Browsing by Author Monk, David
Showing results 12 to 14 of 14
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| Issue Date | Title | Author(s) |
|---|---|---|
| 28-May-2022 | Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances | Pignata, Laura; Cecere, Francesco; Verma, Ankit; Hay Mele, Bruno; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Hernandez Mora, Jose Ramon; Monteagudo Sánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenorio Castano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Cubellis, Maria Vittoria; Perez de Nanclares, Guiomar; Monk, David; Riccio, Andrea; Cerrato, Flavia |
| 1-Jan-2018 | Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains | Monk, David; Morales, Joannella; den Dunnen, Johan T.; Russo, Silvia; Court, Franck; Prawitt, Dirk; Eggermann, Thomas; Beygo, Jasmin; Buiting, Karin; Tumer, Zeynep; Nomenclature group of the European Network for Human Congenital Imprinting Disorders |
| 1-Feb-2023 | Single-cell multi-omic analysis profiles defective genome activation and epigenetic reprogramming associated with human pre-implantation embryo arrest | Hernandez Mora, Jose Ramon; Buhigas, Claudia; Clark, Stephen; Gallego Bonilla, Raquel del; Daskeviciute, Dagne; Monteagudo Sánchez, Ana; Poo Llanillo, Maria Eugenia; Medrano, Jose Vicente; Simón, Carlos; Meseguer, Marcos; Kelsey, Gavin; Monk, David |