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Richard J. Smith

ResearcherPublications, citations & collaboration network

Richard J. Smith is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 1,416 works, 52,853 citations, an h-index of 114 and an i10-index of 683.

1,416
Works
52,853
Citations
114
h-index
683
i10-index

How has Richard J. Smith's publication output changed over time?

ScholarIQpublication output · 1977–2019

Output grew0% over the shown period — from 1 works in 1977 to 1 in 2019.

1
2
3
1
1
2
1
1
19772001200520082013201620172019

What are the most-cited papers on Richard J. Smith?

ScholarIQmost cited works
A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration
Gregory S. Hageman, Don H. Anderson, Lincoln V. Johnson, Lisa S. Hancox, Andrew J. Taiber, Lisa I. Hardisty, Jill L. Hageman, Heather Stockman, James D. Borchardt, Karen M. Gehrs, Richard J. Smith, Giuliana Silvestri, Stephen R. Russell, Caroline C. W. Klaver, Irene Barbazetto, Stanley Chang, Lawrence A. Yannuzzi, Gaetano R. Barile, John C. Merriam, R. Theodore Smith, Adam Olsh, Julie Bergeron, Jana Zernant, Joanna E. Merriam, Bert Gold, Michael Dean, Rando Allikmets
Proceedings of the National Academy of Sciences. 20051,972 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
C3 glomerulopathy: consensus report
Matthew C. Pickering, Vivette D. D’Agati, Carla Nester, Richard J. Smith, Mark Haas, Gerald B. Appel, Charles E. Alpers, Ingeborg M. Bajema, Camille L. Bedrosian, Michael Braun, Mittie K. Doyle, Fádi Fakhouri, Fernando C. Fervenza, Agnes B. Fogo, Véronique Frémeaux‐Bacchi, Daniel P. Gale, Elena Goicoechea de Jorge, Gene Griffin, Claire L. Harris, V. Michael Holers, Sally Johnson, Peter Lavin, Nicholas Medjeral‐Thomas, B. Paul Morgan, Cynthia C. Nast, Laure-Hélène Noël, D K Peters, Santiago Rodrı́guez de Córdoba, Aude Servais, Sanjeev Sethi, Wen-Chao Song, Paul P. Tamburini, Joshua M. Thurman, Michael Zavros, H. Terence Cook
Kidney International. 2013644 CitationsOPEN ACCESS
Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss
Christina Sloan-Heggen, Amanda O. Bierer, A. Eliot Shearer, Diana L. Kolbe, Carla Nishimura, Kathy L. Frees, Sean S. Ephraim, Seiji B. Shibata, Kevin T. Booth, Colleen A. Campbell, Paul T. Ranum, Amy E. Weaver, E. Ann Black-Ziegelbein, Donghong Wang, Héla Azaiez, Richard J. Smith
S199832308. 2016598 CitationsOPEN ACCESS
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, Sandrine Marlin, Françoise Denoyelle, J Waligora, Małgorzata Mueller‐Malesińska, Agneszka Pollak, Rafał Płoski, Alessandra Murgia, Eva Orzan, Pierangela Castorina, Umberto Ambrosetti, Ewa Nowakowska-Szyrwińska, Jerzy Bal, Wojciech Wiszniewski, Andreas Janecke, Doris Nekahm-Heis, Pavel Seeman, O. Bendová, Margaret A. Kenna, Anna Frangulov, Heidi L. Rehm, Mustafa Tekin, Armağan İncesulu, Hans‐Henrik M. Dahl, Desirée du Sart, Lucy Jenkins, Deirdre Lucas, Maria Bitner‐Glindzicz, Karen B. Avraham, Zippora Brownstein, Ignacio del Castillo, Felipe Moreno, Nikolaus Blin, Markus Pfister, István Sziklai, Tímea Tóth, Philip M. Kelley, Edward Cohn, Lionel Van Maldergem, Pascale Hilbert, Anne‐Françoise Roux, M. Mondain, Lies H. Hoefsloot, Cor W. R. J. Cremers, Tuija Löppönen, Heikki Löppönen, Agnete Parving, Karen Grønskov, Iris Schrijver, Joseph Roberson, Francesca Gualandi, Alessandro Martini, Geneviève Lina‐Granade, Nathalie Pallarès-Ruiz, Céu Correia, Graça Fialho, Kim Cryns, Nele Hilgert, Paul Van de Heyning, Carla Nishimura, Richard J. Smith, Guy Van Camp
S134425043. 2005561 CitationsOPEN ACCESS

Related on ScholarIQ

University of Iowa
Institution
A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration
Paper
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
Paper
C3 glomerulopathy: consensus report
Paper
Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss
Paper
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Paper
470M+ articles · free account