about
The somatic genomic landscape of chromophobe renal cell carcinomaStargazin and other transmembrane AMPA receptor regulating proteins interact with synaptic scaffolding protein MAGI-2 in brainFocused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung CancerSomatic cancer variant curation and harmonization through consensus minimum variant level dataGenome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium.Assessing structural variation in a personal genome-towards a human reference diploid genome.Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing.Comprehensive Molecular Characterization of Papillary Renal-Cell CarcinomaSV-STAT accurately detects structural variation via alignment to reference-based assemblies.Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.
P50
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P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0002-5125-0494
@en
name
Caleb F Davis
@ast
Caleb F Davis
@en
Caleb F Davis
@es
Caleb F Davis
@nl
type
label
Caleb F Davis
@ast
Caleb F Davis
@en
Caleb F Davis
@es
Caleb F Davis
@nl
prefLabel
Caleb F Davis
@ast
Caleb F Davis
@en
Caleb F Davis
@es
Caleb F Davis
@nl
P106
P1153
7404361364
P31
P496
0000-0002-5125-0494