Showing 1 - 19 results of 19 for search 'Patrick M. A. Sleiman', query time: 0.04s
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Common and Rare Genetic Risk Factors Converge in Protein Interaction Networks Underlying Schizophrenia by Xiao Chang, Leandro de Araujo Lima, Yichuan Liu, Jin Li, Jin Li, Qingqin Li, Patrick M. A. Sleiman, Patrick M. A. Sleiman, Patrick M. A. Sleiman, Hakon Hakonarson, Hakon Hakonarson, Hakon Hakonarson
Published 2018-09-01
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Target Genes of Autism Risk Loci in Brain Frontal Cortex by Yan Sun, Xueming Yao, Michael E. March, Xinyi Meng, Junyi Li, Zhi Wei, Patrick M.A. Sleiman, Patrick M.A. Sleiman, Patrick M.A. Sleiman, Hakon Hakonarson, Hakon Hakonarson, Hakon Hakonarson, Qianghua Xia, Jin Li
Published 2019-08-01
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Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios by Yichuan Liu, Xiao Chang, Joseph Glessner, Huiqi Qu, Lifeng Tian, Dong Li, Kenny Nguyen, Patrick M. A. Sleiman, Patrick M. A. Sleiman, Hakon Hakonarson, Hakon Hakonarson, Hakon Hakonarson
Published 2019-09-01
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An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities by Isabella Slaby, Heather S. Hain, Debra Abrams, Frank D. Mentch, Joseph T. Glessner, Patrick M. A. Sleiman, Hakon Hakonarson
Published 2022-06-01
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Genetic correlations between COVID-19 and a variety of traits and diseases by Xiao Chang, Yun Li, Kenny Nguyen, Huiqi Qu, Yichuan Liu, Joseph Glessner, Patrick M.A. Sleiman, Hakon Hakonarson
Published 2021-05-01
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Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters by Yichuan Liu, Hui-Qi Qu, Xiao Chang, Lifeng Tian, Jingchun Qu, Joseph Glessner, Patrick M. A. Sleiman, Hakon Hakonarson
Published 2021-03-01
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Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population by Yichuan Liu, Hui-Qi Qu, Jingchun Qu, Xiao Chang, Frank D. Mentch, Kenny Nguyen, Lifeng Tian, Joseph Glessner, Patrick M. A. Sleiman, Hakon Hakonarson
Published 2022-05-01
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Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients by Jingchun Qu, Hui-Qi Qu, Jonathan P. Bradfield, Joseph T. Glessner, Xiao Chang, Lifeng Tian, Michael March, John J. Connolly, Jeffrey D. Roizen, Patrick M. A. Sleiman, Hakon Hakonarson
Published 2021-08-01
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Gene network analysis in a pediatric cohort identifies novel lung function genes. by Bruce A Ong, Jin Li, Joseph M McDonough, Zhi Wei, Cecilia Kim, Rosetta Chiavacci, Frank Mentch, Jason B Caboot, Jonathan Spergel, Julian L Allen, Patrick M A Sleiman, Hakon Hakonarson
Published 2013-01-01
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Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders by Joseph T. Glessner, Munir E. Khan, Xiao Chang, Yichuan Liu, F. George Otieno, Maria Lemma, Isabella Slaby, Heather Hain, Frank Mentch, Jin Li, Charlly Kao, Patrick M. A. Sleiman, Michael E. March, John Connolly, Hakon Hakonarson
Published 2023-04-01
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NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients by Michael E. March, Alvaro Gutierrez-Uzquiza, Asbjorg Osk Snorradottir, Leticia S. Matsuoka, Noelia Fonseca Balvis, Thorgeir Gestsson, Kenny Nguyen, Patrick M. A. Sleiman, Charlly Kao, Helgi J. Isaksson, Birkir Thor Bragason, Elias Olafsson, Astridur Palsdottir, Hakon Hakonarson
Published 2021-03-01
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Copy number variations in alternative splicing gene networks impact lifespan. by Joseph T Glessner, Albert Vernon Smith, Saarene Panossian, Cecilia E Kim, Nagahide Takahashi, Kelly A Thomas, Fengxiang Wang, Kallyn Seidler, Tamara B Harris, Lenore J Launer, Brendan Keating, John Connolly, Patrick M A Sleiman, Joseph D Buxbaum, Struan F A Grant, Vilmundur Gudnason, Hakon Hakonarson
Published 2013-01-01
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Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations by Yun Rose Li, Joseph T. Glessner, Bradley P. Coe, Jin Li, Maede Mohebnasab, Xiao Chang, John Connolly, Charlly Kao, Zhi Wei, Jonathan Bradfield, Cecilia Kim, Cuiping Hou, Munir Khan, Frank Mentch, Haijun Qiu, Marina Bakay, Christopher Cardinale, Maria Lemma, Debra Abrams, Andrew Bridglall-Jhingoor, Meckenzie Behr, Shanell Harrison, George Otieno, Alexandria Thomas, Fengxiang Wang, Rosetta Chiavacci, Lawrence Wu, Dexter Hadley, Elizabeth Goldmuntz, Josephine Elia, John Maris, Robert Grundmeier, Marcella Devoto, Brendan Keating, Michael March, Renata Pellagrino, Struan F. A. Grant, Patrick M. A. Sleiman, Mingyao Li, Evan E. Eichler, Hakon Hakonarson
Published 2020-01-01
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Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 by Sarah Grosche, Ingo Marenholz, Jorge Esparza-Gordillo, Aleix Arnau-Soler, Erola Pairo-Castineira, Franz Rüschendorf, Tarunveer S. Ahluwalia, Catarina Almqvist, Andreas Arnold, Australian Asthma Genetics Consortium (AAGC), Hansjörg Baurecht, Hans Bisgaard, Klaus Bønnelykke, Sara J. Brown, Mariona Bustamante, John A. Curtin, Adnan Custovic, Shyamali C. Dharmage, Ana Esplugues, Mario Falchi, Dietmar Fernandez-Orth, Manuel A. R. Ferreira, Andre Franke, Sascha Gerdes, Christian Gieger, Hakon Hakonarson, Patrick G. Holt, Georg Homuth, Norbert Hubner, Pirro G. Hysi, Marjo-Riitta Jarvelin, Robert Karlsson, Gerard H. Koppelman, Susanne Lau, Manuel Lutz, Patrik K. E. Magnusson, Guy B. Marks, Martina Müller-Nurasyid, Markus M. Nöthen, Lavinia Paternoster, Craig E. Pennell, Annette Peters, Konrad Rawlik, Colin F. Robertson, Elke Rodriguez, Sylvain Sebert, Angela Simpson, Patrick M. A. Sleiman, Marie Standl, Dora Stölzl, Konstantin Strauch, Agnieszka Szwajda, Albert Tenesa, Philip J. Thompson, Vilhelmina Ullemar, Alessia Visconti, Judith M. Vonk, Carol A. Wang, Stephan Weidinger, Matthias Wielscher, Catherine L. Worth, Chen-Jian Xu, Young-Ae Lee
Published 2021-11-01
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