Anna Abramowicz

1.1k citations
8 papers · 686 · 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
    • Connective tissue disorders research 2
    • Genetics and Neurodevelopmental Disorders 1
    • Dermatological and Skeletal Disorders 1

Anna Abramowicz

8 papers receiving 679 citations

Anna Abramowicz's Hit Papers

Splicing mutations in human genetic disorders: examples, detection, and confirmation 2018 · 440 citations
4400+2+5Years since publication100200300400

Peers

Anna Abramowicz
Comparison fields: 5 of 75
  • Molecular Biology 425
  • Genetics 149
  • Neurology 70
  • Immunology 90
  • Cancer Research 38
Replace Luke C. Gandolfo with:
Luke C. Gandolfo Australia
Jana Královičová United Kingdom
Andrea Rivera Germany
Laura Baker United States
Nicholas Bockett New Zealand
Kyoichi Takahashi United States
Marco T. Birke Germany
Alfons Meindl Germany
Elizabeth Kropf United States
Cecily Q. Bernales Canada
Anna Abramowicz relative to Luke C. Gandolfo Australia Luke C. Gandolfo's profile →
Citations per field
00.5×2.7×
Luke C. Gandolfo · 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 →
2018440
2 2015157
3
Neurofibromin in neurofibromatosis type 1 - mutations in NF1gene as a cause of disease.
201461
4 20189
5 20158
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, Cognitive Neuroscience and Immunology, having authored 8 papers that have together received 686 indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (4 papers), RNA modifications and cancer (3 papers), Neurofibromatosis and Schwannoma Cases (2 papers), Connective tissue disorders research (2 papers), Autism Spectrum Disorder Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Galectins and Cancer Biology (1 paper) and Dermatological and Skeletal Disorders (1 paper). The work is most often cited by research in Molecular Biology (425 citations), Genetics (149 citations), Neurology (70 citations), Immunology (90 citations) and Cancer Research (38 citations). Anna Abramowicz has collaborated with scholars based in Poland, United Kingdom and Brazil. Frequent co-authors include Monika Goś, Maria Rita Passos‐Bueno, Somayyeh Fahiminiya, Christina Hung, Alexander A.L. Jorge, Alexsandra C. Malaquias, Chong Ae Kim, Mayana Zatz, Guilherme Lopes Yamamoto and Alexandre C. Pereira. Their work appears in journals such as Genes, Journal of Medical Genetics, American Journal of Medical Genetics Part A, Journal of Applied Genetics and Postępy Higieny i Medycyny Doświadczalnej.

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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