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person:imielm01
Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP
Grant, Struan F A; Li, Mingyao; Bradfield, Jonathan P; Kim, Cecilia E; Annaiah, Kiran; Santa, Erin; Glessner, Joseph T; Casalunovo, Tracy; Frackelton, Edward C; Otieno, F George; Shaner, Julie L; Smith, Ryan M; Imielinski, Marcin; Eckert, Andrew W; Chiavacci, Rosetta M; Berkowitz, Robert I; Hakonarson, Hakon
Recently an association was demonstrated between the single nucleotide polymorphism (SNP), rs9939609, within the FTO locus and obesity as a consequence of a genome wide association (GWA) study of type 2 diabetes in adults. We examined the effects of two perfect surrogates for this SNP plus 11 other SNPs at this locus with respect to our childhood obesity cohort, consisting of both Caucasians and African Americans (AA). Utilizing data from our ongoing GWA study in our cohort of 418 Caucasian obese children (BMI>or=95th percentile), 2,270 Caucasian controls (BMI<95th percentile), 578 AA obese children and 1,424 AA controls, we investigated the association of the previously reported variation at the FTO locus with the childhood form of this disease in both ethnicities. The minor allele frequencies (MAF) of rs8050136 and rs3751812 (perfect surrogates for rs9939609 i.e. both r(2) = 1) in the Caucasian cases were 0.448 and 0.443 respectively while they were 0.391 and 0.386 in Caucasian controls respectively, yielding for both an odds ratio (OR) of 1.27 (95% CI 1.08-1.47; P = 0.0022). Furthermore, the MAFs of rs8050136 and rs3751812 in the AA cases were 0.449 and 0.115 respectively while they were 0.436 and 0.090 in AA controls respectively, yielding an OR of 1.05 (95% CI 0.91-1.21; P = 0.49) and of 1.31 (95% CI 1.050-1.643; P = 0.017) respectively. Investigating all 13 SNPs present on the Illumina HumanHap550 BeadChip in this region of linkage disequilibrium, rs3751812 was the only SNP conferring significant risk in AA. We have therefore replicated and refined the association in an AA cohort and distilled a tag-SNP, rs3751812, which captures the ancestral origin of the actual mutation. As such, variants in the FTO gene confer a similar magnitude of risk of obesity to children as to their adult counterparts and appear to have a global impact.
PMCID:2262153
PMID: 18335027
ISSN: 1932-6203
CID: 5269842
IDENTIFYING HUMAN EPILEPSY SUSCEPTIBILITY ALLELES USING GENOME WIDE ASSOCIATION [Meeting Abstract]
Buono, RJ; Imielinski, M; Sperling, M; Dlugos, D; Privitera, M; French, J; Lo, W; Schachter, SC; Cossette, P; Scattergood, T; Basehore, H; Kim, C; Glessner, J; Chiavacci, R; Lohoff, FW; Berrettini, WH; Ferraro, TN; Hakonarson, H
ISI:000260306600743
ISSN: 0013-9580
CID: 102386
IDENTIFYING HUMAN EPILEPSY SUSCEPTIBILITY ALLELES USING GENOME WIDE ASSOCIATION [Meeting Abstract]
Buono, RJ; Imielinski, M; Sperling, M; Dlugos, D; Privitera, M; French, J; Lo, W; Schachter, SC; Cossette, P; Scattergood, T; Basehore, H; Kim, C; Glessner, J; Chiavacci, R; Lohoff, FW; Berrettini, WH; Ferraro, TN; Hakonarson, H
ISI:000260306601139
ISSN: 0013-9580
CID: 102387
Association of HMGA2 Gene Variation with Height in Specific Pediatric Age Categories
Grant, Struan F. A.; Li, Mingyao; Bradfield, Jonathan P.; Kim, Cecilia E.; Annaiah, Kiran; Santa, Erin; Glessner, Joseph T.; Casalunovo, Tracy; Frackelton, Edward C.; Otieno, F. George; Shaner, Julie L.; Smith, Ryan M.; Eckert, Andrew W.; Imielinski, Marcin; Chiavacci, Rosetta M.; Berkowitz, Robert I.; Hakonarson, Hakon
ISI:000215906500003
ISSN: 1178-6310
CID: 5270492
Metabolic Networks Analysis using Convex Optimization [Meeting Abstract]
Julius, A. Agung; Imielinski, Marcin; Pappas, George J.
ISI:000307311600126
ISSN: 0743-1546
CID: 5270582
Investigating the genomic basis of metabolic robustness through in silico flux analysis [Meeting Abstract]
Imielinski, Marcin; Klitgord, Niels; Belta, Calin
ISI:000307311600131
ISSN: 0743-1546
CID: 5270592
Analysis of lactose metabolism in E. Coli using reachability analysis of hybrid systems
Halász, A; Kumar, V; Imieliński, M; Belta, C; Sokolsky, O; Pathak, S; Rubin, H
We propose an abstraction method for medium-scale biomolecular networks, based on hybrid dynamical systems with continuous multi-affine dynamics. This abstraction method follows naturally from the notion of approximating nonlinear rate laws with continuous piecewise linear functions and can be easily automated. An efficient reachability algorithm is possible for the resulting class of hybrid systems. An efficient reachability algorithm is possible for the resulting class of hybrid systems. An approximation for an ordinary differential equation model of the lac operon is constructed, and it is shown that the abstraction passes the same experimental tests as were used to validate the original model. The well studied biological system exhibits bistability and switching behaviour, arising from positive feedback in the expression mechanism of the lac operon. The switching property of the lac system is an example of the major qualitative features that are the building blocks of higher level, more coarse-grained descriptions. The present approach is useful in helping to correctly identify such properties and in connecting them to the underlying molecular dynamical details. Reachability analysis together with the knowledge of the steady-state structure are used to identify ranges of parameter values for which the system maintains the bistable switching property.
PMID: 17441554
ISSN: 1751-8849
CID: 5637122
Systematic analysis of conservation relations in Escherichia coli genome-scale metabolic network reveals novel growth media. (vol 90, pg 2659, 2006) [Correction]
Imielinski, Marcin; Belta, Calin; Rubin, Harvey; Halasz, Adam
ISI:000247465300036
ISSN: 0006-3495
CID: 5270502
On the computation of minimal cut sets in genome scale metabolic networks [Meeting Abstract]
Imielinski, Marcin; Belta, Calin
ISI:000252258802209
ISSN: 0743-1619
CID: 5270512
Systematic analysis of conservation relations in Escherichia coli genome-scale metabolic network reveals novel growth media
Imielinski, Marcin; Belta, Calin; Rubin, Harvey; Halász, Adam
A biochemical species is called producible in a constraints-based metabolic model if a feasible steady-state flux configuration exists that sustains its nonzero concentration during growth. Extreme semipositive conservation relations (ESCRs) are the simplest semipositive linear combinations of species concentrations that are invariant to all metabolic flux configurations. In this article, we outline a fundamental relationship between the ESCRs of a metabolic network and the producibility of a biochemical species under a nutrient media. We exploit this relationship in an algorithm that systematically enumerates all minimal nutrient sets that render an objective species weakly producible (i.e., producible in the absence of thermodynamic constraints) through a simple traversal of ESCRs. We apply our results to a recent genome scale model of Escherichia coli metabolism, in which we traverse the 51 anhydrous ESCRs of the metabolic network to determine all 928 minimal aqueous nutrient media that render biomass weakly producible. Applying irreversibility constraints, we find 287 of these 928 nutrient sets to be thermodynamically feasible. We also find that an additional 365 of these nutrient sets are thermodynamically feasible in the presence of oxygen. Since biomass producibility is commonly used as a surrogate for growth in genome scale metabolic models, our results represent testable hypotheses of alternate growth media derived from in silico analysis of the E. coli genome scale metabolic network.
PMID: 16461408
ISSN: 0006-3495
CID: 5269832