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Alexandre Xavier

Epigenome-wide association studies: current knowledge, strategies and recommendations
2021 · Maria Pia Campagna, Alexandre Xavier, et al. · Clinical Epigenetics · 228
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Comprehensive mismatch repair gene panel identifies variants in patients with Lynch‐like syndrome
2019 · Alexandre Xavier, Maren Fridtjofsen Olsen, et al. · Molecular Genetics & Genomic Medicine · 49
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TAPES: A tool for assessment and prioritisation in exome studies
2019 · Alexandre Xavier, Rodney J. Scott, et al. · PLoS Computational Biology · 45
Use of multigene‐panel identifies pathogenic variants in several CRC ‐predisposing genes in patients previously tested for Lynch Syndrome
2017 · Maren F. Hansen, Jostein Johansen, et al. · Clinical Genetics · 43
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Evaluation of Cell-Specific Epigenetic Age Acceleration in People With Multiple Sclerosis
2023 · Vicki Maltby, Alexandre Xavier, et al. · Neurology · 33
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Whole-blood methylation signatures are associated with and accurately classify multiple sclerosis disease severity
2022 · Maria Pia Campagna, Alexandre Xavier, et al. · Clinical Epigenetics · 25
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Alteration of DNA Methylation and Epigenetic Scores Associated With Features of Schizophrenia and Common Variant Genetic Risk
2023 · Dylan J. Kiltschewskij, William R. Reay, et al. · Biological Psychiatry · 22
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DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes
2023 · Alexandre Xavier, Vicki E. Maltby, et al. · International Journal of Molecular Sciences · 20
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Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients
2020 · Vicki E. Maltby, Rodney A. Lea, et al. · Scientific Reports · 19
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Parity is associated with long-term differences in DNA methylation at genes related to neural plasticity in multiple sclerosis
2023 · Maria Pia Campagna, Alexandre Xavier, et al. · Clinical Epigenetics · 15
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Epstein–Barr Virus, Lower Vitamin D, Low Sun Exposure, and HLA ‐ DRB1 *1501 Risk Variant Share Common Epigenetic Pathways Leading to Multiple Sclerosis Onset
2025 · Steve Simpson‐Yap, Ellen Morwitch, et al. · Annals of Neurology · 10
HLA-DRB1*15:01 and the MERTK Gene Interact to Selectively Influence the Profile of MERTK-Expressing Monocytes in Both Health and MS
2023 · Michele D. Binder, Eze C. Nwoke, et al. · Neurology Neuroimmunology & Neuroinflammation · 10
Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis
2023 · Alexandre Xavier, Maria Pia Campagna, et al. · Frontiers in Immunology · 10
Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer
2020 · Ashish Kumar Singh, Bente Talseth-Palmer, et al. · PLoS ONE · 10
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p53 Dysregulation in Breast Cancer: Insights on Mutations in the TP53 Network and p53 Isoform Expression
2023 · Luiza Steffens Reinhardt, Kira Groen, et al. · International Journal of Molecular Sciences · 8
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Exome sequencing of familial adenomatous polyposis‐like individuals identifies both known and novel causative genes
2021 · Alexandre Xavier, Rodney J. Scott, et al. · Clinical Genetics · 8
Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing
2023 · Ashish Kumar Singh, Bente Talseth-Palmer, et al. · BMC Medical Genomics · 7
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DNA methylation signatures of Multiple Sclerosis occur independently of genetic risk and are primarily attributed to B cells and monocytes
2023 · Alexandre Xavier, Vicki E Maltby, et al. · Research Square · 4
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Birth history is associated with whole-blood and T-cell methylation patterns in relapse onset multiple sclerosis
2022 · Maria Pia Campagna, Alexandre Xavier, et al. · medRxiv · 3
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X-chromosome methylation patterns in females with multiple sclerosis
2026 · Thomas Calnin, Vicki E Maltby, et al. · medRxiv
Impact of genetic susceptibility on Multiple Sclerosis immune methylome
2025 · Giordano, Antonino, Needhamsen, Maria, et al. · Lirias
Additional file 3 of Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing
2023 · Singh, Ashish Kumar, Talseth-Palmer, Bente, et al. · Figshare
Additional file 4 of Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing
2023 · Singh, Ashish Kumar, Talseth-Palmer, Bente, et al. · Figshare
2326 Differential methylation mediates significant proportions of environmental and lifestyle factors’ associations with MS risk: results from the Ausimmune case-control study
2022 · Steve Simpson-Yap, Ellen Morwitch, et al. · Abstracts
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Author response for "Exome sequencing of familial adenomatous polyposis‐like individuals identifies both known and novel causative genes"
2021 · Alexandre Xavier, Rodney J. Scott, et al.
Works count: 26
Citation count: 569
H-index: 10
I10-index: 14
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