Beata Nowakowska

3.9k total citations
87 papers, 1.5k citations indexed

About

Beata Nowakowska is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Beata Nowakowska has authored 87 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Genetics, 27 papers in Molecular Biology and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Beata Nowakowska's work include Genomic variations and chromosomal abnormalities (38 papers), Prenatal Screening and Diagnostics (16 papers) and Congenital heart defects research (14 papers). Beata Nowakowska is often cited by papers focused on Genomic variations and chromosomal abnormalities (38 papers), Prenatal Screening and Diagnostics (16 papers) and Congenital heart defects research (14 papers). Beata Nowakowska collaborates with scholars based in Poland, United States and Belgium. Beata Nowakowska's co-authors include Barbara Wiśniowiecka‐Kowalnik, Joris Vermeesch, Ewa Obersztyn, Ewa Bocian, Paweł Stankiewicz, Sau Wai Cheung, Maria Boratyńska, Katarzyna Kościelska−Kasprzak, Mirosław Banasik and Marian Klinger and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Beata Nowakowska

80 papers receiving 1.4k citations

Peers

Beata Nowakowska

GENET

SURGE

PPCH

TRANS

Arabella Smith Australia

Güven Lüleci Türkiye

Francesca Faravelli Italy

Dusica Babovic‐Vuksanovic United States

L Perroni Italy

Kerry K. Brown United States

JW Lee South Korea

Abdelaziz Sefiani Morocco

Jacques C. Giltay Netherlands

Pieter van der Vlies Netherlands

Arabella Smith Australia

Beata Nowakowska

1.2k ×1.6

GENET

605 ×1.1

182 ×0.8

SURGE

591 ×2.7

PPCH

47 ×0.2

TRANS

Citations per year, relative to Beata Nowakowska Beata Nowakowska (= 1×) peers Arabella Smith

Countries citing papers authored by Beata Nowakowska

Since Specialization

Citations

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

Fields of papers citing papers by Beata Nowakowska

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beata Nowakowska

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

Grygalewicz, Beata, Lukasz M. Szafron, Renata Woroniecka, et al.. (2025). Cytogenomic and Clinicopathologic Comparison of MYC-Positive and MYC-Negative High-Grade B-Cell Lymphoma With 11q Aberration in the Context of Other Aggressive Lymphomas With MYC Rearrangement. Modern Pathology. 38(8). 100774–100774. 1 indexed citations

Blagowidow, Natalie, Beata Nowakowska, Erica Schindewolf, et al.. (2023). Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14(1). 160–160. 15 indexed citations

Geremek, Maciej, Tomasz Roszkowski, Michał Ciebiera, et al.. (2022). Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience. Genes. 13(5). 724–724. 12 indexed citations

Smyk, Marta, Magdalena Bartnik, Barbara Wiśniowiecka‐Kowalnik, et al.. (2022). Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss. Journal of Assisted Reproduction and Genetics. 39(2). 357–367. 7 indexed citations

Nowakowska, Beata, et al.. (2022). Prenatal diagnosis of acrania/exencephaly/anencephaly sequence (AEAS): additional structural and genetic anomalies. Archives of Gynecology and Obstetrics. 307(1). 293–299. 8 indexed citations

Nowakowska, Beata, et al.. (2021). Genetic Background of Fetal Growth Restriction. International Journal of Molecular Sciences. 23(1). 36–36. 29 indexed citations

Roszkowski, Tomasz, et al.. (2021). Prenatal diagnosis of glutaric acidemia type 2 with the use of exome sequencing — an up-to-date review and new case report. Ginekologia Polska. 92(1). 51–56.

Geremek, Maciej, et al.. (2019). Null variants in AGRN cause lethal fetal akinesia deformation sequence. Clinical Genetics. 97(4). 634–638. 3 indexed citations

Unolt, Marta, Molka Kammoun, Beata Nowakowska, et al.. (2019). Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition. Genetics in Medicine. 22(2). 326–335. 7 indexed citations

10.

Wiśniowiecka‐Kowalnik, Barbara & Beata Nowakowska. (2019). Genetics and epigenetics of autism spectrum disorder—current evidence in the field. Journal of Applied Genetics. 60(1). 37–47. 141 indexed citations

11.

Reich, Adam, Mariusz Gajda, Dmitry Nevozhay, et al.. (2016). Opioid Receptors in Psoriatic Skin: Relationship with Itch. Acta Dermato Venereologica. 97(5). 564–570. 33 indexed citations

12.

Grygalewicz, Beata, Renata Woroniecka, Iwona K. Rzepecka, et al.. (2016). Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8x60K). Molecular Cytogenetics. 9(1). 1–1. 24 indexed citations

13.

Gawliński, Paweł, Renata Posmyk, Tomasz Gambin, et al.. (2016). PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset Encephalopathies. Pediatric Neurology. 60. 83–87. 15 indexed citations

14.

Szymańska, Krystyna, Krzysztof Szczałuba, Agnieszka Ługowska, et al.. (2014). The Analysis of Genetic Aberrations in Children with Inherited Neurometabolic and Neurodevelopmental Disorders. BioMed Research International. 2014. 1–8. 10 indexed citations

15.

Banasik, Mirosław, Maria Boratyńska, Katarzyna Kościelska−Kasprzak, et al.. (2013). The Impact of De Novo Donor-specific Anti-Human Leukocyte Antigen Antibodies on 5-Year Renal Transplant Outcome. Transplantation Proceedings. 45(4). 1449–1452. 29 indexed citations

16.

Robberecht, Caroline, Thierry Voet, Masoud Zamani Esteki, Beata Nowakowska, & Joris Vermeesch. (2012). Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations. Genome Research. 23(3). 411–418. 92 indexed citations

17.

Tsai, Anne Chun-Hui, Beata Nowakowska, Amber N. Pursley, et al.. (2010). Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein–Taybi syndrome detected by aCGH. European Journal of Human Genetics. 19(1). 43–49. 38 indexed citations

18.

Nowakowska, Beata, et al.. (2008). "Nowe połączenia wyrazowe we współczesnej polszczyźnie", Beata Nowakowska, Kraków 2005 : [recenzja] / MNB.. 20. 2 indexed citations

19.

Smyk, Marta, Ewa Obersztyn, Beata Nowakowska, et al.. (2007). Different‐sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(6). 799–806. 47 indexed citations

20.

Smyk, Marta, Ewa Obersztyn, Beata Nowakowska, et al.. (2007). Recurrent SOX9 deletion campomelic dysplasia due to somatic mosaicism in the father. American Journal of Medical Genetics Part A. 143A(8). 866–870. 25 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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