Common variants in polygenic schizophrenia

door Glessner, Joseph T, Hakonarson, Hakon
Gepubliceerd in 2009

ParseCNV integrative copy number variation association software with quality tracking

door Glessner, Joseph T., Li, Jin, Hakonarson, Hakon
Gepubliceerd in 2013

Phasing of Many Thousands of Genotyped Samples

door Williams, Amy L., Patterson, Nick, Glessner, Joseph, Hakonarson, Hakon, Reich, David
Gepubliceerd in 2012

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

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

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

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

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

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

Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries

door Qu, Hui-Qi, Snyder, James, Connolly, John, Glessner, Joseph, Kao, Charlly, Sleiman, Patrick M.A., Hakonarson, Hakon
Gepubliceerd in medRxiv (2022)

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

door Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja
Gepubliceerd in 2007

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

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

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

door Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Gepubliceerd in Congenit Heart Dis (2011)

Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa

door Chang, Xiao, qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Hou, Cuiping, Wang, Fengxiang, Li, Jin, Sleiman, Patrick, Hakonarson, Hakon
Gepubliceerd in J Psychiatr Res (2019)

Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans

door Chang, Xiao, Liu, Yichuan, Mentch, Frank, Glessner, Joseph, Qu, Huiqi, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
Gepubliceerd in Transl Psychiatry (2020)

MONTAGE: a new tool for high-throughput detection of mosaic copy number variation

door Glessner, Joseph T., Chang, Xiao, Liu, Yichuan, Li, Jin, Khan, Munir, Wei, Zhi, Sleiman, Patrick M. A., Hakonarson, Hakon
Gepubliceerd in BMC Genomics (2021)

Genetic correlations between COVID-19 and a variety of traits and diseases

door Chang, Xiao, Li, Yun, Nguyen, Kenny, Qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Sleiman, Patrick M.A., Hakonarson, Hakon
Gepubliceerd in Innovation (Camb) (2021)

Modeling genetic inheritance of copy number variations

door Wang, Kai, Chen, Zhen, Tadesse, Mahlet G., Glessner, Joseph, Grant, Struan F. A., Hakonarson, Hakon, Bucan, Maja, Li, Mingyao
Gepubliceerd in 2008

Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters

door Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Qu, Jingchun, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon
Gepubliceerd in Int J Mol Sci (2021)

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

door Diskin, Sharon J., Li, Mingyao, Hou, Cuiping, Yang, Shuzhang, Glessner, Joseph, Hakonarson, Hakon, Bucan, Maja, Maris, John M., Wang, Kai
Gepubliceerd in 2008

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

door Mitchell, Laura E., Agopian, A.J., Bhalla, Angela, Glessner, Joseph T., Kim, Cecilia E., Swartz, Michael D., Hakonarson, Hakon, Goldmuntz, Elizabeth
Gepubliceerd in Hum Mol Genet (2015)

Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios

door Liu, Yichuan, Chang, Xiao, Glessner, Joseph, Qu, Huiqi, Tian, Lifeng, Li, Dong, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
Gepubliceerd in Front Genet (2019)

Non-coding structural variation differentially impacts attention-deficit hyperactivity disorder (ADHD) gene networks in African American vs Caucasian children

door Liu, Yichuan, Chang, Xiao, Qu, Huiqi, Glessner, Joseph, Tian, Lifeng, Li, Dong, Qiu, Haijun, Sleiman, Patrick M. A., Hakonarson, Hakon
Gepubliceerd in Sci Rep (2020)