Caroline Vance

12.3k citations
42 papers · 4.9k · 1 hit paper · h-index 22

Impact in

  • Neurology top 0.1%
    • Amyotrophic Lateral Sclerosis Research
    • Parkinson's Disease Mechanisms and Treatments
    • Neurological diseases and metabolism
  • Genetics top 0.2%
    • Neurogenetic and Muscular Disorders Research

Papers in

  • Neurology 35
    • Amyotrophic Lateral Sclerosis Research 34
    • Neurological diseases and metabolism 11
    • Parkinson's Disease Mechanisms and Treatments 10
  • Genetics 18
    • Neurogenetic and Muscular Disorders Research 18
Co-authors
Christopher E. Shaw (31 shared papers)Boris Rogelj (10 shared papers)Ammar Al‐Chalabi (11 shared papers)Jemeen Sreedharan (4 shared papers)Christopher C.J. Miller (3 shared papers)Jacqueline de Belleroche (3 shared papers)Ian P. Blair (2 shared papers)Francisco E. Baralle (1 shared paper)
Journals
Neurobiology of Aging (8 papers)Acta Neuropathologica (3 papers)Acta Neuropathologica Communications (3 papers)Brain (3 papers)Human Molecular Genetics (2 papers)
Partner nations
United KingdomUnited StatesItaly

In The Last Decade

Caroline Vance

41 papers receiving 4.8k citations

Caroline Vance's Hit Papers

TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis 2008 · 2.1k citations
2.1k0+6+12Years since publication50010001.5k2.0k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 2008 Science

Peers

Caroline Vance
Comparison fields: 5 of 114
  • Neurology 3.6k
  • Genetics 2.0k
  • Neurology 758
  • Cellular and Molecular Neuroscience 567
  • Molecular Biology 2.1k
Replace Edor Kabashi with:
Edor Kabashi France
Kelly L. Williams Australia
Sandra Almeida United States
Jiou Wang United States
Haifeng Pu United States
Peter E.A. Ash United States
Karen Jansen‐West United States
Diane McKenna‐Yasek United States
Christopher J. Donnelly United States
Alan E. Renton United States
Caroline Vance relative to Edor Kabashi France Edor Kabashi's profile →
Citations per field
00.5×1.5×
Edor Kabashi · 1×
Citations per year

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-authors

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

20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#Work
1
TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
Science ·Jemeen Sreedharan, Ian P. Blair, Vineeta B. Tripathi, 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
Hit paper breakdown →		20082052
2
Hexanucleotide Repeats in ALS/FTD Form Length-Dependent RNA Foci, Sequester RNA Binding Proteins, and Are Neurotoxic
Cell Reports ·Youn‐Bok Lee, Han-Jou Chen, João Peres, Jorge Gomez-Deza, Jan Attig, Maja Štalekar, Claire Troakes, Agnes L. Nishimura, Emma L. Scotter, Caroline Vance, Yoshitsugu Adachi, Valentina Sardone, Jack W. Miller, Bradley Smith, Jean‐Marc Gallo, Jernej Ule, Frank Hirth, Boris Rogelj, Corinne Houart, Christopher E. Shaw
2013369
3
Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2–21.3
Brain ·Caroline Vance, Ammar Al‐Chalabi, Deborah Ruddy, Bradley Smith, Xun Hu, Jemeen Sreedharan, Teepu Siddique, Helenius J. Schelhaas, Benno Küsters, Dirk Troost, Frank Baas, Vianney de Jong, Christopher E. Shaw
2006269
4
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
2012212
5
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
2014212
6
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
2013198
7
Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase
Proceedings of the National Academy of Sciences ·John Mitchell, Praveen Paul, Han-Jou Chen, Alex Morris, Miles Payling, Mario Falchi, James Habgood, Stefania Panoutsou, Sabine Winkler, Veronica Tisato, Amin Hajitou, Bradley Smith, Caroline Vance, Christopher E. Shaw, Nicholas D. Mazarakis, Jacqueline de Belleroche
2010193
8
Carbon In N2 Fixation: Limitation Or Exquisite Adaptation
Annual Review of Plant Physiology and Plant Molecular Biology ·Caroline Vance
1991183
9
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
2011136
10
The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosis
Brain ·Han-Jou Chen, Jacqueline C. Mitchell, Sergey S. Novoselov, Jack W. Miller, Agnes L. Nishimura, Emma L. Scotter, Caroline Vance, Michael E. Cheetham, Christopher E. Shaw
2016132
11
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
2011105
12
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
201790
13
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, Karan Lund, Ammar Al‐Chalabi, Nicola Ticozzi, Vincenzo Silani, Peter C. Sapp, Robert H. Brown, John E. Landers, Safa Al‐Sarraj, Christopher E. Shaw
201484
14
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, Remy Constable, Eva So, Caroline Vance, Emma L. Scotter, Leanne Glover, Tibor Hortobágyi, Eveline S. Arnold, Shuo‐Chien Ling, Melissa McAlonis, Sandrine Da Cruz, Magda Polymenidou, Lino Tessarolo, Don W. Cleveland, Christopher E. Shaw
201583
15
Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice
Human Molecular Genetics ·Eva So, Jacqueline C. Mitchell, Caroline Memmi, George Chennell, Gema Vizcay‐Barrena, Leanne Allison, Christopher E. Shaw, Caroline Vance
201767
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
201162
17
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, Eelco Postumus Meyjes, Frank Baas, Vianney de Jong, Christopher E. Shaw
200356
18
Granule Localization of Glutaminase in Human Neutrophils and the Consequence of Glutamine Utilization for Neutrophil Activity
Journal of Biological Chemistry ·L M Castell, Caroline Vance, Rachel J.M. Abbott, Javier Márquez, Paul Eggleton
200445
19
Co-deposition of SOD1, TDP-43 and p62 proteinopathies in ALS: evidence for multifaceted pathways underlying neurodegeneration
Acta Neuropathologica Communications ·Benjamin G. Trist, Jennifer A. Fifita, Alison Hogan, Natalie Grima, Bradley Smith, Claire Troakes, Caroline Vance, Christopher E. Shaw, Safa Al‐Sarraj, Ian P. Blair, Kay L. Double
202236
20
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
201230

About Caroline Vance

Caroline Vance is a scholar working on Neurology, Genetics, Molecular Biology, Neurology and Physiology, having authored 42 papers that have together received 4.9k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (34 papers), Neurogenetic and Muscular Disorders Research (18 papers), Neurological diseases and metabolism (11 papers), Parkinson's Disease Mechanisms and Treatments (10 papers), Alzheimer's disease research and treatments (5 papers), Genetic Neurodegenerative Diseases (3 papers), RNA Research and Splicing (3 papers) and Prion Diseases and Protein Misfolding (3 papers). The work is most often cited by research in Neurology (3.6k citations), Genetics (2.0k citations), Neurology (758 citations), Cellular and Molecular Neuroscience (567 citations) and Molecular Biology (2.1k 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, Steven Ackerley and P. Nigel Leigh. Their work appears in journals such as Neurobiology of Aging, Acta Neuropathologica, Acta Neuropathologica Communications, 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

Breakdown of academic impact, for papers by Edor KabashiBreakdown of academic impact, for papers by Kelly L. WilliamsBreakdown of academic impact, for papers by Sandra AlmeidaBreakdown of academic impact, for papers by Jiou WangBreakdown of academic impact, for papers by Haifeng PuBreakdown of academic impact, for papers by Peter E.A. AshBreakdown of academic impact, for papers by Karen Jansen‐WestBreakdown of academic impact, for papers by Diane McKenna‐YasekBreakdown of academic impact, for papers by Christopher J. DonnellyBreakdown of academic impact, for papers by Alan E. Renton