Natacha Martin

508 citations

15 papers · 380 indexed · h-index 8

Co-authors: Claudine Junien Catherine Gallou Richard J. Kahnoski Dominique Joly Bruno Costes Pascale Fanen Alexandre Hinzpeter Emmanuelle Girodon
Topics: Cystic Fibrosis Research Advances (6 papers)Epigenetics and DNA Methylation (3 papers)Neonatal Respiratory Health Research (3 papers)
Cited by: Cancer Research Pulmonary and Respiratory Medicine Genetics
Journals: PLoS Genetics Human Mutation Infection Genetics and Evolution
Partner nations: France Italy Switzerland

In The Last Decade

Natacha Martin

15 papers receiving 374 citations

Peers

Countries citing papers authored by Natacha Martin

Since Specialization

Citations

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

Fields of papers citing papers by Natacha Martin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natacha Martin

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Exon identity influences splicing induced by exonic variants and in silico prediction efficacy 2020 ·Journal of Cystic Fibrosis ·Natacha Martin,Anne Bergougnoux,(unknown),B. Chevalier,(unknown),David Baux,Bruno Costes,Pascale Fanen,Caroline Raynal,Isabelle Sermet‐Gaudelus,Emmanuelle Girodon,Magali Taulan‐Cadars,Alexandre Hinzpeter	6
2	Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons 2018 ·ERJ Open Research ·Iwona Pranke,Laure Bidou,Natacha Martin,Sandra Blanchet,Aurélie Hatton,(unknown),(unknown),Bruno Costes,B. Chevalier,Danielle Tondelier,Emmanuelle Girodon,(unknown),Aleksander Edelman,Pascale Fanen,Olivier Namy,Isabelle Sermet‐Gaudelus,Alexandre Hinzpeter	36
3	The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible 2017 ·Clinical Case Reports ·Alexandre Hinzpeter,(unknown),Isabelle Callebaut,Cécile Zordan,Bruno Costes,Julie Guichoux,A. Iron,Didier Lacombe,Natacha Martin,Benoı̂t Arveiler,Pascale Fanen,Patricia Fergelot,Emmanuelle Girodon	4
4	Cisvariants identified in F508del complex alleles modulate CFTR channel rescue by small molecules 2017 ·Human Mutation ·(unknown),(unknown),Natacha Martin,Nathalie Servel,Bruno Costes,(unknown),B. Chevalier,Iwona Pranke,Juliette Simonin,Emmanuelle Girodon,Brice Hoffmann,Jean‐Paul Mornon,Isabelle Callebaut,Isabelle Sermet‐Gaudelus,Pascale Fanen,Aleksander Edelman,Alexandre Hinzpeter	28
5	8 The importance of functional tests to assess the effect of a new CFTR variant when genotype-phenotype correlation is not possible 2016 ·Journal of Cystic Fibrosis ·Alexandre Hinzpeter,(unknown),Cécile Zordan,Bruno Costes,Julie Guichoux,A. Iron,Didier Lacombe,Natacha Martin,Benoı̂t Arveiler,Pascale Fanen,Patricia Fergelot,E. Girodon	1
6	Identification of a Novel 5′ AlternativeCFTRmRNA Isoform in a Patient with Nasal Polyposis andCFTRMutations 2014 ·Human Mutation ·Alexandre Hinzpeter,Alix de Becdelièvre,Éric Bieth,(unknown),François Brémont,Natacha Martin,Bruno Costes,Cathérine Costa,(unknown),(unknown),V. Prulière‐Escabasse,Michel Goossens,Pascale Fanen,Emmanuelle Girodon	2
7	Combined Computational-Experimental Analyses ofCFTRExon Strength Uncover Predictability of Exon-Skipping Level 2013 ·Human Mutation ·(unknown),Alix de Becdelièvre,Lisa Golmard,Christian Vasseur,Cathérine Costa,Asma Chaoui,Natacha Martin,Bruno Costes,Michel Goossens,Emmanuelle Girodon,Pascale Fanen,Alexandre Hinzpeter	25
8	Genetic characterization of Plasmodium falciparum allelic variants infecting mothers at delivery and their children during their first plasmodial infections 2013 ·Infection Genetics and Evolution ·Célia Dechavanne,(unknown),Emmanuelle Renard,Bruno Costes,Natacha Martin,(unknown),(unknown),(unknown),Bich-Tram Huynh,André Garcia,Florence Migot‐Nabias	5
9	Alternative Splicing of In-Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies 2012 ·Human Mutation ·Alexandre Hinzpeter,(unknown),Alix de Becdelièvre,Éric Bieth,Elvira Sondo,Natacha Martin,Bruno Costes,Cathérine Costa,Michel Goossens,Luis J. V. Galietta,Emmanuelle Girodon,Pascale Fanen	10
10	Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier 2010 ·PLoS Genetics ·Alexandre Hinzpeter,(unknown),Elvira Sondo,Cathérine Costa,N. Arous,(unknown),Natacha Martin,Agathe Tarze,Laurence Weiss,Alix de Becdelièvre,Bruno Costes,Michel Goossens,Luis J. V. Galietta,Emmanuelle Girodon,Pascale Fanen	51
11	A rare G6PD variant (c.383T > G; p.128Leu > Arg) with a molecular pathophysiological mechanism similar to that of G6PD A− (68Val > Met, 126Asn > Asp) 2009 ·Blood Cells Molecules and Diseases ·Kamran Moradkhani,Michel Bahuau,Claude Préhu,Natacha Martin,(unknown),Frederic Galactéros,Henri Wajcman	3
12	Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions 2004 ·Human Mutation ·Catherine Gallou,Dominique Chauveau,Richard J. Kahnoski,Dominique Joly,Sophie Giraud,Sylviane Olschwang,Natacha Martin,(unknown),Yves Chrétien,Arnaud Méjean,Jean-Michel Corréas,G Benoît,P Colombeau,Jean‐Pierre Grünfeld,Claudine Junien,Christophe Béroud	68
13	Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions 2004 ·Human Mutation ·Catherine Gallou,Dominique Chauveau,Richard J. Kahnoski,Dominique Joly,Sophie Giraud,Sylviane Olschwang,Natacha Martin,(unknown),Yves Chrétien,Arnaud Méjean,Jean-Michel Corréas,G Benoît,P Colombeau,Jean‐Pierre Grünfeld,Claudine Junien,Christophe Béroud	6
14	Association of GSTT1 non-null and NAT1 slow/rapid genotypes with von Hippel-Lindau tumour suppressor gene transversions in sporadic renal cell carcinoma 2001 ·Pharmacogenetics ·Catherine Gallou,(unknown),Claudine Deloménie,Arnaud Méjean,Natacha Martin,(unknown),Gaël Palais,Raymonde Bouvier,D Droz,Rajagopal Krishnamoorthy,Claudine Junien,Christophe Béroud,Jean‐Marie Dupret	23
15	Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC 1999 ·Human Mutation ·Catherine Gallou,Dominique Joly,(unknown),F. Staroz,Natacha Martin,Georges Tarlet,(unknown),Raymonde Bouvier,D Droz,(unknown),(unknown),Richard J. Kahnoski,Claudine Junien,(unknown)	112

About Natacha Martin

Natacha Martin is a scholar working on Pulmonary and Respiratory Medicine, Cancer Research and Genetics, having authored 15 papers that have together received 380 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (6 papers), Epigenetics and DNA Methylation (3 papers) and Neonatal Respiratory Health Research (3 papers). The work is most often cited by research in Cancer Research (145 citations), Pulmonary and Respiratory Medicine (189 citations) and Genetics (40 citations). Natacha Martin has collaborated with scholars based in France, Italy and Switzerland. Frequent co-authors include Claudine Junien, Catherine Gallou, Richard J. Kahnoski, Dominique Joly, Bruno Costes, Pascale Fanen, Alexandre Hinzpeter, Emmanuelle Girodon, Raymonde Bouvier and D Droz. Their work appears in journals such as PLoS Genetics, Human Mutation and Infection Genetics and Evolution.

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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