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100 years of insulin: celebrating the past, present and future of diabetes therapy

Nature medicine, 2021-07, Vol.27 (7), p.1154-1164

2021

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Genetic scores to stratify risk of developing multiple islet autoantibodies and type 1 diabetes: A prospective study in children

PLoS medicine, 2018-04, Vol.15 (4), p.e1002548

2018

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Preventing type 1 diabetes in childhood

Science (American Association for the Advancement of Science), 2021-07, Vol.373 (6554), p.506-510

2021

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Type 1 diabetes defined by severe insulin deficiency occurs after 30 years of age and is commonly treated as type 2 diabetes

Diabetologia, 2019-07, Vol.62 (7), p.1167-1172

2019

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Analysis of serum Hsp90 as a potential biomarker of β cell autoimmunity in type 1 diabetes

PloS one, 2019-01, Vol.14 (1), p.e0208456-e0208456

2019

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ABCA1. The gatekeeper for eliminating excess tissue cholesterol

Journal of lipid research, 2001-08, Vol.42 (8), p.1173-1179

2001

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Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency

The Journal of experimental medicine, 2024-06, Vol.221 (6)

2024

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Granzyme B is elevated in autoimmune blistering diseases and cleaves key anchoring proteins of the dermal-epidermal junction

Scientific reports, 2018-06, Vol.8 (1), p.9690-11, Article 9690

2018

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Drought intensity alters productivity, carbon allocation and plant nitrogen uptake in fast versus slow grassland communities

The Journal of ecology, 2023-08, Vol.111 (8), p.1681-1699

2023

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Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis

Nature communications, 2024-02, Vol.15 (1), p.1415-1415, Article 1415

2024

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Utility and limitations of monitoring kidney transplants using capillary sampling

Clinical chemistry and laboratory medicine, 2024-08

2024

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Estimating disease prevalence in large datasets using genetic risk scores

Nature communications, 2021-11, Vol.12 (1), p.6441-6441, Article 6441

2021

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1251-P: Aß Classification Defines Four Distinct Forms of Diabetes in Children

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

2022

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1425-P: C-Peptide and Islet Autoantibodies at Diagnosis Predict Long-Term ß-Cell Function and Insulin Dependence in Pediatric Diabetes

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

2023

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Erratum. The Incidence of Adult-Onset Type 1 Diabetes: A Systematic Review From 32 Countries and Regions. Diabetes Care 2022;45:994–1006

Diabetes care, 2023-11, Vol.46 (11), p.2084-2084

2023

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The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway

The Journal of clinical investigation, 1999-10, Vol.104 (8), p.R25-R31

1999

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A foundation model for generalizable disease detection from retinal images

Nature (London), 2023-10, Vol.622 (7981), p.156-163

2023

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155-OR: Genetic Variation and Time to Progression in TN10 (Teplizumab)

Diabetes (New York, N.Y.), 2024-06, Vol.73 (Supplement_1)

2024

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Trial of Decompressive Craniectomy for Traumatic Intracranial Hypertension

The New England journal of medicine, 2016-09, Vol.375 (12), p.1119-1130

2016

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Application of a Genetic Risk Score to Racially Diverse Type 1 Diabetes Populations Demonstrates the Need for Diversity in Risk-Modeling

Scientific reports, 2018-03, Vol.8 (1), p.4529-13, Article 4529

2018

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Investigating hyperkalaemia in adults

BMJ (Online), 2015-10, Vol.351, p.h4762

2015

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1254-P: Genetic Prediction of C-Peptide Trajectory before Type 1 Diabetes Diagnosis in TrialNet

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

2022

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Gfi1 Expression Is Controlled by Five Distinct Regulatory Regions Spread over 100 Kilobases, with Scl/Tal1, Gata2, PU.1, Erg, Meis1, and Runx1 Acting as Upstream Regulators in Early Hematopoietic Cells

Molecular and Cellular Biology, 2010-08, Vol.30 (15), p.3853-3863

2010

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The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

Journal of medical genetics, 2014-03, Vol.51 (3), p.165-169

2014

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Response to Comment on Meek et al. Reappearance of C-Peptide During the Third Trimester in Type 1 Diabetes Pregnancy: Pancreatic Regeneration or Fetal Hyperinsulinism? Diabetes Care 2021;44:1826-1834

Diabetes care, 2022-02, Vol.45 (2), p.e43-e44

2022

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100 years of insulin: celebrating the past, present and future of diabetes therapy

Genetic scores to stratify risk of developing multiple islet autoantibodies and type 1 diabetes: A prospective study in children

Preventing type 1 diabetes in childhood

Type 1 diabetes defined by severe insulin deficiency occurs after 30 years of age and is commonly treated as type 2 diabetes

Analysis of serum Hsp90 as a potential biomarker of β cell autoimmunity in type 1 diabetes

ABCA1. The gatekeeper for eliminating excess tissue cholesterol

Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency

Granzyme B is elevated in autoimmune blistering diseases and cleaves key anchoring proteins of the dermal-epidermal junction

Drought intensity alters productivity, carbon allocation and plant nitrogen uptake in fast versus slow grassland communities

Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis

Utility and limitations of monitoring kidney transplants using capillary sampling

Estimating disease prevalence in large datasets using genetic risk scores

1251-P: Aß Classification Defines Four Distinct Forms of Diabetes in Children

1425-P: C-Peptide and Islet Autoantibodies at Diagnosis Predict Long-Term ß-Cell Function and Insulin Dependence in Pediatric Diabetes

Erratum. The Incidence of Adult-Onset Type 1 Diabetes: A Systematic Review From 32 Countries and Regions. Diabetes Care 2022;45:994–1006

The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway

A foundation model for generalizable disease detection from retinal images

155-OR: Genetic Variation and Time to Progression in TN10 (Teplizumab)

Trial of Decompressive Craniectomy for Traumatic Intracranial Hypertension

Application of a Genetic Risk Score to Racially Diverse Type 1 Diabetes Populations Demonstrates the Need for Diversity in Risk-Modeling

Investigating hyperkalaemia in adults

1254-P: Genetic Prediction of C-Peptide Trajectory before Type 1 Diabetes Diagnosis in TrialNet

Gfi1 Expression Is Controlled by Five Distinct Regulatory Regions Spread over 100 Kilobases, with Scl/Tal1, Gata2, PU.1, Erg, Meis1, and Runx1 Acting as Upstream Regulators in Early Hematopoietic Cells

The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

Response to Comment on Meek et al. Reappearance of C-Peptide During the Third Trimester in Type 1 Diabetes Pregnancy: Pancreatic Regeneration or Fetal Hyperinsulinism? Diabetes Care 2021;44:1826-1834

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