| 36920755 | Inaxaplin for Proteinuric Kidney Disease in Persons with Two <i>APOL1</i> Variants. | N Engl J Med | 2023 |
| 36920755 | Inaxaplin for Proteinuric Kidney Disease in Persons with Two <i>APOL1</i> Variants. | N Engl J Med | 2023 |
| 33402679 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33558525 | Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33283989 | CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia. | N Engl J Med | 2021 |
| 33402679 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33558525 | Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33283989 | CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia. | N Engl J Med | 2021 |
| 31948569 | Functional characterization of tumor antigen-specific T-cells isolated from the tumor microenvironment of sleeping beauty induced murine glioma models. | Methods Enzymol | 2020 |
| 31948569 | Functional characterization of tumor antigen-specific T-cells isolated from the tumor microenvironment of sleeping beauty induced murine glioma models. | Methods Enzymol | 2020 |
| 32000905 | Isolation and characterization of immune cells from the tumor microenvironment of genetically engineered pediatric high-grade glioma models using the sleeping beauty transposon system. | Methods Enzymol | 2020 |
| 32000905 | Isolation and characterization of immune cells from the tumor microenvironment of genetically engineered pediatric high-grade glioma models using the sleeping beauty transposon system. | Methods Enzymol | 2020 |
| 30718883 | Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes. | Eur J Hum Genet | 2019 |
| 31118516 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. | Nature | 2019 |
| 30721028 | High-Density Lipoprotein-Mimicking Nanodiscs for Chemo-immunotherapy against Glioblastoma Multiforme. | ACS Nano | 2019 |
| 30718883 | Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes. | Eur J Hum Genet | 2019 |
| 31118516 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. | Nature | 2019 |
| 30721028 | High-Density Lipoprotein-Mimicking Nanodiscs for Chemo-immunotherapy against Glioblastoma Multiforme. | ACS Nano | 2019 |
| 29048572 | Ventriculoscopic Surgery for Cystic Retrochiasmatic Craniopharyngiomas: Indications, Surgical Technique, and Short-Term Patient Outcomes. | Oper Neurosurg (Hagerstown) | 2018 |
| 29048572 | Ventriculoscopic Surgery for Cystic Retrochiasmatic Craniopharyngiomas: Indications, Surgical Technique, and Short-Term Patient Outcomes. | Oper Neurosurg (Hagerstown) | 2018 |
| 29889582 | Mutant ATRX: uncovering a new therapeutic target for glioma. | Expert Opin Ther Targets | 2018 |
| 29899519 | Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. | Nat Commun | 2018 |
| 29660022 | Molecular ablation of tumor blood vessels inhibits therapeutic effects of radiation and bevacizumab. | Neuro Oncol | 2018 |
| 29421984 | Current state and future prospects of immunotherapy for glioma. | Immunotherapy | 2018 |
| 29279374 | Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. | Proc Natl Acad Sci U S A | 2018 |
| 29360107 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2018 |
| 29889582 | Mutant ATRX: uncovering a new therapeutic target for glioma. | Expert Opin Ther Targets | 2018 |
| 29899519 | Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. | Nat Commun | 2018 |
| 29421984 | Current state and future prospects of immunotherapy for glioma. | Immunotherapy | 2018 |
| 29360107 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2018 |
| 29660022 | Molecular ablation of tumor blood vessels inhibits therapeutic effects of radiation and bevacizumab. | Neuro Oncol | 2018 |
| 29279374 | Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. | Proc Natl Acad Sci U S A | 2018 |
| 27899486 | Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population. | Diabetes | 2017 |
| 28341696 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. | Diabetes | 2017 |
| 28453780 | Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention. | J Clin Endocrinol Metab | 2017 |
| 28838971 | A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes. | Diabetes | 2017 |
| 28666119 | Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms. | Cell | 2017 |
| 28566273 | An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. | Diabetes | 2017 |
| 29257133 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2017 |
| 27899486 | Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population. | Diabetes | 2017 |
| 28453780 | Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention. | J Clin Endocrinol Metab | 2017 |
| 28341696 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. | Diabetes | 2017 |
| 29257133 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2017 |
| 28566273 | An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. | Diabetes | 2017 |
| 28666119 | Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms. | Cell | 2017 |
| 28838971 | A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes. | Diabetes | 2017 |
| 24982446 | Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 Variant. | J Clin Oncol | 2016 |
| 26757982 | Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project. | Eur J Hum Genet | 2016 |
| 27422940 | Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart Study. | Circ Cardiovasc Genet | 2016 |
| 26911676 | Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. | Hum Mol Genet | 2016 |