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Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score

Diabetes care, 2019-03, Vol.42 (3), p.406-415

2019

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Childhood body size directly increases type 1 diabetes risk based on a lifecourse Mendelian randomization approach

Nature communications, 2022-04, Vol.13 (1), p.2337-2337, Article 2337

2022

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Untangling the genetics of beta cell dysfunction and death in type 1 diabetes

Molecular metabolism (Germany), 2024-08, Vol.86, p.101973, Article 101973

2024

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Genetics of type 1 diabetes

Current opinion in genetics & development, 2018-06, Vol.50, p.7-16

2018

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A multi-ancestry genome-wide association study in type 1 diabetes

Human molecular genetics, 2024-05, Vol.33 (11), p.958-968

2024

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Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects

Journal of the American Society of Nephrology, 2016-03, Vol.27 (3), p.814-823

2016

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Human vascularized macrophage-islet organoids to model immune-mediated pancreatic β cell pyroptosis upon viral infection

Cell stem cell, 2024-11, Vol.31 (11), p.1612-1629.e8

2024

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Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 h

Diabetologia, 2024-10, Vol.67 (10), p.2246-2259

2024

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112-OR: Integrative Analysis of Chromatin Accessibility and Genetic Risk in T1D Patients and Controls

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

2020

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Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort

Journal of the American Society of Nephrology, 2016-07, Vol.27 (7), p.1970-1983

2016

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An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts

Nephrology, dialysis, transplantation, 2017-12, Vol.32 (12), p.2051-2058

2017

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APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts

Nephrology, dialysis, transplantation, 2017-06, Vol.32 (6), p.983-990

2017

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PRF1 mutation alters immune system activation, inflammation, and risk of autoimmunity

Multiple sclerosis, 2021-08, Vol.27 (9), p.1332-1340

2021

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GeneVetter: a web tool for quantitative monogenic assessment of rare diseases

Bioinformatics (Oxford, England), 2015-11, Vol.31 (22), p.3682-3684

2015

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Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing

CRISPR journal, 2024-02, Vol.7 (1), p.53-67

2024

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Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability

Pediatric nephrology (Berlin, West), 2017-03, Vol.32 (3), p.467-476

2017

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tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine

BMC bioinformatics, 2016-06, Vol.17 (1), p.233-233, Article 233

2016

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Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability

Pediatric nephrology (Berlin, West), 2017-07, Vol.32 (7), p.1285-1285

2017

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Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes

Journal of the Endocrine Society, 2020-11, Vol.4 (11), p.bvaa121-bvaa121

2020

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Genetic Contribution to the Divergence in Type 1 Diabetes Risk Between Children From the General Population and Children From Affected Families

Diabetes (New York, N.Y.), 2019-04, Vol.68 (4), p.847-857

2019

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SARS-CoV-2 variants, spike mutations and immune escape

Nature reviews. Microbiology, 2021-07, Vol.19 (7), p.409-424

2021

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Maternal treatment with short-chain fatty acids modulates the intestinal microbiota and immunity and ameliorates type 1 diabetes in the offspring

PloS one, 2017-09, Vol.12 (9), p.e0183786-e0183786

2017

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High-resolution mapping of the world's reservoirs and dams for sustainable river-flow management

Frontiers in ecology and the environment, 2011-11, Vol.9 (9), p.494-502

2011

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Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study

The Lancet (British edition), 2013-07, Vol.382 (9888), p.223-233

2013

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Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score

Childhood body size directly increases type 1 diabetes risk based on a lifecourse Mendelian randomization approach

Untangling the genetics of beta cell dysfunction and death in type 1 diabetes

Genetics of type 1 diabetes

Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes

A multi-ancestry genome-wide association study in type 1 diabetes

Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects

Human vascularized macrophage-islet organoids to model immune-mediated pancreatic β cell pyroptosis upon viral infection

Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 h

112-OR: Integrative Analysis of Chromatin Accessibility and Genetic Risk in T1D Patients and Controls

Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort

An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts

APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts

PRF1 mutation alters immune system activation, inflammation, and risk of autoimmunity

GeneVetter: a web tool for quantitative monogenic assessment of rare diseases

Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing

Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability

tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine

Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability

Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes

Genetic Contribution to the Divergence in Type 1 Diabetes Risk Between Children From the General Population and Children From Affected Families

SARS-CoV-2 variants, spike mutations and immune escape

Maternal treatment with short-chain fatty acids modulates the intestinal microbiota and immunity and ameliorates type 1 diabetes in the offspring

High-resolution mapping of the world's reservoirs and dams for sustainable river-flow management

Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study

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