1. Sun ZJ, Ng KH, Liao P, Zhang Y, Ng JL, Liu ID, Tan PH, Chong SS, Chan YH, Liu J, Davila S, Heng CK, Jordan SC, Soong TW, Yap HK. Am J Transplant. 2015 Jul 3. doi: 10.1111/ajt.13378. [Epub ahead of print]
 “Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental Glomerulosclerosis”

2. Bellos E, Kumar V, Lin C, Maggi J, Phua ZY, Cheng C-Y, Cheung G, Hibberd M, Wong TY, Coin LJM and Davila S. co-corresponding author. Nucleic Acids Research. 2014 Sep 16. pii: gku849. [Epub ahead of print]
“cnvCapSeq: detecting copy number variation in long-range targeted resequencing data”

3. Utami KH, Winata CL, Hillmer AM, Aksoy I, Hoang TL, Chew EGY, Mathavan S, Tay SKH, Korzh V, Sarda P, Davila S, Cacheux V, co-corresponding author. Human Mutation. 2014 Aug 18. doi: 10.1002/humu.22636. [Epub ahead of print]
“Impaired development of neural-crest cell derived organs and intellectual disability caused by MED13L haploinsufficiency”

4. Okada Y, Wu D, Trynka G, Raj T, Terao C, Ikari K, Kochi Y, Ohmura K, Suzuki A, Yoshida S, Graham RR, Manoharan A, Ortmann W et al. Nature. 2014 Feb 20;506(7488):376-81. doi: 10.1038/nature12873. Epub 2013 Dec 25.
“Genetics of rheumatoid arthritis contributes to biology and drug discovery”  

5. Khor CC*, Davila S*, Breunis WB, Lee YC, Shimizu C, Wright VJ, Yeung RSM, Tan DEK, Sim KS, Wang JJ, Wong TY, Pang J, Mitchell P, Cimaz R, Dahdah N, Cheung YF, Huang GY, Yang W, Park I-S, Lee J-K, Wu J-Y, Levin M, Burns JC, Burgner D, Kuijpers TW, and Hibberd ML on behalf of the Hong Kong-Shanghai, Korean, Taiwan, U.S. and International, Kawasaki Disease Genetics Consortiums. *equal contribution
Nature Genetics. 2011 Nov 13;43(12):1241-6. doi: 10.1038/ng.981.
“Genome-wide association study identifies FCGR2A as a susceptibility factor for Kawasaki disease”

6. Khor CC, Nguyen Bich CT, Pang J, Davila S, Hoang Truong L, Ong RTH, Dunstan SJ, Wills B, Farrar J, Ta Van T, Tran Thi G, Nguyen Thi NB, Le Trung T, Le Bich L, Nguyen MT, Nguyen THT, Mai Ngoc L, Nguyen MN, Nguyen TH, Nguyen VVC, Tran TT, Tan DEK, Sakuntabhai A, Teo YY, Hibberd ML, Simmons CP.
Nature Genetics. 2011 Oct 16;43(11):1139-41. doi: 10.1038/ng.960.
“Genome-wide association study identifies susceptibility loci for Dengue shock syndrome at MICB and PLCE1”

7. Breunis WB, Davila S, Shimizu C, Oharaseki T, Takahashi K, van Houdt M, Khor CC, Wright VJ, Levin M, Burns JC, Burgner D, Hibberd ML, Kuijpers TW, on behalf of the International Kawasaki Disease Genetics Consortium.
Arthritis & Rheumatism. 2011 Sep 8. doi: 10.1002/art.33316. Epub ahead of print.
“Disruption of vascular homeostasis in Kawasaki Disease patients: involvement of vascular endothelial growth factor and angiopoietins”

8. 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. co-corresponding author
Nature Genetics. 2010 Sep;42(9):772-776. Epub 2010 August 08.
Featured in the same number of Nature Genetics “News & Views” (“Infectious diseases not immune to genome-wide associations” de Bakker PI & Telenti A)
“Genome-wide association study identifies variants in CFH region associated with host susceptibility to meningococcal disease”

9. Shimizu C, Jain S, Davila S, Hibberd ML, Lin KO, Molkara D, Frazer JR, Sun S, Baker AL, Newburger JW, Rowley AH, Stanford T, Shulman ST, Burgner D, Breunis WB, Kuijpers TW, Wright VJ, Levin M, Eleftherohorinou H, Coin L, Popper SJ, Relman DA, Fury W, Lin C, Mellis S, Tremoulet AH, Burns JC.
Circulation Cardiovascular Genetics. 2011; 4;16-25.Epub 2010 Dec 2.
“Transforming growth factor (TGF)-β signaling pathway in patients with Kawasaki disease”
 
10. Ladhani S, Davila S, Heath PT, Ramsay ME, Slack MPE, Hibberd ML, Pollard AJ, Booy R.
Clinical Infectious Diseases. 2010 Oct 1;51(7):761-7.
“Association between single-nucleotide polymorphisms in Mal-TIRAP and interleukin-10 genes and susceptibility to invasive haemophilus influenza serotype b infection in immunized children”

11. Shimizu C, Matsubara T, Onouchi Y, Jain S, Sun S, Nievergelt CM, Shike H, Takegawa T,  Furukawa S、Akagi T, Newburger JW, Baker AL , Burgner D, Hibberd ML, Davila S, Levin M , Mamtani M, He W, Ahuja SK, Burns JC.
Journal of Human Genetics. 2010 Dec;55(12):779-84. Epub 2010 Sep 9.
“Matrix metalloproteinases haplotypes are associated with coronary artery aneurysm formation in patients with Kawasaki disease”

12. Davila S, Froeling FEM, Tan A, Bonnard C, Boland GJ, Snippe H, Hibberd ML, Seielstad M. co-corresponding author. Genes and Immunity. 2010 Apr;11(3):232-8. Epub 2010 Mar 18.
“New Genetic Associations Detected in a Host Response Study to Hepatitis B Vaccine”

13. Davila S, Hibberd ML, Hari Dass R, Wong HEE, Sahiratmadja E, Bonnard C, Alisjahbana B, Szeszko  JS, Balabanova Y, Drobniewski F, van Crevel R, van de Vosse E, Nejentsev S, Ottenhoff THM, Seielstad M. corresponding author. PLoS Genetics. 2008 Oct:4(10):e1000218. Epub 2008 Oct 10.
“Genetic Association and Expression Studies Indicate a Role of Toll-Like Receptor 8 in Pulmonary Tuberculosis”

14. Davila S, Furu L, Gharavi A, Tian X, Onoe T, Qian Q, Li A, Cai Y, Kamath P, King B, Azurmendi P, Tahvanainen P, Kaariainen H, Hockerstedt K, Devuyst O, Pirson Y, Martin R, Lifton R, Tahvanainen E, Torres V, Somlo S.
Nature Genetics. 2004 Jun;36(6):575-7. Epub 2004 May 9.
“Mutations in SEC63 cause autosomal dominant polycystic liver disease”
 
15. Li A, Davila S, Furu L, Qian Q, Tian X, Kamath P, King B, Torres V, Somlo S.
Am J Hum Gen. 2003 Mar;72(3):691-703. Epub 2003 Jan 15. 
“Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease”