Christiaan G. J. Saris

Author

Also Known As

C G J Saris, C. Saris, C.G.J. Saris, Christiaan G J Saris, Christiaan G Saris, Christiaan G. J. Saris, Christiaan G. Saris, Christiaan G.J. Saris, Christiaan GJ Saris, Christiaan Saris

Publications

3.2K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center University Medical Center Utrecht University of Amsterdam University Medical Center Groningen

About

Christiaan G. J. Saris is an author at Radboud University Nijmegen specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	1.2K
2	Engineering	2	2	273
3	Health Sciences	1	1	11
4	Public Health	1	1	12
5	Social Sciences	1	1	19

Christiaan G. J. Saris

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Michael A. van Es, Jan H. Veldink, Christiaan G. J. Saris, Nature Genetics Genome-wide Association StudyNeurodegenerative DiseasesAmyotrophic Lateral SclerosisGeneticsGenetic Epidemiology	2009	402
Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA Rudolf S.N. Fehrmann, Ritsert C. Jansen, Jan H. Veldink, PLoS Genetics	2011	342
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis Michael A. van Es, Paul WJ van Vught, Hylke M. Blauw, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisGeneticsGenetic EpidemiologyGenetic Variation	2007	218
Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients Christiaan G. J. Saris, Steve Horvath, Paul W.J. van Vught, BMC Genomics	2009	211
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study Michael A. van Es, Paul W van Vught, Hylke M. Blauw, The Lancet Neurology Genome-wide Association StudyNeurodegenerative DiseasesAmyotrophic Lateral SclerosisEngineeringMedicine	2007	210
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, Proceedings of the National Academy of Sciences	2009	185
Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials Bas C. Stunnenberg, Joost Raaphorst, Hans Groenewoud, JAMA	2018	129
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen Hylke M. Blauw, Jan H. Veldink, Michael A. van Es, The Lancet Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderGeneticsNeurology	2008	97
KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia Maartje Pennings, Meyke Schouten, Judith van Gaalen, European Journal of Human Genetics	2019	91
Cytosolic 5′-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis James B Lilleker, Anke Rietveld, Stephen R. Pye, Annals of the Rheumatic Diseases	2017	88

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