Natacha Martin

508 total citations
15 papers, 380 citations indexed

About

Natacha Martin is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cancer Research. According to data from OpenAlex, Natacha Martin has authored 15 papers receiving a total of 380 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Pulmonary and Respiratory Medicine and 3 papers in Cancer Research. Recurrent topics in Natacha Martin's work include Cystic Fibrosis Research Advances (6 papers), Epigenetics and DNA Methylation (3 papers) and Neonatal Respiratory Health Research (3 papers). Natacha Martin is often cited by papers focused on Cystic Fibrosis Research Advances (6 papers), Epigenetics and DNA Methylation (3 papers) and Neonatal Respiratory Health Research (3 papers). Natacha Martin collaborates with scholars based in France, Italy and Switzerland. Natacha Martin's 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 and has published in prestigious journals such as PLoS Genetics, Human Mutation and Infection Genetics and Evolution.

In The Last Decade

Natacha Martin

15 papers receiving 374 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Natacha Martin France	8	216	189	145	56	40	15	380
S. J. Lee United Kingdom	8	212 1.0×	170 0.9×	78 0.5×	53 0.9×	20 0.5×	10	465
Yang Cheng China	10	205 0.9×	98 0.5×	105 0.7×	35 0.6×	16 0.4×	26	321
Natalia Dubrowinskaja Germany	13	299 1.4×	154 0.8×	123 0.8×	69 1.2×	20 0.5×	29	465
Moonjoo Han United States	6	282 1.3×	221 1.2×	66 0.5×	42 0.8×	22 0.6×	7	483
Daniel Onofre Vidal Brazil	13	389 1.8×	76 0.4×	226 1.6×	30 0.5×	20 0.5×	31	530
Gloria Lim Canada	7	213 1.0×	93 0.5×	84 0.6×	87 1.6×	19 0.5×	7	332
Iris J.H. van Vlodrop Netherlands	8	374 1.7×	178 0.9×	111 0.8×	18 0.3×	11 0.3×	9	459
Sophie Deveaux France	6	194 0.9×	154 0.8×	61 0.4×	33 0.6×	10 0.3×	6	268
Jiangyi Wang China	12	296 1.4×	119 0.6×	245 1.7×	17 0.3×	11 0.3×	27	429
Lurdes Torres Portugal	11	143 0.7×	70 0.4×	137 0.9×	38 0.7×	32 0.8×	20	328

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

1.

Martin, Natacha, Anne Bergougnoux, B. Chevalier, et al.. (2020). Exon identity influences splicing induced by exonic variants and in silico prediction efficacy. Journal of Cystic Fibrosis. 20(3). 464–472. 6 indexed citations

2.

Pranke, Iwona, Laure Bidou, Natacha Martin, et al.. (2018). Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons. ERJ Open Research. 4(1). 80–2017. 36 indexed citations

3.

Hinzpeter, Alexandre, Isabelle Callebaut, Cécile Zordan, et al.. (2017). The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible. Clinical Case Reports. 5(5). 658–663. 4 indexed citations

4.

Martin, Natacha, Nathalie Servel, Bruno Costes, et al.. (2017). Cisvariants identified in F508del complex alleles modulate CFTR channel rescue by small molecules. Human Mutation. 39(4). 506–514. 28 indexed citations

5.

Hinzpeter, Alexandre, Cécile Zordan, Bruno Costes, et al.. (2016). 8 The importance of functional tests to assess the effect of a new CFTR variant when genotype-phenotype correlation is not possible. Journal of Cystic Fibrosis. 15. S53–S53. 1 indexed citations

6.

Hinzpeter, Alexandre, Alix de Becdelièvre, Éric Bieth, et al.. (2014). Identification of a Novel 5′ AlternativeCFTRmRNA Isoform in a Patient with Nasal Polyposis andCFTRMutations. Human Mutation. 35(7). 805–808. 2 indexed citations

7.

Becdelièvre, Alix de, Lisa Golmard, Christian Vasseur, et al.. (2013). Combined Computational-Experimental Analyses ofCFTRExon Strength Uncover Predictability of Exon-Skipping Level. Human Mutation. 34(6). 873–881. 25 indexed citations

8.

Dechavanne, Célia, Emmanuelle Renard, Bruno Costes, et al.. (2013). Genetic characterization of Plasmodium falciparum allelic variants infecting mothers at delivery and their children during their first plasmodial infections. Infection Genetics and Evolution. 20. 16–25. 5 indexed citations

9.

Hinzpeter, Alexandre, Alix de Becdelièvre, Éric Bieth, et al.. (2012). Alternative Splicing of In-Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies. Human Mutation. 34(2). 287–291. 10 indexed citations

10.

Hinzpeter, Alexandre, Elvira Sondo, Cathérine Costa, et al.. (2010). Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier. PLoS Genetics. 6(10). e1001153–e1001153. 51 indexed citations

11.

Moradkhani, Kamran, Michel Bahuau, Claude Préhu, et al.. (2009). 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). Blood Cells Molecules and Diseases. 43(3). 226–229. 3 indexed citations

12.

Gallou, Catherine, Dominique Chauveau, Richard J. Kahnoski, et al.. (2004). Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions. Human Mutation. 24(3). 215–224. 68 indexed citations

13.

Gallou, Catherine, Dominique Chauveau, Richard J. Kahnoski, et al.. (2004). Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions. Human Mutation. 24(5). 435–436. 6 indexed citations

14.

Gallou, Catherine, Claudine Deloménie, Arnaud Méjean, et al.. (2001). Association of GSTT1 non-null and NAT1 slow/rapid genotypes with von Hippel-Lindau tumour suppressor gene transversions in sporadic renal cell carcinoma. Pharmacogenetics. 11(6). 521–535. 23 indexed citations

15.

Gallou, Catherine, Dominique Joly, F. Staroz, et al.. (1999). Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC. Human Mutation. 13(6). 464–475. 112 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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