All Affiliations
| # | Concept | H-Index | Publications | Citations |
|---|---|---|---|---|
1 | Medicine | 28 | 40 | 5.4K |
2 | Cell Biology | 4 | 4 | 856 |
3 | Health Sciences | 3 | 3 | 88 |
4 | Natural Sciences | 2 | 2 | 134 |
5 | Allergy | 1 | 1 | 365 |
Virginie Verkarre
×
111
Publications
13.5K
Citations
55
H-Index
| Year | Citations | |
|---|---|---|
2007 | 2K | |
2004 | 731 | |
2022 | 690 | |
2015 | 504 | |
2003 | 453 | |
2008 | 365 | |
2013 | 355 | |
2008 | 298 | |
2015 | 294 | |
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. Virginie Verkarre, Jean‐Christophe Fournet, Pascale de Lonlay, Journal of Clinical Investigation Epigenetic ChangeGeneticsPathologyEpigeneticsInsulin Signaling | 1998 | 290 |
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