Author

Yangzhu Du

Observed names: Y Du, Y. Du, Yang-Zhu Du

Observed institutions: National Institutes of Health, Children's Hospital of Philadelphia, University of Helsinki, Philipps University of Marburg, University of Toronto, Wayne State University, Washington University in St. Louis, Hospital for Sick Children, National Human Genome Research Institute, Essen University Hospital, Philadelphia VA Medical Center, Greenwood Genetic Center, New York University, Case Western Reserve University, University of Pennsylvania

ORCID: 0000-0002-1471-8692

Observed ORCID: 0000-0002-1471-8692

OpenAlex ID: A5043676273

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

2003 · Erich Roessler, Yang-Zhu Du, et al. · Proceedings of the National Academy of Sciences · 348

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

1997 · Anand K. Srivastava, Johanna Pispa, et al. · Proceedings of the National Academy of Sciences · 310

SHH mutation is associated with solitary median maxillary central incisor: A study of 13 patients and review of the literature

2001 · Luisa Nanni, Jeffrey E. Ming, et al. · American Journal of Medical Genetics · 173

Variation in Resistin Gene Promoter Not Associated With Polycystic Ovary Syndrome

2003 · Margrit Urbanek, Yangzhu Du, et al. · Diabetes · 85

A longitudinal analysis of SLE patients treated with rituximab (anti-CD20): Factors associated with B lymphocyte recovery

2008 · Jennifer A. Sutter, Jennifer Kwan-Morley, et al. · Clinical Immunology · 62

The concentration of fetal red blood cells in first-trimester pregnant women undergoing uterine aspiration is below the calculated threshold for Rh sensitization

2020 · Sarah Horvath, Patricia Tsao, et al. · Contraception · 46

Regional Localization of 725 Human Chromosome 7-Specific Yeast Artificial Chromosome Clones

1994 · Jürgen Kunz, Stephen W. Scherer, et al. · Genomics · 39

Circulating B cells in type 1 diabetics exhibit fewer maturation-associated phenotypes

2017 · Patrick Hanley, Jennifer A. Sutter, et al. · Clinical Immunology · 37

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The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephaly

2000 · E. Roessler, Y. Du, et al. · Cytogenetic and Genome Research · 27

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Exogenous and Endogenous TLR Ligands Activate Anti-Chromatin and Polyreactive B Cells

2006 · Michele L Fields, Michele H Metzgar, et al. · The Journal of Immunology · 24

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Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform

2020 · Guy Helman, Asako Takanohashi, et al. · Human Mutation · 23

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Duffy antigen receptor and genetic susceptibility of African Americans to acute rejection and delayed function

2004 · Kevin C. Mange, Eline Luning Prak, et al. · Kidney International · 22

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Multiple exon screening using restriction endonuclease fingerprinting (REF): Detection of six novel mutations in the L1 cell adhesion molecule (L1CAM) gene

1998 · Yang-Zhu Du, Anand K. Srivastava, et al. · Human Mutation · 20

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Structure of the human Lanosterol Synthase gene and its analysis as a candidate for holoprosencephaly ( HPE1 )

1999 · E. Roessler, L. Mittaz, et al. · Human Genetics · 14

Membrane association and destabilization by A ggregatibacter actinomycetemcomitans leukotoxin requires changes in secondary structures

2013 · M.J. Walters, A.C. Brown, et al. · Molecular Oral Microbiology · 11

Loss-of-function mutations in the human GLI2 gene cause holoprosencephaly and familial pan-hypopituitarism

2002 · Erich Roessler, Yangzhu Du, et al. · 5

Retinol Binding Protein 4 reactivates latent HIV-1 by triggering canonical NF-κB, JAK/STAT5 and JNK signalling

2025 · Chiara Pastorio, Khumoekae Richard, et al. · Signal Transduction and Targeted Therapy · 4

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Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform

2022 · Guy Helman, Asako Takanohashi, et al. · Human Mutation · 1

Identification of Retinal Proteins that are Nitrated in Elevated Glucose Concentration

2003 · Yangzhu Du, Masaru Miyagi, et al. · Investigative Ophthalmology & Visual Science · 1

Retinol Binding Protein 4 reactivates latent HIV-1 via the JAK/STAT5 and JNK pathways

2025 · Chiara Pastorio, Khumoekae Richard, et al. · bioRxiv (Cold Spring Harbor Laboratory)

Graft-Versus-Host Disease (GVHD) and Senescence-Associated Biomarkers Correlate with Frailty and Survival in Older Adults Undergoing Hematopoietic Cell Transplantation (HCT)

2025 · Ashley D. Hadjis, Honghong Sun, et al. · Transplantation and Cellular Therapy

Structural basis of PTPN18 fingerprint on distinct HER2 tyrosine phosphorylation sites

2013 · H. Wang, F. Yang, et al. · Worldwide Protein Data Bank

Mechanisms of autoimmunity in mice lacking the mer membrane tyrosine kinase

2004 · PL Cohen, Y Du, et al. · Arthritis Research

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Works count: 23

Citation count: 1,252

H-index: 14

I10-index: 15