Claire Redin

3.6k total citations · 1 hit paper
18 papers, 1.3k citations indexed

About

Claire Redin is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Claire Redin has authored 18 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Claire Redin's work include Genetic Syndromes and Imprinting (4 papers), Hedgehog Signaling Pathway Studies (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Claire Redin is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Hedgehog Signaling Pathway Studies (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Claire Redin collaborates with scholars based in France, Switzerland and United States. Claire Redin's co-authors include Jean‐Louis Mandel, Amélie Piton, Jared Rutter, Sihem Boudina, Steven P. Gygi, Carl S. Thummel, Eric B. Taylor, Audrey Boutron, M. Brivet and Noah Dephoure and has published in prestigious journals such as Science, Biological Psychiatry and The American Journal of Human Genetics.

In The Last Decade

Claire Redin

18 papers receiving 1.3k 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.

A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans

2012 644 citations Eric B. Taylor, John C. Schell et al. Science profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Claire Redin France	10	888	482	177	143	123	18	1.3k
Julie R. Jones United States	21	1.1k 1.2×	765 1.6×	95 0.5×	335 2.3×	28 0.2×	55	1.8k
Tie-Shan Tang China	23	1.1k 1.2×	199 0.4×	134 0.8×	66 0.5×	151 1.2×	54	1.6k
Atish Mukherjee United States	14	597 0.7×	425 0.9×	123 0.7×	384 2.7×	300 2.4×	18	1.4k
Kenji Ohe Japan	21	669 0.8×	309 0.6×	93 0.5×	82 0.6×	80 0.7×	74	1.3k
Dirk Prawitt Germany	26	1.2k 1.4×	579 1.2×	147 0.8×	113 0.8×	25 0.2×	49	2.0k
Minoru Asada Japan	19	536 0.6×	89 0.2×	86 0.5×	89 0.6×	37 0.3×	42	1.0k
Anita C. Maiyar United States	14	1.4k 1.5×	326 0.7×	156 0.9×	116 0.8×	35 0.3×	16	1.9k
Shin‐ichiro Takebayashi Japan	22	2.8k 3.2×	586 1.2×	161 0.9×	145 1.0×	25 0.2×	48	3.1k
Salome Gluecksohn‐Waelsch United States	24	1.1k 1.2×	537 1.1×	101 0.6×	186 1.3×	55 0.4×	72	1.8k
John J. Sharp United States	11	679 0.8×	228 0.5×	95 0.5×	193 1.3×	28 0.2×	14	1.5k

Countries citing papers authored by Claire Redin

Since Specialization

Citations

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

Fields of papers citing papers by Claire Redin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claire Redin

This figure shows the co-authorship network connecting the top 25 collaborators of Claire Redin. A scholar is included among the top collaborators of Claire Redin 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 Claire Redin. Claire Redin 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:

18 of 18 papers shown

1.

Hodel, Flavia, Christian W. Thorball, Claire Redin, et al.. (2024). Prevalence of actionable pharmacogenetic variants and high‐risk drug prescriptions: A Swiss hospital‐based cohort study. Clinical and Translational Science. 17(9). e70009–e70009. 6 indexed citations

2.

Redin, Claire, Zahurul A. Bhuiyan, Alessandra Pia Porretta, et al.. (2022). The «Amish» NM_000256.3:c.3330+2T>G splice variant in MYBPC3 associated with hypertrophic cardiomyopathy is an ancient Swiss mutation. European Journal of Medical Genetics. 65(12). 104627–104627. 1 indexed citations

3.

Redin, Claire, et al.. (2020). Pharmacogénomique et aide à la prescription médicamenteuse. Revue Médicale Suisse. 16(716). 2259–2263. 1 indexed citations

4.

Redin, Claire, et al.. (2020). [Pharmacogenomics : a toolbox to improve drug prescription].. PubMed. 16(716). 2259–2263. 3 indexed citations

5.

Zepeda‐Mendoza, Cinthya, Tammy Kammin, David J. Harris, et al.. (2018). Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin. European Journal of Human Genetics. 26(3). 374–381. 4 indexed citations

6.

Quartier, Angélique, Claire Redin, Céline Keime, et al.. (2018). Genes and Pathways Regulated by Androgens in Human Neural Cells, Potential Candidates for the Male Excess in Autism Spectrum Disorder. Biological Psychiatry. 84(4). 239–252. 53 indexed citations

7.

Lohmann, Katja, Claire Redin, Holger Tönnies, et al.. (2017). Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia. JAMA Neurology. 74(7). 806–806. 5 indexed citations

8.

Schaefer, Élise, Corinne Stoetzel, Sophie Scheidecker, et al.. (2016). Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet–Biedl syndrome. Journal of Human Genetics. 61(5). 447–450. 57 indexed citations

9.

Geoffroy, Véronique, Cécile Pizot, Claire Redin, et al.. (2015). VaRank: a simple and powerful tool for ranking genetic variants. PeerJ. 3. e796–e796. 47 indexed citations

10.

Renaud, M., Mathieu Anheim, Erik‐Jan Kamsteeg, et al.. (2014). Autosomal Recessive Cerebellar Ataxia Type 3 Due toANO10Mutations. JAMA Neurology. 71(10). 1305–1305. 32 indexed citations

11.

Piton, Amélie, Claire Redin, & Jean‐Louis Mandel. (2013). XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing. The American Journal of Human Genetics. 93(2). 368–383. 165 indexed citations

12.

Piton, Amélie, Claire Redin, & Jean‐Louis Mandel. (2013). XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing. The American Journal of Human Genetics. 93(2). 406–406. 7 indexed citations

13.

Redin, Claire, Corinne Stoetzel, Inès Ouertani, et al.. (2013). Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis. Clinical Genetics. 85(2). 172–177. 25 indexed citations

14.

Schaefer, Élise, M. Durand, Cathy Obringer, et al.. (2013). Mesoaxial polydactyly is a major feature in Bardet–Biedl syndrome patients with LZTFL1 (BBS17) mutations. Clinical Genetics. 85(5). 476–481. 30 indexed citations

15.

Taylor, Eric B., John C. Schell, Audrey Boutron, et al.. (2012). A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans. Science. 337(6090). 96–100. 644 indexed citations breakdown →

16.

Redin, Claire, Stéphanie Le Gras, Véronique Geoffroy, et al.. (2012). Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes. Journal of Medical Genetics. 49(8). 502–512. 81 indexed citations

17.

Koscinski, Isabelle, Elias Elinati, Claire Redin, et al.. (2011). DPY19L2 Deletion as a Major Cause of Globozoospermia. The American Journal of Human Genetics. 88(3). 344–350. 149 indexed citations

18.

Koscinski, Isabelle, Elias Elinati, Claire Redin, et al.. (2011). DPY19L2 Deletion as a Major Cause of Globozoospermia. The American Journal of Human Genetics. 88(4). 517–517. 4 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