Magdalena Bartnik

1.3k total citations
23 papers, 266 citations indexed

About

Magdalena Bartnik is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Magdalena Bartnik has authored 23 papers receiving a total of 266 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Magdalena Bartnik's work include Genomic variations and chromosomal abnormalities (15 papers), Congenital heart defects research (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Magdalena Bartnik is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Congenital heart defects research (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Magdalena Bartnik collaborates with scholars based in Poland, United States and United Kingdom. Magdalena Bartnik's co-authors include Ewa Bocian, Beata Nowakowska, Ewa Obersztyn, Katarzyna Derwińska, Paweł Stankiewicz, Tadeusz Mazurczak, Barbara Wiśniowiecka‐Kowalnik, J.R. Lupski, Tomasz Gambin and Maciej Sykulski and has published in prestigious journals such as Genetics in Medicine, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Magdalena Bartnik

22 papers receiving 262 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Magdalena Bartnik Poland 10 168 140 56 37 22 23 266
Sandesh C. Sreenath Nagamani United States 6 218 1.3× 194 1.4× 70 1.3× 18 0.5× 17 0.8× 8 349
Molly B. Sheridan United States 8 137 0.8× 118 0.8× 30 0.5× 34 0.9× 17 0.8× 11 281
Nathalie Marle France 11 237 1.4× 170 1.2× 56 1.0× 42 1.1× 19 0.9× 23 373
Eve Õiglane‐Shlik Estonia 10 185 1.1× 177 1.3× 76 1.4× 16 0.4× 13 0.6× 17 320
Mariana Moysés‐Oliveira Brazil 11 206 1.2× 130 0.9× 53 0.9× 35 0.9× 8 0.4× 45 300
Riina Žordania Estonia 12 140 0.8× 182 1.3× 66 1.2× 19 0.5× 11 0.5× 25 350
Heather C Mefford United States 7 220 1.3× 161 1.1× 37 0.7× 29 0.8× 38 1.7× 10 295
Fernando Santos Spain 9 228 1.4× 193 1.4× 84 1.5× 21 0.6× 13 0.6× 13 325
Lucia Perone Italy 12 217 1.3× 198 1.4× 86 1.5× 35 0.9× 19 0.9× 21 361
Claudia Soler‐Alfonso United States 12 135 0.8× 197 1.4× 33 0.6× 15 0.4× 31 1.4× 21 333

Countries citing papers authored by Magdalena Bartnik

Since Specialization
Citations

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

Fields of papers citing papers by Magdalena Bartnik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Magdalena Bartnik

This figure shows the co-authorship network connecting the top 25 collaborators of Magdalena Bartnik. A scholar is included among the top collaborators of Magdalena Bartnik 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 Magdalena Bartnik. Magdalena Bartnik 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.
Woroniecka, Renata, Grzegorz Rymkiewicz, Barbara Pieńkowska‐Grela, et al.. (2023). Cytogenomic features of Richter transformation. Molecular Cytogenetics. 16(1). 31–31. 1 indexed citations
2.
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
3.
Deperas-Kamińska, Marta, Ewa Obersztyn, Nathalie Brison, et al.. (2021). A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC). Molecular Cytogenetics. 14(1). 18–18. 2 indexed citations
4.
Wielgoś, Mirosław, Przemysław Kosiński, Małgorzata Krajewska‐Walasek, et al.. (2021). How does terminal 21q22 deletion really manifest? Delineation based on prenatal diagnosis and literature review. Taiwanese Journal of Obstetrics and Gynecology. 60(6). 1121–1125.
5.
Kutkowska‐Kaźmierczak, Anna, Paweł Gawliński, Wojciech Wiszniewski, et al.. (2020). The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (p.Gln1981*). PubMed. 24(3). 32–36. 2 indexed citations
6.
Pesz, Karolina, Victor Murcia Pienkowski, Agnieszka Pollak, et al.. (2018). Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15. European Journal of Medical Genetics. 61(10). 596–601. 3 indexed citations
7.
8.
Ociepa, Tomasz, et al.. (2018). Prevalence and Risk Factors for Arterial Hypertension Development in Childhood Acute Lymphoblastic Leukemia Survivors. Journal of Pediatric Hematology/Oncology. 41(3). 175–180. 8 indexed citations
9.
10.
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
11.
Smyk, Marta, et al.. (2016). Novel 14q11.2 microduplication including the CHD8 and SUPT16H genes associated with developmental delay. American Journal of Medical Genetics Part A. 170(5). 1325–1329. 11 indexed citations
12.
Leppert, Wojciech, et al.. (2015). Access to the treatment with opioid analgesics in Poland – on the basis of a Conference “ATOME: Polish National Symposium on Access to Opioid Medication”. 7(1). 84–89. 3 indexed citations
13.
Bartnik, Magdalena, Beata Nowakowska, Katarzyna Derwińska, et al.. (2013). Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability. Journal of Applied Genetics. 55(1). 125–144. 26 indexed citations
14.
Sykulski, Maciej, Tomasz Gambin, Magdalena Bartnik, et al.. (2013). Multiple samples aCGH analysis for rare CNVs detection. PubMed. 3(1). 12–12. 3 indexed citations
15.
Derwińska, Katarzyna, Magdalena Bartnik, Barbara Wiśniowiecka‐Kowalnik, et al.. (2013). Assessment of the role of copy-number variants in 150 patients with congenital heart defects.. PubMed. 16(3). 175–82. 21 indexed citations
16.
Bilir, Bülent, Zühal Yapıcı, Cengiz Yalçınkaya, et al.. (2012). High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus–Merzbacher disease. Clinical Genetics. 83(1). 66–72. 9 indexed citations
17.
Wiśniowiecka‐Kowalnik, Barbara, Magdalena Bartnik, Katarzyna Derwińska, et al.. (2012). Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders. European Journal of Human Genetics. 21(6). 620–625. 34 indexed citations
18.
Bartnik, Magdalena, Katarzyna Derwińska, Monika Goś, et al.. (2011). Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females. Genetics in Medicine. 13(5). 447–452. 38 indexed citations
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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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