Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modeling

por Capanu, Marinela, Ionita-Laza, Iuliana
Publicado 2015

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 Applicatio...

por Fardo, David W., Ionita-Laza, Iuliana, Lange, Christoph
Publicado 2009

Cell Type-Specific Annotation and Fine Mapping of Variants Associated With Brain Disorders

por Doostparast Torshizi, Abolfazl, Ionita-Laza, Iuliana, Wang, Kai
Publicado 2020

A SPECTRAL APPROACH INTEGRATING FUNCTIONAL GENOMIC ANNOTATIONS FOR CODING AND NONCODING VARIANTS

por IONITA-LAZA, IULIANA, MCCALLUM, KENNETH, XU, BIN, BUXBAUM, JOSEPH
Publicado 2016

A semi-supervised approach for predicting cell-type specific functional consequences of non-coding variation using MPRAs

por He, Zihuai, Liu, Linxi, Wang, Kai, Ionita-Laza, Iuliana
Publicado 2018

A genome-wide scan statistic framework for whole-genome sequence data analysis

por He, Zihuai, Xu, Bin, Buxbaum, Joseph, Ionita-Laza, Iuliana
Publicado 2019

Rare Variant Analysis for Family-Based Design

por De, Gourab, Yip, Wai-Ki, Ionita-Laza, Iuliana, Laird, Nan
Publicado 2013

Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data

por Huang, Jing, Chen, Yong, Swartz, Michael D, Ionita-Laza, Iuliana
Publicado 2014

Quantile Regression for biomarkers in the UK Biobank

por Wang, Chen, Wang, Tianying, Wei, Ying, Aschard, Hugues, Ionita-Laza, Iuliana
Publicado 2023

A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease

por Ionita-Laza, Iuliana, Buxbaum, Joseph D., Laird, Nan M., Lange, Christoph
Publicado 2011

Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm

por Ding, Yuejing, Cong, Lei, Ionita-Laza, Iuliana, Lo, Shaw-Hwa, Zheng, Tian
Publicado 2007

Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches

por Fan, Ruixue, Huang, Chien-Hsun, Lo, Shaw-Hwa, Zheng, Tian, Ionita-Laza, Iuliana
Publicado 2011

Essential Tremor in a Charcot-Marie-Tooth Type 2C Kindred Does Not Segregate with the TRPV4 R269H Mutation

por Louis, Elan D., Hernandez, Nora, Ottman, Ruth, Ionita-Laza, Iuliana, Clark, Lorraine N.
Publicado 2014

Joint study of genetic regulators for expression traits related to breast cancer

por Zheng, Tian, Wang, Shuang, Cong, Lei, Ding, Yuejing, Ionita-Laza, Iuliana, Lo, Shaw-Hwa
Publicado 2007

Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism

por Ionita-Laza, Iuliana, Capanu, Marinela, De Rubeis, Silvia, McCallum, Kenneth, Buxbaum, Joseph D.
Publicado 2014

Small sample properties of rare variant analysis methods

por Swartz, Michael D, Kim, Taebeom, Niu, Jiangong, Yu, Robert K, Shete, Sanjay, Ionita-Laza, Iuliana
Publicado 2014

BIGKnock: fine-mapping gene-based associations via knockoff analysis of biobank-scale data

por Ma, Shiyang, Wang, Chen, Khan, Atlas, Liu, Linxi, Dalgleish, James, Kiryluk, Krzysztof, He, Zihuai, Ionita-Laza, Iuliana
Publicado 2023

Copy number variation genotyping using family information

por Chu, Jen-hwa, Rogers, Angela, Ionita-Laza, Iuliana, Darvishi, Katayoon, Mills, Ryan E, Lee, Charles, Raby, Benjamin A
Publicado 2013

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia

por Xu, Bin, Ionita-Laza, Iuliana, Roos, J. Louw, Boone, Braden, Woodrick, Scarlet, Sun, Yan, Levy, Shawn, Gogos, Joseph A., Karayiorgou, Maria
Publicado 2012

Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

por Erjavec, Stephanie O., Gelfman, Sahar, Abdelaziz, Alexa R., Lee, Eunice Y., Monga, Isha, Alkelai, Anna, Ionita-Laza, Iuliana, Petukhova, Lynn, Christiano, Angela M.
Publicado 2022