Anna Walczak

661 total citations
19 papers, 271 citations indexed

About

Anna Walczak is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Anna Walczak has authored 19 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Anna Walczak's work include RNA regulation and disease (5 papers), Hereditary Neurological Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Anna Walczak is often cited by papers focused on RNA regulation and disease (5 papers), Hereditary Neurological Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Anna Walczak collaborates with scholars based in Poland, Germany and United Kingdom. Anna Walczak's co-authors include Rafał Płoski, Małgorzata Rydzanicz, Piotr Stawiński, Joanna Kosińska, Agnieszka Pollak, Piotr Gasperowicz, Krystyna Szymańska, Hanna Mierzewska, Krzysztof Szczałuba and Victor Murcia Pienkowski and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Anna Walczak

18 papers receiving 270 citations

Peers

Countries citing papers authored by Anna Walczak

Since Specialization

Citations

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

Fields of papers citing papers by Anna Walczak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Walczak

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels 2025 ·Pediatria i Medycyna Rodzinna ·(unknown), (unknown), Edyta Heropolitańska–Pliszka, Cezary Kowaléwski, (unknown), Anna Walczak, Rafał Płoski, Katarzyna Woźniak	0
2	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
3	Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosis 2022 ·American Journal of Medical Genetics Part A ·Małgorzata Rydzanicz, Wojciech Glinkowski, Anna Walczak, (unknown), Grażyna Kostrzewa, Piotr Gasperowicz, Agnieszka Pollak, Piotr Stawiński, Rafał Płoski	3
4	Brain Tissue Low-Level Mosaicism for MTOR Mutation Causes Smith–Kingsmore Phenotype with Recurrent Hypoglycemia—A Novel Phenotype and a Further Proof for Testing of an Affected Tissue 2021 ·Diagnostics ·Krzysztof Szczałuba, Małgorzata Rydzanicz, Anna Walczak, Joanna Kosińska, (unknown), (unknown), Katarzyna Iwanicka‐Pronicka, Wiesława Grajkowska, Elżbieta Jurkiewicz, Paweł Kowalczyk, Rafał Płoski	3
5	Efficacy and safety of sirolimus therapy in familial hypoinsulinemic hypoglycemia caused by AKT2 mutation inherited from the mosaic father 2021 ·European Journal of Medical Genetics ·(unknown), (unknown), Beata Pyrżak, (unknown), Robert Śmigiel, Anna Walczak, Małgorzata Rydzanicz, Rafał Płoski, Krzysztof Szczałuba	2
6	CLOVES syndrome caused by mosaic mutation in the PIK3CA gene identified in fibroblasts 2021 ·SHILAP Revista de lepidopterología ·(unknown), Małgorzata Rydzanicz, Joanna Kosińska, (unknown), Anna Walczak, Elżbieta Szmida, Anna Rozensztrauch, Rafał Płoski, Robert Śmigiel	1
7	A recurrent de novo variant supports KCNC2 involvement in the pathogenesis of developmental and epileptic encephalopathy 2021 ·American Journal of Medical Genetics Part A ·Małgorzata Rydzanicz, (unknown), Piotr Gasperowicz, Agnieszka Pollak, Grażyna Kostrzewa, Anna Walczak, Magdalena Konarzewska, Rafał Płoski	14
8	Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome 2018 ·Journal of Human Genetics ·Robert Śmigiel, (unknown), (unknown), Victor Murcia Pienkowski, Elżbieta Szmida, Piotr Gasperowicz, Joanna Kosińska, Grażyna Kostrzewa, (unknown), Anna Walczak, (unknown), Małgorzata Rydzanicz, Maria Sąsiadek, Rafał Płoski	15
9	Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines 2018 ·Clinical Genetics ·Krzysztof Szczałuba, (unknown), (unknown), Małgorzata Rydzanicz, Krystyna Szymańska, Wojciech Feleszko, Paweł Włodarski, (unknown), Victor Murcia Pienkowski, Anna Walczak, (unknown), (unknown), (unknown), Piotr Stawiński, Dominika Nowis, Magdalena Dziembowska, Rafał Płoski	12
10	Developmental epileptic encephalopathy with hypomyelination and brain atrophy associated with PTPN23 variants affecting the assembly of UsnRNPs 2018 ·European Journal of Human Genetics ·Robert Śmigiel, (unknown), (unknown), Małgorzata Rydzanicz, Agnieszka Pollak, Anna Walczak, (unknown), Piotr Stawiński, Hanna Mierzewska, Maria Sąsiadek, Oliver J. Gruß, Rafał Płoski	8
11	Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation 2018 ·Clinical Genetics ·Jacek Pilch, (unknown), Anna Walczak, Victor Murcia Pienkowski, (unknown), (unknown), (unknown), Piotr Gasperowicz, Joanna Kosińska, Małgorzata Rydzanicz, Ewa Emich‐Widera, Rafał Płoski	23
12	Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia 2018 ·Human Molecular Genetics ·Robert Śmigiel, Diane L. Sherman, Małgorzata Rydzanicz, Anna Walczak, (unknown), Barbara Królak‐Olejnik, Joanna Kosińska, Piotr Gasperowicz, (unknown), Piotr Stawiński, (unknown), (unknown), (unknown), Paweł Krajewski, Maria Sąsiadek, Peter Brophy, Rafał Płoski	21
13	Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) – A Polish family with novel SACS mutations 2017 ·Neurologia i Neurochirurgia Polska ·(unknown), (unknown), Michał Schinwelski, Małgorzata Rydzanicz, Anna Walczak, (unknown), Rafał Płoski, Jarosław Sławek	12
14	SETD5 loss‐of‐function mutation as a likely cause of a familial syndromic intellectual disability with variable phenotypic expression 2016 ·American Journal of Medical Genetics Part A ·Krzysztof Szczałuba, (unknown), (unknown), Małgorzata Rydzanicz, Anna Walczak, Piotr Stawiński, Bożena Werner, Rafał Płoski	26
15	Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease 2016 ·The American Journal of Human Genetics ·Guy M. Lenk, Krystyna Szymańska, Grażyna Dębska–Vielhaber, Małgorzata Rydzanicz, Anna Walczak, Monika Bekiesińska‐Figatowska, Stefan Vielhaber, Kerstin Hallmann, Piotr Stawiński, (unknown), David Hsu, Wolfram S. Kunz, Miriam H. Meisler, Rafał Płoski	41
16	KIF5A de novo mutation associated with myoclonic seizures and neonatal onset progressive leukoencephalopathy 2016 ·Clinical Genetics ·Małgorzata Rydzanicz, Mateusz Jagła, Joanna Kosińska, (unknown), Adam Sobczak, Agnieszka Pollak, Izabela Herman‐Sucharska, Anna Walczak, Przemko Kwinta, Rafał Płoski	27
17	Spondyloepimetaphyseal dysplasia with neurodegeneration associated with AIFM1 mutation – a novel phenotype of the mitochondrial disease 2016 ·Clinical Genetics ·Hanna Mierzewska, Małgorzata Rydzanicz, Tadeusz Biegański, Joanna Kosińska, Magdalena Mierzewska-Schmidt, Agnieszka Ługowska, Agnieszka Pollak, Piotr Stawiński, Anna Walczak, (unknown), Ewa Obersztyn, Elżbieta Szczepanik, Rafał Płoski	38
18	Inverse Association between Obesity Predisposing FTO Genotype and Completed Suicide 2014 ·PLoS ONE ·Izabela Chojnicka, Sylwia Fudalej, Anna Walczak, (unknown), (unknown), Piotr Stawiński, (unknown), (unknown), Marcin Wojnar, Paweł Krajewski, Rafał Płoski	8
19	Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot–Marie–Tooth disease 2014 ·Journal of the Peripheral Nervous System ·Anna Kostera‐Pruszczyk, Joanna Kosińska, Agnieszka Pollak, Piotr Stawiński, Anna Walczak, (unknown), Anna Potulska‐Chromik, Piotr Szczudlik, Anna Kamińska, Rafał Płoski	12

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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