An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities

por Slaby, Isabella, Hain, Heather S., Abrams, Debra, Mentch, Frank D., Glessner, Joseph T., Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2022

Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development

por Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Mentch, Frank D, Qiu, Haijun, Wang, Xiang, Saeidian, Amir Hossein, Watson, Deborah, Glessner, Joseph, Hakonarson, Hakon
Publicado 2023

Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population

por Liu, Yichuan, Qu, Hui-Qi, Qu, Jingchun, Chang, Xiao, Mentch, Frank D., Nguyen, Kenny, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2022

Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients

por Liu, Yichuan, Qu, Hui-Qi, Mentch, Frank D., Qu, Jingchun, Chang, Xiao, Nguyen, Kenny, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2022

Genomic information of children with malignant brain tumors for the prediction of length of hospitalization

por Liu, Yichuan, Qu, Hui‐Qi, Chang, Xiao, Mentch, Frank D, Qiu, Haijun, Nguyen, Kenny, Wang, Xiang, Saeidian, Amir Hossein, Watson, Deborah, Glessner, Joseph, Hakonarson, Hakon
Publicado 2023

Genome-Wide Association Study of Serum Minerals Levels in Children of Different Ethnic Background

por Chang, Xiao, Li, Jin, Guo, Yiran, Wei, Zhi, Mentch, Frank D., Hou, Cuiping, Zhao, Yan, Qiu, Haijun, Kim, Cecilia, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2015

Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing

por Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Mentch, Frank D, Qiu, Haijun, Nguyen, Kenny, Wang, Xiang, Saeidian, Amir Hossein, Watson, Deborah, Glessner, Joseph, Hakonarson, Hakon
Publicado 2022

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

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

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

por 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.
Publicado 2013

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

por 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
Publicado 2011

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk

por Chang, Xiao, Zhao, Yan, Hou, Cuiping, Glessner, Joseph, McDaniel, Lee, Diamond, Maura A., Thomas, Kelly, Li, Jin, Wei, Zhi, Liu, Yichuan, Guo, Yiran, Mentch, Frank D., Qiu, Haijun, Kim, Cecilia, Evans, Perry, Vaksman, Zalman, Diskin, Sharon J., Attiyeh, Edward F., Sleiman, Patrick, Maris, John M., Hakonarson, Hakon
Publicado 2017

Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic ass...

por Jackson, Kathryn L., Mbagwu, Michael, Pacheco, Jennifer A., Baldridge, Abigail S., Viox, Daniel J., Linneman, James G., Shukla, Sanjay K., Peissig, Peggy L., Borthwick, Kenneth M., Carrell, David A., Bielinski, Suzette J., Kirby, Jacqueline C., Denny, Joshua C., Mentch, Frank D., Vazquez, Lyam M., Rasmussen-Torvik, Laura J., Kho, Abel N.
Publicado 2016

Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants

por Namjou, Bahram, Stanaway, Ian B., Lingren, Todd, Mentch, Frank D., Benoit, Barbara, Dikilitas, Ozan, Niu, Xinnan, Shang, Ning, Shoemaker, Ashley H., Carey, David J., Mirshahi, Tooraj, Singh, Rajbir, Nestor, Jordan G., Hakonarson, Hakon, Denny, Joshua C., Crosslin, David R., Jarvik, Gail P., Kullo, Iftikhar J., Williams, Marc S., Harley, John B.
Publicado 2020

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

por Zhao, Jianhua, Li, Mingyao, Bradfield, Jonathan P, Zhang, Haitao, Mentch, Frank D, Wang, Kai, Sleiman, Patrick M, Kim, Cecilia E, Glessner, Joseph T, Hou, Cuiping, Keating, Brendan J, Thomas, Kelly A, Garris, Maria L, Deliard, Sandra, Frackelton, Edward C, Otieno, F George, Chiavacci, Rosetta M, Berkowitz, Robert I, Hakonarson, Hakon, Grant, Struan FA
Publicado 2010

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

por van Ingen, Gijs, Li, Jin, Goedegebure, André, Pandey, Rahul, Li, Yun Rose, March, Michael E., Jaddoe, Vincent W. V., Bakay, Marina, Mentch, Frank D., Thomas, Kelly, Wei, Zhi, Chang, Xiao, Hain, Heather S., Uitterlinden, André G., Moll, Henriette A., van Duijn, Cornelia M., Rivadeneira, Fernando, Raat, Hein, Baatenburg de Jong, Robert J., Sleiman, Patrick M., van der Schroeff, Marc P., Hakonarson, Hakon
Publicado 2016

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

por Li, Dong, Chang, Xiao, Connolly, John J., Tian, Lifeng, Liu, Yichuan, Bhoj, Elizabeth J., Robinson, Nora, Abrams, Debra, Li, Yun R., Bradfield, Jonathan P., Kim, Cecilia E., Li, Jin, Wang, Fengxiang, Snyder, James, Lemma, Maria, Hou, Cuiping, Wei, Zhi, Guo, Yiran, Qiu, Haijun, Mentch, Frank D., Thomas, Kelly A., Chiavacci, Rosetta M., Cone, Roger, Li, Bingshan, Sleiman, Patrick A., Hakonarson, Hakon
Publicado 2017

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

por Li, Dong, Chang, Xiao, Connolly, John J., Tian, Lifeng, Liu, Yichuan, Bhoj, Elizabeth J., Robinson, Nora, Abrams, Debra, Li, Yun R., Bradfield, Jonathan P., Kim, Cecilia E., Li, Jin, Wang, Fengxiang, Snyder, James, Lemma, Maria, Hou, Cuiping, Wei, Zhi, Guo, Yiran, Qiu, Haijun, Mentch, Frank D., Thomas, Kelly A., Chiavacci, Rosetta M., Cone, Roger, Li, Bingshan, Sleiman, Patrick A., Hakonarson, Hakon
Publicado 2017

Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis

por Li, Jin, Li, Yun R., Glessner, Joseph T., Yang, Jie, March, Michael E., Kao, Charlly, Vaccaro, Courtney N., Bradfield, Jonathan P., Li, Junyi, Mentch, Frank D., Qu, Hui‐Qi, Qi, Xiaohui, Chang, Xiao, Hou, Cuiping, Abrams, Debra J., Qiu, Haijun, Wei, Zhi, Connolly, John J., Wang, Fengxiang, Snyder, James, Flatø, Berit, Thompson, Susan D., Langefeld, Carl D., Lie, Benedicte A., Munro, Jane E., Wise, Carol, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2022

Desiderata for computable representations of electronic health records-driven phenotype algorithms

por Mo, Huan, Thompson, William K, Rasmussen, Luke V, Pacheco, Jennifer A, Jiang, Guoqian, Kiefer, Richard, Zhu, Qian, Xu, Jie, Montague, Enid, Carrell, David S, Lingren, Todd, Mentch, Frank D, Ni, Yizhao, Wehbe, Firas H, Peissig, Peggy L, Tromp, Gerard, Larson, Eric B, Chute, Christopher G, Pathak, Jyotishman, Denny, Joshua C, Speltz, Peter, Kho, Abel N, Jarvik, Gail P, Bejan, Cosmin A, Williams, Marc S, Borthwick, Kenneth, Kitchner, Terrie E, Roden, Dan M, Harris, Paul A
Publicado 2015