Minerva Deanching

608 total citations
13 papers, 419 citations indexed

About

Minerva Deanching is a scholar working on Rheumatology, Physiology and Pathology and Forensic Medicine. According to data from OpenAlex, Minerva Deanching has authored 13 papers receiving a total of 419 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Rheumatology, 6 papers in Physiology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Minerva Deanching's work include Lysosomal Storage Disorders Research (6 papers), Biomedical Research and Pathophysiology (5 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Minerva Deanching is often cited by papers focused on Lysosomal Storage Disorders Research (6 papers), Biomedical Research and Pathophysiology (5 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Minerva Deanching collaborates with scholars based in United States. Minerva Deanching's co-authors include Reuben Matalon, K. Michals, P. Gashkoff, James F. Reynolds, John M. Optiz, Rajinder Kaul, I. Rapin, Toby Johnson, George Hoganson and Chester B. Whitley and has published in prestigious journals such as Genomics, Pediatric Research and American Journal of Medical Genetics.

In The Last Decade

Minerva Deanching

13 papers receiving 411 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Minerva Deanching United States 6 185 183 72 70 63 13 419
P. Gashkoff United States 5 183 1.0× 197 1.1× 73 1.0× 72 1.0× 22 0.3× 6 439
Sylvia Szucs United States 10 265 1.4× 159 0.9× 178 2.5× 107 1.5× 68 1.1× 12 602
Kimberlee Michals Matalon United States 10 155 0.8× 96 0.5× 62 0.9× 130 1.9× 79 1.3× 12 346
Kimberlee Michals‐Matalon United States 12 206 1.1× 113 0.6× 80 1.1× 185 2.6× 91 1.4× 27 386
B. Kruse Germany 9 304 1.6× 92 0.5× 21 0.3× 74 1.1× 113 1.8× 14 531
P Ozand Saudi Arabia 9 197 1.1× 38 0.2× 27 0.4× 107 1.5× 87 1.4× 16 306
Loreta M. Rodrigues United Kingdom 12 149 0.8× 246 1.3× 13 0.2× 17 0.2× 101 1.6× 22 573
U. Holzbach Germany 9 417 2.3× 84 0.5× 84 1.2× 178 2.5× 130 2.1× 11 674
Brian D. Ross United States 6 108 0.6× 207 1.1× 12 0.2× 27 0.4× 34 0.5× 6 421
K. Silver Canada 13 249 1.3× 57 0.3× 24 0.3× 104 1.5× 21 0.3× 15 520

Countries citing papers authored by Minerva Deanching

Since Specialization
Citations

This map shows the geographic impact of Minerva Deanching's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Minerva Deanching with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Minerva Deanching more than expected).

Fields of papers citing papers by Minerva Deanching

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Minerva Deanching. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Minerva Deanching. The network helps show where Minerva Deanching may publish in the future.

Co-authorship network of co-authors of Minerva Deanching

This figure shows the co-authorship network connecting the top 25 collaborators of Minerva Deanching. A scholar is included among the top collaborators of Minerva Deanching based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Minerva Deanching. Minerva Deanching is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Deanching, Minerva, et al.. (2008). 79. Pseudo-deficiency allele of the N-acetylgalactosamine-4-sulfatase gene identified in a family with Maroteaux–Lamy syndrome (mucopolysaccharidosis type VI). Molecular Genetics and Metabolism. 93(2). 34–34. 5 indexed citations
2.
Charnas, Lawrence, Elizabeth Braunlin, Kendra Bjoraker, et al.. (2007). 99 Treatment of multiple sulfatase deficiency with recombinant human arylsulfatase B. Molecular Genetics and Metabolism. 92(4). 31–31. 1 indexed citations
3.
Aronovich, Elena L., K. Paige Carmichael, Hiroki Morizono, et al.. (2000). Canine Heparan Sulfate Sulfamidase and the Molecular Pathology Underlying Sanfilippo Syndrome Type A in Dachshunds. Genomics. 68(1). 80–84. 20 indexed citations
4.
Matalon, Reuben, Rajinder Kaul, K. Michals, et al.. (1989). Aspartoacylase Deficiency: The Enzyme Defect in Canavan Disease. Journal of Inherited Metabolic Disease. 12(S2). 329–331. 59 indexed citations
5.
Matalon, Reuben, K. Michals, Minerva Deanching, et al.. (1988). Aspartoacylase deficiency and N‐acetylaspartic aciduria in patients with canavan disease. American Journal of Medical Genetics. 29(2). 463–471. 296 indexed citations
6.
Matalon, Reuben, et al.. (1986). Carrier detection for sanfilippo A syndrome. Journal of Inherited Metabolic Disease. 11(2). 158–160. 10 indexed citations
7.
Matalon, Reuben, Minerva Deanching, & Kiyoshi Omura. (1983). Hurler, Scheie, and Hurler‐Scheie ‘compound’: Residual activity of α‐l‐iduronidase toward natural substrates suggesting allelic mutations. Journal of Inherited Metabolic Disease. 6(S2). 133–134. 6 indexed citations
8.
Hodach, Albertina E., et al.. (1983). Hunter' syndrome. Ultrastructural features in young children.. PubMed. 107(9). 495–9. 3 indexed citations
9.
Matalon, Reuben, et al.. (1982). Keratan and herparan sulfaturia: glucosamine-6-sulfate deficiency.. PubMed. 12(3). 234–8. 7 indexed citations
10.
Matalon, Reuben, Rebecca S. Wappner, Minerva Deanching, Ingvar Brandt, & Allen L. Horwitz. (1982). Keratan and heparan sulphaturia: a mucopolysaccharidosis with an enzyme defect not previously identified. Journal of Inherited Metabolic Disease. 5(S1). 57–58. 2 indexed citations
11.
Matalon, Reuben, et al.. (1978). 540 A KERATAN AND HEPARAN SULFATURIA - A NEW MUCOPOLYSAC- CHARIDOSIS WITH N-ACETYLGLUCOSAMINE 6− SULFATASE DEFICIENCY. Pediatric Research. 12. 453–453. 4 indexed citations
12.
Matalon, Reuben, Parvin Justice, K. Michals, & Minerva Deanching. (1978). 879 FRUCTOSE-1.6-DIPHOSPHATASE ACTIVITY IN HUMAN TERM PLACENTA. Pediatric Research. 12. 510–510. 1 indexed citations
13.
Matalon, Reuben, Minerva Deanching, & Ira M. Rosenthal. (1977). THE ENZYMIC BASIS FOR THE PHENOTYPIC VARIATION OF HURLER AND SCHEIE SYNDROMES. Pediatric Research. 11(4). 519–519. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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