Huifang Z. Peng

Luoyang Key Laboratory Of Clinical Multiomics And Translational Medicine, Key Laboratory Of Hereditary Rare Diseases Of Health Commission Of Henan Province, Henan Key Laboratory Of Rare Diseases
Luoyang, China

Last Updated: 09/26/2026

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Found 37 publications

The Pathogenicity Analysis of a Hypogonadotropic Hypogonadism Patient With the Novel Variant in the Deep Intronic Region of the PROK2 Gene.

The Pathogenicity Analysis of a Hypogonadotropic Hypogonadism Patient With the Novel Variant in the Deep Intronic Region of the PROK2 Gene.

Journal: Molecular genetics & genomic medicine

Published: January 19, 2026

Case Report: Efficacy and safety of SGLT2 inhibitors in patients with Alström syndrome: a follow-up report of two siblings from the same family.

Case Report: Efficacy and safety of SGLT2 inhibitors in patients with Alström syndrome: a follow-up report of two siblings from the same family.

Journal: Frontiers in endocrinology

Published: January 11, 2026

Functional validation of a non-canonical HNF1B splice-site variant in MODY5.

Functional validation of a non-canonical HNF1B splice-site variant in MODY5.

Journal: Frontiers in endocrinology

Published: December 29, 2025

Metabolomics identifies chenodeoxycholic acid as a protective factor in diabetic foot ulcers.

Metabolomics identifies chenodeoxycholic acid as a protective factor in diabetic foot ulcers.

Journal: Frontiers in endocrinology

Published: November 27, 2025

Rare variants in FAT3 as possible contributors to non-syndromic orofacial cleft risk.

Rare variants in FAT3 as possible contributors to non-syndromic orofacial cleft risk.

Journal: Human genomics

Published: November 17, 2025

Tumor-Derived Exosomal TAGLN2 Promotes Metastasis by Inducing Vascular Permeability and Angiogenesis via the NRP1/SEMA4D/YAP Axis.

Tumor-Derived Exosomal TAGLN2 Promotes Metastasis by Inducing Vascular Permeability and Angiogenesis via the NRP1/SEMA4D/YAP Axis.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: November 02, 2025

Correction: A systematic review and evidence assessment of monogenic gene-disease relationships in human male infertility.

Correction: A systematic review and evidence assessment of monogenic gene-disease relationships in human male infertility.

Journal: Frontiers in endocrinology

Published: August 29, 2025

HER2 deficiency causes a developmental disorder with growth retardation and craniofacial malformations.

HER2 deficiency causes a developmental disorder with growth retardation and craniofacial malformations.

Journal: The Journal of clinical investigation

Published: August 12, 2025

The Xenopus model as a tool for investigating craniofacial developmental disorders.

The Xenopus model as a tool for investigating craniofacial developmental disorders.

Journal: Frontiers in medicine

Published: July 23, 2025

Endocrine metabolism characteristics of Alström syndrome in 25 Chinese patients and identification of a new splice site in the ALMS1 gene.

Endocrine metabolism characteristics of Alström syndrome in 25 Chinese patients and identification of a new splice site in the ALMS1 gene.

Journal: Diabetology & metabolic syndrome

Published: July 11, 2025

Gene therapy for disorders of sex development: current applications and future challenges.

Gene therapy for disorders of sex development: current applications and future challenges.

Journal: Frontiers in genetics

Published: July 07, 2025

A systematic review and evidence assessment of monogenic gene-disease relationships in human male infertility.

A systematic review and evidence assessment of monogenic gene-disease relationships in human male infertility.

Journal: Frontiers in endocrinology

Published: June 09, 2025

Showing 1-12 of 37

Last Updated: 09/26/2026