Tim Hutchin - Concepedia

Author

Tim Hutchin

Birmingham Children's Hospital

Also Known As

T Hutchin, T P Hutchin, T. Hutchin, T. P. Hutchin, TIM P HUTCHIN, Tim Hutchin, Tim P Hutchin, Tim P. Hutchin

Publications

2.5K

Citations

H-Index

Concepts

All Affiliations

Birmingham Children's Hospital St James's University Hospital Centre de Référence Déficits Immunitaires Héréditaires Institut Pasteur University of Leeds

About

Tim Hutchin is an author at Birmingham Children's Hospital specializing in medicine, genetics, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	530
2	Arts	5	5	399
3	Allergy	1	1	13
4	Biology	1	1	26
5	Diabetes	1	1	97

Tim Hutchin

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study Ignacio del Castillo, Miguel A. Moreno‐Pelayo, Francisco Castillo, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyAudiologyEvolutionary Origins	2003	289
A Molecular basis for human hypersensitivity of aminoglyscoside antibiotics Tim Hutchin, lan Haworth, Koichiro Higashi, Nucleic Acids Research	1993	236
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus Elisabeth Verpy, Saber Masmoudi, Ingrid Zwaenepoel, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsNew Gene	2001	191
A mitochondrial DNA clone is associated with increased risk for Alzheimer disease. Tim Hutchin, Gino Cortopassi Proceedings of the National Academy of Sciences	1995	186
Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice Yun Jin Pai, Kit‐Yi Leung, Dawn Savery, Nature Communications	2015	145
A novel mutation in the mitochondrial tRNA<sup>Ser(UCN)</sup> gene in a family with non-syndromic sensorineural hearing impairment Tim Hutchin Journal of Medical Genetics	2000	120
Assessment of the genetic causes of recessive childhood non‐syndromic deafness in the UK – implications for genetic testing Tim Hutchin, NN Coy, Helen E. Conlon, Clinical Genetics	2005	114
The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT Curtis R. Coughlin, Michael A. Swanson, Kathryn E. Kronquist, Genetics in Medicine Metabolic SyndromeMetabolic DisorderGenetic DisorderGeneticsDiabetes	2016	97
Geographical and Ethnic Distribution of Mutations of the Fumarylacetoacetate Hydrolase Gene in Hereditary Tyrosinemia Type 1 Francesca Angileri, Anne Bergeron, Geneviève Morrow, JIMD Reports	2014	69
Genomic deletion within <i>GLDC</i> is a major cause of non-ketotic hyperglycinaemia Jun Kanno, Tim Hutchin, Fumiaki Kamada, Journal of Medical Genetics	2007	65

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