Thomas I Hewat
4PUBLICATIONS
16CO-AUTHORS
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Publications (4)
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|Nov 05, 2022
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism.Matthew N Wakeling, Nick D L Owens, Jessica R Hopkinson
|Oct 14, 2022
Hyperinsulinemic Hypoglycemia Diagnosed in Childhood Can Be Monogenic.Jasmin J Hopkins, Alexandra J Childs, Jayne A L Houghton
|Mar 16, 2022
Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this group.Thomas I Hewat, Thomas W Laver, Jayne A L Houghton
|Oct 11, 2021
Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11.Thomas I Hewat, Daphne Yau, Joseph C S Jerome
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Frequent Collaborators
3 joint publications
Sarah E Flanagan
2 joint publications
Kashyap A Patel
2 joint publications
Thomas W Laver
1 joint publications
Miguel De Los Santos La Torre
1 joint publications
Birgit Rami-Merhar
1 joint publications
Jasmin J Hopkins
1 joint publications
Jayne A L Houghton
1 joint publications
Navoda Atapattu
1 joint publications
Matthew B Johnson
1 joint publications
Matthew N Wakeling
