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Daniel M Jordan

11PUBLICATIONS
119CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseMedical biotechnology diagnostics (incl. biosensors)GenomicsGene expression (incl. microarray and other genome-wide approaches)
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Journal

Publications (11)

Sort by Publication Date:
|Aug 28, 2025
Machine learning-based penetrance of genetic variants.

Iain S Forrest, Ha My T Vy, Ghislain Rocheleau

|Jun 23, 2025
Using large-scale population-based data to improve disease risk assessment of clinical variants.

Iain S Forrest, Kuan-Lin Huang, Julie M Eggington

|Jan 10, 2024
A deep learning transformer model predicts high rates of undiagnosed rare disease in large electronic health systems.

Daniel M Jordan, Ha My T Vy, Ron Do

|May 11, 2023
A machine learning model identifies patients in need of autoimmune disease testing using electronic health records.

Iain S Forrest, Ben O Petrazzini, Áine Duffy

|Nov 03, 2022
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

Guillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki

|Aug 20, 2022
A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank.

Ghislain Rocheleau, Iain S Forrest, Áine Duffy

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Frequent Collaborators

8 joint publications

Ron Do

4 joint publications

Iain S Forrest

3 joint publications

Girish Nadkarni

3 joint publications

Ghislain Rocheleau

3 joint publications

Ha My T Vy

2 joint publications

Ben O Petrazzini

2 joint publications

Kuan-Lin Huang

2 joint publications

Shamil R Sunyaev

2 joint publications

Hong-Hee Won

2 joint publications

Judy H Cho

Frequent Collaborators

8 joint publications

Ron Do

4 joint publications

Iain S Forrest

3 joint publications

Girish Nadkarni

3 joint publications

Ghislain Rocheleau

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