Stéphane Blanchard

4.1k total citations · 1 hit paper
32 papers, 2.9k citations indexed

About

Stéphane Blanchard is a scholar working on Molecular Biology, Sensory Systems and Cell Biology. According to data from OpenAlex, Stéphane Blanchard has authored 32 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 9 papers in Sensory Systems and 8 papers in Cell Biology. Recurrent topics in Stéphane Blanchard's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Pluripotent Stem Cells Research (7 papers) and RNA and protein synthesis mechanisms (6 papers). Stéphane Blanchard is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), Pluripotent Stem Cells Research (7 papers) and RNA and protein synthesis mechanisms (6 papers). Stéphane Blanchard collaborates with scholars based in France, United States and United Kingdom. Stéphane Blanchard's 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 and has published in prestigious journals such as Nature, Nature Communications and Nature Genetics.

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

Stéphane Blanchard

NEURO

GENET

Kimia Kahrizi Iran

Michel Leibovici France

Jiangang Gao China

Konrad Noben‐Trauth United States

Martine Cohen‐Salmon France

Saima Riazuddin United States

Isabelle Perfettini France

Karen P. Steel United Kingdom

Jacqueline Levilliers France

Philomena Mburu United Kingdom

Kimia Kahrizi Iran

Stéphane Blanchard

1.8k ×1.0

826 ×0.6

252 ×0.6

382 ×0.9

NEURO

835 ×2.3

GENET

Citations per year, relative to Stéphane Blanchard Stéphane Blanchard (= 1×) peers Kimia Kahrizi

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

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

20 of 20 papers shown

Moparthi, Satish Babu, Christine Girard-Blanc, Stéphane Blanchard, et al.. (2024). ATG16L1 induces the formation of phagophore-like membrane cups. Nature Structural & Molecular Biology. 31(9). 1448–1459. 11 indexed citations

Blanchard, Stéphane, Jean‐Pierre Bourgeois, Bernd Jagla, et al.. (2023). Functional maturation of human iPSC-derived pyramidal neurons in vivo is dependent on proximity with the host tissue. Frontiers in Cellular Neuroscience. 17. 1259712–1259712. 1 indexed citations

Koukouli, Fani, Stéphane Blanchard, Olivier Féraud, et al.. (2020). Long-term development of human iPSC-derived pyramidal neurons quantified after transplantation into the neonatal mouse cortex. Developmental Biology. 461(1). 86–95. 8 indexed citations

Wetzel, Lisa A., et al.. (2020). TECPR1 promotes aggrephagy by direct recruitment of LC3C autophagosomes to lysosomes. Nature Communications. 11(1). 2993–2993. 39 indexed citations

Blanchard, Stéphane, et al.. (2015). Modeling amyotrophic lateral sclerosis in pure human iPSc-derived motor neurons isolated by a novel FACS double selection technique. Neurobiology of Disease. 82. 269–280. 22 indexed citations

Blanchard, Stéphane, Élise Roy, Stéphanie Bigou, et al.. (2011). Modeling neuronal defects associated with a lysosomal disorder using patient-derived induced pluripotent stem cells. Human Molecular Genetics. 20(18). 3653–3666. 69 indexed citations

Liu, Song, Stéphane Blanchard, Stéphanie Bigou, et al.. (2010). Neurotrophin 3 Improves Delayed Reconstruction of Sensory Pathways After Cervical Dorsal Root Injury. Neurosurgery. 68(2). 450–461. 8 indexed citations

Liu, Song, et al.. (2009). Combination of Microsurgery and Gene Therapy for Spinal Dorsal Root Injury Repair. Molecular Therapy. 17(6). 992–1002. 9 indexed citations

Blanchard, Stéphane, Michaël Hocquemiller, Georg Haase, et al.. (2006). Forced expression of the motor neuron determinant HB9 in neural stem cells affects neurogenesis. Experimental Neurology. 198(1). 167–182. 19 indexed citations

10.

Leibovici, Michel, Elisabeth Verpy, Richard J. Goodyear, et al.. (2005). Initial characterization of kinocilin, a protein of the hair cell kinocilium. Hearing Research. 203(1-2). 144–153. 19 indexed citations

11.

Coimbra, Roney S., Dominique Weil, Stéphane Blanchard, et al.. (2002). A Subtracted cDNA Library from the Zebrafish (Danio rerio) Embryonic Inner Ear: Table 1.. Genome Research. 12(6). 1007–1011. 26 indexed citations

12.

Verpy, Elisabeth, Saber Masmoudi, Ingrid Zwaenepoel, et al.. (2001). Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus. Nature Genetics. 29(3). 345–349. 132 indexed citations

13.

Verpy, Elisabeth, Michel Leibovici, Ingrid Zwaenepoel, et al.. (2000). A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nature Genetics. 26(1). 51–55. 357 indexed citations

14.

Marlin, Sandrine, Stéphane Blanchard, Rima Slim, et al.. (1999). Townes-Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient. Human Mutation. 14(5). 377–377. 6 indexed citations

15.

Weil, Dominique, Stéphane Blanchard, Gallia G. Levy, et al.. (1997). The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. Nature Genetics. 16(2). 191–193. 313 indexed citations

16.

Crozet, Fabien, A. Amraoui, Stéphane Blanchard, et al.. (1997). Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins. Genomics. 40(2). 332–341. 60 indexed citations

17.

Mazel, Didier, Eric Coı̈c, Stéphane Blanchard, William Saurin, & Philippe Marlière. (1997). A survey of polypeptide deformylase function throughout the eubacterial lineage. Journal of Molecular Biology. 266(5). 939–949. 49 indexed citations

18.

Guilford, Parry, Saïda Ben Arab, Stéphane Blanchard, et al.. (1994). A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genetics. 6(1). 24–28. 208 indexed citations

19.

Guilford, Parry, Stéphane Blanchard, Hassan Chaı̈b, et al.. (1994). A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Human Molecular Genetics. 3(6). 989–993. 97 indexed citations

20.

Hardelin, Jean‐Pierre, Jacqueline Levilliers, Stéphane Blanchard, et al.. (1993). Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. Human Molecular Genetics. 2(4). 373–377. 155 indexed citations

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