Aharon Razin

Biochemistry, Genetics and Molecular Biology · Life Sciences

58h-index15.9kcitations144works0.02yr avg
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Research Topics

Epigenetics and DNA Methylation(89), Genetic Syndromes and Imprinting(30), Cancer-related gene regulation(30), DNA and Nucleic Acid Chemistry(20), RNA modifications and cancer(19)

Publications143 total

Improving question answering in programming domain with pretrained language model finetuning using structured diverse online forum data
Scientific and technical journal of information technologies mechanics and optics·2024Open Access
Islet cells share promoter hypomethylation independently of expression, but exhibit cell-type–specific methylation in enhancers
Proceedings of the National Academy of Sciences·2017· 59 citedOpen Access
Annotating the genome by DNA methylation
The International Journal of Developmental Biology·2017· 6 cited
Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study
Journal of Molecular Neuroscience·2016· 10 cited
Identification of tissue-specific cell death using methylation patterns of circulating DNA
Proceedings of the National Academy of Sciences·2016· 608 citedOpen Access
Pattern of methylation of two gene housekeeping functions (DNA methylation/Chinese hamster adenine phosphoribosyltransfers
2016
(DNA-mediated gene transfer/hemimethylated DNA/maintenance Im
2016
Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation
PLoS ONE·2015· 25 citedOpen Access
IKAP Deficiency in an FD Mouse Model and in Oligodendrocyte Precursor Cells Results in Downregulation of Genes Involved in Oligodendrocyte Differentiation and Myelin Formation
PLoS ONE·2014· 12 citedOpen Access
Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patients
Autonomic Neuroscience·2013· 6 cited
Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains
Proceedings of the National Academy of Sciences·2012· 40 citedOpen Access
IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomia
Human Molecular Genetics·2011· 58 cited
Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain
Proceedings of the National Academy of Sciences·2009· 26 citedOpen Access
MeCP2 involvement in the regulation of neuronal  -tubulin production
Human Molecular Genetics·2009· 23 citedOpen Access
<scp>DNA</scp> Methylation: Evolution
Encyclopedia of Life Sciences·2007
MeCP2 Deficiency in the Brain Decreases BDNF Levels by REST/CoREST-Mediated Repression and Increases TRKB Production
Epigenetics·2007· 138 cited
IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination
Human Molecular Genetics·2007· 54 cited
DNA Methylation
Medical intelligence unit·2007· 2 cited
<scp>DNA</scp> Methylation: Evolution
Encyclopedia of Life Sciences·2006
The Prader-Willi/Angelman imprinted domain and its control center
Cytogenetic and Genome Research·2006· 41 cited
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Frequent Co-authors

Howard Cedar(24), Ruth Shemer(9), Tal Kafri(6), Yosef Gruenbaum(6), Moshe Szyf(6), Arthur D. Riggs(5), Reuven Stein(5), Yehudit Birger(3), M. Silber Ariel(2), Michael Brandeis(2), John R. McCarrey(2), Tally Naveh‐Many(2), Dale Frank(2), Yaakov Pollack(2), Abraham Fainsod(2), Shlomo Rottem(2), John W. Sedat(2), N Sciaky-Gallili(2), Gad Glaser(2), Ilana Keshet(2)