Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits

по Oualkacha, Karim, Lakhal-Chaieb, Lajmi, Greenwood, Celia MT
Опубликовано в: Int J Epidemiol (2016)

Pathway analysis for genetic association studies: to do, or not to do? That is the question

по Dufresne, Line, Oualkacha, Karim, Forgetta, Vincenzo, Greenwood, Celia MT
Опубликовано 2014

CpG-set association assessment of lipid concentration changes and DNA methylation

по Zhao, Kaiqiong, Jiang, Lai, Klein, Kathleen, Greenwood, Celia M. T., Oualkacha, Karim
Опубликовано в: BMC Proc (2018)

Joint analysis of multiple blood pressure phenotypes in GAW19 data by using a multivariate rare-variant association test

по Sun, Jianping, Bhatnagar, Sahir R., Oualkacha, Karim, Ciampi, Antonio, Greenwood, Celia M. T.
Опубликовано в: BMC Proc (2016)

Investigating potential causal relationships between SNPs, DNA methylation and HDL

по Jiang, Lai, Zhao, Kaiqiong, Klein, Kathleen, Canty, Angelo J., Oualkacha, Karim, Greenwood, Celia M. T.
Опубликовано в: BMC Proc (2018)

Performance of an allele‐level multi‐locus HLA genotype imputation tool in hematopoietic stem cell donors from Quebec

по Ferradji, Abdelhakim, D'Souza, Yasmin, Saw, Chee Loong, Oualkacha, Karim, Richard, Lucie, Sapir‐Pichhadze, Ruth
Опубликовано в: Immun Inflamm Dis (2017)

Gene Coexpression Analyses Differentiate Networks Associated with Diverse Cancers Harboring TP53 Missense or Null Mutations

по Oros Klein, Kathleen, Oualkacha, Karim, Lafond, Marie-Hélène, Bhatnagar, Sahir, Tonin, Patricia N., Greenwood, Celia M. T.
Опубликовано в: Front Genet (2016)

A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects

по Sun, Jianping, Oualkacha, Karim, Forgetta, Vincenzo, Zheng, Hou-Feng, Brent Richards, J, Ciampi, Antonio, Greenwood, Celia MT
Опубликовано в: Eur J Hum Genet (2016)

Causal modeling in a multi-omic setting: insights from GAW20

по Auerbach, Jonathan, Howey, Richard, Jiang, Lai, Justice, Anne, Li, Liming, Oualkacha, Karim, Sayols-Baixeras, Sergi, Aslibekyan, Stella W.
Опубликовано в: BMC Genet (2018)

Exome-wide rare variant analyses of two bone mineral density phenotypes: the challenges of analyzing rare genetic variation

по Sun, Jianping, Oualkacha, Karim, Forgetta, Vincenzo, Zheng, Hou-Feng, Richards, J. Brent, Evans, Daniel S., Orwoll, Eric, Greenwood, Celia M. T.
Опубликовано в: Sci Rep (2018)

Simultaneous SNP selection and adjustment for population structure in high dimensional prediction models

по Bhatnagar, Sahir R., Yang, Yi, Lu, Tianyuan, Schurr, Erwin, Loredo-Osti, JC, Forest, Marie, Oualkacha, Karim, Greenwood, Celia M. T.
Опубликовано в: PLoS Genet (2020)

Constrained instruments and their application to Mendelian randomization with pleiotropy

по Jiang, Lai, Oualkacha, Karim, Didelez, Vanessa, Ciampi, Antonio, Rosa‐Neto, Pedro, Benedet, Andrea L., Mathotaarachchi, Sulantha, Richards, John Brent, Greenwood, Celia M. T.
Опубликовано в: Genet Epidemiol (2019)

Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemia

по Lajoie, Mathieu, Drouin, Simon, Caron, Maxime, St-Onge, Pascal, Ouimet, Manon, Gioia, Romain, Lafond, Marie-Hélène, Vidal, Ramon, Richer, Chantal, Oualkacha, Karim, Droit, Arnaud, Sinnett, Daniel
Опубликовано в: PLoS One (2017)

On Path to Informing Hierarchy of Eplet Mismatches as Determinants of Kidney Transplant Loss

по Mohammadhassanzadeh, Hossein, Oualkacha, Karim, Zhang, Wenmin, Klement, William, Bourdiec, Amelie, Lamsatfi, Jennat, Yi, Yang, Foster, Bethany, Keown, Paul, Gebel, Howard M., Claas, Frans, Sapir-Pichhadze, Ruth
Опубликовано в: Kidney Int Rep (2021)