Association Analysis of Type 2 Diabetes Loci in Type 1 Diabetes

Por Qu, Hui-Qi, Grant, Struan F.A., Bradfield, Jonathan P., Kim, Cecilia, Frackelton, Edward, Hakonarson, Hakon, Polychronakos, Constantin
Publicado em 2008

Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies

Por Qu, Hui-Qi, Grant, Struan F.A., Bradfield, Jonathan P., Kim, Cecilia, Frackelton, Edward, Hakonarson, Hakon, Polychronakos, Constantin
Publicado em 2009

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

Por Wei, Zhi, Wang, Wei, Bradfield, Jonathan, Li, Jin, Cardinale, Christopher, Frackelton, Edward, Kim, Cecilia, Mentch, Frank, Van Steen, Kristel, Visscher, Peter M., Baldassano, Robert N., Hakonarson, Hakon
Publicado em 2013

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

Por Glessner, Joseph T., Wang, Kai, Sleiman, Patrick M. A., Zhang, Haitao, Kim, Cecilia E., Flory, James H., Bradfield, Jonathan P., Imielinski, Marcin, Frackelton, Edward C., Qiu, Haijun, Mentch, Frank, Grant, Struan F. A., Hakonarson, Hakon
Publicado em 2010

Common variants in HSPB7 and FRMD4B associated with advanced heart failure

Por Cappola, Thomas P., Li, Mingyao, He, Jing, Ky, Bonnie, Gilmore, Joan, Qu, Liming, Keating, Brendan, Reilly, Muredach, Kim, Cecilia E., Glessner, Joseph, Frackelton, Edward, Hakonarson, Hakon, Syed, Faisel, Hindes, Anna, Matkovich, Scot J., Cresci, Sharon, Dorn, Gerald W.
Publicado em 2010

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

Por Matsunami, Nori, Hadley, Dexter, Hensel, Charles H., Christensen, G. Bryce, Kim, Cecilia, Frackelton, Edward, Thomas, Kelly, da Silva, Renata Pellegrino, Stevens, Jeff, Baird, Lisa, Otterud, Brith, Ho, Karen, Varvil, Tena, Leppert, Tami, Lambert, Christophe G., Leppert, Mark, Hakonarson, Hakon
Publicado em 2013

The missense variation landscape of FTO, MC4R and TMEM18 in obese children of African ancestry

Por Deliard, Sandra, Panossian, Saarene, Mentch, Frank D., Kim, Cecilia E., Hou, Cuiping, Frackelton, Edward C., Bradfield, Jonathan P., Glessner, Joseph T., Zhang, Haitao, Wang, Kai, Sleiman, Patrick M.A., Chiavacci, Rosetta M., Berkowitz, Robert I., Hakonarson, Hakon, Zhao, Jianhua, Grant, Struan F.A.
Publicado em 2013

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry

Por Grant, Struan FA, Petri, Michelle, Bradfield, Jonathan P, Kim, Cecilia E, Santa, Erin, Annaiah, Kiran, Frackelton, Edward C, Glessner, Joseph T, Otieno, F George, Shaner, Julie L, Smith, Ryan M, Eckert, Andrew W, Chiavacci, Rosetta M, Imielinski, Marcin, Sullivan, Kathleen E, Hakonarson, Hakon
Publicado em 2009

Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP

Por Grant, Struan F. A., Li, Mingyao, Bradfield, Jonathan P., Kim, Cecilia E., Annaiah, Kiran, Santa, Erin, Glessner, Joseph T., Casalunovo, Tracy, Frackelton, Edward C., Otieno, F. George, Shaner, Julie L., Smith, Ryan M., Imielinski, Marcin, Eckert, Andrew W., Chiavacci, Rosetta M., Berkowitz, Robert I., Hakonarson, Hakon
Publicado em 2008

Examination of All Type 2 Diabetes GWAS Loci Reveals HHEX-IDE as a Locus Influencing Pediatric BMI

Por Zhao, Jianhua, Bradfield, Jonathan P., Zhang, Haitao, Annaiah, Kiran, Wang, Kai, Kim, Cecilia E., Glessner, Joseph T., Frackelton, Edward C., Otieno, F. George, Doran, James, Thomas, Kelly A., Garris, Maria, Hou, Cuiping, Chiavacci, Rosetta M., Li, Mingyao, Berkowitz, Robert I., Hakonarson, Hakon, Grant, Struan F.A.
Publicado em 2010

Examination of Type 2 Diabetes Loci Implicates CDKAL1 as a Birth Weight Gene

Por Zhao, Jianhua, Li, Mingyao, Bradfield, Jonathan P., Wang, Kai, Zhang, Haitao, Sleiman, Patrick, Kim, Cecilia E., Annaiah, Kiran, Glaberson, Wendy, Glessner, Joseph T., Otieno, F. George, Thomas, Kelly A., Garris, Maria, Hou, Cuiping, Frackelton, Edward C., Chiavacci, Rosetta M., Berkowitz, Robert I., Hakonarson, Hakon, Grant, Struan F.A.
Publicado em 2009

The role of obesity-associated loci identified in genome wide association studies in the determination of pediatric BMI

Por Zhao, Jianhua, Bradfield, Jonathan P., Li, Mingyao, Wang, Kai, Zhang, Haitao, Kim, Cecilia E., Annaiah, Kiran, Glessner, Joseph T., Thomas, Kelly, Garris, Maria, Frackelton, Edward C., Otieno, F. George, Shaner, Julie L., Smith, Ryan M., Chiavacci, Rosetta M., Berkowitz, Robert I., Hakonarson, Hakon, Grant, Struan F.A.
Publicado em 2009

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry

Por Grant, Struan F.A., Bradfield, Jonathan P., Zhang, Haitao, Wang, Kai, Kim, Cecilia E., Annaiah, Kiran, Santa, Erin, Glessner, Joseph T., Thomas, Kelly, Garris, Maria, Frackelton, Edward C., Otieno, F. George, Shaner, Julie L., Smith, Ryan M., Imielinski, Marcin, Chiavacci, Rosetta M., Li, Mingyao, Berkowitz, Robert I., Hakonarson, Hakon
Publicado em 2009

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

Por Bradfield, Jonathan P., Qu, Hui-Qi, Wang, Kai, Zhang, Haitao, Sleiman, Patrick M., Kim, Cecilia E., Mentch, Frank D., Qiu, Haijun, Glessner, Joseph T., Thomas, Kelly A., Frackelton, Edward C., Chiavacci, Rosetta M., Imielinski, Marcin, Monos, Dimitri S., Pandey, Rahul, Bakay, Marina, Grant, Struan F. A., Polychronakos, Constantin, Hakonarson, Hakon
Publicado em 2011

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

Por Zhao, Jianhua, Li, Mingyao, Bradfield, Jonathan P, Zhang, Haitao, Mentch, Frank D, Wang, Kai, Sleiman, Patrick M, Kim, Cecilia E, Glessner, Joseph T, Hou, Cuiping, Keating, Brendan J, Thomas, Kelly A, Garris, Maria L, Deliard, Sandra, Frackelton, Edward C, Otieno, F George, Chiavacci, Rosetta M, Berkowitz, Robert I, Hakonarson, Hakon, Grant, Struan FA
Publicado em 2010

Association of the T300A non‐synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease

Por Baldassano, Robert N, Bradfield, Jonathan P, Monos, Dimitri S, Kim, Cecilia E, Glessner, Joseph T, Casalunovo, Tracy, Frackelton, Edward C, Otieno, F George, Kanterakis, Stathis, Shaner, Julie L, Smith, Ryan M, Eckert, Andrew W, Robinson, Luke J, Onyiah, Chioma C, Abrams, Debra J, Chiavacci, Rosetta M, Skraban, Robert, Devoto, Marcella, Grant, Struan F A, Hakonarson, Hakon
Publicado em 2007

A Genome-wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases

Por Glessner, Joseph T., Bradfield, Jonathan P., Wang, Kai, Takahashi, Nagahide, Zhang, Haitao, Sleiman, Patrick M., Mentch, Frank D., Kim, Cecilia E., Hou, Cuiping, Thomas, Kelly A., Garris, Maria L., Deliard, Sandra, Frackelton, Edward C., Otieno, F. George, Zhao, Jianhua, Chiavacci, Rosetta M., Li, Mingyao, Buxbaum, Joseph D., Berkowitz, Robert I., Hakonarson, Hakon, Grant, Struan F.A.
Publicado em 2010

Association of variants of the interleukin-23 receptor (IL23R) gene with susceptibility to pediatric Crohn’s disease

Por Baldassano, Robert N., Bradfield, Jonathan P., Monos, Dimitri S., Kim, Cecilia E., Glessner, Joseph T., Casalunovo, Tracy, Frackelton, Edward C., Otieno, F. George, Kanterakis, Stathis, Shaner, Julie L., Smith, Ryan M., Eckert, Andrew W., Robinson, Luke J., Onyiah, Chioma C., Abrams, Debra J., Chiavacci, Rosetta M., Skraban, Robert, Devoto, Marcella, Grant, Struan F.A., Hakonarson, Hakon
Publicado no Clin Gastroenterol Hepatol (2007)

Examination of genetic variants influencing lipid traits in pediatric populations

Por Wang, Kai, Zhang, Haitao, Mentch, Frank D., Bradfield, Jonathan P., Glessner, Joseph T., Qiu, Haijun, Guo, Yiran, Hou, Cuiping, Frackelton, Edward C., Thomas, Kelly, Bender, Amber, Albano, Anthony, Otieno, George, Garris, Maria, Seidler, Kallyn, Moy, Alexander, Kim, Cecilia E., Keating, Brendan, Chiavacci, Rosetta M., Grundmeier, Robert, Sleiman, Patrick A., Grant, Struan F.A., Hakonarson, Hakon
Publicado no J Pediatr Genet (2012)

Common variants at 5q22associate with pediatric eosinophilic esophagitis

Por Rothenberg, Marc E., Spergel, Jonathan M., Sherrill, Joseph D., Annaiah, Kiran, Martin, Lisa J., Cianferoni, Antonella, Gober, Laura, Kim, Cecilia, Glessner, Joseph, Frackelton, Edward, Thomas, Kelly, Blanchard, Carine, Liacouras, Chris, Verma, Ritu, Aceves, Seema, Collins, Margaret H., Brown-Whitehorn, Terri, Putnam, Phil E., Franciosi, James P., Chiavacci, Rosetta M, Grant, J. Struan F.A., Abonia, J. Pablo, Sleiman, Patrick M.A., Hakonarson, Hakon
Publicado em 2010