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Vanita Vanita
Observed name:
Vanita, Vanita
Institution:
Guru Nanak Dev University
Observed institution:
Guru Nanak Dev University
ORCID:
0000-0003-2251-6641
Observed ORCID:
0000-0003-2251-6641
OpenAlex ID:
A5087954159
A novel mutation in the DNA‐binding domain of MAF at 16q23.1 associated with autosomal dominant “cerulean cataract” in an Indian family
2006
·
Vanita Vanita
, Daljit Singh
, et al.
·
American Journal of Medical Genetics Part A
·
88
Self-assembled vesicle and rod-like aggregates of functionalized perylene diimide: reaction-based near-IR intracellular fluorescent probe for selective detection of palladium
2016
·
Prabhpreet Singh
, Lalit Singh Mittal
, et al.
·
Journal of Materials Chemistry B
·
75
Bay functionalized perylenediimide as a deaggregation based intracellular fluorescent probe for perchlorate
2014
·
Prabhpreet Singh
, Lalit Singh Mittal
, et al.
·
Chemical Communications
·
61
A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.
2006
·
Vanita Vanita
, Jai Rup Singh
, et al.
·
PubMed
·
59
PDF
Genetics of diabetes
2023
·
Shiwali Goyal
, Jyoti Rani
, et al.
·
World Journal of Diabetes
·
49
N,N-dimethylaminoethylaminoanthrone – A chromofluorogenic chemosensor for estimation of Cu2+ in aqueous medium and HeLa cells imaging
2012
·
Ashwani Kumar
, Vanita Vanita
, et al.
·
Sensors and Actuators B Chemical
·
45
A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.
2008
·
Vanita Vanita
, Jai Rup Singh
, et al.
·
PubMed Central
·
45
PDF
The Rise of Type 2 Diabetes in Children and Adolescents: An Emerging Pandemic
2025
·
Shiwali Goyal
, Vanita Vanita
·
Diabetes/Metabolism Research and Reviews
·
44
PDF
Association of aldose reductase gene ( AKR1B1 ) polymorphism with diabetic retinopathy
2016
·
Navdeep Kaur
, Vanita Vanita
·
Diabetes Research and Clinical Practice
·
43
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
2006
·
Vanita Vanita
, Hans Christian Hennies
, et al.
·
PubMed
·
39
PDF
A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
2007
·
Kamlesh Guleria
, Karl Sperling
, et al.
·
PubMed
·
37
Pyridoanthrone-based chromo-fluorogenic amphiphiles for selective CN− detection and their bioimaging application
2019
·
Ashwani Kumar
, Vanita Vanita
, et al.
·
Sensors and Actuators B Chemical
·
36
Pre-clinical and cellular toxicity evaluation of 7-methylxanthine: an investigational drug for the treatment of myopia
2019
·
Harjeet Singh
, Nikhil Shri Sahajpal
, et al.
·
Drug and Chemical Toxicology
·
36
Nanomolar fluorogenic detection of Al(iii) by a series of Schiff bases in an aqueous system and their application in cell imaging
2014
·
Sanyog Sharma
, Maninder Singh Hundal
, et al.
·
Organic & Biomolecular Chemistry
·
36
Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.
2006
·
Vanita Vanita
, James Fielding Hejtmancik
, et al.
·
PubMed
·
34
PDF
Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.
2009
·
Vanita Vanita
, Jai Rup Singh
, et al.
·
PubMed Central
·
30
PDF
A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.
2008
·
Vanita Vanita
, Jai Rup Singh
, et al.
·
PubMed Central
·
29
PDF
Coronene diimide-based self-assembled (fibre-to-disc) fluorescent aggregates for visualization of latent fingerprints
2018
·
Kapil Kumar
, Harminder Singh
, et al.
·
Sensors and Actuators B Chemical
·
27
Clinical and molecular aspects of congenital aniridia – A review of current concepts
2022
·
Shailja Tibrewal
, Ria Ratna
, et al.
·
Indian Journal of Ophthalmology
·
24
A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene.
2007
·
Kamlesh Guleria
, Vanita Vanita
, et al.
·
PubMed Central
·
24
PDF
A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family
2012
·
Seema Saini
, Peter N. Robinson
, et al.
·
Experimental Eye Research
·
22
Nanomolar Cu 2+ Detection in Water Based on Disassembly of AIEgen: Applications in Blood Serum, Cell Imaging and Complex Logic Circuits
2016
·
Prabhpreet Singh
, Harminder Singh
, et al.
·
ChemistrySelect
·
21
Association of RAGE (p.Gly82Ser) and MnSOD (p.Val16Ala) polymorphisms with diabetic retinopathy in T2DM patients from north India
2014
·
Vanita Vanita
·
Diabetes Research and Clinical Practice
·
20
Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort
2019
·
Shruti Passan
, Shiwali Goyal
, et al.
·
Gene
·
18
A novel mutation in the PRPF31 in a North Indian adRP family with incomplete penetrance
2018
·
Sofia Bhatia
, Shiwali Goyal
, et al.
·
Documenta Ophthalmologica
·
18
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Works count:
68
Citation count:
1,106
H-index:
21
I10-index:
31
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