M. Preuss

发表

Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations

Yurii S. Aulchenko, Thomas Meitinger, Ritsert C. Jansen, 2012, PLoS genetics.

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Tanya M. Teslovich, Ayellet V. Segrè, P. Elliott, 2010 .

Edinburgh Research Explorer Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2022 .

Effect of tissue-grouped regulatory variants associated to type 2 diabetes in related secondary outcomes

Michael H. Preuss, J. van Setten, S. W. van der Laan, 2023, Scientific Reports.

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Kyle J. Gaulton, Yoonjung Yoonie Joo, Cassandra N. Spracklen, 2020, Nature Genetics.

Mapping the human genetic architecture of COVID-19

Mattia G. Bergomi, Christopher M. DeBoever, Matthew A. Wiles, 2021, Nature.

Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-Wide Association Meta-analysis Involving More Than 22 000 Cases and 60 000 Controls

D. Absher, T. Assimes, K. Stefánsson, 2010, Circulation. Cardiovascular genetics.

Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

Nicholette D. Palmer, J. Danesh, M. Fornage, 2022, Science advances.

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Ayellet V. Segrè, Cameron D. Palmer, P. Elliott, 2010, Nature.

Genetic analyses of diverse populations improves discovery for complex traits

Stephanie A. Bien, Janina M. Jeff, Sarah C. Nelson, 2019, Nature.

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

Benjamin J. Wright, I. König, A. Ziegler, 2009, Nature Genetics.

Genetic analyses of diverse populations improves discovery for complex traits

Stephanie A. Bien, Janina M. Jeff, Sarah C. Nelson, 2019, Nature.

RANTES/CCL5 and Risk for Coronary Events: Results from the MONICA/KORA Augsburg Case-Cohort, Athero-Express and CARDIoGRAM Studies

Michael H. Preuss, C. Meisinger, N. Klopp, 2011, PloS one.

The association of mannose-binding lectin 2 polymorphisms with outcome in very low birth weight infants

Michael H. Preuss, W. Göpel, P. Nürnberg, 2017, PloS one.

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

Anthony J. Payne, Y. J. Kim, Jason M. Torres, 2018, Nature Genetics.

A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse Ancestries

Aaron F. McDaid, Yan V. Sun, Cassandra N. Spracklen, 2022 .

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits - the Hispanic/Latino Anthropometry Consortium

H. Hakonarson, S. Grant, G. Bedoya, 2021, bioRxiv.

A beginners guide to SNP calling from high-throughput DNA-sequencing data

Daniel M Bader, Michael H. Preuss, A. Altmann, 2012, Human Genetics.

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

Karsten B. Sieber, M. P. Concas, Cassandra N. Spracklen, 2019, Nature Genetics.

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Thomas W. Mühleisen, Benjamin J. Wright, C. Gieger, 2011, Nature Genetics.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2020, Nature Genetics.

Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index

Henrik, Tanya M. Teslovich, Jennie, 2012 .

Host genetic effects in pneumonia

N. Cox, Michael H. Preuss, K. North, 2020, The American Journal of Human Genetics.

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

Anthony J. Payne, Y. J. Kim, Jason M. Torres, 2018, Nature Genetics.

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Alberto Piazza, William Matthai, Flora Peyvandi, 2009, Nature Genetics.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Christian Gieger, Jianxin Shi, Inês Barroso, 2013, Nature Genetics.

A first update on mapping the human genetic architecture of COVID-19

Eurie L. Hong, E. F. Perez, Rachel G Liao, 2022, Nature.

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Karsten B. Sieber, Laurent F. Thomas, Pashupati P. Mishra, 2022, Kidney international.

Rare genetic variants explain missing heritability in smoking

Ivana V. Yang, Dajiang J. Liu, Nicholette D. Palmer, 2022, Nature Human Behaviour.

Genetic architecture of smoking: Evaluating rare variant contribution from deep whole-genome sequencing of up to 26,000 individuals

Ivana V. Yang, David R. Liu, Lisa J. Martin, 2021 .

Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease

Simon C. Potter, Thomas W. Mühleisen, Benjamin J. Wright, 2011, PLoS genetics.

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

M. P. Concas, May E. Montasser, Henry J. Lin, 2022, Nature Communications.