Dr. Rohit Sadanand is a forward-thinking Clinical Geneticist and Pediatrician based in Hyderabad.

Trained at India’s most prestigious medical institutions, he is a pioneer in integrating emerging technologies like Artificial Intelligence and Digital Health into the field of Medical Genetics.

Professional Summary

Dr. Rohit Sadanand is a clinician–scientist specializing in Medical Genetics, with advanced training in Pediatrics and Clinical Genetics. He completed his MBBS at JIPMER, MD Pediatrics at PGIMER, and DM (Medical Genetics) at AIIMS, New Delhi.

His clinical focus includes rare genetic disorders, inborn errors of metabolism, neurogenetic conditions, and undiagnosed syndromes. He has particular expertise in lysosomal storage disorders and biomarker-driven diagnostics, with experience in enzyme replacement therapy, stem cell transplant, and advanced disease-specific biomarkers such as Lyso-Gb1 in Gaucher disease.

Dr. Rohit integrates deep molecular understanding with clinical reasoning, applying genomic tools such as exome sequencing and internationally accepted variant interpretation frameworks to deliver precise diagnoses and actionable insights. His interests extend to genotype–phenotype correlation, variant classification, and the application of AI in genetic medicine.

He is committed to providing evidence-based, compassionate genetic care, bridging advanced genomic science with practical clinical decision-making for families.

Educational Qualifications

• DM in Medical Genetics – AIIMS, New Delhi

• MD in Pediatrics – PGIMER, Chandigarh

• MBBS – JIPMER, Puducherry

Areas of Expertise

• AI & Digital Health in Genetics: Special interest in utilizing Artificial Intelligence and developing specialized applications for genetic data management and patient care.

• Bioinformatics: Applying computational tools to analyze and interpret complex biological data and genomic sequences.

• Inborn Errors of Metabolism (IEM): Diagnosis and long-term management of biochemical genetic disorders with a special focus on lysosomal storage disorders.

• Newborn Screening Follow-up & Interpretation

• Pediatric Genetics: Expert evaluation and management of genetic conditions manifesting in infancy and childhood.

• Clinical Exome & Genome Analysis

• Genomic Interpretation: Translating high-throughput sequencing data into clinically actionable insights.

Practice Location & Timings

• Location: Hyderabad, Telangana

• Hospital: Rainbow Children’s Hospital, Banjara Hills, Hyderabad

• Schedule: Mon/Wed/Fri; 10 AM – 5 PM

Contact & Personal Details

• Email: r1.r7.m5@gmail.com

• Languages: Hindi, English, Telugu