Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Andrew W Eckert"'
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:
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:
Cecilia E. Kim, Tracy Casalunovo, Marcella Devoto, F. George Otieno, Struan F.A. Grant, Robert N. Baldassano, Rosetta M. Chiavacci, Debra J. Abrams, Ryan M. Smith, Luke J. Robinson, Chioma C. Onyiah, Dimitri S. Monos, Julie L. Shaner, Stathis Kanterakis, Jonathan P. Bradfield, Hakon Hakonarson, Robert Skraban, Edward C. Frackelton, Joseph T. Glessner, Andrew W. Eckert
Publikováno v:
Clinical Gastroenterology and Hepatology. 5:972-976
Background & Aims: Recently an association was shown between the single nucleotide polymorphism (SNP), rs11209026, within the interleukin-23 receptor ( IL23R ) locus and Crohn's disease (CD) as a consequence of a genome-wide association study of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72937a07e41bc3beb39e86ced72b0b9b
https://doi.org/10.1016/j.cgh.2007.04.024
https://doi.org/10.1016/j.cgh.2007.04.024
Autor:
Cecilia Kim, Robert C. Seeger, Stefano Monni, Richard H Scott, Edward F. Attiyeh, Shahab Asgharzadeh, Joseph T. Glessner, Eric F. Rappaport, Edward C. Frackelton, Cynthia Winter, Hongzhe Li, Mario Capasso, Carmel McConville, Hakon Hakonarson, Marcella Devoto, John M. Maris, Sharon J. Diskin, Kristina A. Cole, Marci Laudenslager, Wendy B. London, Nazneen Rahman, Jonathan P. Bradfield, Andrew W. Eckert, Cuiping Hou, Tracy Casalunovo, Struan F.A. Grant, Yael P. Mosse
Neuroblastoma is a malignant condition of the developing sympathetic nervous system that most commonly affects young children and is often lethal. Its cause is not known.We performed a genomewide association study by first genotyping blood DNA sample
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfc1fbf1555e07373041a7acf0eaf97a
http://hdl.handle.net/11573/50401
http://hdl.handle.net/11573/50401
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
Autor:
Juan C. Perin, Tracy Casalunovo, Kevin Murphy, F. George Otieno, Chioma C. Onyiah, Chad R. Haldeman-Englert, Livija Medne, Tamim H. Shaikh, Struan F.A. Grant, Hongbo Xie, Xiaowu Gai, Nancy B. Spinner, Elizabeth A. Geiger, Kiran Annaiah, Elvira Dabaghyan, Erin Santa, Robert W. Grundmeier, Ryan O'Hara, Jonathan P. Bradfield, Rosetta M. Chiavacci, Ryan M. Smith, Robert Skraban, Cecilia E. Kim, Hakon Hakonarson, Svetlana Ostapenko, Josephine Elia, Eric F. Rappaport, Andrew W. Eckert, Joseph T. Glessner, Laura K. Conlin, Elizabeth Goldmuntz, Elaine H. Zackai, Julie L. Shaner, Marcin Imielinski, Peter White, Edward C. Frackelton, Monica D’Arcy
Publikováno v:
Genome research. 19(9)
We present a database of copy number variations (CNVs) detected in 2026 disease-free individuals, using high-density, SNP-based oligonucleotide microarrays. This large cohort, comprised mainly of Caucasians (65.2%) and African-Americans (34.2%), was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35d908a6139586be246e685af08dc5bb
https://pubmed.ncbi.nlm.nih.gov/19592680
https://pubmed.ncbi.nlm.nih.gov/19592680
Autor:
Daryl Waggott, Cecilia E. Kim, Julie L. Shaner, Andrew W. Eckert, Rosetta M. Chiavacci, Hakon Hakonarson, Ryan M. Smith, Susan E. Kirsch, Luc Marchand, Robert Skraban, Rosemarie Grabs, Edward C. Frackelton, Struan F.A. Grant, Erin Santa, Constantin Polychronakos, Hui-Qi Qu, Kiran Annaiah, Andrew D. Paterson, Jonathan P. Bradfield, Dimitri S. Monos, Margaret L. Lawson, Robert W. Grundmeier, Marcin Imielinski, Joseph T. Glessner, Charles A. Stanley, F. George Otieno, Shayne Taback
Publikováno v:
Diabetes
OBJECTIVE—Two recent genome-wide association (GWA) studies have revealed novel loci for type 1 diabetes, a common multifactorial disease with a strong genetic component. To fully utilize the GWA data that we had obtained by genotyping 563 type 1 di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb3d61ab8724d1372a6eb51ed291396f
https://pubmed.ncbi.nlm.nih.gov/18840781
https://pubmed.ncbi.nlm.nih.gov/18840781
Autor:
Rosetta M. Chiavacci, Ryan M. Smith, Patrick M. A. Sleiman, Sigfus Gunnlaugsson, Cecilia E. Kim, Marcin Imielinski, F. George Otieno, Hakon Hakonarson, Mark R. Magnusson, Jonathan P. Bradfield, Joseph T. Glessner, Michael M. Grunstein, Robert W. Grundmeier, Struan F.A. Grant, Kiran Annaiah, Maria Garris, Erin Santa, Julian L. Allen, Hans Bisgaard, Kelly A. Thomas, Edward C. Frackelton, Jonathan M. Spergel, Andrew W. Eckert, Wendy Glaberson
Publikováno v:
The Journal of allergy and clinical immunology. 122(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f76c8b2172f98394d53fde235a5986
https://pubmed.ncbi.nlm.nih.gov/18760456
https://pubmed.ncbi.nlm.nih.gov/18760456
Autor:
Cecilia E. Kim, Joseph T. Glessner, Charles A. Stanley, Andrew W. Eckert, Edward C. Frackelton, Susan E. Kirsch, Luke J. Robinson, Robert Skraban, Dimitri S. Monos, Rosetta M. Chiavacci, Ryan M. Smith, F. George Otieno, Rosemarie Grabs, Erin Santa, Julie L. Shaner, Kiran Annaiah, Chioma C. Onyiah, Hui-Qi Qu, Margaret L. Lawson, Hakon Hakonarson, Luc Marchand, Shayne Taback, Jonathan P. Bradfield, Marcella Devoto, Struan F.A. Grant, Tracy Casalunovo, Constantin Polychronakos
Publikováno v:
Diabetes. 57(4)
OBJECTIVE—In stage 1 of our genome-wide association (GWA) study for type 1 diabetes, one locus at 16p13 was detected (P = 1.03 × 10−10) and confirmed in two additional cohorts. Here we describe the results of testing, in these additional cohorts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0498ca9a43cb5630233d436bb8b2947
https://pubmed.ncbi.nlm.nih.gov/18198356
https://pubmed.ncbi.nlm.nih.gov/18198356