Search Results - "Pato, Carlos"

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    Genetic correlation between smoking behaviors and schizophrenia by Hartz, Sarah M, Horton, Amy C, Hancock, Dana B, Baker, Timothy B, Caporaso, Neil E, Chen, Li-Shiun, Hokanson, John E, Lutz, Sharon M, Marazita, Mary L, McNeil, Daniel W, Pato, Carlos N, Pato, Michele T, Johnson, Eric O, Bierut, Laura J

    Published in Schizophrenia research (01-04-2018)
    “…Abstract Nicotine dependence is highly comorbid with schizophrenia, and the etiology of the comorbidity is unknown. To determine whether there is a genetic…”
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    Traumatic events in childhood and adulthood in a diverse-ancestry sample and their role in bipolar disorder by Chen, Qianwei, Kumar, Vandana, Mummini, Swetha, Pato, Carlos N., Pato, Michele T.

    Published in Psychiatry research (01-08-2023)
    “…•Individuals with BD reported having experienced more childhood and lifetime adverse events.•Individuals with BD had a higher prevalence of PTSD.•Among all the…”
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    Comorbidity of severe psychotic disorders with measures of substance use by Hartz, Sarah M, Pato, Carlos N, Medeiros, Helena, Cavazos-Rehg, Patricia, Sobell, Janet L, Knowles, James A, Bierut, Laura J, Pato, Michele T

    Published in JAMA psychiatry (Chicago, Ill.) (01-03-2014)
    “…Although early mortality in severe psychiatric illness is linked to smoking and alcohol, to our knowledge, no studies have comprehensively characterized…”
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    Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia by Jia, Peilin, Wang, Lily, Fanous, Ayman H, Pato, Carlos N, Edwards, Todd L, Zhao, Zhongming

    Published in PLoS computational biology (01-07-2012)
    “…With the recent success of genome-wide association studies (GWAS), a wealth of association data has been accomplished for more than 200 complex…”
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    BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies by Genovese, Giulio, Rockweiler, Nicole B, Gorman, Bryan R, Bigdeli, Tim B, Pato, Michelle T, Pato, Carlos N, Ichihara, Kiku, McCarroll, Steven A

    Published in Bioinformatics (Oxford, England) (02-01-2024)
    “…Abstract Motivation Many genetics studies report results tied to genomic coordinates of a legacy genome assembly. However, as assemblies are updated and…”
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    Consumer beliefs regarding farmed versus wild fish by Claret, Anna, Guerrero, Luis, Ginés, Rafael, Grau, Amàlia, Hernández, M. Dolores, Aguirre, Enaitz, Peleteiro, José Benito, Fernández-Pato, Carlos, Rodríguez-Rodríguez, Carmen

    Published in Appetite (01-08-2014)
    “…•Consumer beliefs about farmed and wild fish were grouped into four categories•Belief patterns were affected by socio-demographic data and objective…”
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    Ancestry-agnostic estimation of DNA sample contamination from sequence reads by Zhang, Fan, Flickinger, Matthew, Taliun, Sarah A Gagliano, Abecasis, Gonçalo R, Scott, Laura J, McCaroll, Steven A, Pato, Carlos N, Boehnke, Michael, Kang, Hyun Min

    Published in Genome research (01-02-2020)
    “…Detecting and estimating DNA sample contamination are important steps to ensure high-quality genotype calls and reliable downstream analysis. Existing methods…”
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    Cultured Mesenchymal Cells from Nasal Turbinate as a Cellular Model of the Neurodevelopmental Component of Schizophrenia Etiology by Tung, Victoria Sook Keng, Mathews, Fasil, Boruk, Marina, Suppa, Gabrielle, Foronjy, Robert, Pato, Michele T, Pato, Carlos N, Knowles, James A, Evgrafov, Oleg V

    “…The study of neurodevelopmental molecular mechanisms in schizophrenia requires the development of adequate biological models such as patient-derived cells and…”
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    Systematic Review and Meta-Analysis on MS-Based Proteomics Applied to Human Peripheral Fluids to Assess Potential Biomarkers of Bipolar Disorder by Rodrigues, Joao E, Martinho, Ana, Santos, Vítor, Santa, Catia, Madeira, Nuno, Martins, Maria J, Pato, Carlos N, Macedo, Antonio, Manadas, Bruno

    “…Bipolar disorder (BD) is a clinically heterogeneous condition, presenting a complex underlying etiopathogenesis that is not sufficiently characterized. Without…”
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    Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans by Carlson, Jedidiah, Locke, Adam E., Flickinger, Matthew, Zawistowski, Matthew, Levy, Shawn, Myers, Richard M., Boehnke, Michael, Kang, Hyun Min, Scott, Laura J., Li, Jun Z., Zöllner, Sebastian

    Published in Nature communications (14-09-2018)
    “…A detailed understanding of the genome-wide variability of single-nucleotide germline mutation rates is essential to studying human genome evolution. Here, we…”
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