Edwin J. Young

2.7k total citations
16 papers, 1.1k citations indexed

About

Edwin J. Young is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Edwin J. Young has authored 16 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Edwin J. Young's work include Glycogen Storage Diseases and Myoclonus (5 papers), Williams Syndrome Research (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Edwin J. Young is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (5 papers), Williams Syndrome Research (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Edwin J. Young collaborates with scholars based in Canada, United States and Estonia. Edwin J. Young's co-authors include Stephen W. Scherer, Lucy R. Osborne, Leonarda Ianzano, Berge A. Minassian, Elayne M. Chan, Cameron Ackerley, Carolyn Β. Mervis, Colleen A. Morris, Martin J. Somerville and Liis Uusküla-Reimand and has published in prestigious journals such as Science, New England Journal of Medicine and Nucleic Acids Research.

In The Last Decade

Edwin J. Young

14 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Edwin J. Young Canada	13	551	538	301	207	109	16	1.1k
Hong Hua Li United States	15	684 1.2×	781 1.5×	51 0.2×	138 0.7×	540 5.0×	16	1.6k
T. Bienvenu France	12	519 0.9×	556 1.0×	88 0.3×	34 0.2×	47 0.4×	29	1.0k
Gökhan Uyanık Germany	17	424 0.8×	731 1.4×	37 0.1×	61 0.3×	61 0.6×	42	1.2k
Mark Bieda United States	13	358 0.6×	980 1.8×	60 0.2×	58 0.3×	66 0.6×	22	1.3k
Rocío G. Urdinguio Spain	19	486 0.9×	1.3k 2.4×	39 0.1×	39 0.2×	126 1.2×	33	1.6k
Gladys Ho Australia	19	855 1.6×	778 1.4×	66 0.2×	35 0.2×	51 0.5×	43	1.4k
Alexandra Afenjar France	16	621 1.1×	521 1.0×	38 0.1×	22 0.1×	55 0.5×	42	1.0k
Muhammad Mahajnah Israel	16	281 0.5×	391 0.7×	56 0.2×	25 0.1×	47 0.4×	55	831
Katrin Õunap Estonia	25	857 1.6×	1.0k 1.9×	107 0.4×	14 0.1×	191 1.8×	106	1.8k

Countries citing papers authored by Edwin J. Young

Since Specialization

Citations

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

Fields of papers citing papers by Edwin J. Young

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edwin J. Young. 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 Edwin J. Young. The network helps show where Edwin J. Young may publish in the future.

Co-authorship network of co-authors of Edwin J. Young

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

All Works

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16 of 16 papers shown

Brown, Pierre Antoine, George S. Charames, Mathieu Lemaire, et al.. (2025). Framework for standardized genetic testing recommendations for chronic kidney disease in Ontario. Genetics in Medicine Open. 3. 103442–103442.

Shugar, Andrea, Anna Szuto, Miriam Weinstein, et al.. (2024). Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmenti. British Journal of Dermatology. 192(5). 933–935.

Young, Edwin J., Yesmino Elia, Esther Assor, et al.. (2021). Mild Idiopathic Infantile Hypercalcemia—Part 1: Biochemical and Genetic Findings. The Journal of Clinical Endocrinology & Metabolism. 106(10). 2915–2937. 13 indexed citations

Tsiplova, Kate, Richard M. Zur, Christian R. Marshall, et al.. (2017). A microcosting and cost–consequence analysis of clinical genomic testing strategies in autism spectrum disorder. Genetics in Medicine. 19(11). 1268–1275. 49 indexed citations

Uusküla-Reimand, Liis, Huayun Hou, Payman Samavarchi‐Tehrani, et al.. (2016). Topoisomerase II beta interacts with cohesin and CTCF at topological domain borders. Genome biology. 17(1). 182–182. 167 indexed citations

Wang, Liguo, Junsheng Chen, Chen Wang, et al.. (2014). MACE: model based analysis of ChIP-exo. Nucleic Acids Research. 42(20). e156–e156. 65 indexed citations

Mervis, Carolyn Β., Emily Lam, Edwin J. Young, et al.. (2012). Duplication of GTF2I Results in Separation Anxiety in Mice and Humans. The American Journal of Human Genetics. 90(6). 1064–1070. 57 indexed citations

Young, Edwin J., et al.. (2010). Enhanced prefrontal serotonin 5-HT1A currents in a mouse model of Williams-Beuren syndrome with low innate anxiety. Journal of Neurodevelopmental Disorders. 2(2). 99–108. 26 indexed citations

Young, Edwin J., Colleen A. Morris, Christian R. Marshall, et al.. (2008). The common inversion of the Williams–Beuren syndrome region at 7q11.23 does not cause clinical symptoms. American Journal of Medical Genetics Part A. 146A(14). 1797–1806. 18 indexed citations

10.

Young, Edwin J., Tatiana V. Lipina, Ariane Mandel, et al.. (2007). Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1‐targeted mice. Genes Brain & Behavior. 7(2). 224–234. 83 indexed citations

11.

Somerville, Martin J., Carolyn Β. Mervis, Edwin J. Young, et al.. (2005). Severe Expressive-Language Delay Related to Duplication of the Williams–Beuren Locus. New England Journal of Medicine. 353(16). 1694–1701. 209 indexed citations

12.

Lohi, Hannes, Edwin J. Young, Clare Rusbridge, et al.. (2005). Expanded Repeat in Canine Epilepsy. Science. 307(5706). 81–81. 137 indexed citations

13.

Ianzano, Leonarda, et al.. (2004). Loss of function of the cytoplasmic isoform of the protein laforin (EPM2A) causes Lafora progressive myoclonus epilepsy. Human Mutation. 23(2). 170–176. 32 indexed citations

14.

Chan, Elayne M., Edwin J. Young, Leonarda Ianzano, et al.. (2003). Mutations in NHLRC1 cause progressive myoclonus epilepsy. Nature Genetics. 35(2). 125–127. 236 indexed citations

15.

Minassian, Berge A., Danielle M. Andrade, Leonarda Ianzano, et al.. (2001). Laforin is a cell membrane and endoplasmic reticulum-associated protein tyrosine phosphatase. Annals of Neurology. 49(2). 271–275. 36 indexed citations

16.

Minassian, Berge A., Danielle M. Andrade, Leonarda Ianzano, et al.. (2001). Laforin is a cell membrane and endoplasmic reticulum–associated protein tyrosine phosphatase. Annals of Neurology. 49(2). 271–275. 4 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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