Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: GENE FREQUENCY - , . Treffer: 96
2017
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
Doi: 10.1038/srep45040
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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
Doi: 10.1097/MEG.0000000000000834
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Plecko, B; Zweier, M; Begemann, A; Mathis, D; Schmitt, B; Striano, P; Baethmann, M; Vari, MS; Beccaria, F; Zara, F; Crowther, LM; Joset, P; Sticht, H; Papuc, SM; Rauch, A
Confirmation of mutations in PROSC as a novel cause of vitamin B 6 -dependent epilepsy.
J Med Genet. 2017; 54(12): 809-814.
Doi: 10.1136/jmedgenet-2017-104521
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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
Doi: 10.1038/ng.3916
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Woischke, C; Schaaf, CW; Yang, HM; Vieth, M; Veits, L; Geddert, H; Märkl, B; Stömmer, P; Schaeffer, DF; Frölich, M; Blum, H; Vosberg, S; Greif, PA; Jung, A; Kirchner, T; Horst, D
In-depth mutational analyses of colorectal neuroendocrine carcinomas with adenoma or adenocarcinoma components.
Mod Pathol. 2017; 30(1): 95-103.
Doi: 10.1038/modpathol.2016.150
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2016
Beheshtian, M; Izadi, N; Kriegshauser, G; Kahrizi, K; Mehr, EP; Rostami, M; Hosseini, M; Azad, M; Montajabiniat, M; Kariminejad, A; Nemeth, S; Oberkanins, C; Najmabadi, H
Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations.
J Genet. 2016; 95(3): 667-674.
Doi: 10.1007/s12041-016-0682-6
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Polin, H; Matzhold, EM; Schlenke, P; Gabriel, C; Danzer, M; Wagner, T
RHD Tyr311Stop encoded by a novel nonsense mutation.
Transfusion. 2016; 56(9):2389-2390
Doi: 10.1111/trf.13702
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2015
Benke, K; Ágg, B; Mátyás, G; Szokolai, V; Harsányi, G; Szilveszter, B; Odler, B; Pólos, M; Maurovich-Horvat, P; Radovits, T; Merkely, B; Nagy, ZB; Szabolcs, Z
Gene polymorphisms as risk factors for predicting the cardiovascular manifestations in Marfan syndrome. Role of folic acid metabolism enzyme gene polymorphisms in Marfan syndrome.
Thromb Haemost. 2015; 114(4): 748-756.
Doi: 10.1160/TH15-02-0096
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Ewald, L; Beate, LW; Stephanie, S; Wilfried, R; Yosuf, el-S
Analysis of a Functional IL-6 Gene Polymorphism in HLAB27 Associated and Intermediate Uveitis Gives New Insight in Disease Pathogenesis and Commonality with Other Autoimmune Diseases.
J Immunol Res. 2015; 2015(7):174062-174062
Doi: 10.1155/2015/174062
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Geiger, O; Hatzl, S; Kashofer, K; Hoefler, G; Wölfler, A; Sill, H; Zebisch, A
Deletion of SPRY4 is a frequent event in secondary acute myeloid leukemia.
Ann Hematol. 2015; 94(11):1923-1924
Doi: 10.1007/s00277-015-2445-5
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Lindner, E; Glatz, W; Schwab, C; El-Shabrawi, Y; Mossböck, G
Analysis of functional polymorphisms in apoptosis-related genes in primary open angle glaucoma.
Mol Vis. 2015; 21(7):1340-1344
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Lindner, E; Weger, M; Ardjomand, N; Renner, W; El-Shabrawi, Y
Associations of Independent IL2RA Gene Variants with Intermediate Uveitis.
PLoS One. 2015; 10(7):e0130737-e0130737
Doi: 10.1371/journal.pone.0130737
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Neumann, M; Vosberg, S; Schlee, C; Heesch, S; Schwartz, S; Gökbuget, N; Hoelzer, D; Graf, A; Krebs, S; Bartram, I; Blum, H; Brüggemann, M; Hecht, J; Bohlander, SK; Greif, PA; Baldus, CD
Mutational spectrum of adult T-ALL.
Oncotarget. 2015; 6(5): 2754-2766.
Doi: 10.18632/oncotarget.2218
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2014
Heidary, M; Auer, M; Ulz, P; Heitzer, E; Petru, E; Gasch, C; Riethdorf, S; Mauermann, O; Lafer, I; Pristauz, G; Lax, S; Pantel, K; Geigl, JB; Speicher, MR
The dynamic range of circulating tumor DNA in metastatic breast cancer.
Breast Cancer Res. 2014; 16(4):421-421
Doi: 10.1186/s13058-014-0421-y
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Heidenreich, B; Nagore, E; Rachakonda, PS; Garcia-Casado, Z; Requena, C; Traves, V; Becker, J; Soufir, N; Hemminki, K; Kumar, R
Telomerase reverse transcriptase promoter mutations in primary cutaneous melanoma.
Nat Commun. 2014; 5(5):3401-3401
Doi: 10.1038/ncomms4401
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Lam, UD; Lerchbaum, E; Schweighofer, N; Trummer, O; Eberhard, K; Genser, B; Pieber, TR; Obermayer-Pietsch, B
Association of MEP1A gene variants with insulin metabolism in central European women with polycystic ovary syndrome.
Gene. 2014; 537(2):245-252
Doi: 10.1016/j.gene.2013.12.055
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Ning, Y; Gerger, A; Zhang, W; Hanna, DL; Yang, D; Winder, T; Wakatsuki, T; Labonte, MJ; Stintzing, S; Volz, N; Sunakawa, Y; Stremitzer, S; El-Khoueiry, R; Lenz, HJ
Plastin polymorphisms predict gender- and stage-specific colon cancer recurrence after adjuvant chemotherapy.
Mol Cancer Ther. 2014; 13(2):528-539
Doi: 10.1158/1535-7163.MCT-13-0646
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Pagava, K; Rauscher, B; Korinteli, IA; Shonvadze, D; Kriegshauser, G; Oberkanins, Ch
Familial Mediterranean fever in Georgia.
Georgian Med News. 2014; 95(230): 79-82.
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Reinthaler, E; Machetanz, G; Hotzy, C; Reindl, M; Fazekas, F; Kristoferitsch, W; Berger, T; Schmied, C; Zimprich, A
No evidence for a role of rare CYP27B1 variants in Austrian multiple sclerosis patients.
MULT SCLER J. 2014; 20(3): 391-392.
Doi: 10.1177/1352458513498130
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Schiekofer, S; Bobak, I; Kleber, ME; Maerz, W; Rudofsky, G; Dugi, KA; Schneider, JG
Association between a gene variant near ataxia telangiectasia mutated and coronary artery disease in men.
Diab Vasc Dis Res. 2014; 11(1):60-63
Doi: 10.1177/1479164113514232
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2013
Behjati, S; Tarpey, PS; Presneau, N; Scheipl, S; Pillay, N; Van Loo, P; Wedge, DC; Cooke, SL; Gundem, G; Davies, H; Nik-Zainal, S; Martin, S; McLaren, S; Goody, V; Goodie, V; Robinson, B; Butler, A; Teague, JW; Halai, D; Khatri, B; Myklebost, O; Baumhoer, D; Jundt, G; Hamoudi, R; Tirabosco, R; Amary, MF; Futreal, PA; Stratton, MR; Campbell, PJ; Flanagan, AM
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.
Nat Genet. 2013; 45(12):1479-1482
Doi: 10.1038/ng.2814
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Friedrich, K; Rupp, C; Hov, JR; Steinebrunner, N; Weiss, KH; Stiehl, A; Brune, M; Schaefer, PK; Schemmer, P; Sauer, P; Schirmacher, P; Runz, H; Karlsen, TH; Stremmel, W; Gotthardt, DN
A frequent PNPLA3 variant is a sex specific disease modifier in PSC patients with bile duct stenosis.
PLoS One. 2013; 8(3):e58734-e58734
Doi: 10.1371/journal.pone.0058734
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Hacker, E; Nagore, E; Cerroni, L; Woods, SL; Hayward, NK; Chapman, B; Montgomery, GW; Soyer, HP; Whiteman, DC;
NRAS and BRAF Mutations in Cutaneous Melanoma and the Association with MC1R Genotype: Findings from Spanish and Austrian Populations.
J INVEST DERMATOL. 2013; 133(4): 1027-1033.
Doi: 10.1038/jid.2012.385
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Köttgen, A; Albrecht, E; Teumer, A; Vitart, V; Krumsiek, J; Hundertmark, C; Pistis, G; Ruggiero, D; Oeaghdha, CM; Haller, T; Yang, Q; Tanaka, T; Johnson, AD; Kutalik, Z; Smith, AV; Shi, J; Struchalin, M; Middelberg, RP; Brown, MJ; Gaffo, AL; Pirastu, N; Li, G; Hayward, C; Zemunik, T; Huffman, J; Yengo, L; Zhao, JH; Demirkan, A; Feitosa, MF; Liu, X; Malerba, G; Lopez, LM; van der Harst, P; Li, X; Kleber, ME; Hicks, AA; Nolte, IM; Johansson, A; Murgia, F; Wild, SH; Bakker, SJ; Peden, JF; Dehghan, A; Steri, M; Tenesa, A; Lagou, V; Salo, P; Mangino, M; Rose, LM; Lehtimäki, T; Woodward, OM; Okada, Y; Tin, A; Müller, C; Oldmeadow, C; Putku, M; Czamara, D; Kraft, P; Frogheri, L; Thun, GA; Grotevendt, A; Gislason, GK; Harris, TB; Launer, LJ; McArdle, P; Shuldiner, AR; Boerwinkle, E; Coresh, J; Schmidt, H; Schallert, M; Martin, NG; Montgomery, GW; Kubo, M; Nakamura, Y; Tanaka, T; Munroe, PB; Samani, NJ; Jacobs, DR; Liu, K; D'Adamo, P; Ulivi, S; Rotter, JI; Psaty, BM; Vollenweider, P; Waeber, G; Campbell, S; Devuyst, O; Navarro, P; Kolcic, I; Hastie, N; Balkau, B; Froguel, P; Esko, T; Salumets, A; Khaw, KT; Langenberg, C; Wareham, NJ; Isaacs, A; Kraja, A; Zhang, Q; Wild, PS; Scott, RJ; Holliday, EG; Org, E; Viigimaa, M; Bandinelli, S; Metter, JE; Lupo, A; Trabetti, E; Sorice, R; Döring, A; Lattka, E; Strauch, K; Theis, F; Waldenberger, M; Wichmann, HE; Davies, G; Gow, AJ; Bruinenberg, M; LifeLines Cohort Study; Stolk, RP; Kooner, JS; Zhang, W; Winkelmann, BR; Boehm, BO; Lucae, S; Penninx, BW; Smit, JH; Curhan, G; Mudgal, P; Plenge, RM; Portas, L; Persico, I; Kirin, M; Wilson, JF; Leach, IM; van Gilst, WH; Goel, A; Ongen, H; Hofman, A; Rivadeneira, F; Uitterlinden, AG; Imboden, M; von Eckardstein, A; Cucca, F; Nagaraja, R; Piras, MG; Nauck, M; Schurmann, C; Budde, K;Ernst, F; Farrington, SM; Theodoratou, E; Prokopenko, I; Stumvoll, M; Jula, A; Perola, M; Salomaa, V; Shin, SY; Spector, TD; Sala, C; Ridker, PM; Kähönen, M; Viikari, J; Hengstenberg, C; Nelson, CP; CARDIoGRAM Consortium;DIAGRAM Consortium;ICBP Consortium MAGIC Consortium;Meschia, JF;Nalls, MA;Sharma, P;Singleton, AB;Kamatani, N;Zeller, T;Burnier, M;Attia, J;Laan, M;Klopp, N;Hillege, HL;Kloiber, S;Choi, H Pirastu, M Tore, S Probst-Hensch, NM Völzke, H; Gudnason, V; Parsa, A; Schmidt, R; Whitfield, JB; Fornage, M; Gasparini, P; Siscovick, DS; Polasek, O; Campbell, H; Rudan, I; Bouatia-Naji, N; Metspalu, A; Loos, RJ; van Duijn, CM; Borecki, IB; Ferrucci, L; Gambaro, G;Deary, IJ; Wolffenbuttel, BH; Chambers, JC; März, W;Pramstaller, PP; Snieder, H; Gyllensten, U; Wright, AF; Navis, G; Watkins, H; Witteman, JCM; Sanna, S; Schipf, S; Dunlop, MG; Tönjes, A; Ripatti, S; Soranzo, N; Toniolo, D; Chasman, DI; Raitakari, O; Kao, WHL; Ciullo, M; Fox, CS; Caulfield, M; Bochud, M; Gieger, C
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
Nat Genet. 2013; 45(2): 145-154.
Doi: 10.1038/ng.2500
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Lajin, B; Alhaj Sakur, A; Alachkar, A
Association between polymorphisms in apoptotic genes and susceptibility for developing breast cancer in Syrian women.
Breast Cancer Res Treat. 2013; 138(2):611-619
Doi: 10.1007/s10549-013-2467-4
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Metzger, S; Walter, C; Riess, O; Roos, RA; Nielsen, JE; Craufurd, D; REGISTRY Investigators of the European Huntington’s Disease Network; Nguyen, HP
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients.
PLoS One. 2013; 8(7):e68951-e68951
Doi: 10.1371/journal.pone.0068951
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Parsa, A; Fuchsberger, C; Köttgen, A; O'Seaghdha, CM; Pattaro, C; de Andrade, M; Chasman, DI; Teumer, A; Endlich, K; Olden, M; Chen, MH; Tin, A; Kim, YJ; Taliun, D; Li, M; Feitosa, M; Gorski, M; Yang, Q; Hundertmark, C; Foster, MC; Glazer, N; Isaacs, A; Rao, M; Smith, AV; O'Connell, JR; Struchalin, M; Tanaka, T; Li, G; Hwang, SJ; Atkinson, EJ; Lohman, K; Cornelis, MC; Johansson, A; Tönjes, A; Dehghan, A; Couraki, V; Holliday, EG; Sorice, R; Kutalik, Z; Lehtimäki, T; Esko, T; Deshmukh, H; Ulivi, S; Chu, AY; Murgia, F; Trompet, S; Imboden, M; Kollerits, B; Pistis, G; Harris, TB; Launer, LJ; Aspelund, T; Eiriksdottir, G; Mitchell, BD; Boerwinkle, E; Schmidt, H; Hofer, E; Hu, F; Demirkan, A; Oostra, BA; Turner, ST; Ding, J; Andrews, JS; Freedman, BI; Giulianini, F; Koenig, W; Illig, T; Döring, A; Wichmann, HE; Zgaga, L; Zemunik, T; Boban, M; Minelli, C; Wheeler, HE; Igl, W; Zaboli, G; Wild, SH; Wright, AF; Campbell, H; Ellinghaus, D; Nöthlings, U; Jacobs, G; Biffar, R; Ernst, F; Homuth, G; Kroemer, HK; Nauck, M; Stracke, S; Völker, U; Völzke, H; Kovacs, P; Stumvoll, M; Mägi, R; Hofman, A; Uitterlinden, AG; Rivadeneira, F; Aulchenko, YS; Polasek, O; Hastie, N; Vitart, V; Helmer, C; Wang, JJ; Stengel, B; Ruggiero, D; Bergmann, S; Kähönen, M; Viikari, J; Nikopensius, T; Province, M; Colhoun, H; Doney, A; Robino, A; Krämer, BK; Portas, L; Ford, I; Buckley, BM; Adam, M; Thun, GA; Paulweber, B; Haun, M; Sala, C; Mitchell, P; Ciullo, M; Vollenweider, P; Raitakari, O; Metspalu, A; Palmer, C; Gasparini, P; Pirastu, M; Jukema, JW; Probst-Hensch, NM; Kronenberg, F; Toniolo, D; Gudnason, V; Shuldiner, AR; Coresh, J; Schmidt, R; Ferrucci, L; van Duijn, CM; Borecki, I; Kardia, SL; Liu, Y; Curhan, GC; Rudan, I; Gyllensten, U; Wilson, JF; Franke, A; Pramstaller, PP; Rettig, R; Prokopenko, I; Witteman, J; Hayward, C; Ridker, PM; Bochud, M; Heid, IM; Siscovick, DS; Fox, CS; Kao, WL; Böger, CA
Common variants in Mendelian kidney disease genes and their association with renal function.
J Am Soc Nephrol. 2013; 24(12):2105-2117
Doi: 10.1681/ASN.2012100983
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Poetsch, M; Preusse-Prange, A; Schwark, T; von Wurmb-Schwark, N
The new guidelines for paternity analysis in Germany-how many STR loci are necessary when investigating duo cases?
Int J Legal Med. 2013; 127(4): 731-734.
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Serum level of IP-10 increases predictive value of IL28B polymorphisms for spontaneous clearance of acute HCV infection.
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Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.
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Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.
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Zimmermann, C; Weger, M; Faschinger, C; Renner, W; Mossböck, G
Role of interleukin 6-174G>C polymorphism
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Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.
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Gugatschka, M; Dehchamani, D; Wascher, TC; Friedrich, G; Renner, W
DNA repair gene ERCC2 polymorphisms and risk of squamous cell carcinoma of the head and neck.
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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.
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Lerchbaum, E; Trummer, O; Giuliani, A; Gruber, HJ; Pieber, TR; Obermayer-Pietsch, B
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IL2RA gene polymorphism rs2104286 A>G seen in multiple sclerosis is associated with intermediate uveitis: possible parallel pathways?
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Maier, R; Steinbrugger, I; Haas, A; Selimovic, M; Renner, W; El-Shabrawi, Y; Werner, C; Wedrich, A; Schmut, O; Weger, M
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The new Powerplex® ESX17 and ESI17 kits in paternity and maternity analyses involving people from Africa--including allele frequencies for three African populations.
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Bahadori, B; Uitz, E; Mayer, A; Harauer, J; Dam, K; Truschnig-Wilders, M; Pilger, E; Renner, W
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