Indraneel Banerjee - Concepedia

Author

Indraneel Banerjee

Royal Manchester Children's Hospital ORCID

Also Known As

Banerjee I, Banerjee, I., I Banerjee, I. Banerjee, Indi Banerjee, Indraneel (Indi) Banerjee, Indraneel Banerjee, Rose Morrissey

264

Publications

3.2K

Citations

H-Index

Concepts

All Affiliations

Royal Manchester Children's Hospital University of Manchester University of Exeter Great Ormond Street Hospital University College London

About

Indraneel Banerjee is an author at Royal Manchester Children's Hospital specializing in medicine, inherited metabolic disease, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	11	227
2	Health Sciences	5	5	114
3	Public Health	4	4	57
4	Engineering	2	2	25
5	Biochemistry	2	2	61

Indraneel Banerjee

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations Sarah E. Flanagan, Ritika R. Kapoor, G Mali, European Journal of Endocrinology	2010	139
Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism Hima Bindu Avatapalle, Indraneel Banerjee, Sajni Shah, Frontiers in Endocrinology	2013	116
Hyperinsulinism–hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype–phenotype correlations Ritika R. Kapoor, Sarah E. Flanagan, Piers Fulton, European Journal of Endocrinology	2009	97
International Guidelines for the Diagnosis and Management of Hyperinsulinism Diva D. De León, Jean Baptiste Arnoux, Indraneel Banerjee, Hormone Research in Paediatrics	2023	91
Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation Sarah E. Flanagan, Weijia Xie, Richard Caswell, The American Journal of Human Genetics	2012	86
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism Indraneel Banerjee, Mars Skae, Sarah E. Flanagan, European Journal of Endocrinology	2011	85
Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time Maria Salomon‐Estebanez, Sarah E. Flanagan, Sian Ellard, Orphanet Journal of Rare Diseases	2016	65
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling Dan Hanson, Philip Murray, Tessa Coulson, Journal of Molecular Endocrinology	2012	57
Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389 Daphne Yau, Thomas W. Laver, Antonia Dastamani, PLoS ONE	2020	57
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism Matthew N. Wakeling, Nick Owens, Jessica R. Hopkinson, Nature Genetics	2022	57

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