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

Year Number of Results
2002 1
2003 2
2004 2
2006 2
2007 3
2008 3
2009 3
2010 1
2011 1
2013 1
2014 1
2015 2
2016 4
2017 3
2018 4
2019 5
2020 4
2021 2
2022 3
2023 4
2024 0

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43 results

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Page 1
Intra- and interchromosomal contact mapping reveals the Igh locus has extensive conformational heterogeneity and interacts with B-lineage genes.
Mielczarek O, Rogers CH, Zhan Y, Matheson LS, Stubbington MJT, Schoenfelder S, Bolland DJ, Javierre BM, Wingett SW, Várnai C, Segonds-Pichon A, Conn SJ, Krueger F, Andrews S, Fraser P, Giorgetti L, Corcoran AE. Mielczarek O, et al. Among authors: rogers ch. Cell Rep. 2023 Sep 26;42(9):113074. doi: 10.1016/j.celrep.2023.113074. Epub 2023 Sep 6. Cell Rep. 2023. PMID: 37676766 Free PMC article.
Optimization of 3D autologous chondrocyte-seeded polyglycolic acid scaffolds to mimic human ear cartilage.
Melgar-Lesmes P, Bosch O, Zubajlo R, Molins G, Comfort S, Luque-Saavedra A, López-Moya M, García-Polite F, Parri Ferrandis FJ, Rogers C, Gelabertó A, Martorell J, Edelman ER, Balcells M. Melgar-Lesmes P, et al. Among authors: rogers c. Biomater Sci. 2023 May 16;11(10):3695-3708. doi: 10.1039/d3bm00035d. Biomater Sci. 2023. PMID: 37022673 Free PMC article.
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.
Baker EK, Arpone M, Bui M, Kraan CM, Ling L, Francis D, Hunter MF, Rogers C, Field MJ, Santa María L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende AM, Amor DJ, Godler DE. Baker EK, et al. Among authors: rogers c. Am J Med Genet A. 2023 Feb;191(2):357-369. doi: 10.1002/ajmg.a.63027. Epub 2022 Nov 8. Am J Med Genet A. 2023. PMID: 36349505 Free PMC article.
Agreement between parents' and clinical researchers' ratings of behavioral problems in children with fragile X syndrome and chromosome 15 imprinting disorders.
Arpone M, Bretherton L, Amor DJ, Hearps SJC, Rogers C, Field MJ, Hunter MF, Santa Maria L, Alliende AM, Slee J, Godler DE, Baker EK. Arpone M, et al. Among authors: rogers c. Res Dev Disabil. 2022 Dec;131:104338. doi: 10.1016/j.ridd.2022.104338. Epub 2022 Sep 28. Res Dev Disabil. 2022. PMID: 36179574
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow.
Godler DE, Ling L, Gamage D, Baker EK, Bui M, Field MJ, Rogers C, Butler MG, Murgia A, Leonardi E, Polli R, Schwartz CE, Skinner CD, Alliende AM, Santa Maria L, Pitt J, Greaves R, Francis D, Oertel R, Wang M, Simons C, Amor DJ. Godler DE, et al. Among authors: rogers c. JAMA Netw Open. 2022 Jan 4;5(1):e2141911. doi: 10.1001/jamanetworkopen.2021.41911. JAMA Netw Open. 2022. PMID: 34982160 Free PMC article.
FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome.
Baker EK, Arpone M, Kraan C, Bui M, Rogers C, Field M, Bretherton L, Ling L, Ure A, Cohen J, Hunter MF, Santa María L, Faundes V, Curotto B, Morales P, Trigo C, Salas I, Alliende A, Amor DJ, Godler DE. Baker EK, et al. Among authors: rogers c. Sci Rep. 2020 Jul 16;10(1):11701. doi: 10.1038/s41598-020-68465-6. Sci Rep. 2020. PMID: 32678152 Free PMC article.
43 results