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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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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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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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index
Hinney, A, Kesselmeier, M, Jall, S, Volckmar, A-L, Föcker, M, Antel, J, Heid, I M, Winkler, T W, Guo, Y, Bergen, A W, Kaye, W, Berrettini, W, Hakonarson, H, Herpertz-Dahlmann, B, de Zwaan, M, Herzog, W, Ehrlich, S, Zipfel, S, Egberts, K M, Adan, R, Brandys, M, van Elburg, A, Boraska Perica, V, Franklin, C S, Tschöp, M H, Zeggini, E, Bulik, C M, Collier, D, Scherag, A, Müller, T D, Hebebrand, J
Published in Molecular psychiatry (01.02.2017)
Published in Molecular psychiatry (01.02.2017)
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Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Medina-Gomez, Carolina, Mullin, Benjamin H., Chesi, Alessandra, Prijatelj, Vid, Kemp, John P., Shochat-Carvalho, Chen, Trajanoska, Katerina, Wang, Carol, Joro, Raimo, Evans, Tavia E., Schraut, Katharina E., Li-Gao, Ruifang, Ahluwalia, Tarunveer S., Zillikens, M. Carola, Zhu, Kun, Mook-Kanamori, Dennis O., Evans, Daniel S., Nethander, Maria, Knol, Maria J., Thorleifsson, Gudmar, Prokic, Ivana, Zemel, Babette, Broer, Linda, McGuigan, Fiona E., van Schoor, Natasja M., Reppe, Sjur, Pawlak, Mikolaj A., Ralston, Stuart H., van der Velde, Nathalie, Lorentzon, Mattias, Stefansson, Kari, Adams, Hieab H. H., Wilson, Scott G., Ikram, M. Arfan, Walsh, John P., Lakka, Timo A., Gautvik, Kaare M., Wilson, James F., Orwoll, Eric S., van Duijn, Cornelia M., Bønnelykke, Klaus, Uitterlinden, Andre G., Styrkársdóttir, Unnur, Akesson, Kristina E., Spector, Timothy D., Tobias, Jonathan H., Ohlsson, Claes, Felix, Janine F., Bisgaard, Hans, Grant, Struan F. A., Richards, J. Brent, Evans, David M., van der Eerden, Bram, van de Peppel, Jeroen, Ackert-Bicknell, Cheryl, Karasik, David, Kague, Erika, Rivadeneira, Fernando
Published in Communications biology (04.07.2023)
Published in Communications biology (04.07.2023)
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Perturbation of the insomnia WDR90 GWAS locus pinpoints rs3752495 as a causal variant influencing distal expression of neighboring gene, PIG-Q
Sonti, Shilpa, Littleton, Sheridan H, Pahl, Matthew C, Zimmerman, Amber J, Chesi, Alessandra, Palermo, Justin, Lasconi, Chiara, Brown, Elizabeth B, Pippin, James A, Wells, Andrew D, Doldur-Balli, Fusun, Pack, Allan I, Gehrman, Phillip R, Keene, Alex C, Grant, S F A
Published in bioRxiv (18.08.2023)
Published in bioRxiv (18.08.2023)
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