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R Gaunt

Showing results (141-150 of 287) with videos related to

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The Journal of Rheumatology|June 3, 2009
A study of relationships between single nucleotide polymorphisms from the growth hormone-insulin-like growth factor axis and bone mass: the Hertfordshire cohort studyElaine M Dennison, Holly E Syddall, Karen A Jameson, et al.
Clinical Epigenetics|October 20, 2017
Epigenome-wide association study of asthma and wheeze in childhood and adolescenceRyan Arathimos, Matthew Suderman, Gemma C Sharp, et al.
Pharmacogenetics and Genomics|May 15, 2007
Haplotype of growth hormone and angiotensin I-converting enzyme genes, serum angiotensin I-converting enzyme and ventricular growth: pathway inference in pharmacogeneticsShuwen Huang, Xiao-He Chen, John R Payne, et al.
Disease Markers|December 7, 2007
Homogeneous assay of rs4343, an ACE I/D proxy, and an analysis in the British Women's Heart and Health Study (BWHHS)Mohammad Reza Abdollahi, Shuwen Huang, Santiago Rodriguez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 25, 2018
Association of copy number variation across the genome with neuropsychiatric traits in the general populationAnna L Guyatt, Evie Stergiakouli, Joanna Martin, et al.
Mitochondrion|August 19, 2017
Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK womenAnna L Guyatt, Kimberley Burrows, Philip A I Guthrie, et al.
International Journal of Epidemiology|January 17, 2017
The epigenetic clock and physical development during childhood and adolescence: longitudinal analysis from a UK birth cohortAndrew J Simpkin, Laura D Howe, Kate Tilling, et al.
Diabetes|March 2, 2017
Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal AnchorHannah R Elliott, Hashem A Shihab, Gabrielle A Lockett, et al.
BMC Medicine|September 4, 2023
Triangulating evidence from observational and Mendelian randomization studies of ketone bodies for cognitive performanceWichanon Sae-Jie, Suangsuda Supasai, Mika Kivimaki, et al.
Annals of Human Genetics|March 6, 2012
From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian PeninsulaMuslim M Alsaadi, Tom R Gaunt, Christopher R Boustred, et al.
Pageof 29

Showing results (141-150 of 287) with videos related to

Sort By:
Pageof 29
The Journal of Rheumatology|June 3, 2009
A study of relationships between single nucleotide polymorphisms from the growth hormone-insulin-like growth factor axis and bone mass: the Hertfordshire cohort studyElaine M Dennison, Holly E Syddall, Karen A Jameson, et al.
Clinical Epigenetics|October 20, 2017
Epigenome-wide association study of asthma and wheeze in childhood and adolescenceRyan Arathimos, Matthew Suderman, Gemma C Sharp, et al.
Pharmacogenetics and Genomics|May 15, 2007
Haplotype of growth hormone and angiotensin I-converting enzyme genes, serum angiotensin I-converting enzyme and ventricular growth: pathway inference in pharmacogeneticsShuwen Huang, Xiao-He Chen, John R Payne, et al.
Disease Markers|December 7, 2007
Homogeneous assay of rs4343, an ACE I/D proxy, and an analysis in the British Women's Heart and Health Study (BWHHS)Mohammad Reza Abdollahi, Shuwen Huang, Santiago Rodriguez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 25, 2018
Association of copy number variation across the genome with neuropsychiatric traits in the general populationAnna L Guyatt, Evie Stergiakouli, Joanna Martin, et al.
Mitochondrion|August 19, 2017
Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK womenAnna L Guyatt, Kimberley Burrows, Philip A I Guthrie, et al.
International Journal of Epidemiology|January 17, 2017
The epigenetic clock and physical development during childhood and adolescence: longitudinal analysis from a UK birth cohortAndrew J Simpkin, Laura D Howe, Kate Tilling, et al.
Diabetes|March 2, 2017
Role of DNA Methylation in Type 2 Diabetes Etiology: Using Genotype as a Causal AnchorHannah R Elliott, Hashem A Shihab, Gabrielle A Lockett, et al.
BMC Medicine|September 4, 2023
Triangulating evidence from observational and Mendelian randomization studies of ketone bodies for cognitive performanceWichanon Sae-Jie, Suangsuda Supasai, Mika Kivimaki, et al.
Annals of Human Genetics|March 6, 2012
From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian PeninsulaMuslim M Alsaadi, Tom R Gaunt, Christopher R Boustred, et al.
Pageof 29