Verena Matejas

2.0k total citations
12 papers, 411 citations indexed

About

Verena Matejas is a scholar working on Nephrology, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Verena Matejas has authored 12 papers receiving a total of 411 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Nephrology, 8 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Verena Matejas's work include Renal Diseases and Glomerulopathies (9 papers), Renal and related cancers (6 papers) and Biomedical Research and Pathophysiology (3 papers). Verena Matejas is often cited by papers focused on Renal Diseases and Glomerulopathies (9 papers), Renal and related cancers (6 papers) and Biomedical Research and Pathophysiology (3 papers). Verena Matejas collaborates with scholars based in Germany, United States and Pakistan. Verena Matejas's co-authors include Martin Zenker, Martin Zenker, Christopher N. Vlangos, Lihadh Al‐Gazali, Iradj Amirlak, Arthur H. Cohen, Mikhail Kagan, Ayşı̇n Bakkaloğlu, Martin Griebel and K Hasselbacher and has published in prestigious journals such as Kidney International, Nephrology Dialysis Transplantation and Pediatric Nephrology.

In The Last Decade

Verena Matejas

11 papers receiving 402 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Verena Matejas Germany 10 306 215 82 80 73 12 411
Rakesh Kumar Verma India 5 244 0.8× 174 0.8× 25 0.3× 80 1.0× 11 0.2× 18 321
Ramiro Nández United States 5 96 0.3× 158 0.7× 50 0.6× 48 0.6× 10 0.1× 6 301
Michael Yau United Kingdom 3 40 0.1× 169 0.8× 8 0.1× 40 0.5× 77 1.1× 4 236
E H Zackai United States 7 36 0.1× 258 1.2× 24 0.3× 213 2.7× 9 0.1× 12 434
Mark V. Clough United States 6 127 0.4× 192 0.9× 4 0.0× 132 1.6× 8 0.1× 8 363
Margherita Baldassarri Italy 10 24 0.1× 120 0.6× 12 0.1× 91 1.1× 61 0.8× 21 281
Fatemehsadat Esteghamat Iran 13 60 0.2× 191 0.9× 64 0.8× 72 0.9× 2 0.0× 17 412
Jouko Meretoja Finland 11 56 0.2× 353 1.6× 112 1.4× 242 3.0× 7 0.1× 15 462
Tahir Naeem Khan Pakistan 11 69 0.2× 118 0.5× 8 0.1× 59 0.7× 2 0.0× 32 308
Josephine Duvall-Young United Kingdom 7 78 0.3× 142 0.7× 5 0.1× 32 0.4× 11 0.2× 9 309

Countries citing papers authored by Verena Matejas

Since Specialization
Citations

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

Fields of papers citing papers by Verena Matejas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Verena Matejas

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

All Works

12 of 12 papers shown
1.
Lehnhardt, A., et al.. (2012). Pierson syndrome in an adolescent girl with nephrotic range proteinuria but a normal GFR. Pediatric Nephrology. 27(5). 865–868. 16 indexed citations
2.
Matejas, Verena, et al.. (2011). Paternal isodisomy of chromosome 3 unmasked by autosomal recessive microcoria‐congenital nephrosis syndrome (Pierson syndrome) in a child with no other phenotypic abnormalities. American Journal of Medical Genetics Part A. 155(10). 2601–2604. 6 indexed citations
3.
Sawyer, Taylor, et al.. (2010). Unique cardiovascular and central nervous system findings in an infant with Pierson (microcoria – congenital nephrosis) Syndrome. Journal of Neonatal-Perinatal Medicine. 3(3). 233–236.
4.
Schoeb, Dominik S., Gil Chernin, Saskia F. Heeringa, et al.. (2010). Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS). Nephrology Dialysis Transplantation. 25(9). 2970–2976. 57 indexed citations
5.
Choi, Hyun Jin, Beom Hee Lee, Ju Hyung Kang, et al.. (2008). Variable phenotype of Pierson syndrome. Pediatric Nephrology. 23(6). 995–1000. 39 indexed citations
6.
Dietrich, A., Verena Matejas, Martin Bitzan, et al.. (2008). Analysis of genes encoding laminin β2 and related proteins in patients with Galloway–Mowat syndrome. Pediatric Nephrology. 23(10). 1779–1786. 9 indexed citations
7.
Wühl, Elke, Jillene Kogan, Aleksandra Żurowska, et al.. (2007). Neurodevelopmental deficits in Pierson (microcoria‐congenital nephrosis) syndrome. American Journal of Medical Genetics Part A. 143A(4). 311–319. 39 indexed citations
8.
Kagan, Mikhail, Arthur H. Cohen, Verena Matejas, Christopher N. Vlangos, & Martin Zenker. (2007). A milder variant of Pierson syndrome. Pediatric Nephrology. 23(2). 323–327. 38 indexed citations
9.
Cavalcanti, Denise P., et al.. (2006). Fraser and Ablepharon macrostomia phenotypes: Concurrence in one family and association with mutatedFRAS1. American Journal of Medical Genetics Part A. 143A(3). 241–247. 17 indexed citations
10.
Matejas, Verena, Lihadh Al‐Gazali, Iradj Amirlak, & Martin Zenker. (2006). A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2. Nephrology Dialysis Transplantation. 21(11). 3283–3286. 38 indexed citations
11.
Matejas, Verena, Kathrin Huehne, Christian T. Thiel, et al.. (2006). Identification of Alu elements mediating a partial PMP22 deletion. Neurogenetics. 7(2). 119–126. 16 indexed citations
12.
Hasselbacher, K, Roger C. Wiggins, Verena Matejas, et al.. (2006). Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Kidney International. 70(6). 1008–1012. 136 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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