Françoise Bergametti

2.9k citations

29 papers · 1.9k indexed · h-index 19

Co-authors: Elisabeth Tournier‐Lasserve Christian Denier Pierre Labauge Catherine Transy Florence Riant Delphine Sitterlin Pierre Tiollais Gwénola Boulday
Topics: Intracranial Aneurysms: Treatment and Complications (8 papers)Cerebrovascular and genetic disorders (8 papers)Vascular Malformations Diagnosis and Treatment (8 papers)
Cited by: Neurology Rheumatology Hepatology
Journals: Brain Neurology Stroke
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 of co-authors of Françoise Bergametti

This figure shows the co-authorship network connecting the top 25 collaborators of Françoise Bergametti. A scholar is included among the top collaborators of Françoise Bergametti based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Françoise Bergametti. Françoise Bergametti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

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