Shalini S Nayak

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Topics

Intellectual Disability

Dna Methylation

Top Venues

American journal of medical genetics. Part A

European journal of human genetics : EJHG

Prenatal diagnosis

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

Publications

Subrahmanya Vasishta, Akkatai S Teli, Akhila Vasudeva, Katta Mohan Girisha, Shalini S Nayak
Early and severe tricuspid valve dysplasia in a fetus with cardiospondylocarpofacial syndrome due to a variant c.616T>G p.(Tyr206Asp) in MAP3K7. Prenatal diagnosis (2023)
Shruti Pande, Purvi Majethia, Karthik Nair, Lakshmi Priya Rao, Selinda Mascarenhas, Namanpreet Kaur, Michelle C do Rosario, Kausthubham Neethukrishna, Ankur Chaurasia, Bhagesh Hunakunti, Nalesh Jadhav, Sruthy Xavier, Jeevan Kumar, Vivekananda Bhat, Gandham SriLakshmi Bhavani, Dhanya Lakshmi Narayanan, B L Yatheesha, Siddaramappa J Patil, Sheela Nampoothiri, Nutan Kamath, Shrikiran Aroor, Ramesh Bhat Y, Leslie E Lewis, Suvasini Sharma, Shruti Bajaj, Naveen Sankhyan, Shahyan Siddiqui, Shalini S Nayak, Stephanie Bielas, Katta Mohan Girisha, Anju Shukla
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India. European journal of human genetics : EJHG (2023)
Shruti Pande, Purvi Majethia, Karthik Nair, Lakshmi Priya Rao, Selinda Mascarenhas, Namanpreet Kaur, Michelle C do Rosario, Kausthubham Neethukrishna, Ankur Chaurasia, Bhagesh Hunakunti, Nalesh Jadhav, Sruthy Xavier, Jeevan Kumar, Vivekananda Bhat, Gandham SriLakshmi Bhavani, Dhanya Lakshmi Narayanan, B L Yatheesha, Siddaramappa J Patil, Sheela Nampoothiri, Nutan Kamath, Shrikiran Aroor, Ramesh Bhat Y, Leslie E Lewis, Suvasini Sharma, Shruti Bajaj, Naveen Sankhyan, Shahyan Siddiqui, Shalini S Nayak, Stephanie Bielas, Katta Mohan Girisha, Anju Shukla
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India. European journal of human genetics : EJHG (2023)
Subrahmanya Vasishta, Akkatai S Teli, Akhila Vasudeva, Katta Mohan Girisha, Shalini S Nayak
Early and severe tricuspid valve dysplasia in a fetus with cardiospondylocarpofacial syndrome due to a variant c.616T>G p.(Tyr206Asp) in MAP3K7. Prenatal diagnosis (2023)
Shalini S Nayak, Robert Harkness, Anju Shukla, Siddharth Banka, William G Newman, Katta Mohan Girisha
Clinically diverse and perinatally lethal syndromes with urorectal septum malformation sequence. American journal of medical genetics. Part A (2022)
Pauline E Schneeberger, Shalini S Nayak, Sigrid Fuchs, Kerstin Kutsche, Katta Mohan Girisha
Roberts syndrome in an Indian patient with humeroradial synostosis, congenital elbow contractures and a novel homozygous splice variant in ESCO2. American journal of medical genetics. Part A 182 (11) (2020)
Periyasamy Radhakrishnan, Anju Shukla, Katta Mohan Girisha, Shalini S Nayak
Biallelic c.1263dupC in DOK7 results in fetal akinesia deformation sequence. American journal of medical genetics. Part A 182 (4) (2019)