Standout Papers
- Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease (2000)
- Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis (1999)
- Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome (2000)
- Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3) (2003)
- Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes (2002)
Immediate Impact
23 by Nobel laureates 30 from Science/Nature 68 standout
Citing Papers
In vivo hematopoietic stem cell modification by mRNA delivery
2023 StandoutScienceNobel
A role of PIEZO1 in iron metabolism in mice and humans
2021 StandoutNobel
Works of Stéphanie Certain being referenced
Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)
2003 Standout
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
2000 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Stéphanie Certain | 1801 | 2127 | 264 | 2427 | 12 | 5.1k | |
| I L Weissman | 1128 | 3347 | 1 | 1792 | 61 | 6.3k | |
| Robert F. Bargatze | 878 | 3179 | 2 | 2389 | 49 | 7.1k | |
| Hattie D. Gresham | 626 | 3267 | 7 | 2687 | 46 | 6.8k | |
| Neil E. Simister | 630 | 2697 | 8 | 2537 | 42 | 6.0k | |
| David C. Scherer | 879 | 3411 | 1 | 3386 | 25 | 7.0k | |
| Alan McClelland | 726 | 679 | 2 | 3339 | 47 | 5.8k | |
| Frank Köntgen | 563 | 4995 | 2 | 3694 | 28 | 9.1k | |
| Stacie M. Anderson | 1291 | 2244 | 2 | 3713 | 82 | 9.7k | |
| J L Cordell | 442 | 1476 | 5 | 1655 | 27 | 5.4k | |
| Mark J. Kiel | 3044 | 1932 | 5 | 2829 | 37 | 7.0k |
All Works
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