R. Ellen Magenis

5.3k citations

71 papers · 3.7k indexed · h-index 32

Molecular Biology top 5%
Genetics top 0.5%
Pediatrics, Perinatology and Child Health top 2%
Cellular and Molecular Neuroscience top 5%
Surgery top 10%

Co-authors: Michael G. Brown Frederick Hecht Joseph Wagstaff Joan H.M. Knoll Charles A. Williams Albert Schinzel Jill Clayton‐Smith Susan B. Olson
Topics: Genomic variations and chromosomal abnormalities (18 papers)Prenatal Screening and Diagnostics (14 papers)Chromosomal and Genetic Variations (10 papers)
Cited by: Genetics Molecular Biology Pediatrics, Perinatology and Child Health
Journals: Nature Science New England Journal of Medicine
Partner nations: United States Canada France

In The Last Decade

R. Ellen Magenis

71 papers receiving 3.6k citations

Peers

Countries citing papers authored by R. Ellen Magenis

Since Specialization

Citations

This map shows the geographic impact of R. Ellen 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. Ellen 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. Ellen Magenis more than expected).

Fields of papers citing papers by R. Ellen Magenis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of R. Ellen Magenis. A scholar is included among the top collaborators of R. Ellen 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. Ellen Magenis. R. Ellen 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

#	Work	Indexed citations
1	Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems 2010 ·The American Journal of Human Genetics ·Stephen R. Williams,Micheala A. Aldred,Vazken M. Der Kaloustian,Fahed Halal,Gordon C. Gowans,D. Ross McLeod,(unknown),Helga V. Toriello,R. Ellen Magenis,Sarah H. Elsea	216
2	Review of disrupted sleep patterns in Smith–Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion 2009 ·American Journal of Medical Genetics Part A ·Eilis Boudreau,Kyle Johnson,Angela R. Jackman,Jan Blancato,Marjan Huizing,Claude Bendavid,MaryPat Jones,Settara C. Chandrasekharappa,Alfred J. Lewy,Ann C. M. Smith,R. Ellen Magenis	36
3	Angelman syndrome 2005: Updated consensus for diagnostic criteria 2006 ·American Journal of Medical Genetics Part A ·Charles A. Williams,Arthur L. Beaudet,Jill Clayton‐Smith,Joan H.M. Knoll,(unknown),Laura Laan,R. Ellen Magenis,A Moncla,Albert Schinzel,Jane Summers,Joseph Wagstaff	420
4	Chondromyxoid fibroma of the nasal cavity with an interstitial insertion between chromosomes 6 and 19 2006 ·Cancer Genetics and Cytogenetics ·(unknown),R. Ellen Magenis,(unknown),(unknown),Atiya Mansoor	15
5	Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm 2005 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Michael G. Brown,Helen J. Lawce,Joseph Gilhooly,Robert S. Wildin,Leesa M. Linck,R. Ellen Magenis,De‐Ann M. Pillers	21
6	Myxoinflammatory fibroblastic sarcoma with complex supernumerary ring chromosomes composed of chromosome 3 segments 2004 ·Cancer Genetics and Cytogenetics ·Atiya Mansoor,(unknown),(unknown),(unknown),Helen J. Lawce,R. Ellen Magenis	38
7	SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development 2001 ·Genes Chromosomes and Cancer ·Kimberly J. Bussey,Helen J. Lawce,(unknown),Xiao Ou Shu,Nyla A. Heerema,Elizabeth J. Perlman,Susan B. Olson,R. Ellen Magenis	36
8	Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations 2001 ·American Journal of Medical Genetics ·Craig R. Warden,De‐Ann M. Pillers,Mary J. Rice,(unknown),(unknown),Brian A. Clark,Joseph Gilhooly,R. Ellen Magenis	12
9	Chromosomes 1 and 12 abnormalities in pediatric germ cell tumors by interphase fluorescence in situ hybridization 2001 ·Cancer Genetics and Cytogenetics ·Kimberly J. Bussey,Helen J. Lawce,(unknown),Xiao Ou Shu,Ron F. Suijkerbuijk,Susan B. Olson,R. Ellen Magenis	19
10	Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development 2001 ·American Journal of Medical Genetics ·Bonnie Jeanne Baty,Susan B. Olson,R. Ellen Magenis,John C. Carey	14
11	Complex translocation (7;22) identified in an epithelioid hemangioendothelioma 1996 ·Cancer Genetics and Cytogenetics ·(unknown),Helen J. Lawce,(unknown),Susan B. Olson,R. Ellen Magenis,Christopher L. Corless	33
12	Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation 1995 ·American Journal of Medical Genetics ·(unknown),De‐Ann M. Pillers,Jacob A. Reiss,Michael G. Brown,R. Ellen Magenis	33
13	Trisomy 11: an association with stem/progenitor cell immunophenotype 1995 ·British Journal of Haematology ·Marilyn L. Slovak,S. Thomas Traweek,Cheryl L. Willman,David R. Head,Kenneth J. Kopecky,R. Ellen Magenis,Frederick R. Appelbaum,Stephen J. Forman	34
14	Chromosomal localization of three human D5 dopamine receptor genes 1992 ·Genomics ·David K. Grandy,(unknown),Yuan Zhang,R. Ellen Magenis,Olivier Civelli	28
15	The human gene fro apurinic/apyrimidinic endonuclease (HAP1): sequence and localization to chromosome 14 band q12 1992 ·Nucleic Acids Research ·(unknown),David K. Grandy,(unknown),R. Ellen Magenis,Leslie Smith,(unknown),(unknown)	16
16	Intrachromosomal location of the telomeric repeat (TTAGGG)n 1991 ·Mammalian Genome ·Bernhard H. F. Weber,Leland Allen,R. Ellen Magenis,Paul J. Goodfellow,Leslie Smith,Michael R. Hayden	28
17	Is angelman syndrome an alternate result of del(15)(qllql3)? 1987 ·American Journal of Medical Genetics ·R. Ellen Magenis,Michael G. Brown,(unknown),Sarojini Budden,Stephen LaFranchi,John M. Opitz,James F. Reynolds,David H. Ledbetter	190
18	Y‐derived sequences detected in a 45,X male by in situ hybridization 1987 ·American Journal of Medical Genetics ·Robert R. Sheehy,Michael G. Brown,Richard J. Warren,M L Schwartzman,R. Ellen Magenis,John M. Opitz,James F. Reynolds	5
19	Fetal karyotype following ascertainment of fetal anomalies by ultrasound 1987 ·Prenatal Diagnosis ·Catherine G. Palmer,Judith H. Miles,Patricia N. Howard‐Peebles,R. Ellen Magenis,Shivanand R. Patil,Jan M. Friedman	33
20	Trisomy 13 (D1) syndrome: Studies on parentalage, sex ratio, and survival 1968 ·The Journal of Pediatrics ·R. Ellen Magenis,Frederick Hecht,Samuel Milham	79

About R. Ellen Magenis

R. Ellen Magenis is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 71 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (14 papers) and Chromosomal and Genetic Variations (10 papers). The work is most often cited by research in Genetics (2.0k citations), Molecular Biology (2.0k citations) and Pediatrics, Perinatology and Child Health (538 citations). R. Ellen Magenis has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Michael G. Brown, Frederick Hecht, Joseph Wagstaff, Joan H.M. Knoll, Charles A. Williams, Albert Schinzel, Jill Clayton‐Smith, Susan B. Olson, Susan B. Olson and John M. Opitz. Their work appears in journals such as Nature, Science and New England Journal of Medicine.

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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