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Search results (68)

« Back to Publications

Genetic substructure in Latin American individuals reveals novel associations, mechanistic insights, and variable polygenic risk score transferability for alcohol traits

Montalvo-Ortiz J. et al, (2026)

Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries.

Rajagopal VM. et al, (2026), Nat Commun, 17

n application of the MR-Horse method to reduce selection bias in genome-wide association studies of disease progression.

Donovan K. et al, (2025), Eur J Hum Genet, 33, 1677 - 1683

Polygenic prediction of coronary heart disease among 130,000 Mexican adults.

Liu T. et al, (2025), Eur J Prev Cardiol

Blood Pressure and Mortality in Mexico City: A Mendelian Randomization Study.

Turner M. et al, (2025), Hypertension, 82, 1896 - 1905

Mendelian randomization study of the effect of body mass index on 52 causes of death among 125 000 Mexican adults with admixed ancestry.

Gnatiuc Friedrichs L. et al, (2025), Int J Epidemiol, 54

Type 2 diabetes and cause-specific mortality in Mexico City: a Mendelian randomisation analysis.

Bragg F. et al, (2025), Lancet Reg Health Am, 45

Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis.

Wen S. et al, (2025), Nat Genet, 57, 572 - 582

ssessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Mitchell J. et al, (2025), Nat Commun, 16

Correction: A deep catalogue of protein-coding variation in 983,578 individuals.

Sun KY. et al, (2025), Nature, 637

Complex relationship between Amerindian ancestry and obesity in the Mexican population

Baca P. et al, (2025), Gaceta Medica De Mexico, 161, 43 - 50

lcohol and mortality in Mexico: prospective study of 150 000 adults.

Trichia E. et al, (2024), Lancet Public Health, 9, e907 - e915

Blood Pressure, eGFR, and Kidney Mortality in Mexico: A Prospective Study of 150,000 Adults

Zhu D., (2024)

deep catalogue of protein-coding variation in 983,578 individuals.

Sun KY. et al, (2024), Nature, 631, 583 - 592

Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Mitchell J. et al, (2024)

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