Dr. GAURI KRISHNA

CONSULTANT - Inherited Metabolic and Genetic Disorder (Adult & Pediatric)

FRCPCH, M. PHIL MED Genetics ( cambridge), Fellowship in Clinical Genetics.

Kannada, Hindi, English Bannerghatta

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Consultation Fee :- ₹ 2150/-

Dr Gauri S Krishna is an internationally published research physician in the field of pediatric and adult inherited metabolic medicine and genetics with over a decade’s experience in medical teaching, writing and statistics. she is expertised is in Pediatrics, inherited metabolic medicine (adult and pediatrics) and medical genetics. She looks after children and adults who have inherited disorders that affect the body’s normal biochemical reactions. She has more than 5 years’ experience as a consultant in two of the leading hospitals in London. She is the quality improvement lead and head of departmental teaching and has worked as the Principal Investigator in four international consortium studies and Sub Principal Investigator in 4 studies (https://orcid.org/0000-0001-5672-4671). She works closely with laboratory scientists, metabolic dietitians, pharmacist specialists and nursing teams. This field is research-active and with the rapid and innovative developments in therapeutics for metabolic disorders.

Awards and Accolades:

Best Oral Presentation: British Inherited Metabolic Disease Group, United Kingdom 2019
“Best Trainee” [out of a cohort of ST4-ST8] East of England Deanery, United Kingdom. 2017
“Best Paediatric Doctor” Cloudnine Hospital, Bengaluru, India. 2013 Highest marks in clinical membership exam in Paediatrics (MD equivalent) Royal college of Paediatrics and child health, UK. 2009
Best thesis award University of Cambridge-Department of medical genetics, UK. 2008
Distinction Paediatrics (MBBS) Rajiv Gandhi University of health sciences, Bengaluru, India.2003

Articles and Blogs:

2023 Improvement in patient outcomes following initiation of burosumab in young adults. Single centre experience: Journal of bone and mineral research (IF: 6.39) (First author) (pre-print)
2021 Long-term cognitive and psychosocial outcomes in adults with phenylketonuria: Journal of inherited metabolic disease (IF: 4.982) (Co-author)
2016 Fibrodysplasia ossificans progressiva: Seven cases of a very rare disorder with heterotopicossification: Journal of inherited metabolic disease (IF: 4.982) (5th author)
2015 Significance of Newborn Screening for Citrullinemia: Journal of Indian perinatology (IF: 0.33) (Corresponding Author)
2010 Antioxidants can inhibit basal autophagy and enhance neurodegeneration in models of polyglutamine disease: Hum Mol Genet 19(17):3413-29 (2010) (IF:6.15) (7th author).
2008 Huntington's disease: from pathology and genetics to potential therapies: Biochem J412(2):191-209 (2008) (IF:4.097) (7th author)
2008 A rational mechanism for combination treatment of Huntington's disease using lithium and rapamycin: Hum Mol Genet 17(2):170-8 (2008) (IF:6.15) (Co-author)