Michael P. Whyte

325 papers receiving 16.6k citations

Michael P. Whyte's Hit Papers

Burosumab Therapy in Children with X-Linked Hypophosphatemia 2018 · 331 citations
3310+14+28Years since publication2505007501000

Peers

Michael P. Whyte
Comparison fields: 5 of 158
  • Endocrinology, Diabetes and Metabolism 6.1k
  • Nephrology 2.6k
  • Rheumatology 4.8k
  • Orthopedics and Sports Medicine 2.7k
  • Oncology 3.2k
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Citations per year

Countries citing papers authored by Michael P. Whyte

Since Specialization
Citations

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

Fields of papers citing papers by Michael P. Whyte

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael P. Whyte. 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 Michael P. Whyte. The network helps show where Michael P. Whyte may publish in the future.

Co-authors

The 25 scholars most cited alongside Michael P. Whyte, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Michael P. Whyte Line = papers co-authored together Michael P. Whyte links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 330 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
Hit paper breakdown →
20041021
2
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
Hit paper breakdown →
1983474
3 1994402
4 2000353
5
Hypophosphatasia — aetiology, nosology, pathogenesis, diagnosis and treatment
Hit paper breakdown →
2016350
6
Burosumab Therapy in Children with X-Linked Hypophosphatemia
Hit paper breakdown →
2018331
7 2003321
8 1999304
9 2002303
10 2015282
11 1988276
12 2010267
13 1995256
14 2003244
15 1985223
16 2007204
17 1992202
18 2015195
19 2002191
20 2015188

About Michael P. Whyte

Michael P. Whyte is a scholar working on Endocrinology, Diabetes and Metabolism, Oncology, Molecular Biology, Genetics and Rheumatology, having authored 330 papers that have together received 17.1k indexed citations. Recurring topics across this work include Alkaline Phosphatase Research Studies (118 papers), Bone health and treatments (103 papers), Parathyroid Disorders and Treatments (52 papers), Heterotopic Ossification and Related Conditions (44 papers), Connective tissue disorders research (41 papers), Vitamin D Research Studies (36 papers), Bone health and osteoporosis research (34 papers) and Bone Metabolism and Diseases (32 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (6.1k citations), Nephrology (2.6k citations), Rheumatology (4.8k citations), Orthopedics and Sports Medicine (2.7k citations) and Oncology (3.2k citations). Michael P. Whyte has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Steven Mumm, William H. McAlister, Stephen P. Coburn, William A. Murphy, José Luís Millán, K N Fedde, Deborah Wenkert, Steven L. Teitelbaum, William S. Sly and Rajesh V. Thakker. Their work appears in journals such as Journal of Bone and Mineral Research, Bone, The Journal of Clinical Endocrinology & Metabolism, The American Journal of Medicine and Journal of Clinical Investigation.

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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