Alteration of DNA Methylation and Epigenetic Scores Associated with Features of Schizophrenia and Common Variant Genetic Risk

- 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.

HLA-DRB1*15:01 and the MERTK Gene Interact to Selectively Influence the Profile of MERTK-Expressing Monocytes in Both Health and MS

- 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

Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing

- Singh, Ashish Kumar, Talseth-Palmer, Bente, Xavier, Alexandre, Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche

DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes

- 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

Evaluation of Cell-Specific Epigenetic Age Acceleration in People With 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

Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis

- 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.

p53 Dysregulation in Breast Cancer: Insights on Mutations in the TP53 Network and p53 Isoform Expression

- Steffens Reinhardt, Luiza, Groen, Kira, Xavier, Alexandre, Avery-Kiejda, Kelly A.

Parity is associated with long-term differences in DNA methylation at genes related to neural plasticity 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

Whole-blood methylation signatures are associated with and accurately classify multiple sclerosis disease severity

- Campagna, Maria Pia, Xavier, Alexandre, Lea, Rodney A., Stankovich, Jim, Maltby, Vicki E., Butzkueven, Helmut, Lechner-Scott, Jeannette, Scott, Rodney J., Jokubaitis, Vilija G.

Epigenome-wide association studies: current knowledge, strategies and recommendations

- Campagna, Maria Pia, Xavier, Alexandre, Lechner-Scott, Jeannette, Maltby, Vicky, Scott, Rodney J., Butzkueven, Helmut, Jokubaitis, Vilija G., Lea, Rodney A.

Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes

- Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente

Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients

- 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

Identification of new causative genes in inherited colorectal cancer

- Xavier, Alexandre

Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer

- Singh, Ashish Kimar, Talseth-Palmer, Bente, McPhillips, Mary, Lavik, Liss Anne Solberg, Xavier, Alexandre, Drablos, Finn, Sjursen, Wenche

Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome

- Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.

TAPES: A tool for assessment and prioritisation in exome studies

- Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente A.

Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome

- 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