Publications by authors named "David Monk"

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and are human placenta-specific imprinted genes associated with germline-inherited maternal DNA methylation.
Dagne Daskeviciute, Becky Sainty, Louise Chappell-Maor, Caitlin Bone, Sarah Russell, David Monk

Epigenetics· December 2025

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Single operator learning curve and insights into the adoption of transoral incisionless fundoplication 2.0 in the UK.
Benjamin Norton, Nasar Aslam, Apostolis Papaefthymiou, Andrea Telese, Margaret Duku, David Monk

Dis Esophagus· November 2025

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Non-canonical imprinting, manifesting as post-fertilization placenta-specific parent-of-origin dependent methylation, is not conserved in humans.
Dagne Daskeviciute, Louise Chappell-Maor, Becky Sainty, Philippe Arnaud, Isabel Iglesias-Platas, David Monk

Hum Mol Genet· March 2025

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Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis.
Deborah J G Mackay, Gabriella Gazdagh, David Monk, Frederic Brioude, Eloise Giabicani

Clin Epigenetics· August 2024

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Is Robotic Surgery the Future for Resectable Esophageal Cancer?: A Systematic Literature Review of Oncological and Clinical Outcomes.
Nikhil Manish Patel, Pranav Harshad Patel, Kai Tai Derek Yeung, David Monk, Borzoueh Mohammadi

Ann Surg Oncol· July 2024

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Differential expression of PPP1R12A transcripts, including those harbouring alternatively spliced micro-exons, in placentae from complicated pregnancies.
Edward Frew, Rebecca Sainty, Louise Chappell-Maor, Caitlin Bone, Dagne Daskeviciute, David Monk

Placenta· June 2024

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Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome.
Neus Baena, David Monk, Cinthia Aguilera, Mario F Fraga, Agustín F Fernández

Clin Epigenetics· May 2024

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The influence of early environment and micronutrient availability on developmental epigenetic programming: lessons from the placenta.
Rebecca Sainty, Matt J Silver, Andrew M Prentice, David Monk

Front Cell Dev Biol· July 2023

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Imprinting disorders.
Thomas Eggermann, David Monk, Guiomar Perez de Nanclares, Masayo Kagami, Eloïse Giabicani

Nat Rev Dis Primers· June 2023

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Single-cell multi-omic analysis profiles defective genome activation and epigenetic reprogramming associated with human pre-implantation embryo arrest.
Jose Ramon Hernandez Mora, Claudia Buhigas, Stephen Clark, Raquel Del Gallego Bonilla, Dagne Daskeviciute, David Monk

Cell Rep· February 2023

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Comparability of 24-hour composite and grab samples for detection of SARS-2-CoV RNA in wastewater.
Brittany L Kmush, David Monk, Hyatt Green, Darcy A Sachs, Teng Zeng

FEMS Microbes· June 2022

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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.
Laura Pignata, Francesco Cecere, Ankit Verma, Bruno Hay Mele, Maria Monticelli, David Monk

Clin Epigenetics· May 2022

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Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndrome.
Joan Sabria-Back, Ana Monteagudo-Sánchez, Marta Sánchez-Delgado, Anne C Ferguson-Smith, Olga Gómez, David Monk

J Med Genet· March 2022

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Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.
Thomas Eggermann, Elzem Yapici, Jet Bliek, Arrate Pereda, Matthias Begemann, David Monk

Clin Epigenetics· March 2022

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Environmentally sensitive hotspots in the methylome of the early human embryo.
Matt J Silver, Ayden Saffari, Noah J Kessler, Gririraj R Chandak, Caroline H D Fall, David Monk

Elife· February 2022

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Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients.
Giovanna Mantovani, Murat Bastepe, David Monk, Luisa de Sanctis, Susanne Thiele

Horm Res Paediatr· July 2021

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Prenatal diagnosis of Kagami-Ogata syndrome.
Cristina Molinet Coll, Joan Sabrià Bach, Montserrat Izquierdo Renau, Ana Alarcón Allen, David Monk

J Clin Ultrasound· June 2021

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The hypomethylation of imprinted genes in IVF/ICSI placenta samples is associated with concomitant changes in histone modifications.
Cécile Choux, Paolo Petazzi, Marta Sanchez-Delgado, José R Hernandez Mora, Ana Monteagudo, David Monk

Epigenetics· December 2020

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The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbances.
Ana Monteagudo-Sánchez, Jose Ramon Hernandez Mora, Carlos Simon, Adam Burton, Jair Tenorio, David Monk

Nucleic Acids Res· November 2020

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Comprehensive analysis of PM20D1 QTL in Alzheimer's disease.
Jose Vicente Sanchez-Mut, Liliane Glauser, David Monk, Johannes Gräff

Clin Epigenetics· February 2020

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A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation.
Hannah Demond, Zahra Anvar, Bahia Namavar Jahromi, Angela Sparago, Ankit Verma, David Monk

Genome Med· December 2019

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A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutations.
Philip Savage, David Monk, Jose R Hernandez Mora, Nick van der Westhuizen, Jennifer Rauw

BMC Cancer· July 2019

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Genomic imprinting disorders: lessons on how genome, epigenome and environment interact.
David Monk, Deborah J G Mackay, Thomas Eggermann, Eamonn R Maher, Andrea Riccio

Nat Rev Genet· April 2019

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Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restriction.
Ana Monteagudo-Sánchez, Marta Sánchez-Delgado, Jose Ramon Hernandez Mora, Nuria Tubío Santamaría, Eduard Gratacós, David Monk

Clin Epigenetics· February 2019

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Wnt/β-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells.
Ilda Theka, Francesco Sottile, Marco Cammisa, Sarah Bonnin, Marta Sanchez-Delgado, David Monk

Sci Rep· January 2019

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