Magdalena Bartnik
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 15
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
- Chronic Lymphocytic Leukemia Research 2
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- Congenital heart defects research 5
- Advanced biosensing and bioanalysis techniques 2
- Co-authors
- Beata Nowakowska (9 shared papers)Ewa Bocian (5 shared papers)Ewa Obersztyn (8 shared papers)Katarzyna Derwińska (5 shared papers)Paweł Stankiewicz (5 shared papers)Tadeusz Mazurczak (4 shared papers)Barbara Wiśniowiecka‐Kowalnik (6 shared papers)Anna Gambin (4 shared papers)
- Journals
- Molecular Cytogenetics (3 papers)Clinical Genetics (3 papers)Journal of Assisted Reproduction and Genetics (1 paper)European Journal of Human Genetics (1 paper)Journal of Pediatric Hematology/Oncology (1 paper)
- Partner nations
- PolandUnited StatesUnited Kingdom
In The Last Decade
Magdalena Bartnik
22 papers receiving 262 citations
Peers
Comparison fields: 5 of 43
- Genetics 168
- Pediatrics, Perinatology and Child Health 56
- Genetics 22
- Molecular Biology 140
- Developmental Neuroscience 6
Countries citing papers authored by Magdalena Bartnik
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
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-authors
The 25 scholars most cited alongside Magdalena Bartnik, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 38 | |
| 2 | 2012 | 34 | |
| 3 | 2013 | 26 | |
| 4 | 2011 | 25 | |
| 5 | 2016 | 24 | |
| 6 | 2010 | 22 | |
| 7 | Assessment of the role of copy-number variants in 150 patients with congenital heart defects. | 2013 | 21 |
| 8 | The usefulness of array comparative genomic hybridization in clinical diagnostics of intellectual disability in children. | 2014 | 12 |
| 9 | 2016 | 11 | |
| 10 | 2012 | 9 | |
| 11 | 2018 | 8 | |
| 12 | 2022 | 7 | |
| 13 | 2018 | 7 | |
| 14 | 2016 | 5 | |
| 15 | Access to the treatment with opioid analgesics in Poland – on the basis of a Conference “ATOME: Polish National Symposium on Access to Opioid Medication” | 2015 | 3 |
| 16 | 2018 | 3 | |
| 17 | 2013 | 3 | |
| 18 | 2020 | 2 | |
| 19 | 2021 | 2 | |
| 20 | 2013 | 2 |
About Magdalena Bartnik
Magdalena Bartnik is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Genetics, having authored 23 papers that have together received 266 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital heart defects research (5 papers), Prenatal Screening and Diagnostics (4 papers), Genomics and Rare Diseases (4 papers), Advanced biosensing and bioanalysis techniques (2 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). The work is most often cited by research in Genetics (168 citations), Pediatrics, Perinatology and Child Health (56 citations), Genetics (22 citations), Molecular Biology (140 citations) and Developmental Neuroscience (6 citations). Magdalena Bartnik has collaborated with scholars based in Poland, United States and United Kingdom. Frequent co-authors include Beata Nowakowska, Ewa Bocian, Ewa Obersztyn, Katarzyna Derwińska, Paweł Stankiewicz, Tadeusz Mazurczak, Barbara Wiśniowiecka‐Kowalnik, Anna Gambin, Chad A. Shaw and Maciej Sykulski. Their work appears in journals such as Molecular Cytogenetics, Clinical Genetics, Journal of Assisted Reproduction and Genetics, European Journal of Human Genetics and Journal of Pediatric Hematology/Oncology.
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.