Hasil Pencarian - Patrick M A Sleiman

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  1. 1
    Common and Rare Genetic Risk Factors Converge in Protein Interaction Networks Underlying Schizophrenia

    Common and Rare Genetic Risk Factors Converge in Protein Interaction Networks Underlying Schizophrenia oleh 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

    Diterbitkan 2018-09-01
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  2. 2
    Target Genes of Autism Risk Loci in Brain Frontal Cortex

    Target Genes of Autism Risk Loci in Brain Frontal Cortex oleh 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

    Diterbitkan 2019-08-01
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  3. 3
    COVID-19 in pediatrics: Genetic susceptibility

    COVID-19 in pediatrics: Genetic susceptibility oleh Joseph T. Glessner, Joseph T. Glessner, Xiao Chang, Frank Mentch, Huiqi Qu, Debra J. Abrams, Alexandria Thomas, Patrick M. A. Sleiman, Patrick M. A. Sleiman, Hakon Hakonarson, Hakon Hakonarson

    Diterbitkan 2022-08-01
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  4. 4
    Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios

    Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios oleh 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

    Diterbitkan 2019-09-01
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  5. 5
    Saudi Arabian CML patient with a novel four‐way translocation at t(9;22;5;2)(q34;q11.2;p13;q44)

    Saudi Arabian CML patient with a novel four‐way translocation at t(9;22;5;2)(q34;q11.2;p13;q44) oleh Walid Dridi, Solaf Kanfar, Patrick M. A. Sleiman, Yichuan Liu, Hakon Hakonarson, Hayaal Rammah, Alia Matrouk

    Diterbitkan 2022-06-01
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  6. 6
    An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities

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

    Diterbitkan 2022-06-01
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  7. 7
    The Long Noncoding RNA Landscape in Amygdala Tissues from Schizophrenia PatientsResearch in Context

    The Long Noncoding RNA Landscape in Amygdala Tissues from Schizophrenia PatientsResearch in Context oleh Tian Tian, Zhi Wei, Xiao Chang, Yichuan Liu, Raquel E. Gur, Patrick M.A. Sleiman, Hakon Hakonarson

    Diterbitkan 2018-08-01
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  8. 8
    MONTAGE: a new tool for high-throughput detection of mosaic copy number variation

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

    Diterbitkan 2021-02-01
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  9. 9
    Genetic correlations between COVID-19 and a variety of traits and diseases

    Genetic correlations between COVID-19 and a variety of traits and diseases oleh Xiao Chang, Yun Li, Kenny Nguyen, Huiqi Qu, Yichuan Liu, Joseph Glessner, Patrick M.A. Sleiman, Hakon Hakonarson

    Diterbitkan 2021-05-01
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  10. 10
    Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters

    Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters oleh Yichuan Liu, Hui-Qi Qu, Xiao Chang, Lifeng Tian, Jingchun Qu, Joseph Glessner, Patrick M. A. Sleiman, Hakon Hakonarson

    Diterbitkan 2021-03-01
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  11. 11
    HIF-1α Pulmonary Phenotype Wide Association Study Unveils a Link to Inflammatory Airway Conditions

    HIF-1α Pulmonary Phenotype Wide Association Study Unveils a Link to Inflammatory Airway Conditions oleh Jelte Kelchtermans, Jelte Kelchtermans, Xiao Chang, Michael E. March, Frank Mentch, Patrick M. A. Sleiman, Hakon Hakonarson, Hakon Hakonarson

    Diterbitkan 2021-09-01
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  12. 12
    Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population

    Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population oleh Yichuan Liu, Hui-Qi Qu, Jingchun Qu, Xiao Chang, Frank D. Mentch, Kenny Nguyen, Lifeng Tian, Joseph Glessner, Patrick M. A. Sleiman, Hakon Hakonarson

    Diterbitkan 2022-05-01
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  13. 13
    Genome-wide association study of serum minerals levels in children of different ethnic background.

    Genome-wide association study of serum minerals levels in children of different ethnic background. oleh Xiao Chang, Jin Li, Yiran Guo, Zhi Wei, Frank D Mentch, Cuiping Hou, Yan Zhao, Haijun Qiu, Cecilia Kim, Patrick M A Sleiman, Hakon Hakonarson

    Diterbitkan 2015-01-01
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  14. 14
    Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients

    Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients oleh 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

    Diterbitkan 2021-08-01
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  15. 15
    Gene network analysis in a pediatric cohort identifies novel lung function genes.

    Gene network analysis in a pediatric cohort identifies novel lung function genes. oleh 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

    Diterbitkan 2013-01-01
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  16. 16
    Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder.

    Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder. oleh Joseph T Glessner, Kai Wang, Patrick M A Sleiman, Haitao Zhang, Cecilia E Kim, James H Flory, Jonathan P Bradfield, Marcin Imielinski, Edward C Frackelton, Haijun Qiu, Frank Mentch, Struan F A Grant, Hakon Hakonarson

    Diterbitkan 2010-12-01
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  17. 17
    Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

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

    Diterbitkan 2017-11-01
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  18. 18
    Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders

    Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders oleh 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

    Diterbitkan 2023-04-01
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  19. 19
    NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients

    NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients oleh 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

    Diterbitkan 2021-03-01
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  20. 20
    Copy number variations in alternative splicing gene networks impact lifespan.

    Copy number variations in alternative splicing gene networks impact lifespan. oleh 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

    Diterbitkan 2013-01-01
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