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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 2 |
2023 | 4 |
2024 | 0 |
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6 results
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Page 1
A scalable approach to characterize pleiotropy across thousands of human diseases and complex traits using GWAS summary statistics.
Am J Hum Genet. 2023 Nov 2;110(11):1863-1874. doi: 10.1016/j.ajhg.2023.09.015. Epub 2023 Oct 24.
Am J Hum Genet. 2023.
PMID: 37879338
Free PMC article.
Leveraging base-pair mammalian constraint to understand genetic variation and human disease.
Sullivan PF, Meadows JRS, Gazal S, Phan BN, Li X, Genereux DP, Dong MX, Bianchi M, Andrews G, Sakthikumar S, Nordin J, Roy A, Christmas MJ, Marinescu VD, Wang C, Wallerman O, Xue J, Yao S, Sun Q, Szatkiewicz J, Wen J, Huckins LM, Lawler A, Keough KC, Zheng Z, Zeng J, Wray NR, Li Y, Johnson J, Chen J; Zoonomia Consortium§; Paten B, Reilly SK, Hughes GM, Weng Z, Pollard KS, Pfenning AR, Forsberg-Nilsson K, Karlsson EK, Lindblad-Toh K.
Sullivan PF, et al.
Science. 2023 Apr 28;380(6643):eabn2937. doi: 10.1126/science.abn2937. Epub 2023 Apr 28.
Science. 2023.
PMID: 37104612
Free PMC article.
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A scalable variational approach to characterize pleiotropic components across thousands of human diseases and complex traits using GWAS summary statistics.
Zhang Z, Jung J, Kim A, Suboc N, Gazal S, Mancuso N.
Zhang Z, et al.
medRxiv [Preprint]. 2023 Mar 29:2023.03.27.23287801. doi: 10.1101/2023.03.27.23287801.
medRxiv. 2023.
PMID: 37034739
Free PMC article.
Updated.
Preprint.
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Leveraging Base Pair Mammalian Constraint to Understand Genetic Variation and Human Disease.
Sullivan PF, Meadows JRS, Gazal S, Phan BN, Li X, Genereux DP, Dong MX, Bianchi M, Andrews G, Sakthikumar S, Nordin J, Roy A, Christmas MJ, Marinescu VD, Wallerman O, Xue JR, Li Y, Yao S, Sun Q, Szatkiewicz J, Wen J, Huckins LM, Lawler AJ, Keough KC, Zheng Z, Zeng J, Wray NR, Johnson J, Chen J; Zoonomia Consortium; Paten B, Reilly SK, Hughes GM, Weng Z, Pollard KS, Pfenning AR, Forsberg-Nilsson K, Karlsson EK, Lindblad-Toh K.
Sullivan PF, et al.
bioRxiv [Preprint]. 2023 Mar 10:2023.03.10.531987. doi: 10.1101/2023.03.10.531987.
bioRxiv. 2023.
PMID: 36945512
Free PMC article.
Updated.
Preprint.
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Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity.
Gazal S, Weissbrod O, Hormozdiari F, Dey KK, Nasser J, Jagadeesh KA, Weiner DJ, Shi H, Fulco CP, O'Connor LJ, Pasaniuc B, Engreitz JM, Price AL.
Gazal S, et al.
Nat Genet. 2022 Jun;54(6):827-836. doi: 10.1038/s41588-022-01087-y. Epub 2022 Jun 6.
Nat Genet. 2022.
PMID: 35668300
Free PMC article.
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Partitioning gene-mediated disease heritability without eQTLs.
Weiner DJ, Gazal S, Robinson EB, O'Connor LJ.
Weiner DJ, et al.
Am J Hum Genet. 2022 Mar 3;109(3):405-416. doi: 10.1016/j.ajhg.2022.01.010. Epub 2022 Feb 9.
Am J Hum Genet. 2022.
PMID: 35143757
Free PMC article.
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