Alexandre Xavier

530 total citations
16 papers, 253 citations indexed

About

Alexandre Xavier is a scholar working on Molecular Biology, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Alexandre Xavier has authored 16 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Cancer Research and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Alexandre Xavier's work include Epigenetics and DNA Methylation (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic factors in colorectal cancer (5 papers). Alexandre Xavier is often cited by papers focused on Epigenetics and DNA Methylation (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic factors in colorectal cancer (5 papers). Alexandre Xavier collaborates with scholars based in Australia, Norway and Sweden. Alexandre Xavier's co-authors include Rodney J. Scott, Bente A. Talseth‐Palmer, Helmut Butzkueven, Jeannette Lechner‐Scott, Vilija Jokubaitis, Rod A. Lea, Jostein Johansen, Wenche Sjursen, Vicki E. Maltby and Finn Drabløs and has published in prestigious journals such as PLoS ONE, Neurology and Scientific Reports.

In The Last Decade

Alexandre Xavier

16 papers receiving 252 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Alexandre Xavier Australia	8	139	82	62	62	43	16	253
Jana Gutwein Germany	6	151 1.1×	97 1.2×	53 0.9×	34 0.5×	32 0.7×	6	272
Tatiana Burjanivová Slovakia	10	126 0.9×	24 0.3×	65 1.0×	76 1.2×	61 1.4×	27	262
Michiya Noguchi Japan	7	199 1.4×	41 0.5×	49 0.8×	48 0.8×	45 1.0×	22	494
Dominique Nadine Markowski Germany	13	133 1.0×	45 0.5×	22 0.4×	63 1.0×	30 0.7×	25	567
Laura G. Baudrin France	7	230 1.7×	54 0.7×	45 0.7×	95 1.5×	121 2.8×	9	414
Ana C. Queirós Spain	8	260 1.9×	19 0.2×	55 0.9×	71 1.1×	38 0.9×	12	355
Lisa Perilli Italy	9	246 1.8×	68 0.8×	30 0.5×	202 3.3×	38 0.9×	11	439
Xianglin Hao China	12	222 1.6×	19 0.2×	27 0.4×	101 1.6×	39 0.9×	22	315
Sebastian Fröhler Germany	8	235 1.7×	30 0.4×	57 0.9×	52 0.8×	45 1.0×	16	350
Borahm Kim South Korea	11	83 0.6×	55 0.7×	84 1.4×	34 0.5×	31 0.7×	21	289

Countries citing papers authored by Alexandre Xavier

Since Specialization

Citations

This map shows the geographic impact of Alexandre Xavier's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Alexandre Xavier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandre Xavier more than expected).

Fields of papers citing papers by Alexandre Xavier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandre Xavier. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Alexandre Xavier. The network helps show where Alexandre Xavier may publish in the future.

Co-authorship network of co-authors of Alexandre Xavier

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandre Xavier. A scholar is included among the top collaborators of Alexandre Xavier based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Alexandre Xavier. Alexandre Xavier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Xavier, Alexandre, Jim Stankovich, Vicki E. Maltby, et al.. (2023). Parity is associated with long-term differences in DNA methylation at genes related to neural plasticity in multiple sclerosis. Clinical Epigenetics. 15(1). 20–20. 6 indexed citations

Xavier, Alexandre, Vicki E. Maltby, Trevor J. Kilpatrick, et al.. (2023). Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis. Frontiers in Immunology. 14. 1162796–1162796. 2 indexed citations

Xavier, Alexandre, Vicki E. Maltby, Ewoud Ewing, et al.. (2023). DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes. International Journal of Molecular Sciences. 24(16). 12576–12576. 7 indexed citations

Reinhardt, Luiza Steffens, et al.. (2023). p53 Dysregulation in Breast Cancer: Insights on Mutations in the TP53 Network and p53 Isoform Expression. International Journal of Molecular Sciences. 24(12). 10078–10078. 2 indexed citations

Maltby, Vicki E., Alexandre Xavier, Ewoud Ewing, et al.. (2023). Evaluation of Cell-Specific Epigenetic Age Acceleration in People With Multiple Sclerosis. Neurology. 101(7). e679–e689. 11 indexed citations

Binder, Michele D., Vivien Li, Alexandre Xavier, et al.. (2023). HLA-DRB1*15:01 and the MERTK Gene Interact to Selectively Influence the Profile of MERTK-Expressing Monocytes in Both Health and MS. Neurology Neuroimmunology & Neuroinflammation. 11(2). e200190–e200190. 3 indexed citations

Reay, William R., Michael P. Geaghan, Joshua Atkins, et al.. (2023). Alteration of DNA Methylation and Epigenetic Scores Associated With Features of Schizophrenia and Common Variant Genetic Risk. Biological Psychiatry. 95(7). 647–661. 12 indexed citations

Singh, Ashish, Bente A. Talseth‐Palmer, Alexandre Xavier, et al.. (2023). Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing. BMC Medical Genomics. 16(1). 126–126. 1 indexed citations

Xavier, Alexandre, Rod A. Lea, Jim Stankovich, et al.. (2022). Whole-blood methylation signatures are associated with and accurately classify multiple sclerosis disease severity. Clinical Epigenetics. 14(1). 194–194. 12 indexed citations

10.

Xavier, Alexandre, Rodney J. Scott, & Bente A. Talseth‐Palmer. (2021). Exome sequencing of familial adenomatous polyposis‐like individuals identifies both known and novel causative genes. Clinical Genetics. 100(4). 478–483. 6 indexed citations

11.

Xavier, Alexandre, Jeannette Lechner‐Scott, Rodney J. Scott, et al.. (2021). Epigenome-wide association studies: current knowledge, strategies and recommendations. Clinical Epigenetics. 13(1). 214–214. 92 indexed citations

12.

Maltby, Vicki E., Rod A. Lea, Alexandre Xavier, et al.. (2020). Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients. Scientific Reports. 10(1). 22217–22217. 8 indexed citations

13.

Singh, Ashish, Bente A. Talseth‐Palmer, Mary McPhillips, et al.. (2020). Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer. PLoS ONE. 15(7). e0235613–e0235613. 4 indexed citations

14.

Xavier, Alexandre, Rodney J. Scott, & Bente A. Talseth‐Palmer. (2019). TAPES: A tool for assessment and prioritisation in exome studies. PLoS Computational Biology. 15(10). e1007453–e1007453. 24 indexed citations

15.

Xavier, Alexandre, Jostein Johansen, Ashish Singh, et al.. (2019). Comprehensive mismatch repair gene panel identifies variants in patients with Lynch‐like syndrome. Molecular Genetics & Genomic Medicine. 7(8). e850–e850. 27 indexed citations

16.

Johansen, Jostein, Inga Bjørnevoll, Bente A. Talseth‐Palmer, et al.. (2017). Use of multigene‐panel identifies pathogenic variants in several CRC‐predisposing genes in patients previously tested for Lynch Syndrome. Clinical Genetics. 92(4). 405–414. 36 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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