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Published in Genome medicine (25.04.2024)
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Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery
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Published in EBioMedicine (01.07.2022)
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Journal Article
Identifying latent genetic interactions in genome-wide association studies using multiple traits
Bass, Andrew J, Bian, Shijia, Wingo, Aliza P, Wingo, Thomas S, Cutler, David J, Epstein, Michael P
Published in bioRxiv (13.09.2023)
Published in bioRxiv (13.09.2023)
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The Quantitative Genetics of Human Disease: 1 Foundations
Cutler, David J., Jodeiry, Kiana, Bass, Andrew J., Epstein, Michael P.
Published in ArXiv.org (29.08.2023)
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Published in ArXiv.org (29.08.2023)
Journal Article
Identifying latent genetic interactions in genome-wide association studies using multiple traits
Bass, Andrew J, Bian, Shijia, Wingo, Aliza P, Wingo, Thomas S, Cutler, David J, Epstein, Michael P
Published in bioRxiv : the preprint server for biology (13.09.2023)
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Published in bioRxiv : the preprint server for biology (13.09.2023)
Journal Article
The Quantitative Genetics of Human Disease: 1 Foundations
Cutler, David J, Jodeiry, Kiana, Bass, Andrew J, Epstein, Michael P
Published in arXiv.org (29.08.2023)
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Published in arXiv.org (29.08.2023)
Paper
Optical Imaging with a Cathepsin B Activated Probe for the Enhanced Detection of Esophageal Adenocarcinoma by Dual Channel Fluorescent Upper GI Endoscopy
Peiman Habibollahi, Jose-Luiz Figueiredo, Pedram Heidari, Austin M Dulak, Yu Imamura, Adam J. Bass, Shuji Ogino, Andrew T Chan, Umar Mahmood
Published in Theranostics (01.01.2012)
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Published in Theranostics (01.01.2012)
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