Psychiatric Genetics

October 2013 - Volume 23 - Issue 5 - Contributor Index

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Arolt, Volker

Evidence of increased risk for major depressive disorder in individuals homozygous for the high-expressing 5-HTTLPR/rs25531 (LA) allele of the serotonin transporter promoter

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Baune, Bernhard T.

Evidence of increased risk for major depressive disorder in individuals homozygous for the high-expressing 5-HTTLPR/rs25531 (LA) allele of the serotonin transporter promoter

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Børglum, Anders D.

An association study between the norepinephrine transporter gene and depression

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Buttenschøn, Henriette N.

An association study between the norepinephrine transporter gene and depression

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Cohen-Woods, Sarah

Evidence of increased risk for major depressive disorder in individuals homozygous for the high-expressing 5-HTTLPR/rs25531 (LA) allele of the serotonin transporter promoter

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Dannlowski, Udo

Evidence of increased risk for major depressive disorder in individuals homozygous for the high-expressing 5-HTTLPR/rs25531 (LA) allele of the serotonin transporter promoter

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Engels, Rutger C.M.E.

Oxytocin receptor gene (OXTR) in relation to loneliness in adolescence: interactions with sex, parental support, and DRD2 and 5-HTTLPR genotypes

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Goossens, Luc

Oxytocin receptor gene (OXTR) in relation to loneliness in adolescence: interactions with sex, parental support, and DRD2 and 5-HTTLPR genotypes

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Grynderup, Matias B.

An association study between the norepinephrine transporter gene and depression

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Hansen, Åse M.

An association study between the norepinephrine transporter gene and depression

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Huang, Yinglin

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Jacobsen, Iben S.

An association study between the norepinephrine transporter gene and depression

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Jin, Qiu

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Kaerlev, Linda

An association study between the norepinephrine transporter gene and depression

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Kanavakis, Emmanuel

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

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Kitsiou-Tzeli, Sophia

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

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Kolstad, Henrik A.

An association study between the norepinephrine transporter gene and depression

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Kordi-Tamandani, Dor Mohammad

Analysis of association between dopamine receptor genes’ methylation and their expression profile with the risk of schizophrenia

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Kourmouli, Niki

Effect of BDNF Val66Met and serotonin transporter 5-HTTLPR polymorphisms on psychopathological characteristics in a sample of university students

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Krogh, Jesper

An association study between the norepinephrine transporter gene and depression

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Li, Jingying

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Li, Jun

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Livaditis, Miltos

Effect of BDNF Val66Met and serotonin transporter 5-HTTLPR polymorphisms on psychopathological characteristics in a sample of university students

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Ma, Hui

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Mamatsiou, Athina

Effect of BDNF Val66Met and serotonin transporter 5-HTTLPR polymorphisms on psychopathological characteristics in a sample of university students

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Mors, Ole

An association study between the norepinephrine transporter gene and depression

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Nordentoft, Merete

An association study between the norepinephrine transporter gene and depression

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Oikonomakis, Vasilis

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

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Pampanos, Andreas

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

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Sahranavard, Roya

Analysis of association between dopamine receptor genes’ methylation and their expression profile with the risk of schizophrenia

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Samakouri, Maria

Effect of BDNF Val66Met and serotonin transporter 5-HTTLPR polymorphisms on psychopathological characteristics in a sample of university students

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Scholte, Ron H.J.

Oxytocin receptor gene (OXTR) in relation to loneliness in adolescence: interactions with sex, parental support, and DRD2 and 5-HTTLPR genotypes

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Silahtaroglu, Asli

An association study between the norepinephrine transporter gene and depression

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Sofocleous, Christalena

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

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Stacey, David

Evidence of increased risk for major depressive disorder in individuals homozygous for the high-expressing 5-HTTLPR/rs25531 (LA) allele of the serotonin transporter promoter

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Thomsen, Jane F.

An association study between the norepinephrine transporter gene and depression

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Toben, Catherine

Evidence of increased risk for major depressive disorder in individuals homozygous for the high-expressing 5-HTTLPR/rs25531 (LA) allele of the serotonin transporter promoter

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Tommerup, Niels

An association study between the norepinephrine transporter gene and depression

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Torkamanzehi, Adam

Analysis of association between dopamine receptor genes’ methylation and their expression profile with the risk of schizophrenia

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Trypsianis, Gregory

Effect of BDNF Val66Met and serotonin transporter 5-HTTLPR polymorphisms on psychopathological characteristics in a sample of university students

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Tümer, Zeynep

An association study between the norepinephrine transporter gene and depression

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van Roekel, Eeske

Oxytocin receptor gene (OXTR) in relation to loneliness in adolescence: interactions with sex, parental support, and DRD2 and 5-HTTLPR genotypes

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Veletza, Stavroula

Effect of BDNF Val66Met and serotonin transporter 5-HTTLPR polymorphisms on psychopathological characteristics in a sample of university students

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Verhagen, Maaike

Oxytocin receptor gene (OXTR) in relation to loneliness in adolescence: interactions with sex, parental support, and DRD2 and 5-HTTLPR genotypes

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Volaki, Konstantina

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

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Vrettou, Christina

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

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Wang, Yuan

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Wu, Lijuan

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Zhao, Xiaofeng

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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Zhu, Gang

Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants

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