Mohammed Tredano

569 total citations
14 papers, 404 citations indexed

About

Mohammed Tredano is a scholar working on Pulmonary and Respiratory Medicine, Surgery and Endocrine and Autonomic Systems. According to data from OpenAlex, Mohammed Tredano has authored 14 papers receiving a total of 404 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pulmonary and Respiratory Medicine, 6 papers in Surgery and 4 papers in Endocrine and Autonomic Systems. Recurrent topics in Mohammed Tredano's work include Neonatal Respiratory Health Research (11 papers), Congenital Diaphragmatic Hernia Studies (6 papers) and Neuroscience of respiration and sleep (4 papers). Mohammed Tredano is often cited by papers focused on Neonatal Respiratory Health Research (11 papers), Congenital Diaphragmatic Hernia Studies (6 papers) and Neuroscience of respiration and sleep (4 papers). Mohammed Tredano collaborates with scholars based in France, Germany and United States. Mohammed Tredano's co-authors include Michel Bahuau, Matthias Griese, Claude Houdayer, Frank Brasch, Jacques Élion, J. de Blic, Michael F. Beers, Rémy Couderc, Surafel Mulugeta and Klaus‐Michael Müller and has published in prestigious journals such as Clinical Chemistry, European Respiratory Journal and Human Mutation.

In The Last Decade

Mohammed Tredano

14 papers receiving 390 citations

Peers

Mohammed Tredano

PRM

SURGE

EAS

GENET

Katsuya Hirata Japan

Yee Him Cheung United States

Gerrit John-Schuster Germany

Darlise DiMatteo United States

Shigenori Iwagaki Japan

Matthew M. Steiner United States

Jean M. Herron United States

Jian Qiu China

Michele Di Candia United Kingdom

George Gershman United States

Katsuya Hirata Japan

Mohammed Tredano

142 ×0.4

PRM

89 ×0.6

SURGE

38 ×0.4

EAS

107 ×1.7

40 ×1.0

GENET

Citations per year, relative to Mohammed Tredano Mohammed Tredano (= 1×) peers Katsuya Hirata

Countries citing papers authored by Mohammed Tredano

Since Specialization

Citations

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

Fields of papers citing papers by Mohammed Tredano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammed Tredano

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

Tredano, Mohammed, D.N. Cooper, Manfred Stuhrmann, et al.. (2005). Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP‐B) deficiency. American Journal of Medical Genetics Part A. 140A(1). 62–69. 16 indexed citations

Griese, Matthias, Mohammed Tredano, Annika Braun, et al.. (2005). Expression profiles of hydrophobic surfactant proteins in children with diffuse chronic lung disease. Respiratory Research. 6(1). 80–80. 18 indexed citations

Tredano, Mohammed, Matthias Griese, Frank Brasch, et al.. (2004). Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease. American Journal of Medical Genetics Part A. 126A(1). 18–26. 94 indexed citations

Brasch, Frank, Matthias Griese, Mohammed Tredano, et al.. (2004). Interstitial lung disease in a baby with ade novomutation in the SFTPC gene. European Respiratory Journal. 24(1). 30–39. 116 indexed citations

Tredano, Mohammed, Matthias Griese, J. de Blic, et al.. (2003). Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: Relationship to SFTPB. American Journal of Medical Genetics Part A. 119A(3). 324–339. 41 indexed citations

Bahuau, Michel, et al.. (2002). FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate. Clinical Genetics. 62(6). 470–473. 33 indexed citations

Tredano, Mohammed, J. de Blic, Matthias Griese, et al.. (2001). Clinical Biological and Genetic Heterogeneity of the Inborn Errors of Pulmonary Surfactant Metabolism. Clinical Chemistry and Laboratory Medicine (CCLM). 39(2). 90–108. 14 indexed citations

Tredano, Mohammed, J. de Blic, Matthias Griese, et al.. (2001). [Clinical, biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolism: SP-B deficiency and alveolar proteinosis].. PubMed. 59(2). 131–48. 3 indexed citations

Griese, Matthias, Mohammed Tredano, & Michel Bahuau. (2001). Pulmonale Alveolarproteinosen. Monatsschrift Kinderheilkunde. 149(11). 1245–1261. 1 indexed citations

10.

Tredano, Mohammed, Patrick Truffert, F. Capron, et al.. (2000). Déficit constitutionnel en protéine B du surfactant pulmonaire: présentation clinique, diagnostic histologique et moléculaire. Archives de Pédiatrie. 7(6). 641–644. 3 indexed citations

11.

Houdayer, Claude, Alban Le Monnier, Marion Gérard, et al.. (1999). Improved Fluorescent PCR-Based Assay for Sizing CGG Repeats at the FRAXA Locus. Clinical Chemistry and Laboratory Medicine (CCLM). 37(4). 397–402. 18 indexed citations

12.

Tredano, Mohammed, Ruurd M. van Elburg, Luc J. I. Zimmermann, et al.. (1999). CompoundSFTPB 1549C?GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency. Human Mutation. 14(6). 502–509. 34 indexed citations

13.

Houdayer, Claude, Myriam Rosenberg‐Bourgin, Mohammed Tredano, et al.. (1999). Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.. PubMed. 42(2). 69–74. 8 indexed citations

14.

Houdayer, Claude, Cécile Cazeneuve, Mohammed Tredano, et al.. (1998). Clinical Evaluation of the CF(12)m Cystic Fibrosis DNA Diagnostic Kit. Clinical Chemistry. 44(6). 1346–1348. 5 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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