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University Hospital Llandough

InstitutionResearch output, impact & collaborations

University Hospital Llandough is a institution indexed in ScholarIQ from OpenAlex.

What is known about University Hospital Llandough?

ScholarIQrecord summary

University Hospital Llandough is a research organisation in Penarth, GB. OpenAlex records 3,303 works and 234,683 citations for it. 648 researchers list it as their most recent affiliation.

How many works does University Hospital Llandough have?

ScholarIQindexed works

University Hospital Llandough has 3,303 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does University Hospital Llandough have?

ScholarIQcitation count

University Hospital Llandough has 234,683 citations in the OpenAlex counts ScholarIQ stores.

How many researchers are at University Hospital Llandough?

ScholarIQresearcher count

University Hospital Llandough has 648 researchers in the ScholarIQ index.

What is the average h-index at University Hospital Llandough?

ScholarIQavg h-index

University Hospital Llandough has an average h-index of 85 in OpenAlex.

What is the ROR of University Hospital Llandough?

ScholarIQror

The ROR for University Hospital Llandough is on the source record.

What is the OpenAlex record for University Hospital Llandough?

ScholarIQopenalex

The OpenAlex for University Hospital Llandough is on the source record.

Who are the most-cited researchers behind University Hospital Llandough?

ScholarIQtop researchers by citations
1
George Kirov · Genetic Associations and Epidemiology
527 works88,410 citations
2
Robert E. Mansel · Breast Cancer Treatment Studies
263 works16,795 citations

What are the most-cited papers on University Hospital Llandough?

ScholarIQmost cited works
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton, David G. Clayton, Lon R. Cardon, Nick Craddock, Panos Deloukas, Audrey Duncanson, Dominic Kwiatkowski, Mark I. McCarthy, Willem H. Ouwehand, Nilesh J. Samani, John A. Todd, Peter Donnelly, Jeffrey C. Barrett, Paul R. Burton, Dan Davison, Peter Donnelly, Doug Easton, David Evans, Hin-Tak Leung, Jonathan L. Marchini, Andrew P. Morris, Chris C. A. Spencer, Martin D. Tobin, Lon R. Cardon, David G. Clayton, Antony Attwood, James P. Boorman, Barbara Cant, Ursula Everson, Judith M. Hussey, Jennifer D. Jolley, Alexandra S. Knight, Kerstin Koch, Elizabeth Meech, Sarah Nutland, C V Prowse, Helen E. Stevens, Niall Taylor, Graham R. Walters, Neil M. Walker, Nicholas A. Watkins, Thilo Winzer, John A. Todd, Willem H. Ouwehand, 1958 Birth Cohort Controls, Richard W. Jones, Wendy L. McArdle, Susan M. Ring, David P. Strachan, Marcus Pembrey, Bipolar Disorder, Gerome Breen, David St Clair, Sian Caesar, Katherine Gordon‐Smith, Lisa Jones, Christine Fraser, Elaine Green, Detelina Grozeva, Marian L. Hamshere, Peter Holmans, Ian Jones, George Kirov, Valentina Moskvina, Ivan Nikolov, Michael O‘Donovan, Michael J. Owen, Nick Craddock, David Collier, Amanda Elkin, Anne Farmer, Richard Williamson, Peter McGuffin, Allan H. Young, I. Nicol Ferrier, Coronary Artery Disease, Stephen G. Ball, Anthony J. Balmforth, Jennifer H. Barrett, D. Timothy Bishop, Mark M. Iles, Azhar Maqbool, Nadira Yuldasheva, Alistair S. Hall, Peter S. Braund, Paul R. Burton, Richard J. Dixon, Massimo Mangino, Suzanne Stevens, Martin D. Tobin, J. Thompson, Nilesh J. Samani, Crohn’s Disease, Francesca Bredin, Mark Tremelling, Miles Parkes, Hazel E. Drummond, Charles W. Lees, Elaine R. Nimmo, Jack Satsangi
Nature. 20079,682 CitationsOPEN ACCESS
Genome-wide association study identifies five new schizophrenia loci
S Ripke, Pamela Sklar, Lizzy Rossin, Douglas M. Ruderfer, Sarah E. Bergen, Mark J Daly, Alan R Sanders, Jubao Duan, P V Gejman, Kenneth S Kendler, Brion S. Maher, Robert Ribble, B Riley, Brandon Wormley, Ayman Fanous, Douglas F Levinson, Madeline Alexander, Jeremy M Silverman, P Holmans, Nicholas Craddock, Sarah Dwyer, Lyudmila Georgieva, Marian Hamshere, George Kirov, Valentina Moskvina, Ivan Nikolov, Nadine Norton, Michael J Owen, Hywel Williams, Nia Williams, Stan Zammit, Michael C O'Donovan, Dan-Yu Lin, Roel A Ophoff, Eric Strengman, Rita M Cantor, Nelson B Freimer, Ole A Andreassen, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Edward Scolnick, S M Purcell, B M Neale, Sven Cichon, Manuel Mattheisen, Markus M Nöthen, David St. Clair, Aiden Corvin, Paul Cormican, Gary Donohoe, Michael Gill, Elaine Kenny, Derek W. Morris, C O'Dushlaine, E M Quinn, Hugh Gurling, Nicholas Bass, Khalid Choudhury, Susmita Datta, Robert Krasucki, Jacob Lawrence, Andrew McQuillin, Jonathan Pimm, Vinay Puri, Werge Tm, Duong Ls, Thomas Hansen, Andrés Ingason, K D Jakobsen, Line Olsen, H Kruuse Rasmussen, Johan H. Thygesen, D Rujescu, Marion Friedl, I Giegling, Annette M Hartmann, H Konnerth, Bettina Konte, Blackwood Dh, Alan Maclean, P. Malloy, Kevin A McGhee, Andrew McIntosh, C Pato, Michele T. Pato, Anil K Malhotra, Todd Lencz, Frank Dudbridge, P M Visscher, D Posthuma, Richard Amdur, H Stefansson, Stacy Steinberg, Kari Stefansson, Bryan Mowry, John J McGrath, Deborah A. Nertney, Vera Golimbet
Nature Genetics. 20111,961 CitationsOPEN ACCESS
Randomized Multicenter Trial of Sentinel Node Biopsy Versus Standard Axillary Treatment in Operable Breast Cancer: The ALMANAC Trial
Robert E. Mansel, Lesley Fallowfield, Mark Kissin, Amit Goyal, Robert G. Newcombe, J. Michael Dixon, Constantinos Yiangou, Kieran Horgan, Nigel Bundred, Ian Monypenny, David England, Mark Sibbering, Tholkifl I. Abdullah, Lester Barr, U Chetty, Dudley H. Sinnett, Anne Fleissig, Dayalan Clarke, Peter J. Ell
JNCI Journal of the National Cancer Institute. 20061,685 Citations
Rare chromosomal deletions and duplications increase risk of schizophrenia
Jennifer Stone, Douglas M. Ruderfer, Pamela Sklar, S M Purcell, Mark J. Daly, Edward M. Scolnick, Mark Daly, Kimberly Chambert, Joshua Korn, Steve McCarroll, Casey Gates, Stacey B. Gabriel, Scott Mahon, Kristen Ardlie, Michael C. O’Donovan, George Kirov, N Craddock, Michael J. Owen, Peter A. Holmans, Nia Williams, L. Georgieva, Ivan Nikolov, N. Norton, H. Williams, Hugh Gurling, Andrew McQuillin, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Vinay Puri, Robert Krasucki, Jacob Lawrence, N J Bass, Douglas H. R. Blackwood, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, AB MacLean, M. Van Beck, Aiden Corvin, M Gill, Derek W. Morris, Colm Ó'Dúshláine, Elaine Kenny, C M Hultman, Paul Lichtenstein, Emma F. Thelander, Carlos N. Pato, Michele T. Pato, Helena Medeiros, Celia Carvalho, A H Fanous, David Conti, James A. Knowles, David St Clair, Soh Leh Kwan, P F Sullivan, P F Sullivan, Stuart MacGregor, Peter M. Visscher, Draga Toncheva, Vihra Milanova, Waddington Jl, Srinivasa Thirumalai, Digby Quested, David Curtis, Caroline Crombie, Gillian Fraser, Nicholas Walker, Frank Middleton, Christopher Morley, Carlos Paz Ferreira, Antonio Macedo, M. Helena Azevedo
Nature. 20081,511 CitationsOPEN ACCESS
A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders.
David Collier, G. Stöber, Tao Li, Armin Heils, Marco Catalano, Daniela Di Bella, María J. Arranz, Robin Murray, Homero Vallada, Dietmar Bengel, C. R. Müller, G.W. Roberts, Enrico Smeraldi, George Kirov, Pak C. Sham, Klaus‐Peter Lesch
PubMed. 1996667 Citations

How much of the research on University Hospital Llandough is open access?

ScholarIQopen access share
67%OPEN ACCESS
Gold
0%
Green
17%
Hybrid
17%
Bronze
33%
Closed
33%

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