Cheryl R. Greenberg

Manitoba Health — Canada

Biochemistry, Genetics and Molecular Biology · Life Sciences

65h-index16.3kcitations709works3.42yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Metabolism and Genetic Disorders(74), Alkaline Phosphatase Research Studies(68), Biochemical and Molecular Research(46), Mitochondrial Function and Pathology(38), Muscle Physiology and Disorders(26)

Publications512 total

The Global Hypophosphatasia Registry: lessons learned from a decade of real-world data
Orphanet Journal of Rare Diseases·2025· 1 citedOpen Access
Correspondence on “Mainstreaming of clinical genetic testing: a conceptual framework” by Mackley et al
Genetics in Medicine·2025Open Access
SUN-741 Bone Mineral Density in Adults With Hypophosphatasia With or Without History of Fractures
Journal of the Endocrine Society·2025Open Access
Biochemical phenotype of hypophosphatasia in asymptomatic individuals carrying <i>ALPL</i> variants
Journal of Bone and Mineral Research·2025· 4 citedOpen Access
Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study
JIMD Reports·2025Open Access
Reprogramming of peripheral blood mononuclear cells from a patient with hypophosphatasia to generate iPSC line (UOMi011-A)
Stem Cell Research·2025Open Access
Generation of a new human iPSC cell line (UOMi010-A) from a patient with hypophosphatasia
Stem Cell Research·2025Open Access
Cognitive decline in an adult with ATR-16 syndrome due to an unbalanced translocation between 11p15.5 and 16p13.3: a case report
Frontiers in Genetics·2025Open Access
Patient-reported outcomes and quality of life in children and adults with hpp treated with asfotase alfa
Endocrine Abstracts·2025
The ALPL gene variant project: results of the first 100 reclassified variants
JBMR Plus·2025· 6 citedOpen Access
Two rare mutations in homozygosity synergize to silence TREX1 in Aicardi-Goutières syndrome
Frontiers in Immunology·2025· 1 citedOpen Access
Disease burden by <i>ALPL</i> variant number in patients with non-life-threatening hypophosphatasia in the Global HPP Registry
Journal of Medical Genetics·2025· 5 citedOpen Access
Coaching Physician Resilience
2024
Longitudinal analysis of culture of patient safety survey results in surgical departments
UNC Libraries·2024Open Access
Review of clinical trials and guidelines for children and youth with mucopolysaccharidosis: outcome selection and measurement
Orphanet Journal of Rare Diseases·2024· 3 citedOpen Access
New insights into the landscape of <i>ALPL</i> gene variants in patients with hypophosphatasia from the Global <scp>HPP</scp> Registry
American Journal of Medical Genetics Part A·2024· 13 citedOpen Access
Professor Philippe Crine: a hero for children with hypophosphatasia
Journal of Bone and Mineral Research·2024Open Access
Co-developing longitudinal patient registries for phenylketonuria and mucopolysaccharidoses in Canada
Molecular Genetics and Metabolism·2024
Correction: Hypophosphatasia diagnosis: current state of the art and proposed diagnostic criteria for children and adults
Osteoporosis International·2024· 1 citedOpen Access
Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry
Orphanet Journal of Rare Diseases·2024· 27 citedOpen Access
page 1 of 26Next →

Frequent Co-authors

Klaus Wrogemann(8), Michael R. Hayden(5), Georg F. Hoffmann(5), Edward Nylen(5), Alberto Burlina(4), Michael P. Whyte(4), Stefan Kölker(4), Stephen I. Goodman(4), David M. Koeller(4), Peter Burgard(4), Tracey Weiler(4), Jorge R. Toro(3), G.M. Glenn(3), Maria L. Turner(3), Paul H. Duray(3), Maria J. Merino(3), Christian P. Pavlovich(3), W. Marston Linehan(3), Berton Zbar(3), James V. Leonard(3)