Melanie A. Jones

University of Leicester — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

20h-index1.5kcitations45works1.52yr avg
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Research Topics

Glycosylation and Glycoproteins Research(6), Genetics, Aging, and Longevity in Model Organisms(6), Neurobiology and Insect Physiology Research(4), Carbohydrate Chemistry and Synthesis(4), Cardiac electrophysiology and arrhythmias(3)

Publications45 total

Developing public health risk messages about antibiotic resistance using metaphors: An international co-design and e-Delphi consensus study
2025Open Access
Risk communication about antimicrobial resistance: a content analysis of metaphor use in global public discourse
Journal of Risk Research·2024· 3 citedOpen Access
The landscape of <scp><i>BRCA1</i></scp> and <scp><i>BRCA2</i></scp> large rearrangements in an international cohort of over 20 000 ovarian tumors identified using next‐generation sequencing
Genes Chromosomes and Cancer·2023· 5 citedOpen Access
Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader–Willi/Angelman syndromes?
Molecular Cytogenetics·2021· 3 citedOpen Access
Selection and Evaluation of Reference Genes for ddPCR-Based Transcript Abundance Studies in Oidiodendron Maius Across Varying Carbon Sources
Research Square (Research Square)·2021· 1 citedOpen Access
Erratum: Lessons from a pair of siblings with BPAN
European Journal of Human Genetics·2016· 6 citedOpen Access
Congenital Disorders of Glycosylation
2016· 1 cited
Lessons from a pair of siblings with BPAN
European Journal of Human Genetics·2015· 40 citedOpen Access
A Novel N-Tetrasaccharide in Patients with Congenital Disorders of Glycosylation, Including Asparagine-Linked Glycosylation Protein 1, Phosphomannomutase 2, and Mannose Phosphate Isomerase Deficiencies
Clinical Chemistry·2015· 63 citedOpen Access
Correction: Corrigendum: Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway
Genetics in Medicine·2014· 1 citedOpen Access
Genetic studies in <i>Drosophila</i> and humans support a model for the concerted function of <i>CISD2</i>, <i>PPT1</i> and <i>CLN3</i> in disease
Biology Open·2014· 12 citedOpen Access
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway
Genetics in Medicine·2014· 236 citedOpen Access
Molecular diagnostic testing for congenital disorders of glycosylation (CDG): Detection rate for single gene testing and next generation sequencing panel testing
Molecular Genetics and Metabolism·2013· 46 cited
Molecular Diagnosis of Congenital Disorders of Glycosylation (CDG)
2013· 2 cited
Mutations in the Glycosylphosphatidylinositol Gene PIGL Cause CHIME Syndrome
The American Journal of Human Genetics·2012· 124 citedOpen Access
DDOST Mutations Identified by Whole-Exome Sequencing Are Implicated in Congenital Disorders of Glycosylation
The American Journal of Human Genetics·2012· 75 citedOpen Access
Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation
Genetics in Medicine·2011· 90 citedOpen Access
Follicular lymphomas without t(14;18) chromosomal translocations exhibit variation in BCL2 protein expression
2011
Drosophila as a model for age-related impairment in locomotor and other behaviors
Experimental Gerontology·2010· 138 cited
Mechanisms Associated with Aging and Age-Related Disease in Drosophila
VCU Scholars Compass (Virginia Commonwealth University)·2010Open Access
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Frequent Co-authors

Madhuri Hegde(9), Mark E. Parry(8), Hudson H. Freeze(6), Mike Grotewiel(5), Devin Rhodenizer(5), Ian Martin(4), Ping He(3), Bobby G. Ng(3), Shruti Bhide(3), Qiuming Gong(3), Zhengfeng Zhou(3), Miao He(3), J. Zonana(3), Angus Clarke(3), Gregory M. Enns(2), Matthew N. Bainbridge(2), Farah Zahir(2), Thomas Bast(2), Rebecca Crimian(2), Kelly Schoch(2)