Genotype: Phenotype correlation in Hirschsprung disease illuminated by comparative RET protein sequence analysis.

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Kashuk CS, Stone EA, Grice EA, Portnoy ME, Green ED, Sidow A, Chakravarti A, McCallion A: Genotype: Phenotype correlation in Hirschsprung disease illuminated by comparative RET protein sequence analysis. Proc Natl Acad Sci (USA) 102:8949-8954, 2005. PMID 15956201.

No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families.

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Mulle JG, Chowdari KV, Nimgaonkar V, Chakravarti A: No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families. Mol Psych 10:431-433, 2005. PMID 15753958.

Evidence for linkage to chromosome 13q32 in an independent sample of schizophrenia families.

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Mulle JG, McDonough JA, Chowdari KV, Nimgaonkar V, Chakravarti A: Evidence for linkage to chromosome 13q32 in an independent sample of schizophrenia families. Mol Psych 10:429-431,2005. PMID 15738936.

IL- 6 Gene Variation is Not Associated with Increased Serum Levels of IL-6, Muscle, Weakness, or Frailty in Older Women.

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Walston J, Arking DE, Fallin D,Li T, Beamer B, Xue Q, Ferrucci L, Fried LP, Chakravarti A: IL- 6 Gene Variation is Not Associated with Increased Serum Levels of IL-6, Muscle, Weakness, or Frailty in Older Women. Exptl Gerontol 40:344-352, 2005. PMID 15820616.

A common, sex-dependent mutation in a putative RET enhancer underlies Hirschsprung disease susceptibility.

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Emison ES, McCallion AS, Kashuk CS, Bush RT, Grice E, Lin S, Portnoy ME, NISC Comparative Sequencing Program, Cutler DJ, Green ED, Chakravarti A: A common, sex-dependent mutation in a putative RET enhancer underlies Hirschsprung disease susceptibility. Nature 434:857-863, 2005. PMID 15829955.

Exhaustive allelic disequilibrium tests are a new approach to genome-wide association studies.

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Lin S, Chakravarti A, Cutler DJ: Exhaustive allelic disequilibrium tests are a new approach to genome-wide association studies. Nat Genet 36:1181-1188, 2004. PMID 15502828.

Haplotype and Missing Data Inference in Nuclear Families.

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Lin S, Chakravarti A, Cutler DJ: Haplotype and Missing Data Inference in Nuclear Families. Genome Res 14:1624-32, 2004. PMID 15256514. PMC509272.

Integrating Ethics and Science in the International HapMap Project.

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The International HapMap Consortium: Integrating Ethics and Science in the International HapMap Project. Nat Rev Genet 5:467-475, 2004. PMID 15153999. PMC2271136.

The Human MitoChip: A high-throughput sequencing microarray for mitochondrial mutation detection.

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Maitra A, Cohen Y, Gillespie SED, Shah N, Sidransky D, Chakravarti A: The Human MitoChip: A high-throughput sequencing microarray for mitochondrial mutation detection. Genome Res 14:812-819, 2004. PMID 15123581. PMC479107.

Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns.

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Mitchell AA, Zwick ME, Chakravarti A, Cutler DJ: Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns. Bioinformatics 20:1022-1032, 2004. PMID 14764571.