Biological phenotypes in the genetics of schizophrenia

Species-specific thermal classification schemes can improve climate related marine resource decisions.

PloS one·2021

A compact high-performance low-field NMR apparatus for measurements on fluids at very high pressures and temperatures.

The Review of scientific instruments·2014

Long-term beneficial effects of adrenal medullary autografts supported by nerve growth factor in Parkinson's disease.

European journal of neurology·2013

Receiving enzyme replacement therapy for a lysosomal storage disorder: a preliminary exploration of the experiences of young patients and their families.

Journal of genetic counseling·2013

A comment on 'social and economic factors in Hong Kong's fertility decline' by Sui-Ying Wat and R. W. Hodge.

Population studies·2011

Recent fertility declines in Hong Kong: the role of the changing age structure.

Population studies·2011

Diversity of Layer 3 Pyramidal Neuron Properties Across Areas of the Primate Neocortex.

Biological psychiatry·2026

Genetic liability to addiction underlies comorbid bipolar and substance use disorders.

Biological psychiatry·2026

Machine Learning-Based Discrimination of Treatment-Resistant Schizophrenia Using Structural Brain Imaging: A Multi-Site Proof-of-Concept Study.

Biological psychiatry·2026

Connectome-based modeling of the suicidal brain: neurobiological substrates, clinical translation and future perspectives.

Biological psychiatry·2026

Cannabis Use and Age-Related Acceleration of Psychosis Onset: A Meta-Analysis.

Biological psychiatry·2026

Normative Modeling of sgACC-DLPFC Functional Connectivity Identifies a Personalized rTMS Target Associated with Clinical Response in Major Depressive Disorder.

Biological psychiatry·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

Biological phenotypes in the genetics of schizophrenia

Related Concept Videos

Species-specific thermal classification schemes can improve climate related marine resource decisions.

A compact high-performance low-field NMR apparatus for measurements on fluids at very high pressures and temperatures.

Long-term beneficial effects of adrenal medullary autografts supported by nerve growth factor in Parkinson's disease.

Receiving enzyme replacement therapy for a lysosomal storage disorder: a preliminary exploration of the experiences of young patients and their families.

A comment on 'social and economic factors in Hong Kong's fertility decline' by Sui-Ying Wat and R. W. Hodge.

Recent fertility declines in Hong Kong: the role of the changing age structure.

Diversity of Layer 3 Pyramidal Neuron Properties Across Areas of the Primate Neocortex.

Genetic liability to addiction underlies comorbid bipolar and substance use disorders.

Machine Learning-Based Discrimination of Treatment-Resistant Schizophrenia Using Structural Brain Imaging: A Multi-Site Proof-of-Concept Study.

Connectome-based modeling of the suicidal brain: neurobiological substrates, clinical translation and future perspectives.

Cannabis Use and Age-Related Acceleration of Psychosis Onset: A Meta-Analysis.

Normative Modeling of sgACC-DLPFC Functional Connectivity Identifies a Personalized rTMS Target Associated with Clinical Response in Major Depressive Disorder.

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

Biological phenotypes in the genetics of schizophrenia

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