Martin Schwarz

6.5k total citations · 1 hit paper
58 papers, 3.1k citations indexed

About

Martin Schwarz is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Martin Schwarz has authored 58 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Pulmonary and Respiratory Medicine, 23 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Martin Schwarz's work include Cystic Fibrosis Research Advances (24 papers), Neonatal Respiratory Health Research (11 papers) and Tracheal and airway disorders (8 papers). Martin Schwarz is often cited by papers focused on Cystic Fibrosis Research Advances (24 papers), Neonatal Respiratory Health Research (11 papers) and Tracheal and airway disorders (8 papers). Martin Schwarz collaborates with scholars based in United Kingdom, Germany and United States. Martin Schwarz's co-authors include Julian I. Schroeder, Geraldine Malone, Maurice Super, John Painter, F. Block, Joan M. Braganza, Zhen‐Ming Pei, Kazuyuki Kuchitsu, John M. Ward and M Super and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Martin Schwarz

57 papers receiving 3.0k citations

Hit Papers

Mutations of the Cystic F... 1998 2026 2007 2016 1998 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Schwarz United Kingdom 25 986 881 669 621 415 58 3.1k
Michio Kuwahara Japan 36 3.4k 3.5× 1.5k 1.6× 206 0.3× 631 1.0× 237 0.6× 102 4.6k
Danièle Evain‐Brion France 38 1.7k 1.7× 303 0.3× 216 0.3× 270 0.4× 201 0.5× 101 4.0k
Lene N. Nejsum Denmark 25 1.9k 1.9× 729 0.8× 246 0.4× 309 0.5× 104 0.3× 75 2.9k
Roger T. Worrell United States 27 1.5k 1.6× 708 0.8× 60 0.1× 343 0.6× 226 0.5× 49 2.5k
Katalin Szászi Canada 37 1.9k 2.0× 322 0.4× 82 0.1× 359 0.6× 270 0.7× 86 3.5k
Paul Shore United Kingdom 28 3.1k 3.1× 154 0.2× 676 1.0× 163 0.3× 598 1.4× 52 4.2k
Sami A. Sanjad Lebanon 16 2.6k 2.6× 703 0.8× 105 0.2× 262 0.4× 106 0.3× 46 3.8k
Michael S. Greer United States 19 886 0.9× 281 0.3× 306 0.5× 154 0.2× 96 0.2× 31 1.6k
William D. Swaim United States 33 1.3k 1.4× 292 0.3× 107 0.2× 368 0.6× 260 0.6× 61 3.4k

Countries citing papers authored by Martin Schwarz

Since Specialization
Citations

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

Fields of papers citing papers by Martin Schwarz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Schwarz

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Schwarz. A scholar is included among the top collaborators of Martin Schwarz 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 Martin Schwarz. Martin Schwarz 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.
Schwarz, Martin, Markéta Havlovičová, Marek Turnovec, et al.. (2024). Body mass index is an overlooked confounding factor in existing clustering studies of 3D facial scans of children with autism spectrum disorder. Scientific Reports. 14(1). 9873–9873. 1 indexed citations
2.
Schwarz, Martin, Eva Froňková, Michael Svatoň, et al.. (2024). Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn’s disease. Molecular Biology Reports. 51(1). 399–399.
3.
Girardet, Anne, Stéphanie Plaza, Martine De Rycke, et al.. (2015). The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus. European Journal of Human Genetics. 24(4). 469–478. 24 indexed citations
4.
Girodon, Emmanuelle, et al.. (2012). Improvement of interpretation in cystic fibrosis clinical laboratory reports: longitudinal analysis of external quality assessment data. European Journal of Human Genetics. 20(12). 1209–1215. 7 indexed citations
5.
Mayell, Sarah, À. Munck, J.V. Craig, et al.. (2008). A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis. Journal of Cystic Fibrosis. 8(1). 71–78. 95 indexed citations
6.
Dequeker, Elisabeth, Manfred Stuhrmann, Michael A. Morris, et al.. (2008). Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders – updated European recommendations. European Journal of Human Genetics. 17(1). 51–65. 163 indexed citations
7.
Malone, Geraldine, Helen Alexandra Shaw, Liviuţa Budişan, et al.. (2008). The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania. Journal of Cystic Fibrosis. 7(5). 423–428. 4 indexed citations
8.
Férec, Claude, Cédric Le Maréchal, M.‐P. Audrézet, et al.. (2004). Analysis of genomic CFTR DNA. Journal of Cystic Fibrosis. 3. 7–10. 7 indexed citations
9.
Arkwright, Peter D., Vera Pravica, Maurice Super, et al.. (2003). End-Organ Dysfunction in Cystic Fibrosis: Association with Angiotensin I Converting Enzyme and Cytokine Gene Polymorphisms. American Journal of Respiratory and Critical Care Medicine. 167(3). 384–389. 53 indexed citations
10.
Schwarz, Martin & Geraldine Malone. (2003). Methods for Screening in Cystic Fibrosis. Humana Press eBooks. 5. 99–120. 3 indexed citations
11.
Lemperle, Gottfried, Martin Schwarz, & Stefan M. Lemperle. (2003). Nail Regeneration by Elongation of the Partially Destroyed Nail Bed. Plastic & Reconstructive Surgery. 111(1). 167–172. 12 indexed citations
12.
Schwarz, Martin & Julian I. Schroeder. (1998). Abscisic acid maintains S‐type anion channel activity in ATP‐depleted Vicia faba guard cells. FEBS Letters. 428(3). 177–182. 37 indexed citations
13.
Popa, Mircea Ioan, Martin Schwarz, G. Hambleton, et al.. (1997). Cystic fibrosis mutations in Romania. European Journal of Pediatrics. 156(3). 212–213. 6 indexed citations
14.
Jordanova, Albena, Luba Kalaydjieva, Alexey Savov, et al.. (1997). SSCP analysis: A blind sensitivity trial. Human Mutation. 10(1). 65–70. 60 indexed citations
15.
Block, F., et al.. (1997). Delayed treatment with rolipram protects against neuronal damage following global ischemia in rats. Neuroreport. 8(17). 3829–3832. 40 indexed citations
16.
Hinnah, Silke C., et al.. (1995). Ion Channels in the Chloroplast Envelope Membrane. Biochemistry. 34(49). 15906–15917. 45 indexed citations
17.
Super, M & Martin Schwarz. (1992). Mutations of the cystic fibrosis gene locus within the population of the Northwest of England. European Journal of Pediatrics. 151(2). 108–111. 16 indexed citations
18.
Schwarz, Martin, Claire Summers, Lesley Heptinstall, et al.. (1991). A Deletion Mutation of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Locus: DeltaI507. Advances in experimental medicine and biology. 290. 393–398. 16 indexed citations
19.
Bauer-Hofmann, R., Albrecht Buchmann, A.S. Wright, & Martin Schwarz. (1990). Mutations in the Ha-ras proto-oncogene in spontaneous and chemically induced liver tumours of the CF1 mouse. Carcinogenesis. 11(10). 1875–1877. 25 indexed citations
20.
Schwarz, Martin, et al.. (1989). Partial deletion 8q without Langer-Giedion syndrome: a recognisable syndrome.. Journal of Medical Genetics. 26(3). 167–171. 8 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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