MRC Epidemiology Unit

 

Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.

Bomba L, Walter K, Guo Q, Surendran P, Kundu K, Nongmaithem S, Karim MA, Stewart ID, Langenberg C, Danesh J, Di Angelantonio E, Roberts DJ, Ouwehand WH, INTERVAL study INTERVAL study, Dunham I, Butterworth AS, Soranzo N

American journal of human genetics. Jun 2021

(DOI : 10.1016/j.ajhg.2022.04.009)

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Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases.

Cai N, Gomez-Duran A, Yonova-Doing E, Kundu K, Burgess AI, Golder ZJ, Calabrese C, Bonder MJ, Camacho M, Lawson RA, Li L, Williams-Gray CH, ICICLE-PD Study Group, Di Angelantonio E, Roberts DJ, Watkins NA, Ouwehand WH, Butterworth AS, Stewart ID, Pietzner M, Wareham NJ, Langenberg C, Danesh J, Walter K, Rothwell PM, Howson JMM, Stegle O, Chinnery PF, Soranzo N

Nature medicine. Oct 2020

(DOI : 10.1038/s41591-021-01441-3)

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