David Monk
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Explore the profile of David Monk including associated specialties, affiliations and a list of published articles.
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2803
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Recent Articles
1.
Daskeviciute D, Chappell-Maor L, Sainty B, Arnaud P, Iglesias-Platas I, Simon C, et al.
Hum Mol Genet
. 2025 Jan;
PMID: 39825493
Genomic imprinting is the parent-of-origin dependent monoallelic expression of genes often associated with regions of germline-derived DNA methylation that are maintained as differentially methylated regions (gDMRs) in somatic tissues. This...
2.
Mackay D, Gazdagh G, Monk D, Brioude F, Giabicani E, Krzyzewska I, et al.
Clin Epigenetics
. 2024 Aug;
16(1):99.
PMID: 39090763
Background: Imprinting disorders are rare diseases resulting from altered expression of imprinted genes, which exhibit parent-of-origin-specific expression patterns regulated through differential DNA methylation. A subgroup of patients with imprinting disorders...
3.
Baena N, Monk D, Aguilera C, Fraga M, Fernandez A, Gabau E, et al.
Clin Epigenetics
. 2024 May;
16(1):62.
PMID: 38715103
Background: Temple syndrome (TS14) is a rare imprinting disorder caused by maternal UPD14, imprinting defects or paternal microdeletions which lead to an increase in the maternal expressed genes and a...
4.
Frew E, Sainty R, Chappell-Maor L, Bone C, Daskeviciute D, Russell S, et al.
Placenta
. 2024 Apr;
151:1-9.
PMID: 38615553
Introduction: Placenta-associated pregnancy complications, including pre-eclampsia (PE) and intrauterine growth restriction (IUGR) are conditions postulated to originate from initial failure of placentation, leading to clinical sequelae indicative of endothelial dysfunction....
5.
Patel N, Patel P, Yeung K, Monk D, Mohammadi B, Mughal M, et al.
Ann Surg Oncol
. 2024 Mar;
31(7):4281-4297.
PMID: 38480565
Background: Radical esophagectomy for resectable esophageal cancer is a major surgical intervention, associated with considerable postoperative morbidity. The introduction of robotic surgical platforms in esophagectomy may enhance advantages of minimally...
6.
Sainty R, Silver M, Prentice A, Monk D
Front Cell Dev Biol
. 2023 Jul;
11:1212199.
PMID: 37484911
DNA methylation is the most commonly studied epigenetic mark in humans, as it is well recognised as a stable, heritable mark that can affect genome function and influence gene expression....
7.
Eggermann T, Monk D, Perez de Nanclares G, Kagami M, Giabicani E, Riccio A, et al.
Nat Rev Dis Primers
. 2023 Jun;
9(1):33.
PMID: 37386011
Imprinting disorders (ImpDis) are congenital conditions that are characterized by disturbances of genomic imprinting. The most common individual ImpDis are Prader-Willi syndrome, Angelman syndrome and Beckwith-Wiedemann syndrome. Individual ImpDis have...
8.
Kmush B, Monk D, Green H, Sachs D, Zeng T, Larsen D
FEMS Microbes
. 2023 Jun;
3:xtac017.
PMID: 37332496
Wastewater surveillance is a cost-effective way to monitor pathogen prevalence and transmission patterns in the entire community. Here, we compare 24-hour composite and grab samples collected during September 2020 from...
9.
Hernandez Mora J, Buhigas C, Clark S, Del Gallego Bonilla R, Daskeviciute D, Monteagudo-Sanchez A, et al.
Cell Rep
. 2023 Feb;
42(2):112100.
PMID: 36763500
During pre-implantation stages of mammalian development, maternally stored material promotes both the erasure of the sperm and oocyte epigenetic profiles and is responsible for concomitant genome activation. Here, we have...
10.
Pignata L, Cecere F, Verma A, Mele B, Monticelli M, Acurzio B, et al.
Clin Epigenetics
. 2022 Jun;
14(1):71.
PMID: 35643636
Background: Beckwith-Wiedemann syndrome (BWS) and Pseudohypoparathyroidism type 1B (PHP1B) are imprinting disorders (ID) caused by deregulation of the imprinted gene clusters located at 11p15.5 and 20q13.32, respectively. In both of...