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Placental microRNA methylome signatures may serve as biomarkers and therapeutic targets for prenatally opioid-exposed infants with neonatal opioid withdrawal syndrome.
Radhakrishna U, Nath SK, Uppala LV, Veerappa A, Forray A, Muvvala SB, Metpally RP, Crist RC, Berrettini WH, Mausi LM, Vishweswaraiah S, Bahado-Singh RO. Radhakrishna U, et al. Among authors: nath sk. Front Genet. 2023 Jun 15;14:1215472. doi: 10.3389/fgene.2023.1215472. eCollection 2023. Front Genet. 2023. PMID: 37434949 Free PMC article.
Expanding the spectrum of γ-secretase gene mutation-associated phenotypes: two novel mutations segregating with familial hidradenitis suppurativa (acne inversa) and acne conglobata.
Ratnamala U, Jhala D, Jain NK, Saiyed NM, Raveendrababu M, Rao MV, Mehta TY, Al-Ali FM, Raval K, Nair S, Chandramohan NK, Kuracha MR, Nath SK, Radhakrishna U. Ratnamala U, et al. Among authors: nath sk. Exp Dermatol. 2016 Apr;25(4):314-6. doi: 10.1111/exd.12911. Epub 2016 Feb 11. Exp Dermatol. 2016. PMID: 26663538 No abstract available.
Maternal opioid use disorder: Placental transcriptome analysis for neonatal opioid withdrawal syndrome.
Radhakrishna U, Nath SK, Vishweswaraiah S, Uppala LV, Forray A, Muvvala SB, Mishra NK, Southekal S, Guda C, Govindamangalam H, Vargas D, Gardella WG, Crist RC, Berrettini WH, Metpally RP, Bahado-Singh RO. Radhakrishna U, et al. Among authors: nath sk. Genomics. 2021 Nov;113(6):3610-3617. doi: 10.1016/j.ygeno.2021.08.001. Epub 2021 Aug 3. Genomics. 2021. PMID: 34352367 Free article.
Placental cytochrome P450 methylomes in infants exposed to prenatal opioids: exploring the effects of neonatal opioid withdrawal syndrome on health horizons.
Radhakrishna U, Sadhasivam S, Radhakrishnan R, Forray A, Muvvala SB, Metpally RP, Patel S, Rawal RM, Vishweswaraiah S, Bahado-Singh RO, Nath SK. Radhakrishna U, et al. Among authors: nath sk. Front Genet. 2024 Jan 4;14:1292148. doi: 10.3389/fgene.2023.1292148. eCollection 2023. Front Genet. 2024. PMID: 38264209 Free PMC article.
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: nath sk. 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
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: nath sk. 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.
Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.
Ratnamala U, Lyle R, Rawal R, Singh R, Vishnupriya S, Himabindu P, Rao V, Aggarwal S, Paluru P, Bartoloni L, Young TL, Paoloni-Giacobino A, Morris MA, Nath SK, Antonarakis SE, Radhakrishna U. Ratnamala U, et al. Among authors: nath sk. Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6814-9. doi: 10.1167/iovs.10-6815. Invest Ophthalmol Vis Sci. 2011. PMID: 21357393 Free PMC article.
264 results