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Expanding the phenotype of CRB2 mutations - A new ciliopathy syndrome?
Jaron R, Rosenfeld N, Zahdeh F, Carmi S, Beni-Adani L, Doviner V, Picard E, Segel R, Zeligson S, Carmel L, Renbaum P, Levy-Lahad E. Jaron R, et al. Among authors: carmel l. Clin Genet. 2016 Dec;90(6):540-544. doi: 10.1111/cge.12764. Epub 2016 May 2. Clin Genet. 2016. PMID: 26925547
Differential DNA methylation of vocal and facial anatomy genes in modern humans.
Gokhman D, Nissim-Rafinia M, Agranat-Tamir L, Housman G, García-Pérez R, Lizano E, Cheronet O, Mallick S, Nieves-Colón MA, Li H, Alpaslan-Roodenberg S, Novak M, Gu H, Osinski JM, Ferrando-Bernal M, Gelabert P, Lipende I, Mjungu D, Kondova I, Bontrop R, Kullmer O, Weber G, Shahar T, Dvir-Ginzberg M, Faerman M, Quillen EE, Meissner A, Lahav Y, Kandel L, Liebergall M, Prada ME, Vidal JM, Gronostajski RM, Stone AC, Yakir B, Lalueza-Fox C, Pinhasi R, Reich D, Marques-Bonet T, Meshorer E, Carmel L. Gokhman D, et al. Among authors: carmel l. Nat Commun. 2020 Mar 4;11(1):1189. doi: 10.1038/s41467-020-15020-6. Nat Commun. 2020. PMID: 32132541 Free PMC article.
The Genomic History of the Bronze Age Southern Levant.
Agranat-Tamir L, Waldman S, Martin MAS, Gokhman D, Mishol N, Eshel T, Cheronet O, Rohland N, Mallick S, Adamski N, Lawson AM, Mah M, Michel M, Oppenheimer J, Stewardson K, Candilio F, Keating D, Gamarra B, Tzur S, Novak M, Kalisher R, Bechar S, Eshed V, Kennett DJ, Faerman M, Yahalom-Mack N, Monge JM, Govrin Y, Erel Y, Yakir B, Pinhasi R, Carmi S, Finkelstein I, Carmel L, Reich D. Agranat-Tamir L, et al. Among authors: carmel l. Cell. 2020 May 28;181(5):1146-1157.e11. doi: 10.1016/j.cell.2020.04.024. Cell. 2020. PMID: 32470400 Free PMC article.
Reconstructing DNA methylation maps of ancient populations.
Barouch A, Mathov Y, Meshorer E, Yakir B, Carmel L. Barouch A, et al. Among authors: carmel l. Nucleic Acids Res. 2024 Feb 28;52(4):1602-1612. doi: 10.1093/nar/gkad1232. Nucleic Acids Res. 2024. PMID: 38261973 Free PMC article.
Inferring Past Environments from Ancient Epigenomes.
Gokhman D, Malul A, Carmel L. Gokhman D, et al. Among authors: carmel l. Mol Biol Evol. 2017 Oct 1;34(10):2429-2438. doi: 10.1093/molbev/msx211. Mol Biol Evol. 2017. PMID: 28957511 Free PMC article.
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.
Zangen D, Kaufman Y, Zeligson S, Perlberg S, Fridman H, Kanaan M, Abdulhadi-Atwan M, Abu Libdeh A, Gussow A, Kisslov I, Carmel L, Renbaum P, Levy-Lahad E. Zangen D, et al. Among authors: carmel l. Am J Hum Genet. 2011 Oct 7;89(4):572-9. doi: 10.1016/j.ajhg.2011.09.006. Epub 2011 Sep 29. Am J Hum Genet. 2011. PMID: 21963259 Free PMC article.
63 results