Anne E Hughes - JoVE Visualize

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Plos One|March 24, 2015

Susceptibility to invasive meningococcal disease: polymorphism of complement system genes and Neisseria meningitidis factor H binding proteinDeclan T Bradley, Thomas W Bourke, Derek J Fairley, et al.

Journal of Bone and Mineral Metabolism|April 21, 2007

Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutationElahe Elahi, Yousef Shafaghati, Sareh Asadi, et al.

Arthritis and Rheumatism|September 18, 2003

Mutations in the amino terminus of ANKH in two US families with calcium pyrophosphate dihydrate crystal deposition diseaseCharlene J Williams, Adrian Pendleton, Gina Bonavita, et al.

BMC Medical Genetics|July 29, 2006

Lack of MEF2A Delta7aa mutation in Irish families with early onset ischaemic heart disease, a family based studyPaul G Horan, Adrian R Allen, Anne E Hughes, et al.

Carcinogenesis|February 6, 2007

A population-based association study of SNPs of GSTP1, MnSOD, GPX2 and Barrett's esophagus and esophageal adenocarcinomaSeamus J Murphy, Anne E Hughes, Chris C Patterson, et al.

Investigative Ophthalmology & Visual Science|November 24, 2005

Retinal vein occlusion, homocysteine, and methylene tetrahydrofolate reductase genotypeStuart J McGimpsey, Jayne V Woodside, Louise Bamford, et al.

Plos Genetics|March 21, 2007

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndromePeter F Zipfel, Matthew Edey, Stefan Heinen, et al.

Circulation. Cardiovascular Genetics|September 19, 2013

A variant in LDLR is associated with abdominal aortic aneurysmDeclan T Bradley, Anne E Hughes, Stephen A Badger, et al.

American Journal of Human Genetics|November 8, 2011

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Matthew J Bown, Gregory T Jones, Seamus C Harrison, et al.

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Showing results (21-30 of 29) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 29 results.

Plos One|March 24, 2015

Susceptibility to invasive meningococcal disease: polymorphism of complement system genes and Neisseria meningitidis factor H binding proteinDeclan T Bradley, Thomas W Bourke, Derek J Fairley, et al.

Journal of Bone and Mineral Metabolism|April 21, 2007

Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutationElahe Elahi, Yousef Shafaghati, Sareh Asadi, et al.

Arthritis and Rheumatism|September 18, 2003

Mutations in the amino terminus of ANKH in two US families with calcium pyrophosphate dihydrate crystal deposition diseaseCharlene J Williams, Adrian Pendleton, Gina Bonavita, et al.

BMC Medical Genetics|July 29, 2006

Lack of MEF2A Delta7aa mutation in Irish families with early onset ischaemic heart disease, a family based studyPaul G Horan, Adrian R Allen, Anne E Hughes, et al.

Carcinogenesis|February 6, 2007

A population-based association study of SNPs of GSTP1, MnSOD, GPX2 and Barrett's esophagus and esophageal adenocarcinomaSeamus J Murphy, Anne E Hughes, Chris C Patterson, et al.

Investigative Ophthalmology & Visual Science|November 24, 2005

Retinal vein occlusion, homocysteine, and methylene tetrahydrofolate reductase genotypeStuart J McGimpsey, Jayne V Woodside, Louise Bamford, et al.

Plos Genetics|March 21, 2007

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndromePeter F Zipfel, Matthew Edey, Stefan Heinen, et al.

Circulation. Cardiovascular Genetics|September 19, 2013

A variant in LDLR is associated with abdominal aortic aneurysmDeclan T Bradley, Anne E Hughes, Stephen A Badger, et al.

American Journal of Human Genetics|November 8, 2011

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Matthew J Bown, Gregory T Jones, Seamus C Harrison, et al.

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