Joanna Kosińska

1.8k citations

54 papers · 891 indexed · h-index 19

Co-authors: Rafał Płoski Małgorzata Rydzanicz Agnieszka Pollak Piotr Stawiński Ewa Pronicka Dorota Piekutowska‐Abramczuk Anna Walczak Elżbieta Jurkiewicz
Topics: Genetics and Neurodevelopmental Disorders (9 papers)Mitochondrial Function and Pathology (8 papers)Genomics and Rare Diseases (6 papers)
Cited by: Clinical Biochemistry Molecular Biology Genetics
Journals: SHILAP Revista de lepidopterologíaPLoS ONE Scientific Reports
Partner nations: Poland United Kingdom Germany

In The Last Decade

Joanna Kosińska

54 papers receiving 886 citations

Peers

Countries citing papers authored by Joanna Kosińska

Since Specialization

Citations

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

Fields of papers citing papers by Joanna Kosińska

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joanna Kosińska

This figure shows the co-authorship network connecting the top 25 collaborators of Joanna Kosińska. A scholar is included among the top collaborators of Joanna Kosińska 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 Joanna Kosińska. Joanna Kosińska 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	Destabilization of mutated human PUS3 protein causes intellectual disability 2022 ·Human Mutation ·Ting‐Yu Lin,Robert Śmigiel,Bożena Kuźniewska,(unknown),Joanna Kosińska,(unknown),Anna Biela,(unknown),(unknown),Izabela Łaczmańska,(unknown),(unknown),(unknown),Monika Goś,Sylwia Rzońca,Magdalena Dziembowska,Rafał Płoski,Sebastian Glatt	20
2	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
3	Case Report: Lennox–Gastaut Epileptic Encephalopathy Responsive to Cannabidiol Treatment Associated With a Novel de novo Mosaic SHANK1 Variant 2021 ·Frontiers in Genetics ·Justyna Paprocka,Szymon Ziętkiewicz,Joanna Kosińska,(unknown),Rafał Płoski	1
4	The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (p.Gln1981) 2020 ·PubMed* ·(unknown),Anna Kutkowska‐Kaźmierczak,Paweł Gawliński,Wojciech Wiszniewski,Monika Goś,Piotr Stawiński,Małgorzata Rydzanicz,Joanna Kosińska,(unknown),(unknown),Magdalena Bartnik,(unknown),Krzysztof Szczałuba,Monika Bekiesińska‐Figatowska,Rafał Płoski,Jerzy Bal,Sylwia Rzońca	2
5	AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant 2020 ·Journal of Applied Genetics ·Krzysztof Szczałuba,Hanna Mierzewska,Robert Śmigiel,Joanna Kosińska,(unknown),(unknown),Piotr Stawiński,Agnieszka Pollak,Małgorzata Rydzanicz,Rafał Płoski	7
6	Single median maxillary central incisor syndrome and variant in SMO gene associated with SHH pathway 2020 ·International Journal of Pediatric Otorhinolaryngology ·Tomasz Zatoński,(unknown),(unknown),(unknown),(unknown),Małgorzata Rydzanicz,Anna Rozensztrauch,Joanna Kosińska,Karolina Dorobisz,Rafał Płoski,Robert Śmigiel	2
7	Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes 2020 ·Neurological Sciences ·Marcin M. Machnicki,Valeria Guglielmi,(unknown),Francesca Gualandi,Lorenzo Verriello,(unknown),Joanna Kosińska,Antonella Sangalli,Małgorzata Rydzanicz,Maria Grazia Romanelli,Marcella Neri,Rafał Płoski,Paola Tonin,Giuliano Tomelleri,Tomasz Stokłosa,Gaetano Vattemi	2
8	Syndromic chorioretinal coloboma associated with heterozygous de novo RARA mutation affecting an amino acid critical for retinoic acid interaction 2019 ·Clinical Genetics ·(unknown),Victor Murcia Pienkowski,Szymon Ziętkiewicz,Małgorzata Rydzanicz,Joanna Kosińska,Piotr Stawiński,(unknown),Rafał Płoski	7
9	Transcriptome-derived investigation of biosynthesis of quinolizidine alkaloids in narrow-leafed lupin (Lupinus angustifolius L.) highlights candidate genes linked to iucundus locus 2019 ·Scientific Reports ·Magdalena Kroc,Grzegorz Koczyk,(unknown),(unknown),(unknown),Paweł Krajewski,Joanna Kosińska,Jan Podkowiński,(unknown),W. Święcicki	33
10	A Novel Monoallelic Nonsense Mutation in the NFKB2 Gene Does Not Cause a Clinical Manifestation 2019 ·Frontiers in Genetics ·Jerzy Kotlinowski,Karolina Bukowska-Straková,(unknown),Joanna Kosińska,(unknown),Piotr Stawiński,Mateusz Wilamowski,Witold Nowak,Alicja Józkowicz,Jarosław Baran,Rafał Płoski,Jolanta Jura	8
11	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
12	Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15 2018 ·European Journal of Medical Genetics ·Karolina Pesz,Victor Murcia Pienkowski,Agnieszka Pollak,Piotr Gasperowicz,Maciej Sykulski,Joanna Kosińska,(unknown),(unknown),Magdalena Bartnik,Beata Nowakowska,Małgorzata Rydzanicz,Maria Sąsiadek,Rafał Płoski	3
13	Novel GNB1 de novo mutation in a patient with neurodevelopmental disorder and cutaneous mastocytosis: Clinical report and literature review 2017 ·European Journal of Medical Genetics ·Krzysztof Szczałuba,(unknown),Krystyna Szymańska,Piotr Gasperowicz,Joanna Kosińska,Małgorzata Rydzanicz,Rafał Płoski	21
14	Isolated Hearing Impairment Caused by SPATA5 Mutations in a Family with Variable Phenotypic Expression 2017 ·Advances in experimental medicine and biology ·Krzysztof Szczałuba,Krystyna Szymańska,Joanna Kosińska,Agnieszka Pollak,Victor Murcia Pienkowski,(unknown),Piotr Stawiński,Małgorzata Rydzanicz,Urszula Demkow,Rafał Płoski	8
15	Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy 2016 ·American Journal of Medical Genetics Part A ·Rafał Płoski,Małgorzata Rydzanicz,(unknown),Maria Franaszczyk,Agnieszka Pollak,Joanna Kosińska,Ewa Michalak,Piotr Stawiński,Lidia Ziółkowska,Zofia T. Bilińska,Bożena Werner	42
16	Further evidence for GRIN2B mutation as the cause of severe epileptic encephalopathy 2016 ·American Journal of Medical Genetics Part A ·Robert Śmigiel,Grażyna Kostrzewa,Joanna Kosińska,Agnieszka Pollak,Piotr Stawiński,Elżbieta Szmida,(unknown),Krystyna Szymańska,Paweł Karpiński,Maria Sąsiadek,Rafał Płoski	22
17	New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre 2016 ·Journal of Translational Medicine ·Ewa Pronicka,Dorota Piekutowska‐Abramczuk,Elżbieta Ciara,Joanna Trubicka,Dariusz Rokicki,Agnieszka Karkucińska‐Więckowska,Magdalena Pajdowska,Elżbieta Jurkiewicz,Paulina Halat,Joanna Kosińska,Agnieszka Pollak,Małgorzata Rydzanicz,Piotr Stawiński,Maciej Pronicki,Małgorzata Krajewska‐Walasek,Rafał Płoski	159
18	Sensitivity of Next-Generation Sequencing Metagenomic Analysis for Detection of RNA and DNA Viruses in Cerebrospinal Fluid: The Confounding Effect of Background Contamination 2016 ·Advances in experimental medicine and biology ·Iwona Bukowska‐Ośko,Karol Perlejewski,Shota Nakamura,Daisuke Motooka,Tomasz Stokowy,Joanna Kosińska,Marta Popiel,Rafał Płoski,Andrzej Horban,(unknown),Kamila Caraballo Cortés,Agnieszka Pawełczyk,Urszula Demkow,Adam Stępień,Marek Radkowski,Tomasz Laskus	49
19	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
20	DIS3 shapes the RNA polymerase II transcriptome in humans by degrading a variety of unwanted transcripts 2015 ·Genome Research ·Teresa Szczepińska,(unknown),Rafał Tomecki,Anna Łabno,Lukasz S. Borowski,Tomasz M. Kuliński,Dorota Adamska,Joanna Kosińska,Andrzej Dziembowski	68

About Joanna Kosińska

Joanna Kosińska is a scholar working on Genetics, Molecular Biology and Cell Biology, having authored 54 papers that have together received 891 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Genomics and Rare Diseases (6 papers). The work is most often cited by research in Clinical Biochemistry (117 citations), Molecular Biology (544 citations) and Genetics (188 citations). Joanna Kosińska has collaborated with scholars based in Poland, United Kingdom and Germany. Frequent co-authors include Rafał Płoski, Małgorzata Rydzanicz, Agnieszka Pollak, Piotr Stawiński, Ewa Pronicka, Dorota Piekutowska‐Abramczuk, Anna Walczak, Elżbieta Jurkiewicz, Dariusz Rokicki and Maciej Pronicki. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

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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