Justin D. Wagner

886 total citations
8 papers, 461 citations indexed

About

Justin D. Wagner is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Justin D. Wagner has authored 8 papers receiving a total of 461 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Epidemiology and 1 paper in Genetics. Recurrent topics in Justin D. Wagner's work include Glycosylation and Glycoproteins Research (1 paper), Down syndrome and intellectual disability research (1 paper) and RNA modifications and cancer (1 paper). Justin D. Wagner is often cited by papers focused on Glycosylation and Glycoproteins Research (1 paper), Down syndrome and intellectual disability research (1 paper) and RNA modifications and cancer (1 paper). Justin D. Wagner collaborates with scholars based in Canada, United States and Australia. Justin D. Wagner's co-authors include Martine Tétreault, David A. Dyment, Carolyn Ziegler, Steve Lin, Laurie J. Morrison, Clifton W. Callaway, Joseph Beyene, Prakesh S. Shah, William H. Gittens and Stéphanie Rey and has published in prestigious journals such as Nature, Human Molecular Genetics and Human Mutation.

In The Last Decade

Justin D. Wagner

8 papers receiving 458 citations

Peers

Countries citing papers authored by Justin D. Wagner

Since Specialization

Citations

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

Fields of papers citing papers by Justin D. Wagner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Justin D. Wagner. 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 Justin D. Wagner. The network helps show where Justin D. Wagner may publish in the future.

Co-authorship network of co-authors of Justin D. Wagner

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy 2017 ·Human Molecular Genetics ·Devon L. Johnstone, (unknown), Yoshiko Murakami, Kristin D. Kernohan, Martine Tétreault, (unknown), Asif Doja, Justin D. Wagner, Lijia Huang, Taila Hartley, Anik St‐Denis, Françoise Le Deist, Jacek Majewski, Dennis E. Bulman, Taroh Kinoshita, David A. Dyment, Kym M. Boycott, Philippe M. Campeau	33
2	Whole-transcriptome sequencing in blood provides a diagnosis of spinal muscular atrophy with progressive myoclonic epilepsy 2017 ·Human Mutation ·Kristin D. Kernohan, Laure Frésard, Zachary Zappala, Taila Hartley, Kevin S. Smith, Justin D. Wagner, Hongbin Xu, Arran McBride, Pierre R. Bourque, Steffany A. L. Bennett, David A. Dyment, Kym M. Boycott, Stephen B. Montgomery, Jodi Warman‐Chardon	20
3	XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia 2016 ·Nature ·Nícolas C. Hoch, Hana Hanzlíková, Stuart L. Rulten, Martine Tétreault, Emilia Komulainen, Limei Ju, P. Hornyak, Zhihong Zeng, William H. Gittens, Stéphanie Rey, Kevin Staras, Grazia M.S. Mancini, Peter J. McKinnon, Zhao‐Qi Wang, Justin D. Wagner, Grace Yoon, Keith W. Caldecott	197
4	Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature 2016 ·BMC Medical Genetics ·(unknown), Daniela Pohl, Erick Sell, Justin D. Wagner, David A. Dyment, Hussein Daoud	35
5	Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2 2015 ·Neuromuscular Disorders ·Justin D. Wagner, Lijia Huang, Martine Tétreault, Jacek Majewski, Kym M. Boycott, Dennis E. Bulman, David A. Dyment, Hugh J. McMillan	20
6	Homozygous mutations inMFN2cause multiple symmetric lipomatosis associated with neuropathy 2015 ·Human Molecular Genetics ·Sarah L. Sawyer, Andy Cheuk‐Him Ng, A. Micheil Innes, Justin D. Wagner, David A. Dyment, Martine Tétreault, Jacek Majewski, Kym M. Boycott, Robert A. Screaton, Garth A. Nicholson	57
7	Adrenaline for out-of-hospital cardiac arrest resuscitation: A systematic review and meta-analysis of randomized controlled trials 2014 ·Resuscitation ·Steve Lin, Clifton W. Callaway, Prakesh S. Shah, Justin D. Wagner, Joseph Beyene, Carolyn Ziegler, Laurie J. Morrison	97
8	Management of difficult airway problems with percutaneous transtracheal ventilation 1988 ·Journal of Oral and Maxillofacial Surgery ·Justin D. Wagner	2

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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