Publications by authors named "Kenny Ee"

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Mediation of Polygenic Asthma Risk Through Gene Expression.
Rakesh Natarajan, Brooke Szczesny, Kanika Kanchan, Erika Esquinca, Meher Preethi Boorgula, Sameer Chavan, Kathleen C Barnes

Allergy· December 2025

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Healthcare professionals' experiences returning monogenic, polygenic, and integrated risk results in the eMERGE study.
Sabrina A Suckiel, Laura Golfinopoulos, Courtney L Scherr, Brenna M Boyd, Wendy K Chung

HGG Adv· 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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Patient and providers' perspectives on using the GUÍA digital tool to enhance genomic results disclosure.
Jacqueline A Odgis, Sabrina A Suckiel, Laura Golfinopoulos, Nicole R Kelly, Katherine E Bonini

Genet Med Open· October 2025

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Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations.
Joshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, Maria Viskadourou, Paula Reventun, Pradeep Natarajan, Paul Scheet

Nat Commun· October 2025

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Implementing integrated genomic risk assessments for breast cancer: lessons learned from the Electronic Medical Records and Genomics study.
Cong Liu, Katherine D Crew, Jennifer Morse, Jodell E Linder, Antonis C Antoniou, Kathleen F Mittendorf

JAMIA Open· October 2025

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SPC: a SPectral Component approach leveraging Identity-by-Descent graphs to address recent population structure in genomic analysis.
Ruhollah Shemirani, Gillian M Belbin, Sinead Cullina, Christa Caggiano, Christopher Gignoux

medRxiv· September 2025

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Prediction and characterization of genetically regulated expression of asthma tissues from African-ancestry populations.
Sarah D Slack, Erika Esquinca, Christopher H Arehart, Meher Preethi Boorgula, Brooke Szczesny, Sameer Chavan, Kathleen C Barnes

J Allergy Clin Immunol· 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, Miryoung Lee

PLoS Genet· September 2025

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A Scalable Framework to Integrate Social Determinants of Health into Disease Risk Models using Biobank Survey Data.
Jane Brown, Abhijith Biji, Kathleen Ferar, Vikas Pejaver, Eimear E Kenny

medRxiv· September 2025

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Investigating the sources of variable impact of pathogenic variants in monogenic metabolic conditions.
Angela Wei, Richard Border, Boyang Fu, Sinéad Cullina, Nadav Brandes

Nat Commun· June 2025

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Ancestry Calibration of Polygenic Risk Scores Improves Risk Stratification and Effect Estimation in African American Adults.
Luciana B Vargas, Mariah C Meyer, Iain R Konigsberg, Aastha Kakar, Patrick M Carry

medRxiv· June 2025

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When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research.
Katherine E Bonini, Lauren R Desrosiers-Battu, Ann Katherine M Foreman, Nuriye N Sahin-Hodoglugil, Mary A Majumder

Genet Med Open· June 2025

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Implementing Integrated Genomic Risk Assessments for Breast Cancer: Lessons Learned from the eMERGE Study.
Cong Liu, Katherine Crew, Jennifer Morse, Jodell E Linder, Antonis C Antoniou, Kathleen F Mittendorf

medRxiv· May 2025

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Current Limitations of Electronic Health Record Systems in Supporting Pragmatic Clinical Trials: Insights from the eMERGE Consortium.
Kavishwar B Wagholikar, Jennifer Allen Pacheco, Adam S Gordon, Atlas Khan, Bahram Namjou Khales

medRxiv· April 2025

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Evolving knowledge of red flag clinical features associated with TTR p.(Val142Ile) in a diverse electronic health-record-linked biobank.
Amy R Kontorovich, Connor B Benson, Alexandra McClellan, Gillian M Belbin, Eimear E Kenny

Genet Med· March 2025

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Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.
Marios K Georgakis, Rainer Malik, Omar El Bounkari, Natalie R Hasbani, Jiang Li, Barry I Freedman

Genome Med· March 2025

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Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood.
Yasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, Fulong Yu, Jason Bacon, Kathleen Barnes, Paul Scheet

Am J Hum Genet· February 2025

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Investigating the Impact of Screen-Sharing Visual Aids during Genomic Results Disclosure via Telehealth in Diverse Families in the TeleKidSeq Pilot Study.
Jacqueline A Odgis, Nicole R Kelly, Monisha Sebastin, Laura Golfinopoulos, Beverly J Insel

Public Health Genomics· 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, Mei-Yueh Lee, Humaira Rasheed, Kristian Hveem

Science· February 2025

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Prediction and Characterization of Genetically Regulated Expression of Target Tissues in Asthma.
Sarah D Slack, Erika Esquinca, Christopher H Arehart, Meher Preethi Boorgula, Brooke Szczesny, Sameer Chavan, Kathleen C Barnes

medRxiv· February 2025

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The PRIMED Consortium: Reducing disparities in polygenic risk assessment.
Iftikhar J Kullo, Matthew P Conomos, Sarah C Nelson, Sally N Adebamowo, Ananyo Choudhury, Pradeep Natarajan

Am J Hum Genet· December 2024

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Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research.
Michelle A Ramos, Katherine E Bonini, Laura Scarimbolo, Nicole R Kelly, Beverly Insel

Am J Hum Genet· December 2024

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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

Cell Genom· November 2024

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Systematic comparison of phenome-wide admixture mapping and genome-wide association in a diverse biobank.
Sinead Cullina, Ruhollah Shemirani, Samira Asgari, Eimear E Kenny

medRxiv· November 2024

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