Disease-associated loci are significantly over-represented among genes bound by transcription factor 7-like 2 (TCF7L2) in vivo
Zhao, J., Schug, J., Li, M., Kaestner, K. H., Grant, S. F. A.
Published in Diabetologia (01.11.2010)
Published in Diabetologia (01.11.2010)
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Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism
Walford, G. A., Green, T., Neale, B., Isakova, T., Rotter, J. I., Grant, S. F. A., Fox, C. S., Pankow, J. S., Wilson, J. G., Meigs, J. B., Siscovick, D. S., Bowden, D. W., Daly, M. J., Florez, J. C.
Published in Diabetologia (01.02.2012)
Published in Diabetologia (01.02.2012)
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Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource
Liu, C. -T., Ng, M. C. Y., Rybin, D., Adeyemo, A., Bielinski, S. J., Boerwinkle, E., Borecki, I., Cade, B., Chen, Y. D. I., Djousse, L., Fornage, M., Goodarzi, M. O., Grant, S. F. A., Guo, X., Harris, T., Kabagambe, E., Kizer, J. R., Liu, Y., Lunetta, K. L., Mukamal, K., Nettleton, J. A., Pankow, J. S., Patel, S. R., Ramos, E., Rasmussen-Torvik, L., Rich, S. S., Rotimi, C. N., Sarpong, D., Shriner, D., Sims, M., Zmuda, J. M., Redline, S., Kao, W. H., Siscovick, D., Florez, J. C., Rotter, J. I., Dupuis, J., Wilson, J. G., Bowden, D. W., Meigs, J. B.
Published in Diabetologia (01.11.2012)
Published in Diabetologia (01.11.2012)
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Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population
Helgadottir, A., Gretarsdottir, S., St. Clair, D., Manolescu, A., Cheung, J., Thorleifsson, G., Pasdar, A., Grant, S.F.A., Whalley, L.J., Hakonarson, H., Thorsteinsdottir, U., Kong, A., Gulcher, J., Stefansson, K., MacLeod, M.J.
Published in American journal of human genetics (01.03.2005)
Published in American journal of human genetics (01.03.2005)
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Remapping the type I diabetes association of the CTLA4 locus
Qu, H-Q, Bradfield, J P, Grant, S F A, Hakonarson, H, Polychronakos, C
Published in Genes and immunity (01.12.2009)
Published in Genes and immunity (01.12.2009)
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Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies
Qu, Hui-Qi, Grant, Struan FA, Bradfield, Jonathan P, Kim, Cecilia, Frackelton, Edward, Hakonarson, Hakon, Polychronakos, Constantin
Published in Journal of medical genetics (01.08.2009)
Published in Journal of medical genetics (01.08.2009)
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Targeted resequencing identifies defective variants of decoy receptor 3 in pediatric-onset inflammatory bowel disease
Cardinale, C J, Wei, Z, Panossian, S, Wang, F, Kim, C E, Mentch, F D, Chiavacci, R M, Kachelries, K E, Pandey, R, Grant, S F A, Baldassano, R N, Hakonarson, H
Published in Genes and immunity (01.10.2013)
Published in Genes and immunity (01.10.2013)
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Influence of SNPSNP interaction on BMI in European American adolescents: findings from the National Longitudinal Study of Adolescent Health
Young, K. L., Graff, M., North, K. E., Richardson, A. S., Bradfield, J. P., Grant, S. F. A., Lange, L. A., Lange, E. M., Harris, K. M., Gordon-Larsen, P.
Published in Pediatric obesity (01.04.2016)
Published in Pediatric obesity (01.04.2016)
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The type I diabetes association of the IL2RA locus
Qu, H-Q, Bradfield, J P, Bélisle, A, Grant, S F A, Hakonarson, H, Polychronakos, C
Published in Genes and immunity (01.12.2009)
Published in Genes and immunity (01.12.2009)
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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, deBerardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S
Published in Molecular psychiatry (01.06.2010)
Published in Molecular psychiatry (01.06.2010)
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FGF21 deficiency is associated with childhood obesity, insulin resistance and hypoadiponectinaemia: The BCAMS Study
Li, G, Yin, J, Fu, J, Li, L, Grant, S.F.A, Li, C, Li, M, Mi, J, Gao, S
Published in Diabetes & metabolism (01.06.2017)
Published in Diabetes & metabolism (01.06.2017)
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Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity
GRANT, Sfa, GLESSNER, J. T, BRADFIELD, J. P, ZHAO, J, TIRONE, J. E, BERKOWITZ, R. I, HAKONARSON, H, SONDHEIMER, N
Published in International Journal of Obesity (01.01.2012)
Published in International Journal of Obesity (01.01.2012)
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Erratum: Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, deBerardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S
Published in Molecular psychiatry (01.11.2010)
Published in Molecular psychiatry (01.11.2010)
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Journal Article
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, Deberardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S
Published in Molecular psychiatry (01.11.2010)
Published in Molecular psychiatry (01.11.2010)
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Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
Medina-Gomez, Carolina, Kemp, John P., Trajanoska, Katerina, Luan, Jian’an, Chesi, Alessandra, Ahluwalia, Tarunveer S., Mook-Kanamori, Dennis O., Ham, Annelies, Hartwig, Fernando P., Evans, Daniel S., Joro, Raimo, Nedeljkovic, Ivana, Zheng, Hou-Feng, Zhu, Kun, Atalay, Mustafa, Liu, Ching-Ti, Nethander, Maria, Broer, Linda, Porleifsson, Gudmar, Mullin, Benjamin H., Handelman, Samuel K., Nalls, Mike A., Jessen, Leon E., Heppe, Denise H.M., Richards, J. Brent, Wang, Carol, Chawes, Bo, Schraut, Katharina E., Amin, Najaf, Wareham, Nick, Karasik, David, Van der Velde, Nathalie, Ikram, M. Arfan, Zemel, Babette S., Zhou, Yanhua, Carlsson, Christian J., Liu, Yongmei, McGuigan, Fiona E., Boer, Cindy G., Bønnelykke, Klaus, Ralston, Stuart H., Robbins, John A., Walsh, John P., Zillikens, M. Carola, Langenberg, Claudia, Li-Gao, Ruifang, Williams, Frances M.K., Harris, Tamara B., Akesson, Kristina, Jackson, Rebecca D., Sigurdsson, Gunnar, den Heijer, Martin, van der Eerden, Bram C.J., van de Peppel, Jeroen, Spector, Timothy D., Pennell, Craig, Horta, Bernardo L., Felix, Janine F., Zhao, Jing Hua, Wilson, Scott G., de Mutsert, Renée, Bisgaard, Hans, Styrkársdóttir, Unnur, Jaddoe, Vincent W., Orwoll, Eric, Lakka, Timo A., Scott, Robert, Grant, Struan F.A., Lorentzon, Mattias, van Duijn, Cornelia M., Wilson, James F., Stefansson, Kari, Psaty, Bruce M., Kiel, Douglas P., Ohlsson, Claes, Ntzani, Evangelia, van Wijnen, Andre J., Forgetta, Vincenzo, Ghanbari, Mohsen, Logan, John G., Williams, Graham R., Bassett, J.H. Duncan, Croucher, Peter I., Evangelou, Evangelos, Uitterlinden, Andre G., Ackert-Bicknell, Cheryl L., Tobias, Jonathan H., Evans, David M., Rivadeneira, Fernando
Published in American journal of human genetics (04.01.2018)
Published in American journal of human genetics (04.01.2018)
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A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Bradfield, Jonathan P, Vogelezang, Suzanne, Felix, Janine F, Chesi, Alessandra, Helgeland, Øyvind, Horikoshi, Momoko, Karhunen, Ville, Lowry, Estelle, Cousminer, Diana L, Ahluwalia, Tarunveer S, Thiering, Elisabeth, Boh, Eileen Tai-Hui, Zafarmand, Mohammad H, Vilor-Tejedor, Natalia, Wang, Carol A, Joro, Raimo, Chen, Zhanghua, Gauderman, William J, Pitkänen, Niina, Parra, Esteban J, Fernandez-Rhodes, Lindsay, Alyass, Akram, Monnereau, Claire, Curtin, John A, Have, Christian T, McCormack, Shana E, Hollensted, Mette, Frithioff-Bøjsøe, Christine, Valladares-Salgado, Adan, Peralta-Romero, Jesus, Teo, Yik-Ying, Standl, Marie, Leinonen, Jaakko T, Holm, Jens-Christian, Peters, Triinu, Vioque, Jesus, Vrijheid, Martine, Simpson, Angela, Custovic, Adnan, Vaudel, Marc, Canouil, Mickaël, Lindi, Virpi, Atalay, Mustafa, Kähönen, Mika, Raitakari, Olli T, van Schaik, Barbera D C, Berkowitz, Robert I, Cole, Shelley A, Voruganti, V Saroja, Wang, Yujie, Highland, Heather M, Comuzzie, Anthony G, Butte, Nancy F, Justice, Anne E, Gahagan, Sheila, Blanco, Estela, Lehtimäki, Terho, Lakka, Timo A, Hebebrand, Johannes, Bonnefond, Amélie, Grarup, Niels, Froguel, Philippe, Lyytikäinen, Leo-Pekka, Cruz, Miguel, Kobes, Sayuko, Hanson, Robert L, Zemel, Babette S, Hinney, Anke, Teo, Koon K, Meyre, David, North, Kari E, Gilliland, Frank D, Bisgaard, Hans, Bustamante, Mariona, Bonnelykke, Klaus, Pennell, Craig E, Rivadeneira, Fernando, Uitterlinden, André G, Baier, Leslie J, Vrijkotte, Tanja G M, Heinrich, Joachim, Sørensen, Thorkild I A, Saw, Seang-Mei, Pedersen, Oluf, Hansen, Torben, Eriksson, Johan, Widén, Elisabeth, McCarthy, Mark I, Njølstad, Pål R, Power, Christine, Hyppönen, Elina, Sebert, Sylvain, Brown, Christopher D, Järvelin, Marjo-Riitta, Timpson, Nicholas J, Johansson, Stefan, Hakonarson, Hakon, Jaddoe, Vincent W V
Published in Human molecular genetics (01.10.2019)
Published in Human molecular genetics (01.10.2019)
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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Manousaki, Despoina, Dudding, Tom, Haworth, Simon, Hsu, Yi-Hsiang, Liu, Ching-Ti, Medina-Gómez, Carolina, Voortman, Trudy, van der Velde, Nathalie, Melhus, Håkan, Robinson-Cohen, Cassianne, Cousminer, Diana L., Nethander, Maria, Vandenput, Liesbeth, Noordam, Raymond, Forgetta, Vincenzo, Greenwood, Celia M.T., Biggs, Mary L., Psaty, Bruce M., Rotter, Jerome I., Zemel, Babette S., Mitchell, Jonathan A., Taylor, Bruce, Lorentzon, Mattias, Karlsson, Magnus, Jaddoe, Vincent V.W., Tiemeier, Henning, Campos-Obando, Natalia, Franco, Oscar H., Utterlinden, Andre G., Broer, Linda, van Schoor, Natasja M., Ham, Annelies C., Ikram, M. Arfan, Karasik, David, de Mutsert, Renée, Rosendaal, Frits R., den Heijer, Martin, Wang, Thomas J., Lind, Lars, Orwoll, Eric S., Mook-Kanamori, Dennis O., Michaëlsson, Karl, Kestenbaum, Bryan, Ohlsson, Claes, Mellström, Dan, de Groot, Lisette C.P.G.M., Grant, Struan F.A., Kiel, Douglas P., Zillikens, M. Carola, Rivadeneira, Fernando, Sawcer, Stephen, Timpson, Nicholas J., Richards, J. Brent
Published in American journal of human genetics (03.08.2017)
Published in American journal of human genetics (03.08.2017)
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DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions
Chen, Yongheng, Chen, Chunxia, Zhang, Zhe, Liu, Chun-Chi, Johnson, Matthew E, Espinoza, Celso A, Edsall, Lee E, Ren, Bing, Zhou, Xianghong Jasmine, Grant, Struan F A, Wells, Andrew D, Chen, Lin
Published in Nucleic acids research (07.01.2015)
Published in Nucleic acids research (07.01.2015)
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