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List of works by Matthieu Moisse

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization

scientific article published on 19 May 2020

Amplification of 1q32.1 Refines the Molecular Classification of Endometrial Carcinoma

scientific article published on 22 September 2017

C9orf72-derived arginine-containing dipeptide repeats associate with axonal transport machinery and impede microtubule-based motility

scientific article published on 09 April 2021

Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

scientific article published in February 2015

Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

preprint

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

scholarly article

DNA methylation profiling of non-small cell lung cancer reveals a COPD-driven immune-related signature

scientific article published on 08 September 2015

Defining Y-SNP variation among the Flemish population (Western Europe) by full genome sequencing.

scientific article published on 28 October 2017

Differentiation but not ALS mutations in FUS rewires motor neuron metabolism

scientific article published on 12 September 2019

Epigenetic effects of carbon nanotubes in human monocytic cells

Evaluation of efficacy and safety markers in a phase II study of metastatic colorectal cancer treated with aflibercept in the first-line setting

scientific article

Expression of FOXP1 and Colorectal Cancer Prognosis

scientific article published on January 2015

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

scientific article published on 4 February 2015

Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

scientific article

Genetic heterogeneity after first-line chemotherapy in high-grade serous ovarian cancer

scientific article published on 13 December 2015

Genetic markers of bevacizumab-induced hypertension

scientific article published on 21 February 2014

Genetic modifiers of CHEK2*1100delC-associated breast cancer risk

scientific article published on 06 October 2016

Genetic variability of VEGF pathway genes in six randomized phase III trials assessing the addition of bevacizumab to standard therapy

scientific article published on 11 July 2014

Genetic variants in VEGF pathway genes in neoadjuvant breast cancer patients receiving bevacizumab: Results from the randomized phase III GeparQuinto study

scientific article published on 23 June 2015

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

scientific article

Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations

scientific article

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

scientific article published in September 2016

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

scientific article published in March 2018

Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions

scientific article

Integrated genome analysis of uterine leiomyosarcoma to identify novel driver genes and targetable pathways.

scientific article

Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients

scientific article published on 21 December 2016

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

scientific article

Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight

article

MicroRNA related polymorphisms and breast cancer risk

scientific article

Mismatch repair deficiency endows tumors with a unique mutation signature and sensitivity to DNA double-strand breaks

scientific article

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients

scientific article

Pipit: visualizing functional impacts of structural variations

scientific article

Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivo

scientific article published on 26 April 2017

Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

Reconsidering the causality of TIA1 mutations in ALS.

scientific article published on 13 December 2017

Salivary DNA Methylation Profiling: Aspects to Consider for Biomarker Identification

scientific article published on 30 November 2016

Somatic copy number alterations predict response to platinum therapy in epithelial ovarian cancer

scientific article published on 2 October 2014

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

scientific article published on 28 January 2022

The Project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public

The effect of SMN gene dosage on ALS risk and disease severity

scientific article published on 02 January 2021

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

scientific article

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