Aradhana Mathur
ScholarGPS® ID: 91609027651138
Affiliation History
Field
Life Sciences
Discipline
Biology and Biological Sciences
Top Specialties
Mutation | Birth Defect | Amyotrophic Lateral Sclerosis
Metrics Summary
Publication Count
22
Predicted Citations
291
Predicted h-index
10
Ranking
Publications and Citation History
Publications based on Top Specialties
Types of Publication
- Publications
- Books
- Patents
- NIH/NSF
Add
Delete
|
---|
Variants in complement genes are uncommon in patients with anti-factor H autoantibody-associated atypical hemolytic uremic syndrome (journal article) Pediatric Nephrology, volume 38, issue 8, pages 2659-2668 (2023). |
The Cleft Palate-Craniofacial Journal, volume 59, issue 11, pages 1329-1339 (2022). |
Distinct and Recognisable Muscle MRI Pattern in a Series of Adults Harbouring an Identical GMPPB Gene Mutation (journal article) Journal of Neuromuscular Diseases, volume 9, issue 1, pages 95-109 (2022). |
neurogenetics, volume 22, issue 4, pages 271-285 (2021). |
Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India (journal article) Indian Pediatrics, volume 58, issue 5, pages 445-451 (2021). |
Brain Communications, volume 3, issue 1 (2021). |
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India (journal article) Human Mutation, volume 41, issue 11, pages 1833-1847 (2020). |
An Indian child with Coats plus syndrome due to mutations in STN1 (journal article) American Journal of Medical Genetics Part A, volume 182, issue 9, pages 2139-2144 (2020). |
C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilection (journal article) Neurobiology of Aging, volume 88 (2020). |
Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population (journal article) eNeurologicalSci, volume 17 (2019). |
Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation (journal article) Clinical Genetics, volume 96, issue 3, pages 271-273 (2019). |
Intrafamilial Variable Phenotype of Complicated Hereditary Spastic Paraplegia, Ataxia and Motor Neuron Disease Linked to a Novel KIF5A C-Terminal Domain Mutation (journal article) SSRN Electronic Journal (2019). |
A founder mutation MLC1 c.736delA associated with megalencephalic leukoencephalopathy with subcortical cysts‐1 in north Indian kindred (journal article) Clinical Genetics, volume 94, issue 2, pages 271-273 (2018). |
A novel mutation in SGSH causing Sanfillipo type 3A Mucopolysaccharidoses in an Indian family (journal article) Molecular Genetics and Metabolism Reports, volume 15 (2018). |
Chemical and genetic stability of methyl chavicol-rich Indian basil (Ocimum basilicum var. CIM-Saumya) micropropagated in vitro (journal article) South African Journal of Botany, volume 113 (2017). |
Biodiversity Offsets and Infrastructure (journal article) Conservation Biology, volume 25, issue 6, pages 1121-1123 (2011). |
World Bank (2010) |
Anticancer Alkaloids of Catharanthus roseus: Transition from Traditional to Modern Medicine (book chapter) In Herbal Medicine: A Cancer Chemopreventive and Therapeutic Perspective Jaypee Brothers Medical Publishers (P) Ltd. (2010) |
CITES and Livelihood (journal article) The Journal of Environment & Development, volume 18, issue 3, pages 291-305 (2009). |
Congenital rubella following inapparent rubella infection. (journal article) The Indian journal of medical research, volume 75 (1982). |