Joseph Glessner

Nature · 2007–2013

A researcher in the Science corpus: 8 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Papers from Joseph Glessner's perspective

Ordered by how strongly the researchers Joseph Glessner trusts endorse each paper. Same corpus, a different order for every researcher.

Large-Scale Copy Number Polymorphism in the Human Genome (Science)
A tiling resolution DNA microarray with complete coverage of the human genome (Nature Genetics)
Fine-scale structural variation of the human genome (Nature Genetics)
Global variation in copy number in the human genome (Nature)
BLAT--the BLAST-like alignment tool. (Genome Research)
Whole genome genotyping technologies on the BeadArray™ platform
The epidemiology of autism spectrum disorders. (Annual Review of Public Health)
[Structural variation in the human genome]. (Yi chuan = Hereditas)
Common deletion polymorphisms in the human genome (Nature Genetics)
Mapping and sequencing of structural variation from eight human genomes (Nature)

Their papers

Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007) — 1,861 citations
De novo mutations in histone modifying genes in congenital heart disease (2013) — 900 citations
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) — 2,780 citations
A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes (2009) — 1,451 citations
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. (2009) — 374 citations
Common genetic variants on 5p14.1 associate with autism spectrum disorders (2009) — 1,008 citations