Genome- wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.

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Carrasquillo MM, McCallion AS, Puffenberger EG, Kashuk CS, Nouri N, Chakravarti A: Genome- wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease. Nat Genet 32:237-244, 2002. PMID 12355085.

Chronic constipation due to Hirschsprung’s disease and desmosis coli in a single family.

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Marshall DG, Meier-Ruge WA, Chakravarti A, Langer JC: Chronic constipation due to Hirschsprung’s disease and desmosis coli in a single family. Pediat Surg Intl 18:110-114, 2002. PMID 11956774.

An evaluation of the assembly of a ~15 Mb region on Human Chromosome 13q32-q33 linked to Bipolar Disorder and Schizophrenia.

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Christian SL, McDonough J, Liu C-Y, Shaikh S, Vlamakis V, Badner JA,Chakravarti A, Gershon ES: An evaluation of the assembly of a ~15 Mb region on Human Chromosome 13q32-q33 linked to Bipolar Disorder and Schizophrenia. Genomics 79:635-656, 2002. PMID 11991713.

Segregation analysis of blood pressure and body mass index in a rural U.S. community.

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Nath SK, Chakravarti A, Chen C-H, Cooper R, Weder A, Schork NJ: Segregation analysis of blood pressure and body mass index in a rural U.S. community. Hum Biol 74:11-23, 2002. PMID 11931572.

Splitting a multigenic disease: segregation at three loci explains sibling recurrence risk in Hirschsprung disease.

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Bolk Gabriel S, Salomon R, Pelet A, Angrist M, Amiel J, Attie-Bitach T, Olson JM, Hofstra R, Buys C, Steffann J, Munnich A, Lyonnet S, Chakravarti A: Splitting a multigenic disease: segregation at three loci explains sibling recurrence risk in Hirschsprung disease. Nat Genet 31:89-93, 2002. PMID 11953745.

Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.

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Blagoev B, Nielsen MM, Angrist M, Chakravarti A, Pandey A: Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene. Gene 284:161-168, 2002. PMID 11891057.

Idiopathic Congenital Central Hypoventilation Syndrome: Evaluation of Brain-Derived Neurotrophic Factor Genomic DNA Sequence Variation.

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Weese-Mayer DE, Bolk S, Silvestri JM, Chakravarti A: Idiopathic Congenital Central Hypoventilation Syndrome: Evaluation of Brain-Derived Neurotrophic Factor Genomic DNA Sequence Variation. Amer J Med Genet 107:306-310, 2002. PMID 11840487.

A genome-wide scan for obesity in African Americans.

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Zhu X, Cooper RS, Luke A, Chen G, Wu X, Chakravarti A, Weder AB: A genome-wide scan for obesity in African Americans. Diabetes 51:541-544, 2002. PMID 11812767.

A graphical tool for polymorphism visualization and characterization.

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Kashuk C, SenGupta S, Eichler E, Chakravarti A: viewGene: A graphical tool for polymorphism visualization and characterization. Genome Res 12:333-338, 2002. PMID 11827953. PMC155269.

The Human Genome Sequence Expedition: Views from the “Base Camp”.

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Green ED, Chakravarti A: The Human Genome Sequence Expedition: Views from the “Base Camp”. Genome Res 11:645-651, 2001. PMID 11337462.