Works matching IS 18687075 AND DT 2021 AND VI 13 AND IP 1


Results: 247
    1

    Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile.

    Published in:
    Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01145-y
    By:
    • Ciolfi, Andrea;
    • Foroutan, Aidin;
    • Capuano, Alessandro;
    • Pedace, Lucia;
    • Travaglini, Lorena;
    • Pizzi, Simone;
    • Andreani, Marco;
    • Miele, Evelina;
    • Invernizzi, Federica;
    • Reale, Chiara;
    • Panteghini, Celeste;
    • Iascone, Maria;
    • Niceta, Marcello;
    • Gavrilova, Ralitza H.;
    • Schultz-Rogers, Laura;
    • Agolini, Emanuele;
    • Bedeschi, Maria Francesca;
    • Prontera, Paolo;
    • Garibaldi, Matteo;
    • Galosi, Serena
    Publication type:
    Article
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    Methylation status of nc886 epiallele reflects periconceptional conditions and is associated with glucose metabolism through nc886 RNAs.

    Published in:
    Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01132-3
    By:
    • Marttila, Saara;
    • Viiri, Leena E.;
    • Mishra, Pashupati P.;
    • Kühnel, Brigitte;
    • Matias-Garcia, Pamela R.;
    • Lyytikäinen, Leo-Pekka;
    • Ceder, Tiina;
    • Mononen, Nina;
    • Rathmann, Wolfgang;
    • Winkelmann, Juliane;
    • Peters, Annette;
    • Kähönen, Mika;
    • Hutri-Kähönen, Nina;
    • Juonala, Markus;
    • Aalto-Setälä, Katriina;
    • Raitakari, Olli;
    • Lehtimäki, Terho;
    • Waldenberger, Melanie;
    • Raitoharju, Emma
    Publication type:
    Article
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    PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations.

    Published in:
    Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01117-2
    By:
    • Cavicchi, Catia;
    • Oussalah, Abderrahim;
    • Falliano, Silvia;
    • Ferri, Lorenzo;
    • Gozzini, Alessia;
    • Gasperini, Serena;
    • Motta, Serena;
    • Rigoldi, Miriam;
    • Parenti, Giancarlo;
    • Tummolo, Albina;
    • Meli, Concetta;
    • Menni, Francesca;
    • Furlan, Francesca;
    • Daniotti, Marta;
    • Malvagia, Sabrina;
    • la Marca, Giancarlo;
    • Chery, Céline;
    • Morange, Pierre-Emmanuel;
    • Tregouet, David;
    • Donati, Maria Alice
    Publication type:
    Article
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    DNAm-based signatures of accelerated aging and mortality in blood are associated with low renal function.

    Published in:
    Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01082-w
    By:
    • Matías-García, Pamela R.;
    • Ward-Caviness, Cavin K.;
    • Raffield, Laura M.;
    • Gao, Xu;
    • Zhang, Yan;
    • Wilson, Rory;
    • Gào, Xīn;
    • Nano, Jana;
    • Bostom, Andrew;
    • Colicino, Elena;
    • Correa, Adolfo;
    • Coull, Brent;
    • Eaton, Charles;
    • Hou, Lifang;
    • Just, Allan C.;
    • Kunze, Sonja;
    • Lange, Leslie;
    • Lange, Ethan;
    • Lin, Xihong;
    • Liu, Simin
    Publication type:
    Article
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    Blood DNA methylation and COVID-19 outcomes.

    Published in:
    Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01102-9
    By:
    • Balnis, Joseph;
    • Madrid, Andy;
    • Hogan, Kirk J.;
    • Drake, Lisa A.;
    • Chieng, Hau C.;
    • Tiwari, Anupama;
    • Vincent, Catherine E.;
    • Chopra, Amit;
    • Vincent, Peter A.;
    • Robek, Michael D.;
    • Singer, Harold A.;
    • Alisch, Reid S.;
    • Jaitovich, Ariel
    Publication type:
    Article
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