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Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Nathalie Chabbert‐Buffet
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710
Publications
5,249
Citation Statements Received
13,416
Citation Statements Given
How they've been cited
8,242
231
4,994
24
How they cite others
31,173
368
12,929
119
Affiliations
Hôpital Tenon
,
Sorbonne Université
Publications
Order By: Most citations
ARMC5
Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome
Assié
1
,
Libé
2
,
Espiard
3
et al.
2013
N Engl J Med
Abstract
Show
432
31
365
1
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Cite
Type and timing of menopausal hormone therapy and breast cancer risk: individual participant meta-analysis of the worldwide epidemiological evidence
Hamajima
1
,
Hirose
2
,
Tajima
3
et al.
2019
The Lancet
Abstract
Show
793
20
344
3
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Add to collection
Cite
Reproductive risk factors and endometrial cancer: the European Prospective Investigation into Cancer and Nutrition
Dossus
1
,
Allen
2
,
Kaaks
3
et al.
2010
Intl Journal of Cancer
Abstract
Show
293
13
285
0
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Cite
Selective progesterone receptor modulators and progesterone antagonists: mechanisms of action and clinical applications
Chabbert‐Buffet
1
,
Méduri
2
,
Bouchard
3
et al.
2005
Abstract
Show
305
4
175
0
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Cite
ARMC5
Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences
Espiard
1
,
Drougat
2
,
Libé
3
et al.
2015
The Journal of Clinical Endocrinology & Metabolism
Abstract
Show
210
16
165
0
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Cite
Diminished ovarian reserve, premature ovarian failure, poor ovarian responder—a plea for universal definitions
Cohen
1
,
Chabbert‐Buffet
2
,
Daraï
3
2015
J Assist Reprod Genet
Abstract
Show
294
1
188
0
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Cite
From Pregnancy to Preeclampsia: A Key Role for Estrogens
Berkane
1
,
Lière
2
,
Oudinet
3
et al.
2017
Abstract
Show
243
6
163
1
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Cite
A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes
Sarfati
1
,
Guiochon‐Mantel
2
,
Rondard
3
et al.
2010
Abstract
Show
148
4
139
0
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Add to collection
Cite
1
2
3