Philippe Couarch

702 total citations
7 papers, 253 citations indexed

About

Philippe Couarch is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Philippe Couarch has authored 7 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in Philippe Couarch's work include Genetics and Neurodevelopmental Disorders (4 papers), Epilepsy research and treatment (2 papers) and Congenital heart defects research (2 papers). Philippe Couarch is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Epilepsy research and treatment (2 papers) and Congenital heart defects research (2 papers). Philippe Couarch collaborates with scholars based in France, Italy and Australia. Philippe Couarch's co-authors include Stéphanie Baulac, Eric Leguern, Alexis Brice, Anne de Septenville, Agnès Camuzat, Bruno Dubois, Isabelle Le Ber, Paola Caroppo, Rita Guerreiro and José Brás and has published in prestigious journals such as Neurology, Neurobiology of Aging and Journal of Molecular Medicine.

In The Last Decade

Philippe Couarch

7 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Philippe Couarch France	7	90	77	66	59	57	7	253
Wotu Tian China	10	47 0.5×	105 1.4×	68 1.0×	73 1.2×	42 0.7×	39	280
Anneke J.A. Kievit Netherlands	10	54 0.6×	139 1.8×	108 1.6×	53 0.9×	103 1.8×	17	352
Luigi Citrigno Italy	11	71 0.8×	160 2.1×	101 1.5×	50 0.8×	34 0.6×	31	356
Hatice Karasoy Türkiye	10	52 0.6×	147 1.9×	131 2.0×	59 1.0×	41 0.7×	26	332
Diane F. van Rappard Netherlands	7	53 0.6×	137 1.8×	26 0.4×	20 0.3×	171 3.0×	7	283
Elisa Bonomi Italy	9	42 0.5×	87 1.1×	69 1.0×	16 0.3×	58 1.0×	13	262
Yongjin Yoo South Korea	9	91 1.0×	156 2.0×	19 0.3×	62 1.1×	48 0.8×	19	291
Lee Darwent United Kingdom	7	53 0.6×	170 2.2×	83 1.3×	47 0.8×	61 1.1×	13	279
Sharon Muggeo Italy	8	91 1.0×	156 2.0×	73 1.1×	22 0.4×	46 0.8×	13	290
Himesha Vandebona Australia	8	72 0.8×	136 1.8×	133 2.0×	38 0.6×	40 0.7×	13	287

Countries citing papers authored by Philippe Couarch

Since Specialization

Citations

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

Fields of papers citing papers by Philippe Couarch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Couarch

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Couarch. A scholar is included among the top collaborators of Philippe Couarch 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 Philippe Couarch. Philippe Couarch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Caroppo, Paola, Agnès Camuzat, Anne de Septenville, et al.. (2015). Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 1(4). 481–486. 30 indexed citations

2.

Ber, Isabelle Le, Anne de Septenville, Rita Guerreiro, et al.. (2014). Homozygous TREM2 mutation in a family with atypical frontotemporal dementia. Neurobiology of Aging. 35(10). 2419.e23–2419.e25. 82 indexed citations

3.

Baulac, Stéphanie, Guy M. Lenk, Bouchra Ouled Amar Bencheikh, et al.. (2014). Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria. Neurology. 82(12). 1068–1075. 64 indexed citations

4.

Couarch, Philippe, Santiago Vernia, Isabelle Gourfinkel‐An, et al.. (2011). Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism. Journal of Molecular Medicine. 89(9). 915–925. 19 indexed citations

5.

Baulac, Stéphanie, Isabelle Gourfinkel‐An, Philippe Couarch, et al.. (2008). A Novel Locus for Generalized Epilepsy With Febrile Seizures Plus in French Families. Archives of Neurology. 65(7). 943–51. 33 indexed citations

6.

Baulac, Stéphanie, Ahmed Bouhouche, Philippe Couarch, et al.. (2008). A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22. Neurogenetics. 10(1). 35–42. 6 indexed citations

7.

Chabrol, E, Isabelle Gourfinkel‐An, Ingrid E. Scheffer, et al.. (2007). Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy. Epilepsy Research. 76(1). 41–48. 19 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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