Publications by authors named "Michael Preuss"

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Cryogenic sample preparation: Comparative analysis of Ga and Xe FIB milling for TEM and APT examination of zirconium.
Ömer Koç, Benjamin M Jenkins, Jack Haley, Christina Hofer, Martin S Meier, Michael Preuss

Ultramicroscopy· November 2025

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Genetic subtyping of obesity reveals biological insights into the uncoupling of adiposity from its cardiometabolic comorbidities.
Nathalie Chami, Zhe Wang, Victor Svenstrup, Virginia Diez Obrero, Daiane Hemerich, Michael H Preuss

Nat Med· November 2025

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Polygenic prediction of body mass index and obesity through the life course and across ancestries.
Roelof A J Smit, Kaitlin H Wade, Qin Hui, Joshua D Arias, Xianyong Yin, Michael H Preuss

Nat Med· September 2025

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Genome-wide association study provides novel insight into the genetic architecture of severe obesity.
Mohanraj Krishnan, Mohammad Yaser Anwar, Anne E Justice, Geetha Chittoor, Hung-Hsin Chen, Michael H Preuss

PLoS Genet· September 2025

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Genome-wide associations with metabolic syndrome among UK Biobank participants reporting use of second-generation antipsychotics.
Nihal El Rouby, Aniwaa Owusu-Obeng, Michael Preuss, Simon Lee, Mingjian Shi

Pharmacotherapy· August 2025

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Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.
Alicia Huerta-Chagoya, Joohyun Kim, Ravi Mandla, Yingchang Lu, Ken Suzuki, Michael Preuss

medRxiv· July 2025

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Global multi-ancestry genetic study elucidates genes and biological pathways associated with thyroid cancer and benign thyroid diseases.
Samantha L White, Maizy S Brasher, Jack Pattee, Wei Zhou, Sinéad Chapman, Michael Preuss

medRxiv· May 2025

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Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits.
Lauren E Petty, Hung-Hsin Chen, Elizabeth G Frankel, Wanying Zhu, Carolina G Downie, Michael Preuss

Nat Commun· April 2025

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Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele.
Xinruo Zhang, Jennifer A Brody, Mariaelisa Graff, Heather M Highland, Nathalie Chami, Michael H Preuss

Nat Commun· April 2025

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Genome Wide Association Study (GWAS) Identifies Novel Genetic Loci for Second-Generation Antipsychotics (SGA)-Induced Metabolic Syndrome (MetS).
Nihal El Rouby, Aniwaa Owusu-Obeng, Michael H Preuss, Simon Lee, Mingjian Shi

Clin Transl Sci· April 2025

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Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases.
Carolina Roselli, Ida Surakka, Morten S Olesen, Gardar Sveinbjornsson, Nicholas A Marston, Michael Preuss

Nat Genet· March 2025

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Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.
Seung Hoan Choi, Sean J Jurgens, Ling Xiao, Matthew C Hill, Christopher M Haggerty, Michael Preuss

Nat Genet· March 2025

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Genetic subtyping of obesity reveals biological insights into the uncoupling of adiposity from its cardiometabolic comorbidities.
Nathalie Chami, Zhe Wang, Victor Svenstrup, Virginia Diez Obrero, Daiane Hemerich, Michael H Preuss

medRxiv· February 2025

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Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas.
Victor Borda, Douglas P Loesch, Bing Guo, Roland Laboulaye, Diego Veliz-Otani, Michael Preuss

Cell Genom· November 2024

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Rare variant contribution to the heritability of coronary artery disease.
Ghislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, Natalie R Hasbani, Alanna C Morrison, Michael H Preuss

Nat Commun· October 2024

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An integrative framework to prioritize genes in more than 500 loci associated with body mass index.
Daiane Hemerich, Victor Svenstrup, Virginia Diez Obrero, Michael Preuss, Arden Moscati

Am J Hum Genet· June 2024

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Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Ken Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, Henry J Taylor, Xianyong Yin, Michael H Preuss

Nature· March 2024

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Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference.
Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou, Daniel F Levey, Dora Koller, Michael H Preuss

Nat Genet· February 2024

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Incidence of adverse respiratory events after adjustment of clear fluid fasting recommendations to 1 h: a prospective, observational, multi-institutional cohort study.
Achim Schmitz, Fabian Kuhn, Jan Hofmann, Walid Habre, Thomas Erb, Michael Preuss

Br J Anaesth· January 2024

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BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability.
Clive J Hoggart, Shing Wan Choi, Judit García-González, Tade Souaiaia, Michael Preuss

Nat Genet· January 2024

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Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Anqi Wang, Jiayi Shen, Alex A Rodriguez, Edward J Saunders, Fei Chen, Michael H Preuss

Nat Genet· December 2023

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Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.
Yasminka A Jakubek, Ying Zhou, Adrienne Stilp, Jason Bacon, Justin W Wong, Michael H Preuss

Nat Genet· November 2023

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Branched chain amino acids harbor distinct and often opposing effects on health and disease.
Christy L Avery, Annie Green Howard, Harold H Lee, Carolina G Downie, Moa P Lee, Michael H Preuss

Commun Med (Lond)· November 2023

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Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Yuxuan Wang, Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A Holdcraft, Michael H Preuss

Am J Hum Genet· October 2023

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