High-throughput variation detection and genotyping using microarrays.

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Cutler DJ, Zwick ME, Carrasquillo MM, Yohn CT, Tobin KP, Kashuk C, Mathews DJ, Shah NA, Eichler EE, Warrington JA, Chakravarti A: High-throughput variation detection and genotyping using microarrays. Genome Res 11:1913-1925, 2001. PMID 11691856. PMC311146.

Absence of colon neoplasia susceptibility variants at the human COX2 locus.

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Wiesner GL, Platzer P, Buxbaum S, Lewis S, MacMillen M, Olechnowicz J, Willis J, Chakravarti A, Elston RC, Markowitz SD: Absence of colon neoplasia susceptibility variants at the human COX2 locus. J Natl Cancer Inst 18:635-639, 2001. PMID 11309440.

Sequence variation within the fragile X locus.

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Mathews DJ, Kashuk C, Brightwell G, Eichler EE, Chakravarti A: Sequence variation within the fragile X locus. Genome Res 11:1382-1391, 2001. PMID 11483579. PMC311115.

The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice.

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Hong H-K, Noveroske JK, Headon DJ, Liu T, Sy M-S, Justice MJ, Chakravarti A: The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice. Genesis 29:163-171, 2001. PMID 11309849.

Lack of association between a biallelic polymorphism in the Adducin gene and blood pressure in Whites and African Americans.

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Schork NJ, Chakravarti A, Thiel B, Fornage M, Jacob HJ, Cai R, Rotimi CN, Cooper RS, Weder AB: Lack of association between a biallelic polymorphism in the Adducin gene and blood pressure in Whites and African Americans. Amer J Hypertension 13:693-698, 2000. PMID 10912755.

Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program.

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Province MA, Boerwinkle E, Chakravarti A, Cooper R, Fornage M, Leppert M, Risch N, Ranade K: Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. J Hypertension 18:867-76, 2000. PMID 10930184.

Linkage disequilibrium analysis of bi-allelic markers, human quantitative trait loci, and threshold-defined cases and controls.

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Schork NJ, Nath SK, Fallin D, Chakravarti A: Linkage disequilibrium analysis of bi-allelic markers, human quantitative trait loci, and threshold-defined cases and controls. Amer J Hum Genet 67:1208-1218, 2000. PMID 11032785. PMC1288563.

Patterns of Genetic Variation in Mendelian and Complex Traits.

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Zwick ME, Cutler DJ, Chakravarti A: Patterns of Genetic Variation in Mendelian and Complex Traits. Annu Rev Genomics Hum Genet 1:387-407, 2000. PMID 11701635.

Patterns of Meiotic Recombination on the Long Arm of Human Chromosome 21.

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Lynn A, Peterson MB, Kashuk C, Cox DR, Antonarakis SE, Chakravarti A: Patterns of Meiotic Recombination on the Long Arm of Human Chromosome 21. Genome Res 10:1319-1332, 2000. PMID 10984450.

Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays.

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Fan J-B, Chen X, Halushka MK, Berno A, Huang X, Ryder T, Lipshutz R, Lockhart DJ, Chakravarti A: Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays. Genome Res 10:853-860, 2000. PMID 10854416. PMC 310915.