A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci
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
Published in PLoS genetics (01.09.2011)
Published in PLoS genetics (01.09.2011)
Get full text
Journal Article
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
Li, Yun R, Li, Jin, Zhao, Sihai D, Bradfield, Jonathan P, Mentch, Frank D, Maggadottir, S Melkorka, Hou, Cuiping, Abrams, Debra J, Chang, Diana, Gao, Feng, Guo, Yiran, Wei, Zhi, Connolly, John J, Cardinale, Christopher J, Bakay, Marina, Glessner, Joseph T, Li, Dong, Kao, Charlly, Thomas, Kelly A, Qiu, Haijun, Chiavacci, Rosetta M, Kim, Cecilia E, Wang, Fengxiang, Snyder, James, Richie, Marylyn D, Flatø, Berit, Førre, Øystein, Denson, Lee A, Thompson, Susan D, Becker, Mara L, Guthery, Stephen L, Latiano, Anna, Perez, Elena, Resnick, Elena, Russell, Richard K, Wilson, David C, Silverberg, Mark S, Annese, Vito, Lie, Benedicte A, Punaro, Marilynn, Dubinsky, Marla C, Monos, Dimitri S, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Kugathasan, Subra, Ellis, Justine A, Munro, Jane E, Sullivan, Kathleen E, Wise, Carol A, Chapel, Helen, Cunningham-Rundles, Charlotte, Grant, Struan F A, Orange, Jordan S, Sleiman, Patrick M A, Behrens, Edward M, Griffiths, Anne M, Satsangi, Jack, Finkel, Terri H, Keinan, Alon, Prak, Eline T Luning, Polychronakos, Constantin, Baldassano, Robert N, Li, Hongzhe, Keating, Brendan J, Hakonarson, Hakon
Published in Nature medicine (01.09.2015)
Published in Nature medicine (01.09.2015)
Get full text
Journal Article
Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Verma, Ritu, Aceves, Seema, Collins, Margaret H, Liacouras, Chris, Sherrill, Joseph D, Martin, Lisa J, Thomas, Kelly, Sleiman, Patrick M A, Spergel, Jonathan M, Franciosi, James P, Grant, Struan F A, Annaiah, Kiran, Hakonarson, Hakon, Brown-Whitehorn, Terri, Putnam, Phil E, Cianferoni, Antonella, Rothenberg, Marc E, Kim, Cecilia, Glessner, Joseph, Frackelton, Edward, Blanchard, Carine, Abonia, J Pablo, Gober, Laura, Chiavacci, Rosetta M
Published in Nature genetics (01.04.2010)
Published in Nature genetics (01.04.2010)
Get full text
Journal Article
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
Elia, Josephine, Glessner, Joseph T, Wang, Kai, Takahashi, Nagahide, Shtir, Corina J, Hadley, Dexter, Sleiman, Patrick M A, Zhang, Haitao, Kim, Cecilia E, Robison, Reid, Lyon, Gholson J, Flory, James H, Bradfield, Jonathan P, Imielinski, Marcin, Hou, Cuiping, Frackelton, Edward C, Chiavacci, Rosetta M, Sakurai, Takeshi, Rabin, Cara, Middleton, Frank A, Thomas, Kelly A, Garris, Maria, Mentch, Frank, Freitag, Christine M, Steinhausen, Hans-Christoph, Todorov, Alexandre A, Reif, Andreas, Rothenberger, Aribert, Franke, Barbara, Mick, Eric O, Roeyers, Herbert, Buitelaar, Jan, Lesch, Klaus-Peter, Banaschewski, Tobias, Ebstein, Richard P, Mulas, Fernando, Oades, Robert D, Sergeant, Joseph, Sonuga-Barke, Edmund, Renner, Tobias J, Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Meyer, Jobst, Pálmason, Haukur, Seitz, Christiane, Loo, Sandra K, Smalley, Susan L, Biederman, Joseph, Kent, Lindsey, Asherson, Philip, Anney, Richard J L, Gaynor, J William, Shaw, Philip, Devoto, Marcella, White, Peter S, Grant, Struan F A, Buxbaum, Joseph D, Rapoport, Judith L, Williams, Nigel M, Nelson, Stanley F, Faraone, Stephen V, Hakonarson, Hakon
Published in Nature genetics (01.01.2012)
Published in Nature genetics (01.01.2012)
Get full text
Journal Article
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations
Li, Yun Rose, Glessner, Joseph T., Coe, Bradley P., Li, Jin, Mohebnasab, Maede, Chang, Xiao, Connolly, John, Kao, Charlly, Wei, Zhi, Bradfield, Jonathan, Kim, Cecilia, Hou, Cuiping, Khan, Munir, Mentch, Frank, Qiu, Haijun, Bakay, Marina, Cardinale, Christopher, Lemma, Maria, Abrams, Debra, Bridglall-Jhingoor, Andrew, Behr, Meckenzie, Harrison, Shanell, Otieno, George, Thomas, Alexandria, Wang, Fengxiang, Chiavacci, Rosetta, Wu, Lawrence, Hadley, Dexter, Goldmuntz, Elizabeth, Elia, Josephine, Maris, John, Grundmeier, Robert, Devoto, Marcella, Keating, Brendan, March, Michael, Pellagrino, Renata, Grant, Struan F. A., Sleiman, Patrick M. A., Li, Mingyao, Eichler, Evan E., Hakonarson, Hakon
Published in Nature communications (14.01.2020)
Published in Nature communications (14.01.2020)
Get full text
Journal Article
A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24
Grant, Struan F.A., PhD, Wang, Kai, PhD, Zhang, Haitao, PhD, Glaberson, Wendy, BA, Annaiah, Kiran, MSc, Kim, Cecilia E., BA, Bradfield, Jonathan P., BS, Glessner, Joseph T., MSc, Thomas, Kelly A., BA, Garris, Maria, BA, Frackelton, Edward C., BA, Otieno, F. George, MSc, Chiavacci, Rosetta M., BSN, Nah, Hyun-Duck, PhD, Kirschner, Richard E., MD, Hakonarson, Hakon, MD, PhD
Published in The Journal of pediatrics (01.12.2009)
Published in The Journal of pediatrics (01.12.2009)
Get full text
Journal Article
Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP
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
Published in PloS one (12.03.2008)
Published in PloS one (12.03.2008)
Get full text
Journal Article
Common variants at five new loci associated with early-onset inflammatory bowel disease
Hakonarson, Hakon, Zhang, Haitao, Grand, Richard, Hou, Cuiping, Silverberg, Mark S, Muise, Aleixo, Stephens, Michael, Annese, Vito, Grundmeier, Robert, Russell, Richard K, Lee, Jessica, Daly, Mark, Griffiths, Anne, Heyman, Melvin B, Latiano, Anna, Kirschner, Barbara, Imielinski, Marcin, Baldassano, Robert N, Cucchiara, Salvatore, Grant, Struan F A, Flory, James H, Monos, Dimitri S, Saeed, Shehzad, Chiavacci, Rosetta M, Bradfield, Jonathan P, Dallapiccola, Bruno, Denson, Lee, Taylor, Kent, McGovern, Dermot, Dubinsky, Marla, Levine, Arie, Castro, Massimo, Abrams, Debra J, Kugathasan, Subra, Otieno, George, Walters, Thomas D, Frackelton, Edward C, Sleiman, Patrick, Van Limbergen, Johan, Wilson, David C, Essers, Jonah, Glessner, Joseph T, Stempak, Joanne, Guthery, Stephen L, Satsangi, Jack, Ferry, George D, Piccoli, David, Wang, Kai, Kim, Cecilia E
Published in Nature genetics (01.12.2009)
Published in Nature genetics (01.12.2009)
Get full text
Journal Article
Web Resource
genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
HAKONARSON, Hakon, GRANT, Struan F. A, LAWSON, Margaret L, ROBINSON, Luke J, SKRABAN, Robert, YANG LU, CHIAVACCI, Rosetta M, STANLEY, Charles A, KIRSCH, Susan E, RAPPAPORT, Eric F, ORANGE, Jordan S, MONOS, Dimitri S, BRADFIELD, Jonathan P, DEVOTO, Marcella, QU, Hui-Qi, POLYCHRONAKOS, Constantin, MARCHAND, Luc, KIM, Cecilia E, GLESSNER, Joseph T, GRABS, Rosemarie, CASALUNOVO, Tracy, TABACK, Shayne P, FRACKELTON, Edward C
Published in Nature (02.08.2007)
Published in Nature (02.08.2007)
Get full text
Journal Article
Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly
Li, Dong, Wenger, Tara L, Seiler, Christoph, March, Michael E, Gutierrez-Uzquiza, Alvaro, Kao, Charlly, Bhoj, Elizabeth, Tian, Lifeng, Rosenbach, Misha, Liu, Yichuan, Robinson, Nora, Behr, Mechenzie, Chiavacci, Rosetta, Hou, Cuiping, Wang, Tiancheng, Bakay, Marina, Pellegrino da Silva, Renata, Perkins, Jonathan A, Sleiman, Patrick, Levine, Michael A, Hicks, Patricia J, Itkin, Maxim, Dori, Yoav, Hakonarson, Hakon
Published in Human molecular genetics (15.09.2018)
Published in Human molecular genetics (15.09.2018)
Get full text
Journal Article
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications
Shaikh, Tamim H, Gai, Xiaowu, Perin, Juan C, Glessner, Joseph T, Xie, Hongbo, Murphy, Kevin, O'Hara, Ryan, Casalunovo, Tracy, Conlin, Laura K, D'Arcy, Monica, Frackelton, Edward C, Geiger, Elizabeth A, Haldeman-Englert, Chad, Imielinski, Marcin, Kim, Cecilia E, Medne, Livija, Annaiah, Kiran, Bradfield, Jonathan P, Dabaghyan, Elvira, Eckert, Andrew, Onyiah, Chioma C, Ostapenko, Svetlana, Otieno, F George, Santa, Erin, Shaner, Julie L, Skraban, Robert, Smith, Ryan M, Elia, Josephine, Goldmuntz, Elizabeth, Spinner, Nancy B, Zackai, Elaine H, Chiavacci, Rosetta M, Grundmeier, Robert, Rappaport, Eric F, Grant, Struan F A, White, Peter S, Hakonarson, Hakon
Published in Genome Research (01.09.2009)
Published in Genome Research (01.09.2009)
Get full text
Journal Article
Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling
Elia, Josephine, Ungal, Grace, Kao, Charlly, Ambrosini, Alexander, De Jesus-Rosario, Nilsa, Larsen, Lene, Chiavacci, Rosetta, Wang, Tiancheng, Kurian, Christine, Titchen, Kanani, Sykes, Brian, Hwang, Sharon, Kumar, Bhumi, Potts, Jacqueline, Davis, Joshua, Malatack, Jeffrey, Slattery, Emma, Moorthy, Ganesh, Zuppa, Athena, Weller, Andrew, Byrne, Enda, Li, Yun R., Kraft, Walter K., Hakonarson, Hakon
Published in Nature communications (16.01.2018)
Published in Nature communications (16.01.2018)
Get full text
Journal Article
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children
Li, Jin, Glessner, Joseph T, Zhang, Haitao, Hou, Cuiping, Wei, Zhi, Bradfield, Jonathan P, Mentch, Frank D, Guo, Yiran, Kim, Cecilia, Xia, Qianghua, Chiavacci, Rosetta M, Thomas, Kelly A, Qiu, Haijun, Grant, Struan F A, Furth, Susan L, Hakonarson, Hakon, Sleiman, Patrick M A
Published in Human molecular genetics (01.04.2013)
Published in Human molecular genetics (01.04.2013)
Get full text
Journal Article
The Role of Obesity-associated Loci Identified in Genome-wide Association Studies in the Determination of Pediatric BMI
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.
Published in Obesity (Silver Spring, Md.) (01.12.2009)
Published in Obesity (Silver Spring, Md.) (01.12.2009)
Get full text
Journal Article
Variants of DENND1B Associated with Asthma in Children
Sleiman, Patrick M.A, Flory, James, Imielinski, Marcin, Bradfield, Jonathan P, Annaiah, Kiran, Willis-Owen, Saffron A.G, Wang, Kai, Rafaels, Nicholas M, Michel, Sven, Bonnelykke, Klaus, Zhang, Haitao, Kim, Cecilia E, Frackelton, Edward C, Glessner, Joseph T, Hou, Cuiping, Otieno, F. George, Santa, Erin, Thomas, Kelly, Smith, Ryan M, Glaberson, Wendy R, Garris, Maria, Chiavacci, Rosetta M, Beaty, Terri H, Ruczinski, Ingo, Orange, Jordan M, Allen, Julian, Spergel, Jonathan M, Grundmeier, Robert, Mathias, Rasika A, Christie, Jason D, von Mutius, Erika, Cookson, William O.C, Kabesch, Michael, Moffatt, Miriam F, Grunstein, Michael M, Barnes, Kathleen C, Devoto, Marcella, Magnusson, Mark, Li, Hongzhe, Grant, Struan F.A, Bisgaard, Hans, Hakonarson, Hakon
Published in The New England journal of medicine (07.01.2010)
Published in The New England journal of medicine (07.01.2010)
Get full text
Journal Article
Genome-wide association identifies diverse causes of common variable immunodeficiency
Orange, Jordan S., MD, PhD, Glessner, Joseph T., MS, Resnick, Elena, MD, Sullivan, Kathleen E., MD, Lucas, Mary, MD, Ferry, Berne, MD, Kim, Cecilia E., BS, Hou, Cuiping, BS, Wang, Fengxiang, BS, Chiavacci, Rosetta, BSN, Kugathasan, Subra, MD, Sleasman, John W., MD, Baldassano, Robert, MD, Perez, Elena E., MD, Chapel, Helen, MD, Cunningham-Rundles, Charlotte, MD, Hakonarson, Hakon, MD, PhD
Published in Journal of allergy and clinical immunology (01.06.2011)
Published in Journal of allergy and clinical immunology (01.06.2011)
Get full text
Journal Article
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
Baldassano, Robert N, Kim, Cecilia E, Chiavacci, Rosetta M, Frackelton, Edward C, Eckert, Andrew W, Abrams, Debra J, Annese, Vito, Bradfield, Jonathan P, Bonkowski, Erin, Annaiah, Kiran, Cucchiara, Salvatore, Shaner, Julie L, Otieno, F George, Grundmeier, Robert, Piccoli, David A, Glessner, Joseph T, Imielinski, Marcin, Monos, Dimitri S, Sleiman, Patrick M A, Tomer, Gitit, Guthery, Stephen L, Smith, Ryan M, Santa, Erin, Willson, Tara, Kugathasan, Subra, Peterson, Nicholas, Mamula, Petar, Grant, Struan F A, Hakonarson, Hakon, Denson, Lee A
Published in Nature genetics (01.10.2008)
Published in Nature genetics (01.10.2008)
Get full text
Journal Article
Body Mass Index (BMI) Trajectories in Infancy Differ by Population Ancestry and May Presage Disparities in Early Childhood Obesity
Roy, Sani M, Chesi, Alessandra, Mentch, Frank, Xiao, Rui, Chiavacci, Rosetta, Mitchell, Jonathan A, Kelly, Andrea, Hakonarson, Hakon, Grant, Struan F.A, Zemel, Babette S, McCormack, Shana E
Published in The journal of clinical endocrinology and metabolism (01.04.2015)
Published in The journal of clinical endocrinology and metabolism (01.04.2015)
Get full text
Journal Article
Genetic sharing and heritability of paediatric age of onset autoimmune diseases
Li, Yun R., Zhao, Sihai D., Li, Jin, Bradfield, Jonathan P., Mohebnasab, Maede, Steel, Laura, Kobie, Julie, Abrams, Debra J., Mentch, Frank D., Glessner, Joseph T., Guo, Yiran, Wei, Zhi, Connolly, John J., Cardinale, Christopher J., Bakay, Marina, Li, Dong, Maggadottir, S. Melkorka, Thomas, Kelly A., Qui, Haijun, Chiavacci, Rosetta M., Kim, Cecilia E., Wang, Fengxiang, Snyder, James, Flatø, Berit, Førre, Øystein, Denson, Lee A., Thompson, Susan D., Becker, Mara L., Guthery, Stephen L., Latiano, Anna, Perez, Elena, Resnick, Elena, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Silverberg, Mark S., Lie, Benedicte A., Punaro, Marilynn, Russell, Richard K., Wilson, David C., Dubinsky, Marla C., Monos, Dimitri S., Annese, Vito, Munro, Jane E., Wise, Carol, Chapel, Helen, Cunningham-Rundles, Charlotte, Orange, Jordan S., Behrens, Edward M., Sullivan, Kathleen E., Kugathasan, Subra, Griffiths, Anne M., Satsangi, Jack, Grant, Struan F. A., Sleiman, Patrick M. A., Finkel, Terri H., Polychronakos, Constantin, Baldassano, Robert N., Luning Prak, Eline T., Ellis, Justine A., Li, Hongzhe, Keating, Brendan J., Hakonarson, Hakon
Published in Nature communications (09.10.2015)
Published in Nature communications (09.10.2015)
Get full text
Journal Article
From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes
Wei, Zhi, Wang, Kai, Qu, Hui-Qi, Zhang, Haitao, Bradfield, Jonathan, Kim, Cecilia, Frackleton, Edward, Hou, Cuiping, Glessner, Joseph T, Chiavacci, Rosetta, Stanley, Charles, Monos, Dimitri, Grant, Struan F A, Polychronakos, Constantin, Hakonarson, Hakon
Published in PLoS genetics (01.10.2009)
Published in PLoS genetics (01.10.2009)
Get full text
Journal Article