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BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome.
Olley G, Ansari M, Bengani H, Grimes GR, Rhodes J, von Kriegsheim A, Blatnik A, Stewart FJ, Wakeling E, Carroll N, Ross A, Park SM; Deciphering Developmental Disorders Study; Bickmore WA, Pradeepa MM, FitzPatrick DR. Olley G, et al. Among authors: carroll n. Nat Genet. 2018 Mar;50(3):329-332. doi: 10.1038/s41588-018-0042-y. Epub 2018 Jan 29. Nat Genet. 2018. PMID: 29379197 Free PMC article.
Publisher Correction: BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome.
Olley G, Ansari M, Bengani H, Grimes GR, Rhodes J, von Kriegsheim A, Blatnik A, Stewart FJ, Wakeling E, Carroll N, Ross A, Park SM, Bickmore WA, Pradeepa MM, FitzPatrick DR; Deciphering Developmental Disorders Study. Olley G, et al. Among authors: carroll n. Nat Genet. 2018 May;50(5):767. doi: 10.1038/s41588-018-0069-0. Nat Genet. 2018. PMID: 29440723
Publisher Correction: BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome.
Olley G, Ansari M, Bengani H, Grimes GR, Rhodes J, von Kriegsheim A, Blatnik A, Stewart FJ, Wakeling E, Carroll N, Ross A, Park SM; Deciphering Developmental Disorders Study; Bickmore WA, Pradeepa MM, FitzPatrick DR. Olley G, et al. Among authors: carroll n. Nat Genet. 2019 Jul;51(7):1192. doi: 10.1038/s41588-019-0448-1. Nat Genet. 2019. PMID: 31168063
Simultaneous adult polycystic kidney disease and Alport syndrome.
Phelan PJ, Fletcher E, Carroll N, Metcalfe W, Turner AN. Phelan PJ, et al. Among authors: carroll n. Nephrology (Carlton). 2016 Aug;21(8):722-3. doi: 10.1111/nep.12661. Nephrology (Carlton). 2016. PMID: 27436620 No abstract available.
Analysis of the MTHFD1 promoter and risk of neural tube defects.
Carroll N, Pangilinan F, Molloy AM, Troendle J, Mills JL, Kirke PN, Brody LC, Scott JM, Parle-McDermott A. Carroll N, et al. Hum Genet. 2009 Apr;125(3):247-56. doi: 10.1007/s00439-008-0616-3. Epub 2009 Jan 8. Hum Genet. 2009. PMID: 19130090 Free PMC article.
A short-sighted approach to high myopia-not just an eye problem.
Burgess FR, Carroll N, Young SL, Schmoll C, Lampe AK, Chan J. Burgess FR, et al. Among authors: carroll n. J AAPOS. 2021 Aug;25(4):247-248. doi: 10.1016/j.jaapos.2021.03.005. Epub 2021 Jun 22. J AAPOS. 2021. PMID: 34166818
Context-dependent effects of CDKN2A and other 9p21 gene losses during the evolution of esophageal cancer.
Ganguli P, Basanta CC, Acha-Sagredo A, Misetic H, Armero M, Mendez A, Zahra A, Devonshire G, Kelly G, Freeman A, Green M, Nye E, Bichisecchi A, Bonfanti P; Oesophageal Cancer Clinical and Molecular Stratification (OCCAMS) Consortium; Rodriguez-Justo M, Spencer J, Fitzgerald RC, Ciccarelli FD. Ganguli P, et al. Nat Cancer. 2025 Jan 3. doi: 10.1038/s43018-024-00876-0. Online ahead of print. Nat Cancer. 2025. PMID: 39753721
504 results