Articles with public access mandates - Iuliana Ionita-LazaLearn more
OverallNIHMRCNSFBMBFDFGNSFCINSERMWellcomeEuropean CommissionGovernment of ItalyHRBVAHHMIAHAAlzheimers's UKNIHRANRAutism Science Foundation, USADOECASAcademy of FinlandTelethonParkinson's UKRCNGovernment of SpainAutism Speaks Inc, USAParkinson's Foundation, USAFlorida Department of Health, USALeducq Foundation, USA
Available somewhere: 84
Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF
YY Ho, I Ionita-Laza, R Ottman
Neurology 78 (8), 563-568, 2012
Mandates: US National Institutes of Health
A statistical framework for mapping risk genes from de novo mutations in whole-genome-sequencing studies
Y Liu, Y Liang, AE Cicek, Z Li, J Li, RA Muhle, M Krenzer, Y Mei, Y Wang, ...
The American Journal of Human Genetics 102 (6), 1031-1047, 2018
Mandates: US National Institutes of Health
Differences in plasma metabolites related to Alzheimer's disease, APOE ε4 status, and ethnicity
B Vardarajan, V Kalia, J Manly, A Brickman, D Reyes‐Dumeyer, ...
Alzheimer's & Dementia: Translational Research & Clinical Interventions 6 (1 …, 2020
Mandates: US National Institutes of Health
Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits
L Liu, A Khan, E Sanchez-Rodriguez, F Zanoni, Y Li, N Steers, O Balderes, ...
Nature communications 13 (1), 6859, 2022
Mandates: US National Institutes of Health, German Research Foundation, Florida …
Identification of putative causal loci in whole-genome sequencing data via knockoff statistics
Z He, L Liu, C Wang, Y Le Guen, J Lee, S Gogarten, F Lu, S Montgomery, ...
Nature communications 12 (1), 3152, 2021
Mandates: US National Institutes of Health
Copy number variation prevalence in known asthma genes and their impact on asthma susceptibility
AJ Rogers, JH Chu, K Darvishi, I Ionita‐Laza, H Lehmann, R Mills, C Lee, ...
Clinical & Experimental Allergy 43 (4), 455-462, 2013
Mandates: US National Institutes of Health
Multitrait GWAS to connect disease variants and biological mechanisms
H Julienne, V Laville, ZR McCaw, Z He, V Guillemot, C Lasry, A Ziyatdinov, ...
PLoS genetics 17 (8), e1009713, 2021
Mandates: US National Institutes of Health, Agence Nationale de la Recherche
CARMA is a new Bayesian model for fine-mapping in genome-wide association meta-analyses
Z Yang, C Wang, L Liu, A Khan, A Lee, B Vardarajan, R Mayeux, K Kiryluk, ...
Nature Genetics 55 (6), 1057-1065, 2023
Mandates: US National Institutes of Health
Genome-wide analysis of common and rare variants via multiple knockoffs at biobank scale, with an application to Alzheimer disease genetics
Z He, Y Le Guen, L Liu, J Lee, S Ma, AC Yang, X Liu, J Rutledge, ...
The American Journal of Human Genetics 108 (12), 2336-2353, 2021
Mandates: US National Institutes of Health, National Institute of Health and Medical …
QRank: a novel quantile regression tool for eQTL discovery
X Song, G Li, Z Zhou, X Wang, I Ionita-Laza, Y Wei
Bioinformatics 33 (14), 2123-2130, 2017
Mandates: US National Institutes of Health
A general and robust framework for secondary traits analysis
X Song, I Ionita-Laza, M Liu, J Reibman, Y Wei
Genetics 202 (4), 1329-1343, 2016
Mandates: US National Science Foundation, US National Institutes of Health
A multi-dimensional integrative scoring framework for predicting functional variants in the human genome
X Li, G Yung, H Zhou, R Sun, Z Li, K Hou, MJ Zhang, Y Liu, T Arapoglou, ...
The American Journal of Human Genetics 109 (3), 446-456, 2022
Mandates: US National Institutes of Health
On quality control measures in genome-wide association studies: a test to assess the genotyping quality of individual probands in family-based association studies and an …
DW Fardo, I Ionita-Laza, C Lange
PLoS Genetics 5 (7), e1000572, 2009
Mandates: US National Institutes of Health
Genetic variants within the serotonin transporter associated with familial risk for major depression
A Talati, G Guffanti, Z Odgerel, I Ionita-Laza, H Malm, A Sourander, ...
Psychiatry research 228 (1), 170-173, 2015
Mandates: US National Institutes of Health
Quantile regression in the secondary analysis of case–control data
Y Wei, X Song, M Liu, I Ionita-Laza, J Reibman
Journal of the American Statistical Association 111 (513), 344-354, 2016
Mandates: US National Science Foundation, US National Institutes of Health
Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
SO Erjavec, S Gelfman, AR Abdelaziz, EY Lee, I Monga, A Alkelai, ...
Nature communications 13 (1), 800, 2022
Mandates: US National Institutes of Health
Copy number variant analysis and genome-wide association study identify loci with large effect for vesicoureteral reflux
M Verbitsky, P Krithivasan, E Batourina, A Khan, SE Graham, M Marasà, ...
Journal of the American Society of Nephrology 32 (4), 805-820, 2021
Mandates: US National Institutes of Health, Health Research Board, Ireland
Linkage disequilibrium mapping of the chromosome 6q21–22.31 bipolar I disorder susceptibility locus
J Fan, I Ionita‐Laza, MB McQueen, B Devlin, S Purcell, SV Faraone, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010
Mandates: US National Institutes of Health
Powerful gene-based testing by integrating long-range chromatin interactions and knockoff genotypes
S Ma, J Dalgleish, J Lee, C Wang, L Liu, R Gill, JD Buxbaum, WK Chung, ...
Proceedings of the National Academy of Sciences 118 (47), e2105191118, 2021
Mandates: US National Institutes of Health, UK Medical Research Council
Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies
D Xu, C Wang, A Khan, N Shang, Z He, A Gordon, IJ Kullo, S Murphy, Y Ni, ...
NPJ Digital Medicine 4 (1), 116, 2021
Mandates: US National Institutes of Health
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