Christel Depienne

18.1k total citations · 1 hit paper
98 papers, 3.2k citations indexed

About

Christel Depienne is a scholar working on Cellular and Molecular Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, Christel Depienne has authored 98 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Cellular and Molecular Neuroscience, 35 papers in Genetics and 31 papers in Molecular Biology. Recurrent topics in Christel Depienne's work include Genetics and Neurodevelopmental Disorders (27 papers), Hereditary Neurological Disorders (21 papers) and Epilepsy research and treatment (20 papers). Christel Depienne is often cited by papers focused on Genetics and Neurodevelopmental Disorders (27 papers), Hereditary Neurological Disorders (21 papers) and Epilepsy research and treatment (20 papers). Christel Depienne collaborates with scholars based in France, Germany and United States. Christel Depienne's co-authors include Giovanni Stévanin, Eric Leguern, Jean‐Louis Mandel, Alexis Brice, Alexandra Dürr, Stephan Klebe, Florence Riant, Isabelle Gourfinkel‐An, Stéphanie Baulac and Emmanuel Roze and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Christel Depienne

93 papers receiving 3.1k citations

Hit Papers

align trajectories sort by overperformance

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.

30 years of repeat expansion disorders: What have we learned and what are the remaining challenges?

2021 187 citations Christel Depienne et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christel Depienne France	33	1.1k	1.1k	836	755	596	98	3.2k
Fritz Zimprich Austria	30	632 0.6×	806 0.7×	375 0.4×	719 1.0×	843 1.4×	102	3.1k
Véronique Rogemond France	46	1.8k 1.6×	1.3k 1.2×	860 1.0×	230 0.3×	3.4k 5.8×	112	5.4k
O. Robain France	31	994 0.9×	1.6k 1.5×	337 0.4×	718 1.0×	234 0.4×	86	3.2k
Marie‐Françoise Belin France	37	1.9k 1.7×	1.3k 1.1×	219 0.3×	120 0.2×	468 0.8×	98	3.7k
Donald E. Born United States	30	968 0.9×	822 0.7×	161 0.2×	477 0.6×	471 0.8×	73	3.2k
Tateki Kikuchi Japan	23	1.6k 1.4×	1.8k 1.6×	613 0.7×	259 0.3×	339 0.6×	80	3.5k
Dietrich Stephan United States	32	520 0.5×	2.3k 2.1×	812 1.0×	84 0.1×	206 0.3×	78	3.9k
Fung‐Chow Chiu United States	26	1.1k 1.0×	1.7k 1.5×	148 0.2×	106 0.1×	398 0.7×	56	3.5k
Tadao Serikawa Japan	36	1.4k 1.2×	2.0k 1.7×	948 1.1×	677 0.9×	209 0.4×	213	3.9k
Xiaoyu Peng United States	14	1.4k 1.2×	1.3k 1.2×	1.5k 1.8×	494 0.7×	4.6k 7.7×	23	5.7k

Countries citing papers authored by Christel Depienne

Since Specialization

Citations

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

Fields of papers citing papers by Christel Depienne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christel Depienne

This figure shows the co-authorship network connecting the top 25 collaborators of Christel Depienne. A scholar is included among the top collaborators of Christel Depienne 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 Christel Depienne. Christel Depienne 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

Corbett, Mark, Christel Depienne, Liana Veneziano, et al.. (2023). Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions. Epilepsia. 64(S1). S14–S21. 11 indexed citations

Tsai, Meng‐Han, Catherine Diao, Sabine Kaya, et al.. (2023). A novel FAME1 repeat configuration in a European family identified using a combined genomics approach. Epilepsia Open. 8(2). 659–665. 10 indexed citations

Trinh, Joanne, Susen Schaake, Björn‐Hergen Laabs, et al.. (2022). Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onset. Brain. 146(3). 1075–1082. 15 indexed citations

Doummar, Diane, Thierry Bienvenu, Perrine Charles, et al.. (2021). Tremor-like subcortical myoclonus in STXBP1 encephalopathy. European Journal of Paediatric Neurology. 34. 62–66. 4 indexed citations

Yigit, Gökhan, Janine Altmüller, Hölger Thiele, et al.. (2021). MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease. European Journal of Medical Genetics. 64(10). 104310–104310. 6 indexed citations

Moretti, Raffaella, Lionel Arnaud, Delphine Bouteiller, et al.. (2021). SCN1A-related epilepsy with recessive inheritance: Two further families. European Journal of Paediatric Neurology. 33. 121–124. 4 indexed citations

Hiatt, Susan M., Michelle L. Thompson, Jeremy W. Prokop, et al.. (2019). Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder. The American Journal of Human Genetics. 104(4). 701–708. 15 indexed citations

Yamada, Elizabeth Sumi, Gesine Respondek, Anderson de Andrade, et al.. (2014). Annonacin, a natural lipophilic mitochondrial complex I inhibitor, increases phosphorylation of tau in the brain of FTDP-17 transgenic mice. Experimental Neurology. 253. 113–125. 37 indexed citations

Mignot, Cyril, Marie‐Laure Moutard, Oriane Trouillard, et al.. (2011). STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients. Epilepsia. 52(10). 1820–1827. 76 indexed citations

10.

Debs, Rabab, Christel Depienne, Agnès Rastetter, et al.. (2010). Biotin-Responsive Basal Ganglia Disease in Ethnic Europeans With Novel SLC19A3 Mutations. Archives of Neurology. 67(1). 126–30. 73 indexed citations

11.

Deback, Claire, Charles‐Édouard Luyt, Sylvain Lespinats, et al.. (2010). Microsatellite analysis of HSV-1 isolates: From oropharynx reactivation toward lung infection in patients undergoing mechanical ventilation. Journal of Clinical Virology. 47(4). 313–320. 15 indexed citations

12.

Riant, Florence, et al.. (2010). De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. Neurology. 75(11). 967–972. 95 indexed citations

13.

Vahedi, Katayoun, Christel Depienne, Florence Riant, et al.. (2009). Elicited repetitive daily blindness. Neurology. 72(13). 1178–1183. 66 indexed citations

14.

Gauvain, Grégory, Isabelle Gourfinkel‐An, Estelle Fédirko, et al.. (2009). Two novelCLCN2mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy. Human Mutation. 30(3). 397–405. 46 indexed citations

15.

Goizet, Cyril, Amir Boukhris, Emeline Mundwiller, et al.. (2008). Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10. Human Mutation. 30(2). E376–E385. 95 indexed citations

16.

Chojnowski, Alexandre, N. Ravisé, Corinne Bachelin, et al.. (2007). Silencing of the Charcot–Marie–Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells. Neurobiology of Disease. 26(2). 323–331. 10 indexed citations

17.

Eugène, Emmanuel, Christel Depienne, Stéphanie Baulac, et al.. (2007). GABA_AReceptor γ2 Subunit Mutations Linked to Human Epileptic Syndromes Differentially Affect Phasic and Tonic Inhibition. Journal of Neuroscience. 27(51). 14108–14116. 67 indexed citations

18.

Höllerhage, Matthias, Marie‐Paule Muriel, Pierre Champy, et al.. (2007). Annonacin, a Natural Mitochondrial Complex I Inhibitor, Causes Tau Pathology in Cultured Neurons. Journal of Neuroscience. 27(29). 7827–7837. 170 indexed citations

19.

Klebe, Stephan, Alexandra Dürr, Naïma Bouslam, et al.. (2007). Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 854–861. 14 indexed citations

20.

Mansky, Louis M., Sandra Prévéral, Erwann Le Rouzic, et al.. (2001). Interaction of Human Immunodeficiency Virus Type 1 Vpr with the HHR23A DNA Repair Protein Does Not Correlate with Multiple Biological Functions of Vpr. Virology. 282(1). 176–185. 23 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.

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