Martine Blayau

2.9k total citations
44 papers, 1.1k citations indexed

About

Martine Blayau is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Martine Blayau has authored 44 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pulmonary and Respiratory Medicine, 12 papers in Molecular Biology and 12 papers in Genetics. Recurrent topics in Martine Blayau's work include Cystic Fibrosis Research Advances (15 papers), Neonatal Respiratory Health Research (8 papers) and Hedgehog Signaling Pathway Studies (6 papers). Martine Blayau is often cited by papers focused on Cystic Fibrosis Research Advances (15 papers), Neonatal Respiratory Health Research (8 papers) and Hedgehog Signaling Pathway Studies (6 papers). Martine Blayau collaborates with scholars based in France, United States and Poland. Martine Blayau's co-authors include Sylvie Odent, Véronique David, Laurent Pasquier, B. Le Marec, Christèle Dubourg, Franck Le Duff, Claude Férec, J. Y. Le Gall, Marie‐Pierre Audrézet and Virginie Scotet and has published in prestigious journals such as Nucleic Acids Research, Human Molecular Genetics and American Journal of Obstetrics and Gynecology.

In The Last Decade

Martine Blayau

42 papers receiving 1.1k citations

Peers

Countries citing papers authored by Martine Blayau

Since Specialization

Citations

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

Fields of papers citing papers by Martine Blayau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martine Blayau

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Highlighting the impact of cascade carrier testing in cystic fibrosis families 2016 ·Journal of Cystic Fibrosis ·I. Duguépéroux, (unknown), Marie‐Pierre Audrézet, G. Rault, I. Frachon, R Bernard, Philippe Parent, Martine Blayau, Sébastien Schmitt, Emmanuelle Génin, Claude Férec, Virginie Scotet	10
2	Cleft lip, cleft palate, hereditary diffuse gastric cancer and germline mutations in CDH1 2012 ·International Journal of Cancer ·Patrick R. Benusiglio, Olivier Caron, Émilie Consolino, Pierre Duvillard, Florence Coulet, Martine Blayau, David Malka	26
3	CFTRmutation combinations producing frequent complex alleles with different clinical and functional outcomes 2012 ·Human Mutation ·(unknown), Emmanuelle Girodon, Caroline Norez, (unknown), (unknown), Alix de Becdelièvre, Thierry Bienvenu, Marie des Georges, (unknown), G. Lalau, Éric Bieth, Martine Blayau, Frédéric Becq, Alain Kitzis, Pascale Fanen, Véronique Ladevèze	17
4	p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study 2010 ·European Journal of Human Genetics ·Céline René, Damien Paulet, Emmanuelle Girodon, Cathérine Costa, G. Lalau, Julie Leclerc, (unknown), Thierry Bienvenu, Martine Blayau, A. Iron, Hervé Mittre, Delphine Feldmann, Caroline Guittard, Mireille Claustres, Marie des Georges	5
5	Colorectal Adenomatous Polyposis Associated with MYH Mutations: Genotype and Phenotype Characteristics 2007 ·Diseases of the Colon & Rectum ·Guillaume Bouguen, Sylvain Manfrédi, Martine Blayau, Catherine Dugast, Bruno Buecher, Dominique Bonneau, Laurent Siproudhis, Véronique David, Jean‐François Bretagne	23
6	Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy 2006 ·Human Mutation ·Christophe Béroud, Sylvie Tuffery‐Giraud, Masafumi Matsuo, Dalil Hamroun, Véronique Humbertclaude, Nicole Monnier, Marie‐Pierre Moizard, Marie‐Antoinette Voelckel, (unknown), Pierre Boisseau, Martine Blayau, Christophe Philippe, Mireille Cossée, Michel Pagès, François Rivier, Olivier Danos, Luis Garcı́a, Mireille Claustres	156
7	Late ovarian relapse of TEL/AML1 positive ALL confirming that TEL deletion is a secondary event in leukemogenesis 2005 ·Leukemia Research ·(unknown), Cathérine Henry, Virginie Gandemer, (unknown), Florence Burtin, Martine Blayau, Jean‐Michel Cayuela, (unknown), (unknown), (unknown), (unknown), (unknown), C. Edan, E. Le Gall, J Goasguen	13
8	Molecular screening ofSHH,ZIC2,SIX3, andTGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations 2004 ·Human Mutation ·(unknown), (unknown), Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, (unknown), Sylvie Odent, (unknown)	104
9	Phenotypic and molecular variability of the holoprosencephalic spectrum 2004 ·American Journal of Medical Genetics Part A ·Leïla Lazaro, Christèle Dubourg, Laurent Pasquier, Franck Le Duff, Martine Blayau, (unknown), (unknown), (unknown), Véronique David, Sylvie Odent	53
10	Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations 2003 ·Human Genetics ·(unknown), Christèle Dubourg, Jocelyne Attia‐Sobol, Jacqueline Vigneron, Martine Blayau, Laurent Pasquier, Leïla Lazaro, Sylvie Odent, Véronique David	40
11	Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France 2003 ·Human Genetics ·Virginie Scotet, Marie‐Pierre Audrézet, Michel Roussey, G. Rault, Martine Blayau, Marc De Braekeleer, Claude Férec	20
12	A new mutation of E-cadherin gene in familial gastric linitis plastica cancer with extra-digestive dissemination 2001 ·European Journal of Gastroenterology & Hepatology ·(unknown), Martine Blayau, Maël Pagenault, (unknown), Jean‐Luc Raoul, Jean‐Pierre Campion, Véronique David, Jean‐François Bretagne	41
13	A new mutation in the six-domain of SIX3 gene causes holoprosencephaly 2000 ·European Journal of Human Genetics ·Laurent Pasquier, Christèle Dubourg, Martine Blayau, (unknown), B. Le Marec, Véronique David, Sylvie Odent	52
14	Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly 1999 ·Human Molecular Genetics ·Sylvie Odent, Tania Attié‐Bitach, Martine Blayau, M Mathieu, (unknown), Anne‐Lise Delezoide, J. Y. Le Gall, B. Le Marec, A Munnich, Véronique David, Michel Vekemans	123
15	Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis 1992 ·Human Genetics ·Joëlle Boretto, Anne‐Marie Jouanolle, Jacqueline Yaouanq, (unknown), (unknown), Martine Blayau, (unknown), André Le Treut, John Clayton, Nicolas Borot, Jean‐Yves Le Gall, Pierre Pontarotti, Véronique David	22
16	Short-term prednisolone followed by recombinant human α-interferon alone or combined with adenine-arabinoside in chronic hepatitis B 1991 ·Journal of Hepatology ·Pierre Brissot, Christian Jacquelinet, Hervé Jouanolle, Véronique David, Dominique Guyader, M. Guéguen, Martine Blayau, Gérard Lescoat, M. Messner, Yves Deugnier	5
17	Dinucleotide repeat polymorphism at the FTHPI locus of chromosome 6 1991 ·Nucleic Acids Research ·(unknown), (unknown), (unknown), Martine Blayau, (unknown), Valentin David	4
18	HLA class I gene polymorphism in genetic hemochromatosis 1990 ·Human Genetics ·Anne‐Marie Jouanolle, Jacqueline Yaouanq, Martine Blayau, (unknown), R Fauchet, M P Font, Jean‐Yves Le Gall, Véronique David	9
19	Ferritin H gene polymorphism in idiopathic hemochromatosis 1989 ·Human Genetics ·Véronique David, (unknown), Jacqueline Yaouanq, Martine Blayau, Laurent Abel, (unknown), (unknown), Jim Drysdale, Jean‐Yves Le Gall, M. K. Simon	16
20	Partial purification and characterization of a serine endopeptidase from rat liver plasma membranes 1986 ·Biochimica et Biophysica Acta (BBA) - General Subjects ·(unknown), (unknown), Martine Blayau, André Le Treut, Jean‐Yves Le Gall	1

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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