Prajnya Ranganath

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 13

Top Venues

Journal of pediatric genetics

Clinical genetics

American journal of medical genetics. Part A

Human mutation

Nizam's Institute of Medical Sciences

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Nizam's Institute of Medical Sciences Dec 16 2011

India

Associate Professor and Head :: Department of Medical Genetics

Publications

T Pragna Lakshmi, Neelam Saini, Mehul A Shah, Swarnalata Gowrishankar, Ashwin B Dalal, Prajnya Ranganath
Short stature and dysmorphic features in Asian Indian siblings with DAAM2-associated steroid-resistant nephrotic syndrome: Expansion of the phenotypic spectrum or a blended phenotype? Clinical genetics 106 (4) (2024)
T Pragna Lakshmi, Neelam Saini, Mehul A Shah, Swarnalata Gowrishankar, Ashwin B Dalal, Prajnya Ranganath
Short stature and dysmorphic features in Asian Indian siblings with DAAM2-associated steroid-resistant nephrotic syndrome: Expansion of the phenotypic spectrum or a blended phenotype? Clinical genetics (2024)
Ritasman Baisya, Prajnya Ranganath, Liza Rajasekhar
PEPD-Related Prolidase Deficiency Presenting as Hyper-immunoglobulin E Syndrome. Journal of clinical immunology 42 (4) (2022)
Prajnya Ranganath, Mallikarjun Patil
Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders. Journal of pediatric genetics 12 (2) (2021)
Prajnya Ranganath, Mallikarjun Patil
Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders. Journal of pediatric genetics 12 (2) (2021)
Prajnya Ranganath, Mallikarjun Patil
Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders. Journal of pediatric genetics 12 (2) (2021)
Ajay Kumar Chaudhary, Aishwarya Gholse, Hampapathalu Adimurthy Nagarajaram, Ashwin Bhikaji Dalal, Neerja Gupta, Atanu Kumar Dutta, Sumita Danda, Rekha Gupta, Hariharan V Sankar, Gandham SriLakshmi Bhavani, Katta Mohan Girisha, Shubha Rao Phadke, Prajnya Ranganath, Murali Dharan Bashyam
Ectodysplasin pathogenic variants affecting the furin-cleavage site and unusual clinical features define X-linked hypohidrotic ectodermal dysplasia in India. American journal of medical genetics. Part A (2021)
Prajnya Ranganath, Mallikarjun Patil
Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders. Journal of pediatric genetics 12 (2) (2021)
N Gayatri, Prajnya Ranganath
Genetic Evaluation of the Parents Following Demise of the Index Case: Report of a Family with Fucosidosis. Journal of obstetrics and gynaecology of India 72 (4) (2021)
Dipti Deshpande, Shailesh Kumar Gupta, Asodu Sandeep Sarma, Prajnya Ranganath, Jamal Md Nurul Jain S, Jayesh Sheth, Mehul Mistri, Neerja Gupta, Madhulika Kabra, Shubha R Phadke, Katta M Girisha, Ratna Dua Puri, Shagun Aggarwal, Chaitanya Datar, Kausik Mandal, Preetha Tilak, Mamta Muranjan, Sunita Bijarnia-Mahay, Radharamadevi Akella, Naresh B Tayade, Akash Ranjan, Ashwin B Dalal
Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiency. Human mutation 42 (10) (2021)
Prajnya Ranganath, Sreeja Perala, Lekshmi Nair, Pramod Kumar Pamu, Aparna Shankar, Sakthivel Murugan, Ashwin Dalal
A newly recognized multiple malformation syndrome with caudal regression associated with a biallelic c.402G>A variant in TBX4. European journal of human genetics : EJHG 28 (5) (2020)
Divya Pasumarthi, Neerja Gupta, Jayesh Sheth, S Jamal Md Nurul Jain, Ikrormi Rungsung, Madhulika Kabra, Prajnya Ranganath, Shagun Aggarwal, Shubha R Phadke, Katta Mohan Girisha, Anju Shukla, Chaitanya Datar, Ishwar C Verma, Ratna Dua Puri, Riddhi Bhavsar, Mehul Mistry, V H Sankar, Kalpana Gowrishankar, Divya Agrawal, Mohandas Nair, Sumita Danda, Jai Prakash Soni, Ashwin Dalal
Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type III. Journal of human genetics 65 (11) (2020)
Gayatri Nerakh, Prajnya Ranganath
Alström Syndrome Presenting as Isolated Dilated Cardiomyopathy. Indian journal of pediatrics 86 (3) (2018)

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Publication Activity (10 Years)

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Prajnya Ranganath