Associations between Hypertension and Genes in the Renin-Angiotensin System.

Zhu X, Chang Y-P C, Yan D, Weder A, Cooper R, Luke A, Donghui K, Chakravarti A: Associations between Hypertension and Genes in the Renin-Angiotensin System. Hypertension 41:1027-1034,2003. PMID 12695419.

Erythrocyte Sodium- Lithium Countertransport and Blood Pressure: A Genome-Wide Linkage Study.

Weder AB, Delgado MC, Zhu X, Gleiberman L, Kan D, Chakravarti A: Erythrocyte Sodium- Lithium Countertransport and Blood Pressure: A Genome-Wide Linkage Study. Hypertension 41:842-846,2003. PMID 12624006.

Phenotype variation in two-locus mouse models of Hirschsprung disease: Tissue-specific interaction between Ret and Ednrb.

McCallion AS, Stames E, Conlon RA, Chakravarti A: Phenotype variation in two-locus mouse models of Hirschsprung disease: Tissue-specific interaction between Ret and Ednrb. Proc Natl Acad Sci (USA) 100:1826-1831, 2003. PMID 12574515. PMC149918.

Undetected Genotyping Errors Cause Apparent Over- Transmission of Common Alleles in the Transmission Disequilibrium Test.

Mitchell AA, Cutler DJ, Chakravarti A: Undetected Genotyping Errors Cause Apparent Over- Transmission of Common Alleles in the Transmission Disequilibrium Test. Amer J Hum Genet 72:598-610, 2003. PMID 12587097. PMC1180236.

A genome wide linkage analysis investigating the determinants of blood pressure in Whites and African Americans.

Thiel BA, Chakravarti A, Cooper RS, Luke A, Lewis SM, Lynn A, Tiwari H, Schork NJ, Weder AB: A genome wide linkage analysis investigating the determinants of blood pressure in Whites and African Americans. Amer J Hypertension 16:151-153, 2003. PMID 12559684.

Linkage disequilibrium and haplotype diversity in the genes of the Renin-Angiotensin system: Findings from the Family Blood Pressure Program.

Zhu X, Yan D, Cooper R, Luke A, Weder A, Chakravarti A: Linkage disequilibrium and haplotype diversity in the genes of the Renin-Angiotensin system: Findings from the Family Blood Pressure Program. Genome Res 13:173-181, 2003. PMID 12566395. PMC420361.

A BDNF Coding Variant is Associated with the NEO Personality Inventory Domain Neuroticism, a Risk Factor for Depression.

Sen S, Nesse RM, Stoltenberg SF, Li S, Gleiberman L, Chakravarti A, Weder AB, Burmeister M: A BDNF Coding Variant is Associated with the NEO Personality Inventory Domain Neuroticism, a Risk Factor for Depression. Neuropsychopharm 28:397-401, 2003. PMID 12589394.

Sequence variations in the public human genome data reflect a bottlenecked population history.

Marth G, Schuler G, Yeh R, Davenport R, Agarwala R, Church D, Wheelan S, Baker J, Ward M, Kholodov M, Phan L, Czabarka, Murval J, Cutler D, Wooding S, Rogers A, Chakravarti A, Harpending H, Kwok P-Y, Sherry S: Sequence variations in the public human genome data reflect a bottlenecked population history. Proc Natl Acad Sci (USA) 100:376-381, 2003. PMID 12502794. PMC140982.

Future of genetics of mood disorders research.

Merikangas K, Chakravarti A, Moldin S, Araj H, Blangero J, Burmeister M, Crabbe J, Depaulo J, Foulks E, Freimer N, Koretz D, Lichtenstein W, Mignot E, Reiss A, Risch N, Takahashi JS: Future of genetics of mood disorders research. Biol Psych 52:457-477, 2002. PMID 12361664.

Haplotype inference in random population samples.

Lin S, Cutler DJ, Zwick ME, Chakravarti A: Haplotype inference in random population samples. Amer J Hum Genet 71:1129-1137, 2002. PMID 12386835. PMC385088.