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Dr. Sameer Bhatia

Associate Consultant
Institute of Medical Genetics & Genomics

Dr. Sameer Bhatia

Associate Consultant
Institute of Medical Genetics & Genomics

Next Generation Medical Genetics Expert And A Senior Paediatrician With More Than 15 Years Of Experience. Special Training In Cancer Genetics, Immuno-Oncology And Precision Medicine From Harvard Medical School, HMX Pro. ECMGG Certified (European Certificate In Medical Genetics And Genomics). NET-LS (Life Sciences) Qualified With All India Rank- 8. Believe In Equitable Distribution Of Resources And Humane Approach With Practical Considerations.

1. Dubey Ak, Sodhi K, Gupta A, Handa R, Bhatia S, Gupta R. Bochdalek Hernia In A Child. Med J Armed Forces India. 2004;60(3):305‐306.
Https://Www.Ncbi.Nlm.Nih.Gov/Pmc/Articles/Pmc4923215/

2. Bhatia S, Holla Rg. Yunis-Varon Syndrome. Indian Pediatr. 2005;42(4):373‐375.
Https://Www.Indianpediatrics.Net/Apr2005/Apr-373-375.Htm

3. Kumar P, Katoch M, Bhatia S, Gupta R. William's Syndrome With Mitral Valve Disease. Med J Armed Forces India. 2014;70(2):189‐191.
Https://Www.Ncbi.Nlm.Nih.Gov/Pmc/Articles/Pmc4017194/

4. Yadav P, Chauhan Vs, Bhat Ps, Agarwal N, Yadav C, Bhatia S. Cross-Sectional Study Of Anxiety Symptoms In Students In Preexamination Period. Ind Psychiatry J. 2017;26(1):56‐63.
Https://Www.Ncbi.Nlm.Nih.Gov/Pmc/Articles/Pmc5810169/

5. Bijarnia-Mahay S, Bhatia S, Arora V. Fructose-1,6-Bisphosphatase Deficiency. 2019 Dec 5. In: Adam Mp, Ardinger Hh, Pagon Ra, Wallace Se, Bean Ljh, Stephens K, Amemiya A, Editors. Genereviews
Https://Pubmed.Ncbi.Nlm.Nih.Gov/31804789/

6. Bhatia S, Bijarnia-Mahay S, Dubey S, Gourie-Devi M. Familial Prion Disease: First Indian Kindred With Gerstmann-Sträussler-Scheinker Syndrome. Neurol India. 2020 Nov-Dec;68(6):1431-1434. Doi: 10.4103/0028-3886.304068. Pmid: 33342883.
Https://Neurologyindia.Com/Article.Asp?Issn=00283886;Year=2020;Volume=68;Issue=6;Spage=1431;Epage=1434;Aulast=Bhatia

7. Bhatia S, Arora V, Verma Ic. A Further Case Of Hypotonia, Ataxia, Developmental Delay And Tooth Enamel Defect Syndrome Due To A Recurrent C-Terminal Binding Protein 1 Mutation [Published Online Ahead Of Print, 2020 Mar 9]. Clin Dysmorphol. 2020;10.1097/
Https://Pubmed.Ncbi.Nlm.Nih.Gov/32167997/

8. Verma Ic, Bhatia S, Arora V. Genetic Testing In Pediatric Epilepsy. Indian J Pediatr. 2020 Oct 22. Doi: 10.1007/S12098-020-03512-8. Epub Ahead Of Print. Pmid: 33090324
Https://Pubmed.Ncbi.Nlm.Nih.Gov/33090324/

9. Pal S, Bhatia S, Bijarnia-Mahay S, Verma Ic, Puri Rd. Challenges In Chronic Genetic Disorders: Lessons From The Covid-19 Pandemic. Indian Pediatr. 2021 Apr 15;58(4):391-392. Doi: 10.1007/S13312-021-2202-X. Pmid: 33883315; Pmcid: Pmc8079848.
Https://Pubmed.Ncbi.Nlm.Nih.Gov/33883315/

Autism, ADHD, Intellectual Disability, Short Stature, Obesity, Physical Deformity, Overgrowth, Recurrent Pregnancy Loss, Aneuploidy Screen Abnormality, Immune Deficiency, Recurrent Infections, Early And Advanced Cancer, Prevention And Screening Of Familial Cancers

Hindi, English, Punjabi

Genetic Counselling, Skin Biopsy, Fetal Evaluation

  1. 2021

    Gold Medal - Doctorate of National Board Medical Genetics

Cancer Genetics, Immuno-Genetics

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