Tim Hutchin

2.5k citations

26 papers · 1.4k indexed · h-index 19

Impact in

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders

Papers in

Sensory Systems 10
- Hearing, Cochlea, Tinnitus, Genetics 10
Clinical Biochemistry 6
- Metabolism and Genetic Disorders 6

Co-authors: Gino Cortopassi N. Saha Mark Stoneking Nathan Fischel‐Ghodsian Koichiro Higashi Howard Cuckle Svetlana Arbuzova Robert F. Mueller
Journals: Journal of Medical Genetics (5 papers)Nature Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)European Journal of Human Genetics (1 paper)Nature Communications (1 paper)
Partner nations: United Kingdom United States Japan

In The Last Decade

Tim Hutchin

26 papers receiving 1.4k citations

Peers

Countries citing papers authored by Tim Hutchin

Since Specialization

Citations

This map shows the geographic impact of Tim Hutchin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tim Hutchin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tim Hutchin more than expected).

Fields of papers citing papers by Tim Hutchin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tim Hutchin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tim Hutchin. The network helps show where Tim Hutchin may publish in the future.

Co-authors

The 25 scholars most cited alongside Tim Hutchin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tim Hutchin Line = papers co-authored together Tim Hutchin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT Genetics in Medicine ·Curtis R. Coughlin, Michael A. Swanson, Kathryn E. Kronquist, Cécile Acquaviva, Tim Hutchin, Pilar Rodríguez‐Pombo, 将嗣犬塚, Elaine Spector, Geralyn Creadon‐Swindell, Danilo X. Llano, Elisa Rahikkala, Jukka S. Moilanen, A. Kharchilava, Gert Matthijs, Николаева Настасья Валерьевна, Celia Pérez‐Cerdá, Magdalena Ugarte, Christine Vianey‐Saban, Gunter Scharer, Johan L.K. Van Hove	2016	56
2	Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice Nature Communications ·Yun Jin Pai, Kit‐Yi Leung, Dawn Savery, Tim Hutchin, Helen Prunty, Simon Heales, Margaret E. Brosnan, John T. Brosnan, Andrew J. Copp, Nicholas D. E. Greene	2015	104
3	Geographical and Ethnic Distribution of Mutations of the Fumarylacetoacetate Hydrolase Gene in Hereditary Tyrosinemia Type 1 JIMD Reports ·Francesca Angileri, Anne Bergeron, Geneviève Morrow, Francine Lettre, George F. Gray, Tim Hutchin, Sarah Ball, Robert M. Tanguay	2014	51
4	Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population International Journal of Pediatric Otorhinolaryngology ·A. V. Kurnosov, Xiaomei Ouyang, Li Du, Denise Yan, Tim Hutchin, Michèle Ramsay, Claire Penn, Xue-Zhong Liu	2011	44
5	Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1 American Journal of Medical Genetics Part A ·Wenqi Zeng, Hanlin Gao, Louise Brueton, Tim Hutchin, George F. Gray, Anupam Chakrapani, S. E. Olpin, Vivian E. Shih	2006	19
6	Assessment of the genetic causes of recessive childhood non‐syndromic deafness in the UK – implications for genetic testing Clinical Genetics ·Tim Hutchin, Brandon L. Rutter, Ilaria Lenci, Elizabeth A.R. Telford, F Palacios Sánchez, Diana C. Blaydon, Graham R. Taylor, Emma L. Coghill, Steve D. M. Brown, Richard C. Trembath, Salih Muminagic, Maria Bitner‐Glindzicz, R. Mueller	2005	93
7	Autosomal Recessive Nonsyndromic Hearing Impairment: an Overview Audiological Medicine ·Tim Hutchin, Elizabeth A.R. Telford, Robert F. Mueller	2003	4
8	Mitochondrial dysfunction and Down's syndrome BioEssays ·Svetlana Arbuzova, Tim Hutchin, Howard Cuckle	2002	66
9	The relative contribution of mutations in the DFNB loci to congenital/early childhood non-syndromal sensorineural hearing impairment/deafness Journal of Medical Genetics ·Nuria Navarro-Coy, Tim Hutchin, Ilaria Lenci, Emma L. Coghill, Anna Middleton, O.I. Klimenko, けよう両澤, Paolo De Angelis, Richard C. Trembath, S. D. M. Brown, R Mueller	2001	2
10	Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus Nature Genetics ·Elisabeth Verpy, Saber Masmoudi, Ingrid Zwaenepoel, Michel Leibovici, Tim Hutchin, Ignacio del Castillo, Sylvie Nouaille, Stéphane Blanchard, 谢梅源, Jean‐Luc Popot, Felipe Moreno, Robert F. Mueller, Christine Petit	2001	132
11	Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction European Journal of Human Genetics ·Tim Hutchin, Nuria Navarro-Coy, Guy Van Camp, Valeria Tiranti, Massimo Zeviani, Markus Schuelke, Michaela Jaksch, Valerie Newton, Robert F. Mueller	2001	20
12	Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment Journal of Medical Genetics ·Tim Hutchin, (unknown), (unknown), (unknown), (unknown), (unknown)	2001	42
13	A novel mutation in the mitochondrial tRNA^Ser(UCN) gene in a family with non-syndromic sensorineural hearing impairment Journal of Medical Genetics ·Tim Hutchin, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2000	97
14	Sensorineural Hearing Loss and the 1555G Mitochondrial DNA Mutation Acta Oto-Laryngologica ·Tim Hutchin	1999	14
15	Mitochondrial DNA Mutations in Alzheimer's Disease Biochemical and Biophysical Research Communications ·Tim Hutchin, Paul R. Heath, R.C.A. Pearson, Alan J. Sinclair	1997	44
16	Mitochondria and Risk for Deafness American Journal of Audiology ·Tim Hutchin, Gino Cortopassi	1995	1
17	A mitochondrial DNA clone is associated with increased risk for Alzheimer disease. Proceedings of the National Academy of Sciences ·Tim Hutchin, Gino Cortopassi	1995	151
18	A molecular and cellular hypothesis for aminoglycoside-induced deafness Hearing Research ·Gino Cortopassi, Tim Hutchin	1994	50
19	Proposed molecular and cellular mechanism for aminoglycoside ototoxicity Antimicrobial Agents and Chemotherapy ·Tim Hutchin, Gino Cortopassi	1994	86
20	A Molecular basis for human hypersensitivity of aminoglyscoside antibiotics Nucleic Acids Research ·Tim Hutchin, Hirangi Mukhi, Koichiro Higashi, Nathan Fischel‐Ghodsian, Mark Stoneking, N. Saha, Sharon H. Carpenter, Gino Cortopassi	1993	187

About Tim Hutchin

Tim Hutchin is a scholar working on Sensory Systems, Clinical Biochemistry, Otorhinolaryngology, Neurology and Endocrine and Autonomic Systems, having authored 26 papers that have together received 1.4k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (10 papers), Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (6 papers), Connexins and lens biology (3 papers), RNA modifications and cancer (3 papers), Vestibular and auditory disorders (3 papers), Biochemical and Molecular Research (2 papers) and Neuroscience of respiration and sleep (2 papers). The work is most often cited by research in Sensory Systems (502 citations), Clinical Biochemistry (333 citations), Otorhinolaryngology (125 citations), Neurology (213 citations) and Biochemistry (112 citations). Tim Hutchin has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include Gino Cortopassi, Gino Cortopassi, N. Saha, Mark Stoneking, Nathan Fischel‐Ghodsian, Koichiro Higashi, Howard Cuckle, Svetlana Arbuzova, Robert F. Mueller and Alan J. Sinclair. Their work appears in journals such as Journal of Medical Genetics, Nature Genetics, Journal of Inherited Metabolic Disease, European Journal of Human Genetics and Nature Communications.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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