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How has David Kavanagh's publication output changed over time?
ScholarIQpublication output · 2005–2024
Output grew200% over the shown period — from 1 works in 2005 to 3 in 2024.
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20052006200720142015201620192024
What are the most-cited papers on David Kavanagh?
ScholarIQmost cited works
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke, B M Neale, Kai-How Farh, Phil Lee, Brendan Bulik‐Sullivan, H Huang, Menachem Fromer, Jacqueline I. Goldstein, Mark J. Daly, Richard A. Belliveau, Sarah E. Bergen, Elizabeth Bevilacqua, Kimberly D. Chambert, Giulio Genovese, Colm Ó'Dúshláine, Edward M. Scolnick, Jordan W. Smoller, Steven A. McCarroll, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Tune H. Pers, J. N. Hirschhorn, Alkes Price, Eli Stahl, Esko T, Aiden Corvin, Paul Cormican, Gary Donohoe, Derek W. Morris, Michael Gill, James T. R. Walters, Peter Holmans, Noa Carrera, Nick Craddock, Valentina Escott‐Price, Lyudmila Georgieva, Marian L. Hamshere, David Kavanagh, Sophie E. Legge, Andrew Pocklington, Alexander Richards, Douglas M. Ruderfer, Nigel Williams, George Kirov, Michael J. Owen, Michael O‘Donovan, David A. Collier, Younes Mokrab, Ingrid Agartz, Erik Söderman, Erik G. Jönsson, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Ole A. Andreassen, Esben Agerbo, Preben Bo Mortensen, Ditte Demontis, Thomas Folkmann Hansen, Manuel Mattheisen, Ole Mors, Line Olsen, H Kruuse Rasmussen, Anders D. Børglum, Werge Tm, Margot Albus, Madeline Alexander, Claudine Laurent, Douglas F. Levinson, Farooq Amin, S Bacanu, Tim B. Bigdeli, Bradley T. Webb, Brandon K. Wormley, Martin Begemann, Christian Hammer, Sergi Papiol, Hannelore Ehrenreich, Béné Jj, Béla Melegh, Anna K. Kähler, Patrik K. E. Magnusson, Christina M. Hultman, Patrick F. Sullivan, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, Joshua L. Roffman, William Byerley, Wiepke Cahn, René S. Kahn, Eric Strengman, Roel A. Ophoff, Guiqing Cai, Buxbaum Jn, Kenneth L. Davis, Elodie Drapeau, Joseph I. Friedman
Nature. 20148,164 CitationsOPEN ACCESS
The ExAC browser: displaying reference data information from over 60 000 exomes
Konrad J. Karczewski, Ben Weisburd, Brett Thomas, Matthew Solomonson, Douglas M. Ruderfer, David Kavanagh, Tymor Hamamsy, Monkol Lek, Kaitlin E. Samocha, Beryl B. Cummings, Daniel Birnbaum, Mark J. Daly, Daniel G. MacArthur
S134668137. 2016841 CitationsOPEN ACCESS
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
Jessica Caprioli, Marina Noris, Simona Brioschi, Gaia Pianetti, Federica Castelletti, Paola Bettinaglio, Caterina Mele, Elena Bresin, Linda Cassis, Sara Gamba, Francesca Porrati, Sara Bucchioni, Giuseppe Monteferrante, Celia J. Fang, M. Kathryn Liszewski, David Kavanagh, John P. Atkinson, Giuseppe Remuzzi, for the International Registry of Recurrent and Familial HUS/TTP
Blood. 2006731 CitationsOPEN ACCESS
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
Timothy H.J. Goodship, H. Terence Cook, Fádi Fakhouri, Fernando C. Fervenza, Véronique Frémeaux‐Bacchi, David Kavanagh, Carla Nester, Marina Noris, Matthew C. Pickering, Santiago Rodrı́guez de Córdoba, Lubka T. Roumenina, Sanjeev Sethi, Richard J. Smith, Charlie E. Alpers, Gerald B. Appel, Gianluigi Ardissino, Gema Ariceta, Mustafa Arıcı, Arvind Bagga, Ingeborg M. Bajema, Miguel Blasco, Linda Burke, Thomas Cairns, M.C. Carratalá, Vivette D. D’Agati, Mohamed R. Daha, An S. De Vriese, Marie‐Agnès Dragon‐Durey, Agnes B. Fogo, Miriam Galbusera, Daniel P. Gale, Hermann Haller, Sally Johnson, Mihály Józsi, Diana Karpman, Lynne D. Lanning, Moglie Le Quintrec, Christoph Licht, Chantal Loirat, Francisco Monfort, B. Paul Morgan, Laure-Hélène Noël, Michelle M. O’Shaughnessy, Marion Rabant, Éric Rondeau, Piero Ruggenenti, Neil Sheerin, Jenna L.H. Smith, Fabrizio Spoleti, Joshua M. Thurman, Nicole C. A. J. van de Kar, Marina Vivarelli, Peter F. Zipfel
Kidney International. 2016703 CitationsOPEN ACCESS
Mutations in Complement Factor I Predispose to Development of Atypical Hemolytic Uremic Syndrome
David Kavanagh, Elizabeth J. Kemp, Elizabeth Mayland, R.J. Winney, Jeremy S. Duffield, Graham Warwick, Anna Richards, Roy Ward, Judith A. Goodship, Timothy H.J. Goodship
Journal of the American Society of Nephrology. 2005476 Citations
Related on ScholarIQ
Newcastle University
Institution
Biological insights from 108 schizophrenia-associated genetic loci
Paper
The ExAC browser: displaying reference data information from over 60 000 exomes
Paper
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
Paper
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
Paper
Mutations in Complement Factor I Predispose to Development of Atypical Hemolytic Uremic Syndrome
Paper