Iuliana Ionita‐Laza

ORCID: 0000-0002-9001-2026

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 34 papers. Top paper: “Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism”.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Cell(2020)10.1016/j.cell.2019.12.036

N/A

9.5DataRank · unranked

2470 citations

Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An +95 more

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Nature Medicine(2021)10.1038/s41591-021-01371-0

N/A

4.7DataRank · unranked

194 citations

Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri, Chen Wang +95 more

Genome-wide polygenic score to predict chronic kidney disease across ancestries

Nature Medicine(2022)10.1038/s41591-022-01869-1

N/A

0.764DataRank · unranked

162 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +34 more

Multitrait GWAS to connect disease variants and biological mechanisms

PLoS Genetics(2021)10.1371/journal.pgen.1009713

N/A

0.550DataRank · unranked

38 citations

Vincent Laville, Zachary R. McCaw, Zihuai He, Vincent Guillemot, Carla Lasry +12 more

A multi-dimensional integrative scoring framework for predicting functional variants in the human genome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.01.017

N/A

0.505DataRank · unranked

28 citations

Godwin Yung, Hufeng Zhou, Ryan Sun, Zilin Li, Kangcheng Hou +7 more

Liability threshold model-based disease risk prediction based on electronic health record phenotypes

Nature Genetics(2025)10.1038/s41588-025-02370-4

N/A

0.292DataRank · unranked

6 citations

Atlas Khan, Chen Wang, Chunhua Weng, Joseph D. Buxbaum, Krzysztof Kiryluk +2 more

Genome-wide polygenic score with APOL1 risk genotypes predicts chronic kidney disease across major continental ancestries

medRxiv(2021)10.1101/2021.10.25.21265398

N/A

0.218DataRank · unranked

2 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +33 more

Genome-wide analysis of common and rare variants via multiple knockoffs at biobank scale, with an application to Alzheimer disease genetics

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.10.009

N/A

0DataRank · unranked

30 citations

Yann Le Guen, Linxi Liu, Justin Lee, Shiyang Ma, Andrew C. Yang +13 more

Powerful gene-based testing by integrating long-range chromatin interactions and knockoff genotypes

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2105191118

N/A

0DataRank · unranked

20 citations

James Dalgleish, Justin Lee, Chen Wang, Linxi Liu, Richard Gill +8 more

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

npj Digital Medicine(2021)10.1038/s41746-021-00488-3

N/A

0DataRank · unranked

17 citations

Chen Wang, Atlas Khan, Ning Shang, Zihuai He, Allan Gordon +9 more

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

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.08.434451

N/A

0DataRank · unranked

4 citations

Linxi Liu, Chen Wang, Yann Le Guen, Justin Lee, Stephanie M. Gogarten +8 more

Powerful gene-based testing by integrating long-range chromatin interactions and knockoff genotypes

medRxiv(2021)10.1101/2021.07.14.21260405

N/A

0DataRank · unranked

4 citations

James Dalgleish, Justin Lee, Chen Wang, Linxi Liu, Richard Gill +8 more

Summary statistics knockoff inference empowers identification of putative causal variants in genome-wide association studies

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.06.471440

N/A

0DataRank · unranked

2 citations

Linxi Liu, Michaël E. Belloy, Yann Le Guen, Aaron Sossin, Xiaoxia Liu +9 more

Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

Nature Communications(2022)10.1038/s41467-022-28343-3

N/A

0DataRank · unranked

34 citations

Sahar Gelfman, A.R. Abdelaziz, Eunice Lee, Isha Monga, Anna Alkelai +4 more

GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

Nature Communications(2022)10.1038/s41467-022-34932-z

N/A

0DataRank · unranked

29 citations

Linxi Liu, Michaël E. Belloy, Yann Le Guen, Aaron Sossin, Xiaoxia Liu +10 more

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

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.013

N/A

0DataRank · unranked

13 citations

Chen Wang, Linxi Liu, Joseph D. Buxbaum, Zihuai He, Iuliana Ionita‐Laza +1 more

Air pollution and decreased bone mineral density among Women's Health Initiative participants

EClinicalMedicine(2023)10.1016/j.eclinm.2023.101864

N/A

0DataRank · unranked

37 citations

Carolyn Crandall, Allison Kupsco, Marianthi‐Anna Kioumourtzoglou, James D. Stewart, Duanping Liao +9 more

Genome-wide discovery for biomarkers using quantile regression at biobank scale

Nature Communications(2024)10.1038/s41467-024-50726-x

N/A

0DataRank · unranked

18 citations

Tianying Wang, Krzysztof Kiryluk, Ying Wei, Hugues Aschard, Iuliana Ionita‐Laza +1 more

linc-ADAIN, a human adipose lincRNA, regulates adipogenesis by modulating KLF5 and IL-8 mRNA stability

Cell Reports(2024)10.1016/j.celrep.2024.114240

N/A

0DataRank · unranked

7 citations

Sebastian Ho, Johana Coronel, Lucie Zhu, Wen Liu, Chenyi Xue +13 more

KnockoffHybrid: A knockoff framework for hybrid analysis of trio and population designs in genome-wide association studies

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.003

N/A

0DataRank · unranked

4 citations

Qi Wang, Chen Wang, Joseph D. Buxbaum, Iuliana Ionita‐Laza, Yi Yang

Local genetic correlation via knockoffs reduces confounding due to cross-trait assortative mating

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.012

N/A

0DataRank · unranked

1 citations

Fan Wang, Richard Border, Joseph D. Buxbaum, Noah Zaitlen, Iuliana Ionita‐Laza +1 more

Beyond guilty by association at scale: searching for causal variants on the basis of genome-wide summary statistics

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.28.582621

N/A

0DataRank · unranked

5 citations

Benjamin B. Chu, James Yang, Jiaqi Gu, Zhaomeng Chen, Linxi Liu +12 more

Air pollution and decreased bone mineral density among Women's Health Initiative participants

Carolina Digital Repository (University of North Carolina at Chapel Hill)(2024)10.17615/93f0-vd23

N/A

0DataRank · unranked

0 citations

Duanping Liao, D. Prada‐Rodríguez, Iuliana Ionita‐Laza, Gary W. Miller, J.D Stewart +9 more

Fine-mapping in admixed populations using CARMA-X, with applications to Latin American studies

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.020

N/A

0DataRank · unranked

4 citations

Chen Wang, Yuridia S. Posadas‐García, Valeria Añorve-Garibay, Badri N. Vardarajan, Andrés Moreno‐Estrada +4 more

Computationally efficient whole-genome quantile regression at biobank scale

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2513007122

N/A

0DataRank · unranked

1 citations

Chen Wang, Tianying Wang, Marco Masala, Edoardo Fiorillo, Marcella Devoto +3 more

Quantile-specific confounding: correction for subtle population stratification via quantile regression

Genetics(2025)10.1093/genetics/iyaf138

N/A

0DataRank · unranked

1 citations

Marco Masala, Edoardo Fiorillo, Marcella Devoto, Francesco Cucca, Iuliana Ionita‐Laza +1 more

Regenie.QRS: computationally efficient whole-genome quantile regression at biobank scale

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.02.651730

N/A

0DataRank · unranked

4 citations

Chen Wang, Tianying Wang, Marco Masala, Edoardo Fiorillo, Marcella Devoto +3 more

Uncovering Heterogeneous Effects via Localized Feature Selection

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.03.657761

N/A

0DataRank · unranked

0 citations

Jiaqi Gu, Zhaomeng Chen, Benjamin B. Chu, Linxi Liu, Tim Morrison +10 more

Differences in plasma metabolites related to Alzheimer's disease, APOE ε4 status, and ethnicity

Alzheimer s & Dementia Translational Research & Clinical Interventions(2020)10.1002/trc2.12025

N/A

0DataRank · unranked

25 citations

Vrinda Kalia, Jennifer J. Manly, Adam M. Brickman, Dolly Reyes‐Dumeyer, Rafael Lantigua +5 more

Co-localization between Sequence Constraint and Epigenomic Information Improves Interpretation of Whole-Genome Sequencing Data

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.03.003

N/A

0DataRank · unranked

4 citations

Chen Wang, Krzysztof Kiryluk, Joseph D. Buxbaum, Iuliana Ionita‐Laza, Danqing Xu

Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain Disorders

Frontiers in Genetics(2020)10.3389/fgene.2020.575928

N/A

0DataRank · unranked

4 citations

Iuliana Ionita‐Laza, Kai Wang, Abolfazl Doostparast Torshizi

Multitrait genetic-phenotype associations to connect disease variants and biological mechanisms

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.26.172999

N/A

0DataRank · unranked

6 citations

Vincent Laville, Zachary R. McCaw, Zihuai He, Vincent Guillemot, Carla Lasry +11 more

Differences in Plasma Metabolites Related to Alzheimer’s Disease, APOE-ε4 status and Ethnicity

medRxiv(2020)10.1101/2020.01.10.20016741

N/A

0DataRank · unranked

1 citations

Vrinda Kalia, Jennifer J. Manly, Adam M. Brickman, Dolly Reyes‐Dumeyer, Rafael Lantigua +5 more

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

Nature Communications(2021)10.1038/s41467-021-22889-4

N/A

0DataRank · unranked

42 citations

Linxi Liu, Chen Wang, Yann Le Guen, Justin Lee, Stephanie M. Gogarten +8 more