Radhakrishna U - Search Results

1

Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region.

Al-Ali FM, Ratnamala U, Mehta TY, Naveed M, Al-Ali MT, Al-Khaja N, Sheth JJ, Master DC, Maiti AK, Chetan GK, Nath SK, Radhakrishna U. Al-Ali FM, et al. Among authors: radhakrishna u. Exp Dermatol. 2010 Sep;19(9):851-3. doi: 10.1111/j.1600-0625.2010.01088.x. Exp Dermatol. 2010. PMID: 20698881

2

Dementia with Lewy bodies post-mortem brains reveal differentially methylated CpG sites with biomarker potential.

Shao X, Vishweswaraiah S, Čuperlović-Culf M, Yilmaz A, Greenwood CMT, Surendra A, McGuinness B, Passmore P, Kehoe PG, Maddens ME, Bennett SAL, Green BD, Radhakrishna U, Graham SF. Shao X, et al. Among authors: radhakrishna u. Commun Biol. 2022 Nov 22;5(1):1279. doi: 10.1038/s42003-022-03965-x. Commun Biol. 2022. PMID: 36418427 Free PMC article.

3

Alzheimer's Precision Neurology: Epigenetics of Cytochrome P450 Genes in Circulating Cell-Free DNA for Disease Prediction and Mechanism.

Bahado-Singh RO, Vishweswaraiah S, Turkoglu O, Graham SF, Radhakrishna U. Bahado-Singh RO, et al. Among authors: radhakrishna u. Int J Mol Sci. 2023 Feb 2;24(3):2876. doi: 10.3390/ijms24032876. Int J Mol Sci. 2023. PMID: 36769199 Free PMC article.

4

Integrative Analysis Unveils the Correlation of Aminoacyl-tRNA Biosynthesis Metabolites with the Methylation of the SEPSECS Gene in Huntington's Disease Brain Tissue.

Vishweswaraiah S, Yilmaz A, Saiyed N, Khalid A, Koladiya PR, Pan X, Macias S, Robinson AC, Mann D, Green BD, Kerševičiūte I, Gordevičius J, Radhakrishna U, Graham SF. Vishweswaraiah S, et al. Among authors: radhakrishna u. Genes (Basel). 2023 Sep 2;14(9):1752. doi: 10.3390/genes14091752. Genes (Basel). 2023. PMID: 37761892 Free PMC article.

5

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

6

Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis.

Naveed M, Al-Ali MT, Murthy SK, Al-Hajali S, Al-Khaja N, Deutsch S, Bottani A, Antonarakis SE, Nath SK, Radhakrishna U. Naveed M, et al. Among authors: radhakrishna u. Am J Med Genet A. 2006 Jul 1;140(13):1440-6. doi: 10.1002/ajmg.a.31239. Am J Med Genet A. 2006. PMID: 16688753

7

Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34.

Radhakrishna U, Ratnamala U, Gaines M, Beiraghi S, Hutchings D, Golla J, Husain SA, Gambhir PS, Sheth JJ, Sheth FJ, Chetan GK, Naveed M, Solanki JV, Patel UC, Master DC, Memon R, Antonarakis GS, Antonarakis SE, Nath SK. Radhakrishna U, et al. Am J Hum Genet. 2006 Sep;79(3):580-5. doi: 10.1086/507487. Epub 2006 Jul 21. Am J Hum Genet. 2006. PMID: 16909398 Free PMC article.

8

Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.

Naveed M, Nath SK, Gaines M, Al-Ali MT, Al-Khaja N, Hutchings D, Golla J, Deutsch S, Bottani A, Antonarakis SE, Ratnamala U, Radhakrishna U. Naveed M, et al. Among authors: radhakrishna u. Am J Hum Genet. 2007 Jan;80(1):105-11. doi: 10.1086/510724. Epub 2006 Nov 29. Am J Hum Genet. 2007. PMID: 17160898 Free PMC article.

9

Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.

Beiraghi S, Nath SK, Gaines M, Mandhyan DD, Hutchings D, Ratnamala U, McElreavey K, Bartoloni L, Antonarakis GS, Antonarakis SE, Radhakrishna U. Beiraghi S, et al. Among authors: radhakrishna u. Am J Hum Genet. 2007 Jul;81(1):180-8. doi: 10.1086/518944. Epub 2007 May 18. Am J Hum Genet. 2007. PMID: 17564975 Free PMC article.

10

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.

Gajecka M, Radhakrishna U, Winters D, Nath SK, Rydzanicz M, Ratnamala U, Ewing K, Molinari A, Pitarque JA, Lee K, Leal SM, Bejjani BA. Gajecka M, et al. Among authors: radhakrishna u. Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1531-9. doi: 10.1167/iovs.08-2173. Epub 2008 Nov 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19011015 Free PMC article.

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