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Human Molecular Genetics|March 21, 1998

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansionJ Del-Favero, L Krols, A Michalik, et al.

Molecular Psychiatry|December 8, 2004

Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association studyI Massat, D Souery, J Del-Favero, et al.

Molecular Psychiatry|June 4, 2014

MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene setsM Strazisar, S Cammaerts, K van der Ven, et al.

Genome Research|November 24, 1999

A high-resolution physical map of human chromosome 21p using yeast artificial chromosomesS Y Wang, M Cruts, J Del-Favero, et al.

Neurology|September 30, 2010

Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.

Neurology|September 30, 2010

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.

Psychological Medicine|July 25, 2003

The serotonin transporter promoter repeat length polymorphism, seasonal affective disorder and seasonalityC Johansson, M Willeit, R Levitan, et al.

Molecular Psychiatry|February 13, 2002

Excess of allele1 for alpha3 subunit GABA receptor gene (GABRA3) in bipolar patients: a multicentric association studyI Massat, D Souery, J Del-Favero, et al.

Molecular Psychiatry|August 30, 2001

Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorderB Lerer, F Macciardi, R H Segman, et al.

Biological Psychiatry|March 29, 2001

Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association studyD Souery, S Van Gestel, I Massat, et al.

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Showing results (31-40 of 40) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 40 results.

Human Molecular Genetics|March 21, 1998

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansionJ Del-Favero, L Krols, A Michalik, et al.

Molecular Psychiatry|December 8, 2004

Molecular Psychiatry|June 4, 2014

MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene setsM Strazisar, S Cammaerts, K van der Ven, et al.

Genome Research|November 24, 1999

A high-resolution physical map of human chromosome 21p using yeast artificial chromosomesS Y Wang, M Cruts, J Del-Favero, et al.

Neurology|September 30, 2010

Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.

Neurology|September 30, 2010

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.

Psychological Medicine|July 25, 2003

The serotonin transporter promoter repeat length polymorphism, seasonal affective disorder and seasonalityC Johansson, M Willeit, R Levitan, et al.

Molecular Psychiatry|February 13, 2002

Excess of allele1 for alpha3 subunit GABA receptor gene (GABRA3) in bipolar patients: a multicentric association studyI Massat, D Souery, J Del-Favero, et al.

Molecular Psychiatry|August 30, 2001

Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorderB Lerer, F Macciardi, R H Segman, et al.

Biological Psychiatry|March 29, 2001

Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association studyD Souery, S Van Gestel, I Massat, et al.

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