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Riku Takei

Showing results (1-10 of 15) with videos related to

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Gout, Urate, and Crystal Deposition Disease|July 3, 2026
Colocalization analysis reveals shared genetic loci contributing to gout and metabolite levelsRiku Takei, Nicholas A Sumpter, Megan P Leask, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Testing for Causal Association between Serum Urate, Gout, and Prostatic Cancer in European MalesSumanth R Chandrupatla, Nicholas Sumpter, Riku Takei, et al.
Journal of Comparative Effectiveness Research|March 18, 2026
Comparison of two-stage methods for count data in Mendelian randomization: a simulation studyMary Appah, Riku Takei, Vinodh Srinivasasainagendra, et al.
Annals of the Rheumatic Diseases|June 7, 2025
Genome-wide association study in chondrocalcinosis reveals ENPP1 as a candidate therapeutic target in calcium pyrophosphate deposition diseaseRiku Takei, Ann Rosenthal, Tristan Pascart, et al.
The Journal of Rheumatology|July 2, 2021
Aotearoa New Zealand Māori and Pacific Population-amplified Gout Risk Variants: <i>CLNK</i> Is a Separate Risk Gene at the <i>SLC2A9</i> LocusAichang Ji, Amara Shaukat, Riku Takei, et al.
Annals of Human Genetics|February 3, 2026
Mitonuclear Discordance and Gout, Type 2 Diabetes and Chronic Kidney Disease in Aotearoa New Zealand Indigenous Māori and Pacific PeopleRachel R Dickerson, Riku Takei, Murray Cadzow, et al.
Journal of Human Genetics|August 12, 2020
Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effectsRiku Takei, Murray Cadzow, David Markie, et al.
Human Molecular Genetics|April 22, 2022
A Polynesian-specific copy number variant encompassing the MICA gene associates with goutKe Wang, Murray Cadzow, Matt Bixley, et al.
BMC Genomics|November 1, 2021
Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populationsAnne-Katrin Emde, Amanda Phipps-Green, Murray Cadzow, et al.
American Journal of Human Genetics|May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Gout, Urate, and Crystal Deposition Disease|July 3, 2026
Colocalization analysis reveals shared genetic loci contributing to gout and metabolite levelsRiku Takei, Nicholas A Sumpter, Megan P Leask, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Testing for Causal Association between Serum Urate, Gout, and Prostatic Cancer in European MalesSumanth R Chandrupatla, Nicholas Sumpter, Riku Takei, et al.
Journal of Comparative Effectiveness Research|March 18, 2026
Comparison of two-stage methods for count data in Mendelian randomization: a simulation studyMary Appah, Riku Takei, Vinodh Srinivasasainagendra, et al.
Annals of the Rheumatic Diseases|June 7, 2025
Genome-wide association study in chondrocalcinosis reveals ENPP1 as a candidate therapeutic target in calcium pyrophosphate deposition diseaseRiku Takei, Ann Rosenthal, Tristan Pascart, et al.
The Journal of Rheumatology|July 2, 2021
Aotearoa New Zealand Māori and Pacific Population-amplified Gout Risk Variants: <i>CLNK</i> Is a Separate Risk Gene at the <i>SLC2A9</i> LocusAichang Ji, Amara Shaukat, Riku Takei, et al.
Annals of Human Genetics|February 3, 2026
Mitonuclear Discordance and Gout, Type 2 Diabetes and Chronic Kidney Disease in Aotearoa New Zealand Indigenous Māori and Pacific PeopleRachel R Dickerson, Riku Takei, Murray Cadzow, et al.
Journal of Human Genetics|August 12, 2020
Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effectsRiku Takei, Murray Cadzow, David Markie, et al.
Human Molecular Genetics|April 22, 2022
A Polynesian-specific copy number variant encompassing the MICA gene associates with goutKe Wang, Murray Cadzow, Matt Bixley, et al.
BMC Genomics|November 1, 2021
Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populationsAnne-Katrin Emde, Amanda Phipps-Green, Murray Cadzow, et al.
American Journal of Human Genetics|May 29, 2018
Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3Sophia R Cameron-Christie, Constance F Wells, Marleen Simon, et al.
Pageof 2