Các bài viết có thể truy cập công khai - Iuliana Ionita-LazaTìm hiểu thêm
Tổng thểNIHMRCNSFBMBFDFGWellcomeNSFCINSERMEuropean CommissionGovernment of ItalyHRBVAHHMIAHAAlzheimers's UKNIHRANRAutism Science Foundation, USADOEFWFCASAcademy of FinlandTelethonParkinson's UKRCNGovernment of SpainResearch Grants Council, Hong KongAutism Speaks Inc, USAParkinson's Foundation, USAFlorida Department of Health, USALeducq Foundation, USA
Không có ở bất kỳ nơi nào: 2
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
Các cơ quan ủy nhiệm: US National Institutes of Health
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
Các cơ quan ủy nhiệm: US National Institutes of Health
Có tại một số nơi: 87
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
Các cơ quan ủy nhiệm: US National Institutes of Health, Howard Hughes Medical Institute, Health …
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
Các cơ quan ủy nhiệm: US National Science Foundation, US National Institutes of Health, Autism …
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
Các cơ quan ủy nhiệm: US National Institutes of Health, Health Research Board, Ireland, UK Medical …
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
Các cơ quan ủy nhiệm: US National Institutes of Health
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
Các cơ quan ủy nhiệm: US National Institutes of Health
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
Các cơ quan ủy nhiệm: US National Institutes of Health
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
Các cơ quan ủy nhiệm: US National Institutes of Health
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
Các cơ quan ủy nhiệm: US National Institutes of Health
Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene
A Takata, B Xu, I Ionita-Laza, JL Roos, JA Gogos, M Karayiorgou
Neuron 82 (4), 773-780, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health
A new testing strategy to identify rare variants with either risk or protective effect on disease
I Ionita-Laza, JD Buxbaum, NM Laird, C Lange
PLoS Genetics 7 (2), e1001289, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
J Xie, L Liu, N Mladkova, Y Li, H Ren, W Wang, Z Cui, L Lin, X Hu, X Yu, ...
Nature communications 11 (1), 1600, 2020
Các cơ quan ủy nhiệm: US National Institutes of Health, Chinese Academy of Sciences, National …
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection
SM Zekavat, SH Lin, AG Bick, A Liu, K Paruchuri, C Wang, MM Uddin, ...
Nature medicine 27 (6), 1012-1024, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health, Howard Hughes Medical Institute, American …
De novo synonymous mutations in regulatory elements contribute to the genetic etiology of autism and schizophrenia
A Takata, I Ionita-Laza, JA Gogos, B Xu, M Karayiorgou
Neuron 89 (5), 940-947, 2016
Các cơ quan ủy nhiệm: US National Institutes of Health
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway
K Kiryluk, Y Li, Z Moldoveanu, H Suzuki, C Reily, P Hou, J Xie, ...
PLoS genetics 13 (2), e1006609, 2017
Các cơ quan ủy nhiệm: US National Institutes of Health
Disease heritability inferred from familial relationships reported in medical records
FCG Polubriaginof, R Vanguri, K Quinnies, GM Belbin, A Yahi, ...
Cell 173 (7), 1692-1704. e11, 2018
Các cơ quan ủy nhiệm: US National Science Foundation, US Department of Energy, US National …
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
Các cơ quan ủy nhiệm: US National Institutes of Health
Rare variant analysis for family-based design
G De, WK Yip, I Ionita-Laza, N Laird
PloS one 8 (1), e48495, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health
Estimating the number of unseen variants in the human genome
I Ionita-Laza, C Lange, N M. Laird
Proceedings of the National Academy of Sciences 106 (13), 5008-5013, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
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