• 2023-current Distinguished Visiting Toh Chin Chye Professor,  Yong Loo Lin School of Medicine, NUS (Singapore) 

• Joint Scientist, KK Women’s and Children’s Hospital (Singapore) 

• 2017-2023 Distinguished Professor of Genetics, Koç University (Turkey) 

• 2016-2020 Professor of Human Genetics, Amsterdam UMC (Netherlands) 

• 2021-2023 Inaugural awardee of Use-Inspired Basic Research Grant, A*STAR (Singapore)

• 2018-2023 Senior Investigator, National Research Foundation (Singapore) 

• 2018-2021 Adjunct Professor, Manipal University (India) 

• 2016-2021 Honorary Professor, Bharath University (India) 

• 2016-2019 Inaugural AAA Fellow, Amsterdam UMC (Netherlands) 

• 2016 The Award for Leading, Educating & Nurturing Talent, A*STAR (Singapore)

• 2013-16 First EMBO Young Investigator based outside Europe, A*STAR (Singapore)

• 2008-2013 Inaugural A*STAR Investigatorship, A*STAR (Singapore)

• 2007-2012 Branco Weiss Fellowship: Society in Science, ETH (Switzerland) 

• 2006 David Sigman Award, UCLA (USA)  

Google scholar

In reverse chronological order on Pubmed

• Chekroun I, Shenbagam S, (...), Reversade B, Alkuraya FS, Alsheikh-Ali A, Abou Tayoun AN. (2025). Genomics of rare diseases in the Greater Middle East. Nature Genetics. 

• Harapas CR, (...), Reversade B. (2022). DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling. Science Immunology.  

• Traspas RM, Teoh TS, (...), Vincent M, Girisha KM, Reversade B. (2022). Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis. Nature Genetics.  

• Szenker-Ravi E, (...), Reversade B. (2022). Discovery of a genetic module essential for assigning left-right asymmetry in humans and ancestral vertebrates. Nature Genetics. 

• Chai G, (...), Reversade B, Gleeson JG. (2021). A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. New England Journal of Medicine.  

• Robinson, KS, Tan DET, Tan KS, Ong HH, (...), Zhong FL, Reversade B.  Enteroviral 3C protease activates the human NLRP1 inflammasome in airway epithelia. Science.  

• Hengel H., (...), Reversade B. (2020). Loss-of-function mutations in UDP- Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy. Nature Communications.  

• Kayserili H, Reversade B. (2018). RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6. Nature.  

• Ho L, (...), Reversade B. (2017). ELABELA deficiency promotes preeclampsia and cardiovascular malformations in mice. Science. 

• Gordon CT, (...), Reversade B. (2017). De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. Nature Genetics. 

• Zhong FL, (...), Reversade B. (2016). Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation. Cell.