Common variants in polygenic schizophrenia

Por Glessner, Joseph T, Hakonarson, Hakon
Publicado em 2009

ParseCNV integrative copy number variation association software with quality tracking

Por Glessner, Joseph T., Li, Jin, Hakonarson, Hakon
Publicado em 2013

Phasing of Many Thousands of Genotyped Samples

Por Williams, Amy L., Patterson, Nick, Glessner, Joseph, Hakonarson, Hakon, Reich, David
Publicado em 2012

Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity

Por Wang, Kai, Li, Wei-Dong, Glessner, Joseph T., Grant, Struan F.A., Hakonarson, Hakon, Price, R. Arlen
Publicado em 2010

GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

Por Sleiman, Patrick, Wang, Dai, Glessner, Joseph, Hadley, Dexter, Gur, Raquel E., Cohen, Nadine, Li, Qingqin, Hakonarson, Hakon
Publicado em 2013

Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects

Por Agopian, A. J., Mitchell, Laura E., Glessner, Joseph, Bhalla, Angela D., Sewda, Anshuman, Hakonarson, Hakon, Goldmuntz, Elizabeth
Publicado em 2014

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Por Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja
Publicado em 2007

Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts

Por Connolly, John J., Glessner, Joseph T., Almoguera, Berta, Crosslin, David R., Jarvik, Gail P., Sleiman, Patrick M., Hakonarson, Hakon
Publicado em 2014

Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies

Por Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Publicado no Congenit Heart Dis (2011)

Modeling genetic inheritance of copy number variations

Por Wang, Kai, Chen, Zhen, Tadesse, Mahlet G., Glessner, Joseph, Grant, Struan F. A., Hakonarson, Hakon, Bucan, Maja, Li, Mingyao
Publicado em 2008

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

Por Diskin, Sharon J., Li, Mingyao, Hou, Cuiping, Yang, Shuzhang, Glessner, Joseph, Hakonarson, Hakon, Bucan, Maja, Maris, John M., Wang, Kai
Publicado em 2008

Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations

Por Mitchell, Laura E., Agopian, A.J., Bhalla, Angela, Glessner, Joseph T., Kim, Cecilia E., Swartz, Michael D., Hakonarson, Hakon, Goldmuntz, Elizabeth
Publicado no Hum Mol Genet (2015)

A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls

Por Li, Wei-Dong, Jiao, Hongxiao, Wang, Kai, Zhang, Clarence, Glessner, Joseph T., Grant, Struan F.A., Zhao, Hongyu, Hakonarson, Hakon, Price, R. Arlen
Publicado em 2013

A Genome-Wide Association Study on Obesity and Obesity-Related Traits

Por Wang, Kai, Li, Wei-Dong, Zhang, Clarence K., Wang, Zuoheng, Glessner, Joseph T., Grant, Struan F. A., Zhao, Hongyu, Hakonarson, Hakon, Price, R. Arlen
Publicado em 2011

Correction: A Genome-Wide Association Study on Obesity and Obesity-Related Traits

Por Wang, Kai, Li, Wei-Dong, Zhang, Clarence K., Wang, Zuoheng, Glessner, Joseph T., Grant, Struan F. A., Zhao, Hongyu, Hakonarson, Hakon, Price, R. Arlen
Publicado em 2012

BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN

Por KIM, DOKYOON, LUCAS, ANASTASIA, GLESSNER, JOSEPH, VERMA, SHEFALI S., BRADFORD, YUKI, LI, RUOWANG, FRASE, ALEX T., HAKONARSON, HAKON, PEISSIG, PEGGY, BRILLIANT, MURRAY, RITCHIE, MARYLYN D.
Publicado no Pac Symp Biocomput (2016)

Association Between a High-Risk Autism Locus on 5p14 and Social Communication Spectrum Phenotypes in the General Population

Por St. Pourcain, Beate, Wang, Kai, Glessner, Joseph T., Golding, Jean, Steer, Colin, Ring, Susan M., Skuse, David H., Grant, Struan F.A., Hakonarson, Hakon, Davey Smith, George
Publicado em 2010

Evidence From Human and Zebrafish That GPC1 Is a Biliary Atresia Susceptibility Gene

Por Cui, Shuang, Leyva-Vega, Melissa, Tsai, Ellen A., Eauclaire, Steven F., Glessner, Joseph T., Hakonarson, Hakon, Devoto, Marcella, Haber, Barbara A., Spinner, Nancy B., Matthews, Randolph P.
Publicado em 2013

CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations

Por Dajani, Rana, Li, Jin, Wei, Zhi, Glessner, Joseph T., Chang, Xiao, Cardinale, Christopher J., Pellegrino, Renata, Wang, Tiancheng, Hakooz, Nancy, Khader, Yousef, Sheshani, Amina, Zandaki, Duaa, Hakonarson, Hakon
Publicado no Sci Rep (2015)

Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy

Por Attiyeh, Edward F., Diskin, Sharon J., Attiyeh, Marc A., Mossé, Yaël P., Hou, Cuiping, Jackson, Eric M., Kim, Cecilia, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., Maris, John M.
Publicado em 2009