The heritability of high myopia: a reanalysis of Goldschmidt's data

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Molecular psychiatry·2018

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

Translational psychiatry·2017

Schizophrenia copy number variants and associative learning.

Molecular psychiatry·2016

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Molecular psychiatry·2016

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Molecular psychiatry·2016

Childhood febrile illness and the risk of myopia in UK Biobank participants.

Eye (London, England)·2016

Safety and efficacy of AAV-based mini- and micro-dystrophin gene therapies in Duchenne muscular dystrophy: a systematic review and meta-analysis of clinical trials.

Journal of medical genetics·2026

Phenotypic manifestations and variant reclassification of germline PTEN variants: a nationwide Danish study.

Journal of medical genetics·2026

Solid tumours in RASopathies: insights from a large monocentric cohort and systematic review of the literature.

Journal of medical genetics·2026

Hypertrophic cardiomyopathy: a genome-wide association meta-analysis and polygenic risk score.

Journal of medical genetics·2026

Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.

Journal of medical genetics·2026

Exploring the clinical and mutational spectrum of MORC2-associated disorders.

Journal of medical genetics·2026

The HEAT Repeat Protein MROH1 Deficiency Leads to Reduced Circulating Thyroid Hormone Levels in Mice.

Endocrinology, diabetes & metabolism·2026

Prenatal stress selectively enhances locomotor hyperactivity in male mice with embryonic loss of Fgfr2.

Frontiers in psychiatry·2026

Single-cell RNA sequencing in diabetic foot ulcers: pathogenesis, biomarkers, and translational potential.

Frontiers in clinical diabetes and healthcare·2026

KAT5: the epigenetic regulator of central nervous system diseases.

Frontiers in molecular neuroscience·2026

Genetic Regulation of DNA Methylation and Its Mediating Role in Blood Pressure: A Genome-Wide Twin Study.

MedComm·2026

Increased Risk of Gout among Patients with Trisomy 21: Insights from a Population-Based Study of over 30,000 Patients with Trisomy 21.

Mediterranean journal of rheumatology·2026

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The heritability of high myopia: a reanalysis of Goldschmidt's data

Related Concept Videos

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

Schizophrenia copy number variants and associative learning.

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

Childhood febrile illness and the risk of myopia in UK Biobank participants.

Safety and efficacy of AAV-based mini- and micro-dystrophin gene therapies in Duchenne muscular dystrophy: a systematic review and meta-analysis of clinical trials.

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Exome sequencing and large-scale analysis of electronic medical record-linked biobank data identify candidate deafness genes.

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The heritability of high myopia: a reanalysis of Goldschmidt's data

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