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Peter C. Sapp

ResearcherPublications, citations & collaboration network

Peter C. Sapp is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Peter C. Sapp have?

ScholarIQindexed works

Peter C. Sapp has 57 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Peter C. Sapp have?

ScholarIQcitation count

Peter C. Sapp has 16,313 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Peter C. Sapp?

ScholarIQh-index

Peter C. Sapp has an h-index of 35 in OpenAlex.

What is the i10-index of Peter C. Sapp?

ScholarIQi10-index

Peter C. Sapp has an i10-index of 45 in OpenAlex.

What is the OpenAlex record for Peter C. Sapp?

ScholarIQopenalex

The OpenAlex for Peter C. Sapp is on the source record.

What are the most-cited papers on Peter C. Sapp?

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
Nature. 19937,074 Citations
Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
Thomas J. Kwiatkowski, Daryl A. Bosco, Aurélie Leclerc, Eric Tamrazian, Charles Vanderburg, C Russ, Adam Davis, James M. Gilchrist, Edward J. Kasarskis, T. L. Munsat, Paul N. Valdmanis, Guy A. Rouleau, Betsy A. Hosler, Pietro Cortelli, Pieter J. de Jong, Yuko Yoshinaga, J. L. Haines, Margaret A. Pericak‐Vance, J Yan, Nicola Ticozzi, Teepu Siddique, D. McKenna‐Yasek, Peter C. Sapp, H. Robert Horvitz, John E. Landers, Robert H. Brown
Science. 20092,568 Citations
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
Science. 2015990 CitationsOPEN ACCESS
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
Nature. 2012601 Citations
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS
Bradley Smith, Nicola Ticozzi, Claudia Fallini, Soragia Athina Gkazi, Simon Topp, Kevin P. Kenna, Emma L. Scotter, Jason Kost, Pamela Keagle, Jack W. Miller, Daniela Calini, Caroline Vance, Eric Danielson, Claire Troakes, Cinzia Tiloca, Safa Al‐Sarraj, Elizabeth Lewis, Andrew King, Claudia Colombrita, Viviana Pensato, Barbara Castellotti, Jacqueline de Belleroche, Frank Baas, Anneloor L.M.A. ten Asbroek, Peter C. Sapp, Diane McKenna‐Yasek, Russell L. McLaughlin, Meraida Polak, Seneshaw Asress, Jesús Esteban‐Pérez, José Luís Muñoz-Blanco, Michael A. Simpson, Wouter van Rheenen, Frank P. Diekstra, Giuseppe Lauria, Stefano Duga, Stefania Corti, Cristina Cereda, Lucia Corrado, Gianni Sorarú, Karen Morrison, Kelly L. Williams, Garth A. Nicholson, Ian P. Blair, Patrick A. Dion, Claire S. Leblond, Guy A. Rouleau, Orla Hardiman, Jan H. Veldink, Leonard H. van den Berg, Ammar Al‐Chalabi, Hardev Pall, Pamela J. Shaw, Martin R. Turner, Kevin Talbot, Franco Taroni, Alberto García‐Redondo, Zheyang Wu, Jonathan D. Glass, Cinzia Gellera, Antonia Ratti, Robert H. Brown, Vincenzo Silani, Christopher E. Shaw, John E. Landers, Sandra D’Alfonso, Letizia Mazzini, Giacomo P. Comi, Roberto Del Bo, Mauro Ceroni, Stella Gagliardi, Giorgia Querin, Cinzia Bertolin
Neuron. 2014370 CitationsOPEN ACCESS

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