Maureen Boxer - Concepedia

Author

Maureen Boxer

Ninewells Hospital

Also Known As

M Boxer, Maureen Boxer

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Ninewells Hospital University of Dundee University College London

About

Maureen Boxer is an author at Ninewells Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	584
2	Natural Sciences	3	3	199
3	Biochemistry	2	2	60
4	Public Health	1	1	28
5	Allergy	1	1	88

Maureen Boxer

Publications

811

Citations

H-Index

Page 1

	Year	Citations
Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias Douglas J. Clarke, Nabil Moghrabi, Gemma Monaghan, Clinica Chimica Acta Allelic VariantMendelian DisorderGenetic DisorderMedicineGenetics	1997	139
Family history of severe cardiovascular disease in Marfan syndrome is associated with increased aortic diameter and decreased survival David I. Silverman, Jonathon Gray, Mary J. Roman, Journal of the American College of Cardiology	1995	107
A molecular genetic service for diagnosing individuals with familial hypercholesterolaemia (FH) in the United Kingdom Karen E. Heath, Steve E. Humphries, Helen Middleton‐Price, European Journal of Human Genetics Genetic TestingFamilial HypercholesterolaemiaMedicinePedigree AnalysisMolecular Genetic Service	2001	106
Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity Victoria J. Green, Munir Pirmohamed, Neil R. Kitteringham, Biochemical Pharmacology Carbamazepine HypersensitivityGenetic AnalysisAllergyMicrosomal Epoxide HydrolaseMedicine	1995	88
Identification of an A-to-G Missense Mutation in Exon 2 of the UGT1 Gene Complex That Causes Crigler-Najjar Syndrome Type 2 Nabil Moghrabi, Douglas J. Clarke, Maureen Boxer, Genomics A-to-g Missense MutationMendelian DisorderUgt1 Gene ComplexGenetic DisorderGenetics	1993	83
Absence of exon 15BRAF germline mutations in familial melanoma Julie Lang, Maureen Boxer, Rona M. MacKie Human Mutation	2003	67
Isolation of a Human YAC Contig Encompassing a Cluster of UGT2 Genes and Its Regional Localization to Chromosome 4q13 Gemma Monaghan, Douglas J. Clarke, Sue Povey, Genomics ChromatinHuman Yac ContigRegional LocalizationDevelopmental BiologyCytogenetics	1994	63
Cosegregation of intragenic markers with a novel mutation that causes Crigler-Najjar syndrome type I: implication in carrier detection and prenatal diagnosis. Nabil Moghrabi, Douglas J. Clarke, Brian Burchell, PubMed	1993	53
Structure of the human UGT2B4 gene encoding a bile acid UDP-glucuronosyltransferase Gemma Monaghan, Brian Burchell, Maureen Boxer Mammalian Genome BiochemistryNatural SciencesLiver PhysiologyGeneticsMedicine	1997	34
Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial marfan syndrome phenotype Cheryl Black, Anne P. Withers, Jonathon Gray, Human Mutation Mendelian DisorderGenetic DisorderMedicineGeneticsGenetic Epidemiology	1998	28

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