Aleksandra Jezela‐Stanek

1.6k total citations
79 papers, 653 citations indexed

About

Aleksandra Jezela‐Stanek is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Aleksandra Jezela‐Stanek has authored 79 papers receiving a total of 653 indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 27 papers in Genetics and 14 papers in Physiology. Recurrent topics in Aleksandra Jezela‐Stanek's work include Lysosomal Storage Disorders Research (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Aleksandra Jezela‐Stanek is often cited by papers focused on Lysosomal Storage Disorders Research (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetics and Neurodevelopmental Disorders (11 papers). Aleksandra Jezela‐Stanek collaborates with scholars based in Poland, United Kingdom and United States. Aleksandra Jezela‐Stanek's co-authors include Elżbieta Ciara, Małgorzata Krajewska‐Walasek, Anna Tylki‐Szymańska, Justyna Paprocka, Stephanie Grünewald, Joanna Chorostowska‐Wynimko, Karolina M. Stępień, Dariusz Rokicki, Krystyńa Chrzańowska and Urszula Lechowicz and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Nutrients.

In The Last Decade

Aleksandra Jezela‐Stanek

73 papers receiving 632 citations

Peers

Countries citing papers authored by Aleksandra Jezela‐Stanek

Since Specialization

Citations

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

Fields of papers citing papers by Aleksandra Jezela‐Stanek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aleksandra Jezela‐Stanek. 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 Aleksandra Jezela‐Stanek. The network helps show where Aleksandra Jezela‐Stanek may publish in the future.

Co-authorship network of co-authors of Aleksandra Jezela‐Stanek

This figure shows the co-authorship network connecting the top 25 collaborators of Aleksandra Jezela‐Stanek. A scholar is included among the top collaborators of Aleksandra Jezela‐Stanek 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 Aleksandra Jezela‐Stanek. Aleksandra Jezela‐Stanek 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

#	Work	Indexed citations
1	Efficacy and Safety of Ketogenic Diet Treatment in Pediatric Patients with Mitochondrial Disease 2024 ·Nutrients ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Dorota Piekutowska‐Abramczuk, (unknown), Elżbieta Ciara, Maciej Jaworski, Aleksandra Jezela‐Stanek, Dariusz Rokicki	2
2	Computational Tools to Assist in Analyzing Effects of the SERPINA1 Gene Variation on Alpha-1 Antitrypsin (AAT) 2024 ·Genes ·(unknown), (unknown), Karolina Mitusińska, Joanna Chorostowska‐Wynimko, Aleksandra Jezela‐Stanek	0
3	Clinical heterogeneity of polish patients with KAT6B–related disorder 2023 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), (unknown), Aleksandra Jezela‐Stanek, Krzysztof Szczałuba, (unknown), (unknown), (unknown), Dorota Jurkiewicz, Piotr Stawiński, Agnieszka Zubkiewicz‐Kucharska, Małgorzata Rydzanicz, Rafał Płoski, Robert Śmigiel	1
4	Biochemical, Genetic and Clinical Diagnostic Approaches to Autism-Associated Inherited Metabolic Disorders 2023 ·Genes ·(unknown), (unknown), Aleksandra Jezela‐Stanek, Elżbieta Ciara, Richard E. Frye, (unknown), Karolina M. Stępień	9
5	The Epidermal Transcriptome Analysis of a Novel c.639_642dup LORICRIN Variant-Delineation of the Loricrin Keratoderma Pathology 2023 ·International Journal of Molecular Sciences ·Katarzyna Wertheim‐Tysarowska, (unknown), Bartłomiej Gielniewski, Bartosz Wojtaś, Alicja Szabelska‐Beręsewicz, (unknown), Adriana Mika, Andrzej Tysarowski, (unknown), Agnieszka Magdalena Rygiel, (unknown), Katarzyna Woźniak, Cezary Kowaléwski, Jolanta Wierzba, Aleksandra Jezela‐Stanek	1
6	Expanding the Knowledge of KIF1A-Dependent Disorders to a Group of Polish Patients 2023 ·Genes ·Justyna Paprocka, Aleksandra Jezela‐Stanek, Robert Śmigiel, Anna Walczak, Hanna Mierzewska, Anna Kutkowska‐Kaźmierczak, Rafał Płoski, Ewa Emich‐Widera, Barbara Steinborn	5
7	Characteristics of Neuroimaging and Behavioural Phenotype in Polish Patients with PIGV-CDG—An Observational Study and Literature Review 2023 ·Genes ·(unknown), Patryk Lipiński, Aleksandra Jezela‐Stanek	1
8	Spectrum of Neurological Symptoms in Glycosylphosphatidylinositol Biosynthesis Defects: Systematic Review 2022 ·Frontiers in Neurology ·Justyna Paprocka, (unknown), (unknown), (unknown), (unknown), Krzysztof Szczałuba, Agnieszka Stembalska, Aleksandra Jezela‐Stanek, Robert Śmigiel	9
9	The fibroblast growth factor 21 concentration in children with mitochondrial disease does not depend on the disease stage, but rather on the disease genotype 2022 ·Pediatric Endocrinology Diabetes and Metabolism ·(unknown), Dariusz Rokicki, (unknown), (unknown), (unknown), Dorota Piekutowska‐Abramczuk, (unknown), Elżbieta Ciara, Maciej Jaworski, Aleksandra Jezela‐Stanek	0
10	Case report: Rare among ultrarare—Clinical odyssey of a new patient with Ogden syndrome 2022 ·Frontiers in Genetics ·(unknown), (unknown), Karolina Chwiałkowska, (unknown), (unknown), (unknown), Urszula Lechowicz, (unknown), Paweł Gajdanowicz, Mirosław Kwaśniewski, Małgorzata Krajewska‐Walasek, Justyna Paprocka, Aleksandra Jezela‐Stanek	5
11	Perinatal manifestations of congenital disorders of glycosylation—A clue to early diagnosis 2022 ·Frontiers in Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), Aleksandra Jezela‐Stanek	2
12	The First Metabolome Analysis in Children with Epilepsy and ALG13-CDG Resulting from c.320A>G Variant 2021 ·Children ·Justyna Paprocka, Aleksandra Jezela‐Stanek, (unknown), Maria Sokół, Patryk Lipiński, Ewa Jamroz, Ewa Emich‐Widera, Anna Tylki‐Szymańska	7
13	Diaphragmatic Hernia as a Prenatal Feature of Glycosylphosphatidylinositol Biosynthesis Defects and the Overlap With Fryns Syndrome – Literature Review 2021 ·Frontiers in Genetics ·Przemysław Kosiński, (unknown), Aleksandra Jezela‐Stanek	3
14	Alpha-1 Antitrypsin Z Variant (AAT PIZ) as a Risk Factor for Intrahepatic Cholestasis of Pregnancy 2021 ·Frontiers in Genetics* ·Przemysław Kosiński, (unknown), Adrianna Mostowska, Paweł Gutaj, Michał Lipa, Ewa Wender-Ożegowska, (unknown), Joanna Chorostowska‐Wynimko, Mirosław Wielgoś, Aleksandra Jezela‐Stanek	2
15	Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants 2019 ·Journal of Neurology ·Francesco Nicita, Fabrizia Stregapede, Alessandra Tessa, Maria Teresa Bassi, Aleksandra Jezela‐Stanek, Guido Primiano, Antonio Pizzuti, Melissa Barghigiani, (unknown), Ginevra Zanni, Serenella Servidei, Guja Astrea, Elena Panzeri, Cristina Maghini, Luciana Losito, Rafał Płoski, Piotr Gasperowicz, Filippo M. Santorelli, Enrico Bertini, Lorena Travaglini	13
16	Novel data on growth phenotype and causative genotypes in 29 patients with Morquio (Morquio-Brailsford) syndrome from Central-Eastern Europe 2019 ·Journal of Applied Genetics ·Aleksandra Jezela‐Stanek, Agnieszka Różdżyńska‐Świątkowska, (unknown), Elżbieta Ciara, (unknown), Anna Tylki‐Szymańska	8
17	Mild phenotype of glutaric aciduria type 1 in polish patients – novel data from a group of 13 cases 2018 ·Metabolic Brain Disease ·(unknown), Aleksandra Jezela‐Stanek, Agnieszka Różdżyńska‐Świątkowska, Elżbieta Jurkiewicz, (unknown), Edyta Szymańska, Dariusz Rokicki, Elżbieta Ciara, Małgorzata Rydzanicz, Piotr Stawiński, Rafał Płoski, Anna Tylki‐Szymańska	7
18	Is diagnosing cardio-facio-cutaneous (CFC) syndrome still a challenge? Delineation of the phenotype in 15 Polish patients with proven mutations, including novel mutations in the BRAF gene 2014 ·European Journal of Medical Genetics ·Elżbieta Ciara, (unknown), Dorota Jurkiewicz, (unknown), Dorota Gieruszczak‐Białek, Agata Skórka, Renata Posmyk, (unknown), (unknown), Krystyńa Chrzańowska, Aleksandra Jezela‐Stanek, Małgorzata Krajewska‐Walasek	10
19	1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay—Additional case and data's review 2012 ·American Journal of Medical Genetics Part A ·Aleksandra Jezela‐Stanek, (unknown), (unknown), (unknown), Małgorzata Krajewska‐Walasek	5
20	Genetic causes of syndromic craniosynostoses 2012 ·European Journal of Paediatric Neurology ·Aleksandra Jezela‐Stanek, Małgorzata Krajewska‐Walasek	15

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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