Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci

por Qu, Hui-Qi, Qu, Jingchun, Bradfield, Jonathan, Marchand, Luc, Glessner, Joseph, Chang, Xiao, March, Michael, Li, Jin, Connolly, John J., Roizen, Jeffrey D., Sleiman, Patrick, Polychronakos, Constantin, Hakonarson, Hakon
Publicado 2021

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

por 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
Publicado 2014

Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection

por Ryan, Sean K., Gonzalez, Michael V., Garifallou, James P., Bennett, Frederick C., Williams, Kimberly S., Sotuyo, Nathaniel P., Mironets, Eugene, Cook, Kieona, Hakonarson, Hakon, Anderson, Stewart A., Jordan-Sciutto, Kelly L.
Publicado 2020

Neuroinflammation and EIF2 Signaling Persist despite Antiretroviral Treatment in an hiPSC Tri-culture Model of HIV Infection

por Ryan, Sean K., Gonzalez, Michael V., Garifallou, James P., Bennett, Frederick C., Williams, Kimberly S., Sotuyo, Nathaniel P., Mironets, Eugene, Cook, Kieona, Hakonarson, Hakon, Anderson, Stewart A., Jordan-Sciutto, Kelly L.
Publicado 2020

Application of exome sequencing to diagnose a novel presentation of the Cornelia de Lange syndrome in an Afro‐Caribbean family

por Thompson, Wayne, Carey, Patrick Z., Donald, Tyhiesia, Nelson, Beverly, Bhoj, Elizabeth J., Li, Dong, Hakonarson, Hakon, Ramirez, Maricela, Elsea, Sarah H., Smith, Janice L., Carey, John C., Sobering, Andrew K.
Publicado 2020

Gene Network Analysis in a Pediatric Cohort Identifies Novel Lung Function Genes

por Ong, Bruce A., Li, Jin, McDonough, Joseph M., Wei, Zhi, Kim, Cecilia, Chiavacci, Rosetta, Mentch, Frank, Caboot, Jason B., Spergel, Jonathan, Allen, Julian L., Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2013

Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders

por Yao, Xueming, Glessner, Joseph T., Li, Junyi, Qi, Xiaohui, Hou, Xiaoyuan, Zhu, Chonggui, Li, Xiaoge, March, Michael E., Yang, Liu, Mentch, Frank D., Hain, Heather S., Meng, Xinyi, Xia, Qianghua, Hakonarson, Hakon, Li, Jin
Publicado 2021

BAG3: Nature’s Quintessential Multi-Functional Protein Functions as a Ubiquitous Intra-Cellular Glue

por Brenner, Caitlyn M., Choudhary, Muaaz, McCormick, Michael G., Cheung, David, Landesberg, Gavin P., Wang, Ju-Fang, Song, Jianliang, Martin, Thomas G., Cheung, Joseph Y., Qu, Hui-Qi, Hakonarson, Hakon, Feldman, Arthur M.
Publicado 2023

From Disease Association to Risk Assessment: An Optimistic View from Genome-Wide Association Studies on Type 1 Diabetes

por Wei, Zhi, Wang, Kai, Qu, Hui-Qi, Zhang, Haitao, Bradfield, Jonathan, Kim, Cecilia, Frackleton, Edward, Hou, Cuiping, Glessner, Joseph T., Chiavacci, Rosetta, Stanley, Charles, Monos, Dimitri, Grant, Struan F. A., Polychronakos, Constantin, Hakonarson, Hakon
Publicado 2009

Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population

por Best, Lyle G., Saxena, Richa, Anderson, Cindy M., Barnes, Michael R., Hakonarson, Hakon, Falcon, Gilbert, Martin, Candelaria, Castillo, Berta Almoguera, Karumanchi, Ananth, Keplin, Kylie, Pearson, Nichole, Lamb, Felicia, Bercier, Shellee, Keating, Brendan J.
Publicado 2013

Correction: Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population

por Best, Lyle G., Saxena, Richa, Anderson, Cindy M., Barnes, Michael R., Hakonarson, Hakon, Falcon, Gilbert, Martin, Candelaria, Castillo, Berta Almoguera, Karumanchi, Ananth, Keplin, Kylie, Pearson, Nichole, Lamb, Felicia, Bercier, Shellee, Keating, Brendan J.
Publicado 2013

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

por 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
Publicado 2015

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

por 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
Publicado 2015

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

por 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
Publicado 2016

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study

por Cardinale, Christopher J., Li, Dong, Tian, Lifeng, Connolly, John J., March, Michael E., Hou, Cuiping, Wang, Fengxiang, Snyder, James, Kim, Cecilia E., Chiavacci, Rosetta M., Sleiman, Patrick M., Burnham, Jon M., Hakonarson, Hakon
Publicado 2016

Treatment of severe Kaposiform Lymphangiomatosis positive for NRAS mutation by MEK-inhibition

por Chowers, Guy, Abebe-Campino, Gadi, Golan, Hana, Vivante, Asaf, Greenberger, Shoshana, Soudack, Michalle, Barkai, Galia, Fox-Fisher, Ilana, Li, Dong, March, Michael, Battig, Mark R., Hakonarson, Hakon, Adams, Denise, Dori, Yoav, Dagan, Adi
Publicado 2022

GATA1 controls numbers of hematopoietic progenitors and their response to autoimmune neuroinflammation

por Hwang, Daniel, Ishikawa, Larissa Lumi Watanabe, Seyedsadr, Maryam S., Mari, Elisabeth, Kasimoglu, Ezgi, Sahin, Ziver, Boehm, Alexandra, Jang, Soohwa, Rasouli, Javad, Vaccaro, Courtney, Gonzalez, Michael, Hakonarson, Hakon, Rostami, Abdolmohamad, Zhang, Guang-Xian, Ciric, Bogoljub
Publicado 2022

Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease

por Stevens, Kristen N., Hakonarson, Hakon, Kim, Cecilia E., Doevendans, Pieter A., Koeleman, Bobby P. C., Mital, Seema, Raue, Jennifer, Glessner, Joseph T., Coles, John G., Moreno, Victor, Granger, Anne, Gruber, Stephen B., Gruber, Peter J.
Publicado 2010

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

por Glessner, Joseph T., Wang, Kai, Sleiman, Patrick M. A., Zhang, Haitao, Kim, Cecilia E., Flory, James H., Bradfield, Jonathan P., Imielinski, Marcin, Frackelton, Edward C., Qiu, Haijun, Mentch, Frank, Grant, Struan F. A., Hakonarson, Hakon
Publicado 2010

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

por St Pourcain, Beate, Skuse, David H, Mandy, William P, Wang, Kai, Hakonarson, Hakon, Timpson, Nicholas J, Evans, David M, Kemp, John P, Ring, Susan M, McArdle, Wendy L, Golding, Jean, Smith, George Davey
Publicado 2014