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NAR Genomics and Bioinformatics|February 1, 2020
JASS: command line and web interface for the joint analysis of GWAS resultsHanna Julienne, Pierre Lechat, Vincent Guillemot, et al.
European Journal of Nuclear Medicine and Molecular Imaging|June 28, 2019
[11C]JNJ54173717, a novel P2X7 receptor radioligand as marker for neuroinflammation: human biodistribution, dosimetry, brain kinetic modelling and quantification of brain P2X7 receptors in patients with Parkinson's disease and healthy volunteersDonatienne Van Weehaeghe, Michel Koole, Mark E Schmidt, et al.
Nucleic Acids Research|April 1, 2025
Long-read whole-genome sequencing-based concurrent haplotyping and aneuploidy profiling of single cellsYan Zhao, Olga Tsuiko, Tatjana Jatsenko, et al.
Microbiology Spectrum|February 27, 2023
Yersiniomics, a Multi-Omics Interactive Database for Yersinia SpeciesPierre Lê-Bury, Karen Druart, Cyril Savin, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 2012
Impact of lactobacilli on orally acquired listeriosisCristel Archambaud, Marie-Anne Nahori, Guillaume Soubigou, et al.
American Journal of Medical Genetics. Part A|May 2, 2015
The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defectsYaojuan Jia, Jacoba J Louw, Jeroen Breckpot, et al.
European Journal of Human Genetics : EJHG|October 29, 2015
Guidelines for diagnostic next-generation sequencingGert Matthijs, Erika Souche, Mariëlle Alders, et al.
Inflammatory Bowel Diseases|December 10, 2024
MIP4IBD: An Easy and Rapid Genotyping-by-Sequencing Assay for the Inflammatory Bowel Diseases Risk LociSare Verstockt, Laurens Hannes, Deborah Sarah Jans, et al.
JIMD Reports|March 17, 2021
SLC37A4-CDG: Second patientMatthew P Wilson, Dulce Quelhas, Elisa Leão-Teles, et al.
Biorxiv : the Preprint Server for Biology|July 1, 2024
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX geneTakfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, et al.
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