Françoise Bergametti

2.9k citations

29 papers · 1.9k indexed · h-index 19

Neurology top 1%
- Intracranial Aneurysms: Treatment and Complications 8
- Cerebrovascular and genetic disorders 8
- Vascular Malformations Diagnosis and Treatment 8
- Intracerebral and Subarachnoid Hemorrhage Research 6
Rheumatology top 5%
- Moyamoya disease diagnosis and treatment 7
Hepatology top 5%
- Hepatitis C virus research 5
Neurology top 10%
- Intracranial Aneurysms: Treatment and Complications 8
- Cerebrovascular and genetic disorders 8
- Vascular Malformations Diagnosis and Treatment 8
- Intracerebral and Subarachnoid Hemorrhage Research 6
Reproductive Medicine top 10%
Epidemiology
- Hepatitis B Virus Studies 6
Genetics
- Connective tissue disorders research 3

Co-authors: Elisabeth Tournier‐Lasserve Christian Denier Pierre Labauge Catherine Transy Florence Riant Delphine Sitterlin Pierre Tiollais Gwénola Boulday
Cited by: Neurology Rheumatology Hepatology
Journals: Brain (1 paper)Neurology (1 paper)Stroke (2 papers)
Partner nations: France Germany United States

In The Last Decade

Françoise Bergametti

29 papers receiving 1.9k citations

Peers

Countries citing papers authored by Françoise Bergametti

Since Specialization

Citations

This map shows the geographic impact of Françoise Bergametti's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Françoise Bergametti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Françoise Bergametti more than expected).

Fields of papers citing papers by Françoise Bergametti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Françoise Bergametti. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Françoise Bergametti. The network helps show where Françoise Bergametti may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Françoise Bergametti, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Françoise Bergametti Line = papers co-authored together Françoise Bergametti links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Biallelic variants in NOS3 and GUCY1A3, the two major genes of the nitric oxide pathway, cause moyamoya cerebral angiopathy Human Genomics ·Stéphanie Guey,Dominique Hervé,Manoëlle Kossorotoff,Guillaume Ha,Chaker Aloui,Françoise Bergametti,Minh Arnould,Hind Guénou,Jessica Hadjadj,Fanny Dubois Teklali,Florence Riant,Jean‐Luc Balligand,Georges Uzan,Bruno O. Villoutreix,Elisabeth Tournier‐Lasserve	2023	5
2	End‐Truncated LAMB1 Causes a Hippocampal Memory Defect and a Leukoencephalopathy Annals of Neurology ·Chaker Aloui,Dominique Hervé,Gaëlle Marenne,Florian Savenier,Kilan Le Guennec,Françoise Bergametti,Edgard Verdura,Thomas Ludwig,Jessica Lebenberg,Waliyde Jabeur,Hélène Morel,Thibault Coste,Geneviève Demarquay,Panagiotis Bachoumas,Julien Cogez,Guillaume Mathey,E Bernard,Hugues Chabriat,Emmanuelle C. Genin,Elisabeth Tournier‐Lasserve	2021	10
3	The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy Genetics in Medicine ·Amélie Pinard,Stéphanie Guey,Dongchuan Guo,Alana C. Cecchi,Natasha Kharas,Stephanie E Wallace,Ellen S. Regalado,Ellen M. Hostetler,Anjail Sharrief,Françoise Bergametti,Manoëlle Kossorotoff,Dominique Hervé,Markus Kraemer,Michael J. Bamshad,Deborah A. Nickerson,Edward R. Smith,Elisabeth Tournier‐Lasserve,Dianna M. Milewicz	2019	34
4	Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy Stroke ·Lou Grangeon,Stéphanie Guey,Jan Claudius Schwitalla,Françoise Bergametti,Minh Arnould,Michaelle Corpechot,Jessica Hadjadj,Florence Riant,Chaker Aloui,Séverine Drunat,Dominique Vidaud,Elisabeth Tournier‐Lasserve,Markus Kraemer	2019	30
5	Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians European Journal of Human Genetics ·Stéphanie Guey,Markus Kraemer,Dominique Hervé,Thomas Ludwig,Manoëlle Kossorotoff,Françoise Bergametti,Jan Claudius Schwitalla,Simone Choi,Lucile Broseus,Isabelle Callebaut,Emmanuelle Génin,Elisabeth Tournier‐Lasserve	2017	84
6	Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene Revue Neurologique ·A. Bisserbe,G. Tertian,C Buffet,Ali G. Turhan,Olivier Lambotte,G. Nasser,P. Alvin,Marion Tardieu,Florence Riant,Françoise Bergametti,Elisabeth Tournier‐Lasserve,Christian Denier	2015	14
7	HeterozygousHTRA1mutations are associated with autosomal dominant cerebral small vessel disease Brain ·Edgard Verdura,Dominique Hervé,Eva Scharrer,Maria del Mar Amador,Lucie Guyant‐Maréchal,Anne Philippi,Astrid Corlobé,Françoise Bergametti,Steven Gazal,Carol Prieto-Morin,Nathalie Beaufort,Benoit Le Bail,Irina Viakhireva,Martin Dichgans,Hugues Chabriat,Christof Haffner,Elisabeth Tournier‐Lasserve	2015	123
8	Can whole-exome sequencing data be used for linkage analysis? European Journal of Human Genetics ·Steven Gazal,Simon Gosset,Edgard Verdura,Françoise Bergametti,Stéphanie Guey,Marie‐Claude Babron,Elisabeth Tournier‐Lasserve	2015	8
9	<b><i>CCM3</i></b> Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas Molecular Syndromology ·Florence Riant,Françoise Bergametti,H.-D. Fournier,Françoise Chapon,Sophie Michalak-Provost,Michaelle Cécillon,Pascal Lejeune,Hassan Hosseini,Chi‐un Choe,Matthias Orth,Christian Bernreuther,Gwénola Boulday,Christian Denier,Pierre Labauge,Elisabeth Tournier‐Lasserve	2013	69
10	Loss of BRCC3 Deubiquitinating Enzyme Leads to Abnormal Angiogenesis and Is Associated with Syndromic Moyamoya The American Journal of Human Genetics ·S. Miskinyte,Matthew G. Butler,Dominique Hervé,Catherine Sarret,Marc Nicolino,Jacob D. Petralia,Françoise Bergametti,Minh Arnould,Van N. Pham,Aniket V. Gore,Konstantinos Spengos,Steven Gazal,France Woimant,Gary K. Steinberg,Brant M. Weinstein,Elisabeth Tournier‐Lasserve	2011	86
11	Recent insights into cerebral cavernous malformations: the molecular genetics of CCM FEBS Journal ·Florence Riant,Françoise Bergametti,Xavier Ayrignac,Gwénola Boulday,Elisabeth Tournier‐Lasserve	2010	135
12	Genetics of cavernous angiomas The Lancet Neurology ·Pierre Labauge,Christian Denier,Françoise Bergametti,Elisabeth Tournier‐Lasserve	2007	225
13	Genotype–phenotype correlations in cerebral cavernous malformations patients Annals of Neurology ·Christian Denier,Pierre Labauge,Françoise Bergametti,Florence Marchelli,Florence Riant,Minh Arnoult,Jacqueline Maciazek,Éric Vicaut,L. Brunereau,Elisabeth Tournier‐Lasserve	2006	171
14	Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations The American Journal of Human Genetics ·Françoise Bergametti,Christian Denier,Pierre Labauge,Minh Arnoult,S. Boetto,Michel Clanet,Philippe Coubes,Bernard Échenne,Rasha Ibrahim,B. Irthum,G Jacquet,M. Lonjon,J.-J. Moreau,J.‐P. Neau,Fabrice Parker,M Trémoulet,Elisabeth Tournier‐Lasserve	2004	334
15	Interaction of Hepatitis B Virus X Protein with Damaged DNA-Binding Protein p127: Structural Analysis and Identification of Antagonists Journal of Biomedical Science ·Françoise Bergametti,Julie Bianchi,Catherine Transy	2002	10
16	A genomic approach of the hepatitis C virus generates a protein interaction map Gene ·Marc Flajolet,G Rotondo,Laurent Daviet,Françoise Bergametti,Geneviève Inchauspé,Pierre Tiollais,Catherine Transy,Pierre Legrain	2000	129
17	UVDDB p127-binding modulates activities and intracellular distribution of Hepatitis B virus X protein Oncogene ·Delphine Sitterlin,Françoise Bergametti,Catherine Transy	2000	47
18	Correct binding of viral X protein to UVDDB-p127 cellular protein is critical for efficient infection by hepatitis B viruses Oncogene ·Delphine Sitterlin,Françoise Bergametti,Pierre Tiollais,Bud C. Tennant,Catherine Transy	2000	57
19	The proapoptotic effect of hepatitis B virus HBx protein correlates with its transactivation activity in stably transfected cell lines Oncogene ·Françoise Bergametti,Sylvie Prigent,Birgit Luber,Annie Benoit,Pierre Tiollais,Alain Sarasin,Catherine Transy	1999	72
20	Subregional mapping of the human gonadotropin-releasing hormone receptor (GnRH-R) gene to 4q between the markers D4S392 and D4S409 Human Genetics ·Marie‐Laure Kottler,Felipe Lorenzo,Françoise Bergametti,P. Commer�on,C Souchier,Raymond Counis	1995	19

About Françoise Bergametti

Françoise Bergametti is a scholar working on Neurology, Hepatology and Rheumatology, having authored 29 papers that have together received 1.9k indexed citations. Recurring topics across this work include Intracranial Aneurysms: Treatment and Complications (8 papers), Cerebrovascular and genetic disorders (8 papers), Vascular Malformations Diagnosis and Treatment (8 papers), Moyamoya disease diagnosis and treatment (7 papers), Intracerebral and Subarachnoid Hemorrhage Research (6 papers), Hepatitis B Virus Studies (6 papers), Hepatitis C virus research (5 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Neurology (1.1k citations), Rheumatology (268 citations) and Hepatology (130 citations). Françoise Bergametti has collaborated with scholars based in France, Germany and United States. Frequent co-authors include Elisabeth Tournier‐Lasserve, Christian Denier, Pierre Labauge, Catherine Transy, Florence Riant, Delphine Sitterlin, Pierre Tiollais, Gwénola Boulday, Xavier Ayrignac and Dominique Hervé. Their work appears in journals such as Brain, Neurology and Stroke.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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