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| 37537905 | Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors. | J Genet Couns | 2024 |
| 36525397 | Identification of Genetic Variation Influencing Metformin Response in a Multiancestry Genome-Wide Association Study in the Diabetes Prevention Program (DPP). | Diabetes | 2023 |
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| 37794253 | Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine. | Nat Med | 2023 |
| 37794142 | The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion. | Commun Med (Lond) | 2023 |
| 37159869 | Association of parity with body mass index and cardiometabolic risk in high-parous women. | Menopause | 2023 |
| 36882501 | Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population. | Mol Psychiatry | 2023 |
| 37131594 | A Systematic Review of the use of Precision Diagnostics in Monogenic Diabetes. | medRxiv | 2023 |
| 37425717 | TM6SF2 Determines Both the Degree of Lipidation and the Number of VLDL Particles Secreted by the Liver. | medRxiv | 2023 |
| 37292813 | Insights from rare variants into the genetic architecture and biology of youth-onset type 2 diabetes. | Res Sq | 2023 |
| 36845305 | Enrollment of underrepresented racial and ethnic groups in the Rare and Atypical Diabetes Network (RADIANT). | J Clin Transl Sci | 2023 |
| 36525397 | Identification of Genetic Variation Influencing Metformin Response in a Multiancestry Genome-Wide Association Study in the Diabetes Prevention Program (DPP). | Diabetes | 2023 |
| 37808701 | Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes. | medRxiv | 2023 |
| 37794253 | Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine. | Nat Med | 2023 |
| 37794142 | The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion. | Commun Med (Lond) | 2023 |
| 37292813 | Insights from rare variants into the genetic architecture and biology of youth-onset type 2 diabetes. | Res Sq | 2023 |
| 37159869 | Association of parity with body mass index and cardiometabolic risk in high-parous women. | Menopause | 2023 |
| 37425717 | TM6SF2 Determines Both the Degree of Lipidation and the Number of VLDL Particles Secreted by the Liver. | medRxiv | 2023 |
| 37131594 | A Systematic Review of the use of Precision Diagnostics in Monogenic Diabetes. | medRxiv | 2023 |
| 36882501 | Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population. | Mol Psychiatry | 2023 |
| 36845305 | Enrollment of underrepresented racial and ethnic groups in the Rare and Atypical Diabetes Network (RADIANT). | J Clin Transl Sci | 2023 |
| 34935254 | Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia. | Eur J Neurol | 2022 |
| 35763601 | Model for Integration of Monogenic Diabetes Diagnosis Into Routine Care: The Personalized Diabetes Medicine Program. | Diabetes Care | 2022 |
| 35442562 | Impact of parental relatedness on reproductive outcomes among the Old Order Amish of Lancaster County. | Am J Med Genet A | 2022 |
| 36208030 | Statistical evidence for high-penetrance MODY-causing genes in a large population-based cohort. | Endocrinol Diabetes Metab | 2022 |
| 34935254 | Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia. | Eur J Neurol | 2022 |
| 35442562 | Impact of parental relatedness on reproductive outcomes among the Old Order Amish of Lancaster County. | Am J Med Genet A | 2022 |
| 35763601 | Model for Integration of Monogenic Diabetes Diagnosis Into Routine Care: The Personalized Diabetes Medicine Program. | Diabetes Care | 2022 |
| 36208030 | Statistical evidence for high-penetrance MODY-causing genes in a large population-based cohort. | Endocrinol Diabetes Metab | 2022 |
| 34108472 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. | Nat Commun | 2021 |
| 33529164 | Monogenic diabetes: a gateway to precision medicine in diabetes. | J Clin Invest | 2021 |
| 34108472 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. | Nat Commun | 2021 |
| 34357114 | Strategies to Integrate Genomic Medicine into Clinical Care: Evidence from the IGNITE Network. | J Pers Med | 2021 |
| 34467620 | The burden of pathogenic variants in clinically actionable genes in a founder population. | Am J Med Genet A | 2021 |
| 34362814 | Monogenic Diabetes in Youth With Presumed Type 2 Diabetes: Results From the Progress in Diabetes Genetics in Youth (ProDiGY) Collaboration. | Diabetes Care | 2021 |
| 33529164 | Monogenic diabetes: a gateway to precision medicine in diabetes. | J Clin Invest | 2021 |
| 34467620 | The burden of pathogenic variants in clinically actionable genes in a founder population. | Am J Med Genet A | 2021 |
| 34362814 | Monogenic Diabetes in Youth With Presumed Type 2 Diabetes: Results From the Progress in Diabetes Genetics in Youth (ProDiGY) Collaboration. | Diabetes Care | 2021 |
| 34357114 | Strategies to Integrate Genomic Medicine into Clinical Care: Evidence from the IGNITE Network. | J Pers Med | 2021 |
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| 32223038 | Perspectives from individuals with familial hypercholesterolemia on direct contact in cascade screening. | J Genet Couns | 2020 |
| 32162750 | Patient perspectives on the diagnostic journey to a monogenic diabetes diagnosis: Barriers and facilitators. | J Genet Couns | 2020 |
| 33141630 | <i>KCNQ1</i> and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine. | Circ Genom Precis Med | 2020 |
| 32739915 | Parkinson's Disease-Related Motor and Nonmotor Symptoms in the Lancaster Amish. | Neuroepidemiology | 2020 |
| 33234182 | Risk factors for <i>Toxoplasma gondii</i> seropositivity in the Old Order Amish. | Epidemiol Infect | 2020 |
| 32843497 | Prevalence, control, and treatment of diabetes, hypertension, and high cholesterol in the Amish. | BMJ Open Diabetes Res Care | 2020 |
| 33164987 | YIPF5 mutations cause neonatal diabetes and microcephaly: progress for precision medicine and mechanistic understanding. | J Clin Invest | 2020 |
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| 33141630 | <i>KCNQ1</i> and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine. | Circ Genom Precis Med | 2020 |