Sonia Davila, PhD

Executive Director – Translational Medicine
Sonia Davila, PhD

Dr. Sonia Davila is the Executive Director of Translational Medicine at Sidra Medicine, a position she has held since December 2023. In this capacity, Dr. Davila leads the Translational Medicine Unit, overseeing all research programs and their implementation in clinical settings.

Dr. Davila’s research interests and expertise encompass infectious and immune-related diseases, as well as rare conditions such as Kawasaki and meningococcal disease.

Prior to joining Sidra Medicine, Dr. Davila was a Deputy Director at the SingHealth Duke-NUS Institute of Precision Medicine (PRISM). She also served as the Research Director at the organization’s Genomic Medicine Centre from 2019 to 2023.

Dr. Davila also previously worked as a Principal Investigator at the Genome Institute of Singapore, where she specialized on human genetic susceptibility to infectious diseases and genetic mutations associated with immune-related disorders.

Dr Davila completed her Graduate Studies in Human genetics from the University of Santiago de Compostela in Spain, where she identified novel mutations in genes causing autosomal dominant polycystic kidney disease unique to Spanish families.

She continued her postdoctoral research at Yale University, leading the discovery of two human genes causing Polycystic Liver Disease (PLD).

Dr. Davila has authored over 70 peer-reviewed publications, which have collectively received more than 10,000 citations, including articles in leading scientific journals.

Sonia Davila is contributing to the advancement of genomic medicine and precision medicine as a practical clinical tool capable of benefitting patients across the globe—no matter how rare their disease.

Selected publications

  1. Genome-wide association study identifies variants in CFH region associated with host susceptibility to meningococcal disease” Nature Genetics. 2010 Sep;42(9):772-776. Epub 2010 August 08.

    Davila S*, Wright VJ, Khor CC, Sim KS, Binder A, Breunis WB, Inwald D, Nadel S, Betts H, Carrol ED, de Groot R, Hermans PWM, Hazelzet J, Emonts M, Lim CC, Kuijpers TW, Martinon-Torres F, Salas A, Zenz W, Levin M*, Hibberd ML*, on behalf of the International Meningococcal Genetics Consortium.

  1. Variation in the CFHR3 gene determines susceptibility to meningococcal disease by controlling factor H levels”. AJHG. 2022, Sep 1:109 (9):1680-1691

    Kumar V, Pouw RB, Autio MI, Sagmeister MG7, Phua ZY, Borghini L, Wright VJ, Pan BF, Tan AKY, Binder A, Brouwer MC, Pinnock E, De Groot R, Hazelzet J, Emonts M, Van Der Flier M, Reiter K, Nöthen MM, Hoffmann P, Schlapbach LJ, EUCLIDS consortium, Bellos E, Anderson S, Secka F, Martinón-Torres F, Salas A, Fink C, Carrol ED, Pollard AJ, Coin LJ, Zenz W, Wouters D, Ang LT, Hibberd ML, Levin M, Kuijpers TW, Davila S*

  1. The Singapore National Medicine Strategy” Nat Genet. 2023 Feb; 55(2):178-186.

    Wong E, Bertin N, Hebrard M, Tirado-Magallanes R, Bellis C, Lim WK, Chua CY, Tong PML, Chua R, Mak K, Lim TM, Cheong WY, Thien KE, Goh KT, Chai JF, Lee J, Sung JJ, Wong TY, Chin CWL, Gluckman PD, Goh LL, Ban KHK, Tan TW; SG10K_Health Consortium; Sim X, Cheng CY, Davila S, Karnani N, Leong KP, Liu J, Prabhakar S, Maurer-Stroh S, Verma CS, Krishnaswamy P, Goh RSM, Chia I, Ho C, Low D, Virabhak S, Yong J, Zheng W, Seow SW, Seck YK, Koh M, Chambers JC, Tai ES, Tan P.