Výsledky vyhledávání - Edward C. Frackelton

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  1. 1
    Large Sample Size, Wide Variant Spectrum, and Advanced Machine-Learning Technique Boost Risk Prediction for Inflammatory Bowel Disease

    Large Sample Size, Wide Variant Spectrum, and Advanced Machine-Learning Technique Boost Risk Prediction for Inflammatory Bowel Disease Autor Zhi Wei, Wei Wang, Jonathan P. Bradfield, Jin Li, Christopher J. Cardinale, Edward C. Frackelton, Cecilia Kim, Frank Mentch, Kristel Van Steen, Peter M. Visscher, Robert N. Baldassano, Hákon Hákonarson

    Vydáno 2013
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    Artigo
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  2. 2
    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 Autor 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

    Vydáno 2010
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    Artigo
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  3. 3
    Assessing the utilization of high-resolution 2-field HLA typing in solid organ transplantation

    Assessing the utilization of high-resolution 2-field HLA typing in solid organ transplantation Autor Yanping Huang, Anh Dinh, S. Heron, Allison Gasiewski, Carolina Kneib, Hilary Mehler, Michael T. Mignogno, Ryan Morlen, Larissa Slavich, Ethan S. Kentzel, Edward C. Frackelton, Jamie L. Duke, Deborah Ferriola, Timothy L. Mosbruger, Olga Timofeeva, Steven S. Geier, Dimitri Monos

    Vydáno 2019
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    Artigo
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  4. 4
    Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population

    Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population Autor Nori Matsunami, Dexter Hadley, Charles H. Hensel, G. Bryce Christensen, Cecilia Kim, Edward C. Frackelton, Kelly Thomas, Renata Pellegrino da Silva, Jeff Stevens, Lisa Baird, Brith Otterud, Karen S. Ho, Tena Varvil, Mark Leppert, Christophe G Lambert, Mark Leppert, Hákon Hákonarson

    Vydáno 2013
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    Artigo
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  5. 5
    Common Variants in <i>HSPB7</i> and <i>FRMD4B</i> Associated With Advanced Heart Failure

    Common Variants in <i>HSPB7</i> and <i>FRMD4B</i> Associated With Advanced Heart Failure Autor Thomas P. Cappola, Mingyao Li, Jing He, Bonnie Ky, Joan Gilmore, Liming Qu, Brendan J. Keating, Muredach P. Reilly, Cecelia E. Kim, Joseph Glessner, Edward C. Frackelton, Hákon Hákonarson, Faisel Syed, Anna Hindes, Scot J. Matkovich, Sharon Cresci, Gerald W. Dorn

    Vydáno 2010
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  6. 6
    A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci

    A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci Autor Jonathan P. Bradfield, Hui‐Qi Qu, Kai Wang, Haitao Zhang, Patrick Sleiman, Chong Ae Kim, Frank Mentch, Haijun Qiu, Joseph Glessner, Kelly Thomas, Edward C. Frackelton, Rosetta Chiavacci, Marcin Imieliński, Dimitri Monos, Rahul Pandey, Marina Bakay, Struan F.A. Grant, Constantin Polychronakos, Hákon Hákonarson

    Vydáno 2011
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    Revisão
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  7. 7
    Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP

    Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP Autor Struan F.A. Grant, Mingyao Li, Jonathan P. Bradfield, Cecilia E. Kim, Kiran Annaiah, Erin Santa, Joseph Glessner, Tracy Casalunovo, Edward C. Frackelton, F. George Otieno, Julie L. Shaner, Ryan M. Smith, Marcin Imieliński, Andrew W. Eckert, Rosetta Chiavacci, Robert I. Berkowitz, Hákon Hákonarson

    Vydáno 2008
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  8. 8
    The Role of Obesity‐associated Loci Identified in Genome‐wide Association Studies in the Determination of Pediatric BMI

    The Role of Obesity‐associated Loci Identified in Genome‐wide Association Studies in the Determination of Pediatric BMI Autor Jianhua Zhao, Jonathan P. Bradfield, Mingyao Li, Kai Wang, Haitao Zhang, Cecilia E. Kim, Kiran Annaiah, Joseph Glessner, Kelly Thomas, Maria Garris, Edward C. Frackelton, F. George Otieno, Julie L. Shaner, Ryan M. Smith, Rosetta Chiavacci, Robert I. Berkowitz, Hákon Hákonarson, Struan F.A. Grant

    Vydáno 2009
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  9. 9
    Examination of Type 2 Diabetes Loci Implicates <i>CDKAL1</i> as a Birth Weight Gene

    Examination of Type 2 Diabetes Loci Implicates <i>CDKAL1</i> as a Birth Weight Gene Autor Jianhua Zhao, Mingyao Li, Jonathan P. Bradfield, Kai Wang, Haitao Zhang, Patrick Sleiman, Chong Ae Kim, Kiran Annaiah, Wendy Glaberson, Joseph Glessner, F. George Otieno, Kelly Thomas, Maria Garris, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Robert I. Berkowitz, Hákon Hákonarson, Struan F.A. Grant

    Vydáno 2009
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  10. 10
    Investigation of the Locus Near <i>MC4R</i> With Childhood Obesity in Americans of European and African Ancestry

    Investigation of the Locus Near <i>MC4R</i> With Childhood Obesity in Americans of European and African Ancestry Autor Struan F.A. Grant, Jonathan P. Bradfield, Haitao Zhang, Kai Wang, Cecilia E. Kim, Kiran Annaiah, Erin Santa, Joseph Glessner, Kelly Thomas, Maria Garris, Edward C. Frackelton, F. George Otieno, Julie L. Shaner, Ryan M. Smith, Marcin Imieliński, Rosetta Chiavacci, Mingyao Li, Robert I. Berkowitz, Hákon Hákonarson

    Vydáno 2009
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  11. 11
    The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

    The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature Autor Jianhua Zhao, Mingyao Li, Jonathan P. Bradfield, Haitao Zhang, Frank Mentch, Kai Wang, Patrick Sleiman, Cecilia E Kim, Joseph Glessner, Cuiping Hou, Brendan J. Keating, Kelly Thomas, Maria Garris, Sandra Deliard, Edward C. Frackelton, F. George Otieno, Rosetta Chiavacci, Robert I. Berkowitz, Hákon Hákonarson, Struan F.A. Grant

    Vydáno 2010
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  12. 12
    A Genome-wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases

    A Genome-wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases Autor Joseph Glessner, Jonathan P. Bradfield, Kai Wang, Nagahide Takahashi, Haitao Zhang, Patrick Sleiman, Frank Mentch, Cecilia E. Kim, Cuiping Hou, Kelly Thomas, Maria Garris, Sandra Deliard, Edward C. Frackelton, F. George Otieno, Jianhua Zhao, Rosetta Chiavacci, Mingyao Li, Joseph D. Buxbaum, Robert I. Berkowitz, Hákon Hákonarson, Struan F.A. Grant

    Vydáno 2010
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  13. 13
    Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

    Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease Autor Robert N. Baldassano, Jonathan P. Bradfield, Dimitri Monos, Changhwan Kim, Joseph Glessner, Tracy Casalunovo, Edward C. Frackelton, F. George Otieno, Stathis Kanterakis, Julie L. Shaner, Richard M. Smith, Andrew W. Eckert, Lozen Robinson, Chioma C. Onyiah, Dominic J. Abrams, Rosetta Chiavacci, Robert Skraban, Marcella Devoto, Struan F.A. Grant, Hákon Hákonarson

    Vydáno 2007
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  14. 14
    Association of Variants of the Interleukin-23 Receptor Gene With Susceptibility to Pediatric Crohn’s Disease

    Association of Variants of the Interleukin-23 Receptor Gene With Susceptibility to Pediatric Crohn’s Disease Autor Robert N. Baldassano, Jonathan P. Bradfield, Dimitri Monos, Chong Ae Kim, Joseph Glessner, Tracy Casalunovo, Edward C. Frackelton, F. George Otieno, Stathis Kanterakis, Julie L. Shaner, Ryan M. Smith, Andrew W. Eckert, Luke J. Robinson, Chioma C. Onyiah, Debra Abrams, Rosetta Chiavacci, Robert Skraban, Marcella Devoto, Struan F.A. Grant, Hákon Hákonarson

    Vydáno 2007
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  15. 15
    Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

    Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes Autor Josephine Elia, Xiaowu Gai, Hongbo Xie, Juan C. Perín, Elizabeth A. Geiger, Joseph Glessner, Monica D’Arcy, Rachel deBerardinis, Edward C. Frackelton, C. Kim, Francesca Lantieri, B M Muganga, L. Wang, Toshinobu Takeda, Eric Rappaport, Struan F.A. Grant, Wade H. Berrettini, Marcella Devoto, Tamim H. Shaikh, Hákon Hákonarson, Peter S. White

    Vydáno 2009
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  16. 16
    ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry

    ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry Autor Patrick Sleiman, Kiran Annaiah, Marcin Imieliński, Jonathan P. Bradfield, Cecilia E. Kim, Edward C. Frackelton, Joseph Glessner, Andrew W. Eckert, F. George Otieno, Erin Santa, Kelly Thomas, Ryan M. Smith, Wendy Glaberson, Maria Garris, Sigfus Gunnlaugsson, Rosetta Chiavacci, Julian L. Allen, Jonathan M. Spergel, Robert W. Grundmeier, Michael Grunstein, Mark Magnusson, Hans Bisgaard, Struan F.A. Grant, Hákon Hákonarson

    Vydáno 2008
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  17. 17
    Common variants at 5q22 associate with pediatric eosinophilic esophagitis

    Common variants at 5q22 associate with pediatric eosinophilic esophagitis Autor Marc E. Rothenberg, Jonathan M. Spergel, Joseph D. Sherrill, Kiran Annaiah, Lisa J. Martin, Antonella Cianferoni, Laura Gober, Cecilia Kim, Joseph Glessner, Edward C. Frackelton, Kelly Thomas, Carine Blanchard, Chris A. Liacouras, Ritu Verma, Seema S. Aceves, Margaret H. Collins, Terri Brown‐Whitehorn, Phil E. Putnam, James P. Franciosi, Rosetta Chiavacci, Struan F.A. Grant, J. Pablo Abonia, Patrick Sleiman, Hákon Hákonarson

    Vydáno 2010
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  18. 18
    Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease

    Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease Autor Kai Wang, Haitao Zhang, Subra Kugathasan, Vito Annese, Jonathan P. Bradfield, Richard K. Russell, Patrick Sleiman, Marcin Imieliński, Joseph Glessner, Cuiping Hou, David C. Wilson, Thomas D. Walters, Cecilia Kim, Edward C. Frackelton, Paolo Lionetti, A. Barabino, Johan Van Limbergen, Stephen L. Guthery, Lee A. Denson, David A. Piccoli, Mingyao Li, Marla Dubinsky, Mark S. Silverberg, Anne M. Griffiths, Struan F.A. Grant, Jack Satsangi, Robert N. Baldassano, Hákon Hákonarson

    Vydáno 2009
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  19. 19
    A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study

    A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study Autor Hákon Hákonarson, Hui‐Qi Qu, Jonathan P. Bradfield, Luc Marchand, Cecilia E. Kim, Joseph Glessner, Rosemarie Grabs, Tracy Casalunovo, Shayne Taback, Edward C. Frackelton, Andrew W. Eckert, Kiran Annaiah, Margaret L. Lawson, F. George Otieno, Erin Santa, Julie L. Shaner, Ryan M. Smith, Chioma C. Onyiah, Robert Skraban, Rosetta Chiavacci, Luke J. Robinson, Charles A. Stanley, Susan Kirsch, Marcella Devoto, Dimitri Monos, Struan F.A. Grant, Constantin Polychronakos

    Vydáno 2008
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  20. 20
    Follow-Up Analysis of Genome-Wide Association Data Identifies Novel Loci for Type 1 Diabetes

    Follow-Up Analysis of Genome-Wide Association Data Identifies Novel Loci for Type 1 Diabetes Autor Struan F.A. Grant, Hui‐Qi Qu, Jonathan P. Bradfield, Luc Marchand, Cecilia E. Kim, Joseph Glessner, Rosemarie Grabs, Shayne Taback, Edward C. Frackelton, Andrew W. Eckert, Kiran Annaiah, Margaret L. Lawson, F. George Otieno, Erin Santa, Julie L. Shaner, Ryan M. Smith, Robert Skraban, Marcin Imieliński, Rosetta Chiavacci, Robert W. Grundmeier, Charles A. Stanley, Susan Kirsch, Daryl Waggott, Andrew D. Paterson, Dimitri Monos, Constantin Polychronakos, Hákon Hákonarson

    Vydáno 2008
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