Articles with public access mandates - Iuliana Ionita-Laza - US National Institutes of HealthLearn more
NoteFor this mandate, articles should be available from specific locations.
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
Not available based on mandate: 12
On the analysis of copy‐number variations in genome‐wide association studies: a translation of the family‐based association test
I Ionita‐Laza, GH Perry, BA Raby, B Klanderman, C Lee, NM Laird, ...
Genetic Epidemiology 32 (3), 273-284, 2008
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, SD Rubeis, JY An, ...
BioRxiv, 484113, 2018
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
K Kiryluk, E Sanchez-Rodriguez, XJ Zhou, F Zanoni, L Liu, N Mladkova, ...
Nature genetics 55 (7), 1091-1105, 2023
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
Statistical challenges in sequence-based association studies with population-and family-based designs
I Ionita-Laza, MH Cho, NM Laird
Statistics in Biosciences 5, 54-70, 2013
Integrated Quantile RAnk Test (iQRAT) for gene-level associations
T Wang, I Ionita-Laza, Y Wei
The Annals of Applied Statistics 16 (3), 1423-1444, 2022
Discovering influential variables: a general computer intensive method for common genetic disorders
T Zheng, H Chernoff, I Hu, I Ionita-Laza, SH Lo
Handbook of statistical bioinformatics, 87-107, 2011
GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy
K Kiryluk, E Sanchez-Rodriguez, X Zhou, F Zanoni, L Liu, N Mladkova, ...
medRxiv, 2021.11. 19.21265383, 2021
Summary statistics knockoff inference empowers identification of putative causal variants in genome-wide association studies
Z He, L Liu, ME Belloy, Y Le Guen, A Sossin, X Liu, X Qi, S Ma, ...
bioRxiv, 2021.12. 06.471440, 2021
Genome-wide polygenic score with APOL1 risk genotypes predicts chronic kidney disease across major continental ancestries
A Khan, MC Turchin, A Patki, V Srinivasasainagendra, N Shang, ...
medRxiv, 2021.10. 25.21265398, 2021
Zihuai He,* Yann Le Guen, Linxi Liu, 4 Justin Lee, 2 Shiyang Ma, 5 Andrew C. Yang, Xiaoxia Liu, Jarod Rutledge, 6 Patricia Moran Losada, Bowen Song, 7 Michael E. Belloy, Robert …
MD Greicius, I Ionita-Laza
A novel quantile regression approach for eQTL discovery
X Song, G Li, I Ionita-Laza, Y Wei
bioRxiv, 070052, 2016
Available based on mandate: 74
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
A spectral approach integrating functional genomic annotations for coding and noncoding variants
I Ionita-Laza, K McCallum, B Xu, JD Buxbaum
Nature genetics 48 (2), 214-220, 2016
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE
L Bertram, C Lange, K Mullin, M Parkinson, M Hsiao, MF Hogan, ...
The American Journal of Human Genetics 83 (5), 623-632, 2008
Sequence kernel association tests for the combined effect of rare and common variants
I Ionita-Laza, S Lee, V Makarov, JD Buxbaum, X Lin
The American Journal of Human Genetics 92 (6), 841-853, 2013
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia
B Xu, I Ionita-Laza, JL Roos, B Boone, S Woodrick, Y Sun, S Levy, ...
Nature genetics 44 (12), 1365-1369, 2012
Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis
I Ionita-Laza, AJ Rogers, C Lange, BA Raby, C Lee
Genomics 93 (1), 22-26, 2009
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