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Results 1-10 of 21 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Epiregulin and EGFR interactions are involved in pain processingMartin, L.J.; Smith, S.B.; Khoutorsky, A.; Magnussen, C.A.; Samoshkin, A.; Sorge, R.E.; Cho, C.; Yosefpour, N.; Sivaselvachandran, S.; Tohyama, S.; Cole, T.; Khuong, T.M.; Mir, E.; Gibson, D.G.; Wieskopf, J.S.; Sotocinal, S.G.; Austin, J.S.; Meloto, C.B.; Gitt, J.H.; Gkogkas, C.; et al.
2017Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traitsJustice, A.; Winkler, T.; Feitosa, M.; Graff, M.; Fisher, V.; Young, K.; Barata, L.; Deng, X.; Czajkowski, J.; Hadley, D.; Ngwa, J.; Ahluwalia, T.; Chu, A.; Heard-Costa, N.; Lim, E.; Perez, J.; Eicher, J.; Kutalik, Z.; Xue, L.; Mahajan, A.; et al.
2012Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22Cicek, M.; Cunningham, J.; Fridley, B.; Serie, D.; Bamlet, W.; Diergaarde, B.; Haile, R.; Le Marchand, L.; Krontiris, T.; Younghusband, H.; Gallinger, S.; Newcomb, P.; Hopper, J.; Jenkins, M.; Casey, G.; Schumacher, F.; Chen, Z.; DeRycke, M.; Templeton, A.; Winship, I.; et al.; Lo, A.
2018Association of serotonin transporter gene AluJb methylation with major depression, amygdala responsiveness, 5-HTTLPR/rs25531 polymorphism, and stressSchneider, I.; Kugel, H.; Redlich, R.; Grotegerd, D.; Bürger, C.; Bürkner, P.-C.; Opel, N.; Dohm, K.; Zaremba, D.; Meinert, S.; Schröder, N.; Straßburg, A.; Schwarte, K.; Schettler, C.; Ambrée, O.; Rust, S.; Domschke, K.; Arolt, V.; Heindel, W.; Baune, B.; et al.
2011Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traitsSpeliotes, E.; Yerges-Armstrong, L.; Wu, J.; Hernaez, R.; Kim, L.; Palmer, C.; Gudnason, V.; Eiriksdottir, G.; Garcia, M.; Launer, L.; Nalls, M.; Clark, J.; Mitchell, B.; Shuldiner, A.; Butler, J.; Tomas, M.; Hoffmann, U.; Hwang, S.; Massaro, J.; O’Donnell, C.; et al.; McCarthy, M.I.
2015Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisRamos-Brossier, M.; Montani, C.; Lebrun, N.; Gritti, L.; Martin, C.; Seminatore-Nole, C.; Toussaint, A.; Moreno, S.; Poirier, K.; Dorseuil, O.; Chelly, J.; Hackett, A.; Gecz, J.; Bieth, E.; Faudet, A.; Heron, D.; Kooy, R.; Loeys, B.; Humeau, Y.; Sala, C.; et al.
2012A genome-wide association search for type 2 diabetes genes in African AmericansPalmer, N.; McDonough, C.; Hicks, P.; Roh, B.; Wing, M.; Sandy An, S.; Hester, J.; Cooke, J.; Bostrom, M.; Rudock, M.; Talbert, M.; Lewis, J.; DIAGRAM Consortium,; MAGIC Consortium,; Ferrara, A.; Lu, L.; Ziegler, J.; Sale, M.; Divers, J.; Shriner, D.; et al.; Kronenberg, F.
2016A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samplesCohen, O.; Weickert, T.; Hess, J.; Paish, L.; McCoy, S.; Rothmond, D.; Galletly, C.; Liu, D.; Weinberg, D.; Huang, X.; Xu, Q.; Shen, Y.; Zhang, D.; Yue, W.; Yan, J.; Wang, L.; Lu, T.; He, L.; Shi, Y.; Xu, M.; et al.
2018A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetesVan Zuydam, N.R.; Ahlqvist, E.; Sandholm, N.; Deshmukh, H.; William Rayner, N.; Abdalla, M.; Ladenvall, C.; Ziemek, D.; Fauman, E.; Robertson, N.R.; McKeigue, P.M.; Valo, E.; Forsblom, C.; Harjutsalo, V.; Perna, A.; Rurali, E.; Loredana Marcovecchio, M.; Igo, R.P.; Salem, R.M.; Perico, N.; et al.
2014Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass IndexHoggart, C.; Venturini, G.; Mangino, M.; Gomez, F.; Ascari, G.; Zhao, J.; Teumer, A.; Winkler, T.; Tšernikova, N.; Luan, J.; Mihailov, E.; Ehret, G.; Zhang, W.; Lamparter, D.; Esko, T.; Macé, A.; Rüeger, S.; Bochud, P.; Barcella, M.; Dauvilliers, Y.; et al.; Visscher, P.

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