Confounded by Sequencing Depth in Association Studies of Rare Alleles

Por Garner, Chad
Publicado em 2011

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

Por Thein, Swee Lay, Menzel, Stephan, Lathrop, Mark, Garner, Chad
Publicado em 2009

Evidence of Genetic Interaction between the β-Globin Complex and Chromosome 8q in the Expression of Fetal Hemoglobin

Por Garner, Chad P., Tatu, Thanusak, Best, Steve, Creary, Lisa, Thein, Swee Lay
Publicado em 2002

Genotype determination for polymorphisms in linkage disequilibrium

Por Yu, Zhaoxia, Garner, Chad, Ziogas, Argyrios, Anton-Culver, Hoda, Schaid, Daniel J
Publicado em 2009

CAD/POLD2 gene expression is associated with poor overall survival and chemoresistance in bladder urothelial carcinoma

Por Givechian, Kevin B., Garner, Chad, Garban, Hermes, Rabizadeh, Shahrooz, Soon-Shiong, Patrick
Publicado no Oncotarget (2018)

The Extent of Linkage Disequilibrium Caused by Selection on G6PD in Humans

Por Saunders, Matthew A., Slatkin, Montgomery, Garner, Chad, Hammer, Michael F., Nachman, Michael W.
Publicado em 2005

An immunogenic NSCLC microenvironment is associated with favorable survival in lung adenocarcinoma

Por Givechian, Kevin B., Garner, Chad, Benz, Steve, Song, Bing, Rabizadeh, Shahrooz, Soon-Shiong, Patrick
Publicado no Oncotarget (2019)

Comprehensive genomic transcriptomic tumor-normal gene panel analysis for enhanced precision in patients with lung cancer

Por Rabizadeh, Shahrooz, Garner, Chad, Sanborn, John Zachary, Benz, Stephen C., Reddy, Sandeep, Soon-Shiong, Patrick
Publicado no Oncotarget (2018)

Linkage Analysis of a Complex Pedigree with Severe Bipolar Disorder, Using a Markov Chain Monte Carlo Method

Por Garner, Chad, McInnes, L. Alison, Service, Susan K., Spesny, Mitzi, Fournier, Eduardo, Leon, Pedro, Freimer, Nelson B.
Publicado em 2001

Association Analysis of the Extended MHC Region in Celiac Disease Implicates Multiple Independent Susceptibility Loci

Por Ahn, Richard, Ding, Yuan Chun, Murray, Joseph, Fasano, Alessio, Green, Peter H. R., Neuhausen, Susan L., Garner, Chad
Publicado em 2012

Identification of an immune gene expression signature associated with favorable clinical features in Treg-enriched patient tumor samples

Por Givechian, Kevin B., Wnuk, Kamil, Garner, Chad, Benz, Stephen, Garban, Hermes, Rabizadeh, Shahrooz, Niazi, Kayvan, Soon-Shiong, Patrick
Publicado no NPJ Genom Med (2018)

Utilization of defined microbial communities enables effective evaluation of meta-genomic assemblies

Por Greenwald, William W., Klitgord, Niels, Seguritan, Victor, Yooseph, Shibu, Venter, J. Craig, Garner, Chad, Nelson, Karen E., Li, Weizhong
Publicado no BMC Genomics (2017)

Genome-Wide Association Study of Celiac Disease in North America Confirms FRMD4B as New Celiac Locus

Por Garner, Chad, Ahn, Richard, Ding, Yuan Chun, Steele, Linda, Stoven, Samantha, Green, Peter H., Fasano, Alessio, Murray, Joseph A., Neuhausen, Susan L.
Publicado em 2014

Genetic variation in IGFBP2 and IGFBP5 is associated with breast cancer in populations of African descent

Por Garner, Chad P., Ding, Yuan C., John, Esther M., Ingles, Sue A., Olopade, Olufunmilayo I., Huo, Dezheng, Adebamowo, Clement, Ogundiran, Temidayo, Neuhausen, Susan L.
Publicado no Hum Genet (2008)

ATR Mutations Promote the Growth of Melannoma Tumors by Modulating the Immune Microenvironment

Por Chen, Chi-Fen, Ruiz-Vega, Rolando, Vasudeva, Priya, Espitia, Francisco, Krasieva, Tatiana B., de Feraudy, Sebastien, Tromberg, Bruce J., Huang, Sharon, Garner, Chad P., Wu, Jie, Hoon, Dave S., Ganesan, Anand K.
Publicado no Cell Rep (2017)

Novel polymorphisms in caspase-8 are associated with breast cancer risk in the California Teachers Study

Por Park, Hannah Lui, Ziogas, Argyrios, Chang, Jenny, Desai, Bhumi, Bessonova, Leona, Garner, Chad, Lee, Eunjung, Neuhausen, Susan L., Wang, Sophia S., Ma, Huiyan, Clague, Jessica, Reynolds, Peggy, Lacey, James V., Bernstein, Leslie, Anton-Culver, Hoda
Publicado no BMC Cancer (2016)

Wnt signaling directs a metabolic program of glycolysis and angiogenesis in colon cancer

Por Pate, Kira T, Stringari, Chiara, Sprowl-Tanio, Stephanie, Wang, Kehui, TeSlaa, Tara, Hoverter, Nate P, McQuade, Miriam M, Garner, Chad, Digman, Michelle A, Teitell, Michael A, Edwards, Robert A, Gratton, Enrico, Waterman, Marian L
Publicado em 2014

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

Por Thein, Swee Lay, Menzel, Stephan, Peng, Xu, Best, Steve, Jiang, Jie, Close, James, Silver, Nicholas, Gerovasilli, Ageliki, Ping, Chen, Yamaguchi, Masao, Wahlberg, Karin, Ulug, Pinar, Spector, Tim D., Garner, Chad, Matsuda, Fumihiko, Farrall, Martin, Lathrop, Mark
Publicado em 2007

Associations between Single Nucleotide Polymorphisms in Iron-Related Genes and Iron Status in Multiethnic Populations

Por McLaren, Christine E., McLachlan, Stela, Garner, Chad P., Vulpe, Chris D., Gordeuk, Victor R., Eckfeldt, John H., Adams, Paul C., Acton, Ronald T., Murray, Joseph A., Leiendecker-Foster, Catherine, Snively, Beverly M., Barcellos, Lisa F., Cook, James D., McLaren, Gordon D.
Publicado em 2012

Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2

Por Menzel, Stephan, Rooks, Helen, Zelenika, Diana, Mtatiro, Siana N, Gnanakulasekaran, Akshala, Drasar, Emma, Cox, Sharon, Liu, Li, Masood, Mariam, Silver, Nicholas, Garner, Chad, Vasavda, Nisha, Howard, Jo, Makani, Julie, Adekile, Adekunle, Pace, Betty, Spector, Tim, Farrall, Martin, Lathrop, Mark, Thein, Swee Lay
Publicado no Ann Hum Genet (2014)