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Indraneel Banerjee

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Wellcome Open Research|August 27, 2020
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndromeIndraneel Banerjee, Senthil Senniappan, Thomas W Laver, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elementsThomas W Laver, Matthew N Wakeling, Richard C Caswell, et al.
Genome Medicine|March 3, 2025
Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severityJasmin J Bennett, Cécile Saint-Martin, Bianca Neumann, et al.
Nature Genetics|November 5, 2022
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinismMatthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, et al.
Hormone Research in Paediatrics|November 26, 2025
EndoCompass Project: Research Roadmap for Diabetes, Obesity, and MetabolismChantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
Frontiers in Endocrinology|November 29, 2023
Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensusM Guftar Shaikh, Angela K Lucas-Herald, Antonia Dastamani, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for diabetes, obesity, and metabolismChantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
The Journal of Infection|June 18, 2023
Reactogenicity, immunogenicity and breakthrough infections following heterologous or fractional second dose COVID-19 vaccination in adolescents (Com-COV3): A randomised controlled trialEimear Kelly, Melanie Greenland, Philip C S de Whalley, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
American Journal of Human Genetics|December 4, 2018
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable ImmunodeficiencyClare V Logan, Jennie E Murray, David A Parry, et al.
Pageof 15

Showing results (141-150 of 150) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 150 results.
Wellcome Open Research|August 27, 2020
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndromeIndraneel Banerjee, Senthil Senniappan, Thomas W Laver, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elementsThomas W Laver, Matthew N Wakeling, Richard C Caswell, et al.
Genome Medicine|March 3, 2025
Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severityJasmin J Bennett, Cécile Saint-Martin, Bianca Neumann, et al.
Nature Genetics|November 5, 2022
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinismMatthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, et al.
Hormone Research in Paediatrics|November 26, 2025
EndoCompass Project: Research Roadmap for Diabetes, Obesity, and MetabolismChantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
Frontiers in Endocrinology|November 29, 2023
Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensusM Guftar Shaikh, Angela K Lucas-Herald, Antonia Dastamani, et al.
European Journal of Endocrinology|October 17, 2025
EndoCompass project: research roadmap for diabetes, obesity, and metabolismChantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
The Journal of Infection|June 18, 2023
Reactogenicity, immunogenicity and breakthrough infections following heterologous or fractional second dose COVID-19 vaccination in adolescents (Com-COV3): A randomised controlled trialEimear Kelly, Melanie Greenland, Philip C S de Whalley, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
American Journal of Human Genetics|December 4, 2018
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable ImmunodeficiencyClare V Logan, Jennie E Murray, David A Parry, et al.
Pageof 15