Standout Papers
- Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein (2004)
- Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. (1983)
- Hypophosphatasia — aetiology, nosology, pathogenesis, diagnosis and treatment (2016)
- Burosumab Therapy in Children with X-Linked Hypophosphatemia (2018)
Immediate Impact
3 by Nobel laureates 13 from Science/Nature 68 standout
Citing Papers
Hallmarks of neurodegenerative diseases
2023 Standout
Molecular Probes, Chemosensors, and Nanosensors for Optical Detection of Biorelevant Molecules and Ions in Aqueous Media and Biofluids
2022 Standout
Works of Michael P. Whyte being referenced
Juvenile Paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation
2013
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
2004 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Michael P. Whyte | 6017 | 3599 | 5891 | 5590 | 324 | 16.5k | |
| José Luís Millán | 6505 | 1134 | 5735 | 4247 | 304 | 15.5k | |
| Ernesto Canalis | 4264 | 5786 | 12163 | 2959 | 308 | 21.3k | |
| H. Fleisch | 2354 | 10380 | 6175 | 2534 | 300 | 19.1k | |
| David J. Baylink | 3706 | 2540 | 5084 | 1113 | 260 | 12.4k | |
| Thomas L. Clemens | 2004 | 3185 | 6733 | 1402 | 153 | 14.9k | |
| David Goltzman | 1789 | 6783 | 8690 | 1533 | 409 | 20.6k | |
| Francis H. Glorieux | 2031 | 7790 | 8094 | 5968 | 320 | 28.4k | |
| L. Darryl Quarles | 1487 | 3206 | 6748 | 1936 | 239 | 17.3k | |
| Louis V. Avioli | 1612 | 2663 | 4461 | 1191 | 269 | 12.3k | |
| Henry M. Kronenberg | 1692 | 7897 | 17473 | 5184 | 237 | 28.3k |
All Works
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