Anna Abramowicz

1.0k citations
8 papers · 636 indexed · 1 hit paper · h-index 6

Impact in

    • RNA modifications and cancer
    • Protein Tyrosine Phosphatases
    • RNA Research and Splicing
    • RNA and protein synthesis mechanisms
    • RNA regulation and disease
    • Genomics and Rare Diseases

Papers in

    • Protein Tyrosine Phosphatases 4
    • RNA modifications and cancer 3
    • RNA Research and Splicing 1
    • Chromatin Remodeling and Cancer 1
    • Connective tissue disorders research 2
    • Dermatological and Skeletal Disorders 1

Anna Abramowicz

8 papers receiving 632 citations

Hit Papers

Splicing mutations in human genetic disorders: examples, detection, and confirmation 2018 · 403 citations
4030+2+5Years since publication100200300400

Peers

Anna Abramowicz
Comparison fields: 5 of 74
  • Molecular Biology 440
  • Genetics 149
  • Immunology 103
  • Neurology 71
  • Cell Biology 44
Replace Adrienne L. Watson with:
Adrienne L. Watson United States
Cynthia Rothblum‐Oviatt United States
Marco T. Birke Germany
Laura Baker United States
Sarah Greenlee United States
Keiko Tadokoro Japan
Wenyi Wu China
Liberty Walker United States
Bert Eussen Netherlands
Cecily Q. Bernales Canada
Anna Abramowicz relative to Adrienne L. Watson United States Adrienne L. Watson's profile →
Citations per field
00.5×1.5×2.1×
Adrienne L. Watson · 1×
Citations per year

Countries citing papers authored by Anna Abramowicz

Since Specialization
Citations

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

Fields of papers citing papers by Anna Abramowicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Anna Abramowicz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anna Abramowicz Line = papers co-authored together Anna Abramowicz links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1
Splicing mutations in human genetic disorders: examples, detection, and confirmation
Hit paper breakdown →
2018403
2 2015149
3
Neurofibromin in neurofibromatosis type 1 - mutations in NF1gene as a cause of disease.
201457
4 20189
5 20157
6
[RAS/MAPK signal transduction pathway and its role in the pathogenesis of Noonan syndrome].
20126
7 20233
8 20162

About Anna Abramowicz

Anna Abramowicz is a scholar working on Molecular Biology, Genetics, Neurology, Immunology and Cognitive Neuroscience, having authored 8 papers that have together received 636 indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (4 papers), RNA modifications and cancer (3 papers), Connective tissue disorders research (2 papers), Galectins and Cancer Biology (2 papers), Neurofibromatosis and Schwannoma Cases (2 papers), Dermatological and Skeletal Disorders (1 paper), RNA Research and Splicing (1 paper) and Chromatin Remodeling and Cancer (1 paper). The work is most often cited by research in Molecular Biology (440 citations), Genetics (149 citations), Immunology (103 citations), Neurology (71 citations) and Cell Biology (44 citations). Anna Abramowicz has collaborated with scholars based in Poland, United Kingdom and United States. Frequent co-authors include Monika Goś, Somayyeh Fahiminiya, Débora Romeo Bertola, Alexander A.L. Jorge, Michel Satya Naslavsky, Mayana Zatz, Ingrid Cristian, Alexandre C. Pereira, Guilherme Lopes Yamamoto and Alexsandra C. Malaquias. Their work appears in journals such as Genes, Journal of Medical Genetics, Postępy Higieny i Medycyny Doświadczalnej, Journal of Applied Genetics and American Journal of Medical Genetics Part A.

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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