Sonia Davila, PhD
Executive Director – Translational Medicine
- Email: sdominguez (@) sidra.org
- Phone: +974 40037369

Sonia completed her undergraduate and graduate studies in Spain. She identified new mutations in genes causing autosomal dominant polycystic kidney disease present only in Spanish families. Upon graduation she moved to Yale University and led the identification of two human genes causing Polycystic Liver Disease (PLD).
In 2004 Sonia joined the Genome Institute of Singapore as a postdoctoral fellow on nephrogenomics. She was rapidly promoted to Research Scientist and to Principal Investigator. Her work focused on human genetic susceptibility to infectious diseases. She has identified genetic mutations involved in immune-related diseases, infectious and autoimmune disorders, rare diseases like Kawasaki and meningococcal disease among others.
In 2016 she started working at SingHealth-Duke NUS AMC to work on clinical implementation of nprecisioonb medicine. She was Deputy Director of SingHealth Duke-NUS Institute of Precision Medicine (PRISM) and Director of Research at the SingHealth Duke-NUS Genomic Medicine Centre.
Sonia joined Sidra Medicine in December 2023 as Executive Director -Translational Medicine.
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
- 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. “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
- 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* “Variation in the CFHR3 gene determines susceptibility to meningococcal disease by controlling factor H levels”. AJHG. 2022, Sep 1:109 (9):1680-1691
- 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. “The Singapore National Medicine Strategy” Nat Genet. 2023 Feb; 55(2):178-186