A Munnich

476 total citations
14 papers, 275 citations indexed

About

A Munnich is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, A Munnich has authored 14 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 5 papers in Physiology. Recurrent topics in A Munnich's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Metabolomics and Mass Spectrometry Studies (2 papers). A Munnich is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Metabolomics and Mass Spectrometry Studies (2 papers). A Munnich collaborates with scholars based in France, Belgium and Italy. A Munnich's co-authors include Agnès Rötig, Jean‐Paul Bonnefont, Pierre Rustin, Thomas Bourgeron, Dominique Chrétien, Nathalie Boddaert, Giuseppe Fiermonte, Laurence Colleaux, Ferdinando Palmieri and Florence Molinari and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and Human Genetics.

In The Last Decade

A Munnich

14 papers receiving 270 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A Munnich France	6	157	109	63	49	32	14	275
Floris C. Hofstede Netherlands	13	292 1.9×	355 3.3×	52 0.8×	121 2.5×	5 0.2×	18	537
Chang-Hung Hsu Taiwan	9	132 0.8×	60 0.6×	45 0.7×	14 0.3×	36 1.1×	13	316
Mary Anne D. Chiong Philippines	10	168 1.1×	142 1.3×	36 0.6×	55 1.1×	8 0.3×	31	295
BN Harding United Kingdom	9	178 1.1×	120 1.1×	14 0.2×	58 1.2×	31 1.0×	12	402
Silvio Ferraris Italy	12	262 1.7×	198 1.8×	42 0.7×	27 0.6×	5 0.2×	12	370
Michelle Levene United Kingdom	8	127 0.8×	80 0.7×	14 0.2×	24 0.5×	16 0.5×	14	234
Daniela Buhaş Canada	10	157 1.0×	109 1.0×	107 1.7×	44 0.9×	7 0.2×	24	286
R. Mercelis Belgium	11	252 1.6×	73 0.7×	16 0.3×	47 1.0×	12 0.4×	15	301
Delphine Héron France	8	90 0.6×	10 0.1×	74 1.2×	50 1.0×	11 0.3×	15	214
David F. Kronn United States	7	156 1.0×	76 0.7×	35 0.6×	62 1.3×	14 0.4×	9	310

Countries citing papers authored by A Munnich

Since Specialization

Citations

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

Fields of papers citing papers by A Munnich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Munnich

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

All Works

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14 of 14 papers shown

Steffann, Julie, A Munnich, & Jean‐Paul Bonnefont. (2011). Tuberous sclerosis (TSC). Atlas of Genetics and Cytogenetics in Oncology and Haematology. 1 indexed citations

Rio, Marlène, Pascale de Lonlay, Vassili Valayannopoulos, et al.. (2010). Mitochondrial ND5 mutations mimicking brainstem tectal glioma. Neurology. 75(1). 93–93. 8 indexed citations

Molinari, Florence, Anna Kamińska, Giuseppe Fiermonte, et al.. (2009). Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts. Clinical Genetics. 76(2). 188–194. 95 indexed citations

Boddaert, Nathalie, Nadia Chabane, Laurence Robel, et al.. (2009). Imagerie anatomique dans l’autisme non syndromique : Étude rétrospective sur 140 IRM. Enfance. 2009(1). 99–99. 1 indexed citations

Romano, S., Nathalie Boddaert, Isabelle Desguerre, et al.. (2006). Molar Tooth Sign and Superior Vermian Dysplasia: A Radiological, Clinical, and Genetic Study. Neuropediatrics. 37(1). 42–45. 18 indexed citations

Faivre, Laurence, A Nivelon‐Chevallier, Philippe Khau Van Kien, et al.. (2001). Mazabraud syndrome in two patients: Clinical overlap with McCune-Albright syndrome. American Journal of Medical Genetics. 99(2). 132–136. 42 indexed citations

Rötig, Agnès, Pascale de Lonlay, Dominique Chrétien, et al.. (1998). Frataxin gene expansion causes aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia. European Journal of Human Genetics. 6. 36–36. 2 indexed citations

Rötig, Agnès, Jean‐Paul Bonnefont, & A Munnich. (1996). Mitochondrial diabetes mellitus.. PubMed. 22(5). 291–8. 39 indexed citations

Chrétien, Dominique, Thomas Bourgeron, Agnès Rötig, A Munnich, & Pierre Rustin. (1990). The measurement of the rotenone-sensitive NADH cytochrome c reductase activity in mitochondria isolated from minute amount of human skeletal muscle. Biochemical and Biophysical Research Communications. 173(1). 26–33. 55 indexed citations

10.

Rötig, Agnès, Jean‐Paul Bonnefont, Marco Colonna, et al.. (1989). Les remaniements du génome mitochondrial dans les déficits énergétiques de l'enfant : de nouvelles maladies de système ?. médecine/sciences. 5(7). 459–459. 2 indexed citations

11.

Rey, F.A., A Munnich, Stanislas Lyonnet, & Jean Rey. (1987). [Classification and heterogeneity of hyperphenylalaninemias linked to a phenylalanine hydroxylase deficiency].. PubMed. 44 Suppl 1. 639–42. 4 indexed citations

12.

Larue, Catherine, A Munnich, C. Charpentier, et al.. (1986). An Extracorporeal Hollow-Fiber Reactor for Phenylketonuria Using Immobilized Phenylalanine Ammonia Lyase. Developmental Pharmacology and Therapeutics. 9(2). 73–81. 3 indexed citations

13.

Munnich, A, et al.. (1983). One gene, several messages. From multifunctional proteins to endogenous opiates. Human Genetics. 64(4). 311–314. 4 indexed citations

14.

Depondt, Eliane, et al.. (1983). [Phenylalanine-restricted diet. The portion-by-weight system].. PubMed. 40 Suppl 1. 251–6. 1 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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