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  1. 1
    The genetics of systemic lupus erythematosus and implications for targeted therapy

    The genetics of systemic lupus erythematosus and implications for targeted therapy por AL Sestak, Barbara G. Fürnrohr, John B. Harley, Joan T. Merrill, Bahram Namjou

    Publicado em 2011
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  2. 2
    Interferon-gamma gene polymorphisms associated with susceptibility to systemic lupus erythematosus

    Interferon-gamma gene polymorphisms associated with susceptibility to systemic lupus erythematosus por Kwang-Woo Kim, Soo‐Kyung Cho, Andrea L. Sestak, Bahram Namjou, Changwon Kang, Sang‐Cheol Bae

    Publicado em 2009
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  3. 3
    Evidence for a Susceptibility Gene, SLEV1, on Chromosome 17p13 in Families with Vitiligo-Related Systemic Lupus Erythematosus

    Evidence for a Susceptibility Gene, SLEV1, on Chromosome 17p13 in Families with Vitiligo-Related Systemic Lupus Erythematosus por Swapan K. Nath, Jennifer A. Kelly, Bahram Namjou, Tom Lam, Gail R. Bruner, R. Hal Scofield, Christopher E. Aston, John B. Harley

    Publicado em 2001
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  4. 4
    46,X,del(X)(q13) Turner's syndrome women with systemic lupus erythematosus in a pedigree multiplex for SLE

    46,X,del(X)(q13) Turner's syndrome women with systemic lupus erythematosus in a pedigree multiplex for SLE por Carisa M. Cooney, Gail R. Bruner, Teresa Aberle, Bahram Namjou‐Khales, Linda K. Myers, Lourdes Feo, S. Li, Alain D’Souza, A Ramirez, John B. Harley, R. Hal Scofield

    Publicado em 2009
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  5. 5
    Autoantibodies targeting glomerular annexin A2 identify patients with proliferative lupus nephritis

    Autoantibodies targeting glomerular annexin A2 identify patients with proliferative lupus nephritis por Dawn J. Caster, Erik A. Korte, Michael L. Merchant, Jon B. Klein, Daniel W. Wilkey, Brad H. Rovin, Dan Birmingham, John B. Harley, Beth L. Cobb, Bahram Namjou, Kenneth R. McLeish, David W. Powell

    Publicado em 2015
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  6. 6
    EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children

    EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children por Bahram Namjou, Mehdi Keddache, Keith Marsolo, Michael Wagner, Todd Lingren, Beth L. Cobb, Cassandra Perry, Stephanie Kennebeck, Ingrid A. Holm, Rongling Li, Nancy A. Crimmins, Lisa J. Martin, Imre Solti, Isaac S. Kohane, John B. Harley

    Publicado em 2013
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  7. 7
    Klinefelter's syndrome (47,XXY) in male systemic lupus erythematosus patients: Support for the notion of a gene‐dose effect from the X chromosome

    Klinefelter's syndrome (47,XXY) in male systemic lupus erythematosus patients: Support for the notion of a gene‐dose effect from the X chromosome por R. Hal Scofield, Gail R. Bruner, Bahram Namjou, Robert P. Kimberly, Rosalind Ramsey‐Goldman, Michelle Petri, John D. Reveille, Graciela S. Alarcón, Luis M. Vilá, Jeff Reid, Bryan Harris, Shibo Li, Jennifer A. Kelly, John B. Harley

    Publicado em 2008
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  8. 8
    Osteopontin and Systemic Lupus Erythematosus Association: A Probable Gene-Gender Interaction

    Osteopontin and Systemic Lupus Erythematosus Association: A Probable Gene-Gender Interaction por Shizhong Han, Joel M. Guthridge, Isaac T. W. Harley, Andrea L. Sestak, Xana Kim-Howard, Kenneth M. Kaufman, Bahram Namjou, Harshal Deshmukh, Gail R. Bruner, Luis R. Espinoza, Gary S. Gilkeson, John B. Harley, Judith A. James, Swapan K. Nath

    Publicado em 2008
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  9. 9
    Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis

    Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis por Bahram Namjou, Keith Marsolo, Robert J. Caroll, Joshua C. Denny, Marylyn D. Ritchie, Shefali S. Verma, Todd Lingren, Aleksey Porollo, Beth L. Cobb, Cassandra Perry, Leah C. Kottyan, Marc E. Rothenberg, Susan D. Thompson, Ingrid A. Holm, Isaac S. Kohane, John B. Harley

    Publicado em 2014
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  10. 10
    Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms

    Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms por Milton Pividori, Sumei Lu, Binglan Li, Chun Su, Matthew E. Johnson, Wei‐Qi Wei, QiPing Feng, Bahram Namjou, Krzysztof Kiryluk, Iftikhar J. Kullo, Yuan Luo, Blair D. Sullivan, Benjamin F. Voight, Carsten Skarke, Marylyn D. Ritchie, Struan F.A. Grant, Casey S. Greene

    Publicado em 2023
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  11. 11
    Imputation and quality control steps for combining multiple genome-wide datasets

    Imputation and quality control steps for combining multiple genome-wide datasets por Shefali S. Verma, Mariza de Andrade, Gerard Tromp, Helena Kuivaniemi, Elizabeth Pugh, Bahram Namjou‐Khales, Shubhabrata Mukherjee, Gail P. Jarvik, Leah C. Kottyan, Amber Burt, Yuki Bradford, Gretta D. Armstrong, Kimberly Derr, Dana C. Crawford, Jonathan L. Haines, Rongling Li, David R. Crosslin, Marylyn D. Ritchie

    Publicado em 2014
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  12. 12
    SLE non-coding genetic risk variant determines the epigenetic dysfunction of an immune cell specific enhancer that controls disease-critical microRNA expression

    SLE non-coding genetic risk variant determines the epigenetic dysfunction of an immune cell specific enhancer that controls disease-critical microRNA expression por Guojun Hou, Isaac T. W. Harley, Xiaoming Lu, Tian Zhou, Ning Xu, Chao Yao, Yuting Qin, Ye Ouyang, Jianyang Ma, Xinyi Zhu, Xiang Yu, Hong Xu, Dai Dai, Huihua Ding, Zhihua Yin, Zhizhong Ye, Jun Deng, Mi Zhou, Yuanjia Tang, Bahram Namjou, Ya Guo, Matthew T. Weirauch, Leah C. Kottyan, John B. Harley, Nan Shen

    Publicado em 2021
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  13. 13
    Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery

    Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery por Tian Zhou, Xinyi Zhu, Zhizhong Ye, Yongfei Wang, Chao Yao, Ning Xu, Mi Zhou, Jianyang Ma, Yuting Qin, Yiwei Shen, Yuanjia Tang, Zhihua Yin, Hong Xu, Yutong Zhang, Xiaoli Zang, Huihua Ding, Wanling Yang, Ya Guo, John B. Harley, Bahram Namjou, Kenneth M. Kaufman, Leah C. Kottyan, Matthew T. Weirauch, Guojun Hou, Nan Shen

    Publicado em 2022
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  14. 14
    Developing an Algorithm to Detect Early Childhood Obesity in Two Tertiary Pediatric Medical Centers

    Developing an Algorithm to Detect Early Childhood Obesity in Two Tertiary Pediatric Medical Centers por Cassandra Brady, Bahram Namjou, Stephanie Kennebeck, Jonathan Bickel, Nandan Patibandla, Yizhao Ni, Sara L. Van Driest, Lixin Chen, Ashton Roach, Beth A. Cobb, Jacqueline Kirby, Joshua C. Denny, Lisa Bailey‐Davis, Marc S. Williams, Keith Marsolo, Imre Solti, Ingrid A. Holm, John B. Harley, Isaac S. Kohane, Guergana Savova, Nancy A. Crimmins, Todd Lingren, Vidhu Thaker

    Publicado em 2016
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  15. 15
    Identification of Four Novel Loci in Asthma in European American and African American Populations

    Identification of Four Novel Loci in Asthma in European American and African American Populations por Berta Almoguera, Lyam Vazquez, Frank Mentch, John J. Connolly, Jennifer A. Pacheco, Agnes S. Sundaresan, Peggy Peissig, James G. Linneman, Catherine A. McCarty, David R. Crosslin, David Carrell, Todd Lingren, Bahram Namjou‐Khales, John B. Harley, Eric B. Larson, Gail P. Jarvik, Murray H. Brilliant, Marc S. Williams, Iftikhar J. Kullo, Erik B. Hysinger, Patrick Sleiman, Hákon Hákonarson

    Publicado em 2016
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  16. 16
    Multiancestral polygenic risk score for pediatric asthma

    Multiancestral polygenic risk score for pediatric asthma por Bahram Namjou, Michael Lape, Edyta Małolepsza, Stanley B. DeVore, Matthew T. Weirauch, Ozan Dikilitas, Gail P. Jarvik, Krzysztof Kiryluk, Iftikhar Kullo, Cong Liu, Yuan Luo, Benjamin A. Satterfield, Jordan W. Smoller, Theresa L. Walunas, John J. Connolly, Patrick Sleiman, Tesfaye B. Mersha, Frank Mentch, Hákon Hákonarson, Cynthia A. Prows, Jocelyn M. Biagini, Gurjit K. Khurana Hershey, Lisa J. Martin, Leah C. Kottyan

    Publicado em 2022
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  17. 17
    Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder

    Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder por Todd Lingren, Pei Chen, Joseph Bochenek, Finale Doshi‐Velez, Patty Manning-Courtney, Julie Bickel, Leah Wildenger Welchons, Judy Reinhold, Nicole Bing, Yizhao Ni, William J. Barbaresi, Frank Mentch, Melissa Basford, Joshua C. Denny, Lyam Vazquez, Cassandra Perry, Bahram Namjou, Haijun Qiu, John J. Connolly, Debra Abrams, Ingrid A. Holm, Beth A. Cobb, Nataline Lingren, Imre Solti, Hákon Hákonarson, Isaac S. Kohane, John B. Harley, Guergana Savova

    Publicado em 2016
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  18. 18
    GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network

    GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network por Bahram Namjou, Todd Lingren, Yongbo Huang, Sreeja Parameswaran, Beth L. Cobb, Ian B. Stanaway, John J. Connolly, Frank Mentch, Barbara Benoit, Xinnan Niu, Wei‐Qi Wei, Robert J. Carroll, Jennifer A. Pacheco, Isaac T. W. Harley, Senad Divanovic, David Carrell, Eric B. Larson, David J. Carey, Shefali S. Verma, Marylyn D. Ritchie, Ali G. Gharavi, Shawn N. Murphy, Marc S. Williams, David R. Crosslin, Gail P. Jarvik, Iftikhar J. Kullo, Hákon Hákonarson, Rongling Li, Stavra A. Xanthakos, John B. Harley

    Publicado em 2019
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  19. 19
    Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience

    Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience por Robyn Fossey, David C. Kochan, Erin Winkler, Joel E. Pacyna, Janet E. Olson, Stephen N. Thibodeau, John J. Connolly, Margaret Harr, Meckenzie Behr, Cynthia A. Prows, Beth L. Cobb, Melanie F. Myers, Nancy Leslie, Bahram Namjou‐Khales, Hila Milo Rasouly, Julia Wynn, Alexander Fedotov, Wendy K. Chung, Ali G. Gharavi, Janet L. Williams, Lynn Pais, Ingrid A. Holm, Sharon Aufox, Maureen E. Smith, Aaron Scrol, Kathleen A. Leppig, Gail P. Jarvik, Georgia L. Wiesner, Rongling Li, Mary Stroud, Jordan W. Smoller, Richard R. Sharp, Iftikhar J. Kullo

    Publicado em 2018
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  20. 20
    High‐density genotyping of STAT4 reveals multiple haplotypic associations with systemic lupus erythematosus in different racial groups

    High‐density genotyping of STAT4 reveals multiple haplotypic associations with systemic lupus erythematosus in different racial groups por Bahram Namjou, Andrea L. Sestak, Don Armstrong, Raphael Zidovetzki, Jennifer A. Kelly, Noam Jacob, Voicu Ciobanu, Kenneth M. Kaufman, Joshua O. Ojwang, Julie T. Ziegler, Francesco P. Quismorio, Andreas Reiff, Barry L. Myones, Joel M. Guthridge, Swapan K. Nath, Gail R. Bruner, Ruth Mehrian‐Shai, Earl D. Silverman, Marisa S. Klein‐Gitelman, Deborah McCurdy, Linda Wagner‐Weiner, James J. Nocton, Chaim Putterman, Sang‐Cheol Bae, Yun Jung Kim, Michelle Petri, John D. Reveille, Timothy J. Vyse, Gary S. Gilkeson, Diane L. Kamen, Marta E. Alarcón‐Riquelme, Patrick M. Gaffney, Kathy L. Moser, Joan T. Merrill, R. Hal Scofield, Judith A. James, Carl D. Langefeld, John B. Harley, Chaim O. Jacob

    Publicado em 2009
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