ParseCNV integrative copy number variation association software with quality tracking

by Glessner, Joseph T., Li, Jin, Hakonarson, Hakon
Published 2013

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

by 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
Published 2015

Phenotype Restricted Genome-Wide Association Study Using a Gene-Centric Approach Identifies Three Low-Risk Neuroblastoma Susceptibility Loci

by Nguyễn, Lễ B., Diskin, Sharon J., Capasso, Mario, Wang, Kai, Diamond, Maura A., Glessner, Joseph, Kim, Cecilia, Attiyeh, Edward F., Mosse, Yael P., Cole, Kristina, Iolascon, Achille, Devoto, Marcella, Hakonarson, Hakon, Li, Hongzhe K., Maris, John M.
Published 2011

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

by Hadley, Dexter, Wu, Zhi-liang, Kao, Charlly, Kini, Akshata, Mohamed-Hadley, Alisha, Thomas, Kelly, Vazquez, Lyam, Qiu, Haijun, Mentch, Frank, Pellegrino, Renata, Kim, Cecilia, Connolly, John, Glessner, Joseph, Hakonarson, Hakon
Published 2014

Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children

by Chang, Xiao, Glessner, Joseph, Tin, Adrienne, Li, Jin, Guo, Yiran, Wei, Zhi, Liu, Yichuan, Mentch, Frank D., Hou, Cuiping, Zhao, Yan, Wang, Tiancheng, Qiu, Haijun, Kim, Cecilia, Sleiman, Patrick M. A., Hakonarson, Hakon
Published 2015

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

by Liu, Yichuan, Li, Yun, March, Michael E., Nguyen, Kenny, Xu, Kexiang, Wang, Fengxiang, Guo, Yiran, Keating, Brendan, Glessner, Joseph, Li, Jiankang, Ganley, Theodore J., Zhang, Jianguo, Deardorff, Matthew A., Xu, Xun, Hakonarson, Hakon
Published 2016

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

by Liu, Yichuan, Li, Yun, March, Michael E., Kenny, Nguyen, Xu, Kexiang, Wang, Fengxiang, Guo, Yiran, Keating, Brendan, Glessner, Joseph, Li, Jiankang, Ganley, Theodore J., Zhang, Jianguo, Deardorff, Matthew A., Xu, Xun, Hakonarson, Hakon
Published 2015

A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci

by Bradfield, Jonathan P., Qu, Hui-Qi, Wang, Kai, Zhang, Haitao, Sleiman, Patrick M., Kim, Cecilia E., Mentch, Frank D., Qiu, Haijun, Glessner, Joseph T., Thomas, Kelly A., Frackelton, Edward C., Chiavacci, Rosetta M., Imielinski, Marcin, Monos, Dimitri S., Pandey, Rahul, Bakay, Marina, Grant, Struan F. A., Polychronakos, Constantin, Hakonarson, Hakon
Published 2011

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry

by Grant, Struan FA, Petri, Michelle, Bradfield, Jonathan P, Kim, Cecilia E, Santa, Erin, Annaiah, Kiran, Frackelton, Edward C, Glessner, Joseph T, Otieno, F George, Shaner, Julie L, Smith, Ryan M, Eckert, Andrew W, Chiavacci, Rosetta M, Imielinski, Marcin, Sullivan, Kathleen E, Hakonarson, Hakon
Published 2009

Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria

by Sajan, Samin A., Fernandez, Liliana, Nieh, Sahar Esmaeeli, Rider, Eric, Bukshpun, Polina, Wakahiro, Mari, Christian, Susan L., Rivière, Jean-Baptiste, Sullivan, Christopher T., Sudi, Jyotsna, Herriges, Michael J., Paciorkowski, Alexander R., Barkovich, A. James, Glessner, Joseph T., Millen, Kathleen J., Hakonarson, Hakon, Dobyns, William B., Sherr, Elliott H.
Published 2013

Copy Number Variations in Alternative Splicing Gene Networks Impact Lifespan

by Glessner, Joseph T., Smith, Albert Vernon, Panossian, Saarene, Kim, Cecilia E., Takahashi, Nagahide, Thomas, Kelly A., Wang, Fengxiang, Seidler, Kallyn, Harris, Tamara B., Launer, Lenore J., Keating, Brendan, Connolly, John, Sleiman, Patrick M. A., Buxbaum, Joseph D., Grant, Struan F. A., Gudnason, Vilmundur, Hakonarson, Hakon
Published 2013

The missense variation landscape of FTO, MC4R and TMEM18 in obese children of African ancestry

by Deliard, Sandra, Panossian, Saarene, Mentch, Frank D., Kim, Cecilia E., Hou, Cuiping, Frackelton, Edward C., Bradfield, Jonathan P., Glessner, Joseph T., Zhang, Haitao, Wang, Kai, Sleiman, Patrick M.A., Chiavacci, Rosetta M., Berkowitz, Robert I., Hakonarson, Hakon, Zhao, Jianhua, Grant, Struan F.A.
Published 2013

Common variation contributes to the genetic architecture of social communication traits

by St Pourcain, Beate, Whitehouse, Andrew J O, Ang, Wei Q, Warrington, Nicole M, Glessner, Joseph T, Wang, Kai, Timpson, Nicholas J, Evans, David M, Kemp, John P, Ring, Susan M, McArdle, Wendy L, Golding, Jean, Hakonarson, Hakon, Pennell, Craig E, Smith, George Davey
Published 2013