Hylke M. Blauw - Concepedia

Author

Hylke M. Blauw

University Medical Center Utrecht

Also Known As

Blauw, H. M., Fernando Rivadeneira, H Blauw, H. M. Blauw, H.M. Blauw, Hylke Blauw, Hylke M Blauw, Hylke M. Blauw

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Utrecht University of California, Los Angeles Utrecht University KU Leuven Umeå University

About

Hylke M. Blauw is an author at University Medical Center Utrecht specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	1.7K
2	Engineering	2	2	273
3	Natural Sciences	2	2	185
4	Public Health	2	2	75
5	Social Sciences	1	1	19

Hylke M. Blauw

Publications

2.2K

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
Embolotherapy of Pulmonary Arteriovenous Malformations: Long-term Results in 112 Patients Johannes J. Mager, Timotheus T. C. Overtoom, Hylke M. Blauw, Journal of Vascular and Interventional Radiology Pulmonary EmbolismThrombosisPulmonary Arteriovenous MalformationsVascular MalformationVascular Surgery	2004	269
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
Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism Bert van der Zwaag, Lude Franke, Martin Poot, PLoS ONE GeneticsMolecular BiologyGene CharacterizationDisease Gene IdentificationGenomics	2009	142
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
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1 Kreshnik Ahmeti, Senda Ajroud‐Driss, Ammar Al‐Chalabi, Neurobiology of Aging Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderGeneticsDegenerative Disease	2012	93
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study Wouter van Rheenen, Frank P. Diekstra, Oliver Harschnitz, PLoS ONE EngineeringTranscriptomics TechnologyNeurochemical BiomarkersGene Expression ProfilingBiostatistics	2018	63

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