M Krawczyński

1.4k total citations
85 papers, 779 citations indexed

About

M Krawczyński is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, M Krawczyński has authored 85 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 31 papers in Genetics and 13 papers in Ophthalmology. Recurrent topics in M Krawczyński's work include Retinal Development and Disorders (18 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Sexual Differentiation and Disorders (10 papers). M Krawczyński is often cited by papers focused on Retinal Development and Disorders (18 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers) and Sexual Differentiation and Disorders (10 papers). M Krawczyński collaborates with scholars based in Poland, Germany and United Kingdom. M Krawczyński's co-authors include Anna Wawrocka, Alicja Krzyżaniak, Jenifer Walkowiak, Michał Witt, Jarosław Walkowiak, Susanne Kohl, Aleksander Jamsheer, S. Faisal Ahmed, Olaf Hiort and Bernd Wissinger and has published in prestigious journals such as Proceedings of the National Academy of Sciences, International Journal of Molecular Sciences and Annals of Oncology.

In The Last Decade

M Krawczyński

77 papers receiving 756 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M Krawczyński Poland 18 470 218 124 115 90 85 779
M. Gonzalés France 16 244 0.5× 131 0.6× 122 1.0× 37 0.3× 30 0.3× 38 617
María‐Luisa Martínez‐Frías Spain 16 251 0.5× 327 1.5× 105 0.8× 37 0.3× 21 0.2× 22 801
Hasan Bağcı Türkiye 17 310 0.7× 91 0.4× 23 0.2× 69 0.6× 40 0.4× 42 667
M D Crawfurd United Kingdom 18 250 0.5× 290 1.3× 43 0.3× 32 0.3× 74 0.8× 33 705
Diana García‐Cruz Mexico 16 272 0.6× 356 1.6× 14 0.1× 37 0.3× 55 0.6× 81 727
Philippe Loget France 16 385 0.8× 291 1.3× 8 0.1× 46 0.4× 58 0.6× 40 749
Margaret Barrow United Kingdom 13 263 0.6× 341 1.6× 15 0.1× 43 0.4× 40 0.4× 18 738
Lakshmi Mehta United States 16 403 0.9× 348 1.6× 15 0.1× 44 0.4× 57 0.6× 46 754
M. S. Pembrey United Kingdom 4 216 0.5× 264 1.2× 13 0.1× 59 0.5× 82 0.9× 7 664
Dilek Aktaş Türkiye 17 423 0.9× 455 2.1× 27 0.2× 43 0.4× 19 0.2× 68 873

Countries citing papers authored by M Krawczyński

Since Specialization
Citations

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

Fields of papers citing papers by M Krawczyński

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Krawczyński

This figure shows the co-authorship network connecting the top 25 collaborators of M Krawczyński. A scholar is included among the top collaborators of M Krawczyński 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 M Krawczyński. M Krawczyński 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.
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Wawrocka, Anna, et al.. (2024). Coexistence of Retinitis Pigmentosa and Ataxia in Patients with PHARC, PCARP, and Oliver–McFarlane Syndromes. International Journal of Molecular Sciences. 25(11). 5759–5759. 2 indexed citations
3.
Walczak‐Sztulpa, Joanna, Anna Wawrocka, Mirosław Andrusiewicz, et al.. (2023). Ciliary phenotyping in renal epithelial cells in a cranioectodermal dysplasia patient with WDR35 variants. Frontiers in Molecular Biosciences. 10. 1285790–1285790. 1 indexed citations
4.
5.
Kmieć, Tomasz, et al.. (2022). Deterioration of visual quality and acuity as the first sign of ceroid lipofuscinosis type 3 (CLN3), a rare neurometabolic disease. Metabolic Brain Disease. 38(2). 709–715. 2 indexed citations
6.
Krawczyński, M, et al.. (2020). Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation. Metabolic Brain Disease. 35(8). 1317–1327. 4 indexed citations
7.
Sanders, Caroline, J. Camille Hall, Arianne B. Dessens, et al.. (2018). Involving Individuals with Disorders of Sex Development and Their Parents in Exploring New Models of Shared Learning: Proceedings from a DSDnet COST Action Workshop. Sexual Development. 12(5). 225–231. 13 indexed citations
8.
Kyriakou, Andreas, Arianne B. Dessens, Jillian Bryce, et al.. (2016). Current models of care for disorders of sex development – results from an International survey of specialist centres. Orphanet Journal of Rare Diseases. 11(1). 155–155. 59 indexed citations
9.
Krawczyński, M, Piotr Stawiński, Jerzy Szaflik, et al.. (2015). Next-generation sequencing of ABCA4: High frequency of complex alleles and novel mutations in patients with retinal dystrophies from Central Europe. Experimental Eye Research. 145. 93–99. 31 indexed citations
10.
Jakubowska, Anna, Jacek Gronwald, M Krawczyński, et al.. (2014). Large deletion causing von Hippel-Lindau disease and hereditary breast cancer syndrome. Hereditary Cancer in Clinical Practice. 12(1). 16–16. 5 indexed citations
11.
Wawrocka, Anna, et al.. (2011). PAX63′ deletion in a family with aniridia. Ophthalmic Genetics. 33(1). 44–48. 19 indexed citations
12.
Krawczyński, Marian, et al.. (2010). Zaburzenia rozwojowe: ilościowa i jakościowa skala problemów klinicznych. Pediatria Polska. 85(1). 10–17. 1 indexed citations
13.
Woźniak, Anna, Marzena Wiśniewska, Renata Glazar, et al.. (2010). Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland. BMC Pediatrics. 10(1). 88–88. 21 indexed citations
14.
Krawczyński, M. (2004). [Genetic ground of primary open angle glaucoma].. PubMed. 106(4-5). 695–8. 1 indexed citations
15.
Krawczyński, M, et al.. (2004). Only neutral polymorphisms found in the TIGR/myocilin gene of 45 Polish patients with primary open-angle glaucoma.. PubMed. 45(2). 275–9. 2 indexed citations
16.
Walkowiak, Jarosław, et al.. (2004). Faecal elastase-1 test is superior to faecal lipase test in the assessment of exocrine pancreatic function in cystic fibrosis. Acta Paediatrica. 93(8). 1042–1045. 3 indexed citations
17.
Krawczyński, M, et al.. (2004). Die Bedeutung der Familienuntersuchung bei der juvenilen Retinoschisis. Der Ophthalmologe. 102(12). 1193–1199. 1 indexed citations
18.
Krawczyński, M. (2003). Genetyka kliniczna dla lekarza praktyka. Przewodnik Lekarza/Guide for GPs. 5(11). 111–116.
19.
Krawczyński, M, Jarosław Walkowiak, & Alicja Krzyżaniak. (2003). Secular changes in body height and weight in children and adolescents in Poznan, Poland, between 1880 and 2000. Acta Paediatrica. 92(3). 277–282. 12 indexed citations
20.
Krawczyński, M, et al.. (1974). [Abnormalities of the urogenital system vascularisation in Turner's syndrome].. PubMed. 29(4). 413–22. 1 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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