Thomas W Laver

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 15

Top Topics

Glycemic Control

Top Venues

European journal of human genetics : EJHG

Wellcome open research

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

Publications

Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Matthew N Wakeling, Richard C Caswell, Benjamin Bunce, Daphne Yau, Jonna M E Männistö, Jayne A L Houghton, Jasmin J Hopkins, Michael N Weedon, Vrinda Saraff, Melanie Kershaw, Engela M Honey, Nuala Murphy, Dinesh Giri, Stuart Nath, Ana Tangari Saredo, Indraneel Banerjee, Khalid Hussain, Nick D L Owens, Sarah E. Flanagan
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. European journal of human genetics : EJHG 32 (7) (2024)
Thomas W Laver, Elisa De Franco, Matthew B Johnson, Kashyap Amratlal Patel, Sian Ellard, Michael N Weedon, Sarah E. Flanagan, Matthew N Wakeling
SavvyCNV: Genome-wide CNV calling from off-target reads. PLoS computational biology 18 (3) (2022)
Thomas W Laver, Matthew N Wakeling, Olivia Knox, Kevin Colclough, Caroline F Wright, Sian Ellard, Andrew T Hattersley, Michael N Weedon, Kashyap Amratlal Patel
Evaluation of Evidence for Pathogenicity Demonstrates That BLK, KLF11, and PAX4 Should Not Be Included in Diagnostic Testing for MODY. Diabetes 71 (5) (2022)
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)
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)
Elisa De Franco, Cécile Saint-Martin, Klaus Brusgaard, Amy E Knight Johnson, Lydia Aguilar-Bryan, Pamela Bowman, Jean-Baptiste Arnoux, Annette Rønholt Larsen, May Sanyoura, Siri Atma W Greeley, Raúl Calzada-León, Bradley Harman, Jayne A L Houghton, Elisa Nishimura-Meguro, Thomas W Laver, Sian Ellard, Daniela Del Gaudio, Henrik Thybo Christesen, Christine Bellanné-Chantelot, Sarah E. Flanagan
Update of variants identified in the pancreatic β-cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes. Human mutation 41 (5) (2020)
Indraneel Banerjee, Senthil Senniappan, Thomas W Laver, Richard C Caswell, Martin Zenker, Klaus Mohnike, Tim Cheetham, Matthew N Wakeling, Dunia Ismail, Belinda Lennerz, Miranda Splitt, Merih Berberoğlu, Susann Empting, Martin Wabitsch, Simone Pötzsch, Prateek Shanmugananda, Zeynep Siklar, Charles F Verge, Michael N Weedon, Sian Ellard, Khalid Hussain, Sarah E. Flanagan
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome. Wellcome open research 4 (2020)
Matthew N Wakeling, Thomas W Laver, Kevin Colclough, Andrew Parish, Sian Ellard, Emma L Baple
Misannotation of multiple-nucleotide variants risks misdiagnosis. Wellcome open research 4 (2019)
Indraneel Banerjee, Senthil Senniappan, Thomas W Laver, Richard C Caswell, Martin Zenker, Klaus Mohnike, Tim Cheetham, Matthew N Wakeling, Dunia Ismail, Belinda Lennerz, Miranda Splitt, Merih Berberoğlu, Susann Empting, Martin Wabitsch, Simone Pötzsch, Prateek Shanmugananda, Zeynep Siklar, Charles F Verge, Michael N Weedon, Sian Ellard, Khalid Hussain, Sarah E. Flanagan
Refinement of the critical genomic region for hypoglycaemia in the Chromosome 9p deletion syndrome. Wellcome open research (2019)
Jonathan M Locke, Cécile Saint-Martin, Thomas W Laver, Kashyap Amratlal Patel, Andrew R Wood, Seth A Sharp, Sian Ellard, Christine Bellanné-Chantelot, Andrew T Hattersley, Lorna W Harries, Michael N Weedon
The Common HNF1A Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY. Diabetes 67 (9) (2018)
Thomas W Laver, Michael N Weedon, Richard Caswell, Khalid Hussain, Sian Ellard, Sarah E Flanagan
Analysis of large-scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia. Human mutation 38 (10) (2017)