A procedure for the efficient collection and processing of pedigree data suitable for genetic analysis

Depression and cognition are associated with lipid dysregulation in both a multigenerational study of depression and the National Health and Nutrition Examination Survey.

Translational psychiatry·2024

Genetic effects influencing risk for major depressive disorder in China and Europe.

Translational psychiatry·2017

Polygenic interactions with environmental adversity in the aetiology of major depressive disorder.

Psychological medicine·2015

The effects on children of depressed mothers' remission and relapse over 9 months.

Psychological medicine·2014

Type I interferon signaling genes in recurrent major depression: increased expression detected by whole-blood RNA sequencing.

Molecular psychiatry·2013

Genotyping serotonin transporter polymorphisms 5-HTTLPR and rs25531 in European- and African-American subjects from the National Institute of Mental Health's Collaborative Center for Genomic Studies.

Translational psychiatry·2013

Impaired low-frequency temporal prediction links to psychomotor dysfunction in depression.

Journal of psychiatric research·2026

When safety fails: A narrative review on attachment in patients with obsessive-compulsive disorder.

Journal of psychiatric research·2026

Transcranial direct current stimulation enhances offline consolidation of implicit sequential learning in individuals with insomnia.

Journal of psychiatric research·2026

Dissociation and antidepressant response to subcutaneous esketamine: A clinical study.

Journal of psychiatric research·2026

Social anxiety and preferred interpersonal distance: The role of estimation bias.

Journal of psychiatric research·2026

Insomnia beyond emotion regulation in adolescent anxiety and depression: A severity-based analysis.

Journal of psychiatric research·2026

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Annals of the Child Neurology Society·2026

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

Pain research & management·2026

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Frontiers in genetics·2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

European journal of human genetics : EJHG·2026

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

Nature communications·2026

A Case of Sotos Syndrome With Right Shoulder Disarticulation Due to a High-Grade Malignant Peripheral Nerve Sheath Tumor in the Right Arm and Shoulder.

Cureus·2026

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A procedure for the efficient collection and processing of pedigree data suitable for genetic analysis

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Depression and cognition are associated with lipid dysregulation in both a multigenerational study of depression and the National Health and Nutrition Examination Survey.

Genetic effects influencing risk for major depressive disorder in China and Europe.

Polygenic interactions with environmental adversity in the aetiology of major depressive disorder.

The effects on children of depressed mothers' remission and relapse over 9 months.

Type I interferon signaling genes in recurrent major depression: increased expression detected by whole-blood RNA sequencing.

Genotyping serotonin transporter polymorphisms 5-HTTLPR and rs25531 in European- and African-American subjects from the National Institute of Mental Health's Collaborative Center for Genomic Studies.

Impaired low-frequency temporal prediction links to psychomotor dysfunction in depression.

When safety fails: A narrative review on attachment in patients with obsessive-compulsive disorder.

Transcranial direct current stimulation enhances offline consolidation of implicit sequential learning in individuals with insomnia.

Dissociation and antidepressant response to subcutaneous esketamine: A clinical study.

Social anxiety and preferred interpersonal distance: The role of estimation bias.

Insomnia beyond emotion regulation in adolescent anxiety and depression: A severity-based analysis.

Complex epilepsy phenotype associated with chromosome 2q24.2-q24.3 deletion involving sodium channel gene cluster.

Purine Metabolism-Related Pathogenic Genes in Trigeminal Neuralgia: A Multiomics Mendelian Randomization Study.

Carrier frequency of autosomal recessive monogenic disorders in the peruvian population.

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis.

A Case of Sotos Syndrome With Right Shoulder Disarticulation Due to a High-Grade Malignant Peripheral Nerve Sheath Tumor in the Right Arm and Shoulder.

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A procedure for the efficient collection and processing of pedigree data suitable for genetic analysis

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