Yuhua Pan

P.R. China
Guangzhou, 510000, China

Last Updated: 09/26/2026

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Found 20 publications

Identification of a rare missense variant in the gene SPATA31H1 associated with hereditary gingival fibromatosis in a large Chinese family.

Identification of a rare missense variant in the gene SPATA31H1 associated with hereditary gingival fibromatosis in a large Chinese family.

Journal: BMC oral health

Published: August 29, 2025

Abemaciclib-associated kidney injuries: A retrospective analysis of the United States Food and Drug Administration adverse events reporting system.

Abemaciclib-associated kidney injuries: A retrospective analysis of the United States Food and Drug Administration adverse events reporting system.

Journal: The Journal of international medical research

Published: March 21, 2025

A novel phex gene variant causes non-syndromic tooth agenesis.

A novel phex gene variant causes non-syndromic tooth agenesis.

Journal: BMC oral health

Published: February 25, 2025

Novel compound heterozygous variants in TGM1 with the lethal neonatal collodion baby and autosomal recessive congenital ichthyosis.

Novel compound heterozygous variants in TGM1 with the lethal neonatal collodion baby and autosomal recessive congenital ichthyosis.

Journal: Archives of dermatological research

Published: December 17, 2024

The dominant negative mutation of PAX9 in nonsyndromic tooth agenesis.

The dominant negative mutation of PAX9 in nonsyndromic tooth agenesis.

Journal: Clinical oral investigations

Published: April 10, 2024

Tumor-to-stroma cd8+ t cells ratio combined with cancer-associated fibroblasts: an innovative approach to predicting lymph node metastases of cervical cancer.

Tumor-to-stroma cd8+ t cells ratio combined with cancer-associated fibroblasts: an innovative approach to predicting lymph node metastases of cervical cancer.

Journal: Journal of cancer research and clinical oncology

Published: October 08, 2023

A novel APC mutation associated with Gardner syndrome in a Chinese family.

A novel APC mutation associated with Gardner syndrome in a Chinese family.

Journal: Gene

Published: September 11, 2023

A comprehensively prognostic and immunological analysis of chloride intracellular channel protein 5 (CLIC5) in pan-cancer and identification in ovarian cancer.

A comprehensively prognostic and immunological analysis of chloride intracellular channel protein 5 (CLIC5) in pan-cancer and identification in ovarian cancer.

Journal: Journal of cancer research and clinical oncology

Published: March 21, 2023

Effectiveness of telehealth interventions on depression symptoms after stroke: A systematic review and meta-analysis.

Effectiveness of telehealth interventions on depression symptoms after stroke: A systematic review and meta-analysis.

Journal: Journal of affective disorders

Published: November 30, 2022

A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia.

A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia.

Journal: European journal of oral sciences

Published: July 25, 2022

Identification of a novel missense heterozygous mutation in the KDF1 gene for non-syndromic congenital anodontia.

Identification of a novel missense heterozygous mutation in the KDF1 gene for non-syndromic congenital anodontia.

Journal: Clinical oral investigations

Published: January 25, 2022

Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia.

Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia.

Journal: Frontiers in pediatrics

Published: September 14, 2021

Showing 1-12 of 20

Last Updated: 09/26/2026