Qiaoyu Y. Cao

399 Wanyuan Road
Shanghai, 201102, China

Last Updated: 09/26/2026

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Found 31 publications

PTPN11 variants in four Chinese patients: a case series and genotype-phenotype analysis.

PTPN11 variants in four Chinese patients: a case series and genotype-phenotype analysis.

Journal: European journal of dermatology : EJD

Published: August 31, 2026

Overlapping Xp21.2 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.

Overlapping Xp21.2 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.

Journal: American journal of human genetics

Published: August 18, 2026

Alopecia Areata Associated With a Dominant AIRE Variant.

Alopecia Areata Associated With a Dominant AIRE Variant.

Journal: The Journal of dermatology

Published: June 19, 2026

Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort.

Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort.

Journal: The British journal of dermatology

Published: May 08, 2026

Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.

Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.

Journal: American journal of human genetics

Published: April 03, 2026

Six cases of ectopic cutaneous ossification associated with GNAS gene variants.

Six cases of ectopic cutaneous ossification associated with GNAS gene variants.

Journal: European journal of dermatology : EJD

Published: September 18, 2025

A Child with Cutaneous-Skeletal Hypophosphatemia Syndrome Caused by a Mosaic HRAS Mutation: Outcome of Treatment with Anti-FGF23 Antibody.

A Child with Cutaneous-Skeletal Hypophosphatemia Syndrome Caused by a Mosaic HRAS Mutation: Outcome of Treatment with Anti-FGF23 Antibody.

Journal: Calcified tissue international

Published: January 07, 2025

SERPINA12 variants harboured in Nagashima-type palmoplantar keratoderma: Potential inflammatory characteristics.

SERPINA12 variants harboured in Nagashima-type palmoplantar keratoderma: Potential inflammatory characteristics.

Journal: Journal of dermatological science

Published: January 07, 2025

Effective therapy with simvastatin compound ointment in palmoplantar keratoderma induced by lanosterol synthase (LSS) gene variants.

Effective therapy with simvastatin compound ointment in palmoplantar keratoderma induced by lanosterol synthase (LSS) gene variants.

Journal: The British journal of dermatology

Published: September 29, 2024

Variations in RASA1 and EPHB4 in Chinese patients with capillary malformation-arteriovenous malformation.

Variations in RASA1 and EPHB4 in Chinese patients with capillary malformation-arteriovenous malformation.

Journal: The Journal of dermatology

Published: July 15, 2024

Large-Scale Cohort Study on the Genetic and Phenotypic Findings of Palmoplantar Keratodermas in the Chinese Population.

Large-Scale Cohort Study on the Genetic and Phenotypic Findings of Palmoplantar Keratodermas in the Chinese Population.

Journal: Experimental dermatology

Published: May 15, 2024

GLMN variants cause skin hyperpigmentation: a promising potential therapeutic target.

GLMN variants cause skin hyperpigmentation: a promising potential therapeutic target.

Journal: The British journal of dermatology

Published: February 29, 2024

Showing 1-12 of 31

Last Updated: 09/26/2026