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Results by year

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

Year Number of Results
1929 1
1938 1
1950 1
1952 2
1957 1
1958 1
1959 6
1960 1
1961 1
1962 3
1963 4
1964 7
1965 5
1966 2
1967 2
1968 4
1970 1
1973 1
1984 1
1988 1
1991 1
1993 1
1994 1
1996 4
1997 3
1998 3
1999 5
2000 7
2001 7
2002 8
2003 6
2004 9
2005 2
2006 3
2007 7
2008 1
2009 4
2010 1
2011 7
2012 8
2013 7
2014 11
2015 2
2016 6
2017 5
2018 11
2019 5
2020 7
2021 7
2022 3
2023 6
2024 2

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196 results

Results by year

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Page 1
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Weiss K, Lazar HP, Kurolap A, Martinez AF, Paperna T, Cohen L, Smeland MF, Whalen S, Heide S, Keren B, Terhal P, Irving M, Takaku M, Roberts JD, Petrovich RM, Schrier Vergano SA, Kenney A, Hove H, DeChene E, Quinonez SC, Colin E, Ziegler A, Rumple M, Jain M, Monteil D, Roeder ER, Nugent K, van Haeringen A, Gambello M, Santani A, Medne L, Krock B, Skraban CM, Zackai EH, Dubbs HA, Smol T, Ghoumid J, Parker MJ, Wright M, Turnpenny P, Clayton-Smith J, Metcalfe K, Kurumizaka H, Gelb BD, Baris Feldman H, Campeau PM, Muenke M, Wade PA, Lachlan K. Weiss K, et al. Among authors: wade pa. Genet Med. 2020 Feb;22(2):389-397. doi: 10.1038/s41436-019-0612-0. Epub 2019 Aug 7. Genet Med. 2020. PMID: 31388190 Free PMC article.
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study; Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM. Snijders Blok L, et al. Among authors: wade pa. Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Nat Commun. 2018. PMID: 30397230 Free PMC article.
The NuRD architecture.
Allen HF, Wade PA, Kutateladze TG. Allen HF, et al. Among authors: wade pa. Cell Mol Life Sci. 2013 Oct;70(19):3513-24. doi: 10.1007/s00018-012-1256-2. Epub 2013 Jan 23. Cell Mol Life Sci. 2013. PMID: 23340908 Free PMC article. Review.
Proteins That Read DNA Methylation.
Shimbo T, Wade PA. Shimbo T, et al. Among authors: wade pa. Adv Exp Med Biol. 2016;945:303-320. doi: 10.1007/978-3-319-43624-1_13. Adv Exp Med Biol. 2016. PMID: 27826844 Review.
Epigenetic remodelling upon FGFR inhibition.
Orlando KA, Wade PA. Orlando KA, et al. Among authors: wade pa. Nat Cell Biol. 2021 Nov;23(11):1115-1116. doi: 10.1038/s41556-021-00782-y. Nat Cell Biol. 2021. PMID: 34737444 No abstract available.
DNA demethylation.
Wolffe AP, Jones PL, Wade PA. Wolffe AP, et al. Among authors: wade pa. Proc Natl Acad Sci U S A. 1999 May 25;96(11):5894-6. doi: 10.1073/pnas.96.11.5894. Proc Natl Acad Sci U S A. 1999. PMID: 10339513 Free PMC article. Review. No abstract available.
Proteins That Read DNA Methylation.
Liu K, Shimbo T, Song X, Wade PA, Min J. Liu K, et al. Among authors: wade pa. Adv Exp Med Biol. 2022;1389:269-293. doi: 10.1007/978-3-031-11454-0_11. Adv Exp Med Biol. 2022. PMID: 36350514
Epigenetics and the adaptive immune response.
Kondilis-Mangum HD, Wade PA. Kondilis-Mangum HD, et al. Among authors: wade pa. Mol Aspects Med. 2013 Jul-Aug;34(4):813-25. doi: 10.1016/j.mam.2012.06.008. Epub 2012 Jul 10. Mol Aspects Med. 2013. PMID: 22789989 Free PMC article. Review.
196 results