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Singh, Ashish Kimar, Talseth-Palmer, Bente, McPhillips, Mary, Lavik, Liss Anne Solberg, Xavier, Alexandre, Drablos, Finn, Sjursen, Wenche. Public Library of Science (PLOS); 2020. Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer.
Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente. Wiley-Blackwell; 2021. Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes.
Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.. John Wiley & Sons; 2019. Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome.
Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente A.. Public Library of Science (PLoS); 2019. TAPES: A tool for assessment and prioritisation in exome studies.
Hansen, Maren F., Johansen, Jostein, Sjursen, Wenche, Sylvander, Anna E., Bjørnevoll, Inga, Talseth-Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn. Wiley-Blackwell; 2017. Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
Campagna, Maria Pia, Xavier, Alexandre, Lechner-Scott, Jeannette, Maltby, Vicky, Scott, Rodney J., Butzkueven, Helmut, Jokubaitis, Vilija G., Lea, Rodney A.. BioMed Central Ltd.; 2021. Epigenome-wide association studies: current knowledge, strategies and recommendations.
Xavier, Alexandre. Identification of new causative genes in inherited colorectal cancer. 2020.
Xavier, Alexandre, Campagna, Maria Pia, Lechner-Scott, Jeannette, Ausimmune Investigator Group,, Maltby, Vicki E., Kilpatrick, Trevor, Taylor, Bruce V., Butzkueven, Helmut, Ponsonby, Anne-Louise, Scott, Rodney J., Jokubaitis, Vilija G., Lea, Rodney A.. Frontiers Research Foundation; 2023. Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis.
Campagna, Maria Pia, Xavier, Alexandre, Lea, Rodney A., Jokubaitis, Vilija G., Stankovich, Jim, Maltby, Vicki E., Slee, Mark, Yeh, Wei Z., Kilpatrick, Trevor, Scott, Rodney J., Butzkueven, Helmut, Lechner-Scott, Jeannette. BioMed Central (BMC); 2023. Parity is associated with long-term differences in DNA methylation at genes related to neural plasticity in multiple sclerosis.
Maltby, Vicki, Xavier, Alexandre, Slee, Mark, van der Mei, Ingrid A., Taylor, Bruce V., Ponsonby, Anne-Louise, Jagodic, Maja, Lea, Rodney, Lechner-Scott, Jeannette, Ewing, Ewoud, Campagna, Maria-Pia, Sampangi, Sandeep, Scott, Rodney J., Butzkueven, Helmut, Jokubaitis, Vilija, Kular, Lara, Bos, Steffan. Wolters Kluwer; 2023. Evaluation of Cell-Specific Epigenetic Age Acceleration in People With Multiple Sclerosis.
Maltby, Vicki E., Lea, Rodney A., Burnard, Sean, Xavier, Alexandre, Van Cao, Thao, White, Nicole, Kennedy, Daniel, Groen, Kira, Sanders, Katherine A., Seeto, Rebecca, Bray, Samara, Gresle, Melissa, Laverick, Louise, Butzkueven, Helmut, Scott, Rodney J., Lechner-Scott, Jeannette. Nature Publishing Group; 2020. Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients.
Xavier, Alexandre, Maltby, Vicki E., Jokubaitis, Vilija G., Kilpatrick, Trevor, Alfredsson, Lars, Jagodic, Maja, Ponsonby, Anne-Louise, Taylor, Bruce V., Scott, Rodney J., Lea, Rodney A., Lechner-Scott, Jeannette, Ewing, Ewoud, Campagna, Maria Pia, Burnard, Sean M., Tegner, Jesper N., Slee, Mark, Butzkueven, Helmut, Kockum, Ingrid, Kular, Lara. MDPI AG; 2023. DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes.
Steffens Reinhardt, Luiza, Groen, Kira, Xavier, Alexandre, Avery-Kiejda, Kelly A.. MDPI AG; 2023. p53 Dysregulation in Breast Cancer: Insights on Mutations in the TP53 Network and p53 Isoform Expression.
Singh, Ashish Kumar, Talseth-Palmer, Bente, Xavier, Alexandre, Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche. BioMed Central (BMC); 2023. Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing.
Binder, Michele D., Nwoke, Eze C., Morwitch, Ellen, Dwyer, Chris, Li, Vivien, Xavier, Alexandre, Lea, Rodney A., Lechner-Scott, Jeannette, Taylor, Bruce V., Ponsonby, Anne-Louise, Kilpatrick, Trevor J., Ausimmune Investigator Group, Dwyer, Chris. Lippincott Williams & Wilkins; 2024. HLA-DRB1*15:01 and the MERTK Gene Interact to Selectively Influence the Profile of MERTK-Expressing Monocytes in Both Health and MS.
Campagna, Maria Pia, Xavier, Alexandre, Lea, Rodney A., Stankovich, Jim, Maltby, Vicki E., Butzkueven, Helmut, Lechner-Scott, Jeannette, Scott, Rodney J., Jokubaitis, Vilija G.. BioMed Central (BMC); 2022. Whole-blood methylation signatures are associated with and accurately classify multiple sclerosis disease severity.
Kiltschewskij, Dylan J., Reay, William R., Cairns, Murray J., Geaghan, Michael P., Atkins, Joshua R., Xavier, Alexandre, Zhang, Xiajie, Watkeys, Oliver J., Carr, Vaughan J., Scott, Rodney J., Green, Melissa J.. Elsevier; 2024. Alteration of DNA Methylation and Epigenetic Scores Associated with Features of Schizophrenia and Common Variant Genetic Risk.