Becky Alhadeff

652 total citations
17 papers, 538 citations indexed

About

Becky Alhadeff is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Becky Alhadeff has authored 17 papers receiving a total of 538 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Genetics. Recurrent topics in Becky Alhadeff's work include Genomics and Chromatin Dynamics (6 papers), DNA Repair Mechanisms (5 papers) and CRISPR and Genetic Engineering (4 papers). Becky Alhadeff is often cited by papers focused on Genomics and Chromatin Dynamics (6 papers), DNA Repair Mechanisms (5 papers) and CRISPR and Genetic Engineering (4 papers). Becky Alhadeff collaborates with scholars based in United States, Italy and United Kingdom. Becky Alhadeff's co-authors include M. Siniscalco, Michele Purrello, Maria Proytcheva, Nathan A. Ellis, Earl E. Henderson, David Lennon, J German, Lloyd J. Old, Nicholas C. Dracopoli and Alan N. Houghton and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and Molecular and Cellular Biology.

In The Last Decade

Becky Alhadeff

17 papers receiving 502 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Becky Alhadeff United States	13	374	183	96	81	62	17	538
J M Parrington United Kingdom	10	537 1.4×	233 1.3×	91 0.9×	78 1.0×	97 1.6×	12	757
Jörg Seidel Germany	8	505 1.4×	284 1.6×	93 1.0×	118 1.5×	112 1.8×	18	767
F. Apiou France	15	517 1.4×	245 1.3×	158 1.6×	144 1.8×	73 1.2×	31	835
Leslie Boghosian-Sell United States	9	320 0.9×	124 0.7×	81 0.8×	105 1.3×	87 1.4×	10	536
Sabita K. Murthy Canada	13	371 1.0×	196 1.1×	83 0.9×	61 0.8×	23 0.4×	25	585
Joseph W. Towner United States	9	324 0.9×	313 1.7×	49 0.5×	179 2.2×	41 0.7×	17	660
H.L. Drwinga United States	6	340 0.9×	148 0.8×	94 1.0×	141 1.7×	83 1.3×	10	598
A. de Capoa Italy	17	546 1.5×	238 1.3×	44 0.5×	53 0.7×	43 0.7×	45	732
Anneke Y. van der Veen Netherlands	15	553 1.5×	304 1.7×	189 2.0×	215 2.7×	37 0.6×	36	872
D K Watson United States	8	344 0.9×	103 0.6×	54 0.6×	77 1.0×	87 1.4×	9	554

Countries citing papers authored by Becky Alhadeff

Since Specialization

Citations

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

Fields of papers citing papers by Becky Alhadeff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Becky Alhadeff

This figure shows the co-authorship network connecting the top 25 collaborators of Becky Alhadeff. A scholar is included among the top collaborators of Becky Alhadeff 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 Becky Alhadeff. Becky Alhadeff 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

Straughen, Joel E., Maria Proytcheva, Becky Alhadeff, et al.. (1996). Physical Mapping of the Bloom Syndrome Region by the Identification of YAC and P1 Clones from Human Chromosome 15 Band q26.1. Genomics. 35(1). 118–128. 12 indexed citations

Ellis, Nathan A., David Lennon, Maria Proytcheva, et al.. (1995). Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells.. PubMed. 57(5). 1019–27. 114 indexed citations

German, James & Becky Alhadeff. (1994). Analysis of Sister‐Chromatid Exchanges. Current Protocols in Human Genetics. 2(1). Unit 8.6–Unit 8.6. 21 indexed citations

Siniscalco, M., I. Oberlé, Paola Melis, et al.. (1991). Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site. American Journal of Medical Genetics. 38(2-3). 357–362. 14 indexed citations

Romani, Massimo, et al.. (1990). Preferential integration of the Ad5/SV40 hybrid virus at the highly recombinogenic human chromosomal site 1p36. Gene. 95(2). 231–241. 23 indexed citations

Purrello, Michele, Becky Alhadeff, K.E. Buckton, et al.. (1987). Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over. Cytogenetic and Genome Research. 44(1). 32–40. 21 indexed citations

Dracopoli, Nicholas C., Becky Alhadeff, Alan N. Houghton, & Lloyd J. Old. (1987). Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma.. PubMed. 47(15). 3995–4000. 67 indexed citations

Purrello, Michele, Becky Alhadeff, Diane Esposito, et al.. (1985). The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.. The EMBO Journal. 4(3). 725–729. 34 indexed citations

Balazs, I., et al.. (1984). Isolation and subregional mapping of a human cDNA clone detecting a common RELP on chromosome 12. Human Genetics. 68(1). 57–61. 12 indexed citations

10.

Alhadeff, Becky & M. Siniscalco. (1984). Complementation Studies in Murine/Human Hybrids Suggest Multiple Etiology for Increased Rate of Sister Chromatid Exchange in Mammalian Cells. PubMed. 29 Pt B. 741–763. 5 indexed citations

11.

Szabó, Piroska E., Michele Purrello, Mariano Rocchi, et al.. (1984). Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.. Proceedings of the National Academy of Sciences. 81(24). 7855–7859. 62 indexed citations

12.

Balazs, I., Michele Purrello, Pablo Rubinstein, Becky Alhadeff, & M. Siniscalco. (1982). Highly polymorphic DNA site D14S1 maps to the region of Burkitt lymphoma translocation and is closely linked to the heavy chain γ1 immunoglobulin locus. Proceedings of the National Academy of Sciences. 79(23). 7395–7399. 17 indexed citations

13.

Stavnezer, Janet, Kenneth B. Marcu, Sonia Sirlin, Becky Alhadeff, & Ulrich Hämmerling. (1982). Rearrangements and deletions of immunoglobulin heavy chain genes in the double-producing B cell lymphoma I.29.. Molecular and Cellular Biology. 2(8). 1002–1013. 23 indexed citations

14.

Stavnezer, Janet, Kenneth B. Marcu, Sonia Sirlin, Becky Alhadeff, & Ulrich Hämmerling. (1982). Rearrangements and Deletions of Immunoglobulin Heavy Chain Genes in the Double-Producing B Cell Lymphoma I.29. Molecular and Cellular Biology. 2(8). 1002–1013. 9 indexed citations

15.

Alhadeff, Becky, et al.. (1980). High rate of sister chromatid exchanges of Bloom’s syndrome chromosomes is corrected in rodent human somatic cell hybrids. Cytogenetic and Genome Research. 27(1). 8–23. 30 indexed citations

16.

Alhadeff, Becky, et al.. (1977). Simultaneous identification of chromatid replication and of human chromosomes in metaphases of man-mouse somatic cell hybrids. Cytogenetic and Genome Research. 19(4). 236–239. 56 indexed citations

17.

Alhadeff, Becky & Cohen Mm. (1976). Frequency and distribution of sister chromatid exchanges in human peripheral lymphocytes.. PubMed. 12(12). 1440–7. 18 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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