Barry L. Barnoski

717 total citations
16 papers, 568 citations indexed

About

Barry L. Barnoski is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Barry L. Barnoski has authored 16 papers receiving a total of 568 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Surgery. Recurrent topics in Barry L. Barnoski's work include Genetics and Neurodevelopmental Disorders (3 papers), Pancreatic function and diabetes (3 papers) and Genetic Syndromes and Imprinting (2 papers). Barry L. Barnoski is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Pancreatic function and diabetes (3 papers) and Genetic Syndromes and Imprinting (2 papers). Barry L. Barnoski collaborates with scholars based in United States, Italy and Germany. Barry L. Barnoski's co-authors include Wen He, Sergei V. Kotenko, Lara S. Izotova, Brian P. Pollack, Sidney Pestka, Peter Eipers, Vincent J. Kidd, Andrew J. Carroll, Jian Han and Beverly S. Emanuel and has published in prestigious journals such as Journal of Biological Chemistry, Blood and The Journal of Immunology.

In The Last Decade

Barry L. Barnoski

15 papers receiving 550 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barry L. Barnoski United States 10 422 132 45 44 33 16 568
Ephrem Chin United States 10 256 0.6× 155 1.2× 25 0.6× 49 1.1× 18 0.5× 16 431
Sika Ristevski Australia 11 359 0.9× 135 1.0× 57 1.3× 59 1.3× 51 1.5× 15 541
Elena Schnabel‐Besson Germany 8 348 0.8× 110 0.8× 27 0.6× 43 1.0× 62 1.9× 17 582
Barbara Pietrucha Poland 12 283 0.7× 114 0.9× 81 1.8× 152 3.5× 19 0.6× 43 556
T Tamaoki Japan 9 316 0.7× 264 2.0× 113 2.5× 35 0.8× 32 1.0× 10 527
Mei‐Chi Cheung United States 8 298 0.7× 139 1.1× 25 0.6× 25 0.6× 35 1.1× 8 597
Yanming Feng United States 11 213 0.5× 111 0.8× 35 0.8× 25 0.6× 32 1.0× 22 400
NP Anagnou United States 14 464 1.1× 125 0.9× 19 0.4× 34 0.8× 12 0.4× 21 657
Gavin R. Oliver United States 13 316 0.7× 127 1.0× 50 1.1× 25 0.6× 42 1.3× 31 496
Sheryl Gere United States 5 466 1.1× 206 1.6× 78 1.7× 34 0.8× 14 0.4× 5 605

Countries citing papers authored by Barry L. Barnoski

Since Specialization
Citations

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

Fields of papers citing papers by Barry L. Barnoski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barry L. Barnoski. 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 Barry L. Barnoski. The network helps show where Barry L. Barnoski may publish in the future.

Co-authorship network of co-authors of Barry L. Barnoski

This figure shows the co-authorship network connecting the top 25 collaborators of Barry L. Barnoski. A scholar is included among the top collaborators of Barry L. Barnoski 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 Barry L. Barnoski. Barry L. Barnoski is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Barnoski, Barry L., Hana Aviv, Vimal Patel, et al.. (2012). Duplication of chromosome 1 [dup(1)(q21q32)] as the sole cytogenetic abnormality in a patient previously treated for AML. Cancer Genetics. 205(12). 665–668. 4 indexed citations
2.
3.
McCorkell, Kelly A., Rita Mancini, Zurab Siprashvili, et al.. (2007). Influence of a nonfragile <i>FHIT</i> transgene on murine tumor susceptibility. Cytogenetic and Genome Research. 118(2-4). 196–203. 1 indexed citations
4.
Martin‐DeLeon, Patricia A., Hong Zhang, Carlos R. Morales, et al.. (2005). Spam1-associated transmission ratio distortion in mice: Elucidating the mechanism. Reproductive Biology and Endocrinology. 3(1). 32–32. 21 indexed citations
5.
Nyman, Lara, Charles L. Hoppel, János Kerner, et al.. (2005). Homozygous carnitine palmitoyltransferase 1a (liver isoform) deficiency is lethal in the mouse. Molecular Genetics and Metabolism. 86(1-2). 179–187. 59 indexed citations
6.
Zhang, Hong, Barry L. Barnoski, Katia Sol‐Church, Deborah L. Stabley, & Patricia A. Martin‐DeLeon. (2005). Murine Spam1 mRNA: Involvement of AU‐rich elements in the 3′UTR and antisense RNA in its tight post‐transcriptional regulation in spermatids. Molecular Reproduction and Development. 73(2). 247–255. 6 indexed citations
7.
Dessain, Scott, et al.. (2004). High efficiency creation of human monoclonal antibody-producing hybridomas. Journal of Immunological Methods. 291(1-2). 109–122. 38 indexed citations
8.
Ottey, Michelle, Teresa Druck, Barry L. Barnoski, et al.. (2004). Fhit-deficient normal and cancer cells are mitomycin C and UVC resistant. British Journal of Cancer. 91(9). 1669–1677. 47 indexed citations
9.
Das, Soma, Christa M. Lese, Minsun Song, et al.. (2000). Partial Paternal Uniparental Disomy of Chromosome 6 in an Infant with Neonatal Diabetes, Macroglossia, and Craniofacial Abnormalities. The American Journal of Human Genetics. 67(6). 1586–1591. 27 indexed citations
10.
11.
Pollack, Brian P., Sergei V. Kotenko, Wen He, et al.. (1999). The Human Homologue of the Yeast Proteins Skb1 and Hsl7p Interacts with Jak Kinases and Contains Protein Methyltransferase Activity. Journal of Biological Chemistry. 274(44). 31531–31542. 240 indexed citations
12.
Li, Li, Qi Wu, Barry L. Barnoski, & Max D. Cooper. (1997). High-Resolution Genetic Map of the Human Glutamyl Aminopeptidase Gene (ENPEP). Genomics. 43(3). 380–383. 5 indexed citations
13.
Rhodes, C. Harker, Katherine M. Call, Marcia L. Budarf, et al.. (1997). Molecular studies of an ependymoma-associated constitutional t(1;22)(p22;q11.2). Cytogenetic and Genome Research. 78(3-4). 247–252. 33 indexed citations
14.
Budarf, Marcia L., et al.. (1995). Assignment of the human hippocampal inward rectifier potassium channel (HIR) gene to 22q13.1. Genomics. 26(3). 625–629. 4 indexed citations
15.
Barnoski, Barry L., et al.. (1994). Structure, chromosomal localization, and methylation pattern of the human mb-1 gene.. The Journal of Immunology. 152(12). 5749–5757. 22 indexed citations
16.
Eipers, Peter, Barry L. Barnoski, Jian Han, Andrew J. Carroll, & Vincent J. Kidd. (1991). Localization of the expressed human p58 protein kinase chromosomal gene to chromosome 1p36 and a highly related sequence to chromosome 15. Genomics. 11(3). 621–629. 47 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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