| 1 | Longitudinal Assessment of Pancreas Volume by MRI Predicts Progression to Stage 3 Type 1 Diabetes | 10.1 | 18 | Citations (PDF) |
| 2 | A loss-of-function mutation in KCNJ11 causing sulfonylurea-sensitive diabetes in early adult life | 8.2 | 8 | Citations (PDF) |
| 3 | Precision treatment of beta-cell monogenic diabetes: a systematic review | 5.1 | 12 | Citations (PDF) |
| 4 | Acute Recurrent Pancreatitis in a Child with INS-related Monogenic Diabetes and a Heterozygous Pathogenic CFTR Mutation | 0.2 | 0 | Citations (PDF) |
| 5 | Novel <i>KDM6A</i> Kabuki Syndrome Mutation With Hyperinsulinemic Hypoglycemia and Pulmonary Hypertension Requiring ECMO | 0.2 | 13 | Citations (PDF) |
| 6 | Development of a standardized MRI protocol for pancreas assessment in humans | 2.4 | 18 | Citations (PDF) |
| 7 | Monogenic Diabetes: From Genetic Insights to Population-Based Precision in Care. Reflections From a <i>Diabetes Care</i> Editors’ Expert Forum | 10.1 | 92 | Citations (PDF) |
| 8 | Update of variants identified in the pancreatic β‐cell K
<sub>ATP</sub>
channel genes
<i>KCNJ11</i>
and
<i>ABCC8</i>
in individuals with congenital hyperinsulinism and diabetes | 3.9 | 153 | Citations (PDF) |
| 9 | Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals | 4.4 | 49 | Citations (PDF) |
| 10 | Precision Medicine: Long-Term Treatment with Sulfonylureas in Patients with Neonatal Diabetes Due to KCNJ11 Mutations | 5.5 | 20 | Citations (PDF) |
| 11 | Iatrogenic Hyperinsulinemia, Not Hyperglycemia, Drives Insulin Resistance in Type 1 Diabetes as Revealed by Comparison With GCK-MODY (MODY2) | 0.5 | 52 | Citations (PDF) |
| 12 | Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA Associated | 0.5 | 32 | Citations (PDF) |
| 13 | 184-LB: Pancreatic Hypoplasia Patients Experience Poor Weight Gain and Labile Diabetes without Diabetic Ketoacidosis (DKA) | 0.5 | 0 | Citations (PDF) |
| 14 | 124-LB: Patients’ Experiences with a Do-It-Yourself Artificial Pancreas and Perspectives of the Endocrinologist’s Role in Supporting Their Use | 0.5 | 0 | Citations (PDF) |
| 15 | Congenital forms of diabetes: the beta-cell and beyond | 3.3 | 20 | Citations (PDF) |
| 16 | Early Intensive Insulin Use May Preserve β-Cell Function in Neonatal Diabetes Due to Mutations in the Proinsulin Gene | 0.2 | 14 | Citations (PDF) |
| 17 | Neonatal Diabetes Mellitus | 1.8 | 168 | Citations (PDF) |
| 18 | Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA | 4.2 | 22 | Citations (PDF) |
| 19 | <i>FOXP3</i>
mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndrome | 4.6 | 29 | Citations (PDF) |
| 20 | Hypoglycemia in sulfonylurea‐treated
<i>KCNJ11</i>
‐neonatal diabetes: Mild‐moderate symptomatic episodes occur infrequently but none involving unconsciousness or seizures | 4.6 | 25 | Citations (PDF) |
| 21 | ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents | 4.6 | 274 | Citations (PDF) |
| 22 | Monogenic diabetes: the impact of making the right diagnosis | 2.4 | 18 | Citations (PDF) |
| 23 | Congenital Diabetes: Comprehensive Genetic Testing Allows for Improved Diagnosis and Treatment of Diabetes and Other Associated Features | 5.5 | 15 | Citations (PDF) |
| 24 | Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry | 2.7 | 57 | Citations (PDF) |
| 25 | Insulin Treatment and Clinical Outcomes in 67 Participants with Infancy-Onset Diabetes | 0.5 | 0 | Citations (PDF) |
| 26 | Management of GCK-MODY in Pregnancy—Does Clinical Practice Follow Current Recommendations? | 0.5 | 1 | Citations (PDF) |
| 27 | White Matter Differences and Neurodevelopment Outcomes in Patients with KATP Channel-Related Diabetes | 0.5 | 0 | Citations (PDF) |
| 28 | Clinical Utility of the T1D Genetic Risk Score—Examples from the U.S. Monogenic Diabetes Registry | 0.5 | 0 | Citations (PDF) |
| 29 | Identifying Patients with GDM at Risk for GCK-MODY | 0.5 | 0 | Citations (PDF) |
| 30 | Case Report: Preservation of Reduced Numbers of Insulin-Positive Cells in Sulfonylurea-Unresponsive <i>KCNJ11</i>-related Diabetes | 4.2 | 24 | Citations (PDF) |
| 31 | Diabetes Presentation in Infancy: High Risk of Diabetic Ketoacidosis | 10.1 | 58 | Citations (PDF) |
| 32 | ADHD, learning difficulties and sleep disturbances associated with <i>KCNJ11</i>
-related neonatal diabetes | 4.6 | 39 | Citations (PDF) |
| 33 | Long Delay in Accurate Diagnosis of Hnf1A-Mody in the us Monogenic Diabetes Registry | 1.8 | 1 | Citations (PDF) |
| 34 | Role of Noninsulin Therapies Alone or in Combination in Chromosome 6q24-Related Transient Neonatal Diabetes: Sulfonylurea Improves but Does Not Always Normalize Insulin Secretion | 10.1 | 29 | Citations (PDF) |
| 35 | Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes | 8.2 | 79 | Citations (PDF) |
| 36 | An online monogenic diabetes discussion group: supporting families and fueling new research | 4.2 | 6 | Citations (PDF) |
| 37 | Response Letter to the Editor | 4.2 | 0 | Citations (PDF) |
| 38 | Neonatal diabetes, gallbladder agenesis, duodenal atresia, and intestinal malrotation caused by a novel homozygous mutation in<i>RFX6</i> | 4.6 | 68 | Citations (PDF) |
| 39 | Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in<i>IER3IP1</i>: insights into the natural history of a rare disorder | 4.6 | 51 | Citations (PDF) |
| 40 | Sulfonylurea Treatment Before Genetic Testing in Neonatal Diabetes: Pros and Cons | 4.2 | 69 | Citations (PDF) |
| 41 | Cost-Effectiveness of MODY Genetic Testing: Translating Genomic Advances Into Practical Health Applications | 10.1 | 130 | Citations (PDF) |
| 42 | Hyperinsulinism in a Neonate | 0.6 | 2 | Citations (PDF) |
| 43 | Successful Transition From Insulin to Sulfonylurea Therapy in a Patient With Monogenic Neonatal Diabetes Owing to a KCNJ11 F333L Mutation | 10.1 | 7 | Citations (PDF) |
| 44 | Gain-of-Function Mutations in the KATP Channel (KCNJ11) Impair Coordinated Hand-Eye Tracking | 2.4 | 7 | Citations (PDF) |
| 45 | Visuomotor Performance in <i>KCNJ11</i>-Related Neonatal Diabetes Is Impaired in Children With DEND-Associated Mutations and May Be Improved by Early Treatment With Sulfonylureas | 10.1 | 98 | Citations (PDF) |
| 46 | Genetics and pathophysiology of neonatal diabetes mellitus | 2.9 | 88 | Citations (PDF) |
| 47 | HLA-DQ haplotypes differ by ethnicity in patients with childhood-onset diabetes | 4.6 | 13 | Citations (PDF) |
| 48 | Neonatal Diabetes: An Expanding List of Genes Allows for Improved Diagnosis and Treatment | 5.5 | 106 | Citations (PDF) |
| 49 | The Cost-Effectiveness of Personalized Genetic Medicine | 10.1 | 86 | Citations (PDF) |
| 50 | Update in neonatal diabetes | 2.3 | 37 | Citations (PDF) |
| 51 | Neonatal diabetes mellitus: A model for personalized medicine | 8.8 | 76 | Citations (PDF) |
| 52 | Tooth Discoloration in Patients With Neonatal Diabetes After Transfer Onto Glibenclamide: A previously unreported side effect | 10.1 | 39 | Citations (PDF) |
| 53 | Diagnosis and treatment of neonatal diabetes: an United States experience† | 4.6 | 121 | Citations (PDF) |
| 54 | Insulin gene mutations as a cause of permanent neonatal diabetes | 7.8 | 520 | Citations (PDF) |
| 55 | Educating Future Leaders of Medical Research: Analysis of Student Opinions and Goals from the MD???PhD SAGE (Students??? Attitudes, Goals, and Education) Survey | 1.5 | 52 | Citations (PDF) |
| 56 | MD-PhD Students in a Major Training Program Show Strong Interest in Becoming Surgeon-Scientists | 1.6 | 18 | Citations (PDF) |
| 57 | The Role of T/B Lymphocyte Collaboration in the Regulation of Autoimmune and Alloimmune Responses | 2.9 | 19 | Citations (PDF) |
| 58 | Specialized CC-chemokine secretion by Th1 cells in destructive autoimmune myocarditis | 6.8 | 17 | Citations (PDF) |
| 59 | Elimination of maternally transmitted autoantibodies prevents diabetes in nonobese diabetic mice | 40.4 | 191 | Citations (PDF) |
| 60 | Impaired Activation of Islet-Reactive CD4 T Cells in Pancreatic Lymph Nodes of B Cell-Deficient Nonobese Diabetic Mice | 0.6 | 62 | Citations (PDF) |
| 61 | In vivo MLR: a novel method for the study of alloimmune responses | 0.7 | 3 | Citations (PDF) |
| 62 | Characterization of the alloimmune response to minor histocompatibility antigens by in vivo MLR | 0.7 | 3 | Citations (PDF) |
| 63 | A DIRECT METHOD FOR THE CALCULATION OF ALLOREACTIVE CD4+ T CELL PRECURSOR FREQUENCY1 | 1.1 | 34 | Citations (PDF) |
| 64 | CD28 COSTIMULATION IN ALLOIMMUNE RESPONSES AGAINST MAJOR AND MINOR HISTOCOMPATIBILITY ANTIGENS | 1.1 | 9 | Citations (PDF) |
| 65 | TRACKING ALLOREACTIVE CELL DIVISION IN VIVO1 | 1.1 | 17 | Citations (PDF) |
