Caroline Vance

12.3k citations

41 papers · 4.8k indexed · 1 hit paper · h-index 22

Neurology top 0.1%
- Amyotrophic Lateral Sclerosis Research 33
- Neurological diseases and metabolism 12
- Parkinson's Disease Mechanisms and Treatments 10
Genetics top 0.2%
- Neurogenetic and Muscular Disorders Research 21
Neurology top 1%
- Amyotrophic Lateral Sclerosis Research 33
- Neurological diseases and metabolism 12
- Parkinson's Disease Mechanisms and Treatments 10
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 3
Molecular Biology top 5%
- Prion Diseases and Protein Misfolding 4
- RNA Research and Splicing 3
Physiology
- Alzheimer's disease research and treatments 5

Co-authors: Christopher E. Shaw Boris Rogelj Ammar Al‐Chalabi Jemeen Sreedharan Christopher C.J. Miller Jacqueline de Belleroche Ian P. Blair Francisco E. Baralle
Cited by: Neurology Genetics
Journals: Neurobiology of Aging (8 papers)Acta Neuropathologica Communications (3 papers)Acta Neuropathologica (3 papers)
Partner nations: United Kingdom United States Italy

In The Last Decade

Caroline Vance

39 papers receiving 4.8k citations

Hit Papers

align trajectories log scale

Peers

Countries citing papers authored by Caroline Vance

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Vance

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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

20 of 20 papers shown

#	Work
1	Targeting lipid droplets in FUS-linked amyotrophic lateral sclerosis mitigates neuronal and astrocytic lipotoxicity Brain ·Laetitia Marcadet,李少钰,S.V. Gaidash,唐博,Cheng Zhan,Оксана Гумінська,Gambo,John W. Kennedy,Claire Troakes,Caroline Vance,Jorge Soliz,Heather D. Durham,Liang Li,Paul A. Dutchak,Chantelle F. Sephton	2025	0
2	A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay Neurobiology of Aging ·Marc Gotkine,Martina de Majo,Chun Hao Wong,Simon Topp,Rachel Michaelson‐Cohen,Silvina Epsztejn‐Litman,Rachel Eiges,Juan D. Jiménez,Moien Kanaan,Febi Iswandi,英仁遠藤,Caroline Vance,Stephen Newhouse,Gerome Breen,Agnes L. Nishimura,Christopher E. Shaw,Bradley Smith	2021	5
3	Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia Neurobiology of Aging ·Soragia Athina Gkazi,Claire Troakes,Simon Topp,Jack W. Miller,Caroline Vance,Jemeen Sreedharan,Ammar Al‐Chalabi,Janine Kirby,Pamela J. Shaw,Safa Al‐Sarraj,Andrew King,Bradley Smith,Christopher E. Shaw	2018	15
4	Review: Modelling the pathology and behaviour of frontotemporal dementia Neuropathology and Applied Neurobiology ·Bautista-Ávila Mirandeli,Jacqueline C. Mitchell,Xiaoqing Wang,Caroline Vance,Sarah Mizielinska	2018	12
5	Amyotrophic lateral sclerosis-like superoxide dismutase 1 proteinopathy is associated with neuronal loss in Parkinson’s disease brain Acta Neuropathologica ·Benjamin G. Trist,Katherine M. Davies,Veronica Cottam,Sian Genoud,Richard Ortega,Stéphane Roudeau,Asunción Carmona,Kasun De Silva,Valerie C. Wasinger,Simon J.G. Lewis,Perminder S. Sachdev,Bradley Smith,Claire Troakes,Caroline Vance,Christopher E. Shaw,Safa Al‐Sarraj,Helen J. Ball,Glenda M. Halliday,Dominic J. Hare,Kay L. Double	2017	85
6	The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients Neurobiology of Aging ·Chun Hao Wong,Simon Topp,Soragia Athina Gkazi,Claire Troakes,Jack W. Miller,Martina de Majo,Janine Kirby,Pamela J. Shaw,Karen Morrison,Jacqueline de Belleroche,Caroline Vance,Ammar Al‐Chalabi,Safa Al‐Sarraj,Christopher E. Shaw,Bradley Smith	2015	14
7	Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS Acta Neuropathologica Communications ·Jacqueline C. Mitchell,Enrique García Torija,Sejal Naik,Caroline Vance,Emma L. Scotter,Leanne Glover,Tibor Hortobágyi,G. Bruno,Shuo‐Chien Ling,巌野沢,Sandrine Da Cruz,Arianne Alves COSTA,Krzysztof Kinowski,Don W. Cleveland,Christopher E. Shaw	2015	78
8	Novel mutations support a role for Profilin 1 in the pathogenesis of ALS Neurobiology of Aging ·Bradley Smith,Caroline Vance,Emma L. Scotter,Claire Troakes,Chun Hao Wong,Simon Topp,Satomi Maekawa,Andrew King,Jacqueline C. Mitchell,张翠玉,Ammar Al‐Chalabi,Nicola Ticozzi,Vincenzo Silani,Peter C. Sapp,Robert H. Brown,John E. Landers,Safa Al‐Sarraj,Christopher E. Shaw	2014	81
9	Differential roles of the ubiquitin proteasome system (UPS) and autophagy in the clearance of soluble and aggregated TDP-43 species Journal of Cell Science ·Emma L. Scotter,Caroline Vance,Agnes L. Nishimura,Youn‐Bok Lee,Han-Jou Chen,Hazel Urwin,Valentina Sardone,Jacqueline C. Mitchell,Boris Rogelj,David C. Rubinsztein,Christopher E. Shaw	2014	211
10	Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population Neurobiology of Aging ·Soocheon Jang,Blaž Koritnik,Lea Leonardis,Leja Dolenc‐Grošelj,Janez Zidar,Bradley Smith,Caroline Vance,Christopher E. Shaw,Boris Rogelj,Damjan Glavač,Metka Ravnik‐Glavač	2014	13
11	ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules Human Molecular Genetics ·Caroline Vance,Emma L. Scotter,Agnes L. Nishimura,Claire Troakes,Jacqueline C. Mitchell,Claudia Kathe,Hazel Urwin,Catherine Manser,Christopher C.J. Miller,Tibor Hortobágyi,Mike Dragunow,Boris Rogelj,Christopher E. Shaw	2013	191
12	Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patients Neurobiology of Aging ·Jack W. Miller,Bradley Smith,Simon Topp,Ammar Al‐Chalabi,Christopher E. Shaw,Caroline Vance	2012	16
13	Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion Acta Neuropathologica ·Jacqueline C. Mitchell,Philip McGoldrick,Caroline Vance,Tibor Hortobágyi,Jemeen Sreedharan,Boris Rogelj,Elizabeth L. Tudor,Bradley Smith,Christian Klasen,Christopher C.J. Miller,Jonathan D. Cooper,Linda Greensmith,Christopher E. Shaw	2012	204
14	Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis‐FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS inclusions Neuropathology and Applied Neurobiology ·Claire Troakes,Tibor Hortobágyi,Caroline Vance,Safa Al‐Sarraj,Boris Rogelj,Christopher E. Shaw	2012	30
15	Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Nicola Ticozzi,Caroline Vance,Aurélie Leclerc,Pamela Keagle,Jonathan D. Glass,D. McKenna‐Yasek,Peter C. Sapp,Vincenzo Silani,Daryl A. Bosco,Christopher E. Shaw,Robert H. Brown,John E. Landers	2011	136
16	Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders Acta Neuropathologica ·Tibor Hortobágyi,Claire Troakes,Agnes L. Nishimura,Caroline Vance,John C. van Swieten,Harro Seelaar,Andrew King,Safa Al‐Sarraj,Boris Rogelj,Christopher E. Shaw	2011	62
17	An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62‐positive, TDP‐43‐negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline Neuropathology ·Claire Troakes,Satomi Maekawa,Lokesh Wijesekera,Boris Rogelj,László Siklós,Christopher Bell,Bradley Smith,Stephen Newhouse,Caroline Vance,Lauren Johnson,Tibor Hortobágyi,Aleksey Shatunov,Ammar Al‐Chalabi,Nigel Leigh,Christopher E. Shaw,Andrew King,Safa Al‐Sarraj	2011	105
18	Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra‐familial variability in age of onset and complex phenotype Clinical Genetics ·Bradley Smith,Steve Bevan,Caroline Vance,P. Renwick,Philip A. Wilkinson,Christos Proukakis,Ferdinando Squitieri,Alfredo Berardelli,Thomas T. Warner,Evan Reid,Christopher E. Shaw	2009	18
19	TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosisbreakdown → Science ·Jemeen Sreedharan,Ian P. Blair,Yu-bao CHEN,Xun Hu,Caroline Vance,Boris Rogelj,Steven Ackerley,Jennifer C. Durnall,Kelly L. Williams,Emanuele Buratti,Francisco E. Baralle,Jacqueline de Belleroche,John D. Mitchell,P. Nigel Leigh,Ammar Al‐Chalabi,Christopher C.J. Miller,Garth A. Nicholson,Christopher E. Shaw	2008	2037
20	Two Families with Familial Amyotrophic Lateral Sclerosis Are Linked to a Novel Locus on Chromosome 16q The American Journal of Human Genetics ·Deborah Ruddy,M. Parton,Ammar Al‐Chalabi,Cathryn M. Lewis,Caroline Vance,Bradley Smith,P. Nigel Leigh,John Powell,Teepu Siddique,Salwiah,Frank Baas,Vianney de Jong,Christopher E. Shaw	2003	56

About Caroline Vance

Caroline Vance is a scholar working on Neurology, Genetics and Neurology, having authored 41 papers that have together received 4.8k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (33 papers), Neurogenetic and Muscular Disorders Research (21 papers), Neurological diseases and metabolism (12 papers), Parkinson's Disease Mechanisms and Treatments (10 papers), Alzheimer's disease research and treatments (5 papers), Prion Diseases and Protein Misfolding (4 papers), Genetic Neurodegenerative Diseases (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Neurology (3.6k citations), Genetics (2.1k citations) and Neurology (836 citations). Caroline Vance has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Christopher E. Shaw, Boris Rogelj, Ammar Al‐Chalabi, Jemeen Sreedharan, Christopher C.J. Miller, Jacqueline de Belleroche, Ian P. Blair, Francisco E. Baralle, Kelly L. Williams and P. Nigel Leigh. Their work appears in journals such as Neurobiology of Aging, Acta Neuropathologica Communications, Acta Neuropathologica, Brain and Human Molecular Genetics.

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