Nataline B. Kardon

938 total citations
26 papers, 640 citations indexed

About

Nataline B. Kardon is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Nataline B. Kardon has authored 26 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 7 papers in Molecular Biology. Recurrent topics in Nataline B. Kardon's work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Acute Myeloid Leukemia Research (6 papers). Nataline B. Kardon is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Acute Myeloid Leukemia Research (6 papers). Nataline B. Kardon collaborates with scholars based in United States, Russia and Qatar. Nataline B. Kardon's co-authors include Kurt Hirschhorn, Brynn Levy, Teresa Dunn, Philip Schulman, Daniel R. Budman, Thomas J. Degnan, Lillian Y. F. Hsu, Vincent Vinciguerra, Robert R. Sheehy and Bradley N. White and has published in prestigious journals such as Science, The Lancet and PEDIATRICS.

In The Last Decade

Nataline B. Kardon

26 papers receiving 612 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nataline B. Kardon United States 13 329 281 232 108 103 26 640
D E Rooney United Kingdom 10 291 0.9× 243 0.9× 245 1.1× 86 0.8× 72 0.7× 14 631
Van den Berghe H Belgium 13 257 0.8× 98 0.3× 267 1.2× 68 0.6× 46 0.4× 45 562
David Peakman United States 15 278 0.8× 192 0.7× 126 0.5× 51 0.5× 84 0.8× 30 636
Michal Daniely Israel 12 225 0.7× 269 1.0× 126 0.5× 57 0.5× 126 1.2× 15 585
Elena Kolomietz Canada 11 269 0.8× 225 0.8× 305 1.3× 104 1.0× 114 1.1× 23 734
P Colombiès France 12 150 0.5× 93 0.3× 127 0.5× 75 0.7× 68 0.7× 64 438
Sara Kaffe United States 16 546 1.7× 399 1.4× 235 1.0× 111 1.0× 26 0.3× 30 768
M. L. Kwee Netherlands 13 320 1.0× 91 0.3× 426 1.8× 57 0.5× 50 0.5× 24 640
Kyohko Abe Japan 14 179 0.5× 94 0.3× 199 0.9× 39 0.4× 45 0.4× 22 604
J. P. M. Geraedts Netherlands 11 153 0.5× 105 0.4× 104 0.4× 77 0.7× 117 1.1× 22 422

Countries citing papers authored by Nataline B. Kardon

Since Specialization
Citations

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

Fields of papers citing papers by Nataline B. Kardon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nataline B. Kardon. 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 Nataline B. Kardon. The network helps show where Nataline B. Kardon may publish in the future.

Co-authorship network of co-authors of Nataline B. Kardon

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

All Works

20 of 20 papers shown
1.
Levy, Brynn, et al.. (2005). Incidence and spectrum of chromosome abnormalities in spontaneous abortions: New insights from a 12-year study. Genetics in Medicine. 7(4). 251–263. 186 indexed citations
2.
Levy, Brynn, Teresa Dunn, Jeffrey H. Kern, Kurt Hirschhorn, & Nataline B. Kardon. (2002). Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat). American Journal of Medical Genetics. 108(3). 192–197. 22 indexed citations
3.
Blum, Robin R., Abolfazl Rahimizadeh, Nataline B. Kardon, Mark Lebwohl, & Huachen Wei. (2001). Genital Lentigines in a 6-Year-Old Boy with a Family History of Cowden's Disease: Clinical and Genetic Evidence of the Linkage between Bannayan–Riley–Ruvacalba Syndrome and Cowden's Disease. Journal of Cutaneous Medicine and Surgery. 5(3). 228–230. 2 indexed citations
4.
Blum, Robin R., Abolfazl Rahimizadeh, Nataline B. Kardon, Mark Lebwohl, & Huachen Wei. (2001). Genital Lentigines in a 6-Year-Old Boy with a Family History of Cowden's Disease: Clinical and Genetic Evidence of the Linkage Between Bannayan-Riley-Ruvacalba Syndrome and Cowden's Disease. Journal of Cutaneous Medicine and Surgery. 5(3). 228–230. 7 indexed citations
5.
Levy, Brynn, Teresa Dunn, Sara Kaffe, Nataline B. Kardon, & Kurt Hirschhorn. (1998). Clinical applications of comparative genomic hybridization. Genetics in Medicine. 1(1). 4–12. 51 indexed citations
6.
Gelb, Bruce D., Judith P. Willner, Teresa Dunn, et al.. (1998). Paternal Uniparental Disomy for Chromosome 1 Revealed by Molecular Analysis of a Patient with Pycnodysostosis. The American Journal of Human Genetics. 62(4). 848–854. 58 indexed citations
7.
Greenberg, Frank, et al.. (1992). Congenital deficiency of α-fetoprotein. American Journal of Obstetrics and Gynecology. 167(2). 509–511. 11 indexed citations
8.
Lichtman, Stuart M., Philip Schulman, Nataline B. Kardon, Steven L. Allen, & Myron Susin. (1988). Monosomy 5 in acute megakaryoblastic leukemia. Cancer Genetics and Cytogenetics. 33(1). 111–117. 5 indexed citations
9.
Kardon, Nataline B., et al.. (1986). Two sporadic cases of amelia/phocomelia with similar phenotype: Rare and unusually symmetrical form of FFU dysostosis or separate entity?. American Journal of Medical Genetics. 25(S2). 239–245. 10 indexed citations
10.
McDermid, Heather E., Alessandra M.V. Duncan, Klaus Brasch, et al.. (1986). Characterization of the Supernumerary Chromosome in Cat Eye Syndrome. Science. 232(4750). 646–648. 119 indexed citations
11.
Schulman, Philip, Nataline B. Kardon, Robert S. Weiner, et al.. (1983). Acquired idiopathic sideroblastic anemia: A new chromosomal abnormality. Cancer Genetics and Cytogenetics. 9(4). 341–345. 13 indexed citations
12.
Kardon, Nataline B., Philip Schulman, Thomas J. Degnan, et al.. (1982). Cytogenetic findings in the dysmyelopoietic syndrome. Cancer. 50(12). 2834–2838. 30 indexed citations
13.
Kolitz, Jonathan E., Philip Schulman, Nataline B. Kardon, et al.. (1981). A complex variant Philadelphia (Ph1) chromosome translocation involving chromosomes No. 11, 14, and 22 in a case of chronic myelogenous leukemia. Cancer Genetics and Cytogenetics. 4(2). 185–188. 7 indexed citations
14.
Kardon, Nataline B., Ernest Lieber, Jessica G. Davis, & Lillian Y. F. Hsu. (1979). Prenatal diagnosis of trisomy 20 mosaicism. Clinical Genetics. 15(3). 267–272. 12 indexed citations
15.
Kardon, Nataline B., et al.. (1977). De novo trisomy 9pter?q13. Human Genetics. 37(2). 149–153. 4 indexed citations
16.
Kardon, Nataline B., et al.. (1977). De novo trisomy 9pter?q13. Human Genetics. 38(2). 249–249. 4 indexed citations
17.
Beratis, Nicholas G., et al.. (1972). Parental mosaicism in trisomy 18.. PubMed. 50(6). 908–11. 18 indexed citations
18.
Kardon, Nataline B., et al.. (1972). Pitfalls in prenatal diagnosis resulting from chromosomal mosaicism. The Journal of Pediatrics. 80(2). 297–299. 12 indexed citations
19.
Beratis, Nicholas G., et al.. (1972). PARENTAL MOSAICISM IN TRISOMY 18. PEDIATRICS. 50(6). 908–911. 14 indexed citations
20.
Kardon, Nataline B., et al.. (1970). TRISOMY 18. The Lancet. 296(7676). 782–782. 13 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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