Jay W. Ellison

3.9k citations

52 papers · 2.6k indexed · 1 hit paper · h-index 23

Genetics top 1%
Molecular Biology top 10%
Pediatrics, Perinatology and Child Health top 2%
Neurology top 5%
Surgery top 10%

Co-authors: Lisa G. Shaffer Jill A. Rosenfeld Larry J. Shapiro L Hood Maike Busch M. Schwab J. Michael Bishop Werner Rosenau
Topics: Genomic variations and chromosomal abnormalities (14 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers)Prenatal Screening and Diagnostics (7 papers)
Cited by: Genetics Gastroenterology Neurology
Journals: Cell Proceedings of the National Academy of Sciences Nucleic Acids Research
Partner nations: United States Argentina United Kingdom

In The Last Decade

Jay W. Ellison

52 papers receiving 2.5k 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.

Enhanced expression of the human gene N-myc consequent to amplification of DNA may contribute to malignant progression of neuroblastoma.

1984 325 citations Jay W. Ellison et al. profile →

Peers

Countries citing papers authored by Jay W. Ellison

Since Specialization

Citations

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

Fields of papers citing papers by Jay W. Ellison

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jay W. Ellison. 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 Jay W. Ellison. The network helps show where Jay W. Ellison may publish in the future.

Co-authorship network of co-authors of Jay W. Ellison

This figure shows the co-authorship network connecting the top 25 collaborators of Jay W. Ellison. A scholar is included among the top collaborators of Jay W. Ellison 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 Jay W. Ellison. Jay W. Ellison 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	Experience Using a Rapid Assay for Aneuploidy and Microdeletion/Microduplication Detection in over 2,900 Prenatal Specimens 2014 ·Fetal Diagnosis and Therapy ·Jill A. Rosenfeld,(unknown),(unknown),(unknown),Lisa D. McDaniel,Roger A. Schultz,Beth S. Torchia,J. Britt Ravnan,Jay W. Ellison,Allan J. Fisher	9
2	Clinical Characterization of a Kindred With a Novel 12-Octapeptide Repeat Insertion in the Prion Protein Gene 2011 ·Archives of Neurology ·(unknown),Bradley F. Boeve,Brendon Boot,Carolyn Orr,Joseph R. Duffy,Bryan K. Woodruff,Anil K. Nair,Jay W. Ellison,Karen M. Kuntz,Kejal Kantarci,Clifford R. Jack,Barbara F. Westmoreland,Julie A. Fields,Matthew Baker,Rosa Rademakers,Joseph E. Parisi,Dennis W. Dickson	21
3	Response to the letter by Collins and Schimke 2011 ·Genetics in Medicine ·(unknown),Justine Coppinger,Blake C. Ballif,Lisa G. Shaffer,Jay W. Ellison,Sulagna C. Saitta,Tracy Stroud,Kandamurugu Manickam,Zheng Fan	2
4	A Non-classical Presentation of Tangier Disease with Three ABCA1 Mutations 2011 ·JIMD Reports ·Muhammad Pervaiz,Gerald T. Gau,Allan S. Jaffe,Amy K. Saenger,Linnea M. Baudhuin,Jay W. Ellison	12
5	Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening 2010 ·Molecular Genetics and Metabolism ·(unknown),Al‐Walid Mohsen,Sara Copeland,Jay W. Ellison,(unknown),Marianne Rohrbach,Berkley R. Powell,Jane Gillis,Dietrich Matern,Jeffrey A. Kant,Jerry Vockley	28
6	Germline TGF‐β receptor mutations and skeletal fragility: A report on two patients with Loeys–Dietz syndrome 2010 ·American Journal of Medical Genetics Part A ·Salman Kirmani,Peter J. Tebben,Aida Lteif,David Gordon,B.L. Clarke,Theresa E. Hefferan,Michael J. Yaszemski,(unknown),Noralane M. Lindor,Jay W. Ellison	31
7	A NovelNDPMutation in an Infant with Unilateral Persistent Fetal Vasculature and Retinal Vasculopathy 2009 ·Ophthalmic Genetics ·(unknown),José S. Pulido,Jay W. Ellison,Polly A. Quiram,Brian G. Mohney	22
8	Aniridia with Preserved Visual Function: A Report of Four Cases with No Mutations in PAX6 2008 ·American Journal of Ophthalmology ·Elias I. Traboulsi,Jay W. Ellison,Jonathan E. Sears,Irene H. Maumenee,(unknown),Brian G. Mohney	11
9	Evidence of Genetic Locus Heterogeneity for Familial Bicuspid Aortic Valve 2007 ·Journal of Surgical Research ·Jay W. Ellison,Marineh Yagubyan,Ramanath Majumdar,Gobinda Sarkar,Mark E. Bolander,Elizabeth J. Atkinson,Maurice Enriquez‐Sarano,Thoralf M. Sundt	19
10	Clinical and molecular genetics of patients with the Carney–Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD 2007 ·European Journal of Human Genetics ·Barbara Pasini,Sarah R. McWhinney,Thalia Bei,Ludmila Matyakhina,Sotirios Stergiopoulos,Michael Muchow,Sosipatros A. Boikos,Barbara Ferrando,Karel Pacák,Guillaume Assié,Éric Baudin,Agnès Chompret,Jay W. Ellison,Jean-Jacques Brière,Pierre Rustin,Anne‐Paule Gimenez‐Roqueplo,Charis Eng,J. Aidan Carney,Constantine A. Stratakis	327
11	Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problems 2007 ·American Journal of Medical Genetics Part A ·Ying Zou,Daniel L. Van Dyke,Jay W. Ellison	6
12	Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies 2005 ·American Journal of Medical Genetics Part A ·Regina Ensenauer,William J. Shaughnessy,Syed M. Jalal,D. Brian Dawson,(unknown),Jay W. Ellison	12
13	PHOG, a candidate gene for involvement in the short stature of Turner syndrome 1997 ·Human Molecular Genetics ·Jay W. Ellison	226
14	Genetic Mapping of the Adenine Nucleotide Translocase-2 Gene (Ant2) to the Mouse Proximal X Chromosome 1996 ·Genomics ·Jay W. Ellison,Eduardo Salido,Larry J. Shapiro	13
15	Rapid evolution of human pseudoautosomal genes and their mouse homologs 1996 ·Mammalian Genome ·Jay W. Ellison,(unknown),Uta Francke,Larry J. Shapiro	51
16	The Ant1 gene maps near Klk3 on proximal mouse Chromosome 8 1996 ·Mammalian Genome ·K. Mills,Jay W. Ellison,Katherine D. Mathews	5
17	Directed isolation of human genes that escape X inactivation 1992 ·Somatic Cell and Molecular Genetics ·Jay W. Ellison,Merry Passage,(unknown),Pauline H. Yen,T. Mohandas,Larry J. Shapiro	30
18	Physical mapping of loci in the distal half of the short arm of the human X chromosome: Implications for the spreading of X-chromosome inactivation 1992 ·Somatic Cell and Molecular Genetics ·(unknown),Merry Passage,Jay W. Ellison,Michael A. Becker,P. H. Yen,Larry J. Shapiro,T. Mohandas	9
19	Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase gene 1992 ·Genomics ·Romeo Carrozzo,Jay W. Ellison,Pauline H. Yen,Patricia Taillon‐Miller,Bernard H. Brownstein,Graziella Persico,Andrea Ballabio,Larry J. Shapiro	10
20	The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolution 1988 ·Cell ·Pauline H. Yen,(unknown),Elizabeth Allen,Siao Ping Tsai,Jay W. Ellison,Lynn Connolly,Katherine Neiswanger,Larry J. Shapiro	154

About Jay W. Ellison

Jay W. Ellison is a scholar working on Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 52 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers) and Prenatal Screening and Diagnostics (7 papers). The work is most often cited by research in Genetics (1.2k citations), Gastroenterology (180 citations) and Neurology (351 citations). Jay W. Ellison has collaborated with scholars based in United States, Argentina and United Kingdom. Frequent co-authors include Lisa G. Shaffer, Jill A. Rosenfeld, Larry J. Shapiro, L Hood, Maike Busch, M. Schwab, J. Michael Bishop, Werner Rosenau, Harold Varmus and Blake C. Ballif. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

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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