Anna Materna‐Kiryluk

2.3k total citations
37 papers, 403 citations indexed

About

Anna Materna‐Kiryluk is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Anna Materna‐Kiryluk has authored 37 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Surgery and 12 papers in Molecular Biology. Recurrent topics in Anna Materna‐Kiryluk's work include Congenital Anomalies and Fetal Surgery (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Anna Materna‐Kiryluk is often cited by papers focused on Congenital Anomalies and Fetal Surgery (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Anna Materna‐Kiryluk collaborates with scholars based in Poland, Germany and Netherlands. Anna Materna‐Kiryluk's co-authors include Anna Latos‐Bieleńska, Magdalena Badura‐Stronka, Barbara Więckowska, Anna Latos‐Bieleńska, Bartłomiej Budny, Aleksander Jamsheer, Krzysztof Kiryluk, Janusz Limon, HH Ropers and Andreas Tzschach and has published in prestigious journals such as Human Molecular Genetics, BMJ Open and Frontiers in Genetics.

In The Last Decade

Anna Materna‐Kiryluk

35 papers receiving 390 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Materna‐Kiryluk Poland 13 170 153 100 91 53 37 403
Jean-Marc Rigot France 15 166 1.0× 267 1.7× 151 1.5× 68 0.7× 18 0.3× 51 732
Elizabeth A. Leeth United States 8 143 0.8× 103 0.7× 115 1.1× 108 1.2× 30 0.6× 11 287
Mónica Aguinaga‐Ríos Mexico 9 93 0.5× 67 0.4× 78 0.8× 99 1.1× 38 0.7× 35 290
Jin Han China 13 160 0.9× 179 1.2× 142 1.4× 246 2.7× 66 1.2× 74 551
M. L. Martínez‐Frías Spain 16 215 1.3× 121 0.8× 244 2.4× 148 1.6× 20 0.4× 31 549
Maria Mercedes de Elejalde United States 11 174 1.0× 70 0.5× 96 1.0× 162 1.8× 26 0.5× 21 342
M. Brun France 8 75 0.4× 83 0.5× 47 0.5× 77 0.8× 44 0.8× 16 235
P. Droullé France 15 110 0.6× 121 0.8× 143 1.4× 394 4.3× 38 0.7× 33 601
Alan G. Howatson United Kingdom 12 62 0.4× 89 0.6× 167 1.7× 85 0.9× 59 1.1× 23 446
M.-P. Vazquez France 12 275 1.6× 221 1.4× 124 1.2× 146 1.6× 28 0.5× 36 473

Countries citing papers authored by Anna Materna‐Kiryluk

Since Specialization
Citations

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

Fields of papers citing papers by Anna Materna‐Kiryluk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Materna‐Kiryluk. 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 Anna Materna‐Kiryluk. The network helps show where Anna Materna‐Kiryluk may publish in the future.

Co-authorship network of co-authors of Anna Materna‐Kiryluk

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Materna‐Kiryluk. A scholar is included among the top collaborators of Anna Materna‐Kiryluk 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 Anna Materna‐Kiryluk. Anna Materna‐Kiryluk 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.
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
2.
Bukowska‐Olech, Ewelina, Anna Sowińska‐Seidler, Dawid Larysz, et al.. (2022). Results from Genetic Studies in Patients Affected with Craniosynostosis: Clinical and Molecular Aspects. Frontiers in Molecular Biosciences. 9. 865494–865494. 3 indexed citations
3.
Dolk, Helen, Maria Loane, Karen Casson, et al.. (2021). Macrolide and lincosamide antibiotic exposure in the first trimester of pregnancy and risk of congenital anomaly: A European case-control study. Reproductive Toxicology. 100. 101–108. 12 indexed citations
4.
Materna‐Kiryluk, Anna, Agnieszka Pollak, Aleksandra Szczawińska-Popłonyk, et al.. (2021). Mosaic IL6ST variant inducing constitutive GP130 cytokine receptor signaling as a cause of neonatal onset immunodeficiency with autoinflammation and dysmorphy. Human Molecular Genetics. 30(3-4). 226–233. 18 indexed citations
5.
Bukowska‐Olech, Ewelina, Anna Materna‐Kiryluk, Joanna Walczak‐Sztulpa, et al.. (2020). Targeted Next-Generation Sequencing in the Diagnosis of Facial Dysostoses. Frontiers in Genetics. 11. 580477–580477. 12 indexed citations
6.
Barišić, Ingeborg, Jorieke E. H. Bergman, Clara Cavero‐Carbonell, et al.. (2018). Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe. European Journal of Medical Genetics. 61(9). 499–507. 22 indexed citations
7.
Wender-Ożegowska, Ewa, Ester Garne, Margery Morgan, et al.. (2018). Insulin analogues use in pregnancy among women with pregestational diabetes mellitus and risk of congenital anomaly: a retrospective population-based cohort study. BMJ Open. 8(2). e014972–e014972. 14 indexed citations
8.
Jamsheer, Aleksander, Aleksandra Jezela‐Stanek, Andrzej Witek, et al.. (2016). Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis. Ginekologia Polska. 87(10). 706–710. 1 indexed citations
9.
Wender-Ożegowska, Ewa, Ester Garne, Margery Morgan, et al.. (2015). Use of insulin analogs in pregestational diabetes and risk of congenital anomalies. University of Southern Denmark Research Portal (University of Southern Denmark). 1 indexed citations
10.
Materna‐Kiryluk, Anna, et al.. (2015). Geospatial clustering of gastroschisis in Poland: Data from the Polish Registryof Congenital Malformations (PRCM). International Journal of Occupational Medicine and Environmental Health. 29(3). 461–470. 14 indexed citations
11.
Materna‐Kiryluk, Anna, Aleksander Jamsheer, Barbara Więckowska, et al.. (2013). Epidemiology of isolated preaxial polydactyly type I: Data from the Polish Registry of Congenital Malformations (PRCM). BMC Pediatrics. 13(1). 26–26. 17 indexed citations
12.
Materna‐Kiryluk, Anna, et al.. (2013). The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1. Pediatric Nephrology. 29(2). 257–267. 13 indexed citations
13.
14.
Materna‐Kiryluk, Anna, et al.. (2011). Maternal reproductive history and the risk of isolated congenital malformations. Paediatric and Perinatal Epidemiology. 25(2). 135–143. 14 indexed citations
15.
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
16.
Budny, Bartłomiej, Magdalena Badura‐Stronka, Anna Materna‐Kiryluk, et al.. (2010). Novel missense mutations in the ubiquitination‐related gene UBE2A cause a recognizable X‐linked mental retardation syndrome. Clinical Genetics. 77(6). 541–551. 40 indexed citations
17.
Badura‐Stronka, Magdalena, Aleksander Jamsheer, Anna Materna‐Kiryluk, et al.. (2009). A novel nonsense mutation in CUL4B gene in three brothers with X‐linked mental retardation syndrome. Clinical Genetics. 77(2). 141–144. 43 indexed citations
18.
Materna‐Kiryluk, Anna, Magdalena Badura‐Stronka, Barbara Więckowska, et al.. (2008). Parental age as a risk factor for isolated congenital malformations in a Polish population. Paediatric and Perinatal Epidemiology. 23(1). 29–40. 55 indexed citations
19.
20.
Walczak, Mieczysław, Anna Materna‐Kiryluk, R. Czajka, et al.. (1998). Prevalence and Forms of Congenital Anomalies in Twins Born in Pomeranian District During the Period from 1.07.1997 to 31.12.1998. Acta geneticae medicae et gemellologiae twin research. 47(3-4). 255–259. 5 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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