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Mohamad Guftar Shaikh

Observed names: G Shaikh, Guftar Shaikh, M G Shaikh, M Guftar Shaikh, M Guftar. Shaikh, M. G. Shaikh, M. Guftar Shaikh, M.G. Shaikh, M.Guftar Shaikh, M. Guftar Shaikh, Mohamad G Shaikh, Mohamad G. Shaikh, Mohamad Shaikh
Observed institutions: Imperial College Healthcare NHS Trust, University of Aberdeen, Edinburgh Napier University, New Cross Hospital, NHS Greater Glasgow and Clyde, Royal Hospital for Children, Hammersmith Hospital, Bristol Royal Hospital for Children, Abu Dhabi Health Services, Birmingham Children's Hospital, Royal Hospital for Sick Children, Queen Elizabeth University Hospital, Royal Manchester Children's Hospital, Royal College of Paediatrics and Child Health, All India Institute of Medical Sciences, University of Glasgow
ORCID: 0000-0002-2316-3334
Observed ORCID: 0000-0002-2316-3334
OpenAlex ID: A5011255066
Role of Gut Microbiota in the Aetiology of Obesity: Proposed Mechanisms and Review of the Literature
2016 · Muhammad Jaffar Khan, Konstantinos Gerasimidis, et al. · Journal of Obesity · 318
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Deficits in Trabecular Bone Microarchitecture in Young Women With Type 1 Diabetes Mellitus
2015 · Naiemh Abdalrahaman, Christie McComb, et al. · Journal of Bone and Mineral Research · 117
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Mechanisms of obesity in Prader–Willi syndrome
2016 · M. J. Khan, K. Gerasimidis, et al. · Pediatric Obesity · 100
Mutation analysis of POUF‐1, PROP‐1 and HESX‐1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo‐optic dysplasia
2005 · L. A. Rainbow, S. A. Rees, et al. · Clinical Endocrinology · 87
Reductions in Basal Metabolic Rate and Physical Activity Contribute to Hypothalamic Obesity
2008 · M. Guftar Shaikh, Richard G. Grundy, et al. · The Journal of Clinical Endocrinology & Metabolism · 76
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years’ Experience in the UK
2021 · Federica Buonocore, Avinaash Maharaj, et al. · Journal of the Endocrine Society · 68
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
2020 · Daphne Yau, Thomas W. Laver, et al. · PLoS ONE · 68
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Vitamin D and Its Effects on Glucose Homeostasis, Cardiovascular Function and Immune Function
2014 · N. El-Fakhri, H. McDevitt, et al. · Hormone Research in Paediatrics · 65
Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita
2008 · M G Shaikh, L Boyes, et al. · Journal of Medical Genetics · 47
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Diazoxide‐induced pulmonary hypertension in hyperinsulinaemic hypoglycaemia: Recommendations from a multicentre study in the United Kingdom
2019 · Suet Ching Chen, Antonia Dastamani, et al. · Clinical Endocrinology · 46
Growth hormone deficiency during young adulthood and the benefits of growth hormone replacement
2016 · M Ahmid, C G Perry, et al. · Endocrine Connections · 43
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The Impact of Growth Hormone Therapy on Adult Height in Noonan Syndrome: A Systematic Review
2015 · Claudio Giacomozzi, Annalisa Deodati, et al. · Hormone Research in Paediatrics · 35
Prader–Willi syndrome: guidance for children and transition into adulthood
2024 · M Guftar Shaikh, Timothy G Barrett, et al. · Endocrine Connections · 34
Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus
2023 · M. Guftar Shaikh, Angela K. Lucas-Herald, et al. · Frontiers in Endocrinology · 31
Diazoxide choline extended‐release tablet in people with Prader‐Willi syndrome: results from long‐term open‐label study
2023 · Jennifer L. Miller, Evelien Gevers, et al. · Obesity · 29
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Hyperleptinaemia rather than fasting hyperinsulinaemia is associated with obesity following hypothalamic damage in children
2008 · M Guftar Shaikh, Richard G Grundy, et al. · European Journal of Endocrinology · 29
An appraisal of current service delivery and future models of care for young people with gender dysphoria
2021 · Stephanie McCallion, Simon Smith, et al. · European Journal of Pediatrics · 26
Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life
2018 · Filiz Mine Çizmecioğlu, Jeremy Huw Jones, et al. · Journal of Clinical Research in Pediatric Endocrinology · 26
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Insights into the pathophysiology of catch-up compared with non-catch-up growth in children born small for gestational age: an integrated analysis of metabolic and transcriptomic data
2014 · A Stevens, C Bonshek, et al. · The Pharmacogenomics Journal · 26
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Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists
2021 · Cordula M. Wolf, Martin Zenker, et al. · European Journal of Medical Genetics · 24
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The use of growth hormone therapy in adults with Prader‐Willi syndrome: A systematic review
2020 · Mikaela Frixou, Diane Vlek, et al. · Clinical Endocrinology · 24
Frequency and aetiology of hypercalcaemia
2016 · J D McNeilly, R Boal, et al. · Archives of Disease in Childhood · 24
Transient Neonatal Hypothyroidism Due to a Maternal Vegan Diet
2003 · M.G. Shaikh, J.M. Anderson, et al. · Journal of Pediatric Endocrinology and Metabolism · 24
Risk factors and management of corticosteroid‐induced hyperglycaemia in paediatric acute lymphoblastic leukaemia
2019 · Kyriacos Gregoriou, Ian Craigie, et al. · Pediatric Blood & Cancer · 21
Increases in Bioactive IGF do not Parallel Increases in Total IGF-I During Growth Hormone Treatment of Children Born SGA
2019 · Mathilde Gersel Wegmann, Rikke Beck Jensen, et al. · The Journal of Clinical Endocrinology & Metabolism · 20
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Works count: 123
Citation count: 1,739
H-index: 23
I10-index: 43
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