Chakravarti A - Search Results

1

Hirschsprung disease, associated syndromes and genetics: a review.

Amiel J, Sproat-Emison E, Garcia-Barcelo M, Lantieri F, Burzynski G, Borrego S, Pelet A, Arnold S, Miao X, Griseri P, Brooks AS, Antinolo G, de Pontual L, Clement-Ziza M, Munnich A, Kashuk C, West K, Wong KK, Lyonnet S, Chakravarti A, Tam PK, Ceccherini I, Hofstra RM, Fernandez R; Hirschsprung Disease Consortium. Amiel J, et al. Among authors: chakravarti a. J Med Genet. 2008 Jan;45(1):1-14. doi: 10.1136/jmg.2007.053959. Epub 2007 Oct 26. J Med Genet. 2008. PMID: 17965226 Review.

2

Segregation at three loci explains familial and population risk in Hirschsprung disease.

Gabriel SB, Salomon R, Pelet A, Angrist M, Amiel J, Fornage M, Attié-Bitach T, Olson JM, Hofstra R, Buys C, Steffann J, Munnich A, Lyonnet S, Chakravarti A. Gabriel SB, et al. Among authors: chakravarti a. Nat Genet. 2002 May;31(1):89-93. doi: 10.1038/ng868. Epub 2002 Apr 15. Nat Genet. 2002. PMID: 11953745

3

A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.

Bolk S, Pelet A, Hofstra RM, Angrist M, Salomon R, Croaker D, Buys CH, Lyonnet S, Chakravarti A. Bolk S, et al. Among authors: chakravarti a. Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):268-73. doi: 10.1073/pnas.97.1.268. Proc Natl Acad Sci U S A. 2000. PMID: 10618407 Free PMC article.

4

Genomic variation in multigenic traits: Hirschsprung disease.

McCallion AS, Emison ES, Kashuk CS, Bush RT, Kenton M, Carrasquillo MM, Jones KW, Kennedy GC, Portnoy ME, Green ED, Chakravarti A. McCallion AS, et al. Among authors: chakravarti a. Cold Spring Harb Symp Quant Biol. 2003;68:373-81. doi: 10.1101/sqb.2003.68.373. Cold Spring Harb Symp Quant Biol. 2003. PMID: 15338639 No abstract available.

5

Sequence variation within the fragile X locus.

Mathews DJ, Kashuk C, Brightwell G, Eichler EE, Chakravarti A. Mathews DJ, et al. Among authors: chakravarti a. Genome Res. 2001 Aug;11(8):1382-91. doi: 10.1101/gr.172601. Genome Res. 2001. PMID: 11483579 Free PMC article.

6

Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes.

Shaw SH, Carrasquillo MM, Kashuk C, Puffenberger EG, Chakravarti A. Shaw SH, et al. Among authors: chakravarti a. Genome Res. 1998 Feb;8(2):111-23. doi: 10.1101/gr.8.2.111. Genome Res. 1998. PMID: 9477339 Free article.

7

Patterns of meiotic recombination on the long arm of human chromosome 21.

Lynn A, Kashuk C, Petersen MB, Bailey JA, Cox DR, Antonarakis SE, Chakravarti A. Lynn A, et al. Among authors: chakravarti a. Genome Res. 2000 Sep;10(9):1319-32. doi: 10.1101/gr.138100. Genome Res. 2000. PMID: 10984450 Free article.

8

Idiopathic congenital central hypoventilation syndrome: evaluation of brain-derived neurotrophic factor genomic DNA sequence variation.

Weese-Mayer DE, Bolk S, Silvestri JM, Chakravarti A. Weese-Mayer DE, et al. Among authors: chakravarti a. Am J Med Genet. 2002 Feb 1;107(4):306-10. doi: 10.1002/ajmg.10133. Am J Med Genet. 2002. PMID: 11840487

9

Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.

Angrist M, Jing S, Bolk S, Bentley K, Nallasamy S, Halushka M, Fox GM, Chakravarti A. Angrist M, et al. Among authors: chakravarti a. Genomics. 1998 Mar 15;48(3):354-62. doi: 10.1006/geno.1997.5191. Genomics. 1998. PMID: 9545641

10

Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.

Angrist M, Bolk S, Bentley K, Nallasamy S, Halushka MK, Chakravarti A. Angrist M, et al. Among authors: chakravarti a. Oncogene. 1998 Dec 10;17(23):3065-70. doi: 10.1038/sj.onc.1202226. Oncogene. 1998. PMID: 9881709

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