Edward Neilan

1.2k total citations
19 papers, 479 citations indexed

About

Edward Neilan is a scholar working on Molecular Biology, Genetics and Sociology and Political Science. According to data from OpenAlex, Edward Neilan has authored 19 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Sociology and Political Science. Recurrent topics in Edward Neilan's work include DNA Repair Mechanisms (4 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Edward Neilan is often cited by papers focused on DNA Repair Mechanisms (4 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Edward Neilan collaborates with scholars based in United States, Taiwan and United Kingdom. Edward Neilan's co-authors include Virginia Kimonis, Philip J. Brooks, Charles D. Smith, Michael Ranes, Aengus Stewart, Probir Chakravarty, Erin Fulchiero, Sarju Mehta, Giles D. Watts and Yuming Wang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Reviews Drug Discovery and Epilepsia.

In The Last Decade

Edward Neilan

18 papers receiving 468 citations

Peers

Countries citing papers authored by Edward Neilan

Since Specialization

Citations

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

Fields of papers citing papers by Edward Neilan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edward Neilan

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Changes in forced vital capacity over ≤ 13 years among patients with late-onset Pompe disease treated with alglucosidase alfa: new modeling of real-world data from the Pompe Registry 2024 ·Journal of Neurology ·Kenneth I. Berger, Yin‐Hsiu Chien, Alberto Dubrovsky, Priya S. Kishnani, Juan Clinton Llerena, Edward Neilan, Mark S. Roberts, Bun Sheng, Julie L. Batista, Magali Periquet, Kathryn M. Wilson, Ans T. van der Ploeg	5
2	The Bespoke Gene Therapy Consortium: facilitating development of AAV gene therapies for rare diseases 2024 ·Nature Reviews Drug Discovery ·Philip J. Brooks, Timothy M. Miller, Frédéric Revah, Junghae Suh, (unknown), (unknown), Timothy K. MacLachlan, Edward Neilan, (unknown), Sadik H. Kassim, (unknown), Joni L. Rutter	13
3	Alglucosidase alfa inhibitory antibodies and clinical correlates in treatment-naive late-onset Pompe disease patients in the late-onset treatment study (LOTS) over 78 weeks: A new post hoc analysis 2019 ·Molecular Genetics and Metabolism ·Vassili Valayannopoulos, Crystal Sung, Quanhong Lei, Meredith C. Foster, Kristina An Haack, (unknown), Christopher Hug, Edward Neilan, Nathan Thibault, Susan Sparks, Susan Richards	1
4	Two Cockayne Syndrome patients with a novel splice site mutation – clinical and metabolic analyses 2018 ·Mechanisms of Ageing and Development ·Inés Sánchez-Román, Sofie Lautrup, Maria D. Aamann, Edward Neilan, John R. Østergaard, Tinna Stevnsner	5
5	Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants 2016 ·JIMD Reports ·Sarah U. Morton, Edward Neilan, Roy W A Peake, Jiahai Shi, Klaus Schmitz‐Abe, Meghan C. Towne, Kyriacos Markianos, Sanjay P. Prabhu, Pankaj B. Agrawal	10
6	Increased oxidative phosphorylation in response to acute and chronic DNA damage 2016 ·PubMed ·Lear E. Brace, Sarah Vose, Kristopher J. Stanya, Rose M. Gathungu, Vasant R. Marur, Alban Longchamp, (unknown), Pedro Mejia, (unknown), Karen Inouye, Roderick T. Bronson, Chih‐Hao Lee, Edward Neilan, Bruce S. Kristal, James R. Mitchell	73
7	Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease 2014 ·Proceedings of the National Academy of Sciences ·Yuming Wang, Probir Chakravarty, Michael Ranes, Gavin Kelly, Philip J. Brooks, Edward Neilan, Aengus Stewart, Giampietro Schiavo, Jesper Q. Svejstrup	80
8	Management of a Woman With Maple Syrup Urine Disease During Pregnancy, Delivery, and Lactation 2014 ·Journal of Parenteral and Enteral Nutrition ·Ann Wessel, Kris M. Mogensen, Frances Rohr, Miriam Erick, Edward Neilan, (unknown), Harvey L. Levy, Kathryn J. Gray, Louise Wilkins‐Haug, Gerard T. Berry	14
9	Newborn Screening for Glutaric Aciduria-II: The New England Experience 2013 ·JIMD Reports ·Inderneel Sahai, Cheryl Garganta, Jeffrey A. Bailey, (unknown), Harvey L. Levy, (unknown), Edward Neilan, Chanika Phornphutkul, David A. Sweetser, (unknown), Roger B. Eaton	12
10	Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy 2012 ·Epilepsia ·Annapurna Poduri, (unknown), Edward Neilan, Princess C. Elhosary, Manju A. Kurian, Esther Meyer, Brenda J. Barry, Omar Khwaja, Mustafa A. Salih, Tommy Stödberg, Ingrid E. Scheffer, Eamonn R. Maher, Mustafa Şahin, Bai‐Lin Wu, Gerard T. Berry, Christopher A. Walsh, Jonathan Picker, Sanjeev V. Kothare	68
11	Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia 2008 ·American Journal of Medical Genetics Part A ·Virginia Kimonis, Sarju Mehta, Erin Fulchiero, Dana Thomasová, Marzia Pasquali, Kym M. Boycott, Edward Neilan, Alex Kartashov, Mark S. Forman, (unknown), (unknown), Steven Mumm, Michael P. Whyte, Charles D. Smith, Giles D. Watts	131
12	Response of Motor Complications in Cockayne Syndrome to Carbidopa-Levodopa 2008 ·Archives of Neurology ·Edward Neilan, Mauricio R. Delgado, (unknown), Sara Y. Kim, (unknown), Bai-Lin Wu, Peter B. Kang	16
13	Peters Anomaly in Association with Multiple Midline Anomalies and a Familial Chromosome 4 Inversion 2006 ·Ophthalmic Genetics ·Edward Neilan, Yana Pikman, Virginia Kimonis	12
14	Gene trap insertional mutagenesis in mice: New vectors and germ Line mutations in two novel genes 1999 ·Transgenic Research ·Edward Neilan, Gregory S. Barsh	2
15	Exposure of Taiwanese adolescents to pornographic media and its impact on sexual attitudes and behaviour 1999 ·Asian Journal of Communication ·Ven‐hwei Lo, Edward Neilan, (unknown), (unknown)	28
16	Television Coverage of the 1995 Legislative election in Taiwan 1998 ·Journal of Broadcasting & Electronic Media ·(unknown), Edward Neilan, (unknown), (unknown)	2
17	Television coverage of the 1995 legislative election in Taiwan: Rise of cable television as a force for balance in media coverage 1998 ·Journal of Broadcasting & Electronic Media ·Ven‐hwei Lo, Edward Neilan, (unknown)	5
18	Dateline Taipei: Foreign journalists’ coverage of Taiwan's first‐ever presidential election 1996 ·Asian Journal of Communication ·Edward Neilan, (unknown), Ven‐hwei Lo	1
19	The Future of the China Market. Prospects for Sino-American Trade. 1975 ·Pacific Affairs ·(unknown), Edward Neilan, (unknown)	1

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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