Prof Vanita Vanita
Professor
| Department of Human Genetics
Guru Nanak Dev University College, Verka
Punjab
Expertise:
Genetics and Heredity
52
Publications
7
Projects
1187
Scopus Citations
764
CrossRef
25 Years 10 Months Total Experience
Scopus
1,187
Citations
23
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CrossRef
764
Citations
17
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Professional Recognition
Post-doctoral Visiting Fellow
2003
National Eye Institute, National Institute of Health, Bethesda, Maryland, USA
Award for Vocational Excellence
2002
Rotary Club Amritsar
Community & Membership
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Personal Details
Doctor of Philosophy
1999
Karnataka Nephrology And Transplant Institute
Professor
Nov 2000 – Present
Guru Nanak Dev University College, Verka
| Department of Human Genetics
Medical and Health Sciences
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Scholarly Work
Molecular Genetic Analysis in Congenital Cataract Patients
OtherThe Neurobiology of Hereditary Retinal Diseases: Genes and Molecular Dysfunctions Underlying Disorders of the Neuroretina
CompletedMolecular Genetic Analyses in Diabetic Retinopathy Cases
CompletedCytokine Gene Polymorphism in Recurrent Pregnancy Loss Cases
CompletedIndo-US collaboration in Genomic Studies on Diabetes
CompletedMolecular and Biochemical Analyses in Congenital Cataract Cases
CompletedStudy of Genomic Diversity of Human Populations of North West India
CompletedMolecular genetic studies in congenital cataract cases
Molecular genetic studies in glaucoma cases
Molecular genetic studies in retinitis pigmentosa cases
Molecular Genetic Analysis in Cases with Retinal Dystrophies
Biochemical Molecular Analysis in Cases with Diabetic Retinopathy
Genetics analyses in patients with glaucoma
Molecular Genetic Analysis in Retinitis Pigmentosa and other Retinal Dystrophy Cases
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Scholarly Publications
Genetic and segregation analysis of congenital cataract in the Indian population
A missense mutation in CRYGD linked with autosomal dominant congenital cataract of aculeiform type
Novel mutation in the γ-S crystallin gene causing autosomal dominant cataract
Scopus: 34
Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
The genetic disease burden and the Molecular Diagnostic Industry in India
A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin
Scopus: 26
A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin
Scopus: 42
A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin
Scopus: 12
Showing 1 to 8 of 52 publications