Jeremy Schwartzentruber
Illumina (United States)(US)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Genomics and Rare Diseases, CRISPR and Genetic Engineering, Bioinformatics and Genomic Networks, RNA modifications and cancer
Most-Cited Works
- → Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma(2012)2,657 cited
- → Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma(2012)1,844 cited
- → Mapping the human genetic architecture of COVID-19(2021)1,104 cited
- → K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas(2012)998 cited
- → Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma(2013)826 cited
- → De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes(2012)745 cited
- → Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics(2020)679 cited
- → An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci(2021)616 cited
- → Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer’s disease risk genes(2021)530 cited
- → Open Targets Platform: supporting systematic drug–target identification and prioritisation(2020)495 cited