Piotr Gasperowicz

726 total citations
23 papers, 312 citations indexed

About

Piotr Gasperowicz is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Piotr Gasperowicz has authored 23 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Surgery. Recurrent topics in Piotr Gasperowicz's work include Genetic Syndromes and Imprinting (3 papers), Genomics and Rare Diseases (3 papers) and RNA regulation and disease (3 papers). Piotr Gasperowicz is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Genomics and Rare Diseases (3 papers) and RNA regulation and disease (3 papers). Piotr Gasperowicz collaborates with scholars based in Poland, Australia and United Kingdom. Piotr Gasperowicz's co-authors include Rafał Płoski, Małgorzata Rydzanicz, Joanna Kosińska, Anna Walczak, Agnieszka Pollak, Maria Barcikowska, Beata Pepłońska, Wojciech Branicki, Magdalena Spólnicka and Cezary Żekanowski and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Piotr Gasperowicz

23 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Piotr Gasperowicz Poland	12	191	74	42	26	25	23	312
Banan Al‐Younes Saudi Arabia	12	222 1.2×	92 1.2×	55 1.3×	13 0.5×	20 0.8×	18	387
Kate Sinclair Australia	10	159 0.8×	36 0.5×	61 1.5×	15 0.6×	12 0.5×	13	356
Fılız Hazan Türkiye	10	183 1.0×	119 1.6×	24 0.6×	7 0.3×	18 0.7×	54	309
Martina Winklmayr Austria	9	213 1.1×	37 0.5×	41 1.0×	12 0.5×	15 0.6×	12	344
Alicia Vaglio United States	7	338 1.8×	159 2.1×	47 1.1×	9 0.3×	48 1.9×	24	548
Jong Hak Won United States	11	221 1.2×	24 0.3×	50 1.2×	10 0.4×	14 0.6×	26	366
Jane Fleming Australia	9	184 1.0×	111 1.5×	57 1.4×	8 0.3×	14 0.6×	30	348
Xun Cheng China	7	269 1.4×	57 0.8×	51 1.2×	7 0.3×	11 0.4×	9	349
Luigina Spaccini Italy	13	208 1.1×	159 2.1×	28 0.7×	7 0.3×	18 0.7×	47	455
Katarzyna Tońska Poland	14	400 2.1×	44 0.6×	46 1.1×	8 0.3×	11 0.4×	40	502

Countries citing papers authored by Piotr Gasperowicz

Since Specialization

Citations

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

Fields of papers citing papers by Piotr Gasperowicz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Piotr Gasperowicz

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

Gasperowicz, Piotr, et al.. (2023). Epigenetic Findings in Twins with Esophageal Atresia. Genes. 14(9). 1822–1822. 2 indexed citations

Misceo, Doriana, Inger‐Lise Mero, Arvind Y. M. Sundaram, et al.. (2023). Novel Loss of Function Variants in CENPF Including a Large Intragenic Deletion in Patients with Strømme Syndrome. Genes. 14(11). 1985–1985. 1 indexed citations

Mrozikiewicz‐Rakowska, Beata, Ilona Szabłowska‐Gadomska, Dominik Cysewski, et al.. (2023). Allogenic Adipose-Derived Stem Cells in Diabetic Foot Ulcer Treatment: Clinical Effectiveness, Safety, Survival in the Wound Site, and Proteomic Impact. International Journal of Molecular Sciences. 24(2). 1472–1472. 15 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

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

Rydzanicz, Małgorzata, Piotr Gasperowicz, Agnieszka Pollak, et al.. (2021). A recurrent de novo variant supports KCNC2 involvement in the pathogenesis of developmental and epileptic encephalopathy. American Journal of Medical Genetics Part A. 185(11). 3384–3389. 14 indexed citations

Rozensztrauch, Anna, Piotr Gasperowicz, Ryszard Ślężak, et al.. (2021). Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report. Frontiers in Pediatrics. 9. 783553–783553. 4 indexed citations

Szczałuba, Krzysztof, Justyna Sicińska, Małgorzata Rydzanicz, et al.. (2020). Intracardiac tumor as a rare manifestation of genetic syndromes—presentation of a family with Gorlin syndrome and a literature review. Journal of Applied Genetics. 61(4). 559–565. 2 indexed citations

Pilch, Jacek, Justyna Paprocka, Małgorzata Rydzanicz, et al.. (2020). Leukoencephalopathy with Calcifications and Cysts—The First Polish Patient with Labrune Syndrome. Brain Sciences. 10(11). 869–869. 3 indexed citations

10.

Nicita, Francesco, Fabrizia Stregapede, Alessandra Tessa, et al.. (2019). Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants. Journal of Neurology. 266(11). 2657–2664. 13 indexed citations

11.

Kabza, Michał, Justyna A. Karolak, Małgorzata Rydzanicz, et al.. (2019). Multiple Differentially Methylated Regions Specific to Keratoconus Explain Known Keratoconus Linkage Loci. Investigative Ophthalmology & Visual Science. 60(5). 1501–1501. 19 indexed citations

12.

Śmigiel, Robert, Victor Murcia Pienkowski, Elżbieta Szmida, et al.. (2018). Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome. Journal of Human Genetics. 63(4). 517–520. 15 indexed citations

13.

Pesz, Karolina, Victor Murcia Pienkowski, Agnieszka Pollak, et al.. (2018). Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15. European Journal of Medical Genetics. 61(10). 596–601. 3 indexed citations

14.

Pilch, Jacek, Anna Walczak, Victor Murcia Pienkowski, et al.. (2018). Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation. Clinical Genetics. 94(3-4). 381–385. 23 indexed citations

15.

Śmigiel, Robert, Diane L. Sherman, Małgorzata Rydzanicz, et al.. (2018). Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia. Human Molecular Genetics. 27(21). 3669–3674. 21 indexed citations

16.

Szczałuba, Krzysztof, Krystyna Szymańska, Piotr Gasperowicz, et al.. (2017). Novel GNB1 de novo mutation in a patient with neurodevelopmental disorder and cutaneous mastocytosis: Clinical report and literature review. European Journal of Medical Genetics. 61(3). 157–160. 21 indexed citations

17.

Spólnicka, Magdalena, Ewelina Pośpiech, Beata Pepłońska, et al.. (2017). DNA methylation in ELOVL2 and C1orf132 correctly predicted chronological age of individuals from three disease groups. International Journal of Legal Medicine. 132(1). 1–11. 76 indexed citations

18.

Madej‐Pilarczyk, Agnieszka, Małgorzata Rydzanicz, Joanna Kosińska, et al.. (2017). A novel de novo COL6A1 mutation emphasizes the role of intron 14 donor splice site defects as a cause of moderate-progressive form of ColVI myopathy – a case report and review of the genotype–phenotype correlation. Folia Neuropathologica. 3(3). 214–220. 4 indexed citations

19.

Truszkowska, Grażyna, Zofia T. Bilińska, Angelika Muchowicz, et al.. (2017). Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy. Scientific Reports. 7(1). 3362–3362. 25 indexed citations

20.

Rydzanicz, Małgorzata, Elżbieta Jurkiewicz, Ewa Jamroz, et al.. (2017). Mild Zellweger syndrome due to a novel PEX6 mutation: correlation between clinical phenotype and in silico prediction of variant pathogenicity. Journal of Applied Genetics. 58(4). 475–480. 13 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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