Publications by authors named "Sebastian Zollner"

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Clinical and Genetic Factors Associated with Intraoperative Minimum Alveolar Concentration Ratio: A Single-center Retrospective Cohort and Genome-wide Association Study.
Nicholas J Douville, Elizabeth S Jewell, Xinyi Zhao, Douglas A Colquhoun, Emily Bertucci-Richter

Anesthesiology· September 2025

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Whole-genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia.
Runjia Li, Sarah A Gagliano Taliun, Kevin Liao, Matthew Flickinger, Janet L Sobell, Sebastian Zollner

HGG Adv· August 2025

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Predictive evidence for the impact of personality styles on depression and functioning in two bipolar disorder cohorts.
Kelly A Ryan, Anastasia K Yocum, Yuhua Zhang, Peisong Han, David F Marshall

J Affect Disord· July 2025

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Expanding biobank pharmacogenomics through machine learning calls of structural variation.
Brett Vanderwerff, Amy L Pasternak, Lars G Fritsche, Emily Bertucci-Richter, Snehal Patil

Genetics· July 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

Nat Commun· 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

Nat Genet· March 2025

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Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia.
Runjia Li, Sarah A Gagliano Taliun, Kevin Liao, Matthew Flickinger, Janet L Sobell, Sebastian Zollner

medRxiv· February 2025

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Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants.
Hongbo Liu, Amin Abedini, Eunji Ha, Ziyuan Ma, Xin Sheng

Science· February 2025

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Variants in the β-globin locus are associated with pneumonia in African American children.
Nadine L N Halligan, Sarah C Hanks, Karen Matsuo, Taylor Martins, Sebastian Zöllner

HGG Adv· January 2025

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The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup.
Yu-Jyun Huang, Nuzulul Kurniansyah, Matthew O Goodman, Brian W Spitzer, Jiongming Wang

medRxiv· December 2024

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FICTURE: scalable segmentation-free analysis of submicron-resolution spatial transcriptomics.
Yichen Si, ChangHee Lee, Yongha Hwang, Jeong H Yun, Weiqiu Cheng

Nat Methods· October 2024

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Multi-ancestry polygenic risk scores for venous thromboembolism.
Yon Ho Jee, Florian Thibord, Alicia Dominguez, Corriene Sept, Kristin Boulier

Hum Mol Genet· September 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

Nature· March 2024

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Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Andrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, Joshua Backman, Joelle Mbatchou

Nature· February 2024

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A Stacking Framework for Polygenic Risk Prediction in Admixed Individuals.
Kevin Liao, Sebastian Zöllner

medRxiv· February 2024

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Multi-ancestry polygenic risk scores for venous thromboembolism.
Yon Ho Jee, Florian Thibord, Alicia Dominguez, Corriene Sept, Kristin Boulier

medRxiv· January 2024

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Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications.
Rosalie B T M Sterenborg, Inga Steinbrenner, Yong Li, Melissa N Bujnis, Tatsuhiko Naito

Nat Commun· January 2024

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Cohort Profile Update: The Heinz C. Prechter Longitudinal Study of Bipolar Disorder.
Anastasia K Yocum, Steve Anderau, Holli Bertram, Helen J Burgess, Amy L Cochran

Int J Epidemiol· December 2023

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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

Nat Genet· December 2023

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Scalable segmentation-free analysis of submicron resolution spatial transcriptomics.
Yichen Si, ChangHee Lee, Yongha Hwang, Jeong H Yun, Weiqiu Cheng

bioRxiv· November 2023

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Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Andrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, Joshua Backman, Joelle Mbatchou

Nature· October 2023

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Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.
Ida Surakka, Kuan-Han Wu, Whitney Hornsby, Brooke N Wolford, Fred Shen

Cell Genom· August 2023

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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

medRxiv· August 2023

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Polygenic prediction of preeclampsia and gestational hypertension.
Michael C Honigberg, Buu Truong, Raiyan R Khan, Brenda Xiao, Laxmi Bhatta

Nat Med· June 2023

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Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.
Nuzulul Kurniansyah, Matthew O Goodman, Alyna T Khan, Jiongming Wang, Elena Feofanova

Nat Commun· June 2023

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