R.E. Magenis

3.4k total citations · 1 hit paper
55 papers, 2.7k citations indexed

About

R.E. Magenis is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, R.E. Magenis has authored 55 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 30 papers in Molecular Biology and 14 papers in Plant Science. Recurrent topics in R.E. Magenis's work include Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (13 papers) and Prenatal Screening and Diagnostics (9 papers). R.E. Magenis is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (13 papers) and Prenatal Screening and Diagnostics (9 papers). R.E. Magenis collaborates with scholars based in United States, Canada and Poland. R.E. Magenis's co-authors include M. Litt, Leland Allen, M. Lalande, Joan H.M. Knoll, John M. Graham, Robert D. Nicholls, E.W. Lovrien, John Chamberlin, James F. Reynolds and John M. Opitz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

R.E. Magenis

55 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1989 432 citations Joan H.M. Knoll, Robert D. Nicholls et al. American Journal of Medical Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R.E. Magenis United States	28	1.5k	1.5k	495	385	366	55	2.7k
R. Ellen Magenis United States	32	2.0k 1.3×	2.0k 1.4×	538 1.1×	469 1.2×	277 0.8×	71	3.7k
Marcia L. Budarf United States	34	1.5k 1.0×	2.9k 2.0×	188 0.4×	181 0.5×	392 1.1×	72	4.0k
E. Schwinger Germany	40	2.0k 1.3×	2.7k 1.8×	794 1.6×	1.3k 3.5×	363 1.0×	210	6.0k
M. W. Partington Canada	33	2.0k 1.3×	1.8k 1.2×	314 0.6×	309 0.8×	91 0.2×	110	3.5k
Hartmut Engels Germany	25	1.3k 0.9×	1.3k 0.9×	267 0.5×	226 0.6×	258 0.7×	66	2.2k
Emma Roberts United Kingdom	18	1.1k 0.7×	2.3k 1.6×	171 0.3×	512 1.3×	263 0.7×	21	3.4k
David A. Koolen Netherlands	22	2.2k 1.4×	1.6k 1.1×	330 0.7×	186 0.5×	337 0.9×	53	3.1k
Sylvain Briault France	23	1.6k 1.0×	1.8k 1.2×	248 0.5×	426 1.1×	140 0.4×	64	3.1k
Susan L. Christian United States	33	3.2k 2.1×	2.3k 1.5×	997 2.0×	354 0.9×	300 0.8×	53	4.4k
Angelo Selicorni Italy	29	1.8k 1.2×	2.5k 1.7×	553 1.1×	191 0.5×	165 0.5×	176	3.8k

Countries citing papers authored by R.E. Magenis

Since Specialization

Citations

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

Fields of papers citing papers by R.E. Magenis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R.E. Magenis. 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 R.E. Magenis. The network helps show where R.E. Magenis may publish in the future.

Co-authorship network of co-authors of R.E. Magenis

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

All Works

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20 of 20 papers shown

O’Dwyer, Michael, Ken Gatter, Marc Loriaux, et al.. (2003). Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate. Leukemia. 17(3). 481–487. 73 indexed citations

Elsea, Sarah H., Smita M. Purandare, Ramesh C. Juyal, et al.. (1997). Definition of the critical interval for Smith-Magenis syndrome. Cytogenetic and Genome Research. 79(3-4). 276–281. 25 indexed citations

Quan, F, et al.. (1995). An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene.. PubMed. 56(5). 1042–51. 46 indexed citations

Magenis, R.E., Leslie Smith, Joseph H. Nadeau, et al.. (1994). Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and human. Mammalian Genome. 5(8). 503–508. 62 indexed citations

Sharma, Vikram, et al.. (1991). Dinucleotide repeat polymorphism at the D14S43 locus. Nucleic Acids Research. 19(7). 1722–1722. 20 indexed citations

Weber, Bernhard H. F., Leland Allen, R.E. Magenis, & Michael R. Hayden. (1991). A low-copy repeat located in subtelomeric regions of 14 different human chromosomal termini. Cytogenetic and Genome Research. 57(4). 179–183. 11 indexed citations

Magenis, R.E., Leland Allen, Mary Helen Black, et al.. (1990). Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences. American Journal of Medical Genetics. 35(3). 333–349. 158 indexed citations

Shohat, Mordechai, Tami Shohat, D L Rimoin, et al.. (1990). Rearrangement of chromosome 15 in the region q11.2→q12 in an individual with obesity syndrome and her normal mother. American Journal of Medical Genetics. 37(2). 173–177. 11 indexed citations

Knoll, Joan H.M., Robert D. Nicholls, R.E. Magenis, et al.. (1989). Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. American Journal of Medical Genetics. 32(2). 285–290. 432 indexed citations breakdown →

10.

Natt, E., et al.. (1989). Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16. Cytogenetic and Genome Research. 50(2-3). 145–148. 77 indexed citations

11.

Smith, Barbara A., Douglas Skarecky, Ulla Bengtsson, et al.. (1988). Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus.. PubMed Central. 42(2). 335–44. 80 indexed citations

12.

Magenis, R.E. & Sheila J. Barton. (1987). Delineation of human prometaphase paracentromeric regions using sequential GTG- and C-banding. Cytogenetic and Genome Research. 45(3-4). 132–140. 2 indexed citations

13.

Affara, Nabeel A., M.A. Ferguson‐Smith, R.E. Magenis, et al.. (1987). Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes. Nucleic Acids Research. 15(18). 7325–7342. 67 indexed citations

14.

Buroker, Norman E., et al.. (1987). A hypervariable repeated sequence on human chromosome 1p36. Human Genetics. 77(2). 175–181. 104 indexed citations

15.

Ferguson‐Smith, M.A., Nabeel A. Affara, & R.E. Magenis. (1987). Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females. Development. 101(Supplement). 41–50. 28 indexed citations

16.

Magenis, R.E., W. Roy Breg, ErnestB. Hook, et al.. (1980). Distribution of sex chromosome complements in 651 patients with turners syndrome. The American Journal of Human Genetics. 32(6). 79. 21 indexed citations

17.

Chamberlin, John, et al.. (1979). The 8p- syndrome. Human Genetics. 47(2). 135–140. 19 indexed citations

18.

Lovrien, E.W., et al.. (1978). Linkage study of antithrombin III. Cytogenetic and Genome Research. 22(1-6). 319–323. 12 indexed citations

19.

Magenis, R.E., et al.. (1978). Exclusion of glutathione reductase from 8pter→8p22 and localization to 8p21. Cytogenetic and Genome Research. 22(1-6). 446–448. 7 indexed citations

20.

Magenis, R.E., et al.. (1978). Linkage relationships of HLA and a familial chromosome 6 inversion (pter→p23::q23→p23::q23→qter): lack of dose effect in duplication-deficient offspring. Cytogenetic and Genome Research. 22(1-6). 418–420. 5 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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