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Usha Dave

Observed names: Dr. Usha Dave,, Dr. Usha Dave, U P Dave, U. Dave, Usha P Dave, Usha P. Dave, Usha Pinakin Dave
OpenAlex ID: A5019314045
Brain-Derived Neurotrophic Factor in children with Autism Spectrum Disorder
2014 · Nikhil J Kasarpalkar, Sweta T Kothari, et al. · Annals of Neurosciences · 77
Cornelia de Lange syndrome in diverse populations
2019 · Leah Dowsett, Antonio R. Porras, et al. · American Journal of Medical Genetics Part A · 52
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms
2023 · Maninder Kaur, Justin Blair, et al. · American Journal of Medical Genetics Part A · 42
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Plasma chitotriosidase activity in children with lysosomal storage disorders
2009 · Jayesh J. Sheth, Frenny J. Sheth, et al. · The Indian Journal of Pediatrics · 40
Evaluation of BR-16 A (mentat) in cognitive and behavioural dysfunction of mentally retarded children—A placebo-controlled study
1993 · Usha P. Dave, Vijaysingh Chauvan, et al. · The Indian Journal of Pediatrics · 36
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
2014 · Chitra Ankleshwaria, Mehul Mistri, et al. · Journal of Human Genetics · 34
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An open-label study to elucidate the effects of standardized Bacopa monnieri extract in the management of symptoms of attention-deficit hyperactivity disorder in children.
2014 · Usha Pinakin Dave, Sunila Rajeev Dingankar, et al. · PubMed · 33
Effect of Prolonged Anticonvulsant Medication in Epileptic Patients: Serum Lipids, Vitamins B6, B12, and Folic Acid, Proteins, and Fine Structure of Liver
1987 · Darab K. Dastur, Usha P. Dave · Epilepsia · 32
Ultrastructural basis of the vasculopathy in and around brain tuberculomas. Possible significance of altered basement membrane.
1977 · D K Dastur, U P Dave · PubMed · 32
Inborn errors of metabolism discovered in Asian department of pediatrics and mental retardation research center
2000 · Chunhua Zhang, Keming Xu, et al. · Journal of Chromatography B Biomedical Sciences and Applications · 24
Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency
2016 · Elsayed Abdelkreem, Radha Rama Devi Akella, et al. · JIMD Reports · 23
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A community genetics approach to population screening in India for mental retardation—a model for developing countries
2005 · U. Dave, N. Shetty, et al. · Annals of Human Biology · 21
Maternal Age and Chromosomal Profile in 160 Down Syndrome Cases – Experience of a Tertiary Genetic Centre from India
2002 · Sanjeev Kothare, Neera Shetty, et al. · International Journal of Human Genetics · 13
Fine structure of cellular and vascular reaction in brain tuberculomas:
1986 · Darab K. Dastur, Usha P. Dave · Pathology - Research and Practice · 9
Chromosomal Abnormalities in Mental Retardation: Indian Experience
2010 · Usha Dave, Dhanlaxmi Shetty · International Journal of Human Genetics · 8
Erratum: Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease
2015 · Chitra Ankleshwaria, Mehul Mistri, et al. · Journal of Human Genetics · 7
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Mutational Screening and Prenatal Diagnosis in Cornelia de Lange syndrome
2013 · Usha Dave, Dhanlaxmi Shetty · The Journal of Obstetrics and Gynecology of India · 6
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Chromosomal Abnormalities in Mental Retardation: Indian Experience
2010 · Usha P. Dave · International Journal of Human Genetics · 5
Hemoglobin Variant Analysis and Its Comparison between Conventional High-performance Liquid Chromatography Using Whole Blood versus Dried Blood Spot: High-performance Liquid Chromatography
2025 · Rabindra Kumar Jena, Sudha Sethy, et al. · Indian Journal of Public Health · 4
Brain-Derived Neurotrophic Factor (BDNF) in Children with Autism Spectrum Disorder
2014 · Nikhil Jayant Kasarpalkar, Sweta Trilok Kothari, et al. · Annals of Neurosciences · 2
Chemical Diagnosis of Congenital Metabolic Disorders by Gas Chromatography / Mass Spectrometry (GC/MS) in India
2001 · Usha P. Dave, Vrajesh Udani, et al. · International Journal of Human Genetics · 2
Phenotypic Evolution in Fabry Disease: Our Experience in Indian Cohort
2024 · Usha Dave, Srilatha Kadali, et al. · Indian Journal of Clinical Biochemistry · 1
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Genetic Counseling in Developmental Disability
2016 · Usha P. Dave · International Journal of Human Genetics · 1
A PCR-based screening method for rapid detection and genetic counseling in Fragile-X syndrome
2010 · Usha Dave, Dhanlaxmi Shetty · Journal of Prenatal Diagnosis and Therapy · 1
Trisomy 9p Syndrome in a Mentally Retarded Female Inherited from Maternal Reciprocal Translocation
2006 · Dhanlaxmi Shetty, K. Desai, et al. · International Journal of Human Genetics · 1
Works count: 38
Citation count: 506
H-index: 13
I10-index: 13
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