The genetics of schizophrenic and schizoid disease

Multiple missense mutations in the diazepam binding inhibitor (DBI) gene identified in schizophrenia but lack of disease association.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2004

Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases.

Psychiatric genetics·2001

Scanning of estrogen receptor alpha (ERalpha) and thyroid hormone receptor alpha (TRalpha) genes in patients with psychiatric diseases: four missense mutations identified in ERalpha gene.

American journal of medical genetics·2001

Identification of single nucleotide polymorphisms (SNPs) and other sequence changes and estimation of nucleotide diversity in coding and flanking regions of the NMDAR1 receptor gene in schizophrenic patients.

Molecular psychiatry·2001

An in-frame deletion in the alpha(2C) adrenergic receptor is common in African--Americans.

Molecular psychiatry·2001

Five missense variants in the amino-terminal domain of the glucocorticoid receptor: no association with puerperal psychosis or schizophrenia.

American journal of medical genetics·2000

Recent strengthening of eastern Pacific ENSO in the last millennium paleorecord.

Science (New York, N.Y.)·2026

Ordering atoms on weak interaction.

Science (New York, N.Y.)·2026

The knotty problem of RNA structure prediction.

Science (New York, N.Y.)·2026

Rethink the cargo, rethink the carrier.

Science (New York, N.Y.)·2026

Direct evaporation of single-crystal metal contacts for 2D semiconductors.

Science (New York, N.Y.)·2026

High-efficiency, long-lived lead-free perovskite light-emitting diodes.

Science (New York, N.Y.)·2026

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

Pharmacology & therapeutics·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Related Experiment Videos

The genetics of schizophrenic and schizoid disease

Related Concept Videos

Multiple missense mutations in the diazepam binding inhibitor (DBI) gene identified in schizophrenia but lack of disease association.

Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases.

Scanning of estrogen receptor alpha (ERalpha) and thyroid hormone receptor alpha (TRalpha) genes in patients with psychiatric diseases: four missense mutations identified in ERalpha gene.

Identification of single nucleotide polymorphisms (SNPs) and other sequence changes and estimation of nucleotide diversity in coding and flanking regions of the NMDAR1 receptor gene in schizophrenic patients.

An in-frame deletion in the alpha(2C) adrenergic receptor is common in African--Americans.

Five missense variants in the amino-terminal domain of the glucocorticoid receptor: no association with puerperal psychosis or schizophrenia.

Recent strengthening of eastern Pacific ENSO in the last millennium paleorecord.

Ordering atoms on weak interaction.

The knotty problem of RNA structure prediction.

Rethink the cargo, rethink the carrier.

Direct evaporation of single-crystal metal contacts for 2D semiconductors.

High-efficiency, long-lived lead-free perovskite light-emitting diodes.

Targeting glycine transporter type 1 (GlyT1) in epilepsy: Pathophysiological rationale and therapeutic perspectives.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Related Experiment Videos

The genetics of schizophrenic and schizoid disease

Related Concept Videos

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