Jan H. Veldink - Concepedia

Author

Jan H. Veldink

Also Known As

A. Tucci, Adriano Chio, André Uitterlinden, Bert A. Hofman, CADISP group, Cathryn M Lewis, David J. Stone, David J. Werring, Franke, Barbara, Ian Blair

558

Publications

44.4K

Citations

106

H-Index

213

Concepts

All Affiliations

University Medical Center Utrecht Utrecht University Radboud University Nijmegen University Medical Center Groningen King's College London

About

Jan H. Veldink is an author at University Medical Center Utrecht specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	80	13.6K
2	Health Sciences	6	6	568
3	Engineering	4	4	1.3K
4	Natural Sciences	2	2	185
5	Nursing	1	1	11

Jan H. Veldink

228

Publications

26.6K

Citations

H-Index

Page 1

	Year	Citations
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression Urmo Võsa, Annique Claringbould, Harm-Jan Westra, Nature Genetics Genome-wide Association StudyGenetic AnalysisMedicineGeneticsLarge-scale Cis-	2021	2K
Systematic identification of trans eQTLs as putative drivers of known disease associations Harm-Jan Westra, Marjolein J. Peters, Tōnu Esko, Nature Genetics Systematic IdentificationAutoimmune DiseaseAllergyMedicineImmunodeficiencies	2013	1.7K
Multiple common variants for celiac disease influencing immune gene expression P Dubois, Gosia Trynka, Lude Franke, Nature Genetics Allelic VariantAutoimmune DiseaseImmunodeficienciesMultiple Common VariantsGenetic Epidemiology	2010	1K
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways Elizabeth T. Cirulli, Brittany N. Lasseigne, Slavé Petrovski, Science EngineeringExome SequencingGeneticsImmunologyDisease Gene Identification	2015	972
Disease variants alter transcription factor levels and methylation of their binding sites Marc Jan Bonder, René Luijk, Daria V. Zhernakova, Nature Genetics Epigenetic ChangeGeneticsDna MethylationEpigenomicsDisease Gene Identification	2016	544
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis Urmo Võsa, Annique Claringbould, Harm-Jan Westra, GeneticsGenetic EpidemiologyHuman PolymorphismMolecular GeneticsGenomics	2018	543
Identification of context-dependent expression quantitative trait loci in whole blood Daria V. Zhernakova, Patrick Deelen, Martijn Vermaat, Nature Genetics Genome-wide Association StudyAllelic VariantQuantitative GeneticsGenotype-phenotype AssociationMedicine	2016	502
Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation Josine L. Min, Gibran Hemani, Eilís Hannon, Nature Genetics BiologyChromatinGenetic EffectsGenome StudyEpigenetic Change	2021	500
Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model Henk-Jan Westeneng, Thomas P. A. Debray, Anne E Visser, The Lancet Neurology Prognostic AssessmentNeurodegenerative DiseasesPersonalised Prediction ModelAmyotrophic Lateral SclerosisDisease Progression	2018	492
Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study Ammar Al‐Chalabi, Andrea Calvo, Adriano Chiò, The Lancet Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderNeuroanatomyMedicine	2014	413

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