J. Stamberg

645 total citations
17 papers, 329 citations indexed

About

J. Stamberg is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, J. Stamberg has authored 17 papers receiving a total of 329 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Plant Science and 6 papers in Molecular Biology. Recurrent topics in J. Stamberg's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (6 papers) and Prenatal Screening and Diagnostics (5 papers). J. Stamberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (6 papers) and Prenatal Screening and Diagnostics (5 papers). J. Stamberg collaborates with scholars based in United States and Denmark. J. Stamberg's co-authors include Emilie H. Mules, Y. Koltin, Paul A. Lemke, Stefán Hreiðarsson, S Pan, L T Hu, Harry Ostrer, John M. Opitz, Lewis Waber and Jeffrey Strovel and has published in prestigious journals such as Gene, British Journal of Haematology and Journal of Medical Genetics.

In The Last Decade

J. Stamberg

16 papers receiving 302 citations

Peers

J. Stamberg

GENET

PPCH

PHEOH

M. Giollant France

de Grouchy J France

Hungshu Wang Canada

Hideaki Chiyo Japan

Florina Raicu Romania

Keiji Hirabayashi Japan

E. Soeda Japan

Anne Bergmann United States

K. E. Brown United Kingdom

V. Pérez‐Infante United States

M. Giollant France

J. Stamberg

150 ×0.9

GENET

183 ×1.2

153 ×2.0

42 ×0.6

PPCH

32 ×0.7

PHEOH

Citations per year, relative to J. Stamberg J. Stamberg (= 1×) peers M. Giollant

Countries citing papers authored by J. Stamberg

Since Specialization

Citations

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

Fields of papers citing papers by J. Stamberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Stamberg

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

All Works

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17 of 17 papers shown

McDevitt, Michael A., Marian Condon, J. Stamberg, Judith E. Karp, & Melissa A. McDiarmid. (2007). Fluorescent in situ hybridization (FISH) in bone marrow and peripheral blood of leukemia patients: Implications for occupational surveillance. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 629(1). 24–31. 5 indexed citations

Bloomfield, C. D., Krzysztof Mrózek, J O Moore, et al.. (2004). Core binding factor acute myeloid leukemia. Cancer and Leukemia Group B (CALGB) Study 8461.. PubMed. 83 Suppl 1. S84–5. 10 indexed citations

Fu, Sidong, Holly Stevenson, Susanne B. Haga, et al.. (2001). Distinct functions of two isoforms of a homeobox gene, BP1 and DLX7, in the regulation of the β-globin gene. Gene. 278(1-2). 131–139. 29 indexed citations

Jalal, S. M., et al.. (2001). Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization. British Journal of Haematology. 112(4). 975–980. 19 indexed citations

Strovel, Jeffrey, J. Stamberg, W. Edward Highsmith, et al.. (2000). Plasma telomerase activity predicts response and relapse in lung cancer. Lung Cancer. 29(1). 258–258. 1 indexed citations

Stamberg, J., et al.. (2000). Severe growth retardation and limb anomalies in a boy with 47,XY,+r(7) and maternal uniparental disomy for chromosome 7. Genetics in Medicine. 2(1). 95–95.

Strovel, Jeffrey, J. Stamberg, & Paul Yarowsky. (1999). Interphase FISH for rapid identification of a Down syndrome animal model. Cytogenetic and Genome Research. 86(3-4). 285–287. 15 indexed citations

Hu, L T, J. Stamberg, & S Pan. (1996). The NAD(P)H:quinone oxidoreductase locus in human colon carcinoma HCT 116 cells resistant to mitomycin C.. PubMed. 56(22). 5253–9. 30 indexed citations

Zaslav, Ann‐Leslie, Bettie M. Steinberg, J. Stamberg, Yue Lin, & A. L. Abramson. (1988). Chromosomal Analysis of Recurrent Laryngeal Papillomas. Archives of Otolaryngology - Head and Neck Surgery. 114(10). 1170–1174. 4 indexed citations

10.

Stamberg, J., et al.. (1988). Duplication 17q mosaicism: an infant with features of Ellis-van Creveld syndrome.. Journal of Medical Genetics. 25(4). 258–260. 19 indexed citations

11.

Ostrer, Harry, et al.. (1984). Two chromosome aberrations in the child of a woman with systemic lupus erythematosus treated with azathioprine and prednisone. American Journal of Medical Genetics. 17(3). 627–632. 32 indexed citations

12.

Mules, Emilie H. & J. Stamberg. (1984). Reproductive outcomes of paracentric inversion carriers: Report of a liveborn dicentric recombinant and literature review. Human Genetics. 67(2). 126–131. 49 indexed citations

13.

Mules, Emilie H., et al.. (1983). Two different structural abnormalities of chromosome 13 in offspring of chromo‐somally normal parents with two fragile sites. Clinical Genetics. 23(5). 380–385. 15 indexed citations

14.

Hreiðarsson, Stefán & J. Stamberg. (1983). Distal monosomy 14 not associated with ring formation.. Journal of Medical Genetics. 20(2). 147–149. 28 indexed citations

15.

Pyeritz, Reed E., et al.. (1982). The marker Xq28 syndrome ("Fragile-X SYndrome") in a retarded man with mitral valve prolapse.. PubMed. 151(5). 231–7. 12 indexed citations

16.

Stamberg, J., et al.. (1981). Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter). Clinical Genetics. 19(2). 122–125. 17 indexed citations

17.

Koltin, Y., J. Stamberg, & Paul A. Lemke. (1972). Genetic structure and evolution of the incompatibility factors in higher fungi. Bacteriological Reviews. 36(2). 156–171. 44 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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