ScholarIQanswers from OpenAlex & ORCID
Lucy R. Wedderburn
ResearcherPublications, citations & collaboration network
Lucy R. Wedderburn is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Lucy R. Wedderburn have?
ScholarIQindexed works
Lucy R. Wedderburn has 572 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Lucy R. Wedderburn have?
ScholarIQcitation count
Lucy R. Wedderburn has 20,820 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Lucy R. Wedderburn?
ScholarIQh-index
Lucy R. Wedderburn has an h-index of 72 in OpenAlex.
What is the i10-index of Lucy R. Wedderburn?
ScholarIQi10-index
Lucy R. Wedderburn has an i10-index of 203 in OpenAlex.
What is the ORCID of Lucy R. Wedderburn?
ScholarIQorcid
The ORCID for Lucy R. Wedderburn is on the source record.
What is the OpenAlex record for Lucy R. Wedderburn?
ScholarIQopenalex
The OpenAlex for Lucy R. Wedderburn is on the source record.
What are the most-cited papers on Lucy R. Wedderburn?
ScholarIQmost cited works
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis
Boston Children's JIA Registry, Anne Hinks, British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group, Childhood Arthritis Prospective Study (CAPS), Childhood Arthritis Response to Medication Study (CHARMS), German Society for Pediatric Rheumatology (GKJR), JIA Gene Expression Study, NIAMS JIA Genetic Registry, TREAT Study, Joanna Cobb, Miranda C. Marion, Sampath Prahalad, Marc Sudman, John Bowes, Paul Martin, Mary E. Comeau, Satria P. Sajuthi, Robert Andrews, Milton R. Brown, Wei‐Min Chen, Patrick Concannon, Panos Deloukas, Sarah Edkins, Stephen Eyre, Patrick M. Gaffney, Stephen L. Guthery, Joel M. Guthridge, Sarah Hunt, Judith A. James, Mehdi Keddache, Kathy L. Moser, Peter A. Nigrović, Suna Önengüt-Gümüşcü, Mitchell Onslow, Carlos D. Rosé, Stephen S. Rich, Kathryn J. A. Steel, Edward K. Wakeland, Carol A. Wallace, Lucy R. Wedderburn, Patricia Woo, John F. Bohnsack, Johannes‐Peter Haas, David N. Glass, Carl D. Langefeld, Wendy Thomson, Susan D. Thompson
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
Damian Smedley, Smedley, Damian, Katherine R. Smith, Martin, Antonio, Thomas, Ellen A, McDonagh, Ellen M, Cipriani, Valentina, Ellingford, Jamie M, Arno, Gavin, Tucci, Arianna, Vandrovcova, Jana, Chan, Georgia, Williams, Hywel J, Ratnaike, Thiloka, Wei, Wei, Stirrups, Kathleen, Ibanez, Kristina, Moutsianas, Loukas, Wielscher, Matthias, Need, Anna, Michael R. Barnes, Letizia Vestito, James Buchanan, Sarah Wordsworth, Sofie Ashford, Rehmström, Karola, Emily Li, Gavin Fuller, Philip Twiss, Olivera Spasić-Bošković, Halsall, Sally, Floto, R Andres, Kenneth Poole, Annette Wagner, Sarju Mehta, Mark Gurnell, Nigel Burrows, Roger James, Christopher J. Penkett, Eleanor Dewhurst, Stefan Gräf, Rutendo Mapeta, Mary Kasanicki, Andrea Haworth, Helen Savage, Melanie Babcock, Martin G. Reese, Mark Bale, Emma L. Baple, C. R. Boustred, Helen Brittain, Anna de Burca, Marta Bleda, A. Devereau, Dina Halai, Eik Haraldsdottir, Zerin Hyder, Dalia Kasperavičiūtė, Christine Patch, Dimitris Polychronopoulos, Angela Matchan, Răzvan Sultana, Mina Ryten, Ana Lisa Taylor Tavares, Carolyn Tregidgo, Clare Turnbull, M. J. Welland, S. M. Wood, Catherine Snow, Eleanor Williams, S. E. A. Leigh, Rebecca E. Foulger, Louise C. Daugherty, Olivia Niblock, Ivone Leong, Caroline F. Wright, Jim Davies, Charles Crichton, James Welch, Kerrie Woods, Lara Abulhoul, Paul Aurora, Detlef Böckenhauer, Alexander Broomfield, Maureen Cleary, Lam, Tanya, Mehul Dattani, Emma Footitt, Vijeya Ganesan, Stephanie Grünewald, Sandrine Compeyrot‐Lacassagne, Francesco Muntoni, Clarissa Pilkington, Rosaline C. M. Quinlivan, Nikhil Thapar, Colin Wallis, Lucy R. Wedderburn, Austen Worth, Teofila Bueser, Cecilia Compton
239th ENMC International Workshop: Classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018
Andrew L. Mammen, Andrew L. Mammen, Yves Allenbach, Werner Stenzel, Olivier Benveniste, Yves Allenbach, Olivier Benveniste, Jan De Bleecker, Olivier Boyer, Livia Casciola‐Rosen, Lisa Christopher‐Stine, Jan Damoiseaux, Cyril Gitiaux, Manabu Fujimoto, Janine A. Lamb, Océane Landon‐Cardinal, Ingrid E. Lundberg, Andrew Mammen, Andrew Mammen, Ichizo Nishino, Josefine Radke, Albert Selva-O’Callaghan, Werner Stenzel, Jiří Vencovský, Marianne de Visser, Guochun Wang, Lucy R. Wedderburn, Victoria P. Werth
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
Simon Rothwell, Robert G. Cooper, Ingrid E. Lundberg, Frederick W. Miller, Peter K. Gregersen, John Bowes, Jiří Vencovský, Katalin Dankó, Vidya Limaye, Albert Selva-O’Callaghan, Michael G. Hanna, Pedro Machado, Lauren M. Pachman, Ann M. Reed, Lisa G. Rider, Joanna Cobb, Hazel Platt, Øyvind Molberg, Olivier Benvéniste, Pernille Mathiesen, Timothy Radstake, Andrea Doria, Jan De Bleecker, Boél De Paepe, Britta Maurer, William Ollier, Leonid Padyukov, Terrance P. OʼHanlon, Annette Lee, Christopher I. Amos, Christian Gieger, Thomas Meitinger, Juliane Winkelmann, Lucy R. Wedderburn, Hector Chinoy, Janine A. Lamb