Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Kiran, Annaiah"'
Autor:
Struan F A Grant, Mingyao Li, Jonathan P Bradfield, Cecilia E Kim, Kiran Annaiah, Erin Santa, Joseph T Glessner, Tracy Casalunovo, Edward C Frackelton, F George Otieno, Julie L Shaner, Ryan M Smith, Marcin Imielinski, Andrew W Eckert, Rosetta M Chiavacci, Robert I Berkowitz, Hakon Hakonarson
Publikováno v:
PLoS ONE, Vol 3, Iss 3, p e1746 (2008)
Recently an association was demonstrated between the single nucleotide polymorphism (SNP), rs9939609, within the FTO locus and obesity as a consequence of a genome wide association (GWA) study of type 2 diabetes in adults. We examined the effects of
Externí odkaz:
https://doaj.org/article/23d313cfac7d4c49879d454db897a2d9
Autor:
Haitao Zhang, Cecilia E. Kim, Joseph T. Glessner, Mingyao Li, F. George Otieno, Julie L. Shaner, Rosetta M. Chiavacci, Hakon Hakonarson, Ryan M. Smith, Kiran Annaiah, Edward C. Frackelton, Robert I. Berkowitz, Struan F.A. Grant, Jonathan P. Bradfield, Kai Wang, Maria Garris, Kelly A. Thomas, Jianhua Zhao
Publikováno v:
Obesity. 17:2254-2257
The prevalence of obesity in children and adults in the United States has increased dramatically over the past decade. Besides environmental factors, genetic factors are known to play an important role in the pathogenesis of obesity. A number of gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dbd9792bc2f113ca293c539fdf4bb78
https://doi.org/10.1038/oby.2009.159
https://doi.org/10.1038/oby.2009.159
Autor:
Rosetta M. Chiavacci, Cuiping Hou, Jonathan P. Bradfield, Haitao Zhang, Kelly A. Thomas, Cecilia E. Kim, Maria Garris, Joseph T. Glessner, Mingyao Li, Robert I. Berkowitz, Hakon Hakonarson, Edward C. Frackelton, F. George Otieno, Struan F.A. Grant, Patrick M. A. Sleiman, Kiran Annaiah, Jianhua Zhao, Kai Wang, Wendy Glaberson
Publikováno v:
Diabetes
OBJECTIVE A number of studies have found that reduced birth weight is associated with type 2 diabetes later in life; however, the underlying mechanism for this correlation remains unresolved. Recently, association has been demonstrated between low bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c437c5e75de8c2d82509bee3a7729935
https://doi.org/10.2337/db09-0506
https://doi.org/10.2337/db09-0506
Autor:
Kai Wang, Rosetta M. Chiavacci, Kiran Annaiah, Ryan M. Smith, Hakon Hakonarson, Kelly A. Thomas, Maria Garris, Erin Santa, Marcin Imielinski, Struan F.A. Grant, Cecilia E. Kim, Jonathan P. Bradfield, Julie L. Shaner, Joseph T. Glessner, Mingyao Li, Robert I. Berkowitz, F. George Otieno, Edward C. Frackelton, Haitao Zhang
Publikováno v:
Obesity. 17:1461-1465
Recently a modest, but consistently, replicated association was demonstrated between obesity and the single nucleotide polymorphism (SNP), rs17782313, 3’ of the MC4R locus as a consequence of a meta-analysis of genome wide association (GWA) studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c097762dc1228f41bfb9b1ae9dc8b299
https://doi.org/10.1038/oby.2009.53
https://doi.org/10.1038/oby.2009.53
Autor:
Joseph Piven, Edward C. Frackelton, Christopher J. McDougle, Patrick M. A. Sleiman, Rosetta M. Chiavacci, John A. Sweeney, Guiqing Cai, Gerard D. Schellenberg, Camille W. Brune, Cuiping Hou, Shana M. Michaels, Rachel M. Game, Wendy Glaberson, Kai Wang, Raphael Bernier, Maja Bucan, Danielle Zurawiecki, Susan E. Levy, Alexander Kolevzon, Hilary Coon, Jeremy M. Silverman, Cecilia E. Kim, Latha Soorya, Nancy J. Minshew, Danielle S. Rudd, David J. Posey, Kacie J. Meyer, James H. Flory, Geraldine Dawson, Emily L. Crawford, Lea K. Davis, Judith Miller, Lambertus Klei, James S. Sutcliffe, Maria Garris, Evdokia Anagnostou, Annette Estes, Marcin Imielinski, Kelly A. Thomas, John I. Nurnberger, Struan F.A. Grant, Thomas H. Wassink, Hakon Hakonarson, Jonathan P. Bradfield, Edwin H. Cook, Bernie Devlin, Frederick G. Otieno, Joseph D. Buxbaum, Shawn Wood, Takeshi Sakurai, Robert T. Schultz, Jeffrey Munson, Thomas Owley, Kiran Annaiah, Joseph T. Glessner, Jennifer Reichert, Haitao Zhang, William M. McMahon, Olena Korvatska
Publikováno v:
Nature. 459:569-573
Autism spectrum disorders (ASDs) are childhood neurodevelopmental disorders with complex genetic origins. Previous studies focusing on candidate genes or genomic regions have identified several copy number variations (CNVs) that are associated with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::843b651f351c30057edfc7d02605efdb
https://doi.org/10.1038/nature07953
https://doi.org/10.1038/nature07953
Autor:
F. George Otieno, Struan F.A. Grant, Andrew W. Eckert, Kathleen E. Sullivan, Rosetta M. Chiavacci, Marcin Imielinski, Ryan M. Smith, Julie L. Shaner, Michelle Petri, Hakon Hakonarson, Edward C. Frackelton, Joseph T. Glessner, Erin Santa, Jonathan P. Bradfield, Kiran Annaiah, Cecilia E. Kim
Publikováno v:
The Application of Clinical Genetics. 2:1-5
Recently an association was demonstrated between the single nucleotide polymorphism (SNP), rs10516487, within the B-cell gene BANK1 and systemic lupus erythematosus (SLE) as a consequence of a genome wide association study of this disease in European
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b9493dcfd0cdc715972038754641c80
https://doi.org/10.2147/tacg.s4089
https://doi.org/10.2147/tacg.s4089
Autor:
David A. Piccoli, Tara Willson, Robert W. Grundmeier, Jonathan P. Bradfield, Dimitri S. Monos, Rosetta M. Chiavacci, Ryan M. Smith, Patrick M. A. Sleiman, Struan F.A. Grant, Petar Mamula, Cecilia E. Kim, Edward C. Frackelton, Joseph T. Glessner, Salvatore Cucchiara, Stephen L. Guthery, Gitit Tomer, Subra Kugathasan, Erin Bonkowski, Andrew W. Eckert, Robert N. Baldassano, Erin Santa, Vito Annese, Kiran Annaiah, Marcin Imielinski, Debra J. Abrams, Lee A. Denson, Julie L. Shaner, Hakon Hakonarson, F. George Otieno, Nicholas Peterson
Publikováno v:
Nature Genetics. 40:1211-1215
Inflammatory bowel disease (IBD) is a common inflammatory disorder with complex etiology that involves both genetic and environmental triggers, including but not limited to defects in bacterial clearance, defective mucosal barrier and persistent dysr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51fc77f2c0dd77d45f89b75aa8172895
https://doi.org/10.1038/ng.203
https://doi.org/10.1038/ng.203
Autor:
Joseph D. Sherrill, Laura M. Gober, Seema S. Aceves, Rosetta M. Chiavacci, Marc E. Rothenberg, James P. Franciosi, Kelly A. Thomas, Edward C. Frackelton, Joseph T. Glessner, Jonathan M. Spergel, J. Pablo Abonia, Margaret H. Collins, Antonella Cianferoni, Hakon Hakonarson, Phil E. Putnam, Cecilia Kim, Lisa J. Martin, Terri F. Brown-Whitehorn, J. Struan F.A. Grant, Carine Blanchard, Kiran Annaiah, Chris A. Liacouras, Patrick M. A. Sleiman, Ritu Verma
Publikováno v:
Nature Genetics. 42:289-291
Eosinophilic esophagitis (EoE) is a polygenic disorder characterized by the accumulation of eosinophils in the esophagus. We carried out a genome-wide association study on clinically and biopsy confirmed EoE patients to identify common variants assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f27a9a72ba452fd92275749a0530613
https://doi.org/10.1038/ng.547
https://doi.org/10.1038/ng.547
Autor:
Rosetta M. Chiavacci, Julian L. Allen, Cecilia E. Kim, Wendy Glaberson, Hans Bisgaard, James H. Flory, Kelly A. Thomas, Robert W. Grundmeier, Patrick M. A. Sleiman, Hou Cuiping, Jason D. Christie, Klaus Bønnelykke, Michael M. Grunstein, Michael Magnusson, Hakon Hakonarson, Hongzhe Li, Struan F.A. Grant, Edward C. Frackelton, Jonathan M. Spergel, Kiran Annaiah, Jonathan P. Bradfield, Maria Garris, Marcin Imielinski, George Otieno, Joseph T. Glessner, Ryan Smith
Publikováno v:
Journal of Allergy and Clinical Immunology. 124:605-607
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c90454600331acb8df574c50962e32d
https://doi.org/10.1016/j.jaci.2009.05.047
https://doi.org/10.1016/j.jaci.2009.05.047
Autor:
Struan Fa, Grant, Michelle, Petri, Jonathan P, Bradfield, Cecilia E, Kim, Erin, Santa, Kiran, Annaiah, Edward C, Frackelton, Joseph T, Glessner, F George, Otieno, Julie L, Shaner, Ryan M, Smith, Andrew W, Eckert, Rosetta M, Chiavacci, Marcin, Imielinski, Kathleen E, Sullivan, Hakon, Hakonarson
Publikováno v:
The Application of Clinical Genetics
Recently an association was demonstrated between the single nucleotide polymorphism (SNP), rs10516487, within the B-cell gene BANK1 and systemic lupus erythematosus (SLE) as a consequence of a genome wide association study of this disease in European
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58f17c154874f70f0a68fe5f3a1c526b
https://pubmed.ncbi.nlm.nih.gov/23776345
https://pubmed.ncbi.nlm.nih.gov/23776345