R.E. Magenis

3.4k citations

55 papers · 2.7k indexed · 1 hit paper · h-index 28

Genetics top 1%
Molecular Biology top 5%
Pediatrics, Perinatology and Child Health top 2%
Cellular and Molecular Neuroscience top 5%
Plant Science top 5%

Co-authors: M. Litt Leland Allen M. Lalande Joan H.M. Knoll John M. Graham Robert D. Nicholls E.W. Lovrien John Chamberlin
Topics: Genomic variations and chromosomal abnormalities (19 papers)Chromosomal and Genetic Variations (13 papers)Prenatal Screening and Diagnostics (9 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research Journal of Clinical Investigation
Partner nations: United States Canada Poland

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

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate 2003 ·Leukemia ·Michael O’Dwyer,Ken Gatter,Marc Loriaux,Brian Druker,Susan B. Olson,R.E. Magenis,Helen J. Lawce,Michael J. Mauro,Richard T. Maziarz,Rita M. Braziel	73
2	Definition of the critical interval for Smith-Magenis syndrome 1997 ·Cytogenetic and Genome Research ·Sarah H. Elsea,Smita M. Purandare,(unknown),Ramesh C. Juyal,Jessica G. Davis,Brenda Finucane,R.E. Magenis,Pragna I. Patel	25
3	An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene. 1995 ·PubMed ·F Quan,J. Zonana,(unknown),Kathryn Peterson,R.E. Magenis,Bradley W. Popovich	46
4	Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and human 1994 ·Mammalian Genome ·R.E. Magenis,Leslie Smith,Joseph H. Nadeau,Keith R. Johnson,Kathleen G. Mountjoy,Roger D. Cone	62
5	Dinucleotide repeat polymorphism at the D14S43 locus 1991 ·Nucleic Acids Research ·Vikram Sharma,Leslie Smith,(unknown),R.E. Magenis,M. Litt	20
6	A low-copy repeat located in subtelomeric regions of 14 different human chromosomal termini 1991 ·Cytogenetic and Genome Research ·Bernhard H. F. Weber,Leland Allen,R.E. Magenis,Michael R. Hayden	11
7	Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences 1990 ·American Journal of Medical Genetics ·R.E. Magenis,(unknown),Leland Allen,Mary Helen Black,Michael G. Brown,Sarojini Budden,Rachel Cohen,Jan M. Friedman,Dagmar K. Kalousek,J. Zonana,D. Borden Lacy,Stephen LaFranchi,Marta Mìrazón Lahr,Jane L. Macfarlane,(unknown)	158
8	Rearrangement of chromosome 15 in the region q11.2→q12 in an individual with obesity syndrome and her normal mother 1990 ·American Journal of Medical Genetics ·Mordechai Shohat,Tami Shohat,D L Rimoin,T. Mohandas,(unknown),R.E. Magenis,Mayer B. Davidson,Julie R. Korenberg	11
9	Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionbreakdown → 1989 ·American Journal of Medical Genetics ·Joan H.M. Knoll,Robert D. Nicholls,R.E. Magenis,John M. Graham,M. Lalande,S.A. Latt,John M. Opitz,James F. Reynolds	432
10	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 1989 ·Cytogenetic and Genome Research ·E. Natt,R.E. Magenis,J. Zimmer,(unknown),Gerd Scherer	77
11	Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus. 1988 ·PubMed Central ·Barbara A. Smith,Douglas Skarecky,Ulla Bengtsson,R.E. Magenis,Nancy J. Carpenter,John J. Wasmuth	80
12	Delineation of human prometaphase paracentromeric regions using sequential GTG- and C-banding 1987 ·Cytogenetic and Genome Research ·R.E. Magenis,Sheila J. Barton	2
13	Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes 1987 ·Nucleic Acids Research ·Nabeel A. Affara,M.A. Ferguson‐Smith,R.E. Magenis,John Tolmie,E. Boyd,Alexander Cooke,Derek J. Jamieson,(unknown),Michael Mitchell,(unknown)	67
14	A hypervariable repeated sequence on human chromosome 1p36 1987 ·Human Genetics ·Norman E. Buroker,Richard K. Bestwick,(unknown),R.E. Magenis,M. Litt	104
15	Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females 1987 ·Development ·M.A. Ferguson‐Smith,Nabeel A. Affara,R.E. Magenis	28
16	Distribution of sex chromosome complements in 651 patients with turners syndrome 1980 ·The American Journal of Human Genetics ·R.E. Magenis,W. Roy Breg,(unknown),ErnestB. Hook,Catherine G. Palmer,László Pásztor,Robert L. Summitt,(unknown)	21
17	The 8p- syndrome 1979 ·Human Genetics ·(unknown),(unknown),John Chamberlin,R.E. Magenis,E.W. Lovrien	19
18	Linkage study of antithrombin III 1978 ·Cytogenetic and Genome Research ·E.W. Lovrien,R.E. Magenis,Marian L. Rivas,(unknown),R. Travis Moreland,Suzanne J. Rowe	12
19	Exclusion of glutathione reductase from 8pter→8p22 and localization to 8p21 1978 ·Cytogenetic and Genome Research ·R.E. Magenis,(unknown),R. Bigley,John Chamberlin,E.W. Lovrien	7
20	Linkage relationships of HLA and a familial chromosome 6 inversion (pter→p23::q23→p23::q23→qter): lack of dose effect in duplication-deficient offspring 1978 ·Cytogenetic and Genome Research ·R.E. Magenis,John Chamberlin,(unknown),E.W. Lovrien	5

About R.E. Magenis

R.E. Magenis is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 55 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (13 papers) and Prenatal Screening and Diagnostics (9 papers). The work is most often cited by research in Genetics (1.5k citations), Pediatrics, Perinatology and Child Health (495 citations) and Molecular Biology (1.5k citations). R.E. Magenis has collaborated with scholars based in United States, Canada and Poland. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

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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