Irit Bar‐Am

2.9k citations
26 papers · 2.4k · 1 hit paper · h-index 15

Impact in

  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
  • Hematology top 5%
    • Acute Myeloid Leukemia Research

Papers in

    • Genomics and Chromatin Dynamics 4
    • DNA Repair Mechanisms 3
    • Gene expression and cancer classification 3
    • Genomic variations and chromosomal abnormalities 11

Irit Bar‐Am

26 papers receiving 2.3k citations

Irit Bar‐Am's Hit Papers

Multicolor Spectral Karyotyping of Human Chromosomes 1996 · 1.4k citations
1.4k0+10+20Years since publication4008001.2k

Peers

Irit Bar‐Am
Comparison fields: 5 of 107
  • Genetics 1.0k
  • Hematology 322
  • Cancer Research 368
  • Biophysics 129
  • Molecular Biology 1.4k
Replace Brigitte Schoell with:
Brigitte Schoell Germany
A. Jauch Germany
Dirk Soenksen United States
Richard A. Young United States
K. D. Zang Germany
Diane Esposito United States
Susana A. Godinho United Kingdom
Sarah Kinston United Kingdom
Steven T. Kosak United States
Joy T. Yang United States
Irit Bar‐Am relative to Brigitte Schoell Germany Brigitte Schoell's profile →
Citations per field
00.5×2.6×
Brigitte Schoell · 1×
Citations per year

Countries citing papers authored by Irit Bar‐Am

Since Specialization
Citations

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

Fields of papers citing papers by Irit Bar‐Am

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Irit Bar‐Am. 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 Irit Bar‐Am. The network helps show where Irit Bar‐Am may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Multicolor Spectral Karyotyping of Human Chromosomes
Hit paper breakdown →
19961433
2 1994370
3 199687
4 200067
5 199865
6 199660
7 199952
8 199831
9 199227
10 200426
11 200524
12 199824
13 199621
14 200317
15 200315
16 199114
17 199514
18 200212
19 200312
20 201712

About Irit Bar‐Am

Irit Bar‐Am is a scholar working on Molecular Biology, Genetics, Plant Science, Cancer Research and Neurology, having authored 26 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers), Genomics and Chromatin Dynamics (4 papers), DNA Repair Mechanisms (3 papers), Cancer Genomics and Diagnostics (3 papers), Gene expression and cancer classification (3 papers), Neuroblastoma Research and Treatments (3 papers) and Acute Myeloid Leukemia Research (3 papers). The work is most often cited by research in Genetics (1.0k citations), Hematology (322 citations), Cancer Research (368 citations), Biophysics (129 citations) and Molecular Biology (1.4k citations). Irit Bar‐Am has collaborated with scholars based in Israel, United States and United Kingdom. Frequent co-authors include Yuval Garini, Thomas Ried, Evelin Schröck, Stanislas du Manoir, Dirk Soenksen, David H. Ledbetter, Timothy Veldman, M.A. Ferguson‐Smith, Brigitte Schoell and Yi Ning. Their work appears in journals such as Genes Chromosomes and Cancer, Genomics, Human Molecular Genetics, Bioimaging and Nucleic Acids Research.

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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