Jasmin J Hopkins
5PUBLICATIONS
11CO-AUTHORS
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Publications (5)
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|Mar 31, 2026
Long-read sequencing enables trio-assisted phasing of de novo variants in the imprinted gene MAGEL2.Thomas W Laver, Preeah Sangha, Lucy Mallin
|Aug 19, 2025
Characterization of congenital hyperinsulinism in Argentina: Clinical features, genetic findings, and treatment outcomes.Gabriela Pacheco, Maria G Bastida, Juan Cáceres
|Apr 14, 2025
REVEL Is Better at Predicting Pathogenicity of Loss-of-Function than Gain-of-Function Variants.Jasmin J Hopkins, Matthew N Wakeling, Matthew B Johnson
|Apr 11, 2024
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements.Thomas W Laver, Matthew N Wakeling, Richard C Caswell
|Oct 14, 2022
Hyperinsulinemic Hypoglycemia Diagnosed in Childhood Can Be Monogenic.Jasmin J Hopkins, Alexandra J Childs, Jayne A L Houghton
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Frequent Collaborators
4 joint publications
Sarah E Flanagan
4 joint publications
Thomas W Laver
2 joint publications
Matthew B Johnson
2 joint publications
Matthew N Wakeling
1 joint publications
Jayne A L Houghton
1 joint publications
Thomas I Hewat
1 joint publications
Navoda Atapattu
1 joint publications
Kashyap A Patel
1 joint publications
Richard C Caswell
1 joint publications
Khalid Hussain
