Veronica Teleanu

3.8k citations
39 papers · 3k · 1 hit paper · h-index 22

Impact in

  • Hematology top 0.5%
    • Acute Myeloid Leukemia Research
    • Multiple Myeloma Research and Treatments
    • Hematopoietic Stem Cell Transplantation
    • Cancer Genomics and Diagnostics

Papers in

    • Acute Myeloid Leukemia Research 22
    • Multiple Myeloma Research and Treatments 4
    • Cancer Genomics and Diagnostics 3

Veronica Teleanu

39 papers receiving 3k citations

Veronica Teleanu's Hit Papers

TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome 2011 · 566 citations
5660+5+10Years since publication100200300400500

Peers

Veronica Teleanu
Comparison fields: 5 of 64
  • Hematology 2.3k
  • Cancer Research 212
  • Genetics 71
  • Oncology 158
  • Health Informatics 15
Replace Amelie Lier with:
Amelie Lier Germany
Jessica Kohlschmidt United States
Deedra Nicolet United States
Carolina Schinke United States
Leylah M. Drusbosky United States
A. Krämer Germany
Prapti Arvind Patel United States
Iulia Cirlan Canada
Constance Regina Baer Germany
Edgar Sioson United States
Veronica Teleanu relative to Amelie Lier Germany Amelie Lier's profile →
Citations per field
00.5×2×2.6×
Amelie Lier · 1×
Citations per year

Countries citing papers authored by Veronica Teleanu

Since Specialization
Citations

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

Fields of papers citing papers by Veronica Teleanu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Veronica Teleanu, 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 Veronica Teleanu Line = papers co-authored together Veronica Teleanu links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.

#Work
1
TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome
Hit paper breakdown →
2011566
2 2014346
3 2013240
4 2016218
5 2018198
6 2021195
7 2017135
8 2011132
9 2019104
10 201594
11 201591
12 201289
13 201889
14 201757
15 201755
16 201754
17 202050
18 202248
19 201642
20 202242

About Veronica Teleanu

Veronica Teleanu is a scholar working on Hematology, Cancer Research, Genetics, Pulmonary and Respiratory Medicine and Gastroenterology, having authored 39 papers that have together received 3k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (22 papers), Multiple Myeloma Research and Treatments (4 papers), Cancer Genomics and Diagnostics (3 papers), Lung Cancer Treatments and Mutations (2 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (2 papers), Acute Lymphoblastic Leukemia research (1 paper), Genomics and Rare Diseases (1 paper) and BRCA gene mutations in cancer (1 paper). The work is most often cited by research in Hematology (2.3k citations), Cancer Research (212 citations), Genetics (71 citations), Oncology (158 citations) and Health Informatics (15 citations). Veronica Teleanu has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Hartmut Doehner, Konstanze Döhner, Arnold Ganser, Richard F. Schlenk, Lars Bullinger, Jürgen Krauter, Gudrun Göhring, Marcus Matthias Schittenhelm, Frank G. Rücker and Jan Krönke. Their work appears in journals such as Blood, Leukemia, Genes Chromosomes and Cancer, Nature Communications and ESMO Open.

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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