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Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L

American journal of human genetics, 2016-06, Vol.98 (6), p.1146-1158

2016

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PRIMUS: Rapid Reconstruction of Pedigrees from Genome-wide Estimates of Identity by Descent

American journal of human genetics, 2014-11, Vol.95 (5), p.553-564

2014

Volltextzugriff (PDF)

Germline BAP1 mutations predispose to malignant mesothelioma

Nature genetics, 2011-10, Vol.43 (10), p.1022-1025

2011

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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Nature genetics, 2018-11, Vol.50 (11), p.1505-1513

2018

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Recommendations for Statistical Reporting in Cardiovascular Medicine: A Special Report From the American Heart Association

Circulation (New York, N.Y.), 2021-07, Vol.144 (4), p.e70

2021

Volltextzugriff (PDF)

Alternative Applications of Genotyping Array Data Using Multivariant Methods

Trends in genetics, 2020-11, Vol.36 (11), p.857-867

2020

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Cross-Tissue and Tissue-Specific eQTLs: Partitioning the Heritability of a Complex Trait

American journal of human genetics, 2014-11, Vol.95 (5), p.521-534

2014

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Revisiting Some Useful Statistical Guidelines in Circulation Research in Response to a Changing Landscape

Circulation research, 2021-05, Vol.128 (11), p.1724-1727

2021

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The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences

Genome research, 2016-12, Vol.26 (12), p.1651

2016

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241-LB: Identification of Novel and Population-Specific Signals for Type 2 Diabetes in Large-Scale Study of Hispanic/Latino Individuals

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

Volltextzugriff (PDF)

Insulin gene mutations as a cause of permanent neonatal diabetes

Proceedings of the National Academy of Sciences - PNAS, 2007-09, Vol.104 (38), p.15040-15044

2007

Volltextzugriff (PDF)

Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease

Frontiers in genetics, 2022-10, Vol.13, p.995488-995488

2022

Volltextzugriff (PDF)

Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D

American journal of human genetics, 2013-01, Vol.92 (1), p.150-156

2013

Volltextzugriff (PDF)

PADRE: Pedigree-Aware Distant-Relationship Estimation

American journal of human genetics, 2016-07, Vol.99 (1), p.154-162

2016

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Gut microbiome features associated with liver fibrosis in Hispanics, a population at high risk for fatty liver disease

Hepatology (Baltimore, Md.), 2022-04, Vol.75 (4), p.955-967

2022

Volltextzugriff (PDF)

Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal

PloS one, 2017-02, Vol.12 (2), p.e0172880-e0172880

2017

Volltextzugriff (PDF)

A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease

Alzheimer's & dementia, 2023-11, Vol.19 (11), p.4886-4895

2023

Volltextzugriff (PDF)

An X Chromosome Transcriptome Wide Association Study Implicates ARMCX6 in Alzheimer's Disease

Journal of Alzheimer's disease, 2024-01, Vol.98 (3), p.1053

2024

Volltextzugriff (PDF)

Critical Evaluation of Data Requires Rigorous but Broadly Based Statistical Inference

Circulation research, 2018-04, Vol.122 (8), p.1049-1051

2018

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Genome-wide Association Study Identifies Novel Risk Loci for Apical Periodontitis

Journal of endodontics, 2023-10, Vol.49 (10), p.1276-1288

2023

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Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes

Human molecular genetics, 2022-09, Vol.31 (18), p.3191-3205

2022

Volltextzugriff (PDF)

303-OR: ADA Presidents' Select Abstract: Transethnic Association Study of Type 2 Diabetes in More than a Million Individuals

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

Volltextzugriff (PDF)

Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering

American journal of human genetics, 2021-12, Vol.108 (12), p.2271-2283

2021

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Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L

PRIMUS: Rapid Reconstruction of Pedigrees from Genome-wide Estimates of Identity by Descent

Germline BAP1 mutations predispose to malignant mesothelioma

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders

Recommendations for Statistical Reporting in Cardiovascular Medicine: A Special Report From the American Heart Association

Alternative Applications of Genotyping Array Data Using Multivariant Methods

Cross-Tissue and Tissue-Specific eQTLs: Partitioning the Heritability of a Complex Trait

Revisiting Some Useful Statistical Guidelines in Circulation Research in Response to a Changing Landscape

A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders

The population genomics of rhesus macaques (Macaca mulatta) based on whole-genome sequences

241-LB: Identification of Novel and Population-Specific Signals for Type 2 Diabetes in Large-Scale Study of Hispanic/Latino Individuals

Insulin gene mutations as a cause of permanent neonatal diabetes

Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease

Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D

PADRE: Pedigree-Aware Distant-Relationship Estimation

Gut microbiome features associated with liver fibrosis in Hispanics, a population at high risk for fatty liver disease

Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal

A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease

An X Chromosome Transcriptome Wide Association Study Implicates ARMCX6 in Alzheimer's Disease

Critical Evaluation of Data Requires Rigorous but Broadly Based Statistical Inference

Genome-wide Association Study Identifies Novel Risk Loci for Apical Periodontitis

Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes

303-OR: ADA Presidents' Select Abstract: Transethnic Association Study of Type 2 Diabetes in More than a Million Individuals

Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering

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