Jay Leonard

587 total citations
12 papers, 406 citations indexed

About

Jay Leonard is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Jay Leonard has authored 12 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Jay Leonard's work include DNA Repair Mechanisms (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Jay Leonard is often cited by papers focused on DNA Repair Mechanisms (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Jay Leonard collaborates with scholars based in United States and United Kingdom. Jay Leonard's co-authors include Steven R. Patierno, John Pierce Wise, Kamila U. Szulc, Babak A. Ardekani, Lynn E. DeLisi, Andrea Maurizio, P.D. Harvey, Jay Nierenberg, B. Saitta and Mahlet G. Tadesse and has published in prestigious journals such as Biology of Reproduction, Genomics and Human Genetics.

In The Last Decade

Jay Leonard

12 papers receiving 393 citations

Peers

Jay Leonard

GENET

SURGE

GENET

HTM

Farkhondeh Behjati Iran

RL Jirtle United States

Mahmoud Y. Issa Egypt

F Ballesta Spain

Cyril Chapman United Kingdom

Matthias Linke Germany

Maria Lucia Scaldaferri Italy

Frederick V. Schaefer United States

Depicha Jindatip Thailand

T. Lukusa Belgium

Farkhondeh Behjati Iran

Jay Leonard

330 ×1.7

271 ×1.6

GENET

53 ×0.8

SURGE

30 ×0.5

GENET

43 ×0.9

HTM

Citations per year, relative to Jay Leonard Jay Leonard (= 1×) peers Farkhondeh Behjati

Countries citing papers authored by Jay Leonard

Since Specialization

Citations

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

Fields of papers citing papers by Jay Leonard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jay Leonard

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

All Works

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12 of 12 papers shown

Kalman, Lisa V., Jay Leonard, Norman P. Gerry, et al.. (2011). Quality Assurance for Duchenne and Becker Muscular Dystrophy Genetic Testing. Journal of Molecular Diagnostics. 13(2). 167–174. 18 indexed citations

Roberson, Elisha, Elizabeth Wohler, Julie Hoover‐Fong, et al.. (2010). Genomic analysis of partial 21q monosomies with variable phenotypes. European Journal of Human Genetics. 19(2). 235–238. 44 indexed citations

Shanske, Alan, Naomi Yachelevich, Leena Ala‐Kokko, Jay Leonard, & Brynn Levy. (2009). Wolf–Hirschhorn syndrome and ectrodactyly: New findings and a review of the literature. American Journal of Medical Genetics Part A. 152A(1). 203–208. 5 indexed citations

Markov, Vladimir, Kenro Kusumi, Mahlet G. Tadesse, et al.. (2007). Identification of Cord Blood-Derived Mesenchymal Stem/stromal Cell Populations with Distinct Growth Kinetics, Differentiation Potentials, and Gene Expression Profiles. Stem Cells and Development. 16(1). 53–74. 75 indexed citations

DeLisi, Lynn E., Andrea Maurizio, Babak A. Ardekani, et al.. (2005). Klinefelter's syndrome (XXY) as a genetic model for psychotic disorders. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 135B(1). 15–23. 125 indexed citations

Robledo, Renato, Patrick K. Bender, Jay Leonard, et al.. (2004). The immunoglobulin λ variable light-chain region in primates has been shaped by multiple, independent, small-scale and large-scale insertion/deletion events. Genomics. 84(4). 678–685. 1 indexed citations

Leonard, Jay, Ann M. Mullinger, John A. Schmidt, Heather J. Cordell, & Robert T. Johnson. (2004). Genome Instability in Ataxia Telangiectasia (A-T) Families: Camptothecin-Induced Damage to Replicating DNA Discriminates between Obligate A-T Heterozygotes, A-T Homozygotes and Controls. Bioscience Reports. 24(6). 617–629. 8 indexed citations

Shanske, Alan, José Carlos Ferreira, Jay Leonard, Peter J. Fuller, & Robert W. Marion. (2001). Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13. American Journal of Medical Genetics. 102(3). 231–236. 32 indexed citations

Xu, Yongsheng, W. Roy Overton, Joel L. Marmar, et al.. (1998). Complete Replication of Human Sperm Genome in Egg Extracts from Xenopus laevis1. Biology of Reproduction. 58(3). 641–647. 5 indexed citations

10.

Wise, John Pierce, Jay Leonard, & Steven R. Patierno. (1992). Clastogenicity of lead chromate particles in hamster and human cells. Mutation Research/Genetic Toxicology. 278(1). 69–79. 79 indexed citations

11.

Leonard, Jay, Robin C. Leonard, & Keith H. Thompson. (1988). Arabinofuranosyl nucleosides induce common fragile sites. Human Genetics. 79(2). 157–162. 4 indexed citations

12.

Leonard, Jay & T. Merz. (1982). Repair of single-strand breaks in normal and trisomic lymphocytes. Mutation Research Letters. 105(6). 417–422. 10 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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