Haozheng Zhang

Jinan, China

Last Updated: 09/26/2026

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Found 11 publications

Detection of pathogenic novel intronic splicing variants in the KIDINS220 gene causes motor developmental delay.

Detection of pathogenic novel intronic splicing variants in the KIDINS220 gene causes motor developmental delay.

Journal: Artificial cells, nanomedicine, and biotechnology

Published: January 12, 2026

Low expression of MKRN1 promotes leukemia cell proliferation.

Low expression of MKRN1 promotes leukemia cell proliferation.

Journal: European journal of medical research

Published: April 10, 2025

Clinical and genetic characteristics of a case of Koolen-De Vries syndrome caused by KANSL1 gene mutation and literature review: A case report.

Clinical and genetic characteristics of a case of Koolen-De Vries syndrome caused by KANSL1 gene mutation and literature review: A case report.

Journal: Medicine

Published: December 10, 2024

Loss of Cep135 causes oligoasthenoteratozoospermia and male infertility in mice.

Loss of Cep135 causes oligoasthenoteratozoospermia and male infertility in mice.

Journal: Cellular and molecular life sciences : CMLS

Published: October 21, 2024

Intron Variant Cause DICER1 Syndrome With Pleuropulmonary Blastoma.

Intron Variant Cause DICER1 Syndrome With Pleuropulmonary Blastoma.

Journal: Human mutation

Published: August 02, 2024

Potential role of ARG1 c.57G > A variant in Argininemia.

Potential role of ARG1 c.57G > A variant in Argininemia.

Journal: Genes & genomics

Published: June 20, 2024

Generation of a transgene-free Induced pluripotent stem (iPS) cell line (JNCHi002-A) from a female heterozygous carrier of the low density lipoprotein receptor (LDLR) gene mutation (c.387delC).

Generation of a transgene-free Induced pluripotent stem (iPS) cell line (JNCHi002-A) from a female heterozygous carrier of the low density lipoprotein receptor (LDLR) gene mutation (c.387delC).

Journal: Stem cell research

Published: May 12, 2024

Clinical feature and genetic mutation of KBG syndrome diagnosed in neonatal period: A case report.

Clinical feature and genetic mutation of KBG syndrome diagnosed in neonatal period: A case report.

Journal: Medicine

Published: October 06, 2023

Combination of Synonymous and Missense Mutations in JAK3 Gene Contributes to Severe Combined Immunodeficiency in One Child.

Combination of Synonymous and Missense Mutations in JAK3 Gene Contributes to Severe Combined Immunodeficiency in One Child.

Journal: Human mutation

Published: June 14, 2023

Clinical and genetic features of luscan-lumish syndrome associated with a novel de novo variant of SETD2 gene: Case report and literature review.

Clinical and genetic features of luscan-lumish syndrome associated with a novel de novo variant of SETD2 gene: Case report and literature review.

Journal: Frontiers in genetics

Published: October 27, 2022

A synonymous mutation in PI4KA impacts the transcription and translation process of gene expression.

A synonymous mutation in PI4KA impacts the transcription and translation process of gene expression.

Journal: Frontiers in immunology

Published: July 06, 2022

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Last Updated: 09/26/2026