Arnold Munnich

3.4k total citations
55 papers, 2.3k citations indexed

About

Arnold Munnich is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Arnold Munnich has authored 55 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Surgery. Recurrent topics in Arnold Munnich's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (8 papers) and ATP Synthase and ATPases Research (5 papers). Arnold Munnich is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (8 papers) and ATP Synthase and ATPases Research (5 papers). Arnold Munnich collaborates with scholars based in France, United Kingdom and United States. Arnold Munnich's co-authors include Pierre Rustin, Agnès Rötig, Daniel Sidi, Stanislas Lyonnet, Jürgen‐Christoph von Kleist-Retzow, Karine Chantrel-Groussard, Valérie Cormier‐Daire, S. Gerber, Jean‐Michel Rozet and Dominique Chrétien and has published in prestigious journals such as Science, The Lancet and Nature Genetics.

In The Last Decade

Arnold Munnich

54 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arnold Munnich France 25 1.6k 580 365 341 237 55 2.3k
Yoshinori Tsurusaki Japan 37 2.6k 1.6× 1.6k 2.8× 181 0.5× 357 1.0× 60 0.3× 146 3.9k
Arjan P.M. de Brouwer Netherlands 30 1.6k 1.0× 923 1.6× 107 0.3× 180 0.5× 59 0.2× 77 2.4k
Scott Noggle United States 27 2.7k 1.6× 326 0.6× 74 0.2× 581 1.7× 61 0.3× 53 3.4k
Elsebet Østergaard Denmark 26 1.6k 1.0× 298 0.5× 808 2.2× 151 0.4× 70 0.3× 67 2.2k
Annick Raas‐Rothschild Israel 34 1.7k 1.0× 898 1.5× 190 0.5× 262 0.8× 28 0.1× 108 3.8k
Kimia Kahrizi Iran 30 1.8k 1.1× 835 1.4× 75 0.2× 203 0.6× 33 0.1× 141 3.0k
Katrin Õunap Estonia 25 1.0k 0.6× 857 1.5× 249 0.7× 91 0.3× 35 0.1× 106 1.8k
Roberta Biancheri Italy 31 1.3k 0.8× 377 0.7× 264 0.7× 350 1.0× 15 0.1× 100 2.5k
Daniel P. Seeburg United States 16 1.4k 0.9× 380 0.7× 93 0.3× 570 1.7× 25 0.1× 26 2.2k
Eduardo Silva Portugal 24 894 0.6× 264 0.5× 62 0.2× 179 0.5× 496 2.1× 60 1.5k

Countries citing papers authored by Arnold Munnich

Since Specialization
Citations

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

Fields of papers citing papers by Arnold Munnich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnold Munnich

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

All Works

20 of 20 papers shown
1.
Thompson, Miles D., Marjan M. Nezarati, Gabriele Gillessen‐Kaesbach, et al.. (2010). Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndrome. American Journal of Medical Genetics Part A. 152A(7). 1661–1669. 36 indexed citations
2.
Huber, Céline, Kim‐Hanh Le Quan Sang, Geneviève Baujat, et al.. (2009). Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum. Journal of Medical Genetics. 48(2). 88–92. 53 indexed citations
3.
Didelot, Gérard, Florence Molinari, P. Tchénio, et al.. (2006). Tequila, a Neurotrypsin Ortholog, Regulates Long-Term Memory Formation in Drosophila. Science. 313(5788). 851–853. 67 indexed citations
4.
Romero, Norma B., Pascale de Lonlay, S. Llense, et al.. (2001). Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with ‘de novo’ duplication of dystrophin gene. Neuromuscular Disorders. 11(5). 494–498. 10 indexed citations
5.
Faivre, Laurence, Jean‐Paul Bonnefont, Stanislas Lyonnet, Arnold Munnich, & Michel Vekemans. (2000). Improvement of cystic fibrosis using antitumoral drugs: a hypothesis. Medical Hypotheses. 54(4). 580–581. 2 indexed citations
6.
Touraine, Renaud, Tania Attié‐Bitach, E. Manceau, et al.. (2000). Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain. The American Journal of Human Genetics. 66(5). 1496–1503. 124 indexed citations
7.
Cabot, Annick, Jean‐Michel Rozet, S. Gerber, et al.. (1999). A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3. The American Journal of Human Genetics. 64(4). 1141–1146. 66 indexed citations
8.
Valnot, Isabelle, Dominique Chrétien, Pascale de Lonlay, et al.. (1999). A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency. Human Genetics. 104(6). 460–466. 81 indexed citations
9.
Rustin, Pierre, Jürgen‐Christoph von Kleist-Retzow, Karine Chantrel-Groussard, et al.. (1999). Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study. The Lancet. 354(9177). 477–479. 274 indexed citations
10.
Amiel, Jeanne, François Doz, M Prieur, et al.. (1998). Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome. Clinical Genetics. 53(4). 278–280. 24 indexed citations
11.
Lonlay-Debeney, Pascale de, Marie‐Christine de Blois, Damien Bonnet, et al.. (1998). Ebstein anomaly associated with rearrangements of chromosomal region 11q. American Journal of Medical Genetics. 80(2). 157–159. 21 indexed citations
12.
Roume, J., M. Le Merrer, Valérie Cormier‐Daire, et al.. (1997). Genetic heterogeneity of Meckel syndrome.. Journal of Medical Genetics. 34(12). 1003–1006. 9 indexed citations
13.
Géromel, Vanna, Béatrice Parfait, Jürgen‐Christoph von Kleist-Retzow, et al.. (1997). The Consequences of a Mild Respiratory Chain Deficiency on Substrate Competitive Oxidation in Human Mitochondria. Biochemical and Biophysical Research Communications. 236(3). 643–646. 22 indexed citations
14.
Feldman, George, Dolores Saavedra, Nathaniel H. Robin, et al.. (1997). A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22. Human Molecular Genetics. 6(11). 1937–1941. 28 indexed citations
15.
Rousseau, F., Jacky Bonaventure, M Le Merrer, P Maroteaux, & Arnold Munnich. (1996). [Mutations of FGFR3 gene cause 3 types of nanisms with variably severity: achondroplasia, thanatophoric nanism and hypochondroplasia].. PubMed. 57(3). 153–153. 5 indexed citations
16.
Rousseau, F., Arnold Munnich, & M Le Merrer. (1994). Not all hypochondroplasia families are linked to chromosome 4p16.3. The American Journal of Human Genetics. 55. 5 indexed citations
17.
Rustin, Pierre, J. Lebidois, Dominique Chrétien, et al.. (1994). Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies. The Journal of Pediatrics. 124(2). 224–228. 60 indexed citations
18.
Kaplan, Josseline, S. Gerber, Dominique Larget‐Piet, et al.. (1993). A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1. Nature Genetics. 5(3). 308–311. 130 indexed citations
19.
Caillaud, Catherine, Laura Vilarinho, Rosário Santos, et al.. (1992). Linkage disequilibrium between phenylketonuria and RFLP haplotype 1 at the phenylalanine hydroxylase locus in Portugal. Human Genetics. 89(1). 69–72. 9 indexed citations
20.
Amédée-Manesme, O, et al.. (1982). [Heterogeneity of leucinosis. Correlations between clinical manifestations, protein tolerance and enzyme deficiency].. PubMed. 39 Suppl 2. 735–40. 3 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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