Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: POLYMORPHISM, SINGLE NUCLEOTIDE - , . Treffer: 331

2019

Berroterán-Infante, N; Tadić, M; Hacker, M; Wadsak, W; Mitterhauser, M Binding Affinity of Some Endogenous and Synthetic TSPO Ligands Regarding the rs6971 Polymorphism.
Int J Mol Sci. 2019; 20(3): [OPEN ACCESS]
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Pfeifer, B; Kapan, DD Estimates of introgression as a function of pairwise distances.
BMC BIOINFORMATICS. 2019; 20(1): 207-207. [OPEN ACCESS]
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Washetine, K; Heeke, S; Ribeyre, C; Bourreau, C; Normand, C; Blons, H; Laurent-Puig, P; Mulot, C; Clermont, D; David, M; Clément, B; Dagher, G; Hofman, P DNAshell Protects DNA Stored at Room Temperature for Downstream Next-Generation Sequencing Studies.
Biopreserv Biobank. 2019; 17(4): 352-354.
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2018

Eriksson, AL; Perry, JRB; Coviello, AD; Delgado, GE; Ferrucci, L; Hoffman, AR; Huhtaniemi, IT; Ikram, MA; Karlsson, MK; Kleber, ME; Laughlin, GA; Liu, Y; Lorentzon, M; Lunetta, KL; Mellström, D; Murabito, JM; Murray, A; Nethander, M; Nielson, CM; Prokopenko, I; Pye, SR; Raffel, LJ; Rivadeneira, F; Srikanth, P; Stolk, L; Teumer, A; Travison, TG; Uitterlinden, AG; Vaidya, D; Vanderschueren, D; Zmuda, JM; März, W; Orwoll, ES; Ouyang, P; Vandenput, L; Wu, FCW; de Jong, FH; Bhasin, S; Kiel, DP; Ohlsson, C Genetic Determinants of Circulating Estrogen Levels and Evidence of a Causal Effect of Estradiol on Bone Density in Men.
J CLIN ENDOCR METAB. 2018; 103(3): 991-1004. [OPEN ACCESS]
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Kimbacher, C; Paar, C; Freystetter, A; Berg, J Cell Line Controls for the Genotyping of a Spectrum of Human Single Nucleotide Polymorphisms in the Clinical Laboratory.
Clin Lab. 2018; 64(5):823-834 [OPEN ACCESS]
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Madar-Shapiro, L; Karady, I; Trahtenherts, A; Syngelaki, A; Akolekar, R; Poon, L; Cohen, R; Sharabi-Nov, A; Huppertz, B; Sammar, M; Juhasz, K; Than, NG; Papp, Z; Romero, R; Nicolaides, KH; Meiri, H Predicting the Risk to Develop Preeclampsia in the First Trimester Combining Promoter Variant -98A/C of LGALS13 (Placental Protein 13), Black Ethnicity, Previous Preeclampsia, Obesity, and Maternal Age.
Fetal Diagn Ther. 2018; 43(4):250-265 [OPEN ACCESS]
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2017

Abbasi, MR; Rifatbegovic, F; Brunner, C; Mann, G; Ziegler, A; Pötschger, U; Crazzolara, R; Ussowicz, M; Benesch, M; Ebetsberger-Dachs, G; Chan, GCF; Jones, N; Ladenstein, R; Ambros, IM; Ambros, PF Impact of Disseminated Neuroblastoma Cells on the Identification of the Relapse-Seeding Clone.
Clin Cancer Res. 2017; 23(15):4224-4232 (- Case Report) [OPEN ACCESS]
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Gorski, M; van der Most, PJ; Teumer, A; Chu, AY; Li, M; Mijatovic, V; Nolte, IM; Cocca, M; Taliun, D; Gomez, F; Li, Y; Tayo, B; Tin, A; Feitosa, MF; Aspelund, T; Attia, J; Biffar, R; Bochud, M; Boerwinkle, E; Borecki, I; Bottinger, EP; Chen, MH; Chouraki, V; Ciullo, M; Coresh, J; Cornelis, MC; Curhan, GC; d'Adamo, AP; Dehghan, A; Dengler, L; Ding, J; Eiriksdottir, G; Endlich, K; Enroth, S; Esko, T; Franco, OH; Gasparini, P; Gieger, C; Girotto, G; Gottesman, O; Gudnason, V; Gyllensten, U; Hancock, SJ; Harris, TB; Helmer, C; Höllerer, S; Hofer, E; Hofman, A; Holliday, EG; Homuth, G; Hu, FB; Huth, C; Hutri-Kähönen, N; Hwang, SJ; Imboden, M; Johansson, Å; Kähönen, M; König, W; Kramer, H; Krämer, BK; Kumar, A; Kutalik, Z; Lambert, JC; Launer, LJ; Lehtimäki, T; de Borst, M; Navis, G; Swertz, M; Liu, Y; Lohman, K; Loos, RJF; Lu, Y; Lyytikäinen, LP; McEvoy, MA; Meisinger, C; Meitinger, T; Metspalu, A; Metzger, M; Mihailov, E; Mitchell, P; Nauck, M; Oldehinkel, AJ; Olden, M; Wjh Penninx, B; Pistis, G; Pramstaller, PP; Probst-Hensch, N; Raitakari, OT; Rettig, R; Ridker, PM; Rivadeneira, F; Robino, A; Rosas, SE; Ruderfer, D; Ruggiero, D; Saba, Y; Sala, C; Schmidt, H; Schmidt, R; Scott, RJ; Sedaghat, S; Smith, AV; Sorice, R; Stengel, B; Stracke, S; Strauch, K; Toniolo, D; Uitterlinden, AG; Ulivi, S; Viikari, JS; Völker, U; Vollenweider, P; Völzke, H; Vuckovic, D; Waldenberger, M; Jin Wang, J; Yang, Q; Chasman, DI; Tromp, G; Snieder, H; Heid, IM; Fox, CS; Köttgen, A; Pattaro, C; Böger, CA; Fuchsberger, C 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Sci Rep. 2017; 7(5):45040-45040 [OPEN ACCESS]
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Hamilton, EMC; Bertini, E; Kalaydjieva, L; Morar, B; Dojčáková, D; Liu, J; Vanderver, A; Curiel, J; Persoon, CM; Diodato, D; Pinelli, L; van der Meij, NL; Plecko, B; Blaser, S; Wolf, NI; Waisfisz, Q; Abbink, TEM; van der Knaap, MS; Recessive H-ABC Research Group UFM1 founder mutation in the Roma population causes recessive variant of H-ABC.
Neurology. 2017; 89(17):1821-1828 [OPEN ACCESS]
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Joshi, PK; Pirastu, N; Kentistou, KA; Fischer, K; Hofer, E; Schraut, KE; Clark, DW; Nutile, T; Barnes, CLK; Timmers, PRHJ; Shen, X; Gandin, I; McDaid, AF; Hansen, TF; Gordon, SD; Giulianini, F; Boutin, TS; Abdellaoui, A; Zhao, W; Medina-Gomez, C; Bartz, TM; Trompet, S; Lange, LA; Raffield, L; van der Spek, A; Galesloot, TE; Proitsi, P; Yanek, LR; Bielak, LF; Payton, A; Murgia, F; Concas, MP; Biino, G; Tajuddin, SM; Seppälä, I; Amin, N; Boerwinkle, E; Børglum, AD; Campbell, A; Demerath, EW; Demuth, I; Faul, JD; Ford, I; Gialluisi, A; Gögele, M; Graff, M; Hingorani, A; Hottenga, JJ; Hougaard, DM; Hurme, MA; Ikram, MA; Jylhä, M; Kuh, D; Ligthart, L; Lill, CM; Lindenberger, U; Lumley, T; Mägi, R; Marques-Vidal, P; Medland, SE; Milani, L; Nagy, R; Ollier, WER; Peyser, PA; Pramstaller, PP; Ridker, PM; Rivadeneira, F; Ruggiero, D; Saba, Y; Schmidt, R; Schmidt, H; Slagboom, PE; Smith, BH; Smith, JA; Sotoodehnia, N; Steinhagen-Thiessen, E; van Rooij, FJA; Verbeek, AL; Vermeulen, SH; Vollenweider, P; Wang, Y; Werge, T; Whitfield, JB; Zonderman, AB; Lehtimäki, T; Evans, MK; Pirastu, M; Fuchsberger, C; Bertram, L; Pendleton, N; Kardia, SLR; Ciullo, M; Becker, DM; Wong, A; Psaty, BM; van Duijn, CM; Wilson, JG; Jukema, JW; Kiemeney, L; Uitterlinden, AG; Franceschini, N; North, KE; Weir, DR; Metspalu, A; Boomsma, DI; Hayward, C; Chasman, D; Martin, NG; Sattar, N; Campbell, H; Esko, T; Kutalik, Z; Wilson, JF Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.
Nat Commun. 2017; 8(1):910-910 [OPEN ACCESS]
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Justice, AE; Winkler, TW; Feitosa, MF; Graff, M; Fisher, VA; Young, K; Barata, L; Deng, X; Czajkowski, J; Hadley, D; Ngwa, JS; Ahluwalia, TS; Chu, AY; Heard-Costa, NL; Lim, E; Perez, J; Eicher, JD; Kutalik, Z; Xue, L; Mahajan, A; Renström, F; Wu, J; Qi, Q; Ahmad, S; Alfred, T; Amin, N; Bielak, LF; Bonnefond, A; Bragg, J; Cadby, G; Chittani, M; Coggeshall, S; Corre, T; Direk, N; Eriksson, J; Fischer, K; Gorski, M; Neergaard Harder, M; Horikoshi, M; Huang, T; Huffman, JE; Jackson, AU; Justesen, JM; Kanoni, S; Kinnunen, L; Kleber, ME; Komulainen, P; Kumari, M; Lim, U; Luan, J; Lyytikäinen, LP; Mangino, M; Manichaikul, A; Marten, J; Middelberg, RPS; Müller-Nurasyid, M; Navarro, P; Pérusse, L; Pervjakova, N; Sarti, C; Smith, AV; Smith, JA; Stančáková, A; Strawbridge, RJ; Stringham, HM; Sung, YJ; Tanaka, T; Teumer, A; Trompet, S; van der Laan, SW; van der Most, PJ; Van Vliet-Ostaptchouk, JV; Vedantam, SL; Verweij, N; Vink, JM; Vitart, V; Wu, Y; Yengo, L; Zhang, W; Hua Zhao, J; Zimmermann, ME; Zubair, N; Abecasis, GR; Adair, LS; Afaq, S; Afzal, U; Bakker, SJL; Bartz, TM; Beilby, J; Bergman, RN; Bergmann, S; Biffar, R; Blangero, J; Boerwinkle, E; Bonnycastle, LL; Bottinger, E; Braga, D; Buckley, BM; Buyske, S; Campbell, H; Chambers, JC; Collins, FS; Curran, JE; de Borst, GJ; de Craen, AJM; de Geus, EJC; Dedoussis, G; Delgado, GE; den Ruijter, HM; Eiriksdottir, G; Eriksson, AL; Esko, T; Faul, JD; Ford, I; Forrester, T; Gertow, K; Gigante, B; Glorioso, N; Gong, J; Grallert, H; Grammer, TB; Grarup, N; Haitjema, S; Hallmans, G; Hamsten, A; Hansen, T; Harris, TB; Hartman, CA; Hassinen, M; Hastie, ND; Heath, AC; Hernandez, D; Hindorff, L; Hocking, LJ; Hollensted, M; Holmen, OL; Homuth, G; Jan Hottenga, J; Huang, J; Hung, J; Hutri-Kähönen, N; Ingelsson, E; James, AL; Jansson, JO; Jarvelin, MR; Jhun, MA; Jørgensen, ME; Juonala, M; Kähönen, M; Karlsson, M; Koistinen, HA; Kolcic, I; Kolovou, G; Kooperberg, C; Krämer, BK; Kuusisto, J; Kvaløy, K; Lakka, TA; Langenberg, C; Launer, LJ; Leander, K; Lee, NR; Lind, L; Lindgren, CM; Linneberg, A; Lobbens, S; Loh, M; Lorentzon, M; Luben, R; Lubke, G; Ludolph-Donislawski, A; Lupoli, S; Madden, PAF; Männikkö, R; Marques-Vidal, P; Martin, NG; McKenzie, CA; McKnight, B; Mellström, D; Menni, C; Montgomery, GW; Musk, AB; Narisu, N; Nauck, M; Nolte, IM; Oldehinkel, AJ; Olden, M; Ong, KK; Padmanabhan, S; Peyser, PA; Pisinger, C; Porteous, DJ; Raitakari, OT; Rankinen, T; Rao, DC; Rasmussen-Torvik, LJ; Rawal, R; Rice, T; Ridker, PM; Rose, LM; Bien, SA; Rudan, I; Sanna, S; Sarzynski, MA; Sattar, N; Savonen, K; Schlessinger, D; Scholtens, S; Schurmann, C; Scott, RA; Sennblad, B; Siemelink, MA; Silbernagel, G; Slagboom, PE; Snieder, H; Staessen, JA; Stott, DJ; Swertz, MA; Swift, AJ; Taylor, KD; Tayo, BO; Thorand, B; Thuillier, D; Tuomilehto, J; Uitterlinden, AG; Vandenput, L; Vohl, MC; Völzke, H; Vonk, JM; Waeber, G; Waldenberger, M; Westendorp, RGJ; Wild, S; Willemsen, G; Wolffenbuttel, BHR; Wong, A; Wright, AF; Zhao, W; Zillikens, MC; Baldassarre, D; Balkau, B; Bandinelli, S; Böger, CA; Boomsma, DI; Bouchard, C; Bruinenberg, M; Chasman, DI; Chen, YD; Chines, PS; Cooper, RS; Cucca, F; Cusi, D; Faire, U; Ferrucci, L; Franks, PW; Froguel, P; Gordon-Larsen, P; Grabe, HJ; Gudnason, V; Haiman, CA; Hayward, C; Hveem, K; Johnson, AD; Wouter Jukema, J; Kardia, SLR; Kivimaki, M; Kooner, JS; Kuh, D; Laakso, M; Lehtimäki, T; Marchand, LL; März, W; McCarthy, MI; Metspalu, A; Morris, AP; Ohlsson, C; Palmer, LJ; Pasterkamp, G; Pedersen, O ... Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Nat Commun. 2017; 8(17):14977-14977 [OPEN ACCESS]
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Kerbert, AJ; Schaapman, JJ; van der Reijden, JJ; Amorós Navarro, À; McCormick, A; van Hoek, B; Arroyo, V; Ginès, P; Jalan, R; Vargas, V; Stauber, R; Verspaget, HW; Coenraad, MJ; CANONIC Study Investigators of the EASL-CLIF Consortium Short article: Impact of genetic variation in the vasopressin 1a receptor on the development of organ failure in patients admitted for acute decompensation of liver cirrhosis.
Eur J Gastroenterol Hepatol. 2017; 29(5):535-538
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Nelson, CP; Goel, A; Butterworth, AS; Kanoni, S; Webb, TR; Marouli, E; Zeng, L; Ntalla, I; Lai, FY; Hopewell, JC; Giannakopoulou, O; Jiang, T; Hamby, SE; Di Angelantonio, E; Assimes, TL; Bottinger, EP; Chambers, JC; Clarke, R; Palmer, CNA; Cubbon, RM; Ellinor, P; Ermel, R; Evangelou, E; Franks, PW; Grace, C; Gu, D; Hingorani, AD; Howson, JMM; Ingelsson, E; Kastrati, A; Kessler, T; Kyriakou, T; Lehtimäki, T; Lu, X; Lu, Y; März, W; McPherson, R; Metspalu, A; Pujades-Rodriguez, M; Ruusalepp, A; Schadt, EE; Schmidt, AF; Sweeting, MJ; Zalloua, PA; AlGhalayini, K; Keavney, BD; Kooner, JS; Loos, RJF; Patel, RS; Rutter, MK; Tomaszewski, M; Tzoulaki, I; Zeggini, E; Erdmann, J; Dedoussis, G; Björkegren, JLM; EPIC-CVD Consortium; CARDIoGRAMplusC4D; UK Biobank CardioMetabolic Consortium CHD working group; Schunkert, H; Farrall, M; Danesh, J; Samani, NJ; Watkins, H; Deloukas, P Association analyses based on false discovery rate implicate new loci for coronary artery disease.
Nat Genet. 2017; 49(9):1385-1391 [OPEN ACCESS]
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Renner, W; Langsenlehner, U; Krenn-Pilko, S; Eder, P; Langsenlehner, T BCL2 genotypes and prostate cancer survival.
Strahlenther Onkol. 2017; 193(6):466-471 [OPEN ACCESS]
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Robinson-Cohen, C; Lutsey, PL; Kleber, ME; Nielson, CM; Mitchell, BD; Bis, JC; Eny, KM; Portas, L; Eriksson, J; Lorentzon, M; Koller, DL; Milaneschi, Y; Teumer, A; Pilz, S; Nethander, M; Selvin, E; Tang, W; Weng, LC; Wong, HS; Lai, D; Peacock, M; Hannemann, A; Völker, U; Homuth, G; Nauk, M; Murgia, F; Pattee, JW; Orwoll, E; Zmuda, JM; Riancho, JA; Wolf, M; Williams, F; Penninx, B; Econs, MJ; Ryan, KA; Ohlsson, C; Paterson, AD; Psaty, BM; Siscovick, DS; Rotter, JI; Pirastu, M; Streeten, E; März, W; Fox, C; Coresh, J; Wallaschofski, H; Pankow, JS; de Boer, IH; Kestenbaum, B Genetic Variants Associated with Circulating Parathyroid Hormone.
J Am Soc Nephrol. 2017; 28(5):1553-1565 [OPEN ACCESS]
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Saleheen, D; Zhao, W; Young, R; Nelson, CP; Ho, W; Ferguson, JF; Rasheed, A; Ou, K; Nurnberg, ST; Bauer, RC; Goel, A; Do, R; Stewart, AFR; Hartiala, J; Zhang, W; Thorleifsson, G; Strawbridge, RJ; Sinisalo, J; Kanoni, S; Sedaghat, S; Marouli, E; Kristiansson, K; Hua Zhao, J; Scott, R; Gauguier, D; Shah, SH; Smith, AV; van Zuydam, N; Cox, AJ; Willenborg, C; Kessler, T; Zeng, L; Province, MA; Ganna, A; Lind, L; Pedersen, NL; White, CC; Joensuu, A; Edi Kleber, M; Hall, AS; März, W; Salomaa, V; O'Donnell, C; Ingelsson, E; Feitosa, MF; Erdmann, J; Bowden, DW; Palmer, CNA; Gudnason, V; Faire, U; Zalloua, P; Wareham, N; Thompson, JR; Kuulasmaa, K; Dedoussis, G; Perola, M; Dehghan, A; Chambers, JC; Kooner, J; Allayee, H; Deloukas, P; McPherson, R; Stefansson, K; Schunkert, H; Kathiresan, S; Farrall, M; Marcel Frossard, P; Rader, DJ; Samani, NJ; Reilly, MP Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions.
Circulation. 2017; 135(24):2336-2353 [OPEN ACCESS]
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Salminen, A; Vlachopoulou, E; Havulinna, AS; Tervahartiala, T; Sattler, W; Lokki, ML; Nieminen, MS; Perola, M; Salomaa, V; Sinisalo, J; Meri, S; Sorsa, T; Pussinen, PJ Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis.
Circ Cardiovasc Genet. 2017; 10(6): [OPEN ACCESS]
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Sims, R; van der Lee, SJ; Naj, AC; Bellenguez, C; Badarinarayan, N; Jakobsdottir, J; Kunkle, BW; Boland, A; Raybould, R; Bis, JC; Martin, ER; Grenier-Boley, B; Heilmann-Heimbach, S; Chouraki, V; Kuzma, AB; Sleegers, K; Vronskaya, M; Ruiz, A; Graham, RR; Olaso, R; Hoffmann, P; Grove, ML; Vardarajan, BN; Hiltunen, M; Nöthen, MM; White, CC; Hamilton-Nelson, KL; Epelbaum, J; Maier, W; Choi, SH; Beecham, GW; Dulary, C; Herms, S; Smith, AV; Funk, CC; Derbois, C; Forstner, AJ; Ahmad, S; Li, H; Bacq, D; Harold, D; Satizabal, CL; Valladares, O; Squassina, A; Thomas, R; Brody, JA; Qu, L; Sánchez-Juan, P; Morgan, T; Wolters, FJ; Zhao, Y; Garcia, FS; Denning, N; Fornage, M; Malamon, J; Naranjo, MCD; Majounie, E; Mosley, TH; Dombroski, B; Wallon, D; Lupton, MK; Dupuis, J; Whitehead, P; Fratiglioni, L; Medway, C; Jian, X; Mukherjee, S; Keller, L; Brown, K; Lin, H; Cantwell, LB; Panza, F; McGuinness, B; Moreno-Grau, S; Burgess, JD; Solfrizzi, V; Proitsi, P; Adams, HH; Allen, M; Seripa, D; Pastor, P; Cupples, LA; Price, ND; Hannequin, D; Frank-García, A; Levy, D; Chakrabarty, P; Caffarra, P; Giegling, I; Beiser, AS; Giedraitis, V; Hampel, H; Garcia, ME; Wang, X; Lannfelt, L; Mecocci, P; Eiriksdottir, G; Crane, PK; Pasquier, F; Boccardi, V; Henández, I; Barber, RC; Scherer, M; Tarraga, L; Adams, PM; Leber, M; Chen, Y; Albert, MS; Riedel-Heller, S; Emilsson, V; Beekly, D; Braae, A; Schmidt, R; Blacker, D; Masullo, C; Schmidt, H; Doody, RS; Spalletta, G; Longstreth, WT; Fairchild, TJ; Bossù, P; Lopez, OL; Frosch, MP; Sacchinelli, E; Ghetti, B; Yang, Q; Huebinger, RM; Jessen, F; Li, S; Kamboh, MI; Morris, J; Sotolongo-Grau, O; Katz, MJ; Corcoran, C; Dunstan, M; Braddel, A; Thomas, C; Meggy, A; Marshall, R; Gerrish, A; Chapman, J; Aguilar, M; Taylor, S; Hill, M; Fairén, MD; Hodges, A; Vellas, B; Soininen, H; Kloszewska, I; Daniilidou, M; Uphill, J; Patel, Y; Hughes, JT; Lord, J; Turton, J; Hartmann, AM; Cecchetti, R; Fenoglio, C; Serpente, M; Arcaro, M; Caltagirone, C; Orfei, MD; Ciaramella, A; Pichler, S; Mayhaus, M; Gu, W; Lleó, A; Fortea, J; Blesa, R; Barber, IS; Brookes, K; Cupidi, C; Maletta, RG; Carrell, D; Sorbi, S; Moebus, S; Urbano, M; Pilotto, A; Kornhuber, J; Bosco, P; Todd, S; Craig, D; Johnston, J; Gill, M; Lawlor, B; Lynch, A; Fox, NC; Hardy, J; ARUK Consortium; Albin, RL; Apostolova, LG; Arnold, SE; Asthana, S; Atwood, CS; Baldwin, CT; Barnes, LL; Barral, S; Beach, TG; Becker, JT; Bigio, EH; Bird, TD; Boeve, BF; Bowen, JD; Boxer, A; Burke, JR; Burns, JM; Buxbaum, JD; Cairns, NJ; Cao, C; Carlson, CS; Carlsson, CM; Carney, RM; Carrasquillo, MM; Carroll, SL; Diaz, CC; Chui, HC; Clark, DG; Cribbs, DH; Crocco, EA; DeCarli, C; Dick, M; Duara, R; Evans, DA; Faber, KM; Fallon, KB; Fardo, DW; Farlow, MR; Ferris, S; Foroud, TM; Galasko, DR; Gearing, M; Geschwind, DH; Gilbert, JR; Graff-Radford, NR; Green, RC; Growdon, JH; Hamilton, RL; Harrell, LE; Honig, LS; Huentelman, MJ; Hulette, CM; Hyman, BT; Jarvik, GP; Abner, E; Jin, LW; Jun, G; Karydas, A; Kaye, JA; Kim, R; Kowall, NW; Kramer, JH; LaFerla, FM; Lah, JJ; Leverenz, JB; Levey, AI; Li, G; Lieberman, AP; Lunetta, KL; Lyketsos, CG; Marson, DC; Martiniuk, F; Mash, DC; Masliah, E; McCormick, WC; McCurry, SM; McDavid, AN; McKee, AC; Mesulam, M; Miller, BL; Miller, CA; Miller, JW; Morris, JC; Murrell, JR; Myers, AJ; O'Bryant, S; Olichney, JM; Pankratz, VS; Parisi, JE; Paulson, HL; Perry, W; Peskind, E; Pierce, A; Poon, WW; Potter, H; Quinn, JF; Raj, A; Raskind, M; Reisberg, B; Reitz, C; Ringman, JM; Robe ... Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Nat Genet. 2017; 49(9):1373-1384 [OPEN ACCESS]
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Stotz, M; Herzog, SA; Pichler, M; Smolle, M; Riedl, J; Rossmann, C; Bezan, A; Stöger, H; Renner, W; Berghold, A; Gerger, A Cancer Stem Cell Gene Variants in CD44 Predict Outcome in Stage II and Stage III Colon Cancer Patients.
Anticancer Res. 2017; 37(4):2011-2018
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Wild, PS; Felix, JF; Schillert, A; Teumer, A; Chen, MH; Leening, MJG; Völker, U; Großmann, V; Brody, JA; Irvin, MR; Shah, SJ; Pramana, S; Lieb, W; Schmidt, R; Stanton, AV; Malzahn, D; Smith, AV; Sundström, J; Minelli, C; Ruggiero, D; Lyytikäinen, LP; Tiller, D; Smith, JG; Monnereau, C; Di Tullio, MR; Musani, SK; Morrison, AC; Pers, TH; Morley, M; Kleber, ME; Aragam, J; Benjamin, EJ; Bis, JC; Bisping, E; Broeckel, U; Cheng, S; Deckers, JW; Del Greco M, F; Edelmann, F; Fornage, M; Franke, L; Friedrich, N; Harris, TB; Hofer, E; Hofman, A; Huang, J; Hughes, AD; Kähönen, M; Investigators, K; Kruppa, J; Lackner, KJ; Lannfelt, L; Laskowski, R; Launer, LJ; Leosdottir, M; Lin, H; Lindgren, CM; Loley, C; MacRae, CA; Mascalzoni, D; Mayet, J; Medenwald, D; Morris, AP; Müller, C; Müller-Nurasyid, M; Nappo, S; Nilsson, PM; Nuding, S; Nutile, T; Peters, A; Pfeufer, A; Pietzner, D; Pramstaller, PP; Raitakari, OT; Rice, KM; Rivadeneira, F; Rotter, JI; Ruohonen, ST; Sacco, RL; Samdarshi, TE; Schmidt, H; Sharp, ASP; Shields, DC; Sorice, R; Sotoodehnia, N; Stricker, BH; Surendran, P; Thom, S; Töglhofer, AM; Uitterlinden, AG; Wachter, R; Völzke, H; Ziegler, A; Münzel, T; März, W; Cappola, TP; Hirschhorn, JN; Mitchell, GF; Smith, NL; Fox, ER; Dueker, ND; Jaddoe, VWV; Melander, O; Russ, M; Lehtimäki, T; Ciullo, M; Hicks, AA; Lind, L; Gudnason, V; Pieske, B; Barron, AJ; Zweiker, R; Schunkert, H; Ingelsson, E; Liu, K; Arnett, DK; Psaty, BM; Blankenberg, S; Larson, MG; Felix, SB; Franco, OH; Zeller, T; Vasan, RS; Dörr, M Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
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Zewinger, S; Kleber, ME; Tragante, V; McCubrey, RO; Schmidt, AF; Direk, K; Laufs, U; Werner, C; Koenig, W; Rothenbacher, D; Mons, U; Breitling, LP; Brenner, H; Jennings, RT; Petrakis, I; Triem, S; Klug, M; Filips, A; Blankenberg, S; Waldeyer, C; Sinning, C; Schnabel, RB; Lackner, KJ; Vlachopoulou, E; Nygård, O; Svingen, GFT; Pedersen, ER; Tell, GS; Sinisalo, J; Nieminen, MS; Laaksonen, R; Trompet, S; Smit, RAJ; Sattar, N; Jukema, JW; Groesdonk, HV; Delgado, G; Stojakovic, T; Pilbrow, AP; Cameron, VA; Richards, AM; Doughty, RN; Gong, Y; Cooper-DeHoff, R; Johnson, J; Scholz, M; Beutner, F; Thiery, J; Smith, JG; Vilmundarson, RO; McPherson, R; Stewart, AFR; Cresci, S; Lenzini, PA; Spertus, JA; Olivieri, O; Girelli, D; Martinelli, NI; Leiherer, A; Saely, CH; Drexel, H; Mündlein, A; Braund, PS; Nelson, CP; Samani, NJ; Kofink, D; Hoefer, IE; Pasterkamp, G; Quyyumi, AA; Ko, YA; Hartiala, JA; Allayee, H; Tang, WHW; Hazen, SL; Eriksson, N; Held, C; Hagström, E; Wallentin, L; Åkerblom, A; Siegbahn, A; Karp, I; Labos, C; Pilote, L; Engert, JC; Brophy, JM; Thanassoulis, G; Bogaty, P; Szczeklik, W; Kaczor, M; Sanak, M; Virani, SS; Ballantyne, CM; Lee, VV; Boerwinkle, E; Holmes, MV; Horne, BD; Hingorani, A; Asselbergs, FW; Patel, RS; GENIUS-CHD consortium; Krämer, BK; Scharnagl, H; Fliser, D; März, W; Speer, T Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study.
Lancet Diabetes Endocrinol. 2017; 5(7):534-543 [OPEN ACCESS]
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2016

Adams, HH; Hibar, DP; Chouraki, V; Stein, JL; Nyquist, PA; Rentería, ME; Trompet, S; Arias-Vasquez, A; Seshadri, S; Desrivières, S; Beecham, AH; Jahanshad, N; Wittfeld, K; Van der Lee, SJ; Abramovic, L; Alhusaini, S; Amin, N; Andersson, M; Arfanakis, K; Aribisala, BS; Armstrong, NJ; Athanasiu, L; Axelsson, T; Beiser, A; Bernard, M; Bis, JC; Blanken, LM; Blanton, SH; Bohlken, MM; Boks, MP; Bralten, J; Brickman, AM; Carmichael, O; Chakravarty, MM; Chauhan, G; Chen, Q; Ching, CR; Cuellar-Partida, G; Braber, AD; Doan, NT; Ehrlich, S; Filippi, I; Ge, T; Giddaluru, S; Goldman, AL; Gottesman, RF; Greven, CU; Grimm, O; Griswold, ME; Guadalupe, T; Hass, J; Haukvik, UK; Hilal, S; Hofer, E; Hoehn, D; Holmes, AJ; Hoogman, M; Janowitz, D; Jia, T; Kasperaviciute, D; Kim, S; Klein, M; Kraemer, B; Lee, PH; Liao, J; Liewald, DC; Lopez, LM; Luciano, M; Macare, C; Marquand, A; Matarin, M; Mather, KA; Mattheisen, M; Mazoyer, B; McKay, DR; McWhirter, R; Milaneschi, Y; Mirza-Schreiber, N; Muetzel, RL; Maniega, SM; Nho, K; Nugent, AC; Loohuis, LM; Oosterlaan, J; Papmeyer, M; Pappa, I; Pirpamer, L; Pudas, S; Pütz, B; Rajan, KB; Ramasamy, A; Richards, JS; Risacher, SL; Roiz-Santiañez, R; Rommelse, N; Rose, EJ; Royle, NA; Rundek, T; Sämann, PG; Satizabal, CL; Schmaal, L; Schork, AJ; Shen, L; Shin, J; Shumskaya, E; Smith, AV; Sprooten, E; Strike, LT; Teumer, A; Thomson, R; Tordesillas-Gutierrez, D; Toro, R; Trabzuni, D; Vaidya, D; Van der Grond, J; Van der Meer, D; Van Donkelaar, MM; Van Eijk, KR; Van Erp, TG; Van Rooij, D; Walton, E; Westlye, LT; Whelan, CD; Windham, BG; Winkler, AM; Woldehawariat, G; Wolf, C; Wolfers, T; Xu, B; Yanek, LR; Yang, J; Zijdenbos, A; Zwiers, MP; Agartz, I; Aggarwal, NT; Almasy, L; Ames, D; Amouyel, P; Andreassen, OA; Arepalli, S; Assareh, AA; Barral, S; Bastin, ME; Becker, DM; Becker, JT; Bennett, DA; Blangero, J; van Bokhoven, H; Boomsma, DI; Brodaty, H; Brouwer, RM; Brunner, HG; Buckner, RL; Buitelaar, JK; Bulayeva, KB; Cahn, W; Calhoun, VD; Cannon, DM; Cavalleri, GL; Chen, C; Cheng, CY; Cichon, S; Cookson, MR; Corvin, A; Crespo-Facorro, B; Curran, JE; Czisch, M; Dale, AM; Davies, GE; De Geus, EJ; De Jager, PL; de Zubicaray, GI; Delanty, N; Depondt, C; DeStefano, AL; Dillman, A; Djurovic, S; Donohoe, G; Drevets, WC; Duggirala, R; Dyer, TD; Erk, S; Espeseth, T; Evans, DA; Fedko, IO; Fernández, G; Ferrucci, L; Fisher, SE; Fleischman, DA; Ford, I; Foroud, TM; Fox, PT; Francks, C; Fukunaga, M; Gibbs, JR; Glahn, DC; Gollub, RL; Göring, HH; Grabe, HJ; Green, RC; Gruber, O; Gudnason, V; Guelfi, S; Hansell, NK; Hardy, J; Hartman, CA; Hashimoto, R; Hegenscheid, K; Heinz, A; Le Hellard, S; Hernandez, DG; Heslenfeld, DJ; Ho, BC; Hoekstra, PJ; Hoffmann, W; Hofman, A; Holsboer, F; Homuth, G; Hosten, N; Hottenga, JJ; Hulshoff Pol, HE; Ikeda, M; Ikram, MK; Jack, CR; Jenkinson, M; Johnson, R; Jönsson, EG; Jukema, JW; Kahn, RS; Kanai, R; Kloszewska, I; Knopman, DS; Kochunov, P; Kwok, JB; Lawrie, SM; Lemaître, H; Liu, X; Longo, DL; Longstreth, WT; Lopez, OL; Lovestone, S; Martinez, O; Martinot, JL; Mattay, VS; McDonald, C; McIntosh, AM; McMahon, KL; McMahon, FJ; Mecocci, P; Melle, I; Meyer-Lindenberg, A; Mohnke, S; Montgomery, GW; Morris, DW; Mosley, TH; Mühleisen, TW; Müller-Myhsok, B; Nalls, MA; Nauck, M; Nichols, TE; Niessen, WJ; Nöthen, MM; Nyberg, L; Ohi, K; Olvera, RL; Ophoff, RA; Pandolfo, M; Paus, T; Pausova, Z; Penninx, BW; Pike, GB; Potkin, SG; Psaty, BM; Reppermund, S; Rietschel, M; Roffman, JL; Romanczuk-Seiferth, N; Rotter, JI; Ryten, M ... Novel genetic loci underlying human intracranial volume identified through genome-wide association.
Nat Neurosci. 2016; 19(12):1569-1582 [OPEN ACCESS]
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Anderson, CD; Falcone, GJ; Phuah, CL; Radmanesh, F; Brouwers, HB; Battey, TW; Biffi, A; Peloso, GM; Liu, DJ; Ayres, AM; Goldstein, JN; Viswanathan, A; Greenberg, SM; Selim, M; Meschia, JF; Brown, DL; Worrall, BB; Silliman, SL; Tirschwell, DL; Flaherty, ML; Kraft, P; Jagiella, JM; Schmidt, H; Hansen, BM; Jimenez-Conde, J; Giralt-Steinhauer, E; Elosua, R; Cuadrado-Godia, E; Soriano, C; van Nieuwenhuizen, KM; Klijn, CJ; Rannikmae, K; Samarasekera, N; Al-Shahi Salman, R; Sudlow, CL; Deary, IJ; Morotti, A; Pezzini, A; Pera, J; Urbanik, A; Pichler, A; Enzinger, C; Norrving, B; Montaner, J; Fernandez-Cadenas, I; Delgado, P; Roquer, J; Lindgren, A; Slowik, A; Schmidt, R; Kidwell, CS; Kittner, SJ; Waddy, SP; Langefeld, CD; Abecasis, G; Willer, CJ; Kathiresan, S; Woo, D; Rosand, J; Global Lipids Genetics Consortium and International Stroke Genetics Consortium Genetic variants in CETP increase risk of intracerebral hemorrhage.
Ann Neurol. 2016; 80(5):730-740 [OPEN ACCESS]
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Barban, N; Jansen, R; de Vlaming, R; Vaez, A; Mandemakers, JJ; Tropf, FC; Shen, X; Wilson, JF; Chasman, DI; Nolte, IM; Tragante, V; van der Laan, SW; Perry, JR; Kong, A; BIOS Consortium; Ahluwalia, TS; Albrecht, E; Yerges-Armstrong, L; Atzmon, G; Auro, K; Ayers, K; Bakshi, A; Ben-Avraham, D; Berger, K; Bergman, A; Bertram, L; Bielak, LF; Bjornsdottir, G; Bonder, MJ; Broer, L; Bui, M; Barbieri, C; Cavadino, A; Chavarro, JE; Turman, C; Concas, MP; Cordell, HJ; Davies, G; Eibich, P; Eriksson, N; Esko, T; Eriksson, J; Falahi, F; Felix, JF; Fontana, MA; Franke, L; Gandin, I; Gaskins, AJ; Gieger, C; Gunderson, EP; Guo, X; Hayward, C; He, C; Hofer, E; Huang, H; Joshi, PK; Kanoni, S; Karlsson, R; Kiechl, S; Kifley, A; Kluttig, A; Kraft, P; Lagou, V; Lecoeur, C; Lahti, J; Li-Gao, R; Lind, PA; Liu, T; Makalic, E; Mamasoula, C; Matteson, L; Mbarek, H; McArdle, PF; McMahon, G; Meddens, SF; Mihailov, E; Miller, M; Missmer, SA; Monnereau, C; van der Most, PJ; Myhre, R; Nalls, MA; Nutile, T; Kalafati, IP; Porcu, E; Prokopenko, I; Rajan, KB; Rich-Edwards, J; Rietveld, CA; Robino, A; Rose, LM; Rueedi, R; Ryan, KA; Saba, Y; Schmidt, D; Smith, JA; Stolk, L; Streeten, E; Tönjes, A; Thorleifsson, G; Ulivi, S; Wedenoja, J; Wellmann, J; Willeit, P; Yao, J; Yengo, L; Zhao, JH; Zhao, W; Zhernakova, DV; Amin, N; Andrews, H; Balkau, B; Barzilai, N; Bergmann, S; Biino, G; Bisgaard, H; Bønnelykke, K; Boomsma, DI; Buring, JE; Campbell, H; Cappellani, S; Ciullo, M; Cox, SR; Cucca, F; Toniolo, D; Davey-Smith, G; Deary, IJ; Dedoussis, G; Deloukas, P; van Duijn, CM; de Geus, EJ; Eriksson, JG; Evans, DA; Faul, JD; Sala, CF; Froguel, P; Gasparini, P; Girotto, G; Grabe, HJ; Greiser, KH; Groenen, PJ; de Haan, HG; Haerting, J; Harris, TB; Heath, AC; Heikkilä, K; Hofman, A; Homuth, G; Holliday, EG; Hopper, J; Hyppönen, E; Jacobsson, B; Jaddoe, VW; Johannesson, M; Jugessur, A; Kähönen, M; Kajantie, E; Kardia, SL; Keavney, B; Kolcic, I; Koponen, P; Kovacs, P; Kronenberg, F; Kutalik, Z; La Bianca, M; Lachance, G; Iacono, WG; Lai, S; Lehtimäki, T; Liewald, DC; LifeLines Cohort Study; Lindgren, CM; Liu, Y; Luben, R; Lucht, M; Luoto, R; Magnus, P; Magnusson, PK; Martin, NG; McGue, M; McQuillan, R; Medland, SE; Meisinger, C; Mellström, D; Metspalu, A; Traglia, M; Milani, L; Mitchell, P; Montgomery, GW; Mook-Kanamori, D; de Mutsert, R; Nohr, EA; Ohlsson, C; Olsen, J; Ong, KK; Paternoster, L; Pattie, A; Penninx, BW; Perola, M; Peyser, PA; Pirastu, M; Polasek, O; Power, C; Kaprio, J; Raffel, LJ; Räikkönen, K; Raitakari, O; Ridker, PM; Ring, SM; Roll, K; Rudan, I; Ruggiero, D; Rujescu, D; Salomaa, V; Schlessinger, D; Schmidt, H; Schmidt, R; Schupf, N; Smit, J; Sorice, R; Spector, TD; Starr, JM; Stöckl, D; Strauch, K; Stumvoll, M; Swertz, MA; Thorsteinsdottir, U; Thurik, AR; Timpson, NJ; Tung, JY; Uitterlinden, AG; Vaccargiu, S; Viikari, J; Vitart, V; Völzke, H; Vollenweider, P; Vuckovic, D; Waage, J; Wagner, GG; Wang, JJ; Wareham, NJ; Weir, DR; Willemsen, G; Willeit, J; Wright, AF; Zondervan, KT; Stefansson, K; Krueger, RF; Lee, JJ; Benjamin, DJ; Cesarini, D; Koellinger, PD; den Hoed, M; Snieder, H; Mills, MC Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
Nat Genet. 2016; 48(12):1462-1472 [OPEN ACCESS]
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Bogen, D; Brunner, C; Walder, D; Ziegler, A; Abbasi, R; Ladenstein, RL; Noguera, R; Martinsson, T; Amann, G; Schilling, FH; Ussowicz, M; Benesch, M; Ambros, PF; Ambros, IM The genetic tumor background is an important determinant for heterogeneous MYCN-amplified neuroblastoma.
Int J Cancer. 2016; 139(1):153-163 [OPEN ACCESS]
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Bonin, S; Donada, M; Bussolati, G; Nardon, E; Annaratone, L; Pichler, M; Chiaravalli, AM; Capella, C; Hoefler, G; Stanta, G A synonymous EGFR polymorphism predicting responsiveness to anti-EGFR therapy in metastatic colorectal cancer patients.
Tumour Biol. 2016; 37(6):7295-7303
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Enko, D; Kriegshäuser, G; Stolba, R; Mangge, H; Brandstetter, D; Mayr, N; Forstner, T; Halwachs-Baumann, G Assessment of vitamin D status and serum CrossLaps levels in adults with primary lactose malabsorption.
Eur J Clin Nutr. 2016; 70(9):1000-1003
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Feichtinger, J; Hernández, I; Fischer, C; Hanscho, M; Auer, N; Hackl, M; Jadhav, V; Baumann, M; Krempl, PM; Schmidl, C; Farlik, M; Schuster, M; Merkel, A; Sommer, A; Heath, S; Rico, D; Bock, C; Thallinger, GG; Borth, N Comprehensive genome and epigenome characterization of CHO cells in response to evolutionary pressures and over time.
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Gandolfi, G; Longo, C; Moscarella, E; Zalaudek, I; Sancisi, V; Raucci, M; Manzotti, G; Gugnoni, M; Piana, S; Argenziano, G; Ciarrocchi, A The extent of whole-genome copy number alterations predicts aggressive features in primary melanomas.
Pigment Cell Melanoma Res. 2016; 29(2):163-175
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Ibrahim-Verbaas, CA; Bressler, J; Debette, S; Schuur, M; Smith, AV; Bis, JC; Davies, G; Trompet, S; Smith, JA; Wolf, C; Chibnik, LB; Liu, Y; Vitart, V; Kirin, M; Petrovic, K; Polasek, O; Zgaga, L; Fawns-Ritchie, C; Hoffmann, P; Karjalainen, J; Lahti, J; Llewellyn, DJ; Schmidt, CO; Mather, KA; Chouraki, V; Sun, Q; Resnick, SM; Rose, LM; Oldmeadow, C; Stewart, M; Smith, BH; Gudnason, V; Yang, Q; Mirza, SS; Jukema, JW; deJager, PL; Harris, TB; Liewald, DC; Amin, N; Coker, LH; Stegle, O; Lopez, OL; Schmidt, R; Teumer, A; Ford, I; Karbalai, N; Becker, JT; Jonsdottir, MK; Au, R; Fehrmann, R; Herms, S; Nalls, M; Zhao, W; Turner, ST; Yaffe, K; Lohman, K; van Swieten, JC; Kardia, S; Knopman, DS; Meeks, WM; Heiss, G; Holliday, EG; Schofield, PW; Tanaka, T; Stott, DJ; Wang, J; Ridker, P; Gow, AJ; Pattie, A; Starr, JM; Hocking, LJ; Armstrong, NJ; McLachlan, S; Shulman, JM; Pilling, LC; Eiriksdottir, G; Scott, RJ; Kochan, NA; Palotie, A; Hsieh, YC; Eriksson, JG; Penman, A; Gottesman, RF; Oostra, BA; Yu, L; DeStefano, AL; Beiser, A; Garcia, M; Rotter, JI; Nöthen, MM; Hofman, A; Slagboom, PE; Westendorp, R; Buckley, BM; Wolf, PA; Uitterlinden, AG; Psaty, BM; Grabe, HJ; Bandinelli, S; Chasman, DI; Grodstein, F; Räikkönen, K; Lambert, JC; Porteous, DJ; Generation Scotland; Price, JF; Sachdev, PS; Ferrucci, L; Attia, JR; Rudan, I; Hayward, C; Wright, AF; Wilson, JF; Cichon, S; Franke, L; Schmidt, H; Ding, J; de Craen, A; Fornage, M; Bennett, DA; Deary, IJ; Ikram, MA; Launer, LJ; Fitzpatrick, AL; Seshadri, S; van Duijn, CM; Mosley, TH GWAS for executive function and processing speed suggests involvement of the CADM2 gene.
Mol Psychiatry. 2016; 21(2):189-197 [OPEN ACCESS]
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Jun, G; Ibrahim-Verbaas, CA; Vronskaya, M; Lambert, JC; Chung, J; Naj, AC; Kunkle, BW; Wang, LS; Bis, JC; Bellenguez, C; Harold, D; Lunetta, KL; Destefano, AL; Grenier-Boley, B; Sims, R; Beecham, GW; Smith, AV; Chouraki, V; Hamilton-Nelson, KL; Ikram, MA; Fievet, N; Denning, N; Martin, ER; Schmidt, H; Kamatani, Y; Dunstan, ML; Valladares, O; Laza, AR; Zelenika, D; Ramirez, A; Foroud, TM; Choi, SH; Boland, A; Becker, T; Kukull, WA; van der Lee, SJ; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, AL; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, DA; Amin, N; Berr, C; Tsolaki, M; Buxbaum, JD; Lopez, OL; Deramecourt, V; Fox, NC; Cantwell, LB; Tárraga, L; Dufouil, C; Hardy, J; Crane, PK; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, TH; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, JF; Hampel, H; Kamboh, MI; de Bruijn, RF; Tzourio, C; Pastor, P; Larson, EB; Rotter, JI; O'Donovan, MC; Montine, TJ; Nalls, MA; Mead, S; Reiman, EM; Jonsson, PV; Holmes, C; St George-Hyslop, PH; Boada, M; Passmore, P; Wendland, JR; Schmidt, R; Morgan, K; Winslow, AR; Powell, JF; Carasquillo, M; Younkin, SG; Jakobsdóttir, J; Kauwe, JS; Wilhelmsen, KC; Rujescu, D; Nöthen, MM; Hofman, A; Jones, L; IGAP Consortium; Haines, JL; Psaty, BM; Van Broeckhoven, C; Holmans, P; Launer, LJ; Mayeux, R; Lathrop, M; Goate, AM; Escott-Price, V; Seshadri, S; Pericak-Vance, MA; Amouyel, P; Williams, J; van Duijn, CM; Schellenberg, GD; Farrer, LA A novel Alzheimer disease locus located near the gene encoding tau protein.
Mol Psychiatry. 2016; 21(1):108-117 [OPEN ACCESS]
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Khan, MA; Khan, S; Windpassinger, C; Badar, M; Nawaz, Z; Mohammad, RM The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.
Ann Hum Genet. 2016; 80(6):342-368 [OPEN ACCESS]
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Khan, MA; Mohan, S; Zubair, M; Windpassinger, C Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome.
BMC Med Genet. 2016; 17(6): 10-10. [OPEN ACCESS]
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Lin, H; Mueller-Nurasyid, M; Smith, AV; Arking, DE; Barnard, J; Bartz, TM; Lunetta, KL; Lohman, K; Kleber, ME; Lubitz, SA; Geelhoed, B; Trompet, S; Niemeijer, MN; Kacprowski, T; Chasman, DI; Klarin, D; Sinner, MF; Waldenberger, M; Meitinger, T; Harris, TB; Launer, LJ; Soliman, EZ; Chen, LY; Smith, JD; Van Wagoner, DR; Rotter, JI; Psaty, BM; Xie, Z; Hendricks, AE; Ding, J; Delgado, GE; Verweij, N; van der Harst, P; Macfarlane, PW; Ford, I; Hofman, A; Uitterlinden, A; Heeringa, J; Franco, OH; Kors, JA; Weiss, S; Völzke, H; Rose, LM; Natarajan, P; Kathiresan, S; Kääb, S; Gudnason, V; Alonso, A; Chung, MK; Heckbert, SR; Benjamin, EJ; Liu, Y; März, W; Rienstra, M; Jukema, JW; Stricker, BH; Dörr, M; Albert, CM; Ellinor, PT Gene-gene Interaction Analyses for Atrial Fibrillation.
Sci Rep. 2016; 6(24):35371-35371 [OPEN ACCESS]
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Wenzl, K; Hofer, S; Troppan, K; Lassnig, M; Steinbauer, E; Wiltgen, M; Zulus, B; Renner, W; Beham-Schmid, C; Neumeister, P; Deutsch, A Higher incidence of the SNP Met 788 Ile in the coding region of A20 in diffuse large B cell lymphomas.
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Balavarca, Y; Pearce, K; Norden, J; Collin, M; Jackson, G; Holler, E; Dressel, R; Kolb, HJ; Greinix, H; Socie, G; Toubert, A; Rocha, V; Gluckman, E; Hromadnikova, I; Sedlacek, P; Wolff, D; Holtick, U; Dickinson, A; Bickeböller, H Predicting survival using clinical risk scores and non-HLA immunogenetics.
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