ScholarIQanswers from OpenAlex
Structural Genomics Consortium
InstitutionResearch output, impact & collaborations
Structural Genomics Consortium is a institution indexed in ScholarIQ from OpenAlex.
What is known about Structural Genomics Consortium?
ScholarIQrecord summary
Structural Genomics Consortium is a research organisation in Toronto, CA. OpenAlex records 1,606 works and 360,491 citations for it. 413 researchers list it as their most recent affiliation.
How many works does Structural Genomics Consortium have?
ScholarIQindexed works
Structural Genomics Consortium has 1,606 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Structural Genomics Consortium have?
ScholarIQcitation count
Structural Genomics Consortium has 360,491 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Structural Genomics Consortium?
ScholarIQresearcher count
Structural Genomics Consortium has 413 researchers in the ScholarIQ index.
What is the average h-index at Structural Genomics Consortium?
ScholarIQavg h-index
Structural Genomics Consortium has an average h-index of 94.5 in OpenAlex.
What is the ROR of Structural Genomics Consortium?
ScholarIQror
The ROR for Structural Genomics Consortium is on the source record.
What is the OpenAlex record for Structural Genomics Consortium?
ScholarIQopenalex
The OpenAlex for Structural Genomics Consortium is on the source record.
What is the Wikidata of Structural Genomics Consortium?
ScholarIQwikidata
The Wikidata for Structural Genomics Consortium is on the source record.
Who are the most-cited researchers behind Structural Genomics Consortium?
ScholarIQtop researchers by citations
What are the most-cited papers on Structural Genomics Consortium?
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
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli, Brittany N. Lasseigne, Slavé Petrovski, Peter C. Sapp, Patrick A. Dion, Claire S. Leblond, Julien Couthouis, Yifan Lu, Quanli Wang, Brian J. Krueger, Zhong Ren, Jonathan Keebler, Yujun Han, Shawn Levy, Braden Boone, Jack R. Wimbish, Lindsay L. Waite, Angela L. Jones, John P. Carulli, Kelly L. Williams, John F. Staropoli, Winnie Xin, Alessandra Chesi, Alya R. Raphael, Diane McKenna‐Yasek, Janet Cady, J.M.B.V. de Jong, Kevin P. Kenna, Bradley Smith, Simon Topp, Jack W. Miller, Soragia Athina Gkazi, Ammar Al‐Chalabi, Leonard H. van den Berg, Jan H. Veldink, Vincenzo Silani, Nicola Ticozzi, Christopher E. Shaw, Robert H. Baloh, Stanley H. Appel, Ericka Simpson, Clotilde Lagier‐Tourenne, Stefan M. Pulst, Summer Gibson, John Q. Trojanowski, Lauren Elman, Leo McCluskey, Murray Grossman, Neil A. Shneider, Wendy K. Chung, John Ravits, Jonathan D. Glass, Katherine B. Sims, Vivianna M. Van Deerlin, Tom Maniatis, Sebastian Hayes, Alban Ordureau, Sharan Swarup, John E. Landers, Frank Baas, Andrew S. Allen, Richard Bedlack, J. Wade Harper, Aaron D. Gitler, Guy A. Rouleau, Robert H. Brown, Matthew B. Harms, Gregory M. Cooper, Tim Harris, R Myers, David B. Goldstein
Diagnostic Utility of Exome Sequencing for Kidney Disease
Emily Groopman, Maddalena Marasà, Sophia Cameron‐Christie, Slavé Petrovski, Vimla S. Aggarwal, Hila Milo Rasouly, Yifu Li, Junying Zhang, Jordan G. Nestor, Priya Krithivasan, Wan Yee Lam, Adele Mitrotti, Stacy Piva, Byum Hee Kil, Debanjana Chatterjee, Rachel Reingold, Drew Bradbury, Michael DiVecchia, Holly Snyder, Xueru Mu, Karla Mehl, Olivia Balderes, David Fasel, Chunhua Weng, Jai Radhakrishnan, Pietro A. Canetta, Gerald B. Appel, Andrew S. Bomback, Wooin Ahn, Natalie Uy, Shumyle Alam, David J. Cohen, Russell J. Crew, Geoffrey K. Dube, Maya K. Rao, Sitharthan Kamalakaran, Brett Copeland, Zhong Ren, Joshua Bridgers, Colin D. Malone, Caroline M. Mebane, Neha Dagaonkar, Bengt Fellström, Carolina Haefliger, Sumit Mohan, Simone Sanna‐Cherchi, Krzysztof Kiryluk, Jan Fleckner, Ruth March, Adam Platt, David B. Goldstein, Ali G. Gharavi
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
Chi-Hong Wu, Claudia Fallini, Nicola Ticozzi, Pamela Keagle, Peter C. Sapp, Katarzyna Piotrowska, Patrick Lowe, Max Koppers, Diane McKenna‐Yasek, Desiree M. Baron, Jason Kost, Paloma González-Pérez, Andrew Fox, Jenni Adams, Franco Taroni, Cinzia Tiloca, Ashley LeClerc, Shawn C. Chafe, Dev Mangroo, Melissa J. Moore, Jill A. Zitzewitz, Zuo-Shang Xu, Leonard H. van den Berg, Jonathan D. Glass, Gabriele Siciliano, Elizabeth T. Cirulli, David B. Goldstein, François Salachas, Vincent Meininger, Wilfried Rossoll, Antonia Ratti, Cinzia Gellera, Daryl A. Bosco, Gary J. Bassell, Vincenzo Silani, Vivian E. Drory, Robert H. Brown, John E. Landers
Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes
J. Claiborne Stephens, David Reich, David Goldstein, Hyoung Doo Shin, Michael W. Smith, Mary Carrington, Cheryl A. Winkler, Gavin Huttley, Rando Allikmets, Lynn M. Schriml, Bernard Gerrard, Michael Malasky, María Dolores Burguete Ramos, Susanne Morlot, Maria Tzetis, Carole Oddoux, Francesco S. di Giovine, George Nasioulas, David Chandler, Michael Aseev, Matthew Hanson, Luba Kalaydjieva, Damjan Glavač, Paolo Gasparini, Emmanouel Kanavakis, Mireille Claustres, Marios Kambouris, Harry Ostrer, Gordon W. Duff, В. С. Баранов, Hiljar Sibul, Andres Metspalu, David Goldman, Nick Martin, David L. Duffy, Jörg Schmidtke, Xavier Estivill, Stephen J. O’Brien, Michael Dean
How much of the research on Structural Genomics Consortium is open access?
ScholarIQopen access share
88%OPEN ACCESS