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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2012 2
2013 1
2014 1
2015 1
2016 4
2017 2
2018 4
2019 4
2020 1
2021 3
2022 5
2023 2
2024 0

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28 results

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Page 1
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorder.
Maia N, Potelle S, Yildirim H, Duvet S, Akula SK, Schulz C, Wiame E, Gheldof A, O'Kane K, Lai A, Sermon K, Proisy M, Loget P, Attié-Bitach T, Quelin C, Fortuna AM, Soares AR, de Brouwer APM, Van Schaftingen E, Nassogne MC, Walsh CA, Stouffs K, Jorge P, Jansen AC, Foulquier F. Maia N, et al. Among authors: gheldof a. Am J Hum Genet. 2022 Feb 3;109(2):345-360. doi: 10.1016/j.ajhg.2021.12.010. Epub 2022 Jan 18. Am J Hum Genet. 2022. PMID: 35045343 Free PMC article.
Cadherins and epithelial-to-mesenchymal transition.
Gheldof A, Berx G. Gheldof A, et al. Prog Mol Biol Transl Sci. 2013;116:317-36. doi: 10.1016/B978-0-12-394311-8.00014-5. Prog Mol Biol Transl Sci. 2013. PMID: 23481201 Review.
A systematic review and evidence assessment of monogenic gene-disease relationships in human female infertility and differences in sex development.
Van Der Kelen A, Okutman Ö, Javey E, Serdarogullari M, Janssens C, Ghosh MS, Dequeker BJH, Perold F, Kastner C, Kieffer E, Segers I, Gheldof A, Hes FJ, Sermon K, Verpoest W, Viville S. Van Der Kelen A, et al. Among authors: gheldof a. Hum Reprod Update. 2023 Mar 1;29(2):218-232. doi: 10.1093/humupd/dmac044. Hum Reprod Update. 2023. PMID: 36571510
EDIR: exome database of interspersed repeats.
Vo Ngoc LDT, Osei R, Dohr K, Olsen C, Seneca S, Gheldof A. Vo Ngoc LDT, et al. Among authors: gheldof a. Bioinformatics. 2023 Jan 1;39(1):btac771. doi: 10.1093/bioinformatics/btac771. Bioinformatics. 2023. PMID: 36453866 Free PMC article.
EMT as the ultimate survival mechanism of cancer cells.
Tiwari N, Gheldof A, Tatari M, Christofori G. Tiwari N, et al. Among authors: gheldof a. Semin Cancer Biol. 2012 Jun;22(3):194-207. doi: 10.1016/j.semcancer.2012.02.013. Epub 2012 Mar 8. Semin Cancer Biol. 2012. PMID: 22406545 Review.
Ascites in infantile onset type II Sialidosis.
Tazi K, Guy-Viterbo V, Gheldof A, Empain A, Paternoster A, De Laet C. Tazi K, et al. Among authors: gheldof a. JIMD Rep. 2022 Jun 3;63(4):316-321. doi: 10.1002/jmd2.12305. eCollection 2022 Jul. JIMD Rep. 2022. PMID: 35822090 Free PMC article.
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres.
Persani L, Cools M, Ioakim S, Faisal Ahmed S, Andonova S, Avbelj-Stefanija M, Baronio F, Bouligand J, Bruggenwirth HT, Davies JH, De Baere E, Dzivite-Krisane I, Fernandez-Alvarez P, Gheldof A, Giavoli C, Gravholt CH, Hiort O, Holterhus PM, Juul A, Krausz C, Lagerstedt-Robinson K, McGowan R, Neumann U, Novelli A, Peyrassol X, Phylactou LA, Rohayem J, Touraine P, Westra D, Vezzoli V, Rossetti R. Persani L, et al. Among authors: gheldof a. Endocr Connect. 2022 Nov 14;11(12):e220367. doi: 10.1530/EC-22-0367. Print 2022 Dec 1. Endocr Connect. 2022. PMID: 36228316 Free PMC article.
Clinical implementation of gene panel testing for lysosomal storage diseases.
Gheldof A, Seneca S, Stouffs K, Lissens W, Jansen A, Laeremans H, Verloo P, Schoonjans AS, Meuwissen M, Barca D, Martens G, De Meirleir L. Gheldof A, et al. Mol Genet Genomic Med. 2019 Feb;7(2):e00527. doi: 10.1002/mgg3.527. Epub 2018 Dec 11. Mol Genet Genomic Med. 2019. PMID: 30548430 Free PMC article.
28 results