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
Family-based association tests for sequence data, and comparisons with population-based association tests
I Ionita-Laza, S Lee, V Makarov, JD Buxbaum, X Lin
European Journal of Human Genetics 21 (10), 1158-1162, 2013
Mandates: US National Institutes of Health
FUN-LDA: a latent dirichlet allocation model for predicting tissue-specific functional effects of noncoding variation: methods and applications
D Backenroth, Z He, K Kiryluk, V Boeva, L Petukhova, E Khurana, ...
The American Journal of Human Genetics 102 (5), 920-942, 2018
Mandates: US National Institutes of Health
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection
NJ Steers, Y Li, Z Drace, JA D’Addario, C Fischman, L Liu, K Xu, YJ Na, ...
New England Journal of Medicine 380 (20), 1918-1928, 2019
Mandates: US National Institutes of Health, UK Medical Research Council, Government of …
Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13. 3 as a susceptibility gene for schizophrenia and autism
I Ionita-Laza, B Xu, V Makarov, JD Buxbaum, JL Roos, JA Gogos, ...
Proceedings of the National Academy of Sciences 111 (1), 343-348, 2014
Mandates: US National Institutes of Health
Genome-wide polygenic score to predict chronic kidney disease across ancestries
A Khan, MC Turchin, A Patki, V Srinivasasainagendra, N Shang, ...
Nature medicine 28 (7), 1412-1420, 2022
Mandates: US National Institutes of Health
Refinement of primate copy number variationhotspots identifies candidate genomic regions evolving under positive selection
O Gokcumen, PL Babb, RC Iskow, Q Zhu, X Shi, RE Mills, I Ionita-Laza, ...
Genome Biology 12, 1-11, 2011
Mandates: US National Institutes of Health
Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets
I Ionita-Laza, V Makarov, JD Buxbaum
The American Journal of Human Genetics 90 (6), 1002-1013, 2012
Mandates: US National Institutes of Health
Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism
I Ionita-Laza, M Capanu, S De Rubeis, K McCallum, JD Buxbaum
PLoS genetics 10 (12), e1004729, 2014
Mandates: US National Institutes of Health
A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs
Z He, L Liu, K Wang, I Ionita-Laza
Nature communications 9 (1), 5199, 2018
Mandates: US National Institutes of Health
Finding disease variants in Mendelian disorders by using sequence data: methods and applications
I Ionita-Laza, V Makarov, S Yoon, B Raby, J Buxbaum, DL Nicolae, X Lin
The American Journal of Human Genetics 89 (6), 701-712, 2011
Mandates: US National Institutes of Health
The interaction of glutathione S‐transferase M1‐null variants with tobacco smoke exposure and the development of childhood asthma
AJ Rogers, C Brasch‐Andersen, I Ionita‐Laza, A Murphy, S Sharma, ...
Clinical & Experimental Allergy 39 (11), 1721-1729, 2009
Mandates: US National Institutes of Health
Returning integrated genomic risk and clinical recommendations: The eMERGE study
JE Linder, A Allworth, HT Bland, PJ Caraballo, RL Chisholm, EW Clayton, ...
Genetics in Medicine 25 (4), 100006, 2023
Mandates: US National Institutes of Health
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
Mandates: US National Science Foundation, US National Institutes of Health, German …
Unified sequence-based association tests allowing for multiple functional annotations and meta-analysis of noncoding variation in metabochip data
Z He, B Xu, S Lee, I Ionita-Laza
The American Journal of Human Genetics 101 (3), 340-352, 2017
Mandates: US National Institutes of Health
Identification of candidate genes for familial early-onset essential tremor
X Liu, N Hernandez, S Kisselev, A Floratos, A Sawle, I Ionita-Laza, ...
European Journal of Human Genetics 24 (7), 1009-1015, 2016
Mandates: US National Institutes of Health, Parkinson's Foundation, USA
Medical records-based chronic kidney disease phenotype for clinical care and “big data” observational and genetic studies
N Shang, A Khan, F Polubriaginof, F Zanoni, K Mehl, D Fasel, PE Drawz, ...
Npj Digital Medicine 4 (1), 70, 2021
Mandates: US National Institutes of Health
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
Mandates: US National Science Foundation, US National Institutes of Health, US …
Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs
I Ionita-Laza, R Ottman
Genetics 189 (3), 1061-1068, 2011
Mandates: US National Institutes of Health
A genome-wide scan statistic framework for whole-genome sequence data analysis
Z He, B Xu, J Buxbaum, I Ionita-Laza
Nature communications 10 (1), 3018, 2019
Mandates: US National Institutes of Health
Does rate of progression run in essential tremor families? Slower vs. faster progressors
ED Louis, N Hernandez, I Ionita-Laza, R Ottman, LN Clark
Parkinsonism & related disorders 19 (3), 363-366, 2013
Mandates: US National Institutes of Health
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