Jawad Khoris

672 total citations
10 papers, 479 citations indexed

About

Jawad Khoris is a scholar working on Neurology, Genetics and Neurology. According to data from OpenAlex, Jawad Khoris has authored 10 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 7 papers in Genetics and 5 papers in Neurology. Recurrent topics in Jawad Khoris's work include Amyotrophic Lateral Sclerosis Research (10 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Neurological diseases and metabolism (5 papers). Jawad Khoris is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (10 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Neurological diseases and metabolism (5 papers). Jawad Khoris collaborates with scholars based in Canada, France and Switzerland. Jawad Khoris's co-authors include Guy A. Rouleau, William Camu, Vincent Meininger, François Salachas, Collette K. Hand, Bruno Moulard, François Gros‐Louis, Philippe Corcia, Pierre Clavelou and William Camu and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Jawad Khoris

10 papers receiving 455 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jawad Khoris Canada 10 433 317 152 151 52 10 479
T. Sagie Israel 3 384 0.9× 259 0.8× 128 0.8× 194 1.3× 65 1.3× 3 539
Petra Tilkin Belgium 7 412 1.0× 226 0.7× 163 1.1× 123 0.8× 58 1.1× 7 494
Asako Tagawa Japan 8 568 1.3× 294 0.9× 120 0.8× 246 1.6× 107 2.1× 26 655
Katie Sidle United Kingdom 6 347 0.8× 188 0.6× 119 0.8× 169 1.1× 97 1.9× 7 452
Joshua D. Kidd United States 9 356 0.8× 167 0.5× 76 0.5× 166 1.1× 75 1.4× 11 504
Stephanie Shepheard Australia 11 334 0.8× 206 0.6× 85 0.6× 166 1.1× 69 1.3× 12 449
Rob Moccia United States 5 486 1.1× 312 1.0× 94 0.6× 334 2.2× 81 1.6× 9 627
Maria Chiara Trolese Italy 11 320 0.7× 190 0.6× 114 0.8× 153 1.0× 62 1.2× 14 419
N. Siddique United States 6 326 0.8× 197 0.6× 108 0.7× 143 0.9× 53 1.0× 8 399
Olubunmi Abel United Kingdom 5 312 0.7× 172 0.5× 101 0.7× 133 0.9× 52 1.0× 6 379

Countries citing papers authored by Jawad Khoris

Since Specialization
Citations

This map shows the geographic impact of Jawad Khoris's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jawad Khoris with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jawad Khoris more than expected).

Fields of papers citing papers by Jawad Khoris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jawad Khoris. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jawad Khoris. The network helps show where Jawad Khoris may publish in the future.

Co-authorship network of co-authors of Jawad Khoris

This figure shows the co-authorship network connecting the top 25 collaborators of Jawad Khoris. A scholar is included among the top collaborators of Jawad Khoris based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jawad Khoris. Jawad Khoris is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Daoud, Hussein, Mike Sabbagh, Véronique Belzil, et al.. (2012). C9orf72 Hexanucleotide Repeat Expansions as the Causative Mutation for Chromosome 9p21–Linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia. Archives of Neurology. 69(9). 1159–63. 22 indexed citations
2.
3.
Hand, Collette K., Rebecca S. Devon, François Gros‐Louis, et al.. (2003). Mutation Screening of the ALS2 Gene in Sporadic and Familial Amyotrophic Lateral Sclerosis. Archives of Neurology. 60(12). 1768–1768. 36 indexed citations
4.
Hand, Collette K., Jawad Khoris, François Salachas, et al.. (2002). A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q. The American Journal of Human Genetics. 70(1). 251–256. 95 indexed citations
5.
Corcia, Philippe, Jawad Khoris, Philippe Couratier, et al.. (2002). SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist. Neurology. 59(9). 1464–1466. 15 indexed citations
6.
Corcia, Philippe, Jawad Khoris, Bertrand de Toffol, et al.. (2002). Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis. Annals of Neurology. 51(2). 243–246. 87 indexed citations
7.
Hand, Collette K., et al.. (2001). Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family. Annals of Neurology. 49(2). 267–271. 59 indexed citations
8.
Khoris, Jawad, Bruno Moulard, Michaela Hayer, et al.. (2000). Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country. European Journal of Neurology. 7(2). 207–211. 29 indexed citations
9.
Camu, William, Jawad Khoris, Bruno Moulard, et al.. (1999). Genetics of familial ALS and consequences for diagnosis. Journal of the Neurological Sciences. 165. S21–S26. 65 indexed citations
10.
Khoris, Jawad, Bruno Moulard, François Salachas, et al.. (1998). Identification of Six Novel SOD1 Gene Mutations in Familial Amyotrophic Lateral Sclerosis. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 25(3). 192–196. 59 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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