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MAX Stéphanie

Département de médecine interne > Service d'oncologie médicale

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Main Referenced Co-authors
Gothot, André  (4)
Bours, Vincent  (3)
Caberg, Jean-Hubert  (3)
Caers, Jo  (3)
Herens, Christian  (3)
Main Referenced Keywords
chromosome (1); cnv (1); complexity (1); copy number (1); exome (1);
Main Referenced Unit & Research Centers
Giga-Cancer - ULiège [BE] (1)
Giga-Genetics - ULiège [BE] (1)
University of Liège, GIGA-Research, Laboratory of Human Genetics, Liège, Belgium (1)
Main Referenced Disciplines
Oncology (2)
Hematology (1)
Genetics & genetic processes (1)

Publications (total 4)

The most downloaded
347 downloads
Wenric, S.* , Sticca, T.* , CABERG, J.-H., Josse, C., Fasquelle, C., HERENS, C., JAMAR, M., MAX, S., GOTHOT, A., CAERS, J., & Bours, V. (2017). Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample. Genetic Epidemiology, 41, 35-40. doi:10.1002/gepi.22019 https://hdl.handle.net/2268/204351

The most cited

2 citations (OpenCitations)

Sticca, T., CABERG, J.-H., Wenric, S., Poulet, C., HERENS, C., JAMAR, M., Josse, C., El Guendi, S., MAX, S., BEGUIN, Y., GOTHOT, A., CAERS, J., & Bours, V. (2017). Genomic Studies of Multiple Myeloma Reveal an Association between X Chromosome Alterations and Genomic Profile Complexity. Genes, Chromosomes and Cancer, 56, 18-27. doi:10.1002/gcc.22397 https://hdl.handle.net/2268/202711

Wenric, S.* , Sticca, T.* , CABERG, J.-H., Josse, C., Fasquelle, C., HERENS, C., JAMAR, M., MAX, S., GOTHOT, A., CAERS, J., & Bours, V. (2017). Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample. Genetic Epidemiology, 41, 35-40. doi:10.1002/gepi.22019
Peer Reviewed verified by ORBi
* These authors have contributed equally to this work.

Sticca, T., CABERG, J.-H., Wenric, S., Poulet, C., HERENS, C., JAMAR, M., Josse, C., El Guendi, S., MAX, S., BEGUIN, Y., GOTHOT, A., CAERS, J., & Bours, V. (2017). Genomic Studies of Multiple Myeloma Reveal an Association between X Chromosome Alterations and Genomic Profile Complexity. Genes, Chromosomes and Cancer, 56, 18-27. doi:10.1002/gcc.22397
Peer Reviewed verified by ORBi

Sticca, T., Wenric, S., CABERG, J.-H., MAX, S., GOTHOT, A., CAERS, J., & Bours, V. (2015). Genomic study of multiple myeloma based on SNP-aCGH and high-throughput exome sequencing.

Max, S., HERENS, C., Schaaf-Lafontaine, N., & GOTHOT, A. (2011). Intégration des informations phénotypiques et génétiques dans le diagnostic et le suivi du myélome. In Cytométrie 2011 (pp. 128-129).

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