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Citation: K. Mykytyn et al., Identification of the gene that, when mutated, causes the human obesity syndrome BBS4, NAT GENET, 28(2), 2001, pp. 188-191

Authors: Nishimura, DY Searby, CC Carmi, R Elbedour, K Van Maldergem, L Fulton, AB Lam, BL Powell, BR Swiderski, RE Bugge, KE Haider, NB Kwitek-Black, AE Ying, LH Duhl, DM Gorman, SW Heon, E Iannaccone, A Bonneau, D Biesecker, LG Jacobson, SG Stone, EM Sheffield, VC

Citation: Dy. Nishimura et al., Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2), HUM MOL GEN, 10(8), 2001, pp. 865-874

Authors: Scott, DA Drury, S Sundstrom, RA Bishop, J Swiderski, RE Carmi, R Ramesh, A Elbedour, K Srisailapathy, CRS Keats, BJ Sheffield, VC Smith, RJH

Citation: Da. Scott et al., Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms ina novel gene, TMEM2, GENE, 246(1-2), 2000, pp. 265-274

Authors: Leiberman, E Pesler, D Parvari, R Elbedour, K Abdul-Latif, H Brown, MR Parks, JS Carmi, R

Citation: E. Leiberman et al., Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiency, AM J MED G, 90(3), 2000, pp. 188-192

Authors: Carmi, R Elbedour, K Wietzman, D Sheffield, V Shoham-Vardi, I

Citation: R. Carmi et al., Lowering the burden of hereditary diseases in a traditional, inbred community: Ethical aspects of genetic research and its application, SCI CONTEXT, 11(3-4), 1998, pp. 391-396