ScholarIQanswers from OpenAlex & ORCID
H. Robert Horvitz
ResearcherPublications, citations & collaboration network
H. Robert Horvitz is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does H. Robert Horvitz have?
ScholarIQindexed works
H. Robert Horvitz has 325 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does H. Robert Horvitz have?
ScholarIQcitation count
H. Robert Horvitz has 75,738 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of H. Robert Horvitz?
ScholarIQh-index
H. Robert Horvitz has an h-index of 125 in OpenAlex.
What is the i10-index of H. Robert Horvitz?
ScholarIQi10-index
H. Robert Horvitz has an i10-index of 235 in OpenAlex.
What is the ORCID of H. Robert Horvitz?
ScholarIQorcid
The ORCID for H. Robert Horvitz is on the source record.
What is the OpenAlex record for H. Robert Horvitz?
ScholarIQopenalex
The OpenAlex for H. Robert Horvitz is on the source record.
What are the most-cited papers on H. Robert Horvitz?
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
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
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
Mitsuya Morita, Ammar Al‐Chalabi, P. M. Andersen, B Hosler, P. Sapp, Elisabet Englund, J. E. Mitchell, James Habgood, Jackie de Belleroche, Jing Xi, Wallaya Jongjaroenprasert, H. Robert Horvitz, Lars‐Gunnar Gunnarsson, Robert H. Brown
Reduced expression of the <i>Kinesin-Associated Protein 3</i> ( <i>KIFAP3</i> ) gene increases survival in sporadic amyotrophic lateral sclerosis
John E. Landers, Judith Melki, Vincent Meininger, Jonathan D. Glass, Leonard H. van den Berg, Michael A. van Es, Peter C. Sapp, Paul W.J. van Vught, Diane McKenna‐Yasek, Hylke M. Blauw, Ting-Jan Cho, Meraida Polak, Lijia Shi, Anne‐Marie Wills, Wendy Broom, Nicola Ticozzi, Vincenzo Silani, Aslıhan Özoğuz, Ildefonso Rodríguez‐Leyva, Jan H. Veldink, Adrian J. Ivinson, Christiaan G. J. Saris, Betsy A. Hosler, Alayna Barnes-Nessa, Nicole Couture, John H. J. Wokke, Thomas J. Kwiatkowski, Roel A. Ophoff, Simon Cronin, Orla Hardiman, Frank P. Diekstra, P. Nigel Leigh, Christopher E. Shaw, Claire L. Simpson, Valerie K. Hansen, John Powell, Philippe Corcia, François Salachas, Simon Heath, Pilar Galán, Georges Franck, H. Robert Horvitz, Mark Lathrop, Shaun Purcell, Ammar Al‐Chalabi, Robert H. Brown