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Citation: S. Ghosh et al., The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes, AM J HU GEN, 67(5), 2000, pp. 1174-1185

Authors: Watanabe, RM Ghosh, S Langefeld, CD Valle, TT Hauser, ER Magnuson, VL Mohlke, KL Silander, K Ally, DS Chines, P Blaschak-Harvan, J Douglas, JA Duren, WL Epstein, MP Fingerlin, TE Kaleta, HS Lange, EM Li, C McEachin, RC Stringham, HM Trager, E White, PP Balow, J Birznieks, G Chang, J Eldridge, W Erdos, MR Karanjawala, ZE Knapp, JI Kudelko, K Martin, C Morales-Mena, A Musick, A Musick, T Pfahl, C Porter, R Rayman, JB Rha, D Segal, L Shapiro, S Sharaf, R Shurtleff, B So, A Tannenbaum, J Te, C Tovar, J Unni, A Welch, C Whiten, R Witt, A Kohtamaki, K Ehnholm, C Eriksson, J Toivanen, L Vidgren, G Nylund, SJ Tuomilehto-Wolf, E Ross, EH Demirchyan, E Hagopian, WA Buchanan, TA Tuomilehto, J Bergman, RN Collins, FS Boehnke, M

Citation: Rm. Watanabe et al., The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci, AM J HU GEN, 67(5), 2000, pp. 1186-1200

Authors: Lopes, J Tardieu, S Silander, K Blair, I Vandenberghe, A Palau, F Ruberg, M Brice, A LeGuern, E

Citation: J. Lopes et al., Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP, HUM MOL GEN, 8(12), 1999, pp. 2285-2292

Authors: Castro, C Gomez-Hernandez, JM Silander, K Barrio, LC

Citation: C. Castro et al., Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations, J NEUROSC, 19(10), 1999, pp. 3752-3760