He Z - Search Results

1

KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design.

Yang Y, Wang C, Liu L, Buxbaum J, He Z, Ionita-Laza I. Yang Y, et al. Among authors: he z. Am J Hum Genet. 2022 Oct 6;109(10):1761-1776. doi: 10.1016/j.ajhg.2022.08.013. Epub 2022 Sep 22. Am J Hum Genet. 2022. PMID: 36150388 Free PMC article.

2

A powerful nonparametric statistical framework for family-based association analyses.

Li M, He Z, Schaid DJ, Cleves MA, Nick TG, Lu Q. Li M, et al. Among authors: he z. Genetics. 2015 May;200(1):69-78. doi: 10.1534/genetics.115.175174. Epub 2015 Mar 5. Genetics. 2015. PMID: 25745024 Free PMC article.

3

Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data.

He Z, Xu B, Lee S, Ionita-Laza I. He Z, et al. Am J Hum Genet. 2017 Sep 7;101(3):340-352. doi: 10.1016/j.ajhg.2017.07.011. Epub 2017 Aug 24. Am J Hum Genet. 2017. PMID: 28844485 Free PMC article.

4

Rare-variant association tests in longitudinal studies, with an application to the Multi-Ethnic Study of Atherosclerosis (MESA).

He Z, Lee S, Zhang M, Smith JA, Guo X, Palmas W, Kardia SLR, Ionita-Laza I, Mukherjee B. He Z, et al. Genet Epidemiol. 2017 Dec;41(8):801-810. doi: 10.1002/gepi.22081. Epub 2017 Oct 27. Genet Epidemiol. 2017. PMID: 29076270 Free PMC article.

5

FUN-LDA: A Latent Dirichlet Allocation Model for Predicting Tissue-Specific Functional Effects of Noncoding Variation: Methods and Applications.

Backenroth D, He Z, Kiryluk K, Boeva V, Pethukova L, Khurana E, Christiano A, Buxbaum JD, Ionita-Laza I. Backenroth D, et al. Among authors: he z. Am J Hum Genet. 2018 May 3;102(5):920-942. doi: 10.1016/j.ajhg.2018.03.026. Am J Hum Genet. 2018. PMID: 29727691 Free PMC article.

6

A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs.

He Z, Liu L, Wang K, Ionita-Laza I. He Z, et al. Nat Commun. 2018 Dec 5;9(1):5199. doi: 10.1038/s41467-018-07349-w. Nat Commun. 2018. PMID: 30518757 Free PMC article.

7

A genome-wide scan statistic framework for whole-genome sequence data analysis.

He Z, Xu B, Buxbaum J, Ionita-Laza I. He Z, et al. Nat Commun. 2019 Jul 9;10(1):3018. doi: 10.1038/s41467-019-11023-0. Nat Commun. 2019. PMID: 31289270 Free PMC article.

8

Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.

He Z, Liu L, Wang C, Le Guen Y, Lee J, Gogarten S, Lu F, Montgomery S, Tang H, Silverman EK, Cho MH, Greicius M, Ionita-Laza I. He Z, et al. Nat Commun. 2021 May 25;12(1):3152. doi: 10.1038/s41467-021-22889-4. Nat Commun. 2021. PMID: 34035245 Free PMC article.

9

Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies.

Xu D, Wang C, Khan A, Shang N, He Z, Gordon A, Kullo IJ, Murphy S, Ni Y, Wei WQ, Gharavi A, Kiryluk K, Weng C, Ionita-Laza I. Xu D, et al. Among authors: he z. NPJ Digit Med. 2021 Jul 23;4(1):116. doi: 10.1038/s41746-021-00488-3. NPJ Digit Med. 2021. PMID: 34302027 Free PMC article.

10

Multitrait GWAS to connect disease variants and biological mechanisms.

Julienne H, Laville V, McCaw ZR, He Z, Guillemot V, Lasry C, Ziyatdinov A, Nerin C, Vaysse A, Lechat P, Ménager H, Le Goff W, Dube MP, Kraft P, Ionita-Laza I, Vilhjálmsson BJ, Aschard H. Julienne H, et al. Among authors: he z. PLoS Genet. 2021 Aug 30;17(8):e1009713. doi: 10.1371/journal.pgen.1009713. eCollection 2021 Aug. PLoS Genet. 2021. PMID: 34460823 Free PMC article.

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