ScholarIQanswers from OpenAlex & ORCID
Deborah J. Smyth
ResearcherPublications, citations & collaboration network
Deborah J. Smyth is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Deborah J. Smyth have?
ScholarIQindexed works
Deborah J. Smyth has 107 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Deborah J. Smyth have?
ScholarIQcitation count
Deborah J. Smyth has 18,836 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Deborah J. Smyth?
ScholarIQh-index
Deborah J. Smyth has an h-index of 55 in OpenAlex.
What is the i10-index of Deborah J. Smyth?
ScholarIQi10-index
Deborah J. Smyth has an i10-index of 82 in OpenAlex.
What is the OpenAlex record for Deborah J. Smyth?
ScholarIQopenalex
The OpenAlex for Deborah J. Smyth is on the source record.
What are the most-cited papers on Deborah J. Smyth?
ScholarIQmost cited works
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
Hironori Ueda, Joanna M. M. Howson, Laura Esposito, J. M. Heward, Snook, Giselle Chamberlain, Daniel B. Rainbow, Kara Hunter, Annabel N. Smith, Gianfranco Di Genova, Mathias Herr, Ingrid Dahlman, Felicity Payne, Deborah J. Smyth, Christopher Lowe, Rebecca C.J. Twells, Sarah Howlett, Barry Healy, Sarah Nutland, Helen Rance, Vin Everett, Luc J Smink, Alexander Lam, Heather J. Cordell, Neil Walker, Cristina Bordin, John S. Hulme, Costantino Motzo, Francesco Cucca, J. Fred Hess, Michael L. Metzker, Jane Rogers, Simon G. Gregory, Amit Allahabadia, Ratnasingam Nithiyananthan, Eva Tuomilehto‐Wolf, Jaakko Tuomilehto, Polly J. Bingley, Kathleen M. Gillespie, Dag E. Undlien, Kjersti S. Rønningen, Cristian Guja, C Ionescu-Tîrgovişte, David A. Savage, Alexander P. Maxwell, D. J. Carson, C. C. Patterson, Jayne A. Franklyn, David Clayton, Laurence B. Peterson, Linda S. Wicker, John A. Todd, Stephen Gough
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Thomas J. Wang, Feng Zhang, J. Brent Richards, Bryan Kestenbaum, Joyce B. J. van Meurs, Diane J. Berry, Douglas P. Kiel, Elizabeth A. Streeten, Claes Ohlsson, Daniel L. Koller, Leena Peltonen, Jason D. Cooper, Paul F. O’Reilly, Denise K. Houston, Nicole L. Glazer, Liesbeth Vandenput, Munro Peacock, Julia Shi, Fernando Rivadeneira, Mark I. McCarthy, Anneli Pouta, Ian H. de Boer, Massimo Mangino, Bernet Kato, Deborah J. Smyth, Sarah L. Booth, Paul F. Jacques, Greg Burke, Mark O. Goodarzi, Ching‐Lung Cheung, Myles Wolf, Kenneth Rice, David Goltzman, Nick Hidiroglou, Martin Ladouceur, Nicholas J. Wareham, Lynne J. Hocking, Deborah Hart, Nigel Arden, Cyrus Cooper, Suneil Malik, William D. Fraser, Anna-Liisa Hartikainen, Guangju Zhai, Helen M. Macdonald, Nita G. Forouhi, Ruth J. F. Loos, David M. Reid, Alan J. Hakim, Elaine Dennison, Ching‐Ti Liu, Chris Power, Helen E. Stevens, Laitinen Jaana, Ramachandran S. Vasan, Nicole Soranzo, Jörg Bojunga, Bruce M. Psaty, Mattias Lorentzon, Tatiana Foroud, Tamara B. Harris, Albert Hofman, John-Olov Jansson, Jane A. Cauley, André G. Uitterlinden, Quince Gibson, Marjo‐Riitta Järvelin, David Karasik, David S. Siscovick, Michael J. Econs, Stephen B. Kritchevsky, José C. Florez, John A. Todd, Josée Dupuis, Elina Hyppönen, Timothy D. Spector
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
Genetics of Type 1 Diabetes in Finland, John A. Todd, Neil Walker, Jason D. Cooper, Deborah J. Smyth, Kate Downes, Vincent Plagnol, Rebecca Bailey, Sergey Nejentsev, Sarah F. Field, Felicity Payne, Christopher E. Lowe, Jeffrey S. Szeszko, Jason P. Hafler, Lauren R Zeitels, Jennie H. M. Yang, Adrian Vella, Sarah Nutland, Helen E. Stevens, Helen Schuilenburg, Gillian Coleman, M Maisuria, William Meadows, Luc J Smink, Barry Healy, Oliver S. Burren, Alex A C Lam, Nigel Ovington, James E. Allen, Ellen Adlem, Hin-Tak Leung, Chris Wallace, Joanna M. M. Howson, Cristian Guja, C Ionescu-Tîrgovişte, Matthew J. Simmonds, J. M. Heward, Stephen Gough, David B. Dunger, Linda S. Wicker, David Clayton
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region
Deborah J. Smyth, Jason D. Cooper, Rebecca Bailey, Sarah Field, Oliver S. Burren, Luc J Smink, Cristian Guja, C Ionescu-Tîrgovişte, Barry Widmer, David B. Dunger, David A. Savage, Neil Walker, David Clayton, John A. Todd
Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage
Ivan L. Ângulo, Oscar Vadas, Fabien Garçon, Edward Banham-Hall, Vincent Plagnol, Timothy Ronan Leahy, Helen Baxendale, Tanya Coulter, James Curtis, Changxin Wu, Katherine G. Blake-Palmer, Olga Perišić, Deborah J. Smyth, Mailis Maes, Christine Fiddler, Jatinder K. Juss, Deirdre Cilliers, Gašper Markelj, Anita Chandra, George E. Farmer, Anna Kielkowska, Jonathan Clark, Sven Kracker, Marianne Debré, Capucine Pïcard, Isabelle Pellier, Nada Jabado, James Morris, Gabriela Barcenas‐Morales, Alain Fischer, Len Stephens, Phillip T. Hawkins, Jeffrey C. Barrett, Mario Abinun, Menna R. Clatworthy, Anne Durandy, Rainer Döffinger, Edwin R. Chilvers, Andrew J. Cant, Dinakantha Kumararatne, Klaus Okkenhaug, Roger Williams, Alison M. Condliffe, Sergey Nejentsev