Identifying rare-variant associations in parent-child trios using a Gaussian support vector machine

por Lu, Ake T, Cantor, Rita M
Publicado 2014

Gene expression in large pedigrees: analytic approaches

por Cantor, Rita M., Cordell, Heather J.
Publicado 2016

Genetic complexity at expression quantitative trait loci

por Cantor, Rita M., Pan, Calvin, Siegmund, Kimberly
Publicado 2016

Co-regulation and multilocus determinants of gene expression in humans

por Kerner, Berit, Bailey, Julia N, Cantor, Rita M
Publicado 2007

Detecting responses to treatment with fenofibrate in pedigrees

por Cherlin, Svetlana, Wang, Maggie Haitian, Bickeböller, Heike, Cantor, Rita M.
Publicado 2018

Support for calcium channel gene defects in autism spectrum disorders

por Lu, Ake Tzu-Hui, Dai, Xiaoxian, Martinez-Agosto, Julian A, Cantor, Rita M
Publicado 2012

Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

por Werling, Donna M, Lowe, Jennifer K, Luo, Rui, Cantor, Rita M, Geschwind, Daniel H
Publicado 2014

ASD Restricted and Repetitive Behaviors Associated at 17q21.33: Genes Prioritized by Expression in Fetal Brains

por Cantor, Rita M., Navarro, Linda, Won, Hyejung, Walker, Rebecca L., Lowe, Jennifer K., Geschwind, Daniel H.
Publicado 2017

Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression

por Link, Jenny C., Hasin-Brumshtein, Yehudit, Cantor, Rita M., Chen, Xuqi, Arnold, Arthur P., Lusis, Aldons J., Reue, Karen
Publicado 2017

“High Density SNP Association Study of the 17q21 Chromosomal Region Linked to Autism Identifies CACNA1G as a Novel Candidate Gene”

por Strom, Samuel P., Stone, Jennifer L., Bosch, John R. ten, Merriman, Barry, Cantor, Rita M., Geschwind, Daniel H., Nelson, Stanley F.
Publicado 2009

Repurposing Dantrolene for Long-Term Combination Therapy to Potentiate Antisense-Mediated DMD Exon Skipping in the mdx Mouse

por Wang, Derek W., Mokhonova, Ekaterina I., Kendall, Genevieve C., Becerra, Diana, Naeini, Yalda B., Cantor, Rita M., Spencer, Melissa J., Nelson, Stanley F., Miceli, M. Carrie
Publicado 2018

Anatomic Brain Asymmetry in Vervet Monkeys

por Fears, Scott C., Scheibel, Kevin, Abaryan, Zvart, Lee, Chris, Service, Susan K., Jorgensen, Matthew J., Fairbanks, Lynn A., Cantor, Rita M., Freimer, Nelson B., Woods, Roger P.
Publicado 2011

Impact of Individual Traits, Saturated Fat, and Protein Source on the Gut Microbiome

por Lang, Jennifer M., Pan, Calvin, Cantor, Rita M., Tang, W. H. Wilson, Garcia-Garcia, Jose Carlos, Kurtz, Ira, Hazen, Stanley L., Bergeron, Nathalie, Krauss, Ronald M., Lusis, Aldons J.
Publicado 2018

DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype

por Wang, Richard T., Barthelemy, Florian, Martin, Ann S., Douine, Emilie D., Eskin, Ascia, Lucas, Ann, Lavigne, Jenifer, Peay, Holly, Khanlou, Negar, Sweeney, Lee, Cantor, Rita M., Miceli, M. Carrie, Nelson, Stanley F.
Publicado 2018

Genome-wide burden of deleterious coding variants increased in schizophrenia

por Loohuis, Loes M. Olde, Vorstman, Jacob A. S., Ori, Anil P., Staats, Kim A., Wang, Tina, Richards, Alexander L., Leonenko, Ganna, Walters, James T., DeYoung, Joseph, Cantor, Rita M., Ophoff, Roel A.
Publicado 2015

GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics

por Tintle, Nathan L., Fardo, David W., de Andrade, Mariza, Aslibekyan, Stella, Bailey, Julia N., Bermejo, Justo Lorenzo, Cantor, Rita M., Ghosh, Saurabh, Melton, Philip, Wang, Xuexia, MacCluer, Jean W., Almasy, Laura
Publicado 2018

Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors

por Almasy, Laura, Amos, Christopher I, Bailey-Wilson, Joan E, Cantor, Rita M, Jaquish, Cashell E, Martinez, Maria, Neuman, Rosalind J, Olson, Jane M, Palmer, Lyle J, Rich, Stephen S, Spence, M Anne, MacCluer, Jean W
Publicado 2003

Online Self-Report Data for Duchenne Muscular Dystrophy Confirms Natural History and Can Be Used to Assess for Therapeutic Benefits

por Wang, Richard T., Silverstein Fadlon, Cheri A., Ulm, J. Wes, Jankovic, Ivana, Eskin, Ascia, Lu, Ake, Rangel Miller, Vanessa, Cantor, Rita M., Li, Ning, Elashoff, Robert, Martin, Anne S., Peay, Holly L., Halnon, Nancy, Nelson, Stanley F.
Publicado 2014

Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals

por Engelman, Corinne D., Greenwood, Celia M. T., Bailey, Julia N., Cantor, Rita M., Kent, Jack W., König, Inke R., Bermejo, Justo Lorenzo, Melton, Phillip E., Santorico, Stephanie A., Schillert, Arne, Wijsman, Ellen M., MacCluer, Jean W., Almasy, Laura
Publicado 2016

Adipose Co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes

por Haas, Blake E, Horvath, Steve, Pietiläinen, Kirsi H, Cantor, Rita M, Nikkola, Elina, Weissglas-Volkov, Daphna, Rissanen, Aila, Civelek, Mete, Cruz-Bautista, Ivette, Riba, Laura, Kuusisto, Johanna, Kaprio, Jaakko, Tusie-Luna, Teresa, Laakso, Markku, Aguilar-Salinas, Carlos A, Pajukanta, Päivi
Publicado 2012