Psychiatric Genetics

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December 2016 - Volume 26 - Issue 6 - Contributor Index

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Sai Shruti, P.

Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders

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Schwab, Sibylle G.

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2

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Seaman, Lauren

Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16–20 October 2015

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Shaik Mohammad, Naushad

Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders

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Shankarappa, Bhagya

Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16–20 October 2015

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Sripo, Thanya

Whole-exome sequencing identifies a novel heterozygous missense variant of the EN2 gene in two unrelated patients with autism spectrum disorder

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Strohmaier, Jana

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2

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Sun, Xinyu

Association of DISC1, BDNF, and COMT polymorphisms with exploratory eye movement of schizophrenia in a Chinese Han population

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