Florence Riant

4.6k citations

61 papers · 2.4k indexed · h-index 29

Impact in

Neurology top 0.5%
- Vascular Malformations Diagnosis and Treatment
- Intracranial Aneurysms: Treatment and Complications
- Cerebrovascular and genetic disorders
- Intracerebral and Subarachnoid Hemorrhage Research
Psychiatry and Mental health top 2%
- Migraine and Headache Studies

Papers in

Neurology 36
- Vascular Malformations Diagnosis and Treatment 16
- Intracranial Aneurysms: Treatment and Complications 13
- Intracerebral and Subarachnoid Hemorrhage Research 12
- Cerebrovascular and genetic disorders 12
- Neurological disorders and treatments 8
Cellular and Molecular Neuroscience 17
- Genetic Neurodegenerative Diseases 17

Co-authors: Elisabeth Tournier‐Lasserve Anne Joutel Françoise Bergametti Pierre Labauge Michaelle Cécillon Christian Denier Jacqueline Maciazek Christel Depienne
Journals: Neurology (6 papers)Developmental Medicine & Child Neurology (3 papers)Journal of Neurology Neurosurgery & Psychiatry (3 papers)Annals of Neurology (3 papers)Stroke (3 papers)
Partner nations: France United States Switzerland

In The Last Decade

Florence Riant

60 papers receiving 2.4k citations

Peers

Countries citing papers authored by Florence Riant

Since Specialization

Citations

This map shows the geographic impact of Florence Riant'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 Florence Riant with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Florence Riant more than expected).

Fields of papers citing papers by Florence Riant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Florence Riant. 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 Florence Riant. The network helps show where Florence Riant may publish in the future.

Co-authors

The 25 scholars most cited alongside Florence Riant, 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 Florence Riant Line = papers co-authored together Florence Riant links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations European Journal of Human Genetics ·Annabelle Chaussenot, Xavier Ayrignac, Nicolas Chatron, Rashmin Kaur, Pierre Labauge, Elisabeth Tournier‐Lasserve, Florence Riant	2024	2
2	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, А.А. Токовенко, Chaker Aloui, Françoise Bergametti, Minh Arnould, Hind Guénou, 健嗣遠藤, Jazhang Feng, Florence Riant, Jean‐Luc Balligand, Georges Uzan, Bruno O. Villoutreix, Elisabeth Tournier‐Lasserve	2023	5
3	Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature review Revue Neurologique ·Chris Cunneen, Philippe Labrune, Peggy Reiner, Mariana Sarov, Forouzan Eskandari, Florence Riant, Elisabeth Tournier‐Lasserve, Hugues Chabriat, Christian Denier	2019	15
4	Benign paroxysmal torticollis, benign paroxysmal vertigo, and benign tonic upward gaze are not benign disorders Developmental Medicine & Child Neurology ·Véronique Humbertclaude, Syafia Farihatul Uzma, Erika Nogué, Nicolas Nagot, Abdoreza Gholipour, B. Tourniaire, Elisabeth Tournier‐Lasserve, Florence Riant, Agathe Roubertie	2018	16
5	Acute-Onset Ataxia and Transient Cerebellar Diffusion Restriction Associated with a PRRT2 Mutation Journal of Stroke and Cerebrovascular Diseases ·Nicolas Legris, Olivier Chassin, Kousar Mohammadidust, Florence Riant, Elisabeth Tournier‐Lasserve, Christian Denier	2018	7
6	Eye movement disorders are an early manifestation of CACNA1A mutations in children Esther Tantsis, Deepak Gill, Lyn R. Griffiths, Sachin Gupta, John A. Lawson, Neven Maksemous, Robert Ouvrier, Florence Riant, Robert L. Smith, Christopher Troedson, Richard Webster, Manoj P. Menezes	2016	2
7	Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene Revue Neurologique ·Hasbulloh Karim Alfauzi, G. Tertian, C Buffet, Ali G. Turhan, Olivier Lambotte, Forouzan Eskandari, P. Alvin, Luca De Marziani, Florence Riant, Françoise Bergametti, Elisabeth Tournier‐Lasserve, Christian Denier	2015	14
8	Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1 Journal of the Neurological Sciences ·K. Rérat, Fabrice Parker, Forouzan Eskandari, Dominique Vidaud, Florence Riant, Elisabeth Tournier‐Lasserve, Christian Denier	2015	6
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, V. Tommasini, 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	CCM molecular screening in a diagnosis context: novel unclassified variants leading to abnormal splicing and importance of large deletions Neurogenetics ·Florence Riant, Michaelle Cécillon, Pascale Saugier-Véber, Elisabeth Tournier‐Lasserve	2013	44
11	PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins European Journal of Paediatric Neurology ·Claudia Castiglioni, Isabel López, Florence Riant, Enrico Bertini, Antonio Terracciano	2012	19
12	Revue généraleAtaxies épisodiques génétiquesHereditary episodic ataxia Revue Neurologique ·Florence Riant, Katayoun Vahedi, Elisabeth Tournier‐Lasserve	2011	5
13	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
14	Elicited repetitive daily blindness Neurology ·Katayoun Vahedi, Christel Depienne, 和田誓一, Florence Riant, A. T. Adesoji, Oriane Trouillard, Alain Gaudric, Michael A. Morris, Eric Leguern, Elisabeth Tournier‐Lasserve, K. S. Zharovtseva	2009	66
15	Activating NOTCH3 mutation in a patient with small-vessel-disease of the Brain Human Mutation ·Charles Fouillade, Hugues Chabriat, Florence Riant, Manuèle Miné, Alexandru Usturoi, Laurent Magy, Marie Germaine Bousser, Elisabeth Tournier‐Lasserve, Anne Joutel	2008	48
16	A novel hereditary small vessel disease of the brain Annals of Neurology ·Steve Verreault, Anne Joutel, Florence Riant, Samantha Dorney-Smith, Mário Rui Silva, Jacqueline Maciazek, Elisabeth Tournier‐Lasserve, Marie‐Germaine Bousser, Hugues Chabriat	2006	21
17	Genotype–phenotype correlations in cerebral cavernous malformations patients Annals of Neurology ·Christian Denier, Pierre Labauge, Françoise Bergametti, Florence Marchelli, Florence Riant, 雑賀光一, Jacqueline Maciazek, Éric Vicaut, L. Brunereau, Elisabeth Tournier‐Lasserve	2006	171
18	ATP1A2 mutations in 11 families with familial hemiplegic migraine Human Mutation ·Florence Riant, Maurizio De Fusco, Paolo Aridon, Anne Ducros, 谷伟, Florence Marchelli, Jacqueline Maciazek, Marie Germaine Bousser, Giorgio Casari, Elisabeth Tournier‐Lasserve	2005	85
19	Clinical features of cerebral cavernous malformations patients with KRIT1 mutations Annals of Neurology ·Christian Denier, Pierre Labauge, L. Brunereau, Florence Riant, Florence Marchelli, 雑賀光一, Michaelle Cécillon, Jacqueline Maciazek, Anne Joutel, Elisabeth Tournier‐Lasserve	2003	73
20	Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations European Journal of Human Genetics ·(unknown), Florence Riant, Christian Denier, Pierre Labauge, Michaelle Cécillon, Jacqueline Maciazek, Anne Joutel, Sophie Laberge, Elisabeth Tournier‐Lasserve	2002	83

About Florence Riant

Florence Riant is a scholar working on Neurology, Cellular and Molecular Neuroscience, Psychiatry and Mental health, Neurology and Rheumatology, having authored 61 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (17 papers), Vascular Malformations Diagnosis and Treatment (16 papers), Intracranial Aneurysms: Treatment and Complications (13 papers), Intracerebral and Subarachnoid Hemorrhage Research (12 papers), Cerebrovascular and genetic disorders (12 papers), Migraine and Headache Studies (9 papers), Moyamoya disease diagnosis and treatment (8 papers) and Neurological disorders and treatments (8 papers). The work is most often cited by research in Neurology (1.3k citations), Psychiatry and Mental health (586 citations), Neurology (308 citations), Immunology and Allergy (192 citations) and Rheumatology (331 citations). Florence Riant has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Elisabeth Tournier‐Lasserve, Anne Joutel, Françoise Bergametti, Pierre Labauge, Michaelle Cécillon, Christian Denier, Jacqueline Maciazek, Christel Depienne, Valérie Domenga and Anne Ducros. Their work appears in journals such as Neurology, Developmental Medicine & Child Neurology, Journal of Neurology Neurosurgery & Psychiatry, Annals of 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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