Publications by authors named "Manolio T"

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Genomic medicine year in review: 2025.
Teri A Manolio, Alauna Rupert, Jahnavi Narula, Carol J Bult, Rex L Chisholm

Am J Hum Genet· December 2025

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Impact of Genetic Risk Factors on Coronary Heart Disease Risk Across the Age Spectrum in Three Major Race/Ethnicity Groups in the United States.
Mohammadreza Naderian, Johanna L Smith, Marwan E Hamed, Ozan Dikilitas, Josh B Cortopassi

medRxiv· November 2025

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Advancing the science of genomic learning healthcare systems.
Teri A Manolio, Renee Rider, Carol J Bult, Rex L Chisholm, Patricia A Deverka

Learn Health Syst· October 2025

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Genomic medicine year in review: 2024.
Teri A Manolio, Jahnavi Narula, Alauna Rupert, Carol J Bult, Rex L Chisholm

Am J Hum Genet· December 2024

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Patterns of pharmacogenetic variation in nine biogeographic groups.
Sophia Hernandez, Lucia A Hindorff, Joannella Morales, Erin M Ramos, Teri A Manolio

Clin Transl Sci· September 2024

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Survey of the training needs of genetic assistants supports the creation of genetic assistant training programs.
Renee A Rider, Luis Cubano, Ebony B Madden, Robb K Rowley, Teri A Manolio

J Genet Couns· August 2024

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Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations.
Niall J Lennon, Leah C Kottyan, Christopher Kachulis, Noura S Abul-Husn, Josh Arias

Nat Med· February 2024

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Genomic medicine year in review: 2023.
Teri A Manolio, Jahnavi Narula, Carol J Bult, Rex L Chisholm, Patricia A Deverka

Am J Hum Genet· December 2023

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Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Jodell E Linder, Ran Tao, Wendy K Chung, Krzysztof Kiryluk, Cong Liu

Am J Hum Genet· November 2023

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eXclusionarY: 10 years later, where are the sex chromosomes in GWASs?
Lei Sun, Zhong Wang, Tianyuan Lu, Teri A Manolio, Andrew D Paterson

Am J Hum Genet· June 2023

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Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations.
Niall J Lennon, Leah C Kottyan, Christopher Kachulis, Noura Abul-Husn, Josh Arias

medRxiv· June 2023

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Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Jodell E Linder, Aimee Allworth, Harris T Bland, Pedro J Caraballo, Rex L Chisholm

Genet Med· April 2023

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Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.
Ozan Dikilitas, Alborz Sherafati, Seyedmohammad Saadatagah, Benjamin A Satterfield, David C Kochan

Circ Genom Precis Med· April 2023

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Development of Competency-based Online Genomic Medicine Training (COGENT).
Susanne B Haga, Wendy K Chung, Luis A Cubano, Timothy B Curry, Philip E Empey

Per Med· January 2023

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Genomic Medicine Year in Review: 2022.
Teri A Manolio, Jahnavi Narula, Carol J Bult, Rex L Chisholm, Patricia A Deverka

Am J Hum Genet· December 2022

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Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results.
Alborz Sherafati, Omar Elsekaily, Seyedmohammad Saadatagah, David C Kochan, Christopher Lee

Genet Med· October 2022

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A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
Ken Wiley, Laura Findley, Madison Goldrich, Tejinder K Rakhra-Burris, Ana Stevens

J Am Med Inform Assoc· July 2022

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The ACMG SF v3.0 gene list increases returnable variant detection by 22% when compared with v2.0 in the ClinSeq cohort.
Jennifer J Johnston, Marie-Luise Brennan, Bailey Radenbaugh, Seeley J Yoo, Sophia M Hernandez

Genet Med· March 2022

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Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Andrew M Glazer, Giovanni Davogustto, Christian M Shaffer, Carlos G Vanoye, Reshma R Desai

Circulation· March 2022

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Genomic medicine year in review: 2021.
Teri A Manolio, Carol J Bult, Rex L Chisholm, Patricia A Deverka, Geoffrey S Ginsburg

Am J Hum Genet· December 2021

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Should all babies have their genome sequenced at birth?
Leslie G Biesecker, Eric D Green, Teri Manolio, Benjamin D Solomon, David Curtis

BMJ· November 2021

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Workshop proceedings: GWAS summary statistics standards and sharing.
Jacqueline A L MacArthur, Annalisa Buniello, Laura W Harris, James Hayhurst, Aoife McMahon

Cell Genom· October 2021

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Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry.
Benjamin A Satterfield, Ozan Dikilitas, Maya S Safarova, Shoa L Clarke, Catherine Tcheandjieu

Circ Genom Precis Med· August 2021

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Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry.
Cong Liu, Nur Zeinomar, Wendy K Chung, Krzysztof Kiryluk, Ali G Gharavi

JAMA Netw Open· August 2021

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Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network.
Sadiya S Khan, Christin Hoell, Lisa M Castillo, John J Connolly, David R Crosslin

Circ Heart Fail· May 2021

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