Pediatric Hospital Medicine
Rady Children's Hospital-San Diego
Osmania University and Medical College, Osmania University and Medical College
Dr Ram Manohar Lohia Hospital
Mount Sinai School of Medicine
UC San Diego
Pediatric Hospital Medicine, Pediatrics
Dr. Manaswitha Khare is a pediatric hospitalist at Rady Children's Hospital-San Diego and an associate physician at UC San Diego School of Medicine.
Dr. Khare completed her medical studies at Osmania Medical College in India. She then received clinical research certification at UC Irvine, where she served as a clinical research fellow, before completing her pediatric residency at the Icahn School of Medicine at Mount Sinai/Elmhurst Hospital. She then completed her pediatric hospital medicine fellowship at UC San Diego in the Division of Pediatric Hospital Medicine.
Dr. Khare is a member of the American Academy of Pediarics, AAP Section of Hospital Medicine, and the Academic Pediatric Association.
Dr. Khare is an accomplished researcher and statistician who has authored numerous publications in peer-reviewed journals, as well as book chapters and multiple oral and poster presentations. In 2011, she was awarded a prestigious NIH/NICHD Rare Diseases Clinical Research Network Training Grant Award that looked at exploring novel therapies for Prader-Willi syndrome. She has a special interest in the field of childhood obesity. Her current work is focused on the pharmacokinetics of commonly prescribed medications in children with obesity.
Takayasu's Arteritis in a Patient With Preexisting Autoimmune Disease.
Holton-Burke R, Laurenzano S, Phillips S, Stover LB, Radhakrishna S, Khare M
Vancomycin Dosing in Children With Overweight or Obesity: A Systematic Review and Meta-analysis.
Khare M, Azim A, Kneese G, Haag M, Weinstein K, Rhee KE, Foster BA
Impact of genetic subtypes of Prader-Willi syndrome with growth hormone therapy on intelligence and body mass index.
Butler MG, Matthews NA, Patel N, Surampalli A, Gold JA, Khare M, Thompson T, Cassidy SB, Kimonis VE
Psychological Impact of Predictive Genetic Testing in VCP Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia.
Surampalli A, Khare M, Kubrussi G, Wencel M, Tanaja J, Donkervoort S, Osann K, Simon M, Wallace D, Smith C, M McInerney-Leo A, Kimonis V
A case report comparing clinical, imaging and neuropsychological assessment findings in twins discordant for the VCP p.R155C mutation.
Surampalli A, Gold BT, Smith C, Castellani RJ, Khare M, Yu H, Nguyen C, Lan M, Wencel M, Wigal S, Caiozzo V, Kimonis V
Effect of genetic subtypes and growth hormone treatment on bone mineral density in Prader-Willi syndrome.
Khare M, Gold JA, Wencel M, Billimek J, Surampalli A, Duarte B, Pontello A, Galassetti P, Cassidy S, Kimonis VE
Cytokine profiling in patients with VCP-associated disease.
Dec E, Rana P, Katheria V, Dec R, Khare M, Nalbandian A, Leu SY, Radom-Aizik S, Llewellyn K, BenMohamed L, Zaldivar F, Kimonis V
Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.
Gold JA, Ruth C, Osann K, Flodman P, McManus B, Lee HS, Donkervoort S, Khare M, Roof E, Dykens E, Miller JL, Driscoll DJ, Butler MG, Heinemann J, Cassidy S, Kimonis VE
Early-onset Alzheimers and cortical vision impairment in a woman with valosin-containing protein disease associated with 2 APOE Îµ4/APOE Îµ4 genotype.
Shamirian S, Nalbandian A, Khare M, Castellani R, Kim R, Kimonis VE
Valosin-containing protein mutation and Parkinson's disease.
Chan N, Le C, Shieh P, Mozaffar T, Khare M, Bronstein J, Kimonis V
See the full listing of this physician's publications on PubMed, a service of the National Library of Medicine.
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