Concepedia
Statistics
Publications
67
Citations
3.9K
H-Index
35
Active since
1997
Affiliations
Queen Mary University of London(Current)
William Harvey Research Institute
University College London
Royal London Hospital
Heartlands Hospital
Louise Metherell is an author at Queen Mary University of London specializing in medicine, pathology, and genetics.
Top concepts
MedicinePathologyGeneticsMolecular BiologyEndocrinologyNatural SciencesMolecular DiagnosticsBiochemistryCell BiologyMicrobiology
Publications per year
1997–2023
Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
Louise Metherell, J. Paul Chapple, Sadani N. Cooray et al. · Nature Genetics · 2005 · 444 citations
Mendelian Disorder, Autoimmune Disease, New Interacting Partner +9
Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency
Eirini Meimaridou, Julia Kowalczyk, Leonardo Guasti et al. · Nature Genetics · 2012 · 260 citations · Full text
Mendelian Disorder, Genetic Disorder, Genetics +6
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans
Claire Hughes, Leonardo Guasti, Eirini Meimaridou et al. · Journal of Clinical Investigation · 2012 · 257 citations · Full text
MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family
Li F. Chan, Tom R. Webb, Teng‐Teng Chung et al. · Proceedings of the National Academy of Sciences · 2009 · 236 citations · Full text
Mc2r Accessory Protein, Molecular Biology, Cellular Physiology +19
Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid Deficiency
Louise Metherell, Danielle Naville, G Halaby et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 159 citations · Full text
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