Immediate Impact
30 standout
Citing Papers
Mitochondrial diseases: from molecular mechanisms to therapeutic advances
2025 Standout
Mitochondria and Brain Disease: A Comprehensive Review of Pathological Mechanisms and Therapeutic Opportunities
2023 Standout
Works of Monique Cordonnier being referenced
TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy.
2012
[Optic neuropathy in Strumpell-Lorrain disease: presentation of a clinical case and literature review].
2002
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Monique Cordonnier | 232 | 41 | 229 | 180 | 56 | 419 | |
| Pinhas Nemet | 246 | 58 | 135 | 266 | 24 | 448 | |
| Şaban Şimşek | 321 | 50 | 109 | 216 | 61 | 486 | |
| Xinping Yu | 248 | 77 | 192 | 152 | 51 | 372 | |
| H Saraux | 291 | 68 | 134 | 93 | 99 | 472 | |
| Osman Melih Ceylan | 259 | 31 | 125 | 211 | 45 | 500 | |
| Daniel Snydacker | 256 | 68 | 88 | 151 | 26 | 478 | |
| An-Guor Wang | 253 | 22 | 103 | 97 | 39 | 449 | |
| Önder Üretmen | 314 | 163 | 179 | 214 | 45 | 459 | |
| Süheyla Köse | 227 | 136 | 168 | 137 | 33 | 372 | |
| Annabella Salerni | 186 | 49 | 141 | 60 | 22 | 387 |
All Works
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