Browsing by Author Monk, David
Showing results 5 to 15 of 15
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Issue Date | Title | Author(s) |
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3-Feb-2020 | Comprehensive analysis of PM20D1 QTL in Alzheimer's disease | Sánchez Mut, Jose Vicente; Glauser, Liliane; Monk, David; Gräff, Johannes |
7-Sep-2017 | Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors | Martín Trujillo, Alex; Vidal, Enrique; Monteagudo Sánchez, Ana; Sánchez Delgado, Marta; Moran, Sebastian; Hernandez Mora, Jose Ramon; Heyn, Holger; Guitart, Miriam; Esteller, Manel; Monk, David |
26-Feb-2019 | Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restriction | Monteagudo Sánchez, Ana; Sánchez Delgado, Marta; Hernandez Mora, Jose Ramon; Tubío Santamaría, Nuria; Gratacós Solsona, Eduard; Esteller, Manel; López de Heredia, Miguel; Nunes Martínez, Virginia; Choux, Cecile; Fauque, Patricia; Perez de Nanclares, Guiomar; Anton, Lauren; Elovitz, Michal A.; Iglesias Platas, Isabel; Monk, David |
6-Jan-2022 | Environmentally sensitive hotspots in the methylome of the early human embryo | Silver, Matt J.; Saffari, Ayden; Kessler, Noah J.; Chandak, Gririraj R.; Fall, Caroline H. D.; Issarapu, Prachand; Dedaniya, Akshay; Betts, Modupeh; Moore, Sophie E.; Routledge, Michael N.; Herceg, Zdenko; Cuenin, Cyrille; Derakhshan, Maria; James, Philip T.; Monk, David; Prentice, Andrew M. |
1-Apr-2014 | Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment | Court, Franck; Tayama, Chiharu; Romanelli, Valeria; Martín Trujillo, Alex; Iglesias Platas, Isabel; Okamura, Kohji; Sugahara, Naoko; Simón, Carlos; Moore, Harry; Harness, Julie V.; Keirstead, Hans; Sanchez-Mut, Jose Vicente; Kaneki, Eisuke; Lapunzina, Pablo; Soejima, Hidenobu; Wake, Norio; Esteller, Manel; Ogata, Tsutomu; Hata, Kenichiro; Nakabayashi, Kazuhiko; Monk, David |
1-Feb-2017 | Human Amniocytes Are Receptive To Chemically Induced Reprogramming To Pluripotency | Hawkins, Kate E.; Moschidou, Dafni; Faccenda, Danilo; Wruck, Wasco; Martín Trujillo, Alex; Hau, Kwan-Leong; Ranzoni, Anna Maria; Sánchez Freire, Veronica V.; Tommasini, Fabio; Eaton, Simon; Coppi, Paolo De; Monk, David; Campanella, Michelangelo; Thrasher, Adrian J.; Adjaye, James; Guillot, Pascale V. |
9-Jan-2014 | Hypermethylation of the alternative AWT1 promoter in hematological malignancies is a highly specific marker for acute myeloid leukemias despite high expression levels | Guillaumet Adkins, Amy; Richter, Julia; Odero, Maria D.; Sandoval, Juan; Agirre, Xabier; Catala, Albert; Esteller, Manel; Prósper, Felipe; Calasanz, María José; Buño, Ismael; Kwo, Mi; Court, Franck; Siebert, Reiner; Monk, David |
7-May-2024 | Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome | Baena, Neus; Monk, David; Aguilera, Cinthia; Fraga, Mario F.; Fernández, Agustín F.; Gabau, Elisabeth; Corripio, Raquel; Capdevila, Nuria; Trujillo, Juan Pablo; Ruiz, Anna; Guitart, Miriam |
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 |