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Lorna W. Harries
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Journal Articles

The Common HNF1A Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY

Jonathan M. Locke, Cécile Saint-Martin, Thomas W. Laver, Kashyap A. Patel, Andrew R. Wood, Seth A. Sharp, Sian Ellard, Christine Bellanné-Chantelot, Andrew T. Hattersley, Lorna W. Harries, Michael N. Weedon
Journal: Diabetes
Diabetes 2018;67(9):1903–1907
https://doi.org/10.2337/db18-0133
Published: 12 June 2018
View article titled, The Common <em>HNF1A</em> Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY
Open the PDF for The Common <em>HNF1A</em> Variant I27L Is a Modifier of Age at Diabetes Diagnosis in Individuals With HNF1A-MODY in another window
Journal Articles

Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations

Brian H. Chen, Marie-France Hivert, Marjolein J. Peters, Luke C. Pilling, John D. Hogan, Lisa M. Pham, Lorna W. Harries, Caroline S. Fox, Stefania Bandinelli, Abbas Dehghan, Dena G. Hernandez, Albert Hofman, Jaeyoung Hong, Roby Joehanes, Andrew D. Johnson, Peter J. Munson, Denis V. Rybin, Andrew B. Singleton, André G. Uitterlinden, Saixia Ying, MAGIC Investigators, David Melzer, Daniel Levy, Joyce B.J. van Meurs, Luigi Ferrucci, Jose C. Florez, Josée Dupuis, James B. Meigs, Eric D. Kolaczyk
Journal: Diabetes
Diabetes 2016;65(12):3794–3804
https://doi.org/10.2337/db16-0470
Published: 13 September 2016
View article titled, Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations
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Includes: Supplementary data
Journal Articles

Targeted Allelic Expression Profiling in Human Islets Identifies cis-Regulatory Effects for Multiple Variants Identified by Type 2 Diabetes Genome-Wide Association Studies

Jonathan M. Locke, Gerald Hysenaj, Andrew R. Wood, Michael N. Weedon, Lorna W. Harries
Journal: Diabetes
Diabetes 2015;64(4):1484–1491
https://doi.org/10.2337/db14-0957
Published: 12 November 2014
View article titled, Targeted Allelic Expression Profiling in Human Islets Identifies <em>cis</em>-Regulatory Effects for Multiple Variants Identified by Type 2 Diabetes Genome-Wide Association Studies
Open the PDF for Targeted Allelic Expression Profiling in Human Islets Identifies <em>cis</em>-Regulatory Effects for Multiple Variants Identified by Type 2 Diabetes Genome-Wide Association Studies in another window
Includes: Supplementary data
Journal Articles

Diabetes Susceptibility in the Canadian Oji-Cree Population Is Moderated by Abnormal mRNA Processing of HNF1A G319S Transcripts

Lorna W. Harries, Melissa J. Sloman, Elizabeth A.C. Sellers, Andrew T. Hattersley, Sian Ellard
Journal: Diabetes
Diabetes 2008;57(7):1978–1982
https://doi.org/10.2337/db07-1633
Published: 01 July 2008
View article titled, Diabetes Susceptibility in the Canadian Oji-Cree Population Is Moderated by Abnormal mRNA Processing of <em>HNF1A</em> G319S Transcripts
Open the PDF for Diabetes Susceptibility in the Canadian Oji-Cree Population Is Moderated by Abnormal mRNA Processing of <em>HNF1A</em> G319S Transcripts in another window
Journal Articles

The Diabetic Phenotype in HNF4A Mutation Carriers Is Moderated By the Expression of HNF4A Isoforms From the P1 Promoter During Fetal Development

Lorna W. Harries, Jonathan M. Locke, Beverley Shields, Neil A. Hanley, Karen Piper Hanley, Anna Steele, Pål R. Njølstad, Sian Ellard, Andrew T. Hattersley
Journal: Diabetes
Diabetes 2008;57(6):1745–1752
https://doi.org/10.2337/db07-1742
Published: 01 June 2008
View article titled, The Diabetic Phenotype in <em>HNF4A</em> Mutation Carriers Is Moderated By the Expression of <em>HNF4A</em> Isoforms From the P1 Promoter During Fetal Development
Open the PDF for The Diabetic Phenotype in <em>HNF4A</em> Mutation Carriers Is Moderated By the Expression of <em>HNF4A</em> Isoforms From the P1 Promoter During Fetal Development in another window
Includes: Supplementary data
Journal Articles

Mosaic Paternal Uniparental Isodisomy and an ABCC8 Gene Mutation in a Patient With Permanent Neonatal Diabetes and Hemihypertrophy

Julian P.H. Shield, Sarah E. Flanagan, Deborah J. Mackay, Lorna W. Harries, Peter Proks, Christophe Girard, Frances M. Ashcroft, I. Karen Temple, Sian Ellard
Journal: Diabetes
Diabetes 2008;57(1):255–258
https://doi.org/10.2337/db07-0999
Published: 01 January 2008
View article titled, Mosaic Paternal Uniparental Isodisomy and an <em>ABCC8</em> Gene Mutation in a Patient With Permanent Neonatal Diabetes and Hemihypertrophy
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Journal Articles

Messenger RNA Transcripts of the Hepatocyte Nuclear Factor-1α Gene Containing Premature Termination Codons Are Subject to Nonsense-Mediated Decay

Lorna W. Harries, Andrew T. Hattersley, Sian Ellard
Journal: Diabetes
Diabetes 2004;53(2):500–504
https://doi.org/10.2337/diabetes.53.2.500
Published: 01 February 2004
View article titled, Messenger RNA Transcripts of the Hepatocyte Nuclear Factor-1α Gene Containing Premature Termination Codons Are Subject to Nonsense-Mediated Decay
Open the PDF for Messenger RNA Transcripts of the Hepatocyte Nuclear Factor-1α Gene Containing Premature Termination Codons Are Subject to Nonsense-Mediated Decay in another window