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Saraswati Nashi
Observed names:
Nashi Saraswati,
Nashi, Saraswati,
S Nashi,
S. Nashi,
SS Nashi,
Saraswati Nashi
show all 6
Institution:
National Institute of Mental Health and Neurosciences
Observed institutions:
University of Ottawa,
Children's Hospital of Eastern Ontario,
Ottawa Hospital,
Swansea University,
Neurology, Inc,
uOttawa Brain and Mind Research Institute,
National Institute of Mental Health and Neurosciences,
Niigata University
show all 8
ORCID:
0000-0002-3184-2345
Observed ORCID:
0000-0002-3184-2345
OpenAlex ID:
A5056673079
Brain and Spinal Cord Lesions in Leprosy: A Magnetic Resonance Imaging–Based Study
2019
·
Kiran Polavarapu
, Veeramani Preethish-Kumar
, et al.
·
American Journal of Tropical Medicine and Hygiene
·
46
Chitotriosidase, a biomarker of amyotrophic lateral sclerosis, accentuates neurodegeneration in spinal motor neurons through neuroinflammation
2020
·
Anu Mary Varghese
, Mausam Ghosh
, et al.
·
Journal of Neuroinflammation
·
44
PDF
Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant
2019
·
Sunitha Balaraju
, Ana Töpf
, et al.
·
European Journal of Human Genetics
·
35
PDF
CASPR2-Related Morvan Syndrome
2020
·
Panda Sudha Swayang
, Atchayaram Nalini
, et al.
·
Neurology Clinical Practice
·
34
Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness
2018
·
David Owen
, Ana Töpf
, et al.
·
American Journal of Medical Genetics Part A
·
34
Neuromuscular disease genetics in under-represented populations: increasing data diversity
2023
·
Lindsay A Wilson
, William L Macken
, et al.
·
Brain
·
32
PDF
Evidence for Mycobacterium leprae Drug Resistance in a Large Cohort of Leprous Neuropathy Patients from India
2020
·
Niranjan Prakash Mahajan
, Mallika Lavania
, et al.
·
American Journal of Tropical Medicine and Hygiene
·
32
PDF
Caregiver burden and quality of life of patients with amyotrophic lateral sclerosis in India
2018
·
Priya Treesa Thomas
, Manjusha G. Warrier
, et al.
·
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
·
27
FDG-PET in Autoimmune Encephalitis
2022
·
Shreyashi Jha
, Chandana Nagaraj
, et al.
·
Annals of Indian Academy of Neurology
·
25
Comparison of Speech Tasks for Automatic Classification of Patients with Amyotrophic Lateral Sclerosis and Healthy Subjects
2018
·
Aravind Illa
, Deep Patel
, et al.
·
IEEE International Conference on Acoustics Speech and Signal Processing
·
25
Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohort
2023
·
Kiran Polavarapu
, Balaraju Sunitha
, et al.
·
Brain
·
24
PDF
In Vivo Evaluation of White Matter Abnormalities in Children with Duchenne Muscular Dystrophy Using DTI
2020
·
V. Preethish-Kumar
, A. Shah
, et al.
·
American Journal of Neuroradiology
·
24
PDF
Mutation pattern in 606 Duchenne muscular dystrophy children with a comparison between familial and non-familial forms: a study in an Indian large single-center cohort
2019
·
Kiran Polavarapu
, Veeramani Preethish-Kumar
, et al.
·
Journal of Neurology
·
24
Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South India
2018
·
Atchayaram Nalini
, Ravinder-Jeet Singh
, et al.
·
Neurology India
·
24
Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndrome
2017
·
Seena Vengalil
, Veeramani Preethish-Kumar
, et al.
·
Neuromuscular Disorders
·
23
Neuroimaging in leprosy: The nerves and beyond
2020
·
Shumyla Jabeen
, Jitender Saini
, et al.
·
Radiology of Infectious Diseases
·
22
PDF
C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilection
2020
·
Uzma Shamim
, Sakshi Ambawat
, et al.
·
Neurobiology of Aging
·
22
Comparing sleep profiles between patients with juvenile myoclonic epilepsy and symptomatic partial epilepsy: Sleep questionnaire-based study
2016
·
Nashi Saraswati
, Chetan Nayak
, et al.
·
Epilepsy & Behavior
·
22
CARASIL families from India with 3 novel null mutations in the HTRA1 gene
2017
·
Veeramani Preethish-Kumar
, Hiroaki Nozaki
, et al.
·
Neurology
·
21
Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoform
2021
·
Veeramani Preethish-Kumar
, Apurva Shah
, et al.
·
Journal of Neurology
·
19
Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome
2021
·
Mainak Bardhan
, Kiran Polavarapu
, et al.
·
Journal of Human Genetics
·
17
A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients
2021
·
Kiran Polavarapu
, Aradhna Mathur
, et al.
·
Neurogenetics
·
16
Family Caregivers’ Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in India
2019
·
Manjusha G. Warrier
, Priya Treesa Thomas
, et al.
·
Journal of Social Work in End-of-Life & Palliative Care
·
16
Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations
2020
·
Shamita Sanga
, Arnab Ghosh
, et al.
·
European Journal of Neurology
·
15
Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent ADSSL1 Missense Variant
2024
·
Dipti Baskar
, Kiran Polavarapu
, et al.
·
Neurology Genetics
·
13
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Works count:
202
Citation count:
980
H-index:
19
I10-index:
32
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