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Publikationen

Suchbegriffe: GENETIC MARKERS - , . Treffer: 35

2020

Zhou, J; Passero, K; Palmiero, NE; Müller-Myhsok, B; Kleber, ME; Maerz, W; Hall, MA Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study.
PLoS One. 2020; 15(9):e0238304-e0238304 Doi: 10.1371/journal.pone.0238304 [OPEN ACCESS]
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2018

Groelz, D; Viertler, C; Pabst, D; Dettmann, N; Zatloukal, K Impact of storage conditions on the quality of nucleic acids in paraffin embedded tissues.
PLoS One. 2018; 13(9):e0203608-e0203608 Doi: 10.1371/journal.pone.0203608 [OPEN ACCESS]
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2017

Gong, JY; Setchell, KDR; Zhao, J; Zhang, W; Wolfe, B; Lu, Y; Lackner, K; Knisely, AS; Wang, NL; Hao, CZ; Zhang, MH; Wang, JS Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry.
J Pediatr Gastroenterol Nutr. 2017; 65(5):561-568 Doi: 10.1097/MPG.0000000000001730
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Perakis, S; Auer, M; Belic, J; Heitzer, E Advances in Circulating Tumor DNA Analysis.
Adv Clin Chem. 2017; 80(10):73-153 Doi: 10.1016/bs.acc.2016.11.005
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Schmidt, N; Grammer, T; Gouni-Berthold, I; Julius, U; Kassner, U; Klose, G; König, C; Laufs, U; Otte, B; Steinhagen-Thiessen, E; Wanner, C; März, W CaRe high - Cascade screening and registry for high cholesterol in Germany.
Atheroscler Suppl. 2017; 30(1):72-76 Doi: 10.1016/j.atherosclerosissup.2017.05.015
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2016

Moreno-Viedma, V; Amor, M; Sarabi, A; Bilban, M; Staffler, G; Zeyda, M; Stulnig, TM Common dysregulated pathways in obese adipose tissue and atherosclerosis.
Cardiovasc Diabetol. 2016; 15(1): 120-120. Doi: 10.1186/s12933-016-0441-2 [OPEN ACCESS]
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2015

Bruns, H; Heil, J; Schultze, D; Al Saeedi, M; Schemmer, P Early markers of reperfusion injury after liver transplantation: association with primary dysfunction.
Hepatobiliary Pancreat Dis Int. 2015; 14(3):246-252 Doi: 10.1016/s1499-3872(15)60384-8
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Muschitz, C; Kocijan, R; Pahr, D; Patsch, JM; Amrein, K; Misof, BM; Kaider, A; Resch, H; Pietschmann, P Ibandronate increases sclerostin levels and bone strength in male patients with idiopathic osteoporosis.
Calcif Tissue Int. 2015; 96(6): 477-489. Doi: 10.1007/s00223-015-0003-8
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Smolle, MA; Pichler, M; Haybaeck, J; Gerger, A Genetic markers of recurrence in colorectal cancer.
Pharmacogenomics. 2015; 16(11):1315-1328 Doi: 10.2217/pgs.15.83
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von Wurmb-Schwark, N; Podruks, E; Schwark, T; Göpel, W; Fimmers, R; Poetsch, M About the power of biostatistics in sibling analysis-comparison of empirical and simulated data.
Int J Legal Med. 2015; 129(6):1201-1209 Doi: 10.1007/s00414-015-1252-9
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2014

Agg, B; Benke, K; Szilveszter, B; Pólos, M; Daróczi, L; Odler, B; Nagy, ZB; Tarr, F; Merkely, B; Szabolcs, Z Possible extracardiac predictors of aortic dissection in Marfan syndrome.
BMC Cardiovasc Disord. 2014; 14(4): 47-47. Doi: 10.1186/1471-2261-14-47 [OPEN ACCESS]
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Amrein, K; Dobnig, H; Wagner, D; Piswanger-Sölkner, C; Pieber, TR; Pilz, S; Tomaschitz, A; Dimai, HP; Fahrleitner-Pammer, A Sclerostin in institutionalized elderly women: associations with quantitative bone ultrasound, bone turnover, fractures, and mortality.
J Am Geriatr Soc. 2014; 62(6):1023-1029 Doi: 10.1111/jgs.12791
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Kocijan, R; Muschitz, C; Fahrleitner-Pammer, A; Amrein, K; Pietschmann, P; Haschka, J; Dinu, S; Kapiotis, S; Resch, H Serum sclerostin levels are decreased in adult patients with different types of osteogenesis imperfecta.
J Clin Endocrinol Metab. 2014; 99(2):E311-E319 Doi: 10.1210/jc.2013-2244 [OPEN ACCESS]
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Lubitz, SA; Lunetta, KL; Lin, H; Arking, DE; Trompet, S; Li, G; Krijthe, BP; Chasman, DI; Barnard, J; Kleber, ME; Dörr, M; Ozaki, K; Smith, AV; Müller-Nurasyid, M; Walter, S; Agarwal, SK; Bis, JC; Brody, JA; Chen, LY; Everett, BM; Ford, I; Franco, OH; Harris, TB; Hofman, A; Kääb, S; Mahida, S; Kathiresan, S; Kubo, M; Launer, LJ; Macfarlane, PW; Magnani, JW; McKnight, B; McManus, DD; Peters, A; Psaty, BM; Rose, LM; Rotter, JI; Silbernagel, G; Smith, JD; Sotoodehnia, N; Stott, DJ; Taylor, KD; Tomaschitz, A; Tsunoda, T; Uitterlinden, AG; Van Wagoner, DR; Völker, U; Völzke, H; Murabito, JM; Sinner, MF; Gudnason, V; Felix, SB; März, W; Chung, M; Albert, CM; Stricker, BH; Tanaka, T; Heckbert, SR; Jukema, JW; Alonso, A; Benjamin, EJ; Ellinor, PT Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.
J Am Coll Cardiol. 2014; 63(12):1200-1210 Doi: 10.1016/j.jacc.2013.12.015 [OPEN ACCESS]
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Pereira, TV; Kimura, L; Suwazono, Y; Nakagawa, H; Daimon, M; Oizumi, T; Kayama, T; Kato, T; Li, L; Chen, S; Gu, D; Renner, W; März, W; Yamada, Y; Bagos, PG; Mingroni-Netto, RC Multivariate meta-analysis of the association of G-protein beta 3 gene (GNB3) haplotypes with cardiovascular phenotypes.
Mol Biol Rep. 2014; 41(5):3113-3125 Doi: 10.1007/s11033-014-3171-0 [OPEN ACCESS]
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2012

Amrein, K; Amrein, S; Drexler, C; Dimai, HP; Dobnig, H; Pfeifer, K; Tomaschitz, A; Pieber, TR; Fahrleitner-Pammer, A Sclerostin and its association with physical activity, age, gender, body composition, and bone mineral content in healthy adults.
J Clin Endocrinol Metab. 2012; 97(1):148-154 Doi: 10.1210/jc.2011-2152 [OPEN ACCESS]
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Bis, JC; DeCarli, C; Smith, AV; van der Lijn, F; Crivello, F; Fornage, M; Debette, S; Shulman, JM; Schmidt, H; Srikanth, V; Schuur, M; Yu, L; Choi, SH; Sigurdsson, S; Verhaaren, BF; DeStefano, AL; Lambert, JC; Jack, CR; Struchalin, M; Stankovich, J; Ibrahim-Verbaas, CA; Fleischman, D; Zijdenbos, A; den Heijer, T; Mazoyer, B; Coker, LH; Enzinger, C; Danoy, P; Amin, N; Arfanakis, K; van Buchem, MA; de Bruijn, RF; Beiser, A; Dufouil, C; Huang, J; Cavalieri, M; Thomson, R; Niessen, WJ; Chibnik, LB; Gislason, GK; Hofman, A; Pikula, A; Amouyel, P; Freeman, KB; Phan, TG; Oostra, BA; Stein, JL; Medland, SE; Vasquez, AA; Hibar, DP; Wright, MJ; Franke, B; Martin, NG; Thompson, PM; Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium; Nalls, MA; Uitterlinden, AG; Au, R; Elbaz, A; Beare, RJ; van Swieten, JC; Lopez, OL; Harris, TB; Chouraki, V; Breteler, MM; De Jager, PL; Becker, JT; Vernooij, MW; Knopman, D; Fazekas, F; Wolf, PA; van der Lugt, A; Gudnason, V; Longstreth, WT; Brown, MA; Bennett, DA; van Duijn, CM; Mosley, TH; Schmidt, R; Tzourio, C; Launer, LJ; Ikram, MA; Seshadri, S; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Nat Genet. 2012; 44(5):545-551 Doi: 10.1038/ng.2237 [OPEN ACCESS]
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Ikram, MA; Fornage, M; Smith, AV; Seshadri, S; Schmidt, R; Debette, S; Vrooman, HA; Sigurdsson, S; Ropele, S; Taal, HR; Mook-Kanamori, DO; Coker, LH; Longstreth, WT; Niessen, WJ; DeStefano, AL; Beiser, A; Zijdenbos, AP; Struchalin, M; Jack, CR; Rivadeneira, F; Uitterlinden, AG; Knopman, DS; Hartikainen, AL; Pennell, CE; Thiering, E; Steegers, EA; Hakonarson, H; Heinrich, J; Palmer, LJ; Jarvelin, MR; McCarthy, MI; Grant, SF; St Pourcain, B; Timpson, NJ; Smith, GD; Sovio, U; Early Growth Genetics Consortium; Nalls, MA; Au, R; Hofman, A; Gudnason, H; van der Lugt, A; Harris, TB; Meeks, WM; Vernooij, MW; van Buchem, MA; Catellier, D; Jaddoe, VW; Gudnason, V; Windham, BG; Wolf, PA; van Duijn, CM; Mosley, TH; Schmidt, H; Launer, LJ; Breteler, MM; DeCarli, C; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium Common variants at 6q22 and 17q21 are associated with intracranial volume.
Nat Genet. 2012; 44(5):539-544 Doi: 10.1038/ng.2245 [OPEN ACCESS]
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Taal, HR; St Pourcain, B; Thiering, E; Das, S; Mook-Kanamori, DO; Warrington, NM; Kaakinen, M; Kreiner-Møller, E; Bradfield, JP; Freathy, RM; Geller, F; Guxens, M; Cousminer, DL; Kerkhof, M; Timpson, NJ; Ikram, MA; Beilin, LJ; Bønnelykke, K; Buxton, JL; Charoen, P; Chawes, BL; Eriksson, J; Evans, DM; Hofman, A; Kemp, JP; Kim, CE; Klopp, N; Lahti, J; Lye, SJ; McMahon, G; Mentch, FD; Müller-Nurasyid, M; O'Reilly, PF; Prokopenko, I; Rivadeneira, F; Steegers, EA; Sunyer, J; Tiesler, C; Yaghootkar, H; Cohorts for Heart and Aging Research in Genetic Epidemiology Consortium; Breteler, MM; Decarli, C; Breteler, MM; Debette, S; Fornage, M; Gudnason, V; Launer, LJ; van der Lugt, A; Mosley, TH; Seshadri, S; Smith, AV; Vernooij, MW; Early Genetics & Lifecourse Epidemiology Consortium; Blakemore, AI; Chiavacci, RM; Feenstra, B; Fernandez-Banet, J; Grant, SF; Hartikainen, AL; van der Heijden, AJ; Iñiguez, C; Lathrop, M; McArdle, WL; Mølgaard, A; Newnham, JP; Palmer, LJ; Palotie, A; Pouta, A; Ring, SM; Sovio, U; Standl, M; Uitterlinden, AG; Wichmann, HE; Vissing, NH; DeCarli, C; van Duijn, CM; McCarthy, MI; Koppelman, GH; Estivill, X; Hattersley, AT; Melbye, M; Bisgaard, H; Pennell, CE; Widen, E; Hakonarson, H; Smith, GD; Heinrich, J; Jarvelin, MR; Jaddoe, VW; Early Growth Genetics Consortium Common variants at 12q15 and 12q24 are associated with infant head circumference.
Nat Genet. 2012; 44(5):532-538 Doi: 10.1038/ng.2238 [OPEN ACCESS]
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2011

Poetsch, M; Kamphausen, T; Bajanowski, T; Schwark, T; von Wurmb-Schwark, N Powerplex® ES versus Powerplex® S5--casework testing of the new screening kit.
Forensic Sci Int Genet. 2011; 5(1): 57-63. Doi: 10.1016/j.fsigen.2009.11.002
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2010

Pichler, M; Beckendorf, J; Winter, E; Kleinert, R; Kniepeiss, D; Hoefler, G Quantitative short-tandem repeat analysis of recipient-derived cells as an additional tool for diagnosing cardiac allograft rejection.
Transplantation. 2010; 89(6): 749-755. Doi: 10.1097/TP.0b013e3181cab05c [OPEN ACCESS]
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2008

Klintschar, M; Reichenpfader, B; Saternus, KS A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome.
J Pediatr. 2008; 153(2): 190-193. Doi: 10.1016/j.jpeds.2008.02.032
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Lin, SF; Price, DL; Chen, CH; Brader, P; Li, S; Gonzalez, L; Zhang, Q; Yu, YA; Chen, N; Szalay, AA; Fong, Y; Wong, RJ Oncolytic vaccinia virotherapy of anaplastic thyroid cancer in vivo.
J Clin Endocrinol Metab. 2008; 93(11):4403-4407 Doi: 10.1210/jc.2008-0316 [OPEN ACCESS]
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Than, NG; Romero, R; Hillermann, R; Cozzi, V; Nie, G; Huppertz, B Prediction of preeclampsia - a workshop report.
Placenta. 2008; 29 Suppl A(2):S83-S85 Doi: 10.1016/j.placenta.2007.10.008 [OPEN ACCESS]
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Wagner, T; Drexler, C; Kröll, W; Jüngling, G; Lanzer, G; Gabriel, C Blood clots in erythrocyte concentrates during transfusion
Anaesthesist. 2008; 57(12): 1167-1171. Doi: 10.1007/s00101-008-1444-5 (- Case Report)
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2007

Fucić, A; Znaor, A; Strnad, M; van der Hel, O; Aleksandrov, A; Miskov, S; Grah, J; Sedlar, M; Jazbec, AM; Ceppi, M; Vermeulen, R; Boffetta, P; Norppa, H; Bonassi, S Chromosome damage and cancer risk in the workplace: the example of cytogenetic surveillance in Croatia.
Toxicol Lett. 2007; 172(1-2): 4-11. Doi: 10.1016/j.toxlet.2007.05.015
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2006

Gourraud, PA; Feolo, M; Hoffman, D; Helmberg, W; Cambon-Thomsen, A The dbMHC microsatellite portal: a public resource for the storage and display of MHC microsatellite information.
TISSUE ANTIGEN 2006 67: 395-401. Doi: 10.1111/j.1399-0039.2006.00600.x
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2005

Eller, P; Schgoer, W; Mueller, T; Tancevski, I; Wehinger, A; Ulmer, H; Foeger, B; Haltmayer, M; Ritsch, A; Patsch, JR Hepatic lipase polymorphism and increased risk of peripheral arterial disease.
J Intern Med. 2005; 258(4):344-348 Doi: 10.1111/j.1365-2796.2005.01549.x [OPEN ACCESS]
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2003

Knez, I; Renner, W; Maier, R; Rehak, P; Rienmüller, R; Pilsl, M; Stanger, O; Mircic, A; Dacar, D; Szalay, Z; Martinovic, I; Vogt, PR; Rigler, B Angiotensin-converting enzyme polymorphisms and their potential impact on left ventricular myocardial geometry after aortic valve surgery.
J Heart Valve Dis. 2003; 12(6):687-695
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Lessig, R; Willuweit, S; Krawczak, M; Wu, FC; Pu, CE; Kim, W; Henke, L; Henke, J; Miranda, J; Hidding, M; Benecke, M; Schmitt, C; Magno, M; Calacal, G; Delfin, FC; de Ungria, MC; Elias, S; Augustin, C; Tun, Z; Honda, K; Kayser, M; Gusmao, L; Amorim, A; Alves, C; Hou, Y; Keyser, C; Ludes, B; Klintschar, M; Immel, UD; Reichenpfader, B; Zaharova, B; Roewer, L Asian online Y-STR Haplotype Reference Database.
Leg Med (Tokyo). 2003; 5 Suppl 1(Pt 3):S160-S163 Doi: 10.1016/S1344-6223(02)00100-1
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1999

Pertl, B; Pieber, D; Lercher-Hartlieb, A; Orescovic, I; Haeusler, M; Winter, R; Kroisel, P; Adinolfi, M Rapid prenatal diagnosis of aneuploidy by quantitative fluorescent PCR on fetal samples from mothers at high risk for chromosome disorders.
Mol Hum Reprod. 1999; 5(12):1176-1179 Doi: 10.1093/molehr/5.12.1176 [OPEN ACCESS]
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Reichenpfader, B; Zehner, R; Klintschar, M Characterization of a highly variable short tandem repeat polymorphism at the D2S1242 locus
ELECTROPHORESIS 1999 20: 514-517. Doi: 10.1002/(SICI)1522-2683(19990301)20:3<514::AID-ELPS514>3.0.CO;2-V
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1998

Klintschar, M; Kozma, Z; al Hammadi, N; Abdull Fatah, M; Nöhammer, C A study on the short tandem repeat systems HumCD4, HumTH01 and HumFIBRA in population samples from Yemen and Egypt.
Int J Legal Med. 1998; 111(2):107-109 Doi: 10.1007%2Fs004140050128
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1993

Taniwaki, M; Speicher, MR; Lengauer, C; Jauch, A; Popp, S; Cremer, T Characterization of two marker chromosomes in a patient with acute nonlymphocytic leukemia by two-color fluorescence in situ hybridization.
Cancer Genet Cytogenet. 1993; 70(2):99-102 Doi: 10.1016/0165-4608(93)90175-L (- Case Report) [OPEN ACCESS]
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1986

Gamperl, R Clonal chromosome aberrations in a case of cutaneous T-cell lymphoma.
Cancer Genet Cytogenet. 1986; 19(3-4):341-344 Doi: 10.1016/0165-4608(86)90064-6 (- Case Report)
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