Alan E. Renton

15.5k citations

43 papers · 2.7k · 2 hit papers · h-index 20

Impact in

Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
Genetics top 1%
- Neurogenetic and Muscular Disorders Research

Papers in

Neurology 17
- Amyotrophic Lateral Sclerosis Research 12
- Parkinson's Disease Mechanisms and Treatments 7
Genetics 14
- Genetic Associations and Epidemiology 10
- Genomics and Rare Diseases 6
- Neurogenetic and Muscular Disorders Research 4

Co-authors: Bryan J. Traynor (13 shared papers)Adriano Chiò (3 shared papers)Nicholas Wood (5 shared papers)Hélène Plun‐Favreau (2 shared papers)L. Miguel Martins (2 shared papers)Alison Goate (16 shared papers)Edoardo Marcora (5 shared papers)Shea J. Andrews (3 shared papers)
Journals: Alzheimer s & Dementia (6 papers)Neurobiology of Aging (4 papers)Molecular Neurodegeneration (3 papers)Human Molecular Genetics (2 papers)Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring (2 papers)
Partner nations: United States United Kingdom Finland

In The Last Decade

Alan E. Renton

43 papers receiving 2.7k citations

Alan E. Renton's Hit Papers

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The complex genetic architecture of Alzheimer's disease: novel insights and future directions 2023 · 183 citations

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Countries citing papers authored by Alan E. Renton

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Citations

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Fields of papers citing papers by Alan E. Renton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alan E. Renton. 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 Alan E. Renton. The network helps show where Alan E. Renton may publish in the future.

Co-authors

The 25 scholars most cited alongside Alan E. Renton, 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 Alan E. Renton Line = papers co-authored together Alan E. Renton links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	State of play in amyotrophic lateral sclerosis genetics Nature Neuroscience ·Alan E. Renton, Adriano Chiò, Bryan J. Traynor Hit paper breakdown →	2013	1149
2	PINK1 cleavage at position A103 by the mitochondrial protease PARL Human Molecular Genetics ·Emma Deas, Hélène Plun‐Favreau, Sonia Gandhi, H. Desmond, (unknown), Samantha H. Y. Loh, Alan E. Renton, (unknown), Alexander J. Whitworth, L. Miguel Martins, Andrey Y. Abramov, Nicholas Wood	2010	400
3	The complex genetic architecture of Alzheimer's disease: novel insights and future directions EBioMedicine ·Shea J. Andrews, Alan E. Renton, Brian Fulton‐Howard, Anna Podlesny‐Drabiniok, Edoardo Marcora, Alison Goate Hit paper breakdown →	2023	183
4	Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress response Cell Death and Differentiation ·Nicoleta Moisoi, Kristina Klupsch, Valentina Fedele, Philip East, Sushant Sharma, Alan E. Renton, Hélène Plun‐Favreau, Richard Edwards, Peter Teismann, Mauro Degli Esposti, Alastair Morrison, Nicholas Wood, Julian Downward, L. Miguel Martins	2008	144
5	Genetic Variants of the α-Synuclein Gene SNCA Are Associated with Multiple System Atrophy PLoS ONE ·Ammar Al‐Chalabi, Alexandra Dürr, Nicholas Wood, Michael Parkinson, Agnès Camuzat, Jean‐Sébastien Hulot, Karen Morrison, Alan E. Renton, Sigurd D. Sussmuth, G. Bernhard Landwehrmeyer, Albert Ludolph, Yves Agid, Alexis Brice, P. Nigel Leigh, Gilbert Bensimon, (unknown)	2009	142
6	The RNA-binding motif 45 (RBM45) protein accumulates in inclusion bodies in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP) patients Acta Neuropathologica ·Mahlon Collins, David Riascos, Tina Kovalik, Jiyan An, Kelly Krupa, Kristin Krupa, Brian L. Hood, Thomas P. Conrads, Alan E. Renton, Bryan J. Traynor, Robert Bowser	2012	64
7	GroupICA dual regression analysis of resting state networks in a behavioral variant of frontotemporal dementia Frontiers in Human Neuroscience ·Riikka Rytty, Juha Nikkinen, Liisa Paavola, Ahmed Abou Elseoud, Virpi Moilanen, Annina Visuri, Osmo Tervonen, Alan E. Renton, Bryan J. Traynor, Vesa Kiviniemi, Anne M. Remes	2013	60
8	Differential DJ-1 gene expression in Parkinson's disease Neurobiology of Disease ·Ravindran Kumaran, Jana Vandrovcová, Connie Luk, Simone Sharma, Alan E. Renton, Nicholas Wood, John Hardy, Andrew J. Lees, Rina Bandopadhyay	2009	43
9	ALS/FTD phenotype in two Sardinian families carrying bothC9ORF72andTARDBPmutations Journal of Neurology Neurosurgery & Psychiatry ·Adriano Chiò, Gabriella Restagno, Maura Brunetti, Irene Ossola, Andrea Calvo, Antonio Canosa, Cristina Moglia, Gianluca Floris, Paolo Tacconi, Francesco Marrosu, Maria Giovanna Marrosu, Maria Rita Murru, Elisa Majounie, Alan E. Renton, Yvegeniya Abramzon, Maura Pugliatti, Maria Alessandra Sotgiu, Bryan J. Traynor, Giuseppe Borghero	2012	42
10	OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes Neurology ·Orly Goldstein, Omri Nayshool, Beatrice Nefussy, Bryan J. Traynor, Alan E. Renton, Mali Gana‐Weisz, Vivian E. Drory, Avi Orr‐Urtreger	2016	38
11	LRRK2 expression in idiopathic and G2019S positive Parkinson's disease subjects: a morphological and quantitative study Neuropathology and Applied Neurobiology ·Simone Sharma, Rina Bandopadhyay, Tammaryn Lashley, Alan E. Renton, Ann E. Kingsbury, Ravindran Kumaran, Constantinos Kallis, Carles Vilariño‐Güell, S. S. O'Sullivan, Andrew J. Lees, Tamás Révész, Nicholas Wood, Janice L. Holton	2011	35
12	Large C9orf72 repeat expansions are not a common cause of Parkinson's disease Neurobiology of Aging ·Elisa Majounie, Yevgeniya Abramzon, Alan E. Renton, Margaux F. Keller, Bryan J. Traynor, Andrew Singleton	2012	35
13	Hippocampal sclerosis dementia with the C9ORF72 hexanucleotide repeat expansion Neurobiology of Aging ·Olga Pletniková, Kelly L. Sloane, Alan E. Renton, Bryan J. Traynor, Barbara J. Crain, Tammy Reid, Tao Zu, Laura P.W. Ranum, Juan C. Troncoso, Peter V. Rabins, Chiadi U. Onyike	2014	35
14	Melatonin receptor type 1A gene linked to Alzheimer’s disease in old age SLEEP ·Sonja Sulkava, Pranuthi Muggalla, Raimo Sulkava, Hanna M. Ollila, Terhi Peuralinna, Liisa Myllykangas, Karri Kaivola, David J. Stone, Bryan J. Traynor, Alan E. Renton, Alberto Rivera, Seppo Helisalmi, Hilkka Soininen, Tuomo Polvikoski, Mikko Hiltunen, Pentti J. Tienari, Henri J. Huttunen, Tiina Paunio	2018	32
15	Clinical Characteristics of C9ORF72-Linked Frontotemporal Lobar Degeneration Dementia and Geriatric Cognitive Disorders Extra ·Anna-Lotta Kaivorinne, Michaela K. Bode, Liisa Paavola, Hannu Tuominen, Mika Kallio, Alan E. Renton, Bryan Traynor, Virpi Moilanen, Anne M. Remes	2013	27
16	Effect of APOE and a polygenic risk score on incident dementia and cognitive decline in a healthy older population Aging Cell ·Moeen Riaz, Aamira Huq, Joanne Ryan, Suzanne G. Orchard, Jane Tiller, Jessica E. Lockery, Robyn L. Woods, Rory Wolfe, Alan E. Renton, Alison Goate, Robert Sebra, Eric E. Schadt, Amy Brodtmann, Raj C. Shah, Elsdon Storey, Anne M. Murray, John J. McNeil, Paul Lacaze	2021	24
17	Beyond association: successes and challenges in linking non-coding genetic variation to functional consequences that modulate Alzheimer’s disease risk Molecular Neurodegeneration ·Gloriia Novikova, Shea J. Andrews, Alan E. Renton, Edoardo Marcora	2021	24
18	17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes Molecular Neurodegeneration ·Kathryn R. Bowles, Derian A. Pugh, Yiyuan Liu, Tulsi Patel, Alan E. Renton, Sara Bandrés‐Ciga, Ziv Gan‐Or, Peter Heutink, Ari Siitonen, Sarah Bertelsen, Jonathan D. Cherry, Celeste M. Karch, Steven J. Frucht, Brian H. Kopell, Inga Peter, Y. J. Park, Alexander W. Charney, Towfique Raj, John F. Crary, Alison Goate	2022	23
19	Functional annotation of genomic variants in studies of late-onset Alzheimer’s disease Bioinformatics ·Mariusz Butkiewicz, Elizabeth Blue, Yuk Yee Leung, Xueqiu Jian, Edoardo Marcora, Alan E. Renton, Amanda B Kuzma, Li-San Wang, Daniel C. Koboldt, Jonathan L. Haines, William S. Bush	2018	20
20	C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten Human Molecular Genetics ·Matthew J. Stopford, Adrian Higginbottom, Guillaume M. Hautbergue, Johnathan Cooper‐Knock, Pádraig J. Mulcahy, Kurt J. De Vos, Alan E. Renton, Hannah A. Pliner, Andrea Calvo, Adriano Chiò, Bryan J. Traynor, Mimoun Azzouz, Paul R. Heath, Janine Kirby, Pamela J. Shaw	2017	20

About Alan E. Renton

Alan E. Renton is a scholar working on Neurology, Genetics, Molecular Biology, Physiology and Genetics, having authored 43 papers that have together received 2.7k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (12 papers), Genetic Associations and Epidemiology (10 papers), Alzheimer's disease research and treatments (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers), Genomics and Rare Diseases (6 papers), Neurogenetic and Muscular Disorders Research (4 papers), Dementia and Cognitive Impairment Research (4 papers) and Bioinformatics and Genomic Networks (4 papers). The work is most often cited by research in Neurology (1.6k citations), Genetics (638 citations), Neurology (482 citations), Cellular and Molecular Neuroscience (344 citations) and Physiology (440 citations). Alan E. Renton has collaborated with scholars based in United States, United Kingdom and Finland. Frequent co-authors include Bryan J. Traynor, Adriano Chiò, Nicholas Wood, Hélène Plun‐Favreau, L. Miguel Martins, Alison Goate, Edoardo Marcora, Shea J. Andrews, Samantha H. Y. Loh and Sonia Gandhi. Their work appears in journals such as Alzheimer s & Dementia, Neurobiology of Aging, Molecular Neurodegeneration, Human Molecular Genetics and Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring.

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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Alan E. Renton

Alan E. Renton's Hit Papers

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