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100 YEARS OF INSULIN: A brief history of diabetes genetics: insights for pancreatic beta-cell development and function

Journal of endocrinology, 2021-07, Vol.250 (3), p.R23-R35

2021

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135-OR: Mapping Cis-Regulatory Programs Affecting Diabetes Risk in Pancreatic Islet Cell Types Using Single-Cell Multimodal Profiling

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

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2050-P: A Multiomics Investigation of a Patient-Derived HNF-1A MODY IPSC Disease Model Reveals Insights into Its Role in Pancreatic Islet Development and Function

Diabetes (New York, N.Y.), 2020-06, Vol.69 (Supplement_1)

2020

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220-LB: Characterizing the Role of 99 Cardiometabolic Candidate Genes Using CRISPR/Cas9, In Vivo Imaging, and Deep Learning in Zebrafish Larvae

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

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249-LB: PAX4 Loss of Function Alters Human Endocrine Cell Development and Influences Diabetes Risk

Diabetes (New York, N.Y.), 2022-06, Vol.71 (Supplement_1)

2022

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25-OR: Investigating a Candidate Causal Allele in Type 2 Diabetes Susceptibility Gene PAM as a Cause of Neonatal Diabetes Mellitus

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

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3-LB: The Type 2 Diabetes-Associated Transcription Factor RREB1 Affects Beta-Cell Function and Development

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

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309-OR: Deep Learning Model of Pancreatic Islet Epigenome Refines Association Signals at Type 2 Diabetes Susceptibility Loci

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

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61-OR: Machine Learning Framework Predicts Metabolic Subphenotypes Using Glucose Dynamics during Oral Glucose Tolerance Test

Diabetes (New York, N.Y.), 2022-06, Vol.71 (Supplement_1)

2022

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Abstract A35: Microenvironmental adaptations drive obesity-associated pancreatic cancer

Cancer research (Chicago, Ill.), 2019-12, Vol.79 (24_Supplement), p.A35-A35

2019

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Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation

European journal of endocrinology, 2008-07, Vol.159 (1), p.27

2008

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Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes

The New England journal of medicine, 2004-09, Vol.351 (14), p.1470-1470

2004

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Activating Mutations in the KCNJ11 Gene Encoding the ATP-Sensitive K+ Channel Subunit Kir6.2 Are Rare in Clinically Defined Type 1 Diabetes Diagnosed Before 2 Years

Diabetes (New York, N.Y.), 2004-11, Vol.53 (11), p.2998-3001

2004

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Activating mutations in the KCNJ11 gene encoding the ATP-sensitive [K.sup.+] channel subunit Kir6.2 are rare in clinically defined type 1 diabetes diagnosed before 2 years

Diabetes (New York, N.Y.), 2004-11, Vol.53 (11), p.2998

2004

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Activating Mutations in the KCNJ11 Gene Encoding the ATP-Sensitive K super(+) Channel Subunit Kir6.2 Are Rare in Clinically Defined Type 1 Diabetes Diagnosed Before 2 Years

Diabetes (New York, N.Y.), 2004-11, Vol.53 (11), p.2998-3001

2004

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Analysis of Differentiation Protocols Defines a Common Pancreatic Progenitor Molecular Signature and Guides Refinement of Endocrine Differentiation

Stem cell reports, 2020-01, Vol.14 (1), p.138-153

2020

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Analysis of the co-operative interaction between the allosterically regulated proteins GK and GKRP using tryptophan fluorescence

Biochemical journal, 2014-05, Vol.459 (3), p.551-564

2014

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Apolipoprotein M can discriminate HNF 1A‐ MODY from Type 1 diabetes

Diabetic medicine, 2013-02, Vol.30 (2), p.246-250

2013

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Apolipoprotein M can discriminate HNF1A-MODY from Type 1 diabetes

Diabetic medicine, 2013-02, Vol.30 (2), p.246-250

2013

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Argonaute2 Mediates Compensatory Expansion of the Pancreatic β Cell

Cell metabolism, 2014-01, Vol.19 (1), p.122-134

2014

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Asian MODY: are we missing an important diagnosis?

Diabetic medicine, 2006-11, Vol.23 (11), p.1257-1260

2006

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Assessment of High-Sensitivity C-Reactive Protein Levels as Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations

Diabetes care, 2010-09, Vol.33 (9), p.1919-1924

2010

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Assessment of the Role of Common Genetic Variation in the Transient Neonatal Diabetes Mellitus (TNDM) Region in Type 2 Diabetes

Diabetes (New York, N.Y.), 2006-08, Vol.55 (8), p.2272-2276

2006

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Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes : A comparative genomic and tagging single nucleotide polymorphism approach

Diabetes (New York, N.Y.), 2006-08, Vol.55 (8), p.2272-2276

2006

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Assessment of the Role of Genetic Variation in the Transient Neonatal Diabetes (TNDM) Region in Type 2 Diabetes: A Comparative Genomic and Haplotype Approach

Diabetes (New York, N.Y.), 2005-06, Vol.54, p.A32

2005

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100 YEARS OF INSULIN: A brief history of diabetes genetics: insights for pancreatic beta-cell development and function

135-OR: Mapping Cis-Regulatory Programs Affecting Diabetes Risk in Pancreatic Islet Cell Types Using Single-Cell Multimodal Profiling

2050-P: A Multiomics Investigation of a Patient-Derived HNF-1A MODY IPSC Disease Model Reveals Insights into Its Role in Pancreatic Islet Development and Function

220-LB: Characterizing the Role of 99 Cardiometabolic Candidate Genes Using CRISPR/Cas9, In Vivo Imaging, and Deep Learning in Zebrafish Larvae

249-LB: PAX4 Loss of Function Alters Human Endocrine Cell Development and Influences Diabetes Risk

25-OR: Investigating a Candidate Causal Allele in Type 2 Diabetes Susceptibility Gene PAM as a Cause of Neonatal Diabetes Mellitus

3-LB: The Type 2 Diabetes-Associated Transcription Factor RREB1 Affects Beta-Cell Function and Development

309-OR: Deep Learning Model of Pancreatic Islet Epigenome Refines Association Signals at Type 2 Diabetes Susceptibility Loci

61-OR: Machine Learning Framework Predicts Metabolic Subphenotypes Using Glucose Dynamics during Oral Glucose Tolerance Test

Abstract A35: Microenvironmental adaptations drive obesity-associated pancreatic cancer

Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation

Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes

Activating Mutations in the KCNJ11 Gene Encoding the ATP-Sensitive K+ Channel Subunit Kir6.2 Are Rare in Clinically Defined Type 1 Diabetes Diagnosed Before 2 Years

Activating mutations in the KCNJ11 gene encoding the ATP-sensitive [K.sup.+] channel subunit Kir6.2 are rare in clinically defined type 1 diabetes diagnosed before 2 years

Activating Mutations in the KCNJ11 Gene Encoding the ATP-Sensitive K super(+) Channel Subunit Kir6.2 Are Rare in Clinically Defined Type 1 Diabetes Diagnosed Before 2 Years

Analysis of Differentiation Protocols Defines a Common Pancreatic Progenitor Molecular Signature and Guides Refinement of Endocrine Differentiation

Analysis of the co-operative interaction between the allosterically regulated proteins GK and GKRP using tryptophan fluorescence

Apolipoprotein M can discriminate HNF 1A‐ MODY from Type 1 diabetes

Apolipoprotein M can discriminate HNF1A-MODY from Type 1 diabetes

Argonaute2 Mediates Compensatory Expansion of the Pancreatic β Cell

Asian MODY: are we missing an important diagnosis?

Assessment of High-Sensitivity C-Reactive Protein Levels as Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations

Assessment of the Role of Common Genetic Variation in the Transient Neonatal Diabetes Mellitus (TNDM) Region in Type 2 Diabetes

Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes : A comparative genomic and tagging single nucleotide polymorphism approach

Assessment of the Role of Genetic Variation in the Transient Neonatal Diabetes (TNDM) Region in Type 2 Diabetes: A Comparative Genomic and Haplotype Approach

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