The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth von Satterthwaite, Theodore D., Connolly, John J., Ruparel, Kosha, Calkins, Monica E., Jackson, Chad, Elliott, Mark A., Roalf, David R., Hopson, Ryan, Prabhakaran, Karthik, Behr, Meckenzie, Qiu, Haijun, Mentch, Frank D., Chiavacci, Rosetta, Sleiman, Patrick M.A., Gur, Ruben C., Hakonarson, Hakon, Gur, Raquel E.

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Identification of novel loci in obstructive sleep apnea in European American and African American children von Quinlan, Courtney M, Chang, Xiao, March, Michael, Mentch, Frank D, Qu, Hui-Qi, Liu, Yichuan, Glessner, Joseph, Sleiman, Patrick M A, Hakonarson, Hakon

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Expanding insights of mitochondrial dysfunction in Parkinson's disease von Wood, Nicholas W, Abou-Sleiman, Patrick M, Muqit, Miratul M. K

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Identification of Four Novel Loci in Asthma in European American and African American Populations von Almoguera, Berta, Vazquez, Lyam, Mentch, Frank, Connolly, John, Pacheco, Jennifer A, Sundaresan, Agnes S, Peissig, Peggy L, Linneman, James G, McCarty, Catherine A, Crosslin, David, Carrell, David S, Lingren, Todd, Namjou-Khales, Bahram, Harley, John B, Larson, Eric, Jarvik, Gail P, Brilliant, Murray, Williams, Marc S, Kullo, Iftikhar J, Hysinger, Erik B, Sleiman, Patrick M A, Hakonarson, Hakon

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Phenome-wide association studies across large population cohorts support drug target validation von Diogo, Dorothée, Tian, Chao, Franklin, Christopher S., Alanne-Kinnunen, Mervi, March, Michael, Spencer, Chris C. A., Vangjeli, Ciara, Weale, Michael E., Mattsson, Hannele, Kilpeläinen, Elina, Sleiman, Patrick M. A., Reilly, Dermot F., McElwee, Joshua, Maranville, Joseph C., Chatterjee, Arnaub K., Bhandari, Aman, Nguyen, Khanh-Dung H., Estrada, Karol, Reeve, Mary-Pat, Hutz, Janna, Bing, Nan, John, Sally, MacArthur, Daniel G., Salomaa, Veikko, Ripatti, Samuli, Hakonarson, Hakon, Daly, Mark J., Palotie, Aarno, Hinds, David A., Donnelly, Peter, Fox, Caroline S., Day-Williams, Aaron G., Plenge, Robert M., Runz, Heiko

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GWAS identifies four novel eosinophilic esophagitis loci von Sleiman, Patrick M. A., Wang, Mei-Lun, Cianferoni, Antonella, Aceves, Seema, Gonsalves, Nirmala, Nadeau, Kari, Bredenoord, Albert J., Furuta, Glenn T., Spergel, Jonathan M., Hakonarson, Hakon

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A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci von 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

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Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients von Liu, Yichuan, Qu, Hui-Qi, Mentch, Frank D., Qu, Jingchun, Chang, Xiao, Nguyen, Kenny, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon

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ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies von Glessner, Joseph T, Li, Jin, Liu, Yichuan, Khan, Munir, Chang, Xiao, Sleiman, Patrick M A, Hakonarson, Hakon

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Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups von Dikilitas, Ozan, Schaid, Daniel J., Kosel, Matthew L., Carroll, Robert J., Chute, Christopher G., Denny, Joshua C., Fedotov, Alex, Feng, QiPing, Hakonarson, Hakon, Jarvik, Gail P., Lee, Ming Ta Michael, Pacheco, Jennifer A., Rowley, Robb, Sleiman, Patrick M., Stein, C. Michael, Sturm, Amy C., Wei, Wei-Qi, Wiesner, Georgia L., Williams, Marc S., Zhang, Yanfei, Manolio, Teri A., Kullo, Iftikhar J.

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The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative von Calkins, Monica E., Merikangas, Kathleen R., Moore, Tyler M., Burstein, Marcy, Behr, Meckenzie A., Satterthwaite, Theodore D., Ruparel, Kosha, Wolf, Daniel H., Roalf, David R., Mentch, Frank D., Qiu, Haijun, Chiavacci, Rosetta, Connolly, John J., Sleiman, Patrick M.A., Gur, Ruben C., Hakonarson, Hakon, Gur, Raquel E.

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Targeting the Complement Alternative Pathway Permits Graft Versus Leukemia Activity while Preventing Graft Versus Host Disease von Nguyen, Hung, Alawieh, Ali, Bastian, David, Kuril, Sandeepkumar, Dai, Min, Daenthanasanmak, Anusara, Zhang, Mengmeng, Iamsawat, Supinya, Schutt, Steven D., Wu, Yongxia, Sleiman, M. Mahdi, Shetty, Akshay, Atkinson, Carl, Sun, Shaoli, Varela, Juan Carlos, Tomlinson, Stephen, Yu, Xue-Zhong

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Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum von Karch, Celeste M, Wen, Natalie, Fan, Chun C, Yokoyama, Jennifer S, Kouri, Naomi, Ross, Owen A, Höglinger, Gunter, Müller, Ulrich, Ferrari, Raffaele, Hardy, John, Schellenberg, Gerard D, Sleiman, Patrick M, Momeni, Parastoo, Hess, Christopher P, Miller, Bruce L, Sharma, Manu, Van Deerlin, Vivianna, Smeland, Olav B, Andreassen, Ole A, Dale, Anders M, Desikan, Rahul S

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NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients von March, Michael E., Gutierrez-Uzquiza, Alvaro, Snorradottir, Asbjorg Osk, Matsuoka, Leticia S., Balvis, Noelia Fonseca, Gestsson, Thorgeir, Nguyen, Kenny, Sleiman, Patrick M. A., Kao, Charlly, Isaksson, Helgi J., Bragason, Birkir Thor, Olafsson, Elias, Palsdottir, Astridur, Hakonarson, Hakon

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MONTAGE: a new tool for high-throughput detection of mosaic copy number variation von Glessner, Joseph T., Chang, Xiao, Liu, Yichuan, Li, Jin, Khan, Munir, Wei, Zhi, Sleiman, Patrick M. A., Hakonarson, Hakon

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Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease von Wang, Kai, Zhang, Haitao, Kugathasan, Subra, Annese, Vito, Bradfield, Jonathan P., Russell, Richard K., Sleiman, Patrick M.A., Imielinski, Marcin, Glessner, Joseph, Hou, Cuiping, Wilson, David C., Walters, Thomas, Kim, Cecilia, Frackelton, Edward C., Lionetti, Paolo, Barabino, Arrigo, Van Limbergen, Johan, Guthery, Stephen, Denson, Lee, Piccoli, David, Li, Mingyao, Dubinsky, Marla, Silverberg, Mark, Griffiths, Anne, Grant, Struan F.A., Satsangi, Jack, Baldassano, Robert, Hakonarson, Hakon

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Heterogeneous Photochemistry of Agrochemicals at the Leaf Surface: A Case Study of Plant Activator Acibenzolar‑S‑methyl von Sleiman, M, de Sainte Claire, P, Richard, C

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Variants of DENND1B Associated with Asthma in Children von Sleiman, Patrick M.A, Flory, James, Imielinski, Marcin, Bradfield, Jonathan P, Annaiah, Kiran, Willis-Owen, Saffron A.G, Wang, Kai, Rafaels, Nicholas M, Michel, Sven, Bonnelykke, Klaus, Zhang, Haitao, Kim, Cecilia E, Frackelton, Edward C, Glessner, Joseph T, Hou, Cuiping, Otieno, F. George, Santa, Erin, Thomas, Kelly, Smith, Ryan M, Glaberson, Wendy R, Garris, Maria, Chiavacci, Rosetta M, Beaty, Terri H, Ruczinski, Ingo, Orange, Jordan M, Allen, Julian, Spergel, Jonathan M, Grundmeier, Robert, Mathias, Rasika A, Christie, Jason D, von Mutius, Erika, Cookson, William O.C, Kabesch, Michael, Moffatt, Miriam F, Grunstein, Michael M, Barnes, Kathleen C, Devoto, Marcella, Magnusson, Mark, Li, Hongzhe, Grant, Struan F.A, Bisgaard, Hans, Hakonarson, Hakon

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An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities von Slaby, Isabella, Hain, Heather S, Abrams, Debra, Mentch, Frank D, Glessner, Joseph T, Sleiman, Patrick M A, Hakonarson, Hakon

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Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder von 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

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