ScholarIQanswers from OpenAlex
Harry Perkins Institute of Medical Research
InstitutionResearch output, impact & collaborations
Harry Perkins Institute of Medical Research is a institution indexed in ScholarIQ from OpenAlex.
What is known about Harry Perkins Institute of Medical Research?
ScholarIQrecord summary
Harry Perkins Institute of Medical Research is a research organisation in Nedlands, AU. OpenAlex records 4,666 works and 512,362 citations for it. 698 researchers list it as their most recent affiliation.
How many works does Harry Perkins Institute of Medical Research have?
ScholarIQindexed works
Harry Perkins Institute of Medical Research has 4,666 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Harry Perkins Institute of Medical Research have?
ScholarIQcitation count
Harry Perkins Institute of Medical Research has 512,362 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Harry Perkins Institute of Medical Research?
ScholarIQresearcher count
Harry Perkins Institute of Medical Research has 698 researchers in the ScholarIQ index.
What is the average h-index at Harry Perkins Institute of Medical Research?
ScholarIQavg h-index
Harry Perkins Institute of Medical Research has an average h-index of 81 in OpenAlex.
What is the ROR of Harry Perkins Institute of Medical Research?
ScholarIQror
The ROR for Harry Perkins Institute of Medical Research is on the source record.
What is the OpenAlex record for Harry Perkins Institute of Medical Research?
ScholarIQopenalex
The OpenAlex for Harry Perkins Institute of Medical Research is on the source record.
Who are the most-cited researchers behind Harry Perkins Institute of Medical Research?
ScholarIQtop researchers by citations
What are the most-cited papers on Harry Perkins Institute of Medical Research?
ScholarIQmost cited works
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
D.R. Rosen, Teepu Siddique, David T. Patterson, Denise A. Figlewicz, Peter C. Sapp, Afif Hentati, Deirdre Donaldson, Jun Goto, J. O'Regan, Han‐Xiang Deng, Zohra Rahmani, Aldis Krizus, Diane McKenna‐Yasek, Annarueber Cayabyab, Sandra M. Gaston, Ralph Berger, Rudolph E. Tanzi, John Halperin, Brian Herzfeldt, R. van den Bergh, W.‐Y. Hung, Thomas D. Bird, Gang Deng, Donald W. Mulder, Celestine Smyth, Nigel G. Laing, Edwin Soriano, Margaret A. Pericak‐Vance, Jonathan Haines, Guy A. Rouleau, James S. Gusella, H. Robert Horvitz, Robert Brown
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care
Eugenio Mercuri, Richard S. Finkel, Francesco Muntoni, Brunhilde Wirth, Jacqueline Montes, Marion Main, Elena Mazzone, Michael G. Vitale, Brian D. Snyder, Susana Quijano‐Roy, Enrico Bertini, Rebecca Hurst Davis, Oscar H. Meyer, Anita K. Simonds, Mary Schroth, Robert J. Graham, Janbernd Kirschner, Susan T. Iannaccone, Thomas O. Crawford, Simon Woods, Ying Qian, Thomas Sejersen, Francesco Muntoni, Brunhilde Wirth, Francesco Danilo Tiziano, Janbernd Kirschner, Eduardo F. Tizzano, Haluk Topaloğlu, Kathy Swoboda, Nigel G. Laing, Saito Kayoko, Thomas W. Prior, Wendy K. Chung, Shou‐Mei Wu, Jacqueline Montes, Elena Mazzone, Marion Main, Caron Coleman, Richard Gee, Allan M. Glanzman, Anna‐Karin Kroksmark, Kristin J. Krosschell, Leslie Nelson, Kristy Rose, Agnieszka Stępień, Carole Vuillerot, Michael G. Vitale, Brian D. Snyder, Susana Quijano-Roy, Jean Dubousset, David M. Farrington, Jack Flynn, Matthew A. Halanski, Carol Hasler, Lotfi Miladi, Christopher Reilly, Benjamin D. Roye, Paul D. Sponseller, Muharrem Yazici, Rebecca Hurst, Enrico Bertini, Stacey Tarrant, Salesa Barja, Simona Bertoli, Thomas O. Crawford, Kevin D. Foust, Barbara Kyle, Lance H. Rodan, Helen Roper, Erin Seffrood, Kathryn J. Swoboda, Agnieszka Szlagatys‐Sidorkiewicz
Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy
Roula Ghaoui, Sandra T. Cooper, Monkol Lek, Kristi Jones, Alastair Corbett, Stephen Reddel, Merrilee Needham, Christina Liang, Leigh B. Waddell, Garth A. Nicholson, Gina O’Grady, Simranpreet Kaur, Royston Ong, Mark R. Davis, Carolyn M. Sue, Nigel G. Laing, Kathryn N. North, Daniel G. MacArthur, Nigel F. Clarke
Consensus Statement on Standard of Care for Congenital Myopathies
Ching H. Wang, James J. Dowling, Kathryn N. North, Mary Schroth, Thomas Sejersen, Frederic Shapiro, Jonathan Bellini, Hali E. Weiss, Marc Guillet, Kimberly Amburgey, Susan Apkon, Enrico Bertini, C. Bönnemann, Nigel F. Clarke, Anne M. Connolly, Brigitte Estournet-Mathiaud, Dominic A. Fitzgerald, Julaine Florence, Richard Gee, Juliana Gurgel‐Giannetti, Allan M. Glanzman, Brittany Hofmeister, Heinz Jungbluth, Anastassios C. Koumbourlis, Nigel G. Laing, Marion Main, Leslie Morrison, Craig F. Munns, Kristy Rose, Pamela M. Schuler, C. Sewry, Kari Storhaug, Mariz Vainzof, Nanci Yuan
How much of the research on Harry Perkins Institute of Medical Research is open access?
ScholarIQopen access share
50%OPEN ACCESS