Sireesha Movva
Overview
Explore the profile of Sireesha Movva including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
141
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Recent Articles
1.
Setia N, Movva S, Balakrishnan P, Biji I, Sawhney J, Puri R, et al.
J Clin Lipidol
. 2020 Feb;
14(1):35-45.
PMID: 32044282
Background: Familial hypercholesterolemia (FH), an autosomal codominant disorder characterized by very high low-density lipoprotein cholesterol, is strongly associated with premature coronary artery disease. Objectives: Molecular landscape of FH in Asian...
2.
Eswarachari V, Kadam P, Movva S, Lingaiah S, Akther R, Kidangan F, et al.
J Matern Fetal Neonatal Med
. 2018 May;
32(24):4177-4180.
PMID: 29793366
Noninvasive prenatal testing (NIPT) is a reliable screening method for fetal aneuploidy detection of trisomy 18, 13, 21 along with few sex chromosome abnormalities monosomy X, XXX, XXY (Klinefelter), XYY...
3.
Vyas B, Puri R, Namboodiri N, Nair M, Sharma D, Movva S, et al.
Am J Med Genet A
. 2016 Apr;
170(6):1510-9.
PMID: 27041150
Long QT syndrome type 1 (LQT1) is the most common type of all Long QT syndromes (LQTS) and occurs due to mutations in KCNQ1. Biallelic mutations with deafness is called...
4.
Ali Khan I, Movva S, Shaik N, Chava S, Jahan P, Mukkavali K, et al.
Meta Gene
. 2015 Jan;
2:299-306.
PMID: 25606412
Background: Type 2 Diabetes Mellitus (T2DM) and Gestational Diabetes Mellitus (GDM) are part of a heterogeneous and complex metabolic group of disorders that share common pathophysiological circumstances, including β-cell dysfunction...
5.
Bijarnia-Mahay S, Movva S, Gupta N, Sharma D, Puri R, Kotecha U, et al.
JIMD Rep
. 2015 Jan;
19:85-93.
PMID: 25595217
Hereditary fructose intolerance (HFI) is a difficult-to-confirm diagnosis, requiring either invasive liver biopsy-enzyme assay or potentially hazardous fructose challenge test or expensive molecular genetic analysis. Therefore, worldwide there has been...
6.
Molecular evaluation of a novel missense mutation & an insertional truncating mutation in SUMF1 gene
Kotecha U, Movva S, Sharma D, Verma J, Puri R, Verma I
Indian J Med Res
. 2014 Sep;
140(1):55-9.
PMID: 25222778
Background & Objectives: Multiple suphphatase deficiency (MSD) is an autosomal recessive disorder affecting the post translational activation of all enzymes of the sulphatase family. To date, approximately 30 different mutations...
7.
Alhomidi M, Vedicherla B, Movva S, Rao P, Ahuja Y, Hasan Q
Tumour Biol
. 2013 May;
34(4):2427-32.
PMID: 23640059
Somatic mutations in mitochondrial DNA (mtDNA) have been demonstrated in various tumors. Mitochondrial D-loop is a non-coding region in the mitochondrial genome, which has essential transcription and replication elements, and...
8.
Bhaskar S, Ganesan M, Chandak G, Mani R, Idris M, Khaja N, et al.
Genet Test Mol Biomarkers
. 2011 Mar;
15(7-8):507-12.
PMID: 21438666
Type 2 diabetes mellitus (T2DM) is a major cause of coronary artery disease (CAD) and is responsible for a great deal of morbidity and mortality in Asian Indians. Several gene...
9.
Latha M, Vaidya S, Movva S, Chava S, Govindan S, Govatati S, et al.
Genet Test Mol Biomarkers
. 2011 Jan;
15(3):181-4.
PMID: 21214494
Background: Endometriosis is a distressing gynecological disorder. Toll-like receptor 4 (TLR4) is specific for recognition of the molecular pattern of gram-negative bacteria. TLR4 is present on the surface of endometrial...
10.
Movva S, Alluri R, Venkatasubramanian S, Vedicherla B, Vattam K, Ahuja Y, et al.
Genet Test Mol Biomarkers
. 2010 Dec;
15(4):257-61.
PMID: 21186995
Diabetes is gradually getting the status of a global epidemic, with India projected as the capital of type 2 diabetes mellitus (T2DM). Nephropathy is an important complication of diabetes and...