Psychiatric Genetics

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December 2016 - Volume 26 - Issue 6 - Contributor Index

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Zhao, Jingjing

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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Zhang, Dai

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

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Zai, Gwyneth

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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Zai, Clement C.

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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Yuen, Ryan K.C.

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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Yue, Weihua

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

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Yang, Xing

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Yang, Lu

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Yan, Hao

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

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Xulu, Khethelo

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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Xi, Shoumin

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Woldbye, David P.D.

Association between genes on chromosome 19p13.2 and panic disorder

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Witt, Stephanie H.

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

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Wang, Lifang

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

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Wang, Chenyao

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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Wang, Bei

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Wang, August G.

Association between genes on chromosome 19p13.2 and panic disorder

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Wagner, Michael

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

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Vereczkei, Andrea

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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Tsetsos, Fotis

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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Sun, Xinyu

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

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Strohmaier, Jana

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

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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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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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Shaik Mohammad, Naushad

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

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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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Schwab, Sibylle G.

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

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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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Rujescu, Dan

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

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Ru, Wenzhao

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Rovaris, Diego L.

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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Rietschel, Marcella

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

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Radha Rama Devi, Akella

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

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Pouget, Jennie G.

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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Pfohl, Marvin A.

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

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Peterson, Roseann E.

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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Patel, Sejal

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Pantavou, Katerina G.

A meta-analysis of FZD3 gene polymorphisms and their association with schizophrenia

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Pan, Chao

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

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Ovenden, Ellen

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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Østergaard, Søren D.

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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O’Brien, Niamh L.

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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Nöthen, Markus M.

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

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Nielsen, Marit N.

Association between genes on chromosome 19p13.2 and panic disorder

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Naik, Usha

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

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Mors, Ole

Association between genes on chromosome 19p13.2 and panic disorder

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Monson, Eric T.

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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Mittal, Kirti

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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Mihaljevic, Marina

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Maier, Wolfgang

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

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Maier, Robert

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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Maffioletti, Elisabetta

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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Ludwig, Michael

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

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Ludwig, Kerstin U.

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

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Lu, Tianlan

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

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Limprasert, Pornprot

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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Li, She

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Lett, Tristram A.

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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Lennertz, Leonard

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

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Lang, Maren

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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Labrie, Viviane

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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Kukshal, Prachi

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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Kruse, Torben A.

Association between genes on chromosome 19p13.2 and panic disorder

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Kristensen, Ann S.

Association between genes on chromosome 19p13.2 and panic disorder

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Krishna Prasad, Chintakindi

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

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Kontou, Panagiota I.

A meta-analysis of FZD3 gene polymorphisms and their association with schizophrenia

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Kirli, Umut

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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Kennedy, James L.

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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Johansen, Oddbjørg

Association between genes on chromosome 19p13.2 and panic disorder

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Hussain, Tajamul

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

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Hofmann, Andrea

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

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Hoffmann, Per

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

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Hnoonual, Areerat

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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Heinemann, Barbara

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

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Hedemand, Anne

Association between genes on chromosome 19p13.2 and panic disorder

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Han, Yonghua

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

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Gregersen, Noomi O.

Association between genes on chromosome 19p13.2 and panic disorder

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Gong, Pingyuan

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Giegling, Ina

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

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Gao, Xiaocai

Investigating the genetic basis of attention to facial expressions: the role of the norepinephrine transporter gene

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Gagliano, Sarah

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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Forstner, Andreas J.

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

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