ScholarIQanswers from OpenAlex
Cardiff and Vale University Health Board
InstitutionResearch output, impact & collaborations
Cardiff and Vale University Health Board is a institution indexed in ScholarIQ from OpenAlex.
What is known about Cardiff and Vale University Health Board?
ScholarIQrecord summary
Cardiff and Vale University Health Board is a research organisation in Cardiff, GB. OpenAlex records 4,034 works and 178,800 citations for it. 1,495 researchers list it as their most recent affiliation.
How many works does Cardiff and Vale University Health Board have?
ScholarIQindexed works
Cardiff and Vale University Health Board has 4,034 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Cardiff and Vale University Health Board have?
ScholarIQcitation count
Cardiff and Vale University Health Board has 178,800 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Cardiff and Vale University Health Board?
ScholarIQresearcher count
Cardiff and Vale University Health Board has 1,495 researchers in the ScholarIQ index.
What is the average h-index at Cardiff and Vale University Health Board?
ScholarIQavg h-index
Cardiff and Vale University Health Board has an average h-index of 46.3 in OpenAlex.
What is the ROR of Cardiff and Vale University Health Board?
ScholarIQror
The ROR for Cardiff and Vale University Health Board is on the source record.
What is the OpenAlex record for Cardiff and Vale University Health Board?
ScholarIQopenalex
The OpenAlex for Cardiff and Vale University Health Board is on the source record.
What is the Wikidata of Cardiff and Vale University Health Board?
ScholarIQwikidata
The Wikidata for Cardiff and Vale University Health Board is on the source record.
Who are the most-cited researchers behind Cardiff and Vale University Health Board?
ScholarIQtop researchers by citations
What are the most-cited papers on Cardiff and Vale University Health Board?
ScholarIQmost cited works
Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
Manuela Neumann, Deepak M. Sampathu, Linda K. Kwong, Adam C. Truax, Matthew C. Micsenyi, Thomas T. Chou, Jennifer Bruce, Theresa Schuck, Murray Grossman, Christopher M. Clark, Leo McCluskey, Bruce L. Miller, Eliezer Masliah, Ian R. Mackenzie, Howard Feldman, W. Feiden, Hans A. Kretzschmar, John Q. Trojanowski, Virginia M.‐Y. Lee
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie, Alan E. Renton, Kin Y. Mok, Elise G.P. Dopper, Adrian J. Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simón‐Sánchez, John C. van Swieten, Yevgeniya Abramzon, Janel O. Johnson, Michael Sendtner, Roger Pamphlett, Richard W. Orrell, Simon Mead, Katie Sidle, Henry Houlden, Jonathan D. Rohrer, Karen Morrison, Hardev Pall, Kevin Talbot, Olaf Ansorge, Dena G. Hernandez, Sampath Arepalli, Mario Sabatelli, Gabriele Mora, Massimo Corbo, Fabio Giannini, Andrea Calvo, Elisabet Englund, Giuseppe Borghero, Gianluca Floris, Anne M. Remes, Hannu Laaksovirta, Leo McCluskey, John Q. Trojanowski, Vivianna M. Van Deerlin, Gerard D. Schellenberg, Michael A. Nalls, Vivian E. Drory, Chin‐Song Lu, Tu‐Hsueh Yeh, Hiroyuki Ishiura, Yuji Takahashi, Shoji Tsuji, Isabelle Le Ber, Alexis Brice, Carsten Drepper, Nigel Williams, Janine Kirby, Pamela J. Shaw, John Hardy, Pentti J. Tienari, Peter Heutink, Huw R. Morris, Stuart Pickering‐Brown, Bryan J. Traynor
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
Janel O. Johnson, Jessica Mandrioli, Michael Benatar, Yevgeniya Abramzon, Vivianna M. Van Deerlin, John Q. Trojanowski, J. Raphael Gibbs, Maura Brunetti, Susan Gronka, Joanne Wuu, Jinhui Ding, Leo McCluskey, Maria Martinez‐Lage, Dana Falcone, Dena Hernández, Sampath Arepalli, Sean Chong, Jennifer C. Schymick, Jeffrey D. Rothstein, Francesco Landi, Yong-Dong Wang, Andrea Calvo, Gabriele Mora, Mario Sabatelli, Maria Rosaria Monsurrò, Stefania Battistini, Fabrizio Salvi, Rossella Spataro, Patrizia Sola, Giuseppe Borghero, Giuliana Galassi, Sonja W. Scholz, J. Paul Taylor, Gabriella Restagno, Adriano Chiò, Bryan J. Traynor
Stages of pTDP‐43 pathology in amyotrophic lateral sclerosis
Johannes Brettschneider, Kelly Del Tredici, Jon B. Toledo, John Robinson, David J. Irwin, Murray Grossman, EunRan Suh, Vivianna M. Van Deerlin, Elisabeth McCarty Wood, Young Min Baek, Linda K. Kwong, Edward B. Lee, Lauren Elman, Leo McCluskey, Lubin Fang, Simone Feldengut, Albert C. Ludolph, Virginia M.‐Y. Lee, Heiko Braak, John Q. Trojanowski
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli, Brittany N. Lasseigne, Slavé Petrovski, Peter C. Sapp, Patrick A. Dion, Claire S. Leblond, Julien Couthouis, Yifan Lu, Quanli Wang, Brian J. Krueger, Zhong Ren, Jonathan Keebler, Yujun Han, Shawn Levy, Braden Boone, Jack R. Wimbish, Lindsay L. Waite, Angela L. Jones, John P. Carulli, Kelly L. Williams, John F. Staropoli, Winnie Xin, Alessandra Chesi, Alya R. Raphael, Diane McKenna‐Yasek, Janet Cady, J.M.B.V. de Jong, Kevin P. Kenna, Bradley Smith, Simon Topp, Jack W. Miller, Soragia Athina Gkazi, Ammar Al‐Chalabi, Leonard H. van den Berg, Jan H. Veldink, Vincenzo Silani, Nicola Ticozzi, Christopher E. Shaw, Robert H. Baloh, Stanley H. Appel, Ericka Simpson, Clotilde Lagier‐Tourenne, Stefan M. Pulst, Summer Gibson, John Q. Trojanowski, Lauren Elman, Leo McCluskey, Murray Grossman, Neil A. Shneider, Wendy K. Chung, John Ravits, Jonathan D. Glass, Katherine B. Sims, Vivianna M. Van Deerlin, Tom Maniatis, Sebastian Hayes, Alban Ordureau, Sharan Swarup, John E. Landers, Frank Baas, Andrew S. Allen, Richard Bedlack, J. Wade Harper, Aaron D. Gitler, Guy A. Rouleau, Robert H. Brown, Matthew B. Harms, Gregory M. Cooper, Tim Harris, R Myers, David B. Goldstein
How much of the research on Cardiff and Vale University Health Board is open access?
ScholarIQopen access share
67%OPEN ACCESS