Wenying Zhang - Cincinnati Childrens Hosp Med Ctr, Univ Cincinnati

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论文共 30 篇作者统计合作学者相似作者

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

Tiziana Coppola, Hannah Hughes,Paul T. Finch,Joshua A. Hess,Steve Wu,Steve Wu,Carlos E. Prada,Carlos E. Prada,Alexander G. Miethke,Alexander G. Miethke,Wenying Zhang,Wenying Zhang,Theodosia A. Kalfa,Theodosia A. Kalfa

Frontiers in Hematology (2024)

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Erythrocyte Disorders Mimicking Congenital Dyserythropoietic Anemia Based on Bone Marrow Pathology Exposed by Genetic Evaluation

Jacopo Ceolan,Katie Seu, Athina Ntoumaziou,Yasmin Elgammal,Sana Emberesh,Lisa Bilston, Donald Richards,Kathryn E. Dickerson,Satheesh Chonat,Natalia Rydz,Carolyn Lutzko,Ammar Husami,Wenying Zhang,Theodosia A. Kalfa

Bloodno. Supplement 1 (2023): 2459-2459

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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

Elizabeth K. Baker,Jingfen Han, William A. Langley, Michael A. Reott Jr.,Barbara E. Hallinan,Robert J. Hopkin,Wenying Zhang

Molecular genetics and genomics : MGGno. 5 (2023): 1185-1199

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Hemolytic anemia and macrothrombocytopenia: A lipid problem

Mary Risinger, Phyllis S. S. Kim, Roberto X. X. Rodriguez,Monica Narvaez Rivas,Kenneth D. R. Setchell,Wenying Zhang,Theodosia A. A. Kalfa

AMERICAN JOURNAL OF HEMATOLOGYno. 8 (2023): 1335-1340

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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

Elizabeth K. Baker,Jingfen Han, William A. Langley, Michael A. Reott,Barbara E. Hallinan,Robert J. Hopkin,Wenying Zhang

Molecular Genetics and Genomicsno. 5 (2023): 1185-1199

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Investigating the Genetic Basis of SURFS and MAS Using An Exome Slice Approach

Michael Matt,Wenying Zhang,Elizabeth Baker,Alexei Grom,Rebecca Marsh,Grant Schulert

JOURNAL OF CLINICAL IMMUNOLOGY（2022）

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Impact of DNA methylation signature exploration for variants of uncertain significance within epigenetic syndromes

Olivia Gittens,Dima Qu'd,Leandra Tolusso,Diana Brightman,Jennifer Kerkhof,Joshua Owens,Howard Saal,Sofia Saenz Ayala,Amelle Shillington,Kimberly Widmeyer,Wenying Zhang,Jacqueline Harris,Matthew Tedder,Bekim Sadikovic,Robert Hopkin,Brittany Simpson

GENETICS IN MEDICINE（2022）

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De novo dhx38 variant associated with congenital dyserythropoietic anemia with ring sideroblasts

Aikaterini Voulgaridou,Ammar Husami,Sana Emberesh,Katie Seu,Lisa Trump,Nathaniel Barasa,Robert Lorsbach,Adam Nelson,Wenying Zhang,Carolyn Lutzko,Theodosia Kalfa

PEDIATRIC BLOOD & CANCER（2022）

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Clinical utility of a 38-gene NGS panel in diagnosing patients with hemolytic anemia: A retrospective review of 435 cases

Xiaolin Hu,Xinjian Wang,Qiaoning Guan,Yaning Wu,Jie Liu,Brian Dawson,Theodosia Kalfa,Wenying Zhang

Genetics in Medicineno. 3 (2022): S263-S263

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