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Genome-wide analysis of copy number variation identifies candidate gene loci associated with the progression of non-alcoholic fatty liver disease.
Zain SM, Mohamed R, Cooper DN, Razali R, Rampal S, Mahadeva S, Chan WK, Anwar A, Rosli NS, Mahfudz AS, Cheah PL, Basu RC, Mohamed Z. Zain SM, et al. Among authors: cooper dn. PLoS One. 2014 Apr 17;9(4):e95604. doi: 10.1371/journal.pone.0095604. eCollection 2014. PLoS One. 2014. PMID: 24743702 Free PMC article.
Prenatal exclusion of severe factor VII deficiency.
Ariffin H, Millar DS, Cooper DN, Chow T, Lin HP. Ariffin H, et al. Among authors: cooper dn. J Pediatr Hematol Oncol. 2003 May;25(5):418-20. doi: 10.1097/00043426-200305000-00014. J Pediatr Hematol Oncol. 2003. PMID: 12759632
Polymorphic pseudogenes in the human genome - a comprehensive assessment.
Lopes-Marques M, Peixoto MJ, Cooper DN, Prata MJ, Azevedo L, Castro LFC. Lopes-Marques M, et al. Among authors: cooper dn. Hum Genet. 2024 Dec;143(12):1465-1479. doi: 10.1007/s00439-024-02715-9. Epub 2024 Nov 2. Hum Genet. 2024. PMID: 39488654 Free PMC article.
VCAT: an integrated variant function annotation tools.
Huang B, Fan C, Chen K, Rao J, Ou P, Tian C, Yang Y, Cooper DN, Zhao H. Huang B, et al. Among authors: cooper dn. Hum Genet. 2024 Nov;143(11):1311-1322. doi: 10.1007/s00439-024-02699-6. Epub 2024 Aug 27. Hum Genet. 2024. PMID: 39192052
Critical assessment of missense variant effect predictors on disease-relevant variant data.
Rastogi R, Chung R, Li S, Li C, Lee K, Woo J, Kim DW, Keum C, Babbi G, Martelli PL, Savojardo C, Casadio R, Chennen K, Weber T, Poch O, Ancien F, Cia G, Pucci F, Raimondi D, Vranken W, Rooman M, Marquet C, Olenyi T, Rost B, Andreoletti G, Kamandula A, Peng Y, Bakolitsa C, Mort M, Cooper DN, Bergquist T, Pejaver V, Liu X, Radivojac P, Brenner SE, Ioannidis NM. Rastogi R, et al. Among authors: cooper dn. bioRxiv [Preprint]. 2024 Jun 8:2024.06.06.597828. doi: 10.1101/2024.06.06.597828. bioRxiv. 2024. PMID: 38895200 Free PMC article. Preprint.
607 results