Biorxiv/in press

https://www.medrxiv.org/content/10.1101/2023.12.04.23299391v1
(12/04/23)
Zhang MJ, Durvasula A, Chiang C, Koch EM, Strober BJ, Shi H, Barton AR, Kim SS, Weissbrod O, Loh P, Gazal S, Sunyaev, Price AL. Pervasive correlations between causal disease effects of proximal SNPs vary with functional annotations and implicate stabilizing selection. medRxiv.

https://www.medrxiv.org/content/10.1101/2024.02.02.24302228v1
(02/04/24)
Peyrot WJ, Panagiotaropoulou GLM, Adams MJ, Awasthi S, Ge T, McIntosh AM, Mitchell BL, Mullins N, O’Connell KS, Penninx BWJH, Posthuma D, Ripke S, Ruderfer DM, Uffelmann E, Vilhjalmsson BJ, Zhu Z, other authors, Smoller JW, Price AL. Distinguishing different psychiatric disorders using DDx-PRS. medRxiv.

https://www.medrxiv.org/content/10.1101/2024.05.13.24307291v1
(05/14/24)
Rossen J, Shi H, Strober BJ, Zhang MJ, Kanai M, McCaw ZR, Liang L, Weissbrod O, Price AL. MultiSuSiE improves multi-ancestry fine-mapping in All of Us whole-genome sequencing data. medRxiv.

https://www.biorxiv.org/content/10.1101/2024.11.07.622307v2
(11/10/24)
Fabiha T, Evergreen I, Kundu S, Pampari A, Abramov S, Boystov A, other authors, Montgomery SB, Engreitz JM, Kundaje A, Tewhey R, Price AL**, Dey K**. A consensus variant-to-function score to functionally prioritize variants for disease. bioRxiv.

https://www.medrxiv.org/content/10.1101/2025.05.05.25327017v2
(05/22/25)
Kerner G, Kamitaki N, Strober B, Price AL. Mapping disease loci to biological processes via joint pleiotropic and epigenomic partitioning. medRxiv.

https://www.medrxiv.org/content/10.1101/2025.06.10.25329261v1
(06/11/25)
Zhao Y, Strober B, Hou K, Kerner G, Danesh J, Gazal S, Cheng W, Inouye M, Price AL**, Jiang X**. Pleiotropic heritability quantifies the shared genetic variance of common diseases. medRxiv