Paul Gissen

14.3k total citations · 1 hit paper
146 papers, 4.6k citations indexed

About

Paul Gissen is a scholar working on Molecular Biology, Physiology and Rheumatology. According to data from OpenAlex, Paul Gissen has authored 146 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 54 papers in Physiology and 30 papers in Rheumatology. Recurrent topics in Paul Gissen's work include Lysosomal Storage Disorders Research (48 papers), Glycogen Storage Diseases and Myoclonus (23 papers) and Metabolism and Genetic Disorders (20 papers). Paul Gissen is often cited by papers focused on Lysosomal Storage Disorders Research (48 papers), Glycogen Storage Diseases and Myoclonus (23 papers) and Metabolism and Genetic Disorders (20 papers). Paul Gissen collaborates with scholars based in United Kingdom, United States and Germany. Paul Gissen's co-authors include Irwin M. Arias, Daniel Little, Manju A. Kurian, Michael J. Devine, Peter T. Clayton, Julien Baruteau, Simon Heales, Martin A. Smith, Eamonn R. Maher and Neil V. Morgan and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Paul Gissen

141 papers receiving 4.5k 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.

Study of Intraventricular Cerliponase Alfa for CLN2 Disease

2018 310 citations Paul Gissen et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Paul Gissen United Kingdom	36	1.9k	1.1k	614	588	585	146	4.6k
Miguel A. Martı́n Spain	42	3.8k 2.0×	985 0.9×	469 0.8×	378 0.6×	691 1.2×	238	6.4k
Gerard A. Lutty United States	60	4.4k 2.3×	779 0.7×	516 0.8×	332 0.6×	407 0.7×	170	10.8k
Maurizio Moggio Italy	44	4.4k 2.3×	883 0.8×	415 0.7×	335 0.6×	1.0k 1.7×	195	6.2k
Yoshikatsu Eto Japan	38	1.7k 0.9×	2.1k 1.9×	673 1.1×	429 0.7×	352 0.6×	225	4.5k
David S. Cassarino United States	29	2.1k 1.1×	776 0.7×	234 0.4×	277 0.5×	615 1.1×	147	4.4k
Hanna Mandel Israel	43	4.0k 2.1×	1.8k 1.5×	534 0.9×	502 0.9×	336 0.6×	176	7.4k
Mariarosa Anna Beatrice Melone Italy	35	1.7k 0.9×	605 0.5×	233 0.4×	233 0.4×	587 1.0×	132	3.5k
Ilsa I. Rovira United States	26	3.4k 1.8×	1.0k 0.9×	445 0.7×	560 1.0×	234 0.4×	33	5.9k
Jakob D. Wikström Sweden	27	4.1k 2.2×	1.5k 1.3×	669 1.1×	840 1.4×	265 0.5×	40	6.1k
Stephan Kemp Netherlands	38	6.3k 3.3×	1.5k 1.3×	237 0.4×	341 0.6×	515 0.9×	110	7.5k

Countries citing papers authored by Paul Gissen

Since Specialization

Citations

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

Fields of papers citing papers by Paul Gissen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Gissen

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Patterson, Marc C., Uma Ramaswami, Aimée Donald, et al.. (2025). Disease-Modifying, Neuroprotective Effect of N-Acetyl- l -Leucine in Adult and Pediatric Patients With Niemann-Pick Disease Type C. Neurology. 105(1). e213589–e213589.

Gissen, Paul, et al.. (2024). P28 A multi-partner approach to approving an innovative treatment. A21.1–A21.

Batzios, Spyros, Emma Footitt, Jonathan W. Mink, et al.. (2024). Evolution of Movement Disorders in Patients With CLN2-Batten Disease Treated With Enzyme Replacement Therapy. Neurology. 103(3). e209615–e209615. 3 indexed citations

Sudhakar, Sniya, Amanda Lam, Philippa B. Mills, et al.. (2024). Clinical Features, Biochemistry, Imaging, and Treatment Response in a Single-Center Cohort With Coenzyme Q ₁₀ Biosynthesis Disorders. Neurology Genetics. 10(6). e200209–e200209. 1 indexed citations

Touramanidou, Loukia, Sonam Gurung, Dany Perocheau, et al.. (2024). Macrophage Inhibitor Clodronate Enhances Liver Transduction of Lentiviral but Not Adeno-Associated Viral Vectors or mRNA Lipid Nanoparticles in Neonatal and Juvenile Mice. Cells. 13(23). 1979–1979. 1 indexed citations

Waddington, Simon N., William H. Peranteau, Ahad A. Rahim, et al.. (2023). Fetal gene therapy. Journal of Inherited Metabolic Disease. 47(1). 192–210. 14 indexed citations

Massaro, Giulia, Wenfei Liu, Simon N. Waddington, et al.. (2021). Gene Therapy for Lysosomal Storage Disorders: Ongoing Studies and Clinical Development. Biomolecules. 11(4). 611–611. 35 indexed citations

Forny, Patrick, Emma Footitt, James Davison, et al.. (2021). Diagnosing Mitochondrial Disorders Remains Challenging in the Omics Era. Neurology Genetics. 7(3). e597–e597. 16 indexed citations

Baruteau, Julien, Sharon C. Cunningham, Berna Şeker Yılmaz, et al.. (2021). Safety and efficacy of an engineered hepatotropic AAV gene therapy for ornithine transcarbamylase deficiency in cynomolgus monkeys. Molecular Therapy — Methods & Clinical Development. 23. 135–146. 23 indexed citations

10.

Perocheau, Dany, Loukia Touramanidou, Sonam Gurung, Paul Gissen, & Julien Baruteau. (2021). Clinical applications for exosomes: Are we there yet?. British Journal of Pharmacology. 178(12). 2375–2392. 96 indexed citations

11.

Brémovà-Ertl, Tatiana, Jens Claaßen, Jordi Gascón‐Bayarri, et al.. (2021). Efficacy and safety of N-acetyl-l-leucine in Niemann–Pick disease type C. Journal of Neurology. 269(3). 1651–1662. 30 indexed citations

12.

Yılmaz, Berna Şeker, Julien Baruteau, Rahimin Affandi Abdul Rahim, & Paul Gissen. (2020). Clinical and Molecular Features of Early Infantile Niemann Pick Type C Disease. International Journal of Molecular Sciences. 21(14). 5059–5059. 21 indexed citations

13.

Counsell, John R., et al.. (2020). Gene therapies targeting the liver. Journal of Hepatology. 74(1). 235–236. 11 indexed citations

14.

Baruteau, Julien, Stephanie Grünewald, Marta Zancolli, et al.. (2019). Urea Cycle Related Amino Acids Measured in Dried Bloodspots Enable Long-Term In Vivo Monitoring and Therapeutic Adjustment. Metabolites. 9(11). 275–275. 3 indexed citations

15.

Baruteau, Julien, Carmen Dı́ez-Fernández, Giusy Ranucci, et al.. (2019). Argininosuccinic aciduria: Recent pathophysiological insights and therapeutic prospects. Journal of Inherited Metabolic Disease. 42(6). 1147–1161. 26 indexed citations

16.

Little, Daniel, Christin Luft, Maëlle Lorvellec, et al.. (2018). A single cell high content assay detects mitochondrial dysfunction in iPSC-derived neurons with mutations in SNCA. Scientific Reports. 8(1). 9033–9033. 44 indexed citations

17.

Baruteau, Julien, Simon N. Waddington, Ian E. Alexander, & Paul Gissen. (2017). Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects. Journal of Inherited Metabolic Disease. 40(4). 497–517. 77 indexed citations

18.

Reid, Emma, Apostolos Papandreou, Suzanne Drury, et al.. (2016). Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. Brain. 139(11). 2844–2854. 27 indexed citations

19.

Sechi, Annalisa, et al.. (2012). INSULIN RESISTANCE AND DIABETES IN GLYCOGEN STORAGE DISEASE: PRESENTATION OF 5 CLINICAL CASES. UCL Discovery (University College London). 1 indexed citations

20.

Hartley, Jane, Nicholas C. Zachos, Ban B. Dawood, et al.. (2010). Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhea of Infancy). Gastroenterology. 138(7). 2388–2398.e2. 96 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.

Explore authors with similar magnitude of impact