ScholarIQanswers from OpenAlex & ORCID
Chris Wallace
ResearcherPublications, citations & collaboration network
Chris Wallace is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Chris Wallace have?
ScholarIQindexed works
Chris Wallace has 343 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Chris Wallace have?
ScholarIQcitation count
Chris Wallace has 43,356 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Chris Wallace?
ScholarIQh-index
Chris Wallace has an h-index of 64 in OpenAlex.
What is the i10-index of Chris Wallace?
ScholarIQi10-index
Chris Wallace has an i10-index of 137 in OpenAlex.
What is the ORCID of Chris Wallace?
ScholarIQorcid
The ORCID for Chris Wallace is on the source record.
What is the OpenAlex record for Chris Wallace?
ScholarIQopenalex
The OpenAlex for Chris Wallace is on the source record.
What are the most-cited papers on Chris Wallace?
ScholarIQmost cited works
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
Genome-wide association study identifies eight loci associated with blood pressure
Christopher Newton‐Cheh, Toby Johnson, Vesela Gateva, Martin D. Tobin, Murielle Bochud, Lachlan Coin, Samer S. Najjar, Jing Hua Zhao, Simon Heath, S. Eyheramendy, Konstantinos A. Papadakis, Benjamin F. Voight, Laura J. Scott, Feng Zhang, Martin Farrall, Toshiko Tanaka, Chris Wallace, John C. Chambers, Kay‐Tee Khaw, Peter M. Nilsson, Pim van der Harst, Silvia Polidoro, Diederick E. Grobbee, N. Charlotte Onland‐Moret, Michiel L. Bots, Louise V. Wain, Katherine S. Elliott, Alexander Teumer, Jian’an Luan, Gavin Lucas, Johanna Kuusisto, Paul R. Burton, David Hadley, Wendy L. McArdle, Morris Brown, Anna F. Dominiczak, Stephen Newhouse, Nilesh J. Samani, John Webster, Eleftheria Zeggini, J. Beckmann, Sven Bergmann, Noha Lim, Kijoung Song, Péter Vollenweider, Gérard Waeber, Dawn Waterworth, Xin Yuan, Leif Groop, Marju Orho‐Melander, Alessandra Allione, Alessandra Di Gregorio, Simonetta Guarrera, Salvatore Panico, Fulvio Ricceri, Valeria Romanazzi, Carlotta Sacerdote, Paolo Vineis, Inês Barroso, Manjinder S. Sandhu, Robert Luben, Gabriel Crawford, Pekka Jousilahti, Markus Perola, Michael Boehnke, Lori L. Bonnycastle, Francis S. Collins, Anne Jackson, Karen L. Mohlke, Heather M. Stringham, Timo T. Valle, Cristen J. Willer, Richard N. Bergman, Mario A. Morken, Angela Döring, Christian Gieger, Thomas Illig, Thomas Meitinger, Elin Org, Arne Pfeufer, H.‐Erich Wichmann, Sekar Kathiresan, Jaume Marrugat, Christopher J. O’Donnell, Stephen M. Schwartz, David S. Siscovick, Isaac Subirana, Nelson B. Freimer, Anna-Liisa Hartikainen, Mark I. McCarthy, Paul F. O’Reilly, Leena Peltonen, Anneli Pouta, Paul E. de Jong, Harold Snieder, Wiek H. van Gilst, Robert Clarke, Anuj Goel, Anders Hamsten, John F. Peden
Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters
Biola M. Javierre, Oliver S. Burren, Steven P. Wilder, Roman Kreuzhuber, Steven M. Hill, Sven Sewitz, Jonathan Cairns, Steven Wingett, Csilla Várnai, Michiel J. Thiecke, Frances Burden, Samantha Farrow, Antony J. Cutler, Karola Rehnström, Kate Downes, Luigi Grassi, Myrto Kostadima, Paula Freire-Pritchett, Fan Wang, Joost H.A. Martens, Bowon Kim, Nilofar Sharifi, Eva M. Janssen‐Megens, Marie‐Laure Yaspo, Matthias Linser, Alexander Kovacsovics, Laura Clarke, David Richardson, Avik Datta, Paul Flicek, Hendrik G. Stunnenberg, John A. Todd, Daniel R. Zerbino, Oliver Stegle, Willem H. Ouwehand, Mattia Frontini, Chris Wallace, Mikhail Spivakov, Peter Fraser
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Gosia Trynka, PreventCD Study Group, Karen A. Hunt, Nicholas Bockett, Jihane Romanos, Vanisha Mistry, Agata Szperl, Sjoerd F. Bakker, Maria Teresa Bardella, Leena Bhaw, Gemma Castillejo, Emilio G. de la Concha, Rodrigo Coutinho de Almeida, Kerith‐Rae Dias, Cleo C. van Diemen, P Dubois, Richard H. Duerr, Sarah Edkins, Lude Franke, Karin Fransén, Javier Gutierrez, Graham Heap, Barbara Hrdličková, Sarah Hunt, Leticia Plaza Izurieta, Valentina Izzo, Leo A. B. Joosten, Cordelia Langford, Maria Cristina Mazzilli, Charles A. Mein, Vandana Midah, Mitja Mitrovič, Barbara Mora, Marinita Morelli, Sarah Nutland, Concepción Núñez, Suna Önengüt-Gümüşcü, Kerra Pearce, Mathieu Platteel, Isabel Polanco, Simon Potter, Carmen Ribes‐Koninckx, Isis Ricaño-Ponce, Stephen S. Rich, Anna Rybak, José Luis Santiago, Sabyasachi Senapati, Ajit Sood, Hania Szajewska, Riccardo Troncone, Jezabel Varadé, Chris Wallace, Victorien M. Wolters, Alexandra Zhernakova, B.K. Thelma, Božena Cukrowská, Elena Urcelay, José Ramón Bilbao, M. L. Mearin, Donatella Barisani, Jeffrey C. Barrett, Vincent Plagnol, Panos Deloukas, Cisca Wijmenga, David A. van Heel
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nick Craddock, Liz Forty, Katherine Gordon‐Smith, Elaine Green, Detelina Grozeva, Ian Jones, George Kirov, Michael O‘Donovan, Michael J. Owen, Ellie Russell, M. E. Hurles, Samuel C. Robson, C. Barnes, Donald F. Conrad, Kathy Stirrups, Jan Aerts, T. Daniel Andrews, Hazel Arbury, Anthony Attwood, Jeffrey C. Barrett, Inês Barroso, Sanjeev S. Bhaskar, John H. Burton, Chris M. Clee, Alison J. Coffey, Andrew Dunham, Sarah Edkins, Tomas Fitzgerald, Emma Gray, Rhian Gwilliam, Naomi Hammond, Husam Hebaishi, Eleanor Howard, Sarah Hunt, Cordelia F. Langford, Kevin Lewis, Kirsten McLay, Michael L. Mimmack, Ifejinelo Onyiah, Kimmo Palin, Michael A. Quail, Richard Redon, Carol Scott, Elilan Somaskantharajah, Armand Valsesia, Eleftheria Zeggini, Nigel P. Carter, Aarno Palotie, Chris Tyler‐Smith, Michael R. Stratton, Panos Deloukas, Dominic Kwiatkowski, Willem H. Ouwehand, Niall J. Cardin, Eleni Giannoulatou, Christopher Holmes, Jonathan Marchini, Christopher Yau, Adam Auton, Simon Myers, Zhan Su, Gil McVean, Peter Donnelly, Richard D. Pearson, Damjan Vukcevic, Jake Byrnes, Mahim Jain, Cecilia M. Lindgren, Julian Maller, Andrew P. Morris, Inga Prokopenko, Nigel W. Rayner, Robertson NP, Adrian V. S. Hill, Mark I. McCarthy, Vincent Plagnol, Oliver S. Burren, Jason D. Cooper, Kate Downes, Matt Hardy, Joanna M. M. Howson, Meeta Maisuria-Armer, Nigel Ovington, Helen Schuilenburg, Debbie J. Smyth, Helen E. Stevens, Neil Walker, Chris Wallace, Matthew Woodburn, John A. Todd, Martin D. Tobin, Louise V. Wain, J. Thompson, Paul R. Burton, Tariq Ahmad, Jennifer D. Jolley, Jennifer G. Sambrook, Jonathan Stephens, Nicholas A. Watkins, Stephen G. Ball