Chakravarti A - Search Results

1

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

2

Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.

Bolk S, Puffenberger EG, Hudson J, Morton DH, Chakravarti A. Bolk S, et al. Among authors: chakravarti a. Am J Hum Genet. 1999 Dec;65(6):1785-90. doi: 10.1086/302687. Am J Hum Genet. 1999. PMID: 10577936 Free PMC article. No abstract available.

3

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

4

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

5

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.

6

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.

7

Segregation analysis of microcephaly.

Cohen T, Zeitune M, McGillivray BC, Hall JG, Lynn AH, Aston CE, Chakravarti A. Cohen T, et al. Among authors: chakravarti a. Am J Med Genet. 1996 Oct 28;65(3):226-34. doi: 10.1002/(SICI)1096-8628(19961028)65:3<226::AID-AJMG11>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 9240749

8

Association study of schizophrenia and the IL-2 receptor beta chain gene.

Nimgaonkar VL, Yang ZW, Zhang XR, Brar JS, Chakravarti A, Ganguli R. Nimgaonkar VL, et al. Among authors: chakravarti a. Am J Med Genet. 1995 Oct 9;60(5):448-51. doi: 10.1002/ajmg.1320600517. Am J Med Genet. 1995. PMID: 8546160

9

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

10

Trend for an association between schizophrenia and D3S1310, a marker in proximity to the dopamine D3 receptor gene.

Jönsson EG, Nimgaonkar VL, Zhang XR, Shaw SH, Burgert E, Crocq MA, Chakravarti A, Sedvall GC. Jönsson EG, et al. Among authors: chakravarti a. Am J Med Genet. 1999 Aug 20;88(4):352-7. Am J Med Genet. 1999. PMID: 10402502

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