Mattia Frontini

发表

Two-step penalised logistic regression for multi-omic data with an application to cardiometabolic syndrome

Alessandra Cabassi, Paul D. W. Kirk, Denis Seyres, 2020, 2008.00235.

Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types

Alfonso Valencia, Nicole Soranzo, Daniel Rico, 2016, bioRxiv.

Transcriptional diversity during lineage commitment of human blood progenitors

Randy J. Read, William J. Astle, Paul Flicek, 2014, Science.

Chromosome contacts in activated T cells identify autoimmune disease candidate genes

Ellen Schofield, Jonathan Cairns, Peter Fraser, 2017, Genome Biology.

Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypes

Christoph Bock, Maik Pietzner, Albert Koulman, 2020, bioRxiv.

Whole genome sequencing of a sporadic primary immunodeficiency cohort

Antonis Pantazis, Keith W. Muir, David J. Williams, 2020, Nature.

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

Jie Huang, William J. Astle, Bengt Sennblad, 2016, Nature Genetics.

Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.

Randy J Read, Karyn Megy, Suthesh Sivapalaratnam, 2019, Blood.

Saturation analysis for whole-genome bisulfite sequencing data

Michael J. Ziller, Alexander Meissner, Simon Heath, 2016, Nature Biotechnology.

Increased DNA methylation variability in type 1 diabetes across three immune effector cell types

Paul Flicek, Nicole Soranzo, Simon Heath, 2016, Nature Communications.