Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi male
Eldar-Geva T., Gross-Tsur V., Hirsch H.J., Altarescu G., Segal R., Zeligson S., Golomb E., Epsztejn-Litman S., Eiges R. (2018).. Mol. Genet.
Genomic Med.  Sep;6(5):811-818.
PMID: 30003711.

Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome. Frontiers in Molecular Neuroscience. Special issue: “The Fragile X Syndrome – Where Do We Go?” 
Mor-Shaked H., Eiges R.
Front. Mol. Neurosci. 2018 Feb 06; 11(31): Ecollection. Review.
 PMID: 29467618.

The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA
Abu Diab M, Mor-Shaked H, Cohen E , Cohen-Hadad Y , Ram O , Epsztejn-Litman S, Eiges R.  (2018).
Genetics. 2018 Dec;210(4):1239-1252.
 PMID: 30396881.

The contribution of pluripotent stem cell (PSC)-based models to the study of FXS. Special issue: “Towards Mechanism-based Treatments for Fragile X Syndrome” 
Abu Diab M. and Eiges R.
Brain Sciences.  Feb 15;9(2). pii: E42. doi: 10.3390/brainsci9020042. Review.
PMID: 30769941.

Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem Cells.
Cohen-Hadad Y, Altarescu G, Eldar-Geva T, Levi-Lahad E, Zhang M, Rogaeva E, Gotkine M, Bartok O, Ashwal-Fluss R, Kadener S, Epsztejn-Litman S, Eiges R.
Stem Cell Reports. 2016 Nov 8;7(5):927-940. PMID: 27773700
Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells.
Mor-Shaked H, Eiges R.
Genes (Basel). 2016 Sep 28;7(10). pii: E77. Review.

Genetic Manipulation of Human Embryonic Stem Cells.
Eiges R.
Methods Mol Biol. 2016;1307:149-72. doi: 10.1007/7651_2014_155.

Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells.
Yanovsky-Dagan S, Mor-Shaked H, Eiges R
World J Stem Cells 2015 Jun 26;7(5):823-38. Review. PMID: 26131313
Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis.
Epsztejn-Litman S, Cohen-Hadad Y., Aharoni S., Altarescu G., Renbaum P., Levy-Lahad E., Schonberger O., Eldar-Geva T., Zeligson S., Eiges R.
PLoS One. 2015Oct 16;10(10):e0138893. PMID: 26473610
Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells.
Yanovsky-Dagan S., Avitzour M., Altarescu G., Renbaum P., Eldar-Geva T.C Schonberger O, Mitrani-Rosenbaum S., Levy-Lahad E., Birnbaum R.Y., Gepstein L., Epsztejn-Litman S, Eiges R.
Stem Cell Reports, 2015Aug 11;5(2):221-31. PMID: 26190529
FMR1 epigenetic silencing commonly occurs in undifferentiated Fragile X affected embryonic stem cells.
Avitzour M., Mor-Shaked H., Yanovsky-Dagan S., Altarescu G., Renbaum P., Eldar-Geva T., Levy-Lahad E., Epsztejn-Litman S., Eiges R.
Stem Cell Reports, 2014 Nov 11;3(5):699-706. PMID: 25418717
The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.
Stelzer Y, Sagi I, Yanuka O, Eiges R, Benvenisty N.
Nat Genet. 2014 Jun;46(6):551-7. doi: 10.1038/ng.2968. Epub 2014 May 11.
Prevention of lysosomal storage diseases and derivation of mutant stem cell lines by preimplantation genetic diagnosis.
Altarescu G, Beeri R, Eiges R, Epsztejn-Litman S, Eldar-Geva T, Elstein D, Zimran A, Margalioth EJ, Levy-Lahad E, Renbaum P.
Mol Biol Int. 2012;2012:797342. doi: 10.1155/2012/797342. Epub 2012 Dec 26.

Female sex bias in human embryonic stem cell lines.
Ben-Yosef D, Amit A, Malcov M, Frumkin T, Ben-Yehudah A, Eldar I, Mey-Raz N, Azem F, Altarescu G, Renbaum P, Beeri R, Varshaver I, Eldar-Geva T, Epsztejn-Litman S, Levy-Lahad E, Eiges R.
Stem Cells Dev. 2012 Feb 10;21(3):363-72. doi: 10.1089/scd.2011.0102. Epub 2011 Jun 24.

GNE is involved in the early development of skeletal and cardiac muscle.
Milman Krentsis I, Sela I, Eiges R, Blanchard V, Berger M, Becker Cohen M, Mitrani-Rosenbaum S.
PLoS One. 2011;6(6):e21389. doi: 10.1371/journal.pone.0021389. Epub 2011 Jun 24.
Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line.
Altarescu G, Renbaum P, Eldar-Geva T, Brooks B, Varshaver I, Avitzour M, Margalioth EJ, Levy-Lahad E, Elstein D, Epsztejn-Litman S, Eiges R.
Prenat Diagn. 2011 Sep;31(9):853-60. doi: 10.1002/pd.2786. Epub 2011 Jun 27.
Genetic manipulation of human embryonic stem cells.
Epsztejn-Litman S, Eiges R.
Methods Mol Biol. 2010;584:387-411. doi: 10.1007/978-1-60761-369-5_21.

PGD-derived human embryonic stem cell lines as a powerful tool for the study of human genetic disorders.
Ben-Yosef D, Malcov M, Eiges R.
Mol Cell Endocrinol. 2008 Jan 30;282(1-2):153-8. doi: 10.1016/j.mce.2007.11.010. Review.

Activation and transposition of endogenous retroviral elements in hypomethylation induced tumors in mice.
Howard G, Eiges R, Gaudet F, Jaenisch R, Eden A.
Oncogene. 2008 Jan 10;27(3):404-8.

Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos.
Eiges R, Urbach A, Malcov M, Frumkin T, Schwartz T, Amit A, Yaron Y, Eden A, Yanuka O, Benvenisty N, Ben-Yosef D.
Cell Stem Cell. 2007 Nov;1(5):568-77. doi: 10.1016/j.stem.2007.09.001.
Genetic manipulation of human embryonic stem cells by transfection.
Eiges R.
Methods Mol Biol. 2006;331:221-39.

Human embryonic stem cells as a powerful tool for studying human embryogenesis.
Dvash T, Ben-Yosef D, Eiges R.
Pediatr Res. 2006 Aug;60(2):111-7. Review.
Temporal gene expression during differentiation of human embryonic stem cells and embryoid bodies.
Dvash T, Mayshar Y, Darr H, McElhaney M, Barker D, Yanuka O, Kotkow KJ, Rubin LL, Benvenisty N, Eiges R.
Hum Reprod. 2004 Dec;19(12):2875-83. Epub 2004 Sep 16.

A molecular view on pluripotent stem cells.
Eiges R, Benvenisty N.
FEBS Lett. 2002 Oct 2;529(1):135-41. Review.

Induced neuronal differentiation of human embryonic stem cells.
Schuldiner M, Eiges R, Eden A, Yanuka O, Itskovitz-Eldor J, Goldstein RS, Benvenisty N.
Brain Res. 2001 Sep 21;913(2):201-5.

Establishment of human embryonic stem cell-transfected clones carrying a marker for undifferentiated cells.
Eiges R, Schuldiner M, Drukker M, Yanuka O, Itskovitz-Eldor J, Benvenisty N.
Curr Biol. 2001 Apr 3;11(7):514-8.