Jay W. Ellison

3.9k total citations · 1 hit paper
52 papers, 2.6k citations indexed

About

Jay W. Ellison is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jay W. Ellison has authored 52 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 24 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jay W. Ellison's 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). Jay W. Ellison is often cited by papers focused on 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). Jay W. Ellison collaborates with scholars based in United States, Argentina and United Kingdom. Jay W. Ellison's 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 and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

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 — A (Enhanced Table)

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

Name	h						Papers	Cites
Jay W. Ellison United States	23	1.2k	1.2k	438	351	308	52	2.6k
Umadevi Tantravahi United States	29	946 0.8×	1.4k 1.1×	416 0.9×	63 0.2×	306 1.0×	67	2.7k
José I. Martı́n-Subero Spain	43	654 0.5×	2.9k 2.4×	223 0.5×	359 1.0×	153 0.5×	147	5.7k
Sahar Mansour United Kingdom	36	1.9k 1.5×	2.2k 1.8×	468 1.1×	107 0.3×	832 2.7×	86	4.7k
Eric Schoenmakers Belgium	34	2.1k 1.7×	2.5k 2.0×	490 1.1×	108 0.3×	698 2.3×	76	5.2k
Theo J.M. Hulsebos Netherlands	32	531 0.4×	2.0k 1.7×	84 0.2×	996 2.8×	127 0.4×	87	3.6k
Beyhan Tüysüz Türkiye	24	988 0.8×	1.4k 1.1×	171 0.4×	107 0.3×	231 0.8×	139	2.5k
Eva Sujansky United States	19	781 0.6×	969 0.8×	342 0.8×	256 0.7×	447 1.5×	30	2.0k
Robert Pilarski United States	28	1.1k 0.9×	1.8k 1.5×	76 0.2×	128 0.4×	290 0.9×	62	3.6k
Roberto Mendoza‐Londono Canada	26	1.2k 0.9×	1.0k 0.8×	151 0.3×	126 0.4×	174 0.6×	85	2.1k
F. Dagna Bricarelli Italy	19	1.8k 1.5×	2.1k 1.7×	271 0.6×	40 0.1×	336 1.1×	51	4.4k

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

Rosenfeld, Jill A., Lisa D. McDaniel, Roger A. Schultz, et al.. (2014). Experience Using a Rapid Assay for Aneuploidy and Microdeletion/Microduplication Detection in over 2,900 Prenatal Specimens. Fetal Diagnosis and Therapy. 36(3). 231–241. 9 indexed citations

Boeve, Bradley F., Brendon Boot, Carolyn Orr, et al.. (2011). Clinical Characterization of a Kindred With a Novel 12-Octapeptide Repeat Insertion in the Prion Protein Gene. Archives of Neurology. 68(9). 1165–1165. 21 indexed citations

Coppinger, Justine, Blake C. Ballif, Lisa G. Shaffer, et al.. (2011). Response to the letter by Collins and Schimke. Genetics in Medicine. 13(11). 982–983. 2 indexed citations

Pervaiz, Muhammad, Gerald T. Gau, Allan S. Jaffe, et al.. (2011). A Non-classical Presentation of Tangier Disease with Three ABCA1 Mutations. JIMD Reports. 4. 109–111. 12 indexed citations

Mohsen, Al‐Walid, Sara Copeland, Jay W. Ellison, et al.. (2010). Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening. Molecular Genetics and Metabolism. 100(4). 333–338. 28 indexed citations

Kirmani, Salman, Peter J. Tebben, Aida Lteif, et al.. (2010). Germline TGF‐β receptor mutations and skeletal fragility: A report on two patients with Loeys–Dietz syndrome. American Journal of Medical Genetics Part A. 152A(4). 1016–1019. 31 indexed citations

Pulido, José S., et al.. (2009). A NovelNDPMutation in an Infant with Unilateral Persistent Fetal Vasculature and Retinal Vasculopathy. Ophthalmic Genetics. 30(2). 99–102. 22 indexed citations

Traboulsi, Elias I., et al.. (2008). Aniridia with Preserved Visual Function: A Report of Four Cases with No Mutations in PAX6. American Journal of Ophthalmology. 145(4). 760–764. 11 indexed citations

Ellison, Jay W., Marineh Yagubyan, Ramanath Majumdar, et al.. (2007). Evidence of Genetic Locus Heterogeneity for Familial Bicuspid Aortic Valve. Journal of Surgical Research. 142(1). 28–31. 19 indexed citations

10.

Pasini, Barbara, Sarah R. McWhinney, Thalia Bei, et al.. (2007). 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. European Journal of Human Genetics. 16(1). 79–88. 327 indexed citations

11.

Zou, Ying, Daniel L. Van Dyke, & Jay W. Ellison. (2007). 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. American Journal of Medical Genetics Part A. 143A(7). 746–751. 6 indexed citations

12.

Ensenauer, Regina, et al.. (2005). Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies. American Journal of Medical Genetics Part A. 134A(2). 202–206. 12 indexed citations

13.

Ellison, Jay W.. (1997). PHOG, a candidate gene for involvement in the short stature of Turner syndrome. Human Molecular Genetics. 6(8). 1341–1347. 226 indexed citations

14.

Ellison, Jay W., Eduardo Salido, & Larry J. Shapiro. (1996). Genetic Mapping of the Adenine Nucleotide Translocase-2 Gene (Ant2) to the Mouse Proximal X Chromosome. Genomics. 36(2). 369–371. 13 indexed citations

15.

Ellison, Jay W., et al.. (1996). Rapid evolution of human pseudoautosomal genes and their mouse homologs. Mammalian Genome. 7(1). 25–30. 51 indexed citations

16.

Mills, K., Jay W. Ellison, & Katherine D. Mathews. (1996). The Ant1 gene maps near Klk3 on proximal mouse Chromosome 8. Mammalian Genome. 7(9). 707–707. 5 indexed citations

17.

Ellison, Jay W., et al.. (1992). Directed isolation of human genes that escape X inactivation. Somatic Cell and Molecular Genetics. 18(3). 259–268. 30 indexed citations

18.

Passage, Merry, Jay W. Ellison, Michael A. Becker, et al.. (1992). 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. Somatic Cell and Molecular Genetics. 18(2). 195–200. 9 indexed citations

19.

Carrozzo, Romeo, Jay W. Ellison, Pauline H. Yen, et al.. (1992). Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase gene. Genomics. 12(1). 7–12. 10 indexed citations

20.

Yen, Pauline H., Elizabeth Allen, Siao Ping Tsai, et al.. (1988). The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolution. Cell. 55(6). 1123–1135. 154 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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