Anna Wawrocka

466 total citations
31 papers, 286 citations indexed

About

Anna Wawrocka is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Anna Wawrocka has authored 31 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 15 papers in Genetics and 9 papers in Ophthalmology. Recurrent topics in Anna Wawrocka's work include Retinal Development and Disorders (10 papers), Genetic and Kidney Cyst Diseases (8 papers) and Renal and related cancers (6 papers). Anna Wawrocka is often cited by papers focused on Retinal Development and Disorders (10 papers), Genetic and Kidney Cyst Diseases (8 papers) and Renal and related cancers (6 papers). Anna Wawrocka collaborates with scholars based in Poland, Germany and Netherlands. Anna Wawrocka's co-authors include M Krawczyński, Aleksander Jamsheer, Joanna Walczak‐Sztulpa, Anna Latos‐Bieleńska, Bartłomiej Budny, Anna Sowińska‐Seidler, Ewelina Bukowska‐Olech, Susanne Kohl, Magdalena Badura‐Stronka and Rafał Płoski and has published in prestigious journals such as International Journal of Molecular Sciences, Cornea and European Journal of Human Genetics.

In The Last Decade

Anna Wawrocka

31 papers receiving 272 citations

Peers

Anna Wawrocka

GENET

OPHTH

RNMI

Cécile Méjécase United Kingdom

Saoud Tahsin Swafiri Spain

Aaron Black United States

Cecinio C. Ronquillo United States

Muhammad Asif Naeem Pakistan

Tatyana A. Vasilyeva Russia

Sarita Rani Patnaik Germany

Tiger Zhou Australia

M. Hermina Strungaru Canada

Lucas Fares‐Taie France

Cécile Méjécase United Kingdom

Anna Wawrocka

247 ×1.1

72 ×0.6

GENET

140 ×1.7

OPHTH

46 ×1.0

RNMI

25 ×0.8

Citations per year, relative to Anna Wawrocka Anna Wawrocka (= 1×) peers Cécile Méjécase

Countries citing papers authored by Anna Wawrocka

Since Specialization

Citations

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

Fields of papers citing papers by Anna Wawrocka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Wawrocka

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

All Works

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20 of 20 papers shown

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

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

Wawrocka, Anna, et al.. (2023). Molecular Re-Diagnosis with Whole-Exome Sequencing Increases the Diagnostic Yield in Patients with Non-Syndromic Retinitis Pigmentosa. Diagnostics. 13(4). 730–730. 3 indexed citations

Sowińska‐Seidler, Anna, et al.. (2022). Molecular background of Leber congenital amaurosis in a Polish cohort of patients—novel variants discovered by NGS. Journal of Applied Genetics. 64(1). 89–104. 4 indexed citations

Walczak‐Sztulpa, Joanna, Anna Wawrocka, Ronald van Beek, et al.. (2022). Identical IFT140 Variants Cause Variable Skeletal Ciliopathy Phenotypes—Challenges for the Accurate Diagnosis. Frontiers in Genetics. 13. 931822–931822. 5 indexed citations

Wawrocka, Anna, Joanna Walczak‐Sztulpa, Magdalena Socha, et al.. (2021). Homozygous microdeletion in the 11p13 region in the patient with isolated form of aniridia: New challenges in the genetic diagnostics of aniridia. American Journal of Medical Genetics Part A. 188(2). 642–647. 2 indexed citations

Raczyńska, Dorota, et al.. (2021). The coincidence of two ultra-rare hereditary eye diseases: gyrate atrophy and Kjer optic atrophy - a surprising diagnosis based on next-generation sequencing. Intractable & Rare Diseases Research. 10(3). 202–206. 3 indexed citations

Wawrocka, Anna, Joanna Walczak‐Sztulpa, Ewelina Bukowska‐Olech, et al.. (2020). Two sisters with microphthalmia and anterior segment dysgenesis secondary to a PAX6 pathogenic variant with clinically healthy parents: a case of gonadal mosaicism?. Japanese Journal of Ophthalmology. 64(2). 134–139. 3 indexed citations

Walczak‐Sztulpa, Joanna, Renata Posmyk, Ewelina Bukowska‐Olech, et al.. (2020). Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease. Orphanet Journal of Rare Diseases. 15(1). 36–36. 12 indexed citations

10.

Walczak‐Sztulpa, Joanna, Anna Wawrocka, Heleen H. Arts, et al.. (2020). Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35. American Journal of Medical Genetics Part A. 182(10). 2417–2425. 8 indexed citations

11.

Wawrocka, Anna, et al.. (2018). Novel CHM mutations in Polish patients with choroideremia – an orphan disease with close perspective of treatment. Orphanet Journal of Rare Diseases. 13(1). 221–221. 3 indexed citations

12.

Wawrocka, Anna & M Krawczyński. (2018). The genetics of aniridia — simple things become complicated. Journal of Applied Genetics. 59(2). 151–159. 34 indexed citations

13.

Chiang, Wei‐Chieh, Anna Wawrocka, Małgorzata Jarmuż‐Szymczak, et al.. (2017). Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 gene. European Journal of Human Genetics. 25(11). 1210–1216. 28 indexed citations

14.

Walczak‐Sztulpa, Joanna, Anna Wawrocka, Ryszard Grenda, et al.. (2017). Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations. American Journal of Medical Genetics Part A. 173(5). 1364–1368. 11 indexed citations

15.

Warowicka, Alicja, et al.. (2015). Fundus albipunctatus: review of the literature and report of a novel RDH5 gene mutation affecting the invariant tyrosine (p.Tyr175Phe). Journal of Applied Genetics. 56(3). 317–327. 22 indexed citations

16.

Wawrocka, Anna, et al.. (2013). 11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia. Journal of Applied Genetics. 54(3). 345–351. 26 indexed citations

17.

Badura‐Stronka, Magdalena, et al.. (2013). Severe manifestation of Leber's hereditary optic neuropathy due to 11778G>A mtDNA mutation in a female with hypoestrogenism due to Perrault syndrome. Mitochondrion. 13(6). 831–834. 14 indexed citations

18.

Wawrocka, Anna, et al.. (2011). PAX63′ deletion in a family with aniridia. Ophthalmic Genetics. 33(1). 44–48. 19 indexed citations

19.

Jamsheer, Aleksander, Marzena Wiśniewska, Andrzej Szpak, et al.. (2009). A novelGJA1 missense mutation in a Polish child with oculodentodigital dysplasia. Journal of Applied Genetics. 50(3). 297–299. 14 indexed citations

20.

Kałużny, Bartłomiej J., Anna Szkulmowska, Maciej Szkulmowski, et al.. (2008). Granular Corneal Dystrophy in 830-nm Spectral Optical Coherence Tomography. Cornea. 27(7). 830–832. 11 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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