Clinical genetics of dementing illness

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

Technology-Based Vestibular Education.

Neurologic clinics·2026

Novel Digital Tools for Clinical Research: Vestibular Simulation for Benign Paroxysmal Positional Vertigo.

Neurologic clinics·2026

Artificial Intelligence and Machine Learning for Eye Movements in Dizziness and Vertigo: A Comprehensive Review.

Neurologic clinics·2026

Diagnostic Decision Support and Automation in Vestibular Diagnosis.

Neurologic clinics·2026

The Digital Evolution of Vestibular Rehabilitation: From Cawthorne-Cooksey to a Digital Future/to Digital Care.

Neurologic clinics·2026

Vestibular Event Monitoring in the Community and Emergency Room.

Neurologic clinics·2026

Emerging roles and mechanistic insights of ASRGL1 in tumorigenesis and cancer progression.

Frontiers in cell and developmental biology·2026

ANOS1 variant and PROK2 upregulation in familial Kallmann syndrome: integrative genetic, transcriptomic, and phenotypic study.

Frontiers in molecular neuroscience·2026

CONDSIAS, a Stress-Triggered Childhood Neurodegeneration: Four Novel ADPRS Variants and a Structured Review of the Reported Phenotype.

Cerebellum (London, England)·2026

Truncating Kabuki Syndrome-associated KMT2D Mutation in FYR Domain Alters Chromatin Accessibility at Neurodevelopmental Loci.

Molecular neurobiology·2026

17q11.2 Duplication (includes NF1 gene): A Scoping Review.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Human induced pluripotent stem cell-derived cortical neurons from monozygotic twins with the Gαo1 K278del mutation reveal disease mechanisms relevant to GNAO1-related encephalopathy.

Epilepsia·2026

Clinical genetics of dementing illness

Related Experiment Videos

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.

Technology-Based Vestibular Education.

Novel Digital Tools for Clinical Research: Vestibular Simulation for Benign Paroxysmal Positional Vertigo.

Artificial Intelligence and Machine Learning for Eye Movements in Dizziness and Vertigo: A Comprehensive Review.

Diagnostic Decision Support and Automation in Vestibular Diagnosis.

The Digital Evolution of Vestibular Rehabilitation: From Cawthorne-Cooksey to a Digital Future/to Digital Care.

Vestibular Event Monitoring in the Community and Emergency Room.

Emerging roles and mechanistic insights of ASRGL1 in tumorigenesis and cancer progression.

ANOS1 variant and PROK2 upregulation in familial Kallmann syndrome: integrative genetic, transcriptomic, and phenotypic study.

CONDSIAS, a Stress-Triggered Childhood Neurodegeneration: Four Novel ADPRS Variants and a Structured Review of the Reported Phenotype.

Truncating Kabuki Syndrome-associated KMT2D Mutation in FYR Domain Alters Chromatin Accessibility at Neurodevelopmental Loci.

17q11.2 Duplication (includes NF1 gene): A Scoping Review.

Human induced pluripotent stem cell-derived cortical neurons from monozygotic twins with the Gαo1 K278del mutation reveal disease mechanisms relevant to GNAO1-related encephalopathy.

Clinical genetics of dementing illness

Related Experiment Videos

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Related Concept Videos

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