Agnieszka Pollak

2.8k total citations
83 papers, 1.2k citations indexed

About

Agnieszka Pollak is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Agnieszka Pollak has authored 83 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 27 papers in Genetics and 13 papers in Sensory Systems. Recurrent topics in Agnieszka Pollak's work include Hearing, Cochlea, Tinnitus, Genetics (13 papers), Mitochondrial Function and Pathology (11 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Agnieszka Pollak is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (13 papers), Mitochondrial Function and Pathology (11 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Agnieszka Pollak collaborates with scholars based in Poland, Germany and Austria. Agnieszka Pollak's co-authors include Rafał Płoski, Małgorzata Rydzanicz, Piotr Stawiński, Joanna Kosińska, Monika Ołdak, Henryk Skarżyńśki, Urszula Lechowicz, Ewa Pronicka, Grażyna Kostrzewa and L Korniszewski and has published in prestigious journals such as PLoS ONE, Brain and Scientific Reports.

In The Last Decade

Agnieszka Pollak

77 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Agnieszka Pollak Poland	19	588	202	201	158	132	83	1.2k
Shin’ichiro Yasunaga Japan	21	741 1.3×	237 1.2×	430 2.1×	31 0.2×	162 1.2×	60	1.7k
Ahmad Abou Tayoun United Arab Emirates	23	892 1.5×	838 4.1×	194 1.0×	65 0.4×	82 0.6×	81	2.0k
Teresa M. Gunn United States	22	717 1.2×	230 1.1×	65 0.3×	44 0.3×	85 0.6×	63	1.6k
Tara M. Riddle United States	11	1.2k 2.1×	126 0.6×	159 0.8×	15 0.1×	62 0.5×	11	1.8k
Ľudevít Kádaši Slovakia	18	446 0.8×	155 0.8×	83 0.4×	147 0.9×	39 0.3×	56	809
Sandra Beer‐Hammer Germany	24	699 1.2×	128 0.6×	94 0.5×	16 0.1×	89 0.7×	56	1.5k
Sergio González Chile	23	789 1.3×	152 0.8×	36 0.2×	17 0.1×	528 4.0×	60	1.9k
Giovanni Di Pasquale United States	18	669 1.1×	589 2.9×	177 0.9×	15 0.1×	25 0.2×	43	1.1k
Seong‐Beom Lee South Korea	25	960 1.6×	131 0.6×	27 0.1×	34 0.2×	58 0.4×	65	2.1k
Anke Seydel Italy	13	986 1.7×	215 1.1×	153 0.8×	13 0.1×	46 0.3×	18	1.4k

Countries citing papers authored by Agnieszka Pollak

Since Specialization

Citations

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

Fields of papers citing papers by Agnieszka Pollak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Agnieszka Pollak

This figure shows the co-authorship network connecting the top 25 collaborators of Agnieszka Pollak. A scholar is included among the top collaborators of Agnieszka Pollak 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 Agnieszka Pollak. Agnieszka Pollak 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

Pollak, Agnieszka, Katarzyna Jończyk‐Potoczna, Grażyna Truszkowska, et al.. (2023). Double Heterozygous Pathogenic Variants in the LOX and PKD1 Genes in a 5-Year-Old Patient with Thoracic Aortic Aneurysm and Polycystic Kidney Disease. Genes. 14(11). 1983–1983. 1 indexed citations

Stembalska, Agnieszka, Małgorzata Rydzanicz, Agnieszka Pollak, et al.. (2022). Prenatal Diagnosis of Jeune Syndrome Caused by Compound Heterozygous Variants in DYNC2H1 Gene—Case Report with Rapid WES Procedure and Differential Diagnosis of Lethal Skeletal Dysplasias. Genes. 13(8). 1339–1339. 4 indexed citations

Stembalska, Agnieszka, Małgorzata Rydzanicz, Wojciech Walas, et al.. (2022). Severe Infantile Axonal Neuropathy with Respiratory Failure Caused by Novel Mutation in X-Linked LAS1L Gene. Genes. 13(5). 725–725. 3 indexed citations

Bobrus‐Chociej, Anna, et al.. (2021). Celiac Disease in Conjunction with Hereditary Fructose Intolerance as a Rare Cause of Liver Steatosis with Mild Hypertransaminasemia—A Case Report. Pediatric Reports. 13(4). 589–593. 3 indexed citations

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

Stembalska, Agnieszka, Małgorzata Rydzanicz, Agnieszka Pollak, et al.. (2021). Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations. Genes. 12(7). 1078–1078. 2 indexed citations

Szczałuba, Krzysztof, Hanna Mierzewska, Robert Śmigiel, et al.. (2020). AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant. Journal of Applied Genetics. 61(2). 213–218. 7 indexed citations

Pollak, Agnieszka, et al.. (2020). Peritoneal dialysis in an adult patient with tetralogy of Fallot diagnosed with incomplete Alagille syndrome. BMC Medical Genetics. 21(1). 195–195. 2 indexed citations

Ołdak, Monika, Agnieszka Pollak, Iwona Stępniak, et al.. (2017). Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome. Journal of Translational Medicine. 15(1). 25–25. 35 indexed citations

10.

Płoski, Rafał, Małgorzata Rydzanicz, Maria Franaszczyk, et al.. (2016). Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy. American Journal of Medical Genetics Part A. 170(12). 3241–3248. 42 indexed citations

11.

Śmigiel, Robert, Grażyna Kostrzewa, Joanna Kosińska, et al.. (2016). Further evidence for GRIN2B mutation as the cause of severe epileptic encephalopathy. American Journal of Medical Genetics Part A. 170(12). 3265–3270. 22 indexed citations

12.

Pollak, Agnieszka, et al.. (2016). Advances in genetic hearing loss: CIB2 gene. European Archives of Oto-Rhino-Laryngology. 274(4). 1791–1795. 9 indexed citations

13.

Rydzanicz, Małgorzata, Mateusz Jagła, Joanna Kosińska, et al.. (2016). KIF5A de novo mutation associated with myoclonic seizures and neonatal onset progressive leukoencephalopathy. Clinical Genetics. 91(5). 769–773. 27 indexed citations

14.

Perlejewski, Karol, Marta Popiel, Tomasz Laskus, et al.. (2015). Next-generation sequencing (NGS) in the identification of encephalitis-causing viruses: Unexpected detection of human herpesvirus 1 while searching for RNA pathogens. Journal of Virological Methods. 226. 1–6. 47 indexed citations

15.

Pollak, Agnieszka, Małgorzata Mueller‐Malesińska, Urszula Lechowicz, et al.. (2012). MTHFR 677T Is a Strong Determinant of the Degree of Hearing Loss Among Polish Males with Postlingual Sensorineural Hearing Impairment. DNA and Cell Biology. 31(7). 1267–1273. 7 indexed citations

16.

Iwanicka‐Pronicka, Katarzyna, Agnieszka Pollak, Agata Skórka, et al.. (2012). Postlingual Hearing Loss as a Mitochondrial 3243A>G Mutation Phenotype. PLoS ONE. 7(10). e44054–e44054. 16 indexed citations

17.

Szaflik, Jerzy, et al.. (2009). Clinical Phenotype of Messmann Corneal Dystrophy With No Mutation in KRT3 and KRT12. Investigative Ophthalmology & Visual Science. 50(13). 5506–5506. 1 indexed citations

18.

Valverde, Alexander, et al.. (2005). Effect of a constant rate infusion of lidocaine on the quality of recovery from sevoflurane or isoflurane general anaesthesia in horses. Equine Veterinary Journal. 37(6). 559–564. 69 indexed citations

19.

Holub, Margareta, et al.. (2005). Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?. Acta Paediatrica. 94(1). 48–52. 9 indexed citations

20.

Pollak, Agnieszka, et al.. (1982). Reduced susceptibility of glycosylated hemoglobin to proteolytic cleavage.. PubMed. 109(4). 621–30. 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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