Michel Bahuau

2.5k total citations
38 papers, 1.1k citations indexed

About

Michel Bahuau is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Michel Bahuau has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 11 papers in Pulmonary and Respiratory Medicine and 10 papers in Molecular Biology. Recurrent topics in Michel Bahuau's work include Cleft Lip and Palate Research (12 papers), Neonatal Respiratory Health Research (9 papers) and Craniofacial Disorders and Treatments (7 papers). Michel Bahuau is often cited by papers focused on Cleft Lip and Palate Research (12 papers), Neonatal Respiratory Health Research (9 papers) and Craniofacial Disorders and Treatments (7 papers). Michel Bahuau collaborates with scholars based in France, Germany and United States. Michel Bahuau's co-authors include Mohammed Tredano, Claude Houdayer, Matthias Griese, Dominique Vidaud, Michel Vidaud, Ivan Bièche, Sylvaine Cordier, Elisabeth Robert‐Gnansia, Christine Francannet and Agnès Nelva and has published in prestigious journals such as Blood, Clinical Chemistry and European Respiratory Journal.

In The Last Decade

Michel Bahuau

37 papers receiving 1.1k citations

Peers

Michel Bahuau
María Dolores Burguete Ramos Spain
Jason D. Engel United States
Georg Eich Switzerland
Nancy R. Schneider United States
Alex Kan Australia
L Koulischer Belgium
Jari Sjöberg Finland
David Carpentieri United States
Asahito Hama Japan
G. Bell United Kingdom
María Dolores Burguete Ramos Spain
Michel Bahuau
Citations per year, relative to Michel Bahuau Michel Bahuau (= 1×) peers María Dolores Burguete Ramos

Countries citing papers authored by Michel Bahuau

Since Specialization
Citations

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

Fields of papers citing papers by Michel Bahuau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michel Bahuau

This figure shows the co-authorship network connecting the top 25 collaborators of Michel Bahuau. A scholar is included among the top collaborators of Michel Bahuau 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 Michel Bahuau. Michel Bahuau 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.
Mamoune, Asmaa, Michel Bahuau, Yamina Hamel, et al.. (2014). A Thermolabile Aldolase A Mutant Causes Fever-Induced Recurrent Rhabdomyolysis without Hemolytic Anemia. PLoS Genetics. 10(11). e1004711–e1004711. 20 indexed citations
2.
Moradkhani, Kamran, Michel Bahuau, Muriel Holder, et al.. (2011). Practical approach for characterization of glucose 6‐phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: Description of seven new G6PD mutants. American Journal of Hematology. 87(2). 208–210. 8 indexed citations
3.
Chevrier, Cécile, Michel Bahuau, Claire Perret, et al.. (2008). Genetic susceptibilities in the association between maternal exposure to tobacco smoke and the risk of nonsyndromic oral cleft. American Journal of Medical Genetics Part A. 146A(18). 2396–2406. 38 indexed citations
4.
Bardakdjian‐Michau, Josiane, et al.. (2008). Neonatal screening for sickle cell disease in France. Journal of Clinical Pathology. 62(1). 31–33. 46 indexed citations
5.
Chevrier, Cécile, Claire Perret, Michel Bahuau, et al.. (2007). Fetal and maternal CYP2E1 genotypes and the risk of nonsyndromic oral clefts. American Journal of Medical Genetics Part A. 143A(12). 1382–1385. 4 indexed citations
6.
Chevrier, Cécile, Claire Perret, Michel Bahuau, et al.. (2007). Fetal and maternalMTHFR C677Tgenotype, maternal folate intake and the risk of nonsyndromic oral clefts. American Journal of Medical Genetics Part A. 143A(3). 248–257. 63 indexed citations
7.
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
8.
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
9.
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
10.
Gajdos, Vincent, Michel Bahuau, Elisabeth Robert‐Gnansia, et al.. (2004). Genetics of nonsyndromic cleft lip with or without cleft palate: is there a Mendelian sub-entity?. Annales de Génétique. 47(1). 29–39. 2 indexed citations
11.
Chevrier, Cécile, Claire Perret, Michel Bahuau, et al.. (2004). Interaction between the ADH1C polymorphism and maternal alcohol intake in the risk of nonsyndromic oral clefts: An evaluation of the contribution of child and maternal genotypes. Birth Defects Research Part A Clinical and Molecular Teratology. 73(2). 114–122. 32 indexed citations
12.
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
13.
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
14.
Houdayer, Claude, Thierry Billette de Villemeur, Michel Bahuau, et al.. (2002). Simple Fluorescent PCR Assay for Discriminating FRAXA Fully Mutated Females from Normal Homozygotes. Genetic Testing. 6(2). 135–139. 7 indexed citations
15.
Bahuau, Michel, et al.. (2002). FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate. Clinical Genetics. 62(6). 470–473. 33 indexed citations
16.
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
17.
Houdayer, Claude, Catherine Bonaïti‐Pellié, V. Soupre, et al.. (2001). Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P). American Journal of Medical Genetics. 104(1). 86–92. 21 indexed citations
18.
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
19.
Houdayer, Claude & Michel Bahuau. (1998). Orofacial cleft defects: inference from nature and nurture.. PubMed. 41(2). 89–117. 13 indexed citations
20.
Bahuau, Michel, Stanislas Lyonnet, Didier Lacombe, et al.. (1993). No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome families. American Journal of Medical Genetics. 46(6). 700–705. 17 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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