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David Monk

Title(s)Adjunct Instructor
Address650 Childs Way
University Park Campus
Los Angeles CA 90089
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. A case of intraplacental gestational choriocarcinoma; characterised by the methylation pattern of the early placenta and an absence of driver mutations. BMC Cancer. 2019 Jul 29; 19(1):744. Savage P, Monk D, Hernandez Mora JR, van der Westhuizen N, Rauw J, Tinker A, Robinson W, Song Q, Seckl MJ, Fisher RA. PMID: 31357948.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    2. Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restriction. Clin Epigenetics. 2019 02 26; 11(1):35. Monteagudo-Sánchez A, Sánchez-Delgado M, Mora JRH, Santamaría NT, Gratacós E, Esteller M, de Heredia ML, Nunes V, Choux C, Fauque P, de Nanclares GP, Anton L, Elovitz MA, Iglesias-Platas I, Monk D. PMID: 30808399.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    3. Wnt/ß-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells. Sci Rep. 2019 01 30; 9(1):948. Theka I, Sottile F, Cammisa M, Bonnin S, Sanchez-Delgado M, Di Vicino U, Neguembor MV, Arumugam K, Aulicino F, Monk D, Riccio A, Cosma MP. PMID: 30700782.
      View in: PubMed   Mentions: 2     Fields:    Translation:AnimalsCells
    4. Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform. Epigenomics. 2018 07; 10(7):941-954. Hernandez Mora JR, Tayama C, Sánchez-Delgado M, Monteagudo-Sánchez A, Hata K, Ogata T, Medrano J, Poo-Llanillo ME, Simón C, Moran S, Esteller M, Tenorio J, Lapunzina P, Kagami M, Monk D, Nakabayashi K. PMID: 29962238.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    5. The Use of Methylation-Sensitive Multiplex Ligation-Dependent Probe Amplification for Quantification of Imprinted Methylation. Methods Mol Biol. 2018; 1766:109-121. Monteagudo-Sánchez A, Garin I, de Nanclares GP, Monk D. PMID: 29605849.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    6. NLRPs, the subcortical maternal complex and genomic imprinting. Reproduction. 2017 12; 154(6):R161-R170. Monk D, Sanchez-Delgado M, Fisher R. PMID: 28916717.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    7. Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors. Nat Commun. 2017 09 07; 8(1):467. Martin-Trujillo A, Vidal E, Monteagudo-Sánchez A, Sanchez-Delgado M, Moran S, Hernandez Mora JR, Heyn H, Guitart M, Esteller M, Monk D. PMID: 28883545.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    8. Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted. Hum Mutat. 2017 06; 38(6):615-620. Alsina Casanova M, Monteagudo-Sánchez A, Rodiguez Guerineau L, Court F, Gazquez Serrano I, Martorell L, Rovira Zurriaga C, Moore GE, Ishida M, Castañon M, Moliner Calderon E, Monk D, Moreno Hernando J. PMID: 28256047.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    9. Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting. PLoS Genet. 2016 Nov; 12(11):e1006427. Sanchez-Delgado M, Court F, Vidal E, Medrano J, Monteagudo-Sánchez A, Martin-Trujillo A, Tayama C, Iglesias-Platas I, Kondova I, Bontrop R, Poo-Llanillo ME, Marques-Bonet T, Nakabayashi K, Simón C, Monk D. PMID: 27835649.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansAnimalsCells
    10. APOA5 genetic and epigenetic variability jointly regulate circulating triacylglycerol levels. Clin Sci (Lond). 2016 11 01; 130(22):2053-2059. Oliva I, Guardiola M, Vallvé JC, Ibarretxe D, Plana N, Masana L, Monk D, Ribalta J. PMID: 27613158.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    11. Diagnosis and management of Silver-Russell syndrome: first international consensus statement. Nat Rev Endocrinol. 2017 02; 13(2):105-124. Wakeling EL, Brioude F, Lokulo-Sodipe O, O'Connell SM, Salem J, Bliek J, Canton AP, Chrzanowska KH, Davies JH, Dias RP, Dubern B, Elbracht M, Giabicani E, Grimberg A, Grønskov K, Hokken-Koelega AC, Jorge AA, Kagami M, Linglart A, Maghnie M, Mohnike K, Monk D, Moore GE, Murray PG, Ogata T, Petit IO, Russo S, Said E, Toumba M, Tümer Z, Binder G, Eggermann T, Harbison MD, Temple IK, Mackay DJ, Netchine I. PMID: 27585961.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    12. Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques. Am J Med Genet A. 2016 10; 170(10):2740-9. Tenorio J, Romanelli V, Martin-Trujillo A, Fernández GM, Segovia M, Perandones C, Pérez Jurado LA, Esteller M, Fraga M, Arias P, Gordo G, Dapía I, Mena R, Palomares M, Pérez de Nanclares G, Nevado J, García-Miñaur S, Santos-Simarro F, Martinez-Glez V, Vallespín E, Monk D, Lapunzina P. PMID: 27480579.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    13. Nongenomic regulation of gene expression. Curr Opin Pediatr. 2016 08; 28(4):521-8. Iglesias-Platas I, Monk D. PMID: 27139000.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    14. Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances. Epigenomics. 2016 06; 8(6):801-16. Bens S, Kolarova J, Beygo J, Buiting K, Caliebe A, Eggermann T, Gillessen-Kaesbach G, Prawitt D, Thiele-Schmitz S, Begemann M, Enklaar T, Gutwein J, Haake A, Paul U, Richter J, Soellner L, Vater I, Monk D, Horsthemke B, Ammerpohl O, Siebert R. PMID: 27323310.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    15. EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome. Eur J Hum Genet. 2016 10; 24(10):1377-87. Eggermann K, Bliek J, Brioude F, Algar E, Buiting K, Russo S, Tümer Z, Monk D, Moore G, Antoniadi T, Macdonald F, Netchine I, Lombardi P, Soellner L, Begemann M, Prawitt D, Maher ER, Mannens M, Riccio A, Weksberg R, Lapunzina P, Grønskov K, Mackay DJ, Eggermann T. PMID: 27165005.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    16. Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects. Clin Epigenetics. 2016; 8:10. Rochtus A, Martin-Trujillo A, Izzi B, Elli F, Garin I, Linglart A, Mantovani G, Perez de Nanclares G, Thiele S, Decallonne B, Van Geet C, Monk D, Freson K. PMID: 26819647.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    17. Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting. PLoS Genet. 2015 Nov; 11(11):e1005644. Sanchez-Delgado M, Martin-Trujillo A, Tayama C, Vidal E, Esteller M, Iglesias-Platas I, Deo N, Barney O, Maclean K, Hata K, Nakabayashi K, Fisher R, Monk D. PMID: 26544189.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansCells
    18. Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling. Eur J Hum Genet. 2016 06; 24(6):784-93. Eggermann T, Brioude F, Russo S, Lombardi MP, Bliek J, Maher ER, Larizza L, Prawitt D, Netchine I, Gonzales M, Grønskov K, Tümer Z, Monk D, Mannens M, Chrzanowska K, Walasek MK, Begemann M, Soellner L, Eggermann K, Tenorio J, Nevado J, Moore GE, Mackay DJ, Temple K, Gillessen-Kaesbach G, Ogata T, Weksberg R, Algar E, Lapunzina P. PMID: 26508573.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    19. Genomic imprinting in the human placenta. Am J Obstet Gynecol. 2015 Oct; 213(4 Suppl):S152-62. Monk D. PMID: 26428495.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansAnimalsCells
    20. Germline-derived DNA methylation and early embryo epigenetic reprogramming: The selected survival of imprints. Int J Biochem Cell Biol. 2015 Oct; 67:128-38. Monk D. PMID: 25966912.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimalsCells
    21. Combined epigenetic and intraspecific variation of the DRD4 and SERT genes influence novelty seeking behavior in great tit Parus major. Epigenetics. 2015; 10(6):516-25. Riyahi S, Sánchez-Delgado M, Calafell F, Monk D, Senar JC. PMID: 25933062.
      View in: PubMed   Mentions: 3     Fields:    Translation:AnimalsCells
    22. The role and interaction of imprinted genes in human fetal growth. Philos Trans R Soc Lond B Biol Sci. 2015 Mar 05; 370(1663):20140074. Moore GE, Ishida M, Demetriou C, Al-Olabi L, Leon LJ, Thomas AC, Abu-Amero S, Frost JM, Stafford JL, Chaoqun Y, Duncan AJ, Baigel R, Brimioulle M, Iglesias-Platas I, Apostolidou S, Aggarwal R, Whittaker JC, Syngelaki A, Nicolaides KH, Regan L, Monk D, Stanier P. PMID: 25602077.
      View in: PubMed   Mentions: 33     Fields:    Translation:Humans
    23. Altered expression of the imprinted transcription factor PLAGL1 deregulates a network of genes in the human IUGR placenta. Hum Mol Genet. 2014 Dec 01; 23(23):6275-85. Iglesias-Platas I, Martin-Trujillo A, Petazzi P, Guillaumet-Adkins A, Esteller M, Monk D. PMID: 24993786.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    24. Screening individuals with intellectual disability, autism and Tourette's syndrome for KCNK9 mutations and aberrant DNA methylation within the 8q24 imprinted cluster. Am J Med Genet B Neuropsychiatr Genet. 2014 Sep; 165B(6):472-8. Sánchez Delgado M, Camprubí C, Tümer Z, Martínez F, Milà M, Monk D. PMID: 24980697.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    25. Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment. Genome Res. 2014 Apr; 24(4):554-69. Court F, Tayama C, Romanelli V, Martin-Trujillo A, Iglesias-Platas I, Okamura K, Sugahara N, Simón C, Moore H, Harness JV, Keirstead H, Sanchez-Mut JV, Kaneki E, Lapunzina P, Soejima H, Wake N, Esteller M, Ogata T, Hata K, Nakabayashi K, Monk D. PMID: 24402520.
      View in: PubMed   Mentions: 93     Fields:    Translation:HumansCells
    26. Stability of genomic imprinting and gestational-age dynamic methylation in complicated pregnancies conceived following assisted reproductive technologies. Biol Reprod. 2013 Sep; 89(3):50. Camprubí C, Iglesias-Platas I, Martin-Trujillo A, Salvador-Alarcon C, Rodriguez MA, Barredo DR, Court F, Monk D. PMID: 23884645.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    27. Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes. Hum Mutat. 2013 Apr; 34(4):595-602. Court F, Martin-Trujillo A, Romanelli V, Garin I, Iglesias-Platas I, Salafsky I, Guitart M, Perez de Nanclares G, Lapunzina P, Monk D. PMID: 23335487.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    28. Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop. Nucleic Acids Res. 2013 Feb 01; 41(4):2171-9. Iglesias-Platas I, Court F, Camprubi C, Sparago A, Guillaumet-Adkins A, Martin-Trujillo A, Riccio A, Moore GE, Monk D. PMID: 23295672.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    29. Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin. PLoS One. 2012; 7(6):e38907. Iglesias-Platas I, Martin-Trujillo A, Cirillo D, Court F, Guillaumet-Adkins A, Camprubi C, Bourc'his D, Hata K, Feil R, Tartaglia G, Arnaud P, Monk D. PMID: 22723905.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    30. Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight. Am J Hum Genet. 2012 Apr 06; 90(4):715-9. Ishida M, Monk D, Duncan AJ, Abu-Amero S, Chong J, Ring SM, Pembrey ME, Hindmarsh PC, Whittaker JC, Stanier P, Moore GE. PMID: 22444668.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    31. Genotype of an individual single nucleotide polymorphism regulates DNA methylation at the TRPC3 alternative promoter. Epigenetics. 2011 Oct 01; 6(10):1236-41. Martin-Trujillo A, Iglesias-Platas I, Coto E, Corral-Juan M, San Nicolás H, Corral J, Volpini V, Matilla-Dueñas A, Monk D. PMID: 21931279.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    32. Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes. Hum Mol Genet. 2011 Aug 15; 20(16):3188-97. Nakabayashi K, Trujillo AM, Tayama C, Camprubi C, Yoshida W, Lapunzina P, Sanchez A, Soejima H, Aburatani H, Nagae G, Ogata T, Hata K, Monk D. PMID: 21593219.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansAnimalsCells
    33. Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes. Nucleic Acids Res. 2011 Jun; 39(11):4577-86. Monk D, Arnaud P, Frost JM, Wood AJ, Cowley M, Martin-Trujillo A, Guillaumet-Adkins A, Iglesias Platas I, Camprubi C, Bourc'his D, Feil R, Moore GE, Oakey RJ. PMID: 21300645.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    34. Deciphering the cancer imprintome. Brief Funct Genomics. 2010 Jul; 9(4):329-39. Monk D. PMID: 20551091.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimalsCells
    35. Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression. Hum Mol Genet. 2009 Aug 15; 18(16):3066-74. Monk D, Arnaud P, Frost J, Hills FA, Stanier P, Feil R, Moore GE. PMID: 19487367.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansCells
    36. Transcript- and tissue-specific imprinting of a tumour suppressor gene. Hum Mol Genet. 2009 Jan 01; 18(1):118-27. Schulz R, McCole RB, Woodfine K, Wood AJ, Chahal M, Monk D, Moore GE, Oakey RJ. PMID: 18836209.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimalsCells
    37. Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues. Hum Mol Genet. 2008 Nov 01; 17(21):3263-70. Parker-Katiraee L, Bousiaki E, Monk D, Moore GE, Nakabayashi K, Scherer SW. PMID: 18678600.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimalsCells
    38. Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing. Genome Res. 2008 Aug; 18(8):1270-81. Monk D, Wagschal A, Arnaud P, Müller PS, Parker-Katiraee L, Bourc'his D, Scherer SW, Feil R, Stanier P, Moore GE. PMID: 18480470.
      View in: PubMed   Mentions: 38     Fields:    Translation:HumansAnimalsCells
    39. Genomic imprinting of Dopa decarboxylase in heart and reciprocal allelic expression with neighboring Grb10. Mol Cell Biol. 2008 Jan; 28(1):386-96. Menheniott TR, Woodfine K, Schulz R, Wood AJ, Monk D, Giraud AS, Baldwin HS, Moore GE, Oakey RJ. PMID: 17967881.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansAnimalsCells
    40. STOX1 is not imprinted and is not likely to be involved in preeclampsia. Nat Genet. 2007 Mar; 39(3):279-80; author reply 280-1. Iglesias-Platas I, Monk D, Jebbink J, Buimer M, Boer K, van der Post J, Hills F, Apostolidou S, Ris-Stalpers C, Stanier P, Moore GE. PMID: 17325670.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    41. A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation. PLoS Genet. 2007 Feb 09; 3(2):e20. Wood AJ, Roberts RG, Monk D, Moore GE, Schulz R, Oakey RJ. PMID: 17291163.
      View in: PubMed   Mentions: 52     Fields:    Translation:HumansAnimalsCells
    42. Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies. Am J Hum Genet. 2006 Nov; 79(5):859-68. Zhou H, Brockington M, Jungbluth H, Monk D, Stanier P, Sewry CA, Moore GE, Muntoni F. PMID: 17033962.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansAnimalsCells
    43. Intrauterine growth restriction--genetic causes and consequences. Semin Fetal Neonatal Med. 2004 Oct; 9(5):371-8. Monk D, Moore GE. PMID: 15691772.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansAnimals
    44. Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis. Mamm Genome. 2003 Dec; 14(12):805-16. Monk D, Smith R, Arnaud P, Preece MA, Stanier P, Beechey CV, Peters J, Kelsey G, Moore GE. PMID: 14724735.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    45. Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark. Hum Mol Genet. 2003 May 01; 12(9):1005-19. Arnaud P, Monk D, Hitchins M, Gordon E, Dean W, Beechey CV, Peters J, Craigen W, Preece M, Stanier P, Moore GE, Kelsey G. PMID: 12700169.
      View in: PubMed   Mentions: 52     Fields:    Translation:HumansAnimalsCells
    46. DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed. Mamm Genome. 2002 Dec; 13(12):686-91. Hitchins MP, Bentley L, Monk D, Beechey C, Peters J, Kelsey G, Ishino F, Preece MA, Stanier P, Moore GE. PMID: 12514746.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    47. Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region. Hum Genet. 2002 Oct; 111(4-5):376-87. Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE. PMID: 12384779.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
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