Anshika Srivastava

Anshika Srivastava

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Anshika Srivastava

Anshika Srivastava

Publications by authors named "Anshika Srivastava"

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29Publications

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Design and analysis of visible photonics resonators coated With CuO thin film.

Nanotechnology 2019 Dec 20. Epub 2019 Dec 20.

ECE, Motilal Nehru National Institute of Technology, Prayagraj, INDIA.

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http://dx.doi.org/10.1088/1361-6528/ab6469DOI Listing
December 2019

Historic migration to South Asia in the last two millennia: A case of Jewish and Parsi populations.

J Biosci 2019 Jul;44(3)

Estonian Biocentre, Institute of Genomics, University of Tartu, Riia 23b, Tartu 51010, Estonia.

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July 2019

Genetic diversity of NDUFV1-dependent mitochondrial complex I deficiency.

Eur J Hum Genet 2018 11 5;26(11):1582-1587. Epub 2018 Jul 5.

Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA.

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http://dx.doi.org/10.1038/s41431-018-0209-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189076PMC
November 2018

Report of four novel variants in ASNS causing asparagine synthetase deficiency and review of literature.

Congenit Anom (Kyoto) 2018 Sep 20;58(5):181-182. Epub 2018 Feb 20.

Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.

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http://dx.doi.org/10.1111/cga.12275DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338226PMC
September 2018

Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome.

Proc Natl Acad Sci U S A 2018 01 8;115(4):E620-E629. Epub 2018 Jan 8.

Molecular Genetics of Development Laboratory, Department of Biological Sciences, University of Quebec at Montreal, Montreal, QC H2X 3Y7, Canada;

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http://www.pnas.org/lookup/doi/10.1073/pnas.1715378115
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http://dx.doi.org/10.1073/pnas.1715378115DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789929PMC
January 2018

Homozygous c.359del variant in MGME1 is associated with early onset cerebellar ataxia.

Eur J Med Genet 2017 Oct 12;60(10):533-535. Epub 2017 Jul 12.

Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2017.07.010DOI Listing
October 2017

Histone H2A Monoubiquitination in Neurodevelopmental Disorders.

Trends Genet 2017 08 29;33(8):566-578. Epub 2017 Jun 29.

Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA; Cell and Molecular Biology Program, University of Michigan Medical School, Ann Arbor, MI, USA. Electronic address:

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http://dx.doi.org/10.1016/j.tig.2017.06.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562288PMC
August 2017

Role of angiotensin II type I (AT1 A1166C) receptor polymorphism in susceptibility of left ventricular dysfunction.

Indian Heart J 2015 May-Jun;67(3):214-21. Epub 2015 May 7.

Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Lucknow 226014, UP, India. Electronic address:

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http://dx.doi.org/10.1016/j.ihj.2015.04.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495590PMC
December 2016

Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.

J Genet 2016 Jun;95(2):263-72

Department of Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Lucknow 226 014, India.

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http://dx.doi.org/10.1007/s12041-016-0623-4DOI Listing
June 2016

A multigenic approach to evaluate genetic variants of PLCE1, LXRs, MMPs, TIMP, and CYP genes in gallbladder cancer predisposition.

Tumour Biol 2014 Sep 27;35(9):8597-606. Epub 2014 May 27.

Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Lucknow, Uttar Pradesh, 226014, India,

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http://dx.doi.org/10.1007/s13277-014-2094-7DOI Listing
September 2014

Genetic predisposition to left ventricular dysfunction: a multigenic and multi-analytical approach.

Gene 2014 Aug 27;546(2):309-17. Epub 2014 May 27.

Department of Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Lucknow 226014, UP, India. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2014.05.060DOI Listing
August 2014

Significant role of ADRB3 rs4994 towards the development of coronary artery disease.

Coron Artery Dis 2014 Jan;25(1):29-34

Departments of aGenetics bCardiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Lucknow, Uttar Pradesh, India.

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https://insights.ovid.com/crossref?an=00019501-201401000-000
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http://dx.doi.org/10.1097/MCA.0000000000000056DOI Listing
January 2014

Role of inflammatory gene polymorphisms in left ventricular dysfunction (LVD) susceptibility in coronary artery disease (CAD) patients.

Cytokine 2013 Mar 26;61(3):856-61. Epub 2013 Jan 26.

Department of Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow 226 014 (UP), India.

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http://dx.doi.org/10.1016/j.cyto.2012.12.020DOI Listing
March 2013

Association of matrix metalloproteinases (MMP2, MMP7 and MMP9) genetic variants with left ventricular dysfunction in coronary artery disease patients.

Clin Chim Acta 2012 Oct 1;413(19-20):1668-74. Epub 2012 Jun 1.

Department of Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences-SGPGIMS, Lucknow-226014 UP, India.

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http://dx.doi.org/10.1016/j.cca.2012.05.012DOI Listing
October 2012

Organic anion transporter 1B1 (SLCO1B1) polymorphism and gallstone formation: High incidence of Exon4 CA genotype in female patients in North India.

Hepatol Res 2011 Jan 25;41(1):71-8. Epub 2010 Oct 25.

Departments of Genetics Gastroenterology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS) Department of Physiology, Chhatrapati Shahuji Maharaj Medical University, Lucknow, India.

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http://dx.doi.org/10.1111/j.1872-034X.2010.00736.xDOI Listing
January 2011

Role of ABCG8 D19H (rs11887534) variant in gallstone susceptibility in northern India.

J Gastroenterol Hepatol 2010 Nov;25(11):1758-62

Departments of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.

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http://dx.doi.org/10.1111/j.1440-1746.2010.06349.xDOI Listing
November 2010

Effect of genetic variant (rs11887534) in ABCG8 gene in coronary artery disease and response to atorvastatin therapy.

Dis Markers 2010 ;28(5):307-13

Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Lucknow, India.

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http://dx.doi.org/10.3233/DMA-2010-0710DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833422PMC
October 2010