World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
55
Citations
11861
World Ranking
14973
National Ranking
6264

Overview

Cynthia J. Curry is affiliated with the University of California, San Francisco, in the United States. Their research spans multiple scientific disciplines, primarily focusing on areas within medicine, biochemistry, genetics and molecular biology, and materials science.

Their work includes contributions to the following main fields of study:

  • Medicine
  • Biochemistry, Genetics and Molecular Biology
  • Materials Science

Within these broader fields, they have focused on specific subfields, including:

  • Surgery
  • Molecular Biology
  • Biomaterials

Their research addresses major topics such as:

  • Peripheral Artery Disease Management
  • Angiogenesis and VEGF in Cancer
  • Electrospun Nanofibers in Biomedical Applications

A notable publication by Cynthia J. Curry is:

  • Growth factor free, peptide-functionalized gelatin hydrogel promotes arteriogenesis and attenuates tissue damage in a murine model of critical limb ischemia, 2023, Biomaterials

This publication reflects the application of biomaterial science in therapeutic contexts related to vascular and tissue regeneration.

Frequent collaborators with Curry include:

  • Sarah M. Sturgeon
  • Brian J. O'Grady
  • A K Yates
  • Andrew Kjar
  • Hayden Paige

Their research has appeared primarily in the journal Biomaterials, indicating a focus on interdisciplinary approaches involving material sciences and their biomedical applications.

Best Publications

  • Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome

    Marco Tartaglia;Len A Pennacchio;Len A Pennacchio;Chen Zhao;Kamlesh K Yadav

  • Evaluation of mental retardation: Recommendations of a consensus conference

    Cynthia J. Curry;Roger E. Stevenson;David Aughton;Janice Byrne

  • Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication

    Megan Y. Dennis;Xander Nuttle;Peter H. Sudmant;Francesca Antonacci

  • Mutations in the Pericentrin (PCNT) Gene Cause Primordial Dwarfism

    Anita Rauch;Christian T. Thiel;Detlev Schindler;Ursula Wick

  • A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases

    Shinya Yamamoto;Manish Jaiswal;Wu Lin Charng;Tomasz Gambin

  • Tenascin–X deficiency is associated with Ehlers–Danlos syndrome

    Grant H. Burch;Yan Gong;Wenhui Liu;Robert W. Dettman

  • WNT1 Mutations in Early-onset Osteoporosis and Osteogenesis Imperfecta

    Christine M. Laine;Kyu Sang Joeng;Philippe M. Campeau;Riku Kiviranta

  • Maternal medications and environmental exposures as risk factors for gastroschisis

    Claudine P. Torfs;Elizabeth A. Katz;Thomas F. Bateson;Phung K. Lam

  • Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

    Jennifer J. Johnston;Isabelle Olivos-Glander;Christina Killoran;Emma Elson

  • Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm.

    Alexander J Doyle;Alexander J Doyle;Alexander J Doyle;Jefferson J Doyle;Seneca L Bessling;Samantha Maragh;Samantha Maragh

  • Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

    Margaret J McMillin;Anita E Beck;Anita E Beck;Jessica X Chong;Kathryn M Shively

  • Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development

    Ashley L. Lennox;Mariah L. Hoye;Ruiji Jiang;Bethany L. Johnson-Kerner

  • Macrocephaly‐Cutis marmorata telangiectatica congenita: A distinct disorder with developmental delay and connective tissue abnormalities

    Cynthia A. Moore;Helga V. Toriello;Dianne N. Abuelo;Marilyn J. Bull

  • Mutations in PIK3R1 Cause SHORT Syndrome

    David A. Dyment;Amanda C. Smith;Diana Alcantara;Jeremy A. Schwartzentruber

  • Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature

    D. R. Witt;H. E. Hoyme;J. Zonana;D. K. Manchester

  • ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.

    Scott E. Hickey;Cynthia J. Curry;Helga V. Toriello

  • Schizencephaly: heterogeneous etiologies in a population of 4 million California births.

    Cynthia J. Curry;Edward J. Lammer;Verne Nelson;Gary M. Shaw

  • PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution

    Ghayda Mirzaa;Andrew E. Timms;Valerio Conti;Evan August Boyle

  • Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28.

    Karen W. Gripp;Cynthia Curry;Ann Haskins Olney;Claudio Sandoval

  • Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

    Jennifer J. Johnston;Julie C. Sapp;Joyce T. Turner;David Amor

Frequent Co-Authors

William B. Dobyns
William B. Dobyns University of Minnesota
John M. Graham
John M. Graham Cedars-Sinai Medical Center
Raoul C.M. Hennekam
Raoul C.M. Hennekam University of Amsterdam
Ian A. Glass
Ian A. Glass University of Washington
A. Micheil Innes
A. Micheil Innes University of Calgary
Kym M. Boycott
Kym M. Boycott Children's Hospital of Eastern Ontario
Jill A. Rosenfeld
Jill A. Rosenfeld Baylor College of Medicine
David A. Dyment
David A. Dyment University of Ottawa
Elaine H. Zackai
Elaine H. Zackai Children's Hospital of Philadelphia
Hakon Hakonarson
Hakon Hakonarson Children's Hospital of Philadelphia

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