Férechté Encha‐Razavi

5.2k citations

64 papers · 1.7k indexed · h-index 21

Developmental Neuroscience top 5%
- Neurogenesis and neuroplasticity mechanisms 5
Genetics top 5%
- Ocular Disorders and Treatments 5
- Genomic variations and chromosomal abnormalities 5
Cell Biology top 5%
Pediatrics, Perinatology and Child Health top 5%
- Fetal and Pediatric Neurological Disorders 19
- Prenatal Screening and Diagnostics 11
Molecular Biology top 10%
- Hedgehog Signaling Pathway Studies 11
- Epigenetics and DNA Methylation 6
- RNA Research and Splicing 6

Co-authors: Tania Attié‐Bitach Michel Vekemans Arnold Münnich Nathalie Boddaert Stanislas Lyonnet Maryse Bonnière Catherine Fallet‐Bianco Yoann Saillour
Cited by: Developmental Neuroscience Genetics Cell Biology
Journals: Proceedings of the National Academy of Sciences (2 papers)Nature Genetics (1 paper)Nature Neuroscience (1 paper)
Partner nations: France United States Switzerland

In The Last Decade

Férechté Encha‐Razavi

60 papers receiving 1.6k citations

Peers

Countries citing papers authored by Férechté Encha‐Razavi

Since Specialization

Citations

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

Fields of papers citing papers by Férechté Encha‐Razavi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Férechté Encha‐Razavi. 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 Férechté Encha‐Razavi. The network helps show where Férechté Encha‐Razavi may publish in the future.

Co-authorship network

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Mapping the developmental profile of ventricular zone–derived neurons in the human cerebellum Proceedings of the National Academy of Sciences ·Anders W. Erickson,Haodan Tan,Liam D. Hendrikse,Jake Millman,Zachary Thomson,Joseph Golser,Omar Khan,Guanyi He,Kathleen Bach,Anusha Mishra,Janja Kopić,Željka Krsnik,Férechté Encha‐Razavi,Giulia Petrilli,Fabien Guimiot,Evelina Silvestri,Kimberly A. Aldinger,Michael D. Taylor,Kathleen J. Millen,Parthiv Haldipur	2025	0
2	Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation Birth Defects Research ·Suzanne Chartier,Lucile Boutaud,Édouard Le Guillou,Caroline Alby,Clarisse Billon,A. Millischer,Catherine Caillaud,Louise Galmiche,Charlotte Mechler,Pascale Sonigo,Nathalie Boddaert,Stanislas Lyonnet,Sophie Rondeau,Christine Bole‐Feysot,Cécile Masson,Y. Ville,Philippe Roth,Isabelle Desguerre,Férechté Encha‐Razavi,Tania Attié‐Bitach	2021	2
3	A clinical and histopathological study of malformations observed in fetuses infected by the Zika virus Brain Pathology ·Aurélie Bèaufrere,Bettina Bessières,Maryse Bonnière,Marine Driessen,Christian Alfano,Thérèse Couderc,Marc Thiry,Nicolas Thelen,Marc Lecuit,Tania Attié‐Bitach,Michel Vekemans,Y. Ville,Laurent Nguyen,Marianne Leruez‐Ville,Férechté Encha‐Razavi	2018	15
4	Prevalence and timing of pregnancy termination for brain malformations: Table 1 Archives of Disease in Childhood Fetal & Neonatal ·Caroline Rouleau,A. Gasner,Nicole Bigi,A. Couture,María Jesús Pérez-Granda,Patricia Blanchet,Jean-Michel Faure,François Rivier,P. Boulot,Annie Laquerrière,Férechté Encha‐Razavi	2011	11
5	PAX2 mutations in fetal renal hypodysplasia American Journal of Medical Genetics Part A ·Jelena Martinovic‐Bouriel,Alexandra Benachi,Maryse Bonnière,Nora Brahimi,Chantal Esculpavit,Nicole Morichon,Michel Vekemans,Corinne Antignac,Rémi Salomon,Férechté Encha‐Razavi,Tania Attié‐Bitach,Marie-Claire Gübler	2010	28
6	Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): Report of 16 fetal cases European Journal of Medical Genetics ·B. Bessières-Grattagliano,B. Foliguet,Louise Devisme,Laurence Lœuillet,Pascale Marcorelles,Maryse Bonnière,A. Laquérrière,Catherine Fallet‐Bianco,Jelena Martinović,S. Zrelli,N. Léticée,Véronique Cayol,Heather Etchevers,Michel Vekemans,Tania Attié‐Bitach,Férechté Encha‐Razavi	2009	11
7	Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia Prenatal Diagnosis ·Geneviève Quenum‐Miraillet,Valérie Malan,Jelena Martinović,Férechté Encha‐Razavi,Bernard Aral,Isabelle Texier,Jean‐Paul Bonnefont,Michel Vekemans,N. Morichon-Delvallez	2008	2
8	Germinal mosaicism and familial recurrence of a SOX2 mutation with highly variable phenotypic expression extending from AEG syndrome to absence of ocular involvement American Journal of Medical Genetics Part A ·Nicolas Chassaing,Brigitte Gilbert‐Dussardier,Florence Nicot,V. Fermeaux,Férechté Encha‐Razavi,Maryse Fiorenza,Annick Toutain,Patrick Calvas	2007	38
9	De novo Subtelomeric Deletion Additional to an Inherited Apparently Balanced Reciprocal Translocation Fetal Diagnosis and Therapy ·(unknown),Eva Pipiras,S. Kanafani,Cyril Touboul,A. Vergnaud,Férechté Encha‐Razavi,M Sinico,Moncef Benkhalifa,Serdar Kasakyan,Stéphane Serero,Jean‐Philippe Wolf,Marion Gérard‐Blanluet,Brigitte Benzacken	2007	3
10	Bilateral periventricular heterotopias in an X‐linked dominant transmission in a family with two affected males American Journal of Medical Genetics Part A ·Marion Gérard‐Blanluet,Volney Sheen,Kalotina Machinis,Jason Neal,Kira Apse,Claude Danan,Martine Sinico,Pierre Brugières,K Mage,Lanto Ratsimbazafy,Annie Elbez,Jean‐Claude Janaud,Serge Amselem,Christopher A. Walsh,Férechté Encha‐Razavi	2006	20
11	Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy The American Journal of Human Genetics ·Florence Molinari,Annick Raas‐Rothschild,Marlène Rio,Giuseppe Fiermonte,Férechté Encha‐Razavi,Luigi Palmieri,Ferdinando Palmieri,Ziva Ben‐Neriah,Noman Kadhom,Michel Vekemans,Tania Attié‐Bitach,Arnold Münnich,Pierre Rustin,Laurence Colleaux	2005	115
12	Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2 Prenatal Diagnosis ·Agnès Guichet,Stéphane Triau,Catherine Lépinard,Chantal Esculapavit,F. Biquard,Philippe Descamps,Férechté Encha‐Razavi,Dominique Bonneau	2004	20
13	Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development Gene Expression Patterns ·Marie‐Laure Sobrier,Tania Attié‐Bitach,Irène Netchine,Férechté Encha‐Razavi,Michel Vekemans,Serge Amselem	2004	43
14	Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different American Journal of Medical Genetics Part A ·Géraldine Viot,Pascale Sonigo,Isabelle Simon,Brigitte Simon‐Bouy,Frédéric Chadeyron,Chérif Beldjord,Julia Tantau,Jelena Martinović,Chantal Esculpavit,Françis Brunelle,Arnold Münnich,Michel Vekemans,Férechté Encha‐Razavi	2003	23
15	Unusual Variant of Holoprosencephaly in Monosomy 13q Pediatric and Developmental Pathology ·Pascale Marcorelles,Philippe Loget,Catherine Fallet‐Bianco,Jo x EB lle Roume,Férechté Encha‐Razavi,Anne‐Lise Delezoide	2002	20
16	Mosaic trisomy 9 and lobar holoprosencephaly American Journal of Medical Genetics ·Marion Gérard‐Blanluet,Claude Danan,Martine Sinico,F. Lelong,E. Borghi,Gilles Dassieu,Jean‐Claude Janaud,Sylvie Odent,Férechté Encha‐Razavi	2002	12
17	Cerebro‐osseous‐digital syndrome: Four new cases of a lethal skeletal dysplasia—distinct from Neu‐Laxova syndrome American Journal of Medical Genetics ·Alison M. Elliott,Marie Gonzalès,Jean‐Claude Hoeffel,Martine Le Merrer,P Maroteaux,Férechté Encha‐Razavi,Nicole Joyé,Colette Berchel,C. P. Fliegel,David J. Aughton,Kelly Beaudry‐Rodgers,Farnez Hasteh,Michael Nerlich,William R. Wilcox,David L. Rimoin,Ralph S. Lachman,Peter Freisinger	2002	1
18	Expression of the SMADIP1 gene during early human development Mechanisms of Development ·Yolanda Espinosa‐Parrilla,Jeanne Amiel,Joëlle Augé,Férechté Encha‐Razavi,Arnold Münnich,Stanislas Lyonnet,Michel Vekemans,Tania Attié‐Bitach	2002	27
19	Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain The American Journal of Human Genetics ·Renaud Touraine,Tania Attié‐Bitach,E. Manceau,Eckhard Korsch,Pierre Sarda,Véronique Pingault,Férechté Encha‐Razavi,Anna Pelet,Joëlle Augé,A Nivelon‐Chevallier,A. M. Holschneider,Marc Munnes,Walter Doerfler,Michel Goossens,Arnold Munnich,Michel Vekemans,Stanislas Lyonnet	2000	124
20	Expression of the SOX10 gene during human development FEBS Letters ·Nadège Bondurand,Alexandra Kobetz,Véronique Pingault,N Lemort,Férechté Encha‐Razavi,G Couly,Derk E. Goerich,Michael Wegner,Marc Abitbol,Michel Goossens	1998	94

About Férechté Encha‐Razavi

Férechté Encha‐Razavi is a scholar working on Pediatrics, Perinatology and Child Health, Developmental Neuroscience and Genetics, having authored 64 papers that have together received 1.7k indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (19 papers), Hedgehog Signaling Pathway Studies (11 papers), Prenatal Screening and Diagnostics (11 papers), Epigenetics and DNA Methylation (6 papers), RNA Research and Splicing (6 papers), Ocular Disorders and Treatments (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Neurogenesis and neuroplasticity mechanisms (5 papers). The work is most often cited by research in Developmental Neuroscience (172 citations), Genetics (529 citations) and Cell Biology (298 citations). Férechté Encha‐Razavi has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Tania Attié‐Bitach, Michel Vekemans, Arnold Münnich, Nathalie Boddaert, Stanislas Lyonnet, Maryse Bonnière, Catherine Fallet‐Bianco, Yoann Saillour, Jamel Chelly and Michel Goossens. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Nature Neuroscience.

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.

Explore authors with similar magnitude of impact