检索结果 - Joseph Glessner

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  1. 1
    ParseCNV integrative copy number variation association software with quality tracking

    ParseCNV integrative copy number variation association software with quality tracking 由 Joseph Glessner, Jin Li, Hákon Hákonarson

    出版 2013
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  2. 2
    Phasing of Many Thousands of Genotyped Samples

    Phasing of Many Thousands of Genotyped Samples 由 Amy L. Williams, Hon‐Cheong So, Joseph Glessner, Hákon Hákonarson, David Reich

    出版 2012
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  3. 3
    Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity

    Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity 由 Kai Wang, Weidong Li, Joseph Glessner, Struan F.A. Grant, Hákon Hákonarson, R. Arlen Price

    出版 2010
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  4. 4
    Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies

    Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies 由 Elizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, Hákon Hákonarson, Jaclyn A. Biegel, Peter S. White, Xiaowu Gai, Tamim H. Shaikh

    出版 2011
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  5. 5
    PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

    PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data 由 Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F.A. Grant, Hákon Hákonarson, Maja Bućan

    出版 2007
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  6. 6
    Modeling genetic inheritance of copy number variations

    Modeling genetic inheritance of copy number variations 由 Kai Wang, Zhen Chen, Mahlet G. Tadesse, Joseph Glessner, Struan F.A. Grant, Hákon Hákonarson, Maja Bućan, Mingyao Li

    出版 2008
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  7. 7
    Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

    Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms 由 Sharon J. Diskin, Mingyao Li, Cuiping Hou, Shuzhang Yang, Joseph Glessner, Hákon Hákonarson, Maja Bućan, John M. Maris, Kai Wang

    出版 2008
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  8. 8
    A Genome-Wide Association Study on Obesity and Obesity-Related Traits

    A Genome-Wide Association Study on Obesity and Obesity-Related Traits 由 Kai Wang, Weidong Li, Hu Zhang, Zuoheng Wang, Joseph Glessner, Struan F.A. Grant, Hongyu Zhao, Hákon Hákonarson, R. Arlen Price

    出版 2011
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  9. 9
    GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

    GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus 由 Patrick Sleiman, Dai Wang, Joseph Glessner, Dexter Hadley, Raquel E. Gur, Nadine Cohen, Qingqin S. Li, Hákon Hákonarson, Patrick Sleiman, Joseph Glessner, Dexter Hadley, Charlly Kao, Zhi-liang Wu, Cecilia Kim, Kelly Thomas, Hákon Hákonarson, Dai Wang, Reyna Favis, Dong-Jing Fu, Hedy Chung, Adam Savitz, Srihari Gopal, Nadine Cohen, Qingqin S. Li

    出版 2013
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  10. 10
    CANOES: detecting rare copy number variants from whole exome sequencing data

    CANOES: detecting rare copy number variants from whole exome sequencing data 由 Daniel Backenroth, Jason Homsy, Laura Rodriguez Murillo, Joseph Glessner, Edwin Lin, Martina Brueckner, Richard P. Lifton, Elizabeth Goldmuntz, Wendy K. Chung, Yufeng Shen

    出版 2014
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  11. 11
    Evidence From Human and Zebrafish That GPC1 Is a Biliary Atresia Susceptibility Gene

    Evidence From Human and Zebrafish That GPC1 Is a Biliary Atresia Susceptibility Gene 由 Shuang Cui, Melissa Leyva‐Vega, Ellen Tsai, Steven F. EauClaire, Joseph Glessner, Hákon Hákonarson, Marcella Devoto, Barbara Haber, Nancy B. Spinner, Randolph P. Matthews

    出版 2013
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  12. 12
    Association Between a High-Risk Autism Locus on 5p14 and Social Communication Spectrum Phenotypes in the General Population

    Association Between a High-Risk Autism Locus on 5p14 and Social Communication Spectrum Phenotypes in the General Population 由 Beaté St Pourcain, Kai Wang, Joseph Glessner, Jean Golding, Colin Steer, Susan M. Ring, David Skuse, Struan F.A. Grant, Hákon Hákonarson, George Davey Smith

    出版 2010
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  13. 13
    Methylome-wide analysis in systemic microbial-induced experimental periodontal disease in mice with different susceptibility

    Methylome-wide analysis in systemic microbial-induced experimental periodontal disease in mice with different susceptibility 由 Cristhiam de Jesus Hernandez Martinez, Joseph Glessner, Lívia Sertori Finoti, Pedro Henrique Félix Silva, Michel Reis Messora, Ricardo D. Coletta, Hákon Hákonarson, Daniela Bazan Palioto

    出版 2024
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  14. 14
    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 由 Joseph Glessner, Jin Li, Dai Wang, Michael March, Leandro Lima, Akshatha Desai, Dexter Hadley, Charlly Kao, Raquel E. Gur, Nadine Cohen, Patrick Sleiman, Qingqin S. Li, Hákon Hákonarson

    出版 2017
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  15. 15
    Genome wide association (GWA) predictors of anti-TNFα therapeutic responsiveness in pediatric inflammatory bowel disease

    Genome wide association (GWA) predictors of anti-TNFα therapeutic responsiveness in pediatric inflammatory bowel disease 由 Marla C. Dubinsky, Ling Mei, Madison Friedman, Tanvi Dhere, Talin Haritunians, Hákon Hákonarson, Cecilia Kim, Joseph Glessner, Stephan R. Targan, Dermot McGovern, Kent D. Taylor, Jerome I. Rotter

    出版 2009
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  16. 16
    Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy

    Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy 由 Edward F. Attiyeh, Sharon J. Diskin, Marc A. Attiyeh, Yaël P. Mossé, Cuiping Hou, Eric M. Jackson, Cecilia Kim, Joseph Glessner, Hákon Hákonarson, Jaclyn A. Biegel, John M. Maris

    出版 2009
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  17. 17
    Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders

    Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders 由 Xueming Yao, Joseph Glessner, Junyi Li, Xiaohui Qi, Xiaoyuan Hou, Chonggui Zhu, Xiaoge Li, Michael March, Liu Yang, Frank Mentch, Heather S. Hain, Xinyi Meng, Qianghua Xia, Hákon Hákonarson, Jin Li

    出版 2021
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  18. 18
    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 由 Joseph Glessner, Kai Wang, Patrick Sleiman, Haitao Zhang, Cecilia E. Kim, James H. Flory, Jonathan P. Bradfield, Marcin Imieliński, Edward C. Frackelton, Haijun Qiu, Frank Mentch, Struan F.A. Grant, Hákon Hákonarson

    出版 2010
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  19. 19
    A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci

    A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci 由 Xiao Chang, Michael March, Frank Mentch, Kenny Nguyen, Joseph Glessner, Hui‐Qi Qu, Yichuan Liu, G.T. Furuta, Seema S. Aceves, Nirmala Gonsalves, Kari C. Nadeau, Antonella Cianferoni, Jonathan M. Spergel, Patrick Sleiman, Hákon Hákonarson

    出版 2021
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  20. 20
    Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease

    Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease 由 Kristen N. Stevens, Hákon Hákonarson, Chong Ae Kim, Pieter A. Doevendans, Bobby P. C. Koeleman, Seema Mital, Jennifer Raue, Joseph Glessner, John G. Coles, Vı́ctor Moreno, Anne Granger, Stephen B. Gruber, Peter J. Gruber

    出版 2010
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