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Neha S. Bhatia, MD, MA
Accepting New Patients
Meet Neha S. Bhatia, MD, MA
Title(s)
Medical Geneticist; Assistant Professor, Tufts University School of Medicine
Department + Services
Pediatrics, Genetics and Metabolism
Clinical Focus Areas
Dysmorphology, clinical genetics
Seeing Patients In
Boston, 617-636-8100
Request Appointment
| Programs + Specialties |
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| Training + Education |
Stony Brook University School of Medicine; Internship and Residency: Pediatrics, Jacobi Medical Center
Fellowship: Medical Genetics, The Children's Hospital of Montefiore
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| Board Certifications |
Pediatrics, Genetics and Genomics |
| NPI # |
1528360104 |
| Gender |
Female |
| Language(s) |
Hindi |
| Accepted Insurances |
View Accepted Insurances at Tufts MC + Tufts Children's Hospital
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Tufts Children's Hospital
Floating Building, 3rd Floor
755 Washington Street
Boston, MA 02111
Phone #: 617-636-8100
Fax #: 617-636-0745
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Bhatia NS, Ying JY, Bonnard C, Kuan J-L, Brett M, Heming W, Cham BW, Chin HL, Bosso-Lefevre C, Dharuman P, Escande-Beillard N, Devasia AG, Goh J, Kam S, Liew W, Lin G, Lim E, Jain K, Alvin Ng Yu-Jin, Subramanian D, Min X, Yuen-Ming T, Tawari N, Tiang Z, Ting TW, Tohari S, Tong, CK, Lezhava A, Ng SB, Law HY, Venkatesh B, Tomar S, Sethi R, Tan G, Shanmugasundaram A, God DL, Lai PS, Lai A, Tan ES, Ng I, Reversades B, Foo R, Tan EC, Jamuar SS (manuscript under review). Phenotype-Driven Genomic Sequencing Significantly Improves Diagnostic Yield in a Resource Constrained Setting – The Singapore Experience
Ting CY, Bhatia NS, Lim JY, et al. Further delineation of CDC45-related Meier-Gorlin syndrome with craniosynostosis and review of literature. European Journal of Medical Genetics, 2019;S1769-7212(18)30728-6. Cited in PubMed: PMID: 30986546
Lim JY*, Bhatia NS*, Vasanwala RF, Chay PL, Lim KB, Khoo PC, Schwarze U, Jamuar SS. A Novel Ser40Trp variant in IFITM5 in a family with osteogenesis imperfecta and review of the literature. Clinical Dysmorphology, 2019;28(3):120-125 (*contributed equally) Cited in PubMed: PMID: 30985308
Bhatia NS, Lim JY, Brett MS, Tan EC, Law HY, Thomas B, Choo J, Lai AHM, Jamuar SS. Chromosome 12q24.31 microdeletion and congenital heart disease: a case report and review of the literature. Clinical Dysmorphology (2019); 28:53-56. Cited in PubMed; PMID: 30507726
Mazzocco MMM, Singh Bhatia N, Lesniak-Karpiak K. Visuospatial skills and their association with math performance in girls with fragile X or Turner Syndrome. Child Neuropsychology (2006); 12: 87-110. Cited in PubMed; PMID: 16754531
American Academy of Pediatrics
American College of Medical Genetics
American Society of Human Genetics
