Researcher Profile

Allison Ashley-Koch

Publications

4,853

Citations

Co-Authors

Active Years

Publications

Open Access Journal Article Genome Biology Sep 09, 2025

Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals

Margaret Sunitha Selvaraj · Xihao Li · Zilin Li · Eric Van Buren +440 more

10.1186/s13059-025-03698-0 3 citations

Journal Article Nature Apr 08, 2022

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Vassily Trubetskoy · Antonio F. Pardiñas · Ting Qi · Georgia Panagiotaropoulou +584 more

10.1038/s41586-022-04434-5 2,398 citations

Journal Article Nature Genetics Mar 01, 2022

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Pierrick Wainschtein · Deepti Jain · Zhili Zheng · Stella Aslibekyan +451 more

10.1038/s41588-021-00997-7 304 citations

Open Access Journal Article Nature Communications Oct 11, 2022

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Margaret Sunitha Selvaraj · Xihao Li · Zilin Li · Akhil Pampana +429 more

10.1038/s41467-022-33510-7 67 citations

Journal Article Nature Methods Oct 27, 2022

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

Zilin Li · Xihao Li · Hufeng Zhou · Sheila M. Gaynor +508 more

10.1038/s41592-022-01640-x 104 citations

Journal Article Nature Genetics Oct 01, 2021

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Yang Luo · Masahiro Kanai · Wanson Choi · Xinyi Li +428 more

10.1038/s41588-021-00935-7 161 citations

Journal Article Nature Genetics Aug 24, 2020

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Xihao Li · Zilin Li · Hufeng Zhou · Sheila M. Gaynor +428 more

10.1038/s41588-020-0676-4 256 citations

Open Access Journal Article PLoS ONE Sep 24, 2020

Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients

Luke Hebert · Paul Hillman · Craig Baker · Michael Brown +5 more

10.1371/journal.pone.0239083 12 citations

Journal Article Nature Oct 14, 2020

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Alexander G. Bick · Joshua S. Weinstock · Satish K. Nandakumar · Charles P. Fulco +408 more

10.1038/s41586-020-2819-2 675 citations

Open Access Journal Article Chest Dec 01, 2019

Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

Priyadarshini Kachroo · Julian Hecker · Bo L. Chawes · Tarunveer S. Ahluwalia +347 more

10.1016/j.chest.2019.08.2202 6 citations

Journal Article Nature Genetics Jan 11, 2016

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma

Jessica N. Cooke Bailey · Stephanie J Loomis · Jae H Kang · R Rand Allingham +77 more

10.1038/ng.3482 238 citations

Journal Article American Journal of Epidemiology Feb 28, 2007

HLA-DR15 Haplotype and Multiple Sclerosis: A HuGE Review

Hollie Schmidt · Dhelia Williamson · Allison Ashley-Koch

10.1093/aje/kwk118 174 citations

Open Access Journal Article The American Journal of Human Genetics Nov 01, 2002

A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)

Evan Reid · Mark Kloos · Allison Ashley-Koch · Lori Hughes +8 more

10.1086/344210 455 citations

Publication Timeline

2025

2022

2021

2020

2019

2016

2007

2002

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