Renée Bernstein

609 total citations
26 papers, 466 citations indexed

About

Renée Bernstein is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Renée Bernstein has authored 26 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Plant Science and 8 papers in Molecular Biology. Recurrent topics in Renée Bernstein's work include Chromosomal and Genetic Variations (9 papers), Acute Myeloid Leukemia Research (6 papers) and Prenatal Screening and Diagnostics (6 papers). Renée Bernstein is often cited by papers focused on Chromosomal and Genetic Variations (9 papers), Acute Myeloid Leukemia Research (6 papers) and Prenatal Screening and Diagnostics (6 papers). Renée Bernstein collaborates with scholars based in South Africa and United States. Renée Bernstein's co-authors include M. R. Pinto, Stephen S. Wachtel, Gloria C. Koo, B. Mendelow, Lorna G. Macdougall, W. R. Bezwoda, Preben Philip, Trefor Jenkins, Yoshimi Ueshima and John M. Opitz and has published in prestigious journals such as Science, JAMA and British Journal of Haematology.

In The Last Decade

Renée Bernstein

26 papers receiving 448 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Renée Bernstein South Africa 13 241 195 163 71 64 26 466
J.W. Wessels Netherlands 8 216 0.9× 173 0.9× 173 1.1× 85 1.2× 39 0.6× 10 445
Sparkes Rs United States 11 143 0.6× 132 0.7× 122 0.7× 73 1.0× 72 1.1× 30 382
P. Mollevanger Netherlands 13 196 0.8× 189 1.0× 65 0.4× 51 0.7× 59 0.9× 19 428
Mauri Keinänen Finland 11 216 0.9× 91 0.5× 255 1.6× 80 1.1× 31 0.5× 14 466
Shunsuke Kimura Japan 13 203 0.8× 144 0.7× 95 0.6× 67 0.9× 67 1.0× 40 476
Barbara Adler‐Brecher United States 7 462 1.9× 163 0.8× 197 1.2× 47 0.7× 67 1.0× 9 677
W.L. Neuman United States 10 251 1.0× 101 0.5× 131 0.8× 46 0.6× 39 0.6× 18 476
Paolo Guanciali Franchi Italy 14 220 0.9× 298 1.5× 80 0.5× 54 0.8× 80 1.3× 31 484
Lorna M. Webber Australia 7 176 0.7× 89 0.5× 120 0.7× 53 0.7× 18 0.3× 11 372
WB Bias United States 9 134 0.6× 132 0.7× 277 1.7× 120 1.7× 57 0.9× 14 537

Countries citing papers authored by Renée Bernstein

Since Specialization
Citations

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

Fields of papers citing papers by Renée Bernstein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renée Bernstein

This figure shows the co-authorship network connecting the top 25 collaborators of Renée Bernstein. A scholar is included among the top collaborators of Renée Bernstein 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 Renée Bernstein. Renée Bernstein 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.
Bernstein, Renée, Paul M. Zeltzer, Fritz Lin, & Philip M. Carpenter. (1994). Trisomy 11 and other nonrandom trisomies in congenital fibrosarcoma. Cancer Genetics and Cytogenetics. 78(1). 82–86. 16 indexed citations
2.
Bernstein, Renée, et al.. (1993). Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridization. American Journal of Medical Genetics. 46(1). 77–82. 5 indexed citations
3.
Bernstein, Renée, et al.. (1992). Prenatal application of fluorescent in situ hybridization (FISH) for identification of a mosaic Y‐chromosome marker, IDIC(Yp). Prenatal Diagnosis. 12(9). 709–716. 9 indexed citations
4.
Castle, David, H Isaacs, Michèle Ramsay, & Renée Bernstein. (1992). Hereditary motor and sensory neuropathy type I, associated with aplasia cutis congenital possible X‐linked inheritance. Clinical Genetics. 41(2). 108–110. 2 indexed citations
5.
Steinhaus, Kathryn A., Renée Bernstein, & Maureen Bocian. (1991). Importance of accurate diagnosis in counseling for neural tube defects diagnosed prenatally. Clinical Genetics. 39(5). 355–361. 2 indexed citations
6.
Macdougall, Lorna G., et al.. (1990). Fanconi anemia in black African children. American Journal of Medical Genetics. 36(4). 408–413. 16 indexed citations
7.
Lambson, Bronwen E., Renée Bernstein, & B. Mendelow. (1990). Chromosomal evolution in secretory and nonsecretory subline of MOPC 21. Somatic Cell and Molecular Genetics. 16(1). 91–95. 2 indexed citations
8.
Shen, Violet, et al.. (1990). Absence of isochromosome 12p in a pineal region malignant germ cell tumor. Cancer Genetics and Cytogenetics. 50(1). 153–160. 24 indexed citations
9.
Bernstein, Renée, et al.. (1989). Loss of the Y chromosome associated with translocation t(6;9)(p23;q34) in a patient with acute nonlymphocytic leukemia. Cancer Genetics and Cytogenetics. 39(1). 81–87. 10 indexed citations
10.
Castle, David, Renée Bernstein, John M. Optiz, & James F. Reynolds. (1988). Cytogenetic analysis of 688 couples experiencing multiple spontaneous abortions. American Journal of Medical Genetics. 29(3). 549–556. 28 indexed citations
11.
Bernstein, Renée, et al.. (1988). Fanconi's anemia—Chromosome breakage studies in homozygotes and heterozygotes. Cancer Genetics and Cytogenetics. 33(2). 175–183. 26 indexed citations
12.
Willem, Pascale, M. R. Pinto, & Renée Bernstein. (1988). Translocation t(1;7) revisited. Cancer Genetics and Cytogenetics. 36(1). 45–54. 14 indexed citations
13.
Bernstein, Renée, et al.. (1987). Fanconi anemia: Another disease of unusually high prevalence in the Afrikaans population of South africa. American Journal of Medical Genetics. 27(4). 793–797. 46 indexed citations
14.
Macdougall, Lorna G., et al.. (1986). Acute Childhood Leukemia in Johannesburg. Journal of Pediatric Hematology/Oncology. 8(1). 43–51. 17 indexed citations
15.
Bernstein, Renée, et al.. (1986). Acute promyelocytic transformation of chronic myeloid leukaemia with an isochromosome 17q. British Journal of Haematology. 64(4). 751–756. 7 indexed citations
16.
Bernstein, Renée, M. R. Pinto, Jennifer G.R. Kromberg, et al.. (1985). Segregation patterns and phenotypes of unbalanced offspring in a large family with (10;18) chromosome translocation. American Journal of Medical Genetics. 22(4). 727–742. 2 indexed citations
17.
Bernstein, Renée, Preben Philip, & Yoshimi Ueshima. (1984). Abnormalities of Chromosome 7 Resulting in Monosomy 7 or in Deletion of the Long Arm (7q-): Review of Translocations, Breakpoints, and Associated Abnormalities. Cancer Genetics and Cytogenetics. 11(3). 300–303. 40 indexed citations
18.
Bernstein, Renée. (1981). The Y Chromosome and Primary Sexual Differentiation. JAMA. 245(19). 1953–1953. 3 indexed citations
19.
Bernstein, Renée, et al.. (1980). Cytogenetic findings in chronic myeloid leukemia (CML); evaluation of karyotype, blast morphology, and survival in the acute phase. Cancer Genetics and Cytogenetics. 2(1). 23–37. 42 indexed citations
20.
Bernstein, Renée, Gloria C. Koo, & Stephen S. Wachtel. (1980). Abnormality of the X Chromosome in Human 46,XY Female Siblings with Dysgenetic Ovaries. Science. 207(4432). 768–769. 62 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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