Neuregulin 1: genetic support for schizophrenia subtypes

Cannabis use and cognitive biases in people with first-episode psychosis and their siblings.

Psychological medicine·2024

Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing.

Journal of the European Academy of Dermatology and Venereology : JEADV·2024

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.

Scientific reports·2017

Impact of deep brain stimulation of the ventral anterior limb of the internal capsule on cognition in depression.

Psychological medicine·2017

Subcortical volumetric abnormalities in bipolar disorder.

Molecular psychiatry·2016

Hostility in schizophrenia: An integrated analysis of the combined Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) and the European First Episode Schizophrenia Trial (EUFEST) studies.

European psychiatry : the journal of the Association of European Psychiatrists·2015

Psychedelics and astrocytes: a hypothesis-driven perspective on neuro-glial integration, network plasticity, and neuroimmune reprogramming.

Molecular psychiatry·2026

Molecular alterations in chondrolectin-containing somatostatin neurons in schizophrenia differ based on circuit context.

Molecular psychiatry·2026

Maternal NKG2D-mediated immune activation shapes fetal neural development.

Molecular psychiatry·2026

Neuroinflammation as molecular landscape of post-operative delirium revealed by live human brain multi-omics profiling.

Molecular psychiatry·2026

Accelerated DMN-targeted cTBS improves processing speed deficits in schizophrenia.

Molecular psychiatry·2026

The HDAC inhibitor sodium butyrate moderately enhances long-term fear extinction memory retrieval in humans.

Molecular psychiatry·2026

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Frontiers in genetics·2026

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

Frontiers in pediatrics·2026

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Seizure·2026

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Neuregulin 1: genetic support for schizophrenia subtypes

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Cannabis use and cognitive biases in people with first-episode psychosis and their siblings.

Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing.

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.

Impact of deep brain stimulation of the ventral anterior limb of the internal capsule on cognition in depression.

Subcortical volumetric abnormalities in bipolar disorder.

Hostility in schizophrenia: An integrated analysis of the combined Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) and the European First Episode Schizophrenia Trial (EUFEST) studies.

Psychedelics and astrocytes: a hypothesis-driven perspective on neuro-glial integration, network plasticity, and neuroimmune reprogramming.

Molecular alterations in chondrolectin-containing somatostatin neurons in schizophrenia differ based on circuit context.

Maternal NKG2D-mediated immune activation shapes fetal neural development.

Neuroinflammation as molecular landscape of post-operative delirium revealed by live human brain multi-omics profiling.

Accelerated DMN-targeted cTBS improves processing speed deficits in schizophrenia.

The HDAC inhibitor sodium butyrate moderately enhances long-term fear extinction memory retrieval in humans.

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

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Neuregulin 1: genetic support for schizophrenia subtypes

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