. No abstract available.


The oxytocin receptor gene predicts brain activity during an emotion recognition task in autism.

Uzefovsky F, Bethlehem RAI, Shamay-Tsoory S, Ruigrok A, Holt R, Spencer M, Chura L, Warrier V, Chakrabarti B, Bullmore E, Suckling J, Floris D, Baron-Cohen S.

Mol Autism. 2019 Mar 12;10:12. doi: 10.1186/s13229-019-0258-4. eCollection 2019.


Large-scale associations between the leukocyte transcriptome and BOLD responses to speech differ in autism early language outcome subtypes.

Lombardo MV, Pramparo T, Gazestani V, Warrier V, Bethlehem RAI, Carter Barnes C, Lopez L, Lewis NE, Eyler L, Pierce K, Courchesne E.

Nat Neurosci. 2018 Dec;21(12):1680-1688. doi: 10.1038/s41593-018-0281-3. Epub 2018 Nov 26.


Testing the Empathizing-Systemizing theory of sex differences and the Extreme Male Brain theory of autism in half a million people.

Greenberg DM, Warrier V, Allison C, Baron-Cohen S.

Proc Natl Acad Sci U S A. 2018 Nov 27;115(48):12152-12157. doi: 10.1073/pnas.1811032115. Epub 2018 Nov 12.


Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.

Warrier V, Toro R, Chakrabarti B; iPSYCH-Broad autism group, Børglum AD, Grove J; 23andMe Research Team, Hinds DA, Bourgeron T, Baron-Cohen S.

Transl Psychiatry. 2018 Mar 12;8(1):35. doi: 10.1038/s41398-017-0082-6.


Synaptic and transcriptionally downregulated genes are associated with cortical thickness differences in autism.

Romero-Garcia R, Warrier V, Bullmore ET, Baron-Cohen S, Bethlehem RAI.

Mol Psychiatry. 2019 Jul;24(7):1053-1064. doi: 10.1038/s41380-018-0023-7. Epub 2018 Feb 26.


Genetic contribution to 'theory of mind' in adolescence.

Warrier V, Baron-Cohen S.

Sci Rep. 2018 Feb 22;8(1):3465. doi: 10.1038/s41598-018-21737-8.


Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition.

Warrier V, Grasby KL, Uzefovsky F, Toro R, Smith P, Chakrabarti B, Khadake J, Mawbey-Adamson E, Litterman N, Hottenga JJ, Lubke G, Boomsma DI, Martin NG, Hatemi PK, Medland SE, Hinds DA, Bourgeron T, Baron-Cohen S.

Mol Psychiatry. 2018 Jun;23(6):1402-1409. doi: 10.1038/mp.2017.122. Epub 2017 Jun 6.


Digital necrosis with squamous cell carcinoma of the tonsil.

Warrier V, Ahmad A, Alshatti Y, Jafar A.

Int Med Case Rep J. 2016 Jun 27;9:159-62. doi: 10.2147/IMCRJ.S106861. eCollection 2016.


A comprehensive meta-analysis of common genetic variants in autism spectrum conditions.

Warrier V, Chee V, Smith P, Chakrabarti B, Baron-Cohen S.

Mol Autism. 2015 Aug 28;6:49. doi: 10.1186/s13229-015-0041-0. eCollection 2015.


A Pooled Genome-Wide Association Study of Asperger Syndrome.

Warrier V, Chakrabarti B, Murphy L, Chan A, Craig I, Mallya U, Lakatošová S, Rehnstrom K, Peltonen L, Wheelwright S, Allison C, Fisher SE, Baron-Cohen S.

PLoS One. 2015 Jul 15;10(7):e0131202. doi: 10.1371/journal.pone.0131202. eCollection 2015.


Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome.

Di Napoli A, Warrier V, Baron-Cohen S, Chakrabarti B.

Mol Autism. 2015 Feb 27;6:9. doi: 10.1186/s13229-015-0009-0. eCollection 2015.


Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome.

Di Napoli A, Warrier V, Baron-Cohen S, Chakrabarti B.

Mol Autism. 2014 Sep 16;5(1):48. doi: 10.1186/2040-2392-5-48. eCollection 2014.


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.

Baron-Cohen S, Murphy L, Chakrabarti B, Craig I, Mallya U, Lakatošová S, Rehnstrom K, Peltonen L, Wheelwright S, Allison C, Fisher SE, Warrier V.

PLoS One. 2014 May 6;9(5):e96374. doi: 10.1371/journal.pone.0096374. eCollection 2014.


Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome.

Durdiaková J, Warrier V, Baron-Cohen S, Chakrabarti B.

Mol Autism. 2014 Mar 31;5(1):25. doi: 10.1186/2040-2392-5-25.


STX1A and Asperger syndrome: a replication study.

Durdiaková J, Warrier V, Banerjee-Basu S, Baron-Cohen S, Chakrabarti B.

Mol Autism. 2014 Feb 18;5(1):14. doi: 10.1186/2040-2392-5-14.


Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism.

Warrier V, Baron-Cohen S, Chakrabarti B.

Mol Autism. 2013 Dec 9;4(1):48. doi: 10.1186/2040-2392-4-48.


CLN6 disease caused by the same mutation originating in Pakistan has varying pathology.

Guerreiro R, Bras JT, Vieira M, Warrier V, Agrawal S, Stewart H, Anderson G, Mole SE.

Eur J Paediatr Neurol. 2013 Nov;17(6):657-60. doi: 10.1016/j.ejpn.2013.04.011. Epub 2013 Jun 2.


Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses.

Warrier V, Vieira M, Mole SE.

Biochim Biophys Acta. 2013 Nov;1832(11):1827-30. doi: 10.1016/j.bbadis.2013.03.017. Epub 2013 Mar 28. Review.

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