Hot off the Press 
'Hot off the Press' is a daily listing of the most recent articles in epigenetics and imprinting, collected from the PubMed database and sorted by the date added to PubMed (not necessarily by official publication date). You can also suscribe to an RSS feed.
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Semi-automated IT-scATAC-seq profiles cell-specific chromatin accessibility in differentiation and peripheral blood populations
Jin W, Ma J, Rong L, Huang S, Li T, Jin G, Zhou Z
Nat Commun (Mar 2025)
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Comparative epigenomics to clinical trials in human breast cancer and canine mammary tumor
Jeong SJ, Lee KH, Cho JY
Anim Cells Syst (Seoul) (2025)
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Long non coding RNA function in epigenetic memory with a particular emphasis on genomic imprinting and X chromosome inactivation
Le LTT
Gene (Apr 2025)
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Programmable mRNA therapeutics for controlled epigenomic modulation of single and multiplexed gene expression in diverse diseases
O'Donnell CW, Farelli JD, Belaghzal H, Chen J, Beech L, Sullivan J, Morrison-Smith C, Siecinski S, Katz A, Mildrum S, Gurnani M, Dhanania P, Webb CR, Castello Coatti G, Rumale P, Costa DFG, Gibson MI, Wang YE, Newman JV, McCauley TG
Nat Commun (Mar 2025)
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GWAS for Defining the Pathogenesis of Hypertension: Have They Delivered?
Alexander MR, Edwards TL, Harrison DG
Hypertension (Apr 2025)
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A timely assessment of the state of transcriptomic and epigenomic profiling in OA: opportunities for advancements
Craft AM, Rice SJ, De Bari C, Kapoor M
Osteoarthritis Cartilage (Mar 2025)
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Ripple Effects of Early Life Stress on Vascular Health
Kellum CE, Kelly GC, Pollock JS
Hypertension (Apr 2025)
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Extensive epigenomic dysregulation is a hallmark of homologous recombination deficiency in triple-negative breast cancer
Chen Y, Salas LA, Marotti JD, Jenkins NP, Cheng C, Miller TW, Kettenbach AN, Christensen BC
Int J Cancer (Mar 2025)
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Reframing Formalin: A Molecular Opportunity Enabling Historical Epigenomics and Retrospective Gene Expression Studies
Holleley CE, Hahn EE
Mol Ecol Resour (Apr 2025)
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Host-microbe multi-omics and succinotype profiling have prognostic value for future relapse in patients with inflammatory bowel disease
O'Sullivan J, Patel S, Leventhal GE, Fitzgerald RS, Laserna-Mendieta EJ, Huseyin CE, Konstantinidou N, Rutherford E, Lavelle A, Dabbagh K, DeSantis TZ, Shanahan F, Temko A, Iwai S, Claesson MJ
Gut Microbes (Dec 2025)
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Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome
Braga BL, da Cunha Scalco R, Homma TK, Freire BL, Cellin LP, Canton APM, Lerario AM, de Assis Funari MF, de Souza V, Bertola DR, Malaquias AC, Mendonca BB, de Lima Jorge AA
Clin Genet (Apr 2025)
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Parental origin of transgene modulates amyloid-β plaque burden in the 5xFAD mouse model of Alzheimer's disease
Sasmita AO, Ong EC, Nazarenko T, Mao S, Komarek L, Thalmann M, Hantakova V, Spieth L, Berghoff SA, Barr HJ, Hingerl M, Börensen F, Hirrlinger J, Simons M, Stevens B, Depp C, Nave KA
Neuron (Mar 2025)
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Genome-wide methylation association study in monozygotic twins discordant for curve severity of adolescent idiopathic scoliosis
Wu Z, Dai Z, Feng Z, Qiu Y, Zhu Z, Xu L
Spine J (Apr 2025)
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Unraveling the intricate molecular landscape and potential biomarkers in lung adenocarcinoma through integrative epigenomic and transcriptomic profiling
Mukherjee A, Boonbangyang M, K S M
Sci Rep (Mar 2025)
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Embryo-restricted responses to maternal IL-17A promote neurodevelopmental disorders in mouse offspring
Andruszewski D, Uhlfelder DC, Desiato G, Regen T, Schelmbauer C, Blanfeld M, Scherer L, Radyushkin K, Pozzi D, Waisman A, Mufazalov IA
Mol Psychiatry (Apr 2025)
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Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene
Vimercati A, Tannorella P, Guzzetti S, Calzari L, Gentilini D, Manfredini E, Gori G, Gaudino R, Antona V, Piccione M, Daolio C, Auricchio R, Sirchia F, Minelli A, Rossi E, Bellini M, Biasucci G, Raucci AR, Pozzobon G, Patti G, Napoli F, Larizza L, Maghnie M, Russo S
J Clin Endocrinol Metab (Mar 2025)
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Mechanisms of Impaired Wound Healing in Type 2 Diabetes: The Role of Epigenetic Factors
Bauer TM, Moon J, Shadiow J, Buckley S, Gallagher KA
Arterioscler Thromb Vasc Biol (Mar 2025)
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Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases
Sinha S, Rabea F, Ramaswamy S, Chekroun I, El Naofal M, Jain R, Alfalasi R, Halabi N, Yaslam S, Sheikh Hassani M, Shenbagam S, Taylor A, Uddin M, Almarri MA, Du Plessis S, Alsheikh-Ali A, Abou Tayoun A
Nat Commun (Mar 2025)
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Non-canonical imprinting, manifesting as post-fertilization placenta-specific parent-of-origin dependent methylation, is not conserved in humans
Daskeviciute D, Chappell-Maor L, Sainty B, Arnaud P, Iglesias-Platas I, Simon C, Okae H, Arima T, Vassena R, Lartey J, Monk D
Hum Mol Genet (Mar 2025)
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FDPSM: Feature-Driven Prediction Modeling of Pathogenic Synonymous Mutations
Jin F, Cheng N, Wang L, Ye B, Xia J
J Chem Inf Model (Mar 2025)
