Terry M. Reade

600 total citations
8 papers, 375 citations indexed

About

Terry M. Reade is a scholar working on Nephrology, Oncology and Molecular Biology. According to data from OpenAlex, Terry M. Reade has authored 8 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Nephrology, 3 papers in Oncology and 2 papers in Molecular Biology. Recurrent topics in Terry M. Reade's work include Parathyroid Disorders and Treatments (4 papers), Bone health and treatments (3 papers) and Genomics and Rare Diseases (1 paper). Terry M. Reade is often cited by papers focused on Parathyroid Disorders and Treatments (4 papers), Bone health and treatments (3 papers) and Genomics and Rare Diseases (1 paper). Terry M. Reade collaborates with scholars based in Canada. Terry M. Reade's co-authors include Charles R. Scriver, Francis H. Glorieux, Hy Goldman, C. R. Scriver, Jonathan B. Kronick, Paul Goodyer, Sigrid Jéquier, Carol L. Clow, David E.C. Cole and Edgar Delvin and has published in prestigious journals such as New England Journal of Medicine, The Journal of Clinical Endocrinology & Metabolism and The Journal of Pediatrics.

In The Last Decade

Terry M. Reade

8 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Terry M. Reade Canada 7 210 100 88 68 61 8 375
Philip G. Rose United States 11 102 0.5× 82 0.8× 66 0.8× 126 1.9× 39 0.6× 14 487
Daniela Gabizon Israel 6 199 0.9× 109 1.1× 38 0.4× 77 1.1× 82 1.3× 9 316
Adel B. Korkor United States 9 289 1.4× 136 1.4× 85 1.0× 107 1.6× 81 1.3× 14 459
Ruth Samuel Israel 5 271 1.3× 94 0.9× 75 0.9× 99 1.5× 113 1.9× 6 394
Quanle Qi United States 7 361 1.7× 124 1.2× 257 2.9× 71 1.0× 69 1.1× 7 574
Kyoko Nagasue Japan 10 464 2.2× 119 1.2× 85 1.0× 144 2.1× 86 1.4× 11 621
Ph. Bordier France 9 136 0.6× 98 1.0× 163 1.9× 43 0.6× 65 1.1× 11 447
A. Mariè France 8 182 0.9× 48 0.5× 48 0.5× 40 0.6× 20 0.3× 19 277
L. F. Hill United Kingdom 10 103 0.5× 132 1.3× 56 0.6× 61 0.9× 40 0.7× 18 335
Arnold J. Felsenfeld United States 9 614 2.9× 179 1.8× 113 1.3× 158 2.3× 105 1.7× 10 681

Countries citing papers authored by Terry M. Reade

Since Specialization
Citations

This map shows the geographic impact of Terry M. Reade'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 Terry M. Reade with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Terry M. Reade more than expected).

Fields of papers citing papers by Terry M. Reade

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Terry M. Reade. 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 Terry M. Reade. The network helps show where Terry M. Reade may publish in the future.

Co-authorship network of co-authors of Terry M. Reade

This figure shows the co-authorship network connecting the top 25 collaborators of Terry M. Reade. A scholar is included among the top collaborators of Terry M. Reade 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 Terry M. Reade. Terry M. Reade is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
1.
Schwartz, Steven O., C. R. Scriver, Terry M. Reade, & E D Shields. (1988). Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: Further evidence that they are different diseases. Oral Surgery Oral Medicine Oral Pathology. 66(3). 310–314. 19 indexed citations
2.
Scriver, C. R., Barbara E. Mahon, Harvey L. Levy, et al.. (1987). The Hartnup phenotype: Mendelian transport disorder, multifactorial disease.. PubMed. 40(5). 401–12. 49 indexed citations
3.
Goodyer, Paul, Jonathan B. Kronick, Sigrid Jéquier, Terry M. Reade, & Charles R. Scriver. (1987). Nephrocalcinosis and its relationship to treatment of hereditary rickets. The Journal of Pediatrics. 111(5). 700–704. 63 indexed citations
4.
Scriver, Charles R., Carol L. Clow, Terry M. Reade, et al.. (1985). Ontogeny modifies manifestations of cystinuria genes: Implications for counseling. The Journal of Pediatrics. 106(3). 411–416. 25 indexed citations
5.
Kronick, Jonathan B., Paul Goodyer, Sigrid Jéquier, & Terry M. Reade. (1984). ULTRASOUND DIAGNOSIS OF NEPHROCALCINOSIS DURING TREATMENT OF HEREDITARY RICKETS. Pediatric Research. 18. 364A–364A. 1 indexed citations
6.
Marie, Pierre J., C. R. Scriver, David E.C. Cole, et al.. (1981). X-Linked Hypophosphatemia: Effect of Calcitriol on Renal Handling of Phosphate, Serum Phosphate, and Bone Mineralization*. The Journal of Clinical Endocrinology & Metabolism. 52(3). 463–472. 66 indexed citations
7.
Glorieux, Francis H., et al.. (1972). Use of Phosphate and Vitamin D to Prevent Dwarfism and Rickets in X-Linked Hypophosphatemia. New England Journal of Medicine. 287(10). 481–487. 134 indexed citations
8.
Clow, Carol L., Terry M. Reade, & Charles R. Scriver. (1971). Management of Hereditary Metabolic Disease. New England Journal of Medicine. 284(23). 1292–1298. 18 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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