日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

DNA methylation analysis in patients with neurodevelopmental disorders improves variant interpretation and reveals complexity

对神经发育障碍患者进行DNA甲基化分析,可以提高变异解读的准确性并揭示其复杂性。

Trajkova, Slavica; Kerkhof, Jennifer; Rossi Sebastiano, Matteo; Pavinato, Lisa; Ferrero, Enza; Giovenino, Chiara; Carli, Diana; Di Gregorio, Eleonora; Marinoni, Roberta; Mandrile, Giorgia; Palermo, Flavia; Carestiato, Silvia; Cardaropoli, Simona; Pullano, Verdiana; Rinninella, Antonina; Giorgio, Elisa; Pippucci, Tommaso; Dimartino, Paola; Rzasa, Jessica; Rooney, Kathleen; McConkey, Haley; Petlichkovski, Aleksandar; Pasini, Barbara; Sukarova-Angelovska, Elena; Campbell, Christopher M; Metcalfe, Kay; Jenkinson, Sarah; Banka, Siddharth; Mussa, Alessandro; Ferrero, Giovanni Battista; Sadikovic, Bekim; Brusco, Alfredo

Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes.

未解决的神经发育疾病病例中 X 染色体失活偏倚可指导对 X 连锁基因的重新评估

Giovenino Chiara, Trajkova Slavica, Pavinato Lisa, Cardaropoli Simona, Pullano Verdiana, Ferrero Enza, Sukarova-Angelovska Elena, Carestiato Silvia, Salmin Paola, Rinninella Antonina, Battaglia Anthony, Bertoli Luca, Fadda Antonio, Palermo Flavia, Carli Diana, Mussa Alessandro, Dimartino Paola, Bruselles Alessandro, Froukh Tawfiq, Mandrile Giorgia, Pasini Barbara, De Rubeis Silvia, Buxbaum Joseph D, Pippucci Tommaso, Tartaglia Marco, Rossato Marzia, Delledonne Massimo, Ferrero Giovanni Battista, Brusco Alfredo