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Ankita Narang
Ankita Narang
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Title
Cited by
Cited by
Year
Integrating transcriptome and proteome profiling: Strategies and applications
D Kumar, G Bansal, A Narang, T Basak, T Abbas, D Dash
Proteomics 16 (19), 2533-2544, 2016
1712016
Genomics of rare genetic diseases—experiences from India
S Sivasubbu, V Scaria
Human genomics 13 (1), 52, 2019
522019
Deletion of the APOBEC3B gene strongly impacts susceptibility to falciparum malaria
P Jha, S Sinha, K Kanchan, T Qidwai, A Narang, PK Singh, SS Pati, ...
Infection, Genetics and Evolution 12 (1), 142-148, 2012
432012
IGVBrowser–a genomic variation resource from diverse Indian populations
A Narang, RD Roy, A Chaurasia, A Mukhopadhyay, M Mukerji, ...
Database 2010, baq022, 2010
422010
Ayurgenomics for stratified medicine: TRISUTRA consortium initiative across ethnically and geographically diverse Indian populations
B Prasher, B Varma, A Kumar, BK Khuntia, R Pandey, A Narang, P Tiwari, ...
Journal of ethnopharmacology 197, 274-293, 2017
352017
Recent admixture in an Indian population of African ancestry
A Narang, P Jha, V Rawat, A Mukhopadhayay, D Dash, A Basu, M Mukerji
The American Journal of Human Genetics 89 (1), 111-120, 2011
352011
Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families
M Faruq, A Narang, R Kumari, R Pandey, A Garg, M Behari, D Dash, ...
Clinical Genetics 86 (4), 335-341, 2014
292014
Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders
C Okhuijsen-Pfeifer, MZ van der Horst, CA Bousman, B Lin, KR van Eijk, ...
Translational Psychiatry 12 (1), 145, 2022
202022
Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations
RW Thergaonkar, A Narang, BS Gurjar, P Tiwari, M Puraswani, H Saini, ...
Clinical and Experimental Nephrology 22, 653-660, 2018
142018
Extensive copy number variations in admixed Indian population of African ancestry: potential involvement in adaptation
A Narang, P Jha, D Kumar, R Kutum, AK Mondal, ...
Genome biology and evolution 6 (12), 3171-3181, 2014
142014
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India
A Narang, B Uppilli, A Vivekanand, S Naushin, A Yadav, K Singhal, ...
Human Mutation 41 (11), 1833-1847, 2020
132020
Genome and transcriptome analysis of the mealybug Maconellicoccus hirsutus: Correlation with its unique phenotypes
S Kohli, P Gulati, A Narang, J Maini, KV Shamsudheen, R Pandey, ...
Genomics 113 (4), 2483-2494, 2021
92021
A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7‐CAG Expansion Loci in the Indian and Mexican Population
M Faruq, JJ Magaña, V Suroliya, A Narang, NM Murillo‐Melo, ...
Annals of Human Genetics 81 (5), 197-204, 2017
92017
Associations between polygenic risk score loading, psychosis liability, and clozapine use among individuals with schizophrenia
BD Lin, J Pinzón-Espinosa, E Blouzard, MZ van der Horst, ...
JAMA psychiatry 80 (2), 181-185, 2023
82023
Whole exome sequencing in healthy individuals of extreme constitution types reveals differential disease risk: a novel approach towards predictive medicine
T Abbas, G Chaturvedi, P Prakrithi, AK Pathak, R Kutum, P Dakle, ...
Journal of Personalized Medicine 12 (3), 489, 2022
72022
Mining histone methyltransferases and demethylases from whole genome sequence
P Gulati, S Kohli, A Narang, V Brahmachari
Journal of biosciences 45, 1-17, 2020
42020
VitiVar: A locus specific database of vitiligo associated genes and variations
I Gupta, A Narang, P Singh, V Manchanda, S Khanna, M Mukerji, ...
Gene 721, 100018, 2019
42019
Generation of two human induced pluripotent stem cell lines from peripheral blood mononuclear cells of clozapine-tolerant and clozapine-induced myocarditis patients with …
N Vaziri, D Marques, X Wang, P Machiraju, A Narang, K Vlahos, ...
Stem Cell Research 63, 102877, 2022
32022
Genome and transcriptome analysis of the mealybug Maconellicoccus hirsutus: A model for genomic Imprinting
S Kohli, P Gulati, J Maini, S KV, R Pandey, V Scaria, S Sivasubbu, ...
bioRxiv, 2020.05. 22.110437, 2020
22020
Genetic differences between extreme and composite constitution types from whole exome sequences reveal actionable variations
T Abbas, R Kutum, R Pandey, P Dakle, A Narang, V Manchanda, R Patil, ...
bioRxiv, 2020.04. 24.059006, 2020
22020
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Articles 1–20