Publications by authors named "Ira Hall"

Claim this Profile

Mentions over time

Mentions by platform

Video Views

436,181

Total Likes

15,405

Extended Reach

2,337,788

Social Features

248
G
Genealogy based trait association with LOCATER boosts power at loci with allelic heterogeneity.
Xinxin Wang, Ryan Christ, Erica Young, Chul Joo Kang, Indraniel Das, Ira M Hall

medRxiv· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clade Distillation for Genome-wide Association Studies.
Ryan Christ, Xinxin Wang, Louis J M Aslett, David Steinsaltz, Ira Hall

Genetics· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Single cell variant to enhancer to gene map for coronary artery disease.
Junedh M Amrute, Paul C Lee, Ittai Eres, Chang Jie Mick Lee, Andrea Bredemeyer, Ira M Hall

medRxiv· November 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies.
Derek Shyr, Rounak Dey, Xihao Li, Hufeng Zhou, Eric Boerwinkle, Ira Hall

Am J Hum Genet· October 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification.
Paul S de Vries, Matthew P Conomos, Kuldeep Singh, Christopher J Nicholson, Deepti Jain, Ira M Hall

Nat Cardiovasc Res· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A draft human pangenome reference.
Wen-Wei Liao, Mobin Asri, Jana Ebler, Daniel Doerr, Marina Haukness, Tobias Marschall, Ira M Hall

Nature· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Semi-automated assembly of high-quality diploid human reference genomes.
Erich D Jarvis, Giulio Formenti, Arang Rhie, Andrea Guarracino, Chentao Yang, Tobias Marschall, Ira Hall

Nature· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.
Xianyong Yin, Debraj Bose, Annie Kwon, Sarah C Hanks, Anne U Jackson, Ira M Hall

Am J Hum Genet· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios.
Marta Byrska-Bishop, Uday S Evani, Xuefang Zhao, Anna O Basile, Haley J Abel, Ira M Hall

Cell· September 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Human Pangenome Project: a global resource to map genomic diversity.
Ting Wang, Lucinda Antonacci-Fulton, Kerstin Howe, Heather A Lawson, Julian K Lucas, Tobias Marschall, Ira M Hall

Nature· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.
Xianyong Yin, Lap Sum Chan, Debraj Bose, Anne U Jackson, Peter VandeHaar, Ira M Hall

Nat Commun· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space.
Michael C Schatz, Anthony A Philippakis, Enis Afgan, Eric Banks, Vincent J Carey, Ira M Hall

Cell Genom· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Structural variants are a major source of gene expression differences in humans and often affect multiple nearby genes.
Alexandra J Scott, Colby Chiang, Ira M Hall

Genome Res· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
Elmo Christian Saarentaus, Aki Samuli Havulinna, Nina Mars, Ari Ahola-Olli, Tuomo Tapio Johannes Kiiskinen, Ira M Hall

Mol Psychiatry· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
Liron Ganel, Lei Chen, Ryan Christ, Jagadish Vangipurapu, Erica Young, Ira M Hall

Hum Genomics· June 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease.
Olivia M de Goede, Daniel C Nachun, Nicole M Ferraro, Michael J Gloudemans, Abhiram S Rao, Ira M Hall

Cell· May 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Haplotype-resolved diverse human genomes and integrated analysis of structural variation.
Peter Ebert, Peter A Audano, Qihui Zhu, Bernardo Rodriguez-Martin, David Porubsky, Ira M Hall, Tobias Marschall

Science· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association of structural variation with cardiometabolic traits in Finns.
Lei Chen, Haley J Abel, Indraniel Das, David E Larson, Liron Ganel, Ira M Hall

Am J Hum Genet· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Telomere-to-telomere assembly of a complete human X chromosome.
Karen H Miga, Sergey Koren, Arang Rhie, Mitchell R Vollger, Ariel Gershman, Ira Hall

Nature· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Transcriptomic signatures across human tissues identify functional rare genetic variation.
Nicole M Ferraro, Benjamin J Strober, Jonah Einson, Nathan S Abell, Francois Aguet, Ira Hall

Science· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mapping and characterization of structural variation in 17,795 human genomes.
Haley J Abel, David E Larson, Allison A Regier, Colby Chiang, Indraniel Das, Ira M Hall

Nature· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
svtools: population-scale analysis of structural variation.
David E Larson, Haley J Abel, Colby Chiang, Abhijit Badve, Indraniel Das, Ira M Hall

Bioinformatics· November 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.
Adam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, Susan K Service, Aki S Havulinna, Ira M Hall

Nature· November 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome sequencing of Finnish isolates enhances rare-variant association power.
Adam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, Susan K Service, Aki S Havulinna, Ira M Hall

Nature· August 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis