Irit Bar‐Am

2.9k total citations · 1 hit paper
26 papers, 2.3k citations indexed

About

Irit Bar‐Am is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Irit Bar‐Am has authored 26 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Plant Science. Recurrent topics in Irit Bar‐Am's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers) and Gene expression and cancer classification (4 papers). Irit Bar‐Am is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers) and Gene expression and cancer classification (4 papers). Irit Bar‐Am collaborates with scholars based in Israel, United States and United Kingdom. Irit Bar‐Am's co-authors include Yuval Garini, Evelin Schröck, Stanislas du Manoir, Thomas Ried, David H. Ledbetter, Dirk Soenksen, Timothy Veldman, M.A. Ferguson‐Smith, Brigitte Schoell and Johannes Wienberg and has published in prestigious journals such as Science, Nucleic Acids Research and Oncogene.

In The Last Decade

Irit Bar‐Am

26 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Multicolor Spectral Karyotyping of Human Chromosomes

1996 1.3k citations Evelin Schröck, Stanislas du Manoir et al. Science profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Irit Bar‐Am Israel	15	1.4k	967	498	379	312	26	2.3k
Brigitte Schoell Germany	14	1.3k 0.9×	1.0k 1.1×	502 1.0×	503 1.3×	118 0.4×	16	2.2k
A. Jauch Germany	28	1.7k 1.2×	596 0.6×	372 0.7×	437 1.2×	533 1.7×	50	2.6k
Dirk Soenksen United States	7	803 0.6×	839 0.9×	431 0.9×	245 0.6×	117 0.4×	12	1.5k
K. D. Zang Germany	34	1.4k 1.0×	662 0.7×	388 0.8×	421 1.1×	147 0.5×	144	3.7k
Richard A. Young United States	11	5.5k 4.0×	611 0.6×	357 0.7×	792 2.1×	238 0.8×	11	6.2k
Diane Esposito United States	10	1.7k 1.2×	636 0.7×	176 0.4×	1.5k 4.0×	49 0.2×	12	2.8k
Douglas Tkachuk United States	14	1.1k 0.8×	327 0.3×	187 0.4×	123 0.3×	734 2.4×	17	2.0k
Susana A. Godinho United Kingdom	15	2.6k 1.8×	589 0.6×	346 0.7×	440 1.2×	44 0.1×	27	3.5k
Sandra Hanks United Kingdom	16	1.7k 1.2×	1.2k 1.2×	124 0.2×	517 1.4×	41 0.1×	20	2.4k
Joy T. Yang United States	18	2.0k 1.4×	165 0.2×	115 0.2×	305 0.8×	254 0.8×	20	3.3k

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-authorship network of co-authors of Irit Bar‐Am

This figure shows the co-authorship network connecting the top 25 collaborators of Irit Bar‐Am. A scholar is included among the top collaborators of Irit Bar‐Am based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Irit Bar‐Am. Irit Bar‐Am is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Sagie, Shira, et al.. (2017). Non-random length distribution of individual telomeres in immunodeficiency, centromeric instability and facial anomalies syndrome, type I. Human Molecular Genetics. 26(21). 4244–4256. 12 indexed citations

Brenner, Ori, Ninette Amariglio, Nechama I. Smorodinsky, et al.. (2005). Impaired genomic stability and increased oxidative stress exacerbate different features of Ataxia-telangiectasia. Human Molecular Genetics. 14(19). 2929–2943. 23 indexed citations

Stark, Batia, Marta Jeison, Drorit Luria, et al.. (2004). Classical and molecular cytogenetic abnormalities and outcome of childhood acute myeloid leukaemia: report from a referral centre in Israel. British Journal of Haematology. 126(3). 320–337. 25 indexed citations

Stark, Batia, Marta Jeison, Irit Bar‐Am, et al.. (2003). der(11)t(11;17): a distinct cytogenetic pathway of advanced stage neuroblastoma (NBL) – detected by spectral karyotyping (SKY). Cancer Letters. 197(1-2). 75–79. 12 indexed citations

Kakazu, Naoki, et al.. (2003). A new chromosome banding technique, spectral color banding (SCAN), for full characterization of chromosomal abnormalities. Genes Chromosomes and Cancer. 37(4). 412–416. 12 indexed citations

Steinlein, Claus, et al.. (2003). Multicolor spectral karyotyping of rat chromosomes. Cytogenetic and Genome Research. 103(1-2). 163–168. 15 indexed citations

Stark, Batia, Marta Jeison, Irit Bar‐Am, et al.. (2002). Distinct cytogenetic pathways of advanced‐stage neuroblastoma tumors, detected by spectral karyotyping. Genes Chromosomes and Cancer. 34(3). 313–324. 12 indexed citations

Stark, Batia, Marta Jeison, Shifra Ash, et al.. (2000). Apparently Unrelated Clones Shown by Spectral Karyotyping to Represent Clonal Evolution of Cryptic t(10;11)(p13;q23) in a Patient with Acute Monoblastic Leukemia. Cancer Genetics and Cytogenetics. 120(2). 105–110. 10 indexed citations

Spitzer, Daniel, et al.. (2000). Karyotypic dissection of Hodgkin's disease cell lines reveals ectopic subtelomeres and ribosomal DNA at sites of multiple jumping translocations and genomic amplification. Leukemia. 14(10). 1803–1814. 65 indexed citations

10.

Garini, Yuval, et al.. (1999). Signal to noise analysis of multiple color fluorescence imaging microscopy. Cytometry. 35(3). 214–226. 48 indexed citations

11.

Rothmann, Chana, et al.. (1998). Spectral imaging for quantitative histology and cytogenetics.. PubMed. 13(3). 921–6. 22 indexed citations

12.

Gele, Mireille Van, Nadine Van Roy, Salve G. Ronan, et al.. (1998). Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas. Genes Chromosomes and Cancer. 23(1). 67–71. 29 indexed citations

13.

Regev, Aviv, et al.. (1998). Telomeric repeats on small polydisperse circular DNA (spcDNA) and genomic instability. Oncogene. 17(26). 3455–3461. 65 indexed citations

14.

Levanon, Ditsa, Yael Bernstein, Varda Negreanu, et al.. (1996). A Large Variety of Alternatively Spliced and Differentially Expressed mRNAs Are Encoded by the Human Acute Myeloid Leukemia Gene AML1. DNA and Cell Biology. 15(3). 175–185. 85 indexed citations

15.

Schröck, Evelin, Stanislas du Manoir, Timothy Veldman, et al.. (1996). Multicolor Spectral Karyotyping of Human Chromosomes. Science. 273(5274). 494–497. 1318 indexed citations breakdown →

16.

Bar‐Am, Irit, Lydia Avivi, & Mia Horowitz. (1996). Assignment of the human prosaposin gene (PSAP) to 10q22.1 by fluorescence in situ hybridization. Cytogenetic and Genome Research. 72(4). 316–318(1996. 5 indexed citations

17.

Levanon, Ditsa, Varda Negreanu, Yael Bernstein, et al.. (1994). AML1, AML2, and AML3, the Human Members of the runt domain Gene-Family: cDNA Structure, Expression, and Chromosomal Localization. Genomics. 23(2). 425–432. 361 indexed citations

18.

Bar‐Am, Irit, Orna Mor, Yosef Shiloh, Lydia Avivi, & Herman Yeger. (1992). Detection of amplified dna sequences in human tumor cell lines by fluorescence in situ hybridization. Genes Chromosomes and Cancer. 4(4). 314–320. 26 indexed citations

19.

Shiloh, Yosef, Orna Mor, Irit Bar‐Am, et al.. (1992). DNA sequences amplified in cancer cells: an interface between tumor biology and human genome analysis. Mutation Research/Reviews in Genetic Toxicology. 276(3). 329–337. 3 indexed citations

20.

Yaniv, A., et al.. (1991). A novel approach for establishing common or random integration loci for retroviral genomes. Nucleic Acids Research. 19(15). 4299–4299. 1 indexed citations

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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