Chakravarti A - Search Results

1

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.

2

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.

3

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.

4

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

Carrasquillo MM, Zlotogora J, Barges S, Chakravarti A. Carrasquillo MM, et al. Among authors: chakravarti a. Hum Mol Genet. 1997 Nov;6(12):2163-72. doi: 10.1093/hmg/6.12.2163. Hum Mol Genet. 1997. PMID: 9328482

5

High-throughput variation detection and genotyping using microarrays.

Cutler DJ, Zwick ME, Carrasquillo MM, Yohn CT, Tobin KP, Kashuk C, Mathews DJ, Shah NA, Eichler EE, Warrington JA, Chakravarti A. Cutler DJ, et al. Among authors: chakravarti a. Genome Res. 2001 Nov;11(11):1913-25. doi: 10.1101/gr.197201. Genome Res. 2001. PMID: 11691856 Free PMC article.

6

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.

7

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

8

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.

9

A DNA polymorphism discovery resource for research on human genetic variation.

Collins FS, Brooks LD, Chakravarti A. Collins FS, et al. Among authors: chakravarti a. Genome Res. 1998 Dec;8(12):1229-31. doi: 10.1101/gr.8.12.1229. Genome Res. 1998. PMID: 9872978 Free article. No abstract available.

10

Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects.

Schork NJ, Nath SK, Fallin D, Chakravarti A. Schork NJ, et al. Among authors: chakravarti a. Am J Hum Genet. 2000 Nov;67(5):1208-18. doi: 10.1086/321201. Epub 2000 Oct 13. Am J Hum Genet. 2000. PMID: 11032785 Free PMC article.

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