Birmingham Children's Hospital

Institution (Healthcare)

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Birmingham Children's Hospital

Publications

446.5K

Citations

813

Authors

1.2K

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About

Birmingham Children's Hospital is a healthcare institution in Birmingham, United Kingdom known for medicine, pediatrics, and pathology.

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Birmingham Children's Hospital

Publications

446.5K

Citations

Page 1

	Year	Citations
Human Hypertension Caused by Mutations in WNK Kinases Frederick H. Wilson, Sandra Disse-Nicodème, Keith A. Choate, Science	2001	1.5K
Neurodevelopmental outcome at 2 years of age after general anaesthesia and awake-regional anaesthesia in infancy (GAS): an international multicentre, randomised controlled trial Andrew Davidson, Nicola Disma, Jurgen C. de Graaff, The Lancet Infant Brain DevelopmentNeonatologyPediatric NeurosurgeryMedicineCognitive Development	2015	1.1K
International Pediatric Multiple Sclerosis Study Group criteria for pediatric multiple sclerosis and immune-mediated central nervous system demyelinating disorders: revisions to the 2007 definitions Lauren Krupp, Marc Tardieu, Maria Pia Amato, Multiple Sclerosis Journal	2013	1.1K
PIM2: a revised version of the Paediatric Index of Mortality Intensive Care Medicine Epidemiological TrendEpidemiologyPediatric EpidemiologyPediatricsPaediatric Index	2003	1K
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature Gillian Rice, Paul R. Kasher, Gabriella Forte, Nature Genetics Autoimmune DiseaseGenetic DisorderGeneticsPathogenesisImmunology	2012	916
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III David B. Simon, Ranjit S. Bindra, Traci A. Mansfield, Nature Genetics ChannelopathiesGenetic DisorderChloride Channel GeneGeneticsPathogenesis	1997	863
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data Sebastian Köhler, Sandra C. Doelken, Chris Mungall, Nucleic Acids Research EngineeringGeneticsUpdated Hpo DatabaseGenetic EpidemiologyMolecular Biology	2013	834
EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome Marc Délepine, Marc Nicolino, Timothy Barrett, Nature Genetics Wolcott-rallison SyndromeTranscriptional RegulationSignal TransductionTranslational BiologyGenetic Disorder	2000	815
European Resuscitation Council Guidelines for Resuscitation 2015 Anatolij Truhlář, Charles D. Deakin, Jasmeet Soar, Resuscitation Neonatal ResuscitationTrauma ResuscitationCardiopulmonary ResuscitationEmergency Medicine InjuryMedicine	2015	812
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation Edith C. H. Friesema, Annette Grueters, Heike Biebermann, The Lancet Mendelian DisorderGenetic DisorderGeneticsThyroid DiseaseFragile X Spectrum	2004	697

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