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A. Menelaou · SciRah

Researcher profile · Semantic Scholar

A. Menelaou

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A. Menelaou — researcher profile on SciRah

h-index: 12
Works: 17
Citations: 22K

Most-cited papers

A global reference for human genetic variation
Taras K. Oleksyk, Adam Gonçalo R. David M. Richard M. Gonçalo R. David R. Auton Abecasis Altshuler Durbin Abecasis Bentley C, Adam Gonçalo R. Auton Abecasis, Adam Auton +496 more
2015Nature17K citations Open access
Semantic Scholar
An integrated map of structural variation in 2,504 human genomes
P. Sudmant, T. Rausch, E. Gardner, R. Handsaker +78 more
2015Nature2,278 citations Open access
Semantic Scholar
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W. van Rheenen, A. Shatunov, Annelot M. Dekker, R. Mclaughlin +173 more
2016Nature Genetics558 citations Open access
Semantic Scholar
Genome-wide patterns and properties of de novo mutations in humans
L. Francioli, P. Polak, A. Koren, A. Menelaou +14 more
2015Nature Genetics395 citations Open access
Semantic Scholar
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C Androniki Sara L Freerk Pier Francesco Clara C P Francioli Menelaou Pulit van Dijk Palamara Elbers, L. Francioli, A. Menelaou, S. Pulit +82 more
2014Nature Genetics308 citations Open access
Semantic Scholar
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci
R. Betz, L. Petukhova, S. Ripke, Hai-Liang Huang +29 more
2015Nature Communications290 citations Open access
Semantic Scholar
The Genome of the Netherlands: design, and project goals
D. Boomsma, C. Wijmenga, E. Slagboom, M. Swertz +48 more
2013European Journal of Human Genetics289 citations Open access
Semantic Scholar
Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands'
Patrick Deelen, A. Menelaou, E. V. van Leeuwen, A. Kanterakis +19 more
2014European Journal of Human Genetics111 citations Open access
Semantic Scholar
High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms
M. Kurki, E. Gaál, J. Kettunen, T. Lappalainen +31 more
2014PLoS Genetics71 citations Open access
Semantic Scholar
Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
E. V. van Leeuwen, L. Karssen, J. Deelen, A. Isaacs +68 more
2015Nature Communications56 citations Open access
Semantic Scholar
Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold
A. Menelaou, J. Marchini
2013Bioinform.52 citations Open access
Semantic Scholar
Genomic and functional overlap between somatic and germline chromosomal rearrangements.
S. van Heesch, M. Simonis, Markus J. van Roosmalen, V. Pillalamarri +26 more
2014Cell Reports27 citations Open access
Semantic Scholar
Association Claims in the Sequencing Era
S. Pulit, M. Leusink, A. Menelaou, P. de Bakker
2014Genes12 citations Open access
Semantic Scholar
WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene
Lilit Nersisyan, M. Nikoghosyan, A. Arakelyan, L. Francioli +83 more
2019Scientific Reports10 citations Open access
Semantic Scholar
The Genome of the Netherlands design, and project goals
D. Boomsma, C. Wijmenga, E. Slagboom, M. Swertz +48 more
4 citations
Semantic Scholar
Peer Review #1 of "Local ancestry prediction with PyLAE (v0.2)"
Nikita Moshkov, А. Е. Сметанин, T. Tatarinova, Alexander Smetanin +496 more
20210 citations Open access
Semantic Scholar
LD-based SNP and genotype calling from next-generation sequencing reads
A. Menelaou
20120 citations
Semantic Scholar

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