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Issue Date
Title
Author(s)
2013
Common variants in mendelian kidney disease genes and their association with renal function
Parsa, A.
;
Fuchsberger, C.
;
Köttgen, A.
;
O'Seaghdha, C.
;
Pattaro, C.
;
De Andrade, M.
;
Chasman, D.
;
Teumer, A.
;
Endlich, K.
;
Olden, M.
;
Chen, M.
;
Tin, A.
;
Kim, Y.
;
Taliun, D.
;
Li, M.
;
Feitosa, M.
;
Gorski, M.
;
Yang, Q.
;
Hundertmark, C.
;
Foster, M.
;
et al.
2011
Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development
Sovio, U.
;
Mook-Kanamori, D.
;
Warrington, N.
;
Lawrence, R.
;
Briollais, L.
;
Palmer, C.
;
Cecil, J.
;
Sandling, J.
;
Syvanen, A.
;
Kaakinen, M.
;
Beilin, L.
;
Millwood, I.
;
Bennett, A.
;
Laitneen, J.
;
Pouta, A.
;
Molitor, J.
;
Smith, G.
;
Ben-Shlomo, Y.
;
Jaddoe, V.
;
Palmer, L.
;
et al.
;
Gibson, G.
2015
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
Painter, J.
;
O'Mara, T.
;
Batra, J.
;
Cheng, T.
;
Lose, F.
;
Dennis, J.
;
Michailidou, K.
;
Tyrer, J.
;
Ahmed, S.
;
Ferguson, K.
;
Healey, C.
;
Kaufmann, S.
;
Hillman, K.
;
Walpole, C.
;
Moya, L.
;
Pollock, P.
;
Jones, A.
;
Howarth, K.
;
Martin, L.
;
Gorman, M.
;
et al.
2015
Genetic heritage of the balto-slavic speaking populations: a synthesis of autosomal, mitochondrial and Y-chromosomal data
Kushniarevich, A.
;
Utevska, O.
;
Chuhryaeva, M.
;
Agdzhoyan, A.
;
Dibirova, K.
;
Uktveryte, I.
;
Möls, M.
;
Mulahasanovic, L.
;
Pshenichnov, A.
;
Frolova, S.
;
Shanko, A.
;
Metspalu, E.
;
Reidla, M.
;
Tambets, K.
;
Tamm, E.
;
Koshel, S.
;
Zaporozhchenko, V.
;
Atramentova, L.
;
Kučinskas, V.
;
Davydenko, O.
;
et al.
;
Calafell, F.
2012
FTO genotype is associated with phenotypic variability of body mass index
Yang, J.
;
Loos, R.
;
Powell, J.
;
Medland, S.
;
Speliotes, E.
;
Chasman, D.
;
Rose, L.
;
Thorleifsson, G.
;
Steinthorsdottir, V.
;
Mägi, R.
;
Waite, L.
;
Smith, A.
;
Yerges-Armstrong, L.
;
Monda, K.
;
Hadley, D.
;
Mahajan, A.
;
Li, G.
;
Kapur, K.
;
Vitart, V.
;
Huffman, J.
;
et al.
2011
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
Strawbridge, R.
;
Dupuis, J.
;
Prokopenko, I.
;
Barker, A.
;
Ahlqvist, E.
;
Rybin, D.
;
Petrie, J.
;
Travers, M.
;
Bouatia-Naji, N.
;
Dimas, A.
;
Nica, A.
;
Wheeler, E.
;
Chen, H.
;
Voight, B.
;
Taneera, J.
;
Kanoni, S.
;
Peden, J.
;
Turrini, F.
;
Gustafsson, S.
;
Zabena, C.
;
et al.
2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
Cavalleri, G.
;
Weale, M.
;
Shianna, K.
;
Singh, R.
;
Lynch, J.
;
Grinton, B.
;
Szoeke, C.
;
Murphy, K.
;
Kinirons, P.
;
O'Rourke, D.
;
Ge, D.
;
Depondt, C.
;
Claeys, K.
;
Pandolfo, M.
;
Gumbs, C.
;
Walley, N.
;
McNamara, J.
;
Mulley, J.
;
Linney, K.
;
Sheffield, L.
;
et al.
2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy
Cavalleri, G.
;
Walley, N.
;
Soranzo, N.
;
Mulley, J.
;
Doherty, C.
;
Kapoor, A.
;
Depondt, C.
;
Lynch, J.
;
Scheffer, I.
;
Heils, A.
;
Gehrmann, A.
;
Kinirons, P.
;
Gandhi, S.
;
Satishchandra, P.
;
Wood, N.
;
Anand, A.
;
Sander, T.
;
Berkovic, S.
;
Delanty, N.
;
Goldstein, D.
;
et al.
2008
The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4610 cases amongst 18637 participants
Lawlor, D.
;
Harbord, R.
;
Timpson, N.
;
Lowe, G.
;
Rumley, A.
;
Gaunt, T.
;
Baker, I.
;
Yarnell, J.
;
Kivimaki, M.
;
Kumari, M.
;
Norman, P.
;
Jamrozik, K.
;
Hankey, G.
;
Almeida, O.
;
Flicker, L.
;
Warrington, N.
;
Marmot, M.
;
Ben-Shlomo, Y.
;
Palmer, L.
;
Day, I.
;
et al.
;
Keavney, B.
Discover
Author
2
Ben-Shlomo, Y.
2
Cavalleri, G.
2
Chasman, D.
2
Depondt, C.
2
Kinirons, P.
2
Lynch, J.
2
Mulley, J.
2
Palmer, L.
2
Walley, N.
2
Warrington, N.
.
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Case-Control Studies
3
Genome-Wide Association Study
3
Male
3
White People
2
Adult
2
Alleles
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Alpha-Ketoglutarate-Dependent Dio...
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