58 papers found
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study
The genetic structure of Norway
Recommendations for the FAIRification of genomic track metadata
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research
Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database
Mutational dynamics and immune evasion in diffuse large B-cell lymphoma explored in a relapse-enriched patient series
Loss of Snord116 impacts lateral hypothalamus, sleep and food-related behaviors
Ancient genomes from Iceland reveal the making of a human population
Personal Cancer Genome Reporter: Variant Interpretation Report For Precision Oncology
Hi-C-constrained physical models of human chromosomes recover functionally-related properties of genome organization
Transcriptomic Profiling of Tumor Aggressiveness in Sporadic Nonfunctioning Pancreatic Neuroendocrine Neoplasms
Pre-diagnostic serum levels of EGFR and ErbB2 and genetic glioma risk variants: a nested case-control study
Galaxy Portal: interacting with the galaxy platform through mobile devices
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
P17.94glioma Gwas Hits - Markers for Risk or for Prognosis?
Melanoma brain colonization involves the emergence of a brain-adaptive phenotype
Cell sampling and global nucleic acid amplification.
Protein arrays: a versatile toolbox for target identification and monitoring of patient immune responses.
MUTYH Mutations Do Not Cause HNPCC or Late Onset Familial Colorectal Cancer
Sampling Effects on Gene Expression Data from a Human Tumour Xenograft
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