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From mouse to human: evolutionary genomics analysis of human orthologs of essential genes

PLoS genetics, 2013-05, Vol.9 (5), p.e1003484-e1003484

2013

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Detecting Long-Term Balancing Selection Using Allele Frequency Correlation

Molecular biology and evolution, 2017-11, Vol.34 (11), p.2996-3005

2017

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Regularized sequence-context mutational trees capture variation in mutation rates across the human genome

PLoS genetics, 2023-07, Vol.19 (7), p.e1010807-e1010807

2023

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Genetics of height and risk of atrial fibrillation: A Mendelian randomization study

PLoS medicine, 2020-10, Vol.17 (10), p.e1003288-e1003288

2020

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Testing for an unusual distribution of rare variants

PLoS genetics, 2011-03, Vol.7 (3), p.e1001322-e1001322

2011

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Keen on the tenure track job, are you? Know these things, you should

Genome Biology, 2019-01, Vol.20 (1), p.6-6, Article 6

Voight, Benjamin F

2019

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A map of recent positive selection in the human genome

PLoS biology, 2006-03, Vol.4 (3), p.e72-e72

2006

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A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis

Nature communications, 2021-08, Vol.12 (1), p.5078-17, Article 5078

2021

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The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study

PLoS medicine, 2020-09, Vol.17 (9), p.e1003302

2020

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Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Nature genetics, 2014-04, Vol.46 (4), p.357

2014

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Pervasive sharing of genetic effects in autoimmune disease

PLoS genetics, 2011-08, Vol.7 (8), p.e1002254-e1002254

2011

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Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments

Nature genetics, 2021-09, Vol.53 (9), p.1322

2021

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Prioritizing the Role of Major Lipoproteins and Subfractions as Risk Factors for Peripheral Artery Disease

Circulation (New York, N.Y.), 2021-08, Vol.144 (5), p.353-364

2021

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Single-Cell Analysis Reveals that Noncoding RNAs Contribute to Clonal Heterogeneity by Modulating Transcription Factor Recruitment

Molecular cell, 2012-02, Vol.45 (4), p.470-482

2012

Volltextzugriff (PDF)

TSABL: Trait Specific Annotation Based Locus predictor

BMC genomics, 2022-06, Vol.23 (1), p.444-444, Article 444

2022

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Mendelian randomization analyses clarify the effects of height on cardiovascular diseases

PloS one, 2024-07, Vol.19 (7), p.e0298786

2024

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Characterization of the genome and silk-gland transcriptomes of Darwin's bark spider (Caerostris darwini)

PloS one, 2022-06, Vol.17 (6), p.e0268660-e0268660

2022

Volltextzugriff (PDF)

Dissecting an adiposity locus with an arsenal of genomics

Genome Biology, 2018-06, Vol.19 (1), p.74-74, Article 74

2018

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Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approach

BMC bioinformatics, 2022-10, Vol.23 (1), p.420-420, Article 420

2022

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Genetic Variation Determines PPARγ Function and Anti-diabetic Drug Response In Vivo

Cell, 2015-07, Vol.162 (1), p.33-44

2015

Volltextzugriff (PDF)

An expanded sequence context model broadly explains variability in polymorphism levels across the human genome

Nature genetics, 2016-04, Vol.48 (4), p.349

2016

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Convergent adaptation of human lactase persistence in Africa and Europe

Nature genetics, 2007-01, Vol.39 (1), p.31-40

2007

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A central role for GRB10 in regulation of islet function in man

PLoS genetics, 2014-04, Vol.10 (4), p.e1004235-e1004235

2014

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Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypes

BMC medical genomics, 2020-06, Vol.13 (1), p.89-89, Article 89

2020

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Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

PLoS genetics, 2012-05, Vol.8 (5), p.e1002741-e1002741

2012

Volltextzugriff (PDF)

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From mouse to human: evolutionary genomics analysis of human orthologs of essential genes

Detecting Long-Term Balancing Selection Using Allele Frequency Correlation

Regularized sequence-context mutational trees capture variation in mutation rates across the human genome

Genetics of height and risk of atrial fibrillation: A Mendelian randomization study

Testing for an unusual distribution of rare variants

Keen on the tenure track job, are you? Know these things, you should

A map of recent positive selection in the human genome

A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis

The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Pervasive sharing of genetic effects in autoimmune disease

Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments

Prioritizing the Role of Major Lipoproteins and Subfractions as Risk Factors for Peripheral Artery Disease

Single-Cell Analysis Reveals that Noncoding RNAs Contribute to Clonal Heterogeneity by Modulating Transcription Factor Recruitment

TSABL: Trait Specific Annotation Based Locus predictor

Mendelian randomization analyses clarify the effects of height on cardiovascular diseases

Characterization of the genome and silk-gland transcriptomes of Darwin's bark spider (Caerostris darwini)

Dissecting an adiposity locus with an arsenal of genomics

Estimating the effect size of a hidden causal factor between SNPs and a continuous trait: a mediation model approach

Genetic Variation Determines PPARγ Function and Anti-diabetic Drug Response In Vivo

An expanded sequence context model broadly explains variability in polymorphism levels across the human genome

Convergent adaptation of human lactase persistence in Africa and Europe

A central role for GRB10 in regulation of islet function in man

Genetic colocalization atlas points to common regulatory sites and genes for hematopoietic traits and hematopoietic contributions to disease phenotypes

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

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