Iuliana Ionita-Laza
Iuliana Ionita-Laza
Associate Professor of Biostatistics, Columbia University
Email verificata su columbia.edu - Home page
TitoloCitata daAnno
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, AE Cicek, ...
Nature 515 (7526), 209, 2014
12842014
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
3982008
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, 2012
3632012
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
2832013
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, 2016
2142016
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
2072009
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
1532011
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
1002014
Genomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scan
I Ionita-Laza, MB McQueen, NM Laird, C Lange
The American Journal of Human Genetics 81 (3), 607-614, 2007
942007
Rare variant analysis for family-based design
G De, WK Yip, I Ionita-Laza, N Laird
PloS one 8 (1), e48495, 2013
842013
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, 2013
742013
Estimating the number of unseen variants in the human genome
I Ionita-Laza, C Lange, NM Laird
Proceedings of the National Academy of Sciences 106 (13), 5008-5013, 2009
682009
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
652008
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
642016
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
612014
Refinement of primate copy number variation hotspots 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 (5), R52, 2011
552011
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
542012
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
452011
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
392017
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
382014
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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