Vanita Vanita - Concepedia

Author

Vanita Vanita

Guru Nanak Dev University ORCID

Also Known As

Vanita Vanita, Vanita, Vanita

Publications

Citations

H-Index

Concepts

All Affiliations

Guru Nanak Dev University Punjab Technical University Charité - Universitätsmedizin Berlin Humboldt-Universität zu Berlin Satguru Partap Singh Hospital

About

Vanita Vanita is an author at Guru Nanak Dev University specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	207
2	Engineering	3	3	107
3	Natural Sciences	1	1	17
4	Public Health	1	1	21
5	Biochemistry	1	1	43

Vanita Vanita

Publications

882

Citations

H-Index

Page 1

	Year	Citations
A novel mutation in the DNA‐binding domain of <i>MAF</i> at 16q23.1 associated with autosomal dominant “cerulean cataract” in an Indian family Vanita Vanita, Daljit Singh, Peter N. Robinson, American Journal of Medical Genetics Part A	2006	90
Self-assembled vesicle and rod-like aggregates of functionalized perylene diimide: reaction-based near-IR intracellular fluorescent probe for selective detection of palladium Prabhpreet Singh, Lalit Singh Mittal, Vanita Vanita, Journal of Materials Chemistry B	2016	70
Bay functionalized perylenediimide as a deaggregation based intracellular fluorescent probe for perchlorate Prabhpreet Singh, Lalit Singh Mittal, Vanita Vanita, Chemical Communications	2014	58
A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family. Vanita Vanita, Jai Rup Singh, J. Fielding Hejtmancik, PubMed	2006	58
A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin. Vanita Vanita, Jai Rup Singh, Daljit Singh, PubMed	2008	44
N,N-dimethylaminoethylaminoanthrone – A chromofluorogenic chemosensor for estimation of Cu2+ in aqueous medium and HeLa cells imaging Ashwani Kumar, Vanita Vanita, Amandeep Walia, Sensors and Actuators B Chemical A Chromofluorogenic ChemosensorAqueous MediumEngineeringBiochemistryChemical Image	2012	43
A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family. Kamlesh Guleria, Karl Sperling, Daljit Singh, PubMed	2007	38
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin. Vanita Vanita, Hans Christian Hennies, Daljit Singh, PubMed	2006	38
Association of aldose reductase gene ( AKR1B1 ) polymorphism with diabetic retinopathy Navdeep Kaur, Vanita Vanita Diabetes Research and Clinical Practice Metabolic SyndromeDiabetic RetinopathyOcular DiseaseOphthalmologyGenetics	2016	37
Pyridoanthrone-based chromo-fluorogenic amphiphiles for selective CN− detection and their bioimaging application Ashwani Kumar, Vanita Vanita, Amandeep Walia, Sensors and Actuators B Chemical Pyridoanthrone-based Chromo-fluorogenic AmphiphilesEngineeringBioconjugationBiomedical AnalysisBioimaging	2019	37

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