Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alexandra I F Blakemore

Showing results (21-30 of 55) with videos related to

Pageof 6
Sort By:
Psychiatric Genetics|October 16, 2009
Association study of serotonergic gene variants with antipsychotic-induced adverse reactionsIsmail Al-Janabi, Maria J Arranz, Alexandra I F Blakemore, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|March 11, 2016
Body composition of the host influences dendritic cell phenotype in patients treated for colorectal cancerGeorge Malietzis, Gui Han Lee, Hafid O Al-Hassi, et al.
International Journal of Obesity (2005)|January 31, 2024
Oligogenic inheritance in severe adult obesitySumaya Almansoori, Suzanne I Alsters, Andrianos M Yiorkas, et al.
Clinical Chemistry|June 17, 2011
Accurate single-nucleotide polymorphism allele assignment in trisomic or duplicated regions by using a single base-extension assay with MALDI-TOF mass spectrometryAnne L Trewick, Julia S El-Sayed Moustafa, Adam J de Smith, et al.
Plos One|June 12, 2014
Multiple measures of adiposity are associated with mean leukocyte telomere length in the northern Finland birth cohort 1966Jessica L Buxton, Shikta Das, Alina Rodriguez, et al.
Nature Methods|June 1, 2010
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVsLachlan J M Coin, Julian E Asher, Robin G Walters, et al.
Annals of Human Genetics|March 16, 2011
Investigation of the HIN200 locus in UK SLE families identifies novel copy number variantsMichelle M A Fernando, Adam J de Smith, Lachlan Coin, et al.
Bioinformatics (Oxford, England)|May 7, 2011
famCNV: copy number variant association for quantitative traits in familiesHariklia Eleftherohorinou, Johanna C Andersson-Assarsson, Robin G Walters, et al.
Human Molecular Genetics|August 2, 2007
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseasesAdam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Journal of Affective Disorders|March 18, 2023
Depression mediates the relationship between alexithymia and obesity in the Northern Finland Birth Cohort 1966 (NFBC1966)Nurul Hanis Ramzi, Juha Auvinen, Juha Veijola, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Psychiatric Genetics|October 16, 2009
Association study of serotonergic gene variants with antipsychotic-induced adverse reactionsIsmail Al-Janabi, Maria J Arranz, Alexandra I F Blakemore, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine|March 11, 2016
Body composition of the host influences dendritic cell phenotype in patients treated for colorectal cancerGeorge Malietzis, Gui Han Lee, Hafid O Al-Hassi, et al.
International Journal of Obesity (2005)|January 31, 2024
Oligogenic inheritance in severe adult obesitySumaya Almansoori, Suzanne I Alsters, Andrianos M Yiorkas, et al.
Clinical Chemistry|June 17, 2011
Accurate single-nucleotide polymorphism allele assignment in trisomic or duplicated regions by using a single base-extension assay with MALDI-TOF mass spectrometryAnne L Trewick, Julia S El-Sayed Moustafa, Adam J de Smith, et al.
Plos One|June 12, 2014
Multiple measures of adiposity are associated with mean leukocyte telomere length in the northern Finland birth cohort 1966Jessica L Buxton, Shikta Das, Alina Rodriguez, et al.
Nature Methods|June 1, 2010
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVsLachlan J M Coin, Julian E Asher, Robin G Walters, et al.
Annals of Human Genetics|March 16, 2011
Investigation of the HIN200 locus in UK SLE families identifies novel copy number variantsMichelle M A Fernando, Adam J de Smith, Lachlan Coin, et al.
Bioinformatics (Oxford, England)|May 7, 2011
famCNV: copy number variant association for quantitative traits in familiesHariklia Eleftherohorinou, Johanna C Andersson-Assarsson, Robin G Walters, et al.
Human Molecular Genetics|August 2, 2007
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseasesAdam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Journal of Affective Disorders|March 18, 2023
Depression mediates the relationship between alexithymia and obesity in the Northern Finland Birth Cohort 1966 (NFBC1966)Nurul Hanis Ramzi, Juha Auvinen, Juha Veijola, et al.
Pageof 6