R. Takei

发表

A genome-wide association analysis of 2,622,830 individuals reveals new pathogenic pathways in gout.

Yu, Abhishek, Yamamoto, 2022, medRxiv.

Correction to: Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects

T. Merriman, Hyon K. Choi, Yongyong Shi, 2020, Journal of human genetics.

Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects

T. Merriman, Hyon K. Choi, Yongyong Shi, 2020, Journal of Human Genetics.

Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations

Stephane E. Castel, Anne-Katrin Emde, T. Merriman, 2021, BMC Genomics.

A Polynesian-specific copy number variant encompassing the MICA gene associates with gout

T. Merriman, Zhiqiang Li, M. Bixley, 2022, Human Molecular Genetics.

Correspondence on ‘Variants in urate transporters, ADH1B, GCKR and MEPE genes associated with transition from asymptomatic hyperuricaemia to gout: results of the first gout versus asymptomatic hyperuricaemia GWAS in Caucasians using data from the UK Biobank’

T. Merriman, M. Cadzow, A. Phipps-Green, 2021, Annals of the Rheumatic Diseases.

A Polynesian-specific copy number variant encompassing the MHC Class I Polypeptide-related Sequence A (MICA) gene associates with gout.

T. Merriman, Yongyong Shi, Zhiqiang Li, 2022, Human molecular genetics.

Association of Gout Polygenic Risk Score With Age at Disease Onset and Tophaceous Disease in European and Polynesian Men With Gout

L. Joosten, A. Vazquez, T. Merriman, 2022, Arthritis & rheumatology.

Novel genetic loci in adolescent-onset gout derived from whole genome sequencing of a Chinese cohort

C. Li, Y. Li, N. Dalbeth, 2023, medRxiv.

A Polynesian-specific missense CETP variant alters the lipid profile

D. Weeks, T. Merriman, M. Bixley, 2023, HGG advances.

Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.

D. Sillence, S. Robertson, M. Bahlo, 2018, American journal of human genetics.

University of Groningen Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH 3

D. Sillence, S. Robertson, M. Bahlo, 2018 .

A population-specific missense variant rs1597000001 in CETP promotes a favorable lipid profile and reduces CETP activity.

D. Weeks, T. Merriman, P. Wilcox, 2021, medRxiv.