Férechté Encha‐Razavi

5.2k citations

64 papers · 1.7k indexed · h-index 21

Molecular Biology top 10%
Genetics top 5%
Pediatrics, Perinatology and Child Health top 5%
Cell Biology top 5%
Surgery

Co-authors: Tania Attié‐Bitach Michel Vekemans Arnold Münnich Nathalie Boddaert Stanislas Lyonnet Maryse Bonnière Catherine Fallet‐Bianco Yoann Saillour
Topics: Fetal and Pediatric Neurological Disorders (19 papers)Hedgehog Signaling Pathway Studies (11 papers)Prenatal Screening and Diagnostics (11 papers)
Cited by: Developmental Neuroscience Genetics Cell Biology
Journals: Proceedings of the National Academy of Sciences Nature Genetics Nature Neuroscience
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 of co-authors of Férechté Encha‐Razavi

This figure shows the co-authorship network connecting the top 25 collaborators of Férechté Encha‐Razavi. A scholar is included among the top collaborators of Férechté Encha‐Razavi 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 Férechté Encha‐Razavi. Férechté Encha‐Razavi 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	Mapping the developmental profile of ventricular zone–derived neurons in the human cerebellum 2025 ·Proceedings of the National Academy of Sciences ·Anders W. Erickson,(unknown),Liam D. Hendrikse,(unknown),Zachary Thomson,(unknown),Omar Khan,(unknown),(unknown),Anusha Mishra,(unknown),Željka Krsnik,Férechté Encha‐Razavi,(unknown),Fabien Guimiot,Evelina Silvestri,Kimberly A. Aldinger,Michael D. Taylor,Kathleen J. Millen,Parthiv Haldipur	0
2	Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation 2021 ·Birth Defects Research ·Suzanne Chartier,Lucile Boutaud,(unknown),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	2
3	A clinical and histopathological study of malformations observed in fetuses infected by the Zika virus 2018 ·Brain Pathology ·Aurélie Bèaufrere,Bettina Bessières,Maryse Bonnière,(unknown),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	15
4	Prevalence and timing of pregnancy termination for brain malformations: Table 1 2011 ·Archives of Disease in Childhood Fetal & Neonatal ·Caroline Rouleau,(unknown),Nicole Bigi,A. Couture,María Jesús Pérez-Granda,Patricia Blanchet,Jean-Michel Faure,François Rivier,P. Boulot,Annie Laquerrière,Férechté Encha‐Razavi	11
5	PAX2 mutations in fetal renal hypodysplasia 2010 ·American Journal of Medical Genetics Part A ·(unknown),Alexandra Benachi,Maryse Bonnière,(unknown),Chantal Esculpavit,Nicole Morichon,Michel Vekemans,Corinne Antignac,Rémi Salomon,Férechté Encha‐Razavi,Tania Attié‐Bitach,Marie-Claire Gübler	28
6	Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): Report of 16 fetal cases 2009 ·European Journal of Medical Genetics ·(unknown),B. Foliguet,Louise Devisme,Laurence Lœuillet,Pascale Marcorelles,Maryse Bonnière,A. Laquérrière,Catherine Fallet‐Bianco,Jelena Martinović,(unknown),(unknown),Véronique Cayol,Heather Etchevers,Michel Vekemans,Tania Attié‐Bitach,Férechté Encha‐Razavi	11
7	Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia 2008 ·Prenatal Diagnosis ·(unknown),Valérie Malan,Jelena Martinović,Férechté Encha‐Razavi,Bernard Aral,Isabelle Texier,Jean‐Paul Bonnefont,Michel Vekemans,N. Morichon-Delvallez	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 2007 ·American Journal of Medical Genetics Part A ·Nicolas Chassaing,Brigitte Gilbert‐Dussardier,Florence Nicot,V. Fermeaux,Férechté Encha‐Razavi,(unknown),Annick Toutain,Patrick Calvas	38
9	De novo Subtelomeric Deletion Additional to an Inherited Apparently Balanced Reciprocal Translocation 2007 ·Fetal Diagnosis and Therapy ·(unknown),Eva Pipiras,(unknown),Cyril Touboul,(unknown),Férechté Encha‐Razavi,(unknown),Moncef Benkhalifa,(unknown),Stéphane Serero,Jean‐Philippe Wolf,Marion Gérard‐Blanluet,Brigitte Benzacken	3
10	Bilateral periventricular heterotopias in an X‐linked dominant transmission in a family with two affected males 2006 ·American Journal of Medical Genetics Part A ·Marion Gérard‐Blanluet,Volney Sheen,(unknown),Jason Neal,Kira Apse,Claude Danan,Martine Sinico,Pierre Brugières,(unknown),(unknown),(unknown),(unknown),Serge Amselem,Christopher A. Walsh,Férechté Encha‐Razavi	20
11	Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy 2005 ·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	115
12	Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2 2004 ·Prenatal Diagnosis ·Agnès Guichet,Stéphane Triau,(unknown),(unknown),F. Biquard,Philippe Descamps,Férechté Encha‐Razavi,Dominique Bonneau	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 2004 ·Gene Expression Patterns ·Marie‐Laure Sobrier,Tania Attié‐Bitach,Irène Netchine,Férechté Encha‐Razavi,Michel Vekemans,Serge Amselem	43
14	Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different 2003 ·American Journal of Medical Genetics Part A ·Géraldine Viot,Pascale Sonigo,Isabelle Simon,Brigitte Simon‐Bouy,(unknown),Chérif Beldjord,Julia Tantau,Jelena Martinović,Chantal Esculpavit,Françis Brunelle,Arnold Münnich,Michel Vekemans,Férechté Encha‐Razavi	23
15	Unusual Variant of Holoprosencephaly in Monosomy 13q 2002 ·Pediatric and Developmental Pathology ·Pascale Marcorelles,Philippe Loget,Catherine Fallet‐Bianco,(unknown),Férechté Encha‐Razavi,Anne‐Lise Delezoide	20
16	Mosaic trisomy 9 and lobar holoprosencephaly 2002 ·American Journal of Medical Genetics ·Marion Gérard‐Blanluet,Claude Danan,Martine Sinico,F. Lelong,(unknown),Gilles Dassieu,(unknown),Sylvie Odent,Férechté Encha‐Razavi	12
17	Cerebro‐osseous‐digital syndrome: Four new cases of a lethal skeletal dysplasia—distinct from Neu‐Laxova syndrome 2002 ·American Journal of Medical Genetics ·Alison M. Elliott,Marie Gonzalès,(unknown),Martine Le Merrer,P Maroteaux,Férechté Encha‐Razavi,Nicole Joyé,(unknown),(unknown),David J. Aughton,(unknown),(unknown),Michael Nerlich,William R. Wilcox,David L. Rimoin,Ralph S. Lachman,Peter Freisinger	1
18	Expression of the SMADIP1 gene during early human development 2002 ·Mechanisms of Development ·Yolanda Espinosa‐Parrilla,Jeanne Amiel,Joëlle Augé,Férechté Encha‐Razavi,Arnold Münnich,Stanislas Lyonnet,Michel Vekemans,Tania Attié‐Bitach	27
19	Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain 2000 ·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,(unknown),Michel Goossens,Arnold Munnich,(unknown),Stanislas Lyonnet	124
20	Expression of the SOX10 gene during human development 1998 ·FEBS Letters ·Nadège Bondurand,Alexandra Kobetz,Véronique Pingault,N Lemort,Férechté Encha‐Razavi,G Couly,(unknown),Michael Wegner,Marc Abitbol,Michel Goossens	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) and Prenatal Screening and Diagnostics (11 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.

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