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Page 1
A cookbook for DNase Hi-C.
Gridina M, Mozheiko E, Valeev E, Nazarenko LP, Lopatkina ME, Markova ZG, Yablonskaya MI, Voinova VY, Shilova NV, Lebedev IN, Fishman V. Gridina M, et al. Epigenetics Chromatin. 2021 Mar 20;14(1):15. doi: 10.1186/s13072-021-00389-5. Epigenetics Chromatin. 2021. PMID: 33743768 Free PMC article.
Predicting Genome Architecture: Challenges and Solutions.
Belokopytova P, Fishman V. Belokopytova P, et al. Front Genet. 2021 Jan 22;11:617202. doi: 10.3389/fgene.2020.617202. eCollection 2020. Front Genet. 2021. PMID: 33552135 Free PMC article. Review.
Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene.
Gridina MM, Matveeva NM, Fishman VS, Menzorov AG, Kizilova HA, Beregovoy NA, Kovrigin II, Pristyazhnyuk IE, Oscorbin IP, Filipenko ML, Kashevarova AA, Skryabin NA, Nikitina TV, Sazhenova EA, Nazarenko LP, Lebedev IN, Serov OL. Gridina MM, et al. Among authors: fishman vs. Mol Neurobiol. 2018 Aug;55(8):6533-6546. doi: 10.1007/s12035-017-0851-5. Epub 2018 Jan 11. Mol Neurobiol. 2018. PMID: 29327201
A mosaic intragenic microduplication of LAMA1 and a constitutional 18p11.32 microduplication in a patient with keratosis pilaris and intellectual disability.
Kashevarova AA, Nazarenko LP, Skryabin NA, Nikitina TV, Vasilyev SA, Tolmacheva EN, Lopatkina ME, Salyukova OA, Chechetkina NN, Vorotelyak EA, Kalabusheva EP, Fishman VS, Kzhyshkowska J, Graziano C, Magini P, Romeo G, Lebedev IN. Kashevarova AA, et al. Among authors: fishman vs. Am J Med Genet A. 2018 Nov;176(11):2395-2403. doi: 10.1002/ajmg.a.40478. Epub 2018 Sep 23. Am J Med Genet A. 2018. PMID: 30244536
Quantitative prediction of enhancer-promoter interactions.
Belokopytova PS, Nuriddinov MA, Mozheiko EA, Fishman D, Fishman V. Belokopytova PS, et al. Genome Res. 2020 Jan;30(1):72-84. doi: 10.1101/gr.249367.119. Epub 2019 Dec 2. Genome Res. 2020. PMID: 31804952 Free PMC article.
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay.
Vasilyev SA, Skryabin NA, Kashevarova AA, Tolmacheva EN, Savchenko RR, Vasilyeva OY, Lopatkina ME, Zarubin AA, Fishman VS, Belyaeva EO, Filippova MO, Shorina AR, Maslennikov AB, Shestovskikh OL, Gayner TA, Čulić V, Vulić R, Nazarenko LP, Lebedev IN. Vasilyev SA, et al. Among authors: fishman vs. Cytogenet Genome Res. 2021;161(3-4):105-119. doi: 10.1159/000514491. Epub 2021 Apr 13. Cytogenet Genome Res. 2021. PMID: 33849037 Free article.
43 results