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 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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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes von Glessner, Joseph T., Wang, Kai, Cai, Guiqing, Korvatska, Olena, Kim, Cecilia E., Wood, Shawn, Zhang, Haitao, Estes, Annette, Brune, Camille W., Bradfield, Jonathan P., Imielinski, Marcin, Frackelton, Edward C., Reichert, Jennifer, Crawford, Emily L., Munson, Jeffrey, Sleiman, Patrick M. A., Chiavacci, Rosetta, Annaiah, Kiran, Thomas, Kelly, Hou, Cuiping, Glaberson, Wendy, Flory, James, Otieno, Frederick, Garris, Maria, Soorya, Latha, Klei, Lambertus, Piven, Joseph, Meyer, Kacie J., Anagnostou, Evdokia, Sakurai, Takeshi, Game, Rachel M., Rudd, Danielle S., Zurawiecki, Danielle, McDougle, Christopher J., Davis, Lea K., Miller, Judith, Posey, David J., Michaels, Shana, Kolevzon, Alexander, Silverman, Jeremy M., Bernier, Raphael, Levy, Susan E., Schultz, Robert T., Dawson, Geraldine, Owley, Thomas, McMahon, William M., Wassink, Thomas H., Sweeney, John A., Nurnberger, John I., Coon, Hilary, Sutcliffe, James S., Minshew, Nancy J., Grant, Struan F. A., Bucan, Maja, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Schellenberg, Gerard D., Hakonarson, Hakon

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Common genetic variants on 5p14.1 associate with autism spectrum disorders von Wang, Kai, Zhang, Haitao, Ma, Deqiong, Bucan, Maja, Glessner, Joseph T., Abrahams, Brett S., Salyakina, Daria, Imielinski, Marcin, Bradfield, Jonathan P., Sleiman, Patrick M. A., Kim, Cecilia E., Hou, Cuiping, Frackelton, Edward, Chiavacci, Rosetta, Takahashi, Nagahide, Sakurai, Takeshi, Rappaport, Eric, Lajonchere, Clara M., Munson, Jeffrey, Estes, Annette, Korvatska, Olena, Piven, Joseph, Sonnenblick, Lisa I., Alvarez Retuerto, Ana I., Herman, Edward I., Dong, Hongmei, Hutman, Ted, Sigman, Marian, Ozonoff, Sally, Klin, Ami, Owley, Thomas, Sweeney, John A., Brune, Camille W., Cantor, Rita M., Bernier, Raphael, Gilbert, John R., Cuccaro, Michael L., McMahon, William M., Miller, Judith, State, Matthew W., Wassink, Thomas H., Coon, Hilary, Levy, Susan E., Schultz, Robert T., Nurnberger, John I., Haines, Jonathan L., Sutcliffe, James S., Cook, Edwin H., Minshew, Nancy J., Buxbaum, Joseph D., Dawson, Geraldine, Grant, Struan F. A., Geschwind, Daniel H., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Hakonarson, Hakon

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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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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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Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients von Qu, Jingchun, Qu, Hui-Qi, Bradfield, Jonathan P., Glessner, Joseph T., Chang, Xiao, Tian, Lifeng, March, Michael, Connolly, John J., Roizen, Jeffrey D., Sleiman, Patrick M. A., Hakonarson, Hakon

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Mendelian Randomization in the Era of Genomewide Association Studies von SLEIMAN, Patrick M. A, GRANT, Struan F. A

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Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population von Liu, Yichuan, Qu, Hui-Qi, Qu, Jingchun, Chang, Xiao, Mentch, Frank D, Nguyen, Kenny, Tian, Lifeng, Glessner, Joseph, 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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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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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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Strong synaptic transmission impact by copy number variations in schizophrenia von Glessner, Joseph T., Reilly, Muredach P., Kim, Cecilia E., Takahashi, Nagahide, Albano, Anthony, Hou, Cuiping, Bradfield, Jonathan P., Zhang, Haitao, Sleiman, Patrick M. A., Flory, James H., Imielinski, Marcin, Frackelton, Edward C., Chiavacci, Rosetta, Thomas, Kelly A., Garris, Maria, Otieno, Frederick G., Davidson, Michael, Weiser, Mark, Reichenberg, Abraham, Davis, Kenneth L., Friedman, Joseph I., Cappola, Thomas P., Margulies, Kenneth B., Rader, Daniel J., Grant, Struan F. A., Buxbaum, Joseph D., Gur, Raquel E., Hakonarson, Hakon, Lupski, James R.

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Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders von Glessner, Joseph T, Li, Jin, Wang, Dai, March, Michael, Lima, Leandro, Desai, Akshatha, Hadley, Dexter, Kao, Charlly, Gur, Raquel E, Cohen, Nadine, Sleiman, Patrick M A, Li, Qingqin, Hakonarson, Hakon

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Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects von Wang, Kai, Baldassano, Robert, Zhang, Haitao, Qu, Hui-Qi, Imielinski, Marcin, Kugathasan, Subra, Annese, Vito, Dubinsky, Marla, Rotter, Jerome I., Russell, Richard K., Bradfield, Jonathan P., Sleiman, Patrick M.A., Glessner, Joseph T., Walters, Thomas, Hou, Cuiping, Kim, Cecilia, Frackelton, Edward C., Garris, Maria, Doran, James, Romano, Claudio, Catassi, Carlo, Van Limbergen, Johan, Guthery, Stephen L., Denson, Lee, Piccoli, David, Silverberg, Mark S., Stanley, Charles A., Monos, Dimitri, Wilson, David C., Griffiths, Anne, Grant, Struan F.A., Satsangi, Jack, Polychronakos, Constantin, Hakonarson, Hakon

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Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders von Glessner, Joseph T, Khan, Munir E, Chang, Xiao, Liu, Yichuan, Otieno, F George, Lemma, Maria, Slaby, Isabella, Hain, Heather, Mentch, Frank, Li, Jin, Kao, Charlly, Sleiman, Patrick M A, March, Michael E, Connolly, John, Hakonarson, Hakon

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Genome-wide association study of serum minerals levels in children of different ethnic background von 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

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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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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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