Haplotype analysis of distantly related populations implicates corneodesmosin in psoriasis susceptibility

[Genetic counselling and testing in pulmonary arterial hypertension - A consensus statement on behalf of the International Consortium for Genetic Studies in PAH - French version].

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MC3R links nutritional state to childhood growth and the timing of puberty.

Nature·2021

Anakinra for palmoplantar pustulosis: results from a randomized, double-blind, multicentre, two-staged, adaptive placebo-controlled trial (APRICOT).

The British journal of dermatology·2021

Risk-mitigating behaviours in people with inflammatory skin and joint disease during the COVID-19 pandemic differ by treatment type: a cross-sectional patient survey.

The British journal of dermatology·2020

Prenatal exposure to maternal cigarette smoking and structural properties of the human corpus callosum.

NeuroImage·2019

A standardization approach to compare treatment safety and effectiveness outcomes between clinical trials and real-world populations in psoriasis.

The British journal of dermatology·2019

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

Association between miR-21 polymorphism and the risk of primary dental caries in preschool children.

Odontology·2026

Beyond gene editing: the age of chromosome-scale genome engineering.

Trends in genetics : TIG·2026

Metabolic syndrome risk occurs at relatively low adiposity levels in Korean adults.

Nutrition research (New York, N.Y.)·2026

Deconvolving DNA mixtures with Demixtify.

Forensic science international. Genetics·2026

Insulin resistance mediates the relationship between cardiovascular-kidney-metabolic syndrome and depression: A cross-sectional analysis.

Heart & lung : the journal of critical care·2026

Ras-MAPK somatic variants in mesial temporal lobe epilepsy.

Current opinion in genetics & development·2026

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Haplotype analysis of distantly related populations implicates corneodesmosin in psoriasis susceptibility

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[Genetic counselling and testing in pulmonary arterial hypertension - A consensus statement on behalf of the International Consortium for Genetic Studies in PAH - French version].

MC3R links nutritional state to childhood growth and the timing of puberty.

Anakinra for palmoplantar pustulosis: results from a randomized, double-blind, multicentre, two-staged, adaptive placebo-controlled trial (APRICOT).

Risk-mitigating behaviours in people with inflammatory skin and joint disease during the COVID-19 pandemic differ by treatment type: a cross-sectional patient survey.

Prenatal exposure to maternal cigarette smoking and structural properties of the human corpus callosum.

A standardization approach to compare treatment safety and effectiveness outcomes between clinical trials and real-world populations in psoriasis.

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.

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

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

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

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

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

Association between miR-21 polymorphism and the risk of primary dental caries in preschool children.

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