Radhakrishna U - Search Results

1

The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.

Radhakrishna U, Bornholdt D, Scott HS, Patel UC, Rossier C, Engel H, Bottani A, Chandal D, Blouin JL, Solanki JV, Grzeschik KH, Antonarakis SE. Radhakrishna U, et al. Am J Hum Genet. 1999 Sep;65(3):645-55. doi: 10.1086/302557. Am J Hum Genet. 1999. PMID: 10441570 Free PMC article.

2

An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36.

Radhakrishna U, Blouin JL, Solanki JV, Dhoriani GM, Antonarakis SE. Radhakrishna U, et al. Am J Med Genet. 1996 Dec 11;66(2):209-15. doi: 10.1002/(SICI)1096-8628(19961211)66:2<209::AID-AJMG17>3.0.CO;2-X. Am J Med Genet. 1996. PMID: 8958333

3

Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

Radhakrishna U, Blouin JL, Mehenni H, Patel UC, Patel MN, Solanki JV, Antonarakis SE. Radhakrishna U, et al. Am J Hum Genet. 1997 Mar;60(3):597-604. Am J Hum Genet. 1997. PMID: 9042919 Free PMC article.

4

The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region.

Radhakrishna U, Blouin JL, Mehenni H, Mehta TY, Sheth FJ, Sheth JJ, Solanki JV, Antonarakis SE. Radhakrishna U, et al. Am J Med Genet. 1997 Jul 11;71(1):80-6. doi: 10.1002/(sici)1096-8628(19970711)71:1<80::aid-ajmg15>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9215774

5

Mutation in GLI3 in postaxial polydactyly type A.

Radhakrishna U, Wild A, Grzeschik KH, Antonarakis SE. Radhakrishna U, et al. Nat Genet. 1997 Nov;17(3):269-71. doi: 10.1038/ng1197-269. Nat Genet. 1997. PMID: 9354785 No abstract available.

6

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

Mehenni H, Blouin JL, Radhakrishna U, Bhardwaj SS, Bhardwaj K, Dixit VB, Richards KF, Bermejo-Fenoll A, Leal AS, Raval RC, Antonarakis SE. Mehenni H, et al. Among authors: radhakrishna u. Am J Hum Genet. 1997 Dec;61(6):1327-34. doi: 10.1086/301644. Am J Hum Genet. 1997. PMID: 9399902 Free PMC article.

7

An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree.

Radhakrishna U, Senol S, Herken H, Gucuyener K, Gehrig C, Blouin JL, Akarsu NA, Antonarakis SE. Radhakrishna U, et al. Eur J Hum Genet. 2001 Jan;9(1):39-44. doi: 10.1038/sj.ejhg.5200584. Eur J Hum Genet. 2001. PMID: 11175298

8

Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.

Lyle R, Radhakrishna U, Blouin JL, Gagos S, Everman DB, Gehrig C, Delozier-Blanchet C, Solanki JV, Patel UC, Nath SK, Gurrieri F, Neri G, Schwartz CE, Antonarakis SE. Lyle R, et al. Among authors: radhakrishna u. Am J Med Genet A. 2006 Jul 1;140(13):1384-95. doi: 10.1002/ajmg.a.31247. Am J Med Genet A. 2006. PMID: 16691619

9

Polydactyly: a study of a five generation Indian family.

Radhakrishna U, Multani AS, Solanki JV, Shah VC, Chinoy NJ. Radhakrishna U, et al. J Med Genet. 1993 Apr;30(4):296-9. doi: 10.1136/jmg.30.4.296. J Med Genet. 1993. PMID: 8487274 Free PMC article.

10

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.

Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thornquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, Balk KG, Neufeld K, Swartz KL, DeMarchi N, Papadimitriou GN, Dikeos DG, Stefanis CN, Chakravarti A, Childs B, Housman DE, Kazazian HH, Antonarakis S, Pulver AE. Blouin JL, et al. Among authors: radhakrishna u. Nat Genet. 1998 Sep;20(1):70-3. doi: 10.1038/1734. Nat Genet. 1998. PMID: 9731535

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