Patryk Lipiński

746 total citations
52 papers, 326 citations indexed

About

Patryk Lipiński is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Patryk Lipiński has authored 52 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 18 papers in Physiology and 15 papers in Genetics. Recurrent topics in Patryk Lipiński's work include Lysosomal Storage Disorders Research (17 papers), Glycosylation and Glycoproteins Research (9 papers) and Liver Disease Diagnosis and Treatment (8 papers). Patryk Lipiński is often cited by papers focused on Lysosomal Storage Disorders Research (17 papers), Glycosylation and Glycoproteins Research (9 papers) and Liver Disease Diagnosis and Treatment (8 papers). Patryk Lipiński collaborates with scholars based in Poland, Russia and Lithuania. Patryk Lipiński's co-authors include Anna Tylki‐Szymańska, Piotr Socha, Irena Jankowska, Elżbieta Ciara, Joanna Cielecka–Kuszyk, Agnieszka Różdżyńska‐Świątkowska, Agnieszka Ługowska, Rafał Płoski, Aleksandra Jezela‐Stanek and Joanna Pawłowska and has published in prestigious journals such as International Journal of Molecular Sciences, Nutrients and Journal of Pediatric Gastroenterology and Nutrition.

In The Last Decade

Patryk Lipiński

45 papers receiving 324 citations

Peers

Patryk Lipiński
Ruqaiah Altassan Saudi Arabia
N. Leslie United States
Dimitar K. Gavrilov United States
Y.T. Chen United States
J. A. Barranger United States
Hisayuki Hiraiwa United States
C J Pan United States
Ruqaiah Altassan Saudi Arabia
Patryk Lipiński
Citations per year, relative to Patryk Lipiński Patryk Lipiński (= 1×) peers Ruqaiah Altassan

Countries citing papers authored by Patryk Lipiński

Since Specialization
Citations

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

Fields of papers citing papers by Patryk Lipiński

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patryk Lipiński

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

All Works

20 of 20 papers shown
1.
Lipiński, Patryk, et al.. (2024). Effects of GBA1 Variants and Prenatal Exposition on the Glucosylsphingosine (Lyso-Gb1) Levels in Gaucher Disease Carriers. International Journal of Molecular Sciences. 25(22). 12021–12021. 1 indexed citations
2.
Lipiński, Patryk, et al.. (2024). Body Height of MPS I and II Patients after Hematopoietic Stem Cell Transplantation: The Impact of Dermatan Sulphate. Diagnostics. 14(17). 1956–1956. 2 indexed citations
3.
Lipiński, Patryk, et al.. (2024). Case report: Early (molecular) diagnosis is the clue: report on ALDH7A1 deficiency in newborns. Frontiers in Genetics. 15. 1464556–1464556.
4.
Lipiński, Patryk, Elżbieta Ciara, Dorota Jurkiewicz, et al.. (2023). DCDC2-Related Ciliopathy: Report of Six Polish Patients, Novel DCDC2 Variant, and Literature Review of Reported Cases. Diagnostics. 13(11). 1917–1917. 1 indexed citations
6.
Dubiela, Paweł, et al.. (2023). Alpha-Synuclein mRNA Level Found Dependent on L444P Variant in Carriers and Gaucher Disease Patients on Enzyme Replacement Therapy. Biomolecules. 13(4). 644–644. 3 indexed citations
7.
Paprocka, Justyna, Aleksandra Jezela‐Stanek, Maria Sokół, et al.. (2021). The First Metabolome Analysis in Children with Epilepsy and ALG13-CDG Resulting from c.320A>G Variant. Children. 8(3). 251–251. 7 indexed citations
8.
Lipiński, Patryk, et al.. (2021). Long-term outcome of patients with alpha-mannosidosis – A single center study. Molecular Genetics and Metabolism Reports. 30. 100826–100826. 14 indexed citations
9.
Lipiński, Patryk, et al.. (2021). Pediatric Liver Disease Patients and Secondary Glycosylation Abnormalities. Frontiers in Pediatrics. 8. 613224–613224. 4 indexed citations
10.
Lipiński, Patryk, Dorota Piekutowska‐Abramczuk, Elżbieta Jurkiewicz, et al.. (2021). NBAS deficiency due to biallelic c.2809C > G variant presenting with recurrent acute liver failure with severe hyperammonemia, acquired microcephaly and progressive brain atrophy. Metabolic Brain Disease. 36(7). 2169–2172. 4 indexed citations
11.
Lipiński, Patryk & Anna Tylki‐Szymańska. (2021). Zaburzenie homeostazy lipidowej w deficycie lizosomalnej lipazy – patomechanizm, diagnostyka i leczenie. Postępy Biochemii. 67(3). 231–235. 1 indexed citations
12.
Lipiński, Patryk, Maja Klaudel‐Dreszler, Elżbieta Ciara, et al.. (2021). Sterol 27-Hydroxylase Deficiency as a Cause of Neonatal Cholestasis: Report of 2 Cases and Review of the Literature. Frontiers in Pediatrics. 8. 616582–616582. 7 indexed citations
13.
Pajdowska, Magdalena, et al.. (2021). Transferrin isoform analysis from dried blood spots and serum samples by gel isoelectric focusing for screening congenital disorders of glycosylation. Acta Biochimica Polonica. 68(1). 139–142. 2 indexed citations
14.
Lipiński, Patryk, et al.. (2021). Congenital disorders of glycosylation: Prevalence, incidence and mutational spectrum in the Polish population. Molecular Genetics and Metabolism Reports. 27. 100726–100726. 11 indexed citations
15.
Lipiński, Patryk, Dorota Jurkiewicz, Elżbieta Ciara, et al.. (2020). Neonatal cholestasis due to citrin deficiency: diagnostic pitfalls. Acta Biochimica Polonica. 67(2). 225–228. 4 indexed citations
16.
Lipiński, Patryk, et al.. (2020). Progressive macrophage accumulation in lysosomal acid lipase deficiency. Molecular Genetics and Metabolism Reports. 23. 100594–100594. 7 indexed citations
17.
Lipiński, Patryk, Elżbieta Ciara, Dorota Jurkiewicz, et al.. (2020). Targeted Next-Generation Sequencing in Diagnostic Approach to Monogenic Cholestatic Liver Disorders—Single-Center Experience. Frontiers in Pediatrics. 8. 414–414. 14 indexed citations
18.
Jankowska, Irena, Piotr Czubkowski, Patryk Lipiński, et al.. (2020). Acute liver failure due to DGUOK deficiency–is liver transplantation justified?. Clinics and Research in Hepatology and Gastroenterology. 45(1). 101408–101408. 16 indexed citations
19.
Cielecka–Kuszyk, Joanna, Patryk Lipiński, Sylwia Szymańska, Hor Ismail, & Irena Jankowska. (2019). Long-term follow-up in children with progressive familial intrahepatic cholestasis type 2 after partial external biliary diversion with focus on histopathological features. Polish Journal of Pathology. 70(2). 79–83. 5 indexed citations
20.
Lipiński, Patryk, et al.. (2017). Newborn presentation of Niemann–Pick disease type C – Difficulties and limitations of diagnostic methods. Pediatrics & Neonatology. 59(3). 317–318. 3 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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