Glenn Anderson

3.4k citations

41 papers · 1.6k indexed · h-index 21

Impact in

Physiology top 5%
- Lysosomal Storage Disorders Research
- Diet and metabolism studies
- Calcium signaling and nucleotide metabolism
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders

Papers in

Physiology 17
- Lysosomal Storage Disorders Research 14
Cell Biology 6
- Cellular transport and secretion 5

Co-authors: Hans H. Goebel Alessandro Simonati Thomas S. Jacques Shamima Rahman Sara Mole J. Helen Cross Neil J. Sebire M. Malone
Journals: Neurology (3 papers)Brain (2 papers)Acta Neuropathologica (2 papers)European Journal of Paediatric Neurology (2 papers)Clinical Infectious Diseases (1 paper)
Partner nations: United Kingdom United States India

In The Last Decade

Glenn Anderson

39 papers receiving 1.6k citations

Peers

Countries citing papers authored by Glenn Anderson

Since Specialization

Citations

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

Fields of papers citing papers by Glenn Anderson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Glenn Anderson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Glenn Anderson Line = papers co-authored together Glenn Anderson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Maculopathy and adult‐onset ataxia in patients with biallelic MFSD8 variants Molecular Genetics & Genomic Medicine ·Sigurd Dobloug, Ulrika Kjellström, Glenn Anderson, Emily Gardner, Sara Mole, Jayesh Sheth, Andreas Puschmann	2024	2
2	Buffy Coat Score as a Biomarker of Treatment Response in Neuronal Ceroid Lipofuscinosis Type 2 Brain Sciences ·Siyamini Sivananthan, Laura Lee, Glenn Anderson, Barbara Csányi, Ruth Williams, Paul Gissen	2023	0
3	Sirtuin 5 depletion impairs mitochondrial function in human proximal tubular epithelial cells Scientific Reports ·Timo N. Haschler, Harry Horsley, Monika Bałys, Glenn Anderson, Jan‐Willem Taanman, Robert J. Unwin, Jill T. Norman	2021	30
4	Immunotherapy-responsive childhood neurodegeneration with systemic and central nervous system inflammation European Journal of Paediatric Neurology ·Mário Sá, Yael Hacohen, Lucy Alderson, W.K. Chong, Glenn Anderson, Thomas S. Jacques, David Neubauer, Elżbieta Szczepanik, Ming Lim, Marios Kaliakatsos	2018	1
5	Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis The Lancet Neurology ·Sara Mole, Glenn Anderson, Heather Band, Samuel F. Berkovic, Jonathan D. Cooper, Sophia-Martha kleine Holthaus, Tristan R. McKay, Diego L. Medina, Rahimin Affandi Abdul Rahim, Angela Schulz, Alexander J. Smith	2018	115
6	SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20 Human Molecular Genetics ·Dale Bryant, Yang Liu, Sanchari Datta, Hanaa Hariri, Marian Seda, Glenn Anderson, Emma Peskett, Charalambos Demetriou, Sérgio B. Sousa, Dagan Jenkins, Peter T. Clayton, Maria Bitner‐Glindzicz, Gudrun E. Moore, W. Mike Henne, Philip Stanier	2018	52
7	Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay Journal of Inherited Metabolic Disease ·Emma Reid, Hywel Williams, Glenn Anderson, Malika Benatti, Kling Chong, Chela James, Louise Ocaka, (unknown), Cheryl Hemingway, Daniel Little, Richard J. P. Brown, Alasdair Parker, Simon Holden, Emma Footitt, Shamima Rahman, Paul Gissen, Philippa B. Mills, Peter T. Clayton	2017	15
8	Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1 The Journal of Experimental Medicine ·Ariane Standing, Dessislava Malinova, Ying Hong, Julien Record, Dale Moulding, Michael P. Blundell, Karolin Nowak, Hannah E. Jones, Ebun Omoyinmi, Kimberly Gilmour, Alan Medlar, Horia Stanescu, Robert Kleta, Glenn Anderson, Sira Nanthapisal, Sónia Gomes, Nigel Klein, Despina Eleftheriou, Adrian J. Thrasher, Paul Brogan	2016	105
9	Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes Brain ·Emma Reid, Apostolos Papandreou, Suzanne Drury, C. R. Boustred, Wyatt W. Yue, Yehani Wedatilake, Clare Beesley, Thomas S. Jacques, Glenn Anderson, Lara Abulhoul, Alexander Broomfield, Maureen Cleary, Stephanie Grünewald, Sophia Varadkar, Nicholas Lench, Shamima Rahman, Paul Gissen, Peter T. Clayton, Philippa B. Mills	2016	27
10	The interaction of carbon nanotubes with an in vitro blood-brain barrier model and mouse brain in vivo Biomaterials ·Houmam Kafa, Julie Wang, Noelia Rubio, Kerrie Venner, Glenn Anderson, Elzbieta Pach, Belén Ballesteros, Jane E. Preston, N. Joan Abbott, Khuloud T. Al‐Jamal	2015	155
11	Pale Body-Like Inclusion Formation and Neurodegeneration following Depletion of 26S Proteasomes in Mouse Brain Neurones are Independent of α-Synuclein PLoS ONE ·Simon Paine, Glenn Anderson, Karen Bedford, Karen Lawler, R. John Mayer, James Lowe, Lynn Bedford	2013	25
12	Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem‐cell phenotype British Journal of Dermatology ·Veronica A. Kinsler, Glenn Anderson, B. Latimer, D. Natarajan, Eugene Healy, Gudrun E. Moore, Neil J. Sebire	2013	17
13	CLN6 disease caused by the same mutation originating in Pakistan has varying pathology European Journal of Paediatric Neurology ·Rita Guerreiro, José Brás, Mariana Vieira, Varun Warrier, Shakti Agrawal, Helen Stewart, Glenn Anderson, Sara Mole	2013	10
14	mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis Acta Neuropathologica ·Shireena A. Yasin, Abu M. Ali, Mathew Tata, Simon Picker, Glenn Anderson, Elizabeth C. Latimer‐Bowman, Sarah Leigh Nicholson, William Harkness, J. Helen Cross, Simon Paine, Thomas S. Jacques	2013	65
15	Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing European Journal of Human Genetics ·Mariacristina Scoto, Tom Cullup, Sebahattin Çırak, (unknown), (unknown), Long Feng, (unknown), Glenn Anderson, Stephen Abbs, (unknown), Heinz Jungbluth, Francesco Muntoni	2013	0
16	Human pathology in NCL Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Glenn Anderson, Hans H. Goebel, Alessandro Simonati	2012	158
17	Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell Acta Neuropathologica ·Shireena A. Yasin, K Latak, Francesca Becherini, Anita Ganapathi, Khadijah Miller, Oliver Campos, Simon Picker, Nelly Bier, Martin A. Smith, Maria Thom, Glenn Anderson, J. Helen Cross, William Harkness, Brian Harding, Thomas S. Jacques	2010	41
18	Electron Microscopy of Chorionic Villus Samples for Prenatal Diagnosis of Lysosomal Storage Disorders Ultrastructural Pathology ·Darren Fowler, Glenn Anderson, Ashok Vellodi, M. Malone, Neil J. Sebire	2007	16
19	Diagnosis of Neuronal Ceroid Lipofuscinosis (Batten Disease) by Electron Microscopy in Peripheral Blood Specimens Ultrastructural Pathology ·Glenn Anderson, V. V. Smith, Ivan Brooke, M. Malone, Neil J. Sebire	2006	11
20	Laryngeal candidiasis: A cause of airway obstruction in the immunocompromised child The Journal of Laryngology & Otology ·Edward Fisher, Aurelia Richards, Glenn Anderson, David Albert	1992	13

About Glenn Anderson

Glenn Anderson is a scholar working on Physiology, Physiology, Cell Biology, Epidemiology and Clinical Biochemistry, having authored 41 papers that have together received 1.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (14 papers), Mitochondrial Function and Pathology (5 papers), Autophagy in Disease and Therapy (5 papers), Cellular transport and secretion (5 papers), Carbohydrate Chemistry and Synthesis (4 papers), Hydraulic Fracturing and Reservoir Analysis (3 papers), Genetic and Kidney Cyst Diseases (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Physiology (644 citations), Physiology (103 citations), Clinical Biochemistry (148 citations), Cell Biology (307 citations) and Rheumatology (143 citations). Glenn Anderson has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Hans H. Goebel, Alessandro Simonati, Thomas S. Jacques, Shamima Rahman, Sara Mole, J. Helen Cross, Neil J. Sebire, M. Malone, Simon Paine and Houmam Kafa. Their work appears in journals such as Neurology, Brain, Acta Neuropathologica, European Journal of Paediatric Neurology and Clinical Infectious Diseases.

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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