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Surya Balakrishnan
Observed name:
Balakrishnan, Surya
Institutions:
Apollo Hospitals,
Apollo Hospitals,
Apollo Hospitals,
Panimalar Medical College Hospital & Research Institute,
PSG College of Arts & Science
Observed institutions:
Apollo Hospitals,
Nizam's Institute of Medical Sciences,
Centre for Cellular and Molecular Biology,
Apollo Hospitals,
Apollo Hospitals,
Panimalar Medical College Hospital & Research Institute,
PSG College of Arts & Science,
Centre for DNA Fingerprinting and Diagnostics
show all 8
ORCID:
0000-0001-8563-8553
Observed ORCID:
0000-0001-8563-8553
OpenAlex ID:
A5062482131
Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphism
2018
·
Venugopal S. Vineeth
, Aneek Das Bhowmik
, et al.
·
Journal of Human Genetics
·
15
Clinical and Molecular Spectrum of Degenerative Cerebellar Ataxia: A Single Centre Study
2022
·
Surya Balakrishnan
, Shagun Aggarwal
, et al.
·
Neurology India
·
8
Report of an unusual association of hydrosyringomyelia with Gabriele-de Vries syndrome in an Asian-Indian patient
2021
·
Surya Balakrishnan
, Prajnya Ranganath
·
Clinical Dysmorphology
·
8
Prenatal onset GAPO syndrome with a novel ANTXR1 variant in an Indian child: Expansion of the phenotype & literature review
2024
·
Surya Balakrishnan
, Iravathy Goud
, et al.
·
European Journal of Medical Genetics
·
3
Mosaic paternal uniparental isodisomy of 15q11-q13 region causing Angelman phenotype
2019
·
Dhanya Lakshmi Narayanan
, Prajnya Ranganath
, et al.
·
Clinical Dysmorphology
·
2
Ecogenomic profiling of spatial variations in sediment microbial communities of a freshwater lake
2026
·
Surya Balakrishnan
, Bharathkumar Rajagopal
, et al.
·
Cleaner Water
·
1
A new case of SUPT16H-associated syndromic neurodevelopmental delay
2024
·
Surya Balakrishnan
, Mouneesha Rachamadugu
, et al.
·
Clinical Dysmorphology
·
1
Atypical Hemolytic-uremic Syndrome with Postrenal Transplant Recurrence Due to a Novel Frameshift Variant in Complement Factor H
2023
·
Surya Balakrishnan
, Satyanarayana Garre
·
Apollo Medicine
·
1
Novel ASAH1 Variant in an Indian Boy with Biochemical Evidence of Reduced Alpha Ceramidase Activity
2026
·
Surya Balakrishnan
, Sudarshan Reddy
, et al.
·
Genetic Clinics
Mitigating Genetic Diagnostic Errors and Unwarranted Cascade Testing: Two Illustrative Cases
2026
·
Surya Balakrishnan
, Ambika Gupta
, et al.
·
Apollo Medicine
Enhancing Collaboration, Providing Care, and Fostering Change: A 3-C Approach to Evaluate the Impact of Family Adoption Program in Undergraduate Competency-based Medical Education Curriculum
2026
·
Krishna Mohan Surapaneni
, Suguna Elayaperumal
, et al.
·
Indian Journal of Public Health
Genotype-Phenotype Insights from a Rare Case of 2q37.2 Microdeletion Syndrome in an Indian Boy
2026
·
Surya Balakrishnan
, Khyati Arora
, et al.
·
Genetic Clinics
9p13.3 Syndrome: A Rare and Unusual Genetic Cause of Tremor in a Young Indian Boy
2026
·
Surya Balakrishnan
, Soumya Sharma
, et al.
·
Apollo Medicine
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Works count:
16
Citation count:
39
H-index:
3
I10-index:
1
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