M. Barth

733 total citations
17 papers, 423 citations indexed

About

M. Barth is a scholar working on Molecular Biology, Physiology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. Barth has authored 17 papers receiving a total of 423 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Physiology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. Barth's work include Lysosomal Storage Disorders Research (5 papers), Glycosylation and Glycoproteins Research (3 papers) and Metabolism and Genetic Disorders (3 papers). M. Barth is often cited by papers focused on Lysosomal Storage Disorders Research (5 papers), Glycosylation and Glycoproteins Research (3 papers) and Metabolism and Genetic Disorders (3 papers). M. Barth collaborates with scholars based in France, United Kingdom and Germany. M. Barth's co-authors include Anthony H. Fensom, Ann Harris, Dominique Bonneau, Alice Goldenberg, Patrizia Amati‐Bonneau, Nathalie Le Meur, Véronique David, Thierry Frébourg, Stéphane Auvin and Muriel Holder‐Espinasse and has published in prestigious journals such as Investigative Ophthalmology & Visual Science, Journal of Medical Genetics and Human Genetics.

In The Last Decade

M. Barth

17 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Barth France 12 217 140 128 58 57 17 423
Shinjiro Akaboshi Japan 16 317 1.5× 68 0.5× 237 1.9× 31 0.5× 53 0.9× 27 592
M. Pineda Spain 13 285 1.3× 118 0.8× 67 0.5× 48 0.8× 38 0.7× 26 533
Mar O’Callaghan Spain 12 273 1.3× 98 0.7× 125 1.0× 23 0.4× 43 0.8× 26 489
Deborah Barbouth United States 11 285 1.3× 412 2.9× 118 0.9× 54 0.9× 43 0.8× 32 678
Krystyna Szymańska Poland 14 218 1.0× 177 1.3× 47 0.4× 29 0.5× 41 0.7× 48 485
Iris Noyman Israel 9 207 1.0× 64 0.5× 72 0.6× 55 0.9× 32 0.6× 26 455
Kazushi Miya Japan 11 204 0.9× 94 0.7× 76 0.6× 96 1.7× 31 0.5× 20 500
Giulia Massaro United Kingdom 10 189 0.9× 86 0.6× 163 1.3× 34 0.6× 80 1.4× 17 391
Cíntia Barros Santos-Rebouças Brazil 17 378 1.7× 311 2.2× 100 0.8× 40 0.7× 36 0.6× 64 767
Charlotte Thiels Germany 11 225 1.0× 46 0.3× 66 0.5× 32 0.6× 22 0.4× 25 399

Countries citing papers authored by M. Barth

Since Specialization
Citations

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

Fields of papers citing papers by M. Barth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Barth

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

All Works

17 of 17 papers shown
1.
Eichler, Florian, et al.. (2022). Understanding caregiver descriptions of initial signs and symptoms to improve diagnosis of metachromatic leukodystrophy. Orphanet Journal of Rare Diseases. 17(1). 370–370. 8 indexed citations
2.
Spitz, Marie‐Aude, Sylvain Roche, Bénédicte Héron, et al.. (2016). Chronic Diarrhea in l-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French Patients. JIMD Reports. 31. 85–93. 13 indexed citations
3.
Buchholz, Annick, et al.. (2015). Pädiatrische Einschätzung von elterlichen Belastungen und Unterstützungsbedarf. Prävention und Gesundheitsförderung. 10(4). 314–319. 4 indexed citations
4.
Chaussenot, Annabelle, Cécile Rouzier, M.P. Quéré, et al.. (2014). Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1‐related disorders. Clinical Genetics. 87(5). 430–439. 35 indexed citations
5.
Zieger, Barbara, et al.. (2013). A Prospective Randomised Control Study: Reduction of Children's Pain Expectation Using a Picture Book during Blood Withdrawal. Klinische Pädiatrie. 225(3). 110–114. 5 indexed citations
6.
Barth, M., Valérie Serre, Laurence Hubert, et al.. (2011). Kinetic Analyses Guide the Therapeutic Decision in a Novel Form of Moderate Aromatic Acid Decarboxylase Deficiency. JIMD Reports. 3. 25–32. 20 indexed citations
7.
Colin, Estelle, Renaud Touraine, J.‐M. Levaillant, et al.. (2011). Binder phenotype in mothers affected with autoimmune disorders. The Journal of Maternal-Fetal & Neonatal Medicine. 25(8). 1413–1418. 11 indexed citations
8.
Meur, Nathalie Le, Muriel Holder‐Espinasse, Sylvie Jaillard, et al.. (2009). MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. Journal of Medical Genetics. 47(1). 22–29. 150 indexed citations
9.
Findl, Oliver, et al.. (1999). Accommodation induced biometric changes in the human eye. Investigative Ophthalmology & Visual Science. 40(4). 6071–6. 1 indexed citations
10.
Barth, M., Chris Ward, Ann Harris, Ahmed Saad, & Anthony H. Fensom. (1994). Frequency of arylsulphatase A pseudodeficiency associated mutations in a healthy population.. Journal of Medical Genetics. 31(9). 667–671. 34 indexed citations
11.
Barth, M., Anthony H. Fensom, & Ann Harris. (1994). The arylsulphatase A gene and molecular genetics of metachromatic leucodystrophy.. Journal of Medical Genetics. 31(9). 663–666. 13 indexed citations
12.
Zlotogora, Joël, et al.. (1994). A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophy.. Journal of Medical Genetics. 31(9). 672–674. 19 indexed citations
13.
Barth, M., Anthony H. Fensom, & Ann Harris. (1993). Prevalence of common mutations in the arylsulphatase A gene in metachromatic leukodystrophy patients diagnosed in Britain. Human Genetics. 91(1). 73–7. 33 indexed citations
14.
Walley, Andrew J., M. Barth, Ian O. Ellis, Anthony H. Fensom, & Adrian L. Harris. (1993). Gaucher's disease in the United Kingdom: screening non-Jewish patients for the two common mutations.. Journal of Medical Genetics. 30(4). 280–283. 23 indexed citations
15.
Giugliani, Roberto, et al.. (1991). Seven‐year experience of a reference laboratory for detection of inborn errors of metabolism in Brazil. Journal of Inherited Metabolic Disease. 14(3). 400–402. 6 indexed citations
16.
Viana, Marcos Borato, et al.. (1990). Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosis.. Journal of Medical Genetics. 27(8). 499–504. 32 indexed citations
17.
Rumpf, K. W., M. Barth, M. Blech, et al.. (1984). Bezafibrat-induzierte Myolyse und Myoglobinurie bei Patienten mit eingeschränkter Nierenfunktion. Journal of Molecular Medicine. 62(8). 346–348. 16 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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