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Klannemark, M
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Vohl, MC
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Lane, CR
Schaffner, SF
Bolk, S
Brewer, C
Tuomi, T
Gaudet, D
Hudson, TJ
Daly, M
Groop, L
Lander, ES
Citation: D. Altshuler et al., The common PPAR gamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes, NAT GENET, 26(1), 2000, pp. 76-80
Authors:
Hirschhorn, JN
Sklar, P
Lindblad-Toh, K
Lim, YM
Ruiz-Gutierrez, M
Bolk, S
Langhorst, B
Schaffner, S
Winchester, E
Lander, ES
Citation: Jn. Hirschhorn et al., SBE-TAGS: An array-based method for efficient single-nucleotide polymorphism genotyping, P NAS US, 97(22), 2000, pp. 12164-12169
Authors:
Bolk, S
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Hofstra, RMW
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Salomon, R
Croaker, D
Buys, CHCM
Lyonnet, S
Chakravarti, A
Citation: S. Bolk et al., A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus, P NAS US, 97(1), 2000, pp. 268-273
Authors:
Bolk, S
Puffenberger, EG
Hudson, J
Morton, DH
Chakravarti, A
Citation: S. Bolk et al., Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the Old Order Mennonites, AM J HU GEN, 65(6), 1999, pp. 1785-1790
Authors:
Angrist, M
Bolk, S
Bentley, K
Nallasamy, S
Halushka, MK
Chakravarti, A
Citation: M. Angrist et al., Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease, ONCOGENE, 17(23), 1998, pp. 3065-3070