Renata Glazar

410 total citations
7 papers, 259 citations indexed

About

Renata Glazar is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Renata Glazar has authored 7 papers receiving a total of 259 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Epidemiology. Recurrent topics in Renata Glazar's work include Bone health and treatments (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and Nail Diseases and Treatments (1 paper). Renata Glazar is often cited by papers focused on Bone health and treatments (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and Nail Diseases and Treatments (1 paper). Renata Glazar collaborates with scholars based in Poland, United States and Australia. Renata Glazar's co-authors include Anna Latos‐Bieleńska, Piotr Rogala, Ulpu Seppänen, Leena Ala‐Kokko, Łukasz Kołodziej, Jaana Lohiniva, Merja Perälä, Tim D. Spector, Malwina Czarny‐Ratajczak and K. Kozlowski and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

Renata Glazar

7 papers receiving 254 citations

Peers

Renata Glazar

MB

GENET

RHEUM

IA

RM

Katinka A. Vigh‐Conrad United States

Temuujin Dansranjavin Germany

Jeannette Connerney United States

M.-F. de Tand France

Jerry Shapiro United States

Pawan Dhami United Kingdom

Renqian Du China

M van Rooijen Netherlands

Lara Cresswell United Kingdom

H.G. Slager Netherlands

Katinka A. Vigh‐Conrad United States

Renata Glazar

128 ×0.8

MB

78 ×0.6

GENET

14 ×0.2

RHEUM

11 ×0.3

IA

47 ×1.2

RM

Citations per year, relative to Renata Glazar Renata Glazar (= 1×) peers Katinka A. Vigh‐Conrad

Countries citing papers authored by Renata Glazar

Since Specialization

Citations

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

Fields of papers citing papers by Renata Glazar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renata Glazar

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

All Works

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7 of 7 papers shown

1.

Walczak‐Sztulpa, Joanna, Anna Wawrocka, Ewelina Bukowska‐Olech, et al.. (2022). WDR35 variants in a cranioectodermal dysplasia patient with early onset end‐stage renal disease and retinal dystrophy. American Journal of Medical Genetics Part A. 188(10). 3071–3077. 2 indexed citations

2.

Sowińska‐Seidler, Anna, Ewelina Bukowska‐Olech, Magdalena Socha, et al.. (2019). Functional analysis of novel RUNX2 mutations identified in patients with cleidocranial dysplasia. Clinical Genetics. 96(5). 429–438. 16 indexed citations

3.

Piersiala, Krzysztof, et al.. (2017). Acrofacial dysostosis suggesting Nager syndrome in newborn – Diagnostic and therapeutic difficulties. Pediatria Polska. 92(5). 619–622. 2 indexed citations

4.

Jamsheer, Aleksander, Tomasz Żemojtel, Mateusz Kolanczyk, et al.. (2013). Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion. Journal of Medical Genetics. 50(9). 579–584. 25 indexed citations

5.

Kusz-Zamelczyk, Kamila, Marcin Piotr Sajek, Anna Spik, et al.. (2013). Mutations of NANOS1, a human homologue of the Drosophila morphogen, are associated with a lack of germ cells in testes or severe oligo-astheno-teratozoospermia. Journal of Medical Genetics. 50(3). 187–193. 59 indexed citations

6.

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

7.

Czarny‐Ratajczak, Malwina, Jaana Lohiniva, Piotr Rogala, et al.. (2001). A Mutation in COL9A1 Causes Multiple Epiphyseal Dysplasia: Further Evidence for Locus Heterogeneity. The American Journal of Human Genetics. 69(5). 969–980. 134 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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