Ritika R. Kapoor - Publications, H-index & Citations

Ritika R. Kapoor

University College London

26H指数

115论文数

2.8K被引数

收录论文 33

发表时间

The oxytocin system in patients with craniopharyngioma: A systematic review 颅咽管瘤患者的催产素系统: 系统评价

FRONTIERS IN NEUROENDOCRINOLOGY

IF6.7

2025-01-01

OAAI

Mann, Amy; Kalitsi, Jennifer; Jani, Khushali; Martins, Daniel; Kapoor, Ritika R.; Paloyelis, Yannis

Low-dose diazoxide therapy in hyperinsulinaemic hypoglycaemia

CLINICAL ENDOCRINOLOGY

IF2.4

2023-12-07

OAAI

Ng, Amy Yi-Lin; Agrawal, Pankaj; Vijayan, Roopa; Arya, Ved B.; Kapoor, Ritika R.; Shah, Pratik

Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus 先天性高胰岛素血症网络化管理中的标准化实践：英国国家级协作共识

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-10-30

OAAI

Shaikh, M. Guftar; Lucas-Herald, Angela K.; Dastamani, Antonia; Salomon Estebanez, Maria; Senniappan, Senthil; Abid, Noina; Ahmad, Sumera; Alexander, Sophie; Avatapalle, Bindu; Awan, Neelam; Blair, Hester; Boyle, Roisin; Chesover, Alexander; Cochrane, Barbara; Craigie, Ross; Cunjamalay, Annaruby; Dearman, Sarah; De Coppi, Paolo; Erlandson-Parry, Karen; Flanagan, Sarah E.; Gilbert, Clare; Gilligan, Niamh; Hall, Caroline; Houghton, Jayne; Kapoor, Ritika; Mcdevitt, Helen; Mohamed, Zainab; Morgan, Kate; Nicholson, Jacqueline; Nikiforovski, Ana; O'Shea, Elaine; Shah, Pratik; Wilson, Kirsty; Worth, Chris; Worthington, Sarah; Banerjee, Indraneel

Neurodevelopmental impairments in children with septo-optic dysplasia spectrum conditions: a systematic review 视光发育不良儿童的神经发育障碍: 系统评价

MOLECULAR AUTISM

IF5.5

2023-07-25

OAAI

Mann, Amy; Aghababaie, Arameh; Kalitsi, Jennifer; Martins, Daniel; Paloyelis, Yannis; Kapoor, Ritika R.

Autoimmune Encephalitis and Autism Spectrum Disorder

FRONTIERS IN PSYCHIATRY

IF3.2

2021-12-17

OAAI

Whiteley, Paul; Marlow, Ben; Kapoor, Ritika R.; Blagojevic-Stokic, Natasa; Sala, Regina

Prolactinoma in childhood and adolescence-Tumour size at presentation predicts management strategy: Single centre series and a systematic review and meta-analysis

CLINICAL ENDOCRINOLOGY

IF2.4

2020-12-26

PREAI

Arya, Ved Bhushan; Aylwin, Simon J. B.; Hulse, Tony; Ajzensztejn, Michal; Kalitsi, Jennifer; Kalogirou, Nicolas; Bodi, Istvan; Thomas, Nick; Hampton, Tim; Kapoor, Ritika R.; Buchanan, Charles R.

Hyperinsulinemic hypoglycemia in children and adolescents: Recent advances in understanding of pathophysiology and management

REVIEWS IN ENDOCRINE & METABOLIC DISORDERS

IF8

2020-03-17

OAAI

Guemes, Maria; Rahman, Sofia Asim; Kapoor, Ritika R.; Flanagan, Sarah; Houghton, Jayne A. L.; Misra, Shivani; Oliver, Nick; Dattani, Mehul Tulsidas; Shah, Pratik

Genetic causes of hypopituitarism

ARCHIVES OF MEDICAL SCIENCE

IF3.3

2020-01-01

OAAI

Parkin, Katherine; Kapoor, Ritika; Bhat, Ravindra; Greenough, Anne

Hyperinsulinaemic hypoglycaemia in deoxyguanosine kinase deficiency

CLINICAL ENDOCRINOLOGY

IF2.4

2019-09-11

PREAI

Arya, Ved Bhushan; Dhawan, Anil; Kapoor, Ritika R.

Transient neonatal hyperinsulinaemic hypoglycaemia: perinatal predictors of length and cost of stay

EUROPEAN JOURNAL OF PEDIATRICS

IF2.6

2018-09-19

PREAI

Kozen, Kazune; Dassios, Theodore; Kametas, Nick; Kapoor, Ritika R.; Greenough, Anne

Acceptability of Robot Assistant in Management of Type 1 Diabetes in Children

DIABETES TECHNOLOGY & THERAPEUTICS

IF6.3

2016-09-01

PREAI

Al-Taee, Majid A.; Kapoor, Ritika; Garrett, Christopher; Choudhary, Pratik

Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients 沃尔科特-拉里森综合征中的齿状突骨: 4例患者的病例系列

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2016-02-10

OAAI

Dias, R. P.; Buchanan, C. R.; Thomas, N.; Lim, S.; Solanki, G.; Connor, S. E. J.; Barrett, T. G.; Kapoor, R. R.

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism

EUROPEAN JOURNAL OF ENDOCRINOLOGY

IF5.2

2013-04-01

200

OAAI

Kapoor, Ritika R.; Flanagan, Sarah E.; Arya, Ved Bhushan; Shield, Julian P.; Ellard, Sian; Hussain, Khalid

Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age

ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION

IF3.6

2013-01-29

OAAI

Arya, Ved Bhushan; Flanagan, Sarah E.; Kumaran, Anitha; Shield, Julian P.; Ellard, Sian; Hussain, Khalid; Kapoor, Ritika R.

Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2012-05-14

OAAI

Heslegrave, Amanda J.; Kapoor, Ritika R.; Eaton, Simon; Chadefaux, Bernadette; Akcay, Teoman; Simsek, Enver; Flanagan, Sarah E.; Ellard, Sian; Hussain, Khalid

Congenital hyperinsulinism: marked clinical heterogeneity in siblings with identical mutations in the ABCC8 gene

CLINICAL ENDOCRINOLOGY

IF2.4

2012-01-04

PREAI

Kapoor, Ritika R.; Flanagan, Sarah E.; Ellard, Sian; Hussain, Khalid

The Heterogeneity of Focal Forms of Congenital Hyperinsulinism

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2012-01-01

OAAI

Ismail, Dunia; Kapoor, Ritika R.; Smith, Virpi V.; Ashworth, Michael; Blankenstein, Oliver; Pierro, Agostino; Flanagan, Sarah E.; Ellard, Sian; Hussain, Khalid

Partial ABCC8 gene deletion mutations causing diazoxide-unresponsive hyperinsulinaemic hypoglycaemia

PEDIATRIC DIABETES

IF5.6

2011-10-07

OAAI

Flanagan, S. E.; Damhuis, A.; Banerjee, I.; Rokicki, D.; Jefferies, C.; Kapoor, R. R.; Hussain, K.; Ellard, S.

Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations

DIABETOLOGIA

IF10.2

2011-06-15

OAAI

Kapoor, R. R.; Flanagan, S. E.; James, C. T.; McKiernan, J.; Thomas, A. M.; Harmer, S. C.; Shield, J. P.; Tinker, A.; Ellard, S.; Hussain, K.

Genome-Wide Homozygosity Analysis Reveals HADH Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in Consanguineous Pedigrees

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2011-03-01

OAAI

Flanagan, Sarah E.; Patch, Ann-Marie; Locke, Jonathan M.; Akcay, Teoman; Simsek, Enver; Alaei, Mohammadreza; Yekta, Zeinab; Desai, Meena; Kapoor, Ritika R.; Hussain, Khalid; Ellard, Sian

研究方向