Authors: Mykytyn, K Braun, T Carmi, R Haider, NB Searby, CC Shastri, M Beck, G Wright, AF Iannaccone, A Elbedour, K Riise, R Baldi, A Raas-Rothschild, A Gorman, SW Duhl, DM Jacobson, SG Casavant, T Stone, EM Sheffield, VC

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: Nishimura, DY Searby, CC Alward, WL Walton, D Craig, JE Mackey, DA Kawase, K Kanis, AB Patil, SR Stone, EM Sheffield, VC

Citation: Dy. Nishimura et al., A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye, AM J HU GEN, 68(2), 2001, pp. 364-372