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The role of imprinted genes in humans.
Ishida M, Moore GE. Ishida M, et al. Mol Aspects Med. 2013 Jul-Aug;34(4):826-40. doi: 10.1016/j.mam.2012.06.009. Epub 2012 Jul 4. Mol Aspects Med. 2013. PMID: 22771538 Free article. Review.
Genome-wide methylation analysis in Silver-Russell syndrome patients.
Prickett AR, Ishida M, Böhm S, Frost JM, Puszyk W, Abu-Amero S, Stanier P, Schulz R, Moore GE, Oakey RJ. Prickett AR, et al. Among authors: ishida m. Hum Genet. 2015 Mar;134(3):317-332. doi: 10.1007/s00439-014-1526-1. Epub 2015 Jan 7. Hum Genet. 2015. PMID: 25563730 Free PMC article.
Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood.
Lokulo-Sodipe O, Ballard L, Child J, Inskip HM, Byrne CD, Ishida M, Moore GE, Wakeling EL, Fenwick A, Mackay DJG, Davies JH, Temple IK. Lokulo-Sodipe O, et al. Among authors: ishida m. J Med Genet. 2020 Oct;57(10):683-691. doi: 10.1136/jmedgenet-2019-106561. Epub 2020 Feb 13. J Med Genet. 2020. PMID: 32054688 Free PMC article.
Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.
Alsina Casanova M, Monteagudo-Sánchez A, Rodiguez Guerineau L, Court F, Gazquez Serrano I, Martorell L, Rovira Zurriaga C, Moore GE, Ishida M, Castañon M, Moliner Calderon E, Monk D, Moreno Hernando J. Alsina Casanova M, et al. Among authors: ishida m. Hum Mutat. 2017 Jun;38(6):615-620. doi: 10.1002/humu.23213. Epub 2017 Mar 24. Hum Mutat. 2017. PMID: 28256047
The speech gene FOXP2 is not imprinted.
Thomas AC, Frost JM, Ishida M, Vargha-Khadem F, Moore GE, Stanier P. Thomas AC, et al. Among authors: ishida m. J Med Genet. 2012 Nov;49(11):669-70. doi: 10.1136/jmedgenet-2012-101242. Epub 2012 Oct 2. J Med Genet. 2012. PMID: 23033221 No abstract available.
The role and interaction of imprinted genes in human fetal growth.
Moore GE, Ishida M, Demetriou C, Al-Olabi L, Leon LJ, Thomas AC, Abu-Amero S, Frost JM, Stafford JL, Chaoqun Y, Duncan AJ, Baigel R, Brimioulle M, Iglesias-Platas I, Apostolidou S, Aggarwal R, Whittaker JC, Syngelaki A, Nicolaides KH, Regan L, Monk D, Stanier P. Moore GE, et al. Among authors: ishida m. Philos Trans R Soc Lond B Biol Sci. 2015 Mar 5;370(1663):20140074. doi: 10.1098/rstb.2014.0074. Philos Trans R Soc Lond B Biol Sci. 2015. PMID: 25602077 Free PMC article. Review.
Analysis of CDKN1C in fetal growth restriction and pregnancy loss.
Suntharalingham JP, Ishida M, Buonocore F, Del Valle I, Solanky N, Demetriou C, Regan L, Moore GE, Achermann JC. Suntharalingham JP, et al. Among authors: ishida m. F1000Res. 2019 Jan 23;8:90. doi: 10.12688/f1000research.15016.2. eCollection 2019. F1000Res. 2019. PMID: 31497289 Free PMC article. Review.
Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome.
Suntharalingham JP, Ishida M, Del Valle I, Stalman SE, Solanky N, Wakeling E, Moore GE, Achermann JC, Buonocore F. Suntharalingham JP, et al. Among authors: ishida m. Front Endocrinol (Lausanne). 2022 Aug 18;13:953707. doi: 10.3389/fendo.2022.953707. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36060959 Free PMC article.
2,571 results