Stéphane Blanchard

4.1k citations

32 papers · 2.9k indexed · 1 hit paper · h-index 20

Molecular Biology top 5%
Sensory Systems top 0.1%
Cell Biology top 5%
Neurology top 2%
Genetics top 5%

Co-authors: Christine Petit Jacqueline Levilliers Fabienne Lévi-Acobas Parry Guilford Mohamed Drira Dominique Weil Michael D. Weston F A Gibson
Topics: Hearing, Cochlea, Tinnitus, Genetics (9 papers)Pluripotent Stem Cells Research (7 papers)RNA and protein synthesis mechanisms (6 papers)
Cited by: Sensory Systems Neurology Otorhinolaryngology
Journals: Nature Nature Communications Nature Genetics
Partner nations: France United States United Kingdom

In The Last Decade

Stéphane Blanchard

32 papers receiving 2.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Defective myosin VIIA gene responsible for Usher syndrome type IB

1995 819 citations Stéphane Blanchard, Parry Guilford et al. profile →

Peers

Countries citing papers authored by Stéphane Blanchard

Since Specialization

Citations

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

Fields of papers citing papers by Stéphane Blanchard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphane Blanchard

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphane Blanchard. A scholar is included among the top collaborators of Stéphane Blanchard 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 Stéphane Blanchard. Stéphane Blanchard 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	ATG16L1 induces the formation of phagophore-like membrane cups 2024 ·Nature Structural & Molecular Biology ·(unknown),Satish Babu Moparthi,Christine Girard-Blanc,(unknown),Stéphane Blanchard,(unknown),(unknown),Audrey Salles,(unknown),Stéphane Vassilopoulos,Thomas Wollert	11
2	Functional maturation of human iPSC-derived pyramidal neurons in vivo is dependent on proximity with the host tissue 2023 ·Frontiers in Cellular Neuroscience ·(unknown),(unknown),(unknown),Stéphane Blanchard,Jean‐Pierre Bourgeois,Bernd Jagla,Baptiste Saudemont,(unknown),Stéphanie Pons,Uwe Maskos	1
3	Long-term development of human iPSC-derived pyramidal neurons quantified after transplantation into the neonatal mouse cortex 2020 ·Developmental Biology ·(unknown),Fani Koukouli,Stéphane Blanchard,(unknown),(unknown),(unknown),Olivier Féraud,Annelise Bennaceur‐Griscelli,Matthias Groszer,Uwe Maskos	8
4	TECPR1 promotes aggrephagy by direct recruitment of LC3C autophagosomes to lysosomes 2020 ·Nature Communications ·Lisa A. Wetzel,Stéphane Blanchard,(unknown),Viola Beier,Anna Kaufmann,Thomas Wollert	39
5	Modeling amyotrophic lateral sclerosis in pure human iPSc-derived motor neurons isolated by a novel FACS double selection technique 2015 ·Neurobiology of Disease ·(unknown),(unknown),Stéphane Blanchard,(unknown),Boris Lamotte d’Incamps,(unknown),Gilbert Baillat,Delphine Bohl,Georg Haase	22
6	Modeling neuronal defects associated with a lysosomal disorder using patient-derived induced pluripotent stem cells 2011 ·Human Molecular Genetics ·(unknown),Stéphane Blanchard,(unknown),Élise Roy,Stéphanie Bigou,Roseline Froissart,Isabelle Rouvet,Sandrine Vitry,Jean Michel Heard,Delphine Bohl	69
7	Neurotrophin 3 Improves Delayed Reconstruction of Sensory Pathways After Cervical Dorsal Root Injury 2010 ·Neurosurgery ·Song Liu,Stéphane Blanchard,Stéphanie Bigou,Sandrine Vitry,Delphine Bohl,Jean‐Michel Heard	8
8	Combination of Microsurgery and Gene Therapy for Spinal Dorsal Root Injury Repair 2009 ·Molecular Therapy ·Song Liu,Delphine Bohl,Stéphane Blanchard,(unknown),Gérard Saïd,Jean‐Michel Heard	9
9	Forced expression of the motor neuron determinant HB9 in neural stem cells affects neurogenesis 2006 ·Experimental Neurology ·(unknown),Stéphane Blanchard,Michaël Hocquemiller,Georg Haase,Song Liu,Anne Nosjean,Jean Michel Heard,Delphine Bohl	19
10	Initial characterization of kinocilin, a protein of the hair cell kinocilium 2005 ·Hearing Research ·Michel Leibovici,Elisabeth Verpy,Richard J. Goodyear,Ingrid Zwaenepoel,Stéphane Blanchard,(unknown),Guy P. Richardson,Christine Petit	19
11	A Subtracted cDNA Library from the Zebrafish (Danio rerio) Embryonic Inner Ear: Table 1. 2002 ·Genome Research ·Roney S. Coimbra,Dominique Weil,(unknown),Stéphane Blanchard,Michael H. Levi,Jean‐Pierre Hardelin,Jean Weissenbach,Christine Petit	26
12	Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus 2001 ·Nature Genetics ·Elisabeth Verpy,Saber Masmoudi,Ingrid Zwaenepoel,Michel Leibovici,Tim Hutchin,Ignacio del Castillo,Sylvie Nouaille,Stéphane Blanchard,(unknown),Jean‐Luc Popot,Felipe Moreno,Robert F. Mueller,Christine Petit	132
13	A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C 2000 ·Nature Genetics ·Elisabeth Verpy,Michel Leibovici,Ingrid Zwaenepoel,Xue-Zhong Liu,Andreas Gal,Nabiha Salem,Ahmad M. Mansour,Stéphane Blanchard,Ichiro Kobayashi,Bronya J.B. Keats,Rima Slim,Christine Petit	357
14	Townes-Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient 1999 ·Human Mutation ·Sandrine Marlin,Stéphane Blanchard,Rima Slim,Didier Lacombe,Françoise Denoyelle,(unknown),Elisa Calzolari,Valérie Drouin‐Garraud,(unknown),A Fourmaintraux,Nicole Philip,Jean‐Edmond Toublanc,Christine Petit	6
15	The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene 1997 ·Nature Genetics ·Dominique Weil,(unknown),Stéphane Blanchard,Gallia G. Levy,Fabienne Lévi-Acobas,Mohamed Drira,Hammadi Ayadi,Christine Petit	313
16	Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins 1997 ·Genomics ·Fabien Crozet,A. Amraoui,Stéphane Blanchard,Marc Lenoir,Chantal Ripoll,Philippe Vago,Christian Hamel,Cécile Fizames,Fabienne Lévi-Acobas,D. Depétris,Marie‐Geneviève Mattéi,Dominique Weil,Rémy Pujol,Christine Petit	60
17	A survey of polypeptide deformylase function throughout the eubacterial lineage 1997 ·Journal of Molecular Biology ·Didier Mazel,Eric Coı̈c,Stéphane Blanchard,William Saurin,Philippe Marlière	49
18	A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q 1994 ·Nature Genetics ·Parry Guilford,Saïda Ben Arab,Stéphane Blanchard,Jacqueline Levilliers,Jean Weissenbach,(unknown),Christine Petit	208
19	A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene 1994 ·Human Molecular Genetics ·Parry Guilford,(unknown),Stéphane Blanchard,Hassan Chaı̈b,Denis Le Paslier,Jean Weissenbach,Mohamed Drira,Christine Petit	97
20	Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome 1993 ·Human Molecular Genetics ·Jean‐Pierre Hardelin,Jacqueline Levilliers,Stéphane Blanchard,Jean‐Claude Carel,M Leuténegger,(unknown),Pierre Bouloux,Christine Petit	155

About Stéphane Blanchard

Stéphane Blanchard is a scholar working on Sensory Systems, Cell Biology and Developmental Neuroscience, having authored 32 papers that have together received 2.9k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Pluripotent Stem Cells Research (7 papers) and RNA and protein synthesis mechanisms (6 papers). The work is most often cited by research in Sensory Systems (1.4k citations), Neurology (406 citations) and Otorhinolaryngology (170 citations). Stéphane Blanchard has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Christine Petit, Jacqueline Levilliers, Fabienne Lévi-Acobas, Parry Guilford, Mohamed Drira, Dominique Weil, Michael D. Weston, F A Gibson, Anabel Varela and James Walsh. Their work appears in journals such as Nature, Nature Communications and Nature Genetics.

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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