Wenying Zhang

department of pediatrics university of cincinnati college of medicine cincinnati ohio usa

United States

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Articles (18)

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2025

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2025

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2021

Collaborators (5)

Kimberly Gilmour

Clinical Lead and Director of Cell Therapy and Chief of Laboratory Medicine

Great Ormond Street Institute of Child Health

UNITED KINGDOM

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margaret collins

University of Cincinnati College of Medicine

UNITED STATES

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Theodosia Kalfa

Professor

Cincinnati Children's Hospital Medical Center

UNITED STATES

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Alexandra Demcsak

Adjunct Assistant Professor

University of California, Los Angeles

UNITED STATES

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Miklós Sahin-Tóth

Professor

University of California, Los Angeles

UNITED STATES

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Wenying Zhang

Research Interests

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Articles (18)

Advances on the genetic basis of red cell membrane disorders.

Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variants.

The phenotypic spectrum of the Cornelia de Lange-like "Alazami-Yuan syndrome": A case report of the 7th diagnosed individual and review of the literature.

Case Report: A novel missense variant in <i>ZC4H2</i>, c.196C>T p.(Leu66Phe), is associated with a mild, ZC4H2-related X-linked syndromic intellectual disability (ZARD) phenotype.

Case report: Childhood erythrocytosis due to hypermanganesemia caused by homozygous SLC30A10 mutation

Detection of a novel gross deletion in the UNC13D gene ends the diagnostic odyssey for a family with familial hemophagocytic lymphohistiocytosis 3.

Novel chymotrypsin C (CTRC) variants from real-world genetic testing of pediatric chronic pancreatitis cases

Clinical, Immunologic, and Genetic Characteristics in Patients With Syndrome of Undifferentiated Recurrent Fevers.

Genetic Testing in Patients with Autoimmune Lymphoproliferative Syndrome: Experience of 802 Patients at Cincinnati Children's Hospital Medical Center.

The Role of Pancreatitis Risk Genes in Endocrine Insufficiency Development After Acute Pancreatitis in Children.

Hemolytic anemia and macrothrombocytopenia: A lipid problem?

Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group.

RNA sequencing reveals a complete picture of a homozygous missense variant in a patient with VPS13D movement disorder: a case report and review of the literature.

Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.

Desmoplakin and periplakin genetically and functionally contribute to eosinophilic esophagitis

Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center.

Combining whole exome sequencing with in silico analysis and clinical data to identify candidate variants in pediatric left ventricular noncompaction.

Epilepsy phenotypes associated with MAP1B-related brain malformations.

Collaborators (5)

Kimberly Gilmour

margaret collins

Theodosia Kalfa

Alexandra Demcsak

Miklós Sahin-Tóth

Make your next move.

Wenying Zhang

Research Interests

Explore related searches

Contact this professor

Articles (18)

Advances on the genetic basis of red cell membrane disorders.

Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variants.

The phenotypic spectrum of the Cornelia de Lange-like "Alazami-Yuan syndrome": A case report of the 7th diagnosed individual and review of the literature.

Case Report: A novel missense variant in &lt;i&gt;ZC4H2&lt;/i&gt;, c.196C&gt;T p.(Leu66Phe), is associated with a mild, ZC4H2-related X-linked syndromic intellectual disability (ZARD) phenotype.

Case report: Childhood erythrocytosis due to hypermanganesemia caused by homozygous SLC30A10 mutation

Detection of a novel gross deletion in the UNC13D gene ends the diagnostic odyssey for a family with familial hemophagocytic lymphohistiocytosis 3.

Novel chymotrypsin C (CTRC) variants from real-world genetic testing of pediatric chronic pancreatitis cases

Clinical, Immunologic, and Genetic Characteristics in Patients With Syndrome of Undifferentiated Recurrent Fevers.

Genetic Testing in Patients with Autoimmune Lymphoproliferative Syndrome: Experience of 802 Patients at Cincinnati Children's Hospital Medical Center.

The Role of Pancreatitis Risk Genes in Endocrine Insufficiency Development After Acute Pancreatitis in Children.

Hemolytic anemia and macrothrombocytopenia: A lipid problem?

Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group.

RNA sequencing reveals a complete picture of a homozygous missense variant in a patient with VPS13D movement disorder: a case report and review of the literature.

Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.

Desmoplakin and periplakin genetically and functionally contribute to eosinophilic esophagitis

Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center.

Combining whole exome sequencing with in silico analysis and clinical data to identify candidate variants in pediatric left ventricular noncompaction.

Epilepsy phenotypes associated with MAP1B-related brain malformations.

Collaborators (5)

Kimberly Gilmour

margaret collins

Theodosia Kalfa

Alexandra Demcsak

Miklós Sahin-Tóth

Make your next move.

Case Report: A novel missense variant in <i>ZC4H2</i>, c.196C>T p.(Leu66Phe), is associated with a mild, ZC4H2-related X-linked syndromic intellectual disability (ZARD) phenotype.