Suchergebnisse - "Li, Xihao"

PubPharm (24)

1

MagicalRsq-X : A cross-cohort transferable genotype imputation quality metric

enthalten in: American journal of human genetics | 2024

von Sun, Q. | Yang, Y. | Rosen, J. | +24

2

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis

enthalten in: Circulation. Genomic and precision medicine | 2023

von Hasbani, N. | Westerman, K. | Kwak, S. | +59

3

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

enthalten in: American journal of human genetics | 2023

von Wang, Y. | Selvaraj, M. | Li, X. | +72

UpdateOf: medRxiv. 2023 Jun 29;:. - PMID 37425772

4

Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations

enthalten in: Nature communications | 2023

von Feofanova, E. | Brown, M. | Alkis, T. | +33

ErratumIn: Nat Commun. 2023 Oct 19;14(1):6611. - PMID 37857625

5

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

enthalten in: Nature genetics | 2023

von Li, X. | Quick, C. | Zhou, H. | +158

6

FAVOR : functional annotation of variants online resource and annotator for variation across the human genome

enthalten in: Nucleic acids research | 2023

von Zhou, H. | Arapoglou, T. | Li, X. | +22

7

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

enthalten in: Nature methods | 2022

von Li, Z. | Li, X. | Zhou, H. | +167

CommentIn: Nat Methods. 2022 Dec;19(12):1532-1533. - PMID 36316564

8

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

enthalten in: Nature communications | 2022

von Selvaraj, M. | Li, X. | Li, Z. | +183

9

Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer

enthalten in: Nature genetics | 2022

von Byun, J. | Han, Y. | Li, Y. | +82

10

STAAR workflow : a cloud-based workflow for scalable and reproducible rare variant analysis

enthalten in: Bioinformatics (Oxford, England) | 2022

von Gaynor, S. | Westerman, K. | Ackovic, L. | +5