Genome-Wide Association Study of Serum Minerals Levels in Children of Different Ethnic Background

Por Chang, Xiao, Li, Jin, Guo, Yiran, Wei, Zhi, Mentch, Frank D., Hou, Cuiping, Zhao, Yan, Qiu, Haijun, Kim, Cecilia, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado no PLoS One (2015)

Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children

Por Chang, Xiao, Glessner, Joseph, Tin, Adrienne, Li, Jin, Guo, Yiran, Wei, Zhi, Liu, Yichuan, Mentch, Frank D., Hou, Cuiping, Zhao, Yan, Wang, Tiancheng, Qiu, Haijun, Kim, Cecilia, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado no Sci Rep (2015)

Age group and sex differences in performance on a computerized neurocognitive battery in children age 8–21

Por Gur, Ruben C., Richard, Jan, Calkins, Monica E., Chiavacci, Rosetta, Hansen, John A., Bilker, Warren B., Loughead, James, Connolly, John J., Qiu, Haijun, Mentch, Frank D., Abou-Sleiman, Patrick M., Hakonarson, Hakon, Gur, Raquel E.
Publicado em 2012

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

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children

Por 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.
Publicado em 2013

The Philadelphia Neurodevelopmental Cohort: A Publicly Available Resource for the Study of Normal and Abnormal Brain Development in Youth

Por Satterthwaite, Theodore D., Connolly, John J., Ruparel, Kosha, Calkins, Monica E., Jackson, Chad, Elliott, Mark A., Roalf, David R., Hopson, Ryan, Prabhakaran, Karthik, Behr, Meckenzie, Qiu, Haijun, Mentch, Frank D., Chiavacci, Rosetta, Sleiman, Patrick M. A., Gur, Ruben C., Hakonarson, Hakon, Gur, Raquel E.
Publicado no Neuroimage (2015)

The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative

Por Calkins, Monica E., Merikangas, Kathleen R., Moore, Tyler M., Burstein, Marcy, Behr, Meckenzie A, Satterthwaite, Theodore D., Ruparel, Kosha, Wolf, Daniel H., Roalf, David R., Mentch, Frank D., Qiu, Haijun, Chiavacci, Rosetta, Connolly, John J., Sleiman, Patrick M.A., Gur, Ruben C., Hakonarson, Hakon, Gur, Raquel E.
Publicado no J Child Psychol Psychiatry (2015)

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

Rare variants at 16p11.2 are associated with common variable immunodeficiency

Por Maggadottir, S. Melkorka, Li, Jin, Glessner, Joseph T., Li, Yun Rose, Wei, Zhi, Chang, Xiao, Mentch, Frank D, Thomas, Kelly A, Kim, Cecilia E., Zhao, Yan, Hou, Cuiping, Wang, Fengxiang, Jørgensen, Silje F., Perez, Elena E., Sullivan, Kathleen E., Orange, Jordan Scott, Karlsen, Tom H., Chapel, Helen, Cunningham-Rundles, Charlotte, Hakonarson, Hakon
Publicado no J Allergy Clin Immunol (2015)

Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic ass...

Por Jackson, Kathryn L., Mbagwu, Michael, Pacheco, Jennifer A., Baldridge, Abigail S., Viox, Daniel J., Linneman, James G., Shukla, Sanjay K., Peissig, Peggy L., Borthwick, Kenneth M., Carrell, David A., Bielinski, Suzette J., Kirby, Jacqueline C., Denny, Joshua C., Mentch, Frank D., Vazquez, Lyam M., Rasmussen-Torvik, Laura J., Kho, Abel N.
Publicado no BMC Infect Dis (2016)

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

AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate

Por Falk, Marni J., Li, Dong, Gai, Xiaowu, McCormick, Elizabeth, Place, Emily, Lasorsa, Francesco M., Otieno, Frederick G., Hou, Cuiping, Kim, Cecilia E., Abdel-Magid, Nada, Vazquez, Lyam, Mentch, Frank D., Chiavacci, Rosetta, Liang, Jinlong, Liu, Xuanzhu, Jiang, Hui, Giannuzzi, Giulia, Marsh, Eric D., Yiran, Guo, Tian, Lifeng, Palmieri, Ferdinando, Hakonarson, Hakon
Publicado em 2014

Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate

Por Falk, Marni J., Li, Dong, Gai, Xiaowu, McCormick, Elizabeth, Place, Emily, Lasorsa, Francesco M., Otieno, Frederick G., Hou, Cuiping, Kim, Cecilia E., Abdel-Magid, Nada, Vazquez, Lyam, Mentch, Frank D., Chiavacci, Rosetta, Liang, Jinlong, Liu, Xuanzhu, Jiang, Hui, Giannuzzi, Giulia, Marsh, Eric D., Guo, Yiran, Tian, Lifeng, Palmieri, Ferdinando, Hakonarson, Hakon
Publicado em 2014

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

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)

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

Por van Ingen, Gijs, Li, Jin, Goedegebure, André, Pandey, Rahul, Li, Yun Rose, March, Michael E., Jaddoe, Vincent W. V., Bakay, Marina, Mentch, Frank D., Thomas, Kelly, Wei, Zhi, Chang, Xiao, Hain, Heather S., Uitterlinden, André G., Moll, Henriette A., van Duijn, Cornelia M., Rivadeneira, Fernando, Raat, Hein, Baatenburg de Jong, Robert J., Sleiman, Patrick M., van der Schroeff, Marc P., Hakonarson, Hakon
Publicado no Nat Commun (2016)

Desiderata for computable representations of electronic health records-driven phenotype algorithms

Por Mo, Huan, Thompson, William K, Rasmussen, Luke V, Pacheco, Jennifer A, Jiang, Guoqian, Kiefer, Richard, Zhu, Qian, Xu, Jie, Montague, Enid, Carrell, David S, Lingren, Todd, Mentch, Frank D, Ni, Yizhao, Wehbe, Firas H, Peissig, Peggy L, Tromp, Gerard, Larson, Eric B, Chute, Christopher G, Pathak, Jyotishman, Denny, Joshua C, Speltz, Peter, Kho, Abel N, Jarvik, Gail P, Bejan, Cosmin A, Williams, Marc S, Borthwick, Kenneth, Kitchner, Terrie E, Roden, Dan M, Harris, Paul A
Publicado no J Am Med Inform Assoc (2015)

A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways

Por Bustamante, Mariona, Standl, Marie, Bassat, Quique, Vilor-Tejedor, Natalia, Medina-Gomez, Carolina, Bonilla, Carolina, Ahluwalia, Tarunveer S., Bacelis, Jonas, Bradfield, Jonathan P., Tiesler, Carla M.T., Rivadeneira, Fernando, Ring, Susan, Vissing, Nadja H., Fink, Nadia R., Jugessur, Astanand, Mentch, Frank D., Ballester, Ferran, Kriebel, Jennifer, Kiefte-de Jong, Jessica C., Wolsk, Helene M., Llop, Sabrina, Thiering, Elisabeth, Beth, Systke A., Timpson, Nicholas J., Andersen, Josefine, Schulz, Holger, Jaddoe, Vincent W.V., Evans, David M., Waage, Johannes, Hakonarson, Hakon, Grant, Struan F.A., Jacobsson, Bo, Bønnelykke, Klaus, Bisgaard, Hans, Davey Smith, George, Moll, Henriette A., Heinrich, Joachim, Estivill, Xavier, Sunyer, Jordi
Publicado no Hum Mol Genet (2016)

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Por 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
Publicado no Nat Commun (2015)

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Por 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
Publicado no Nat Med (2015)