Thomas I Hewat

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 4

Top Topics

Top Venues

European journal of endocrinology

Nature genetics

Pediatric diabetes

The Journal of clinical endocrinology and metabolism

This page only lists publications with an associated author ORCID identifier.

Publications

Matthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, Matthew B Johnson, Jayne A L Houghton, Antonia Dastamani, Christine S Flaxman, Rebecca C Wyatt, Thomas I Hewat, Jasmin J Hopkins, Thomas W Laver, Rachel van Heugten, Michael N Weedon, Elisa De Franco, Kashyap A Patel, Sian Ellard, Noel G Morgan, Edmund Cheesman, Indraneel Banerjee, Andrew T Hattersley, Mark J Dunne, null null, Sarah J Richardson, Sarah E. Flanagan
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism. Nature genetics 54 (11) (2022)
Thomas I Hewat, Thomas W Laver, Jayne A L Houghton, Jonna M E Männistö, Sabah Alvi, Stephen P Brearey, Declan Cody, Antonia Dastamani, Miguel Angel De Los Santos-La Torre, Nuala Murphy, Birgit M Rami-Merhar, Birgit Wefers, Hanna Huopio, Indraneel Banerjee, Matthew B Johnson, Sarah E. Flanagan
Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this group. Pediatric diabetes 23 (4) (2022)
Jasmin J Hopkins, Alexandra J Childs, Jayne A L Houghton, Thomas I Hewat, Navoda Atapattu, Matthew B Johnson, Kashyap Amratlal Patel, Thomas W Laver, Sarah E. Flanagan
Hyperinsulinaemic hypoglycaemia diagnosed in childhood can be monogenic. The Journal of clinical endocrinology and metabolism (2022)
Thomas I Hewat, Daphne Yau, Joseph C S Jerome, Thomas W Laver, Jayne A L Houghton, Beverley M Shields, Sarah E Flanagan, Kashyap Amratlal Patel
Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11. European journal of endocrinology 185 (6) (2021)