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Search Items: GENETICS, . hits: 265

2019

Adams, HHH; Roshchupkin, GV; DeCarli, C; Franke, B; Grabe, HJ; Habes, M; Jahanshad, N; Medland, SE; Niessen, W; Satizabal, CL; Schmidt, R; Seshadri, S; Teumer, A; Thompson, PM; Vernooij, MW; Wittfeld, K; Ikram, MA Full exploitation of high dimensionality in brain imaging: The JPND working group statement and findings.
Alzheimers Dement (Amst). 2019; 11:286-290 [OPEN ACCESS]
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Aspelund, T; Grübler, MR; Smith, AV; Gudmundsson, EF; Keppel, M; Cotch, MF; Harris, TB; Jorde, R; Grimnes, G; Joakimsen, R; Schirmer, H; Wilsgaard, T; Mathiesen, EB; Njølstad, I; Løchen, ML; März, W; Kleber, ME; Tomaschitz, A; Grove-Laugesen, D; Rejnmark, L; Swart, KMA; Brouwer, IA; Lips, P; van Schoor, NM; Sempos, CT; Durazo-Arvizu, RA; Škrabáková, Z; Dowling, KG; Cashman, KD; Kiely, M; Pilz, S; Gudnason, V; Eiriksdottir, G Effect of Genetically Low 25-Hydroxyvitamin D on Mortality Risk: Mendelian Randomization Analysis in 3 Large European Cohorts.
Nutrients. 2019; 11(1): [OPEN ACCESS]
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Bengesser, SA; Mörkl, S; Painold, A; Dalkner, N; Birner, A; Fellendorf, FT; Platzer, M; Queissner, R; Hamm, C; Maget, A; Pilz, R; Rieger, A; Wagner-Skacel, J; Reininghaus, B; Kapfhammer, HP; Petek, E; Kashofer, K; Halwachs, B; Holzer, P; Waha, A; Reininghaus, EZ Epigenetics of the molecular clock and bacterial diversity in bipolar disorder.
Psychoneuroendocrinology. 2019; 101(1):160-166
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Budde, M; Anderson-Schmidt, H; Gade, K; Reich-Erkelenz, D; Adorjan, K; Kalman, JL; Senner, F; Papiol, S; Andlauer, TFM; Comes, AL; Schulte, EC; Klöhn-Saghatolislam, F; Gryaznova, A; Hake, M; Bartholdi, K; Flatau, L; Reitt, M; Quast, S; Stegmaier, S; Meyers, M; Emons, B; Haußleiter, IS; Juckel, G; Nieratschker, V; Dannlowski, U; Schaupp, SK; Schmauß, M; Zimmermann, J; Reimer, J; Schulz, S; Wiltfang, J; Reininghaus, E; Anghelescu, IG; Arolt, V; Baune, BT; Konrad, C; Thiel, A; Fallgatter, AJ; Figge, C; von Hagen, M; Koller, M; Lang, FU; Wigand, ME; Becker, T; Jäger, M; Dietrich, DE; Stierl, S; Scherk, H; Spitzer, C; Folkerts, H; Witt, SH; Degenhardt, F; Forstner, AJ; Rietschel, M; Nöthen, MM; Falkai, P; Schulze, TG; Heilbronner, U A longitudinal approach to biological psychiatric research: The PsyCourse study.
Am J Med Genet B Neuropsychiatr Genet. 2019; 180(2):89-102 [OPEN ACCESS]
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Kalman, JL; Papiol, S; Forstner, AJ; Heilbronner, U; Degenhardt, F; Strohmaier, J; Adli, M; Adorjan, K; Akula, N; Alda, M; Anderson-Schmidt, H; Andlauer, TF; Anghelescu, IG; Ardau, R; Arias, B; Arolt, V; Aubry, JM; Backlund, L; Bartholdi, K; Bauer, M; Baune, BT; Becker, T; Bellivier, F; Benabarre, A; Bengesser, S; Bhattacharjee, AK; Biernacka, JM; Birner, A; Brichant-Petitjean, C; Budde, M; Cervantes, P; Chillotti, C; Cichon, S; Clark, SR; Colom, F; Comes, AL; Cruceanu, C; Czerski, PM; Dannlowski, U; Dayer, A; Del Zompo, M; DePaulo, JR; Dietrich, DE; Étain, B; Ethofer, T; Falkai, P; Fallgatter, A; Figge, C; Flatau, L; Folkerts, H; Frisen, L; Frye, MA; Fullerton, JM; Gade, K; Gard, S; Garnham, JS; Goes, FS; Grigoroiu-Serbanescu, M; Gryaznova, A; Hake, M; Hauser, J; Herms, S; Hoffmann, P; Hou, L; Jäger, M; Jamain, S; Jiménez, E; Juckel, G; Kahn, JP; Kassem, L; Kelsoe, J; Kittel-Schneider, S; Kliwicki, S; Klohn-Sagatholislam, F; Koller, M; König, B; Konrad, C; Lackner, N; Laje, G; Landén, M; Lang, FU; Lavebratt, C; Leboyer, M; Leckband, SG; Maj, M; Manchia, M; Martinsson, L; McCarthy, MJ; McElroy, SL; McMahon, FJ; Mitchell, PB; Mitjans, M; Mondimore, FM; Monteleone, P; Nieratschker, V; Nievergelt, CM; Novák, T; Ösby, U; Pfennig, A; Potash, JB; Reich-Erkelenz, D; Reif, A; Reimer, J; Reininghaus, E; Reitt, M; Ripke, S; Rouleau, GA; Rybakowski, JK; Schalling, M; Scherk, H; Schmauß, M; Schofield, PR; Schubert, KO; Schulte, EC; Schulz, S; Senner, F; Severino, G; Shekhtman, T; Shilling, PD; Simhandl, C; Slaney, CM; Spitzer, C; Squassina, A; Stamm, T; Stegmaier, S; Stierl, S; Stopkova, P; Thiel, A; Tighe, SK; Tortorella, A; Turecki, G; Vieta, E; Veeh, J; von Hagen, M; Wigand, ME; Wiltfang, J; Witt, S; Wright, A; Zandi, PP; Zimmermann, J; Nöthen, M; Rietschel, M; Schulze, TG Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study.
Bipolar Disord. 2019; 21(1):68-75 [OPEN ACCESS]
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Kunkle, BW; Grenier-Boley, B; Sims, R; Bis, JC; Damotte, V; Naj, AC; Boland, A; Vronskaya, M; van der Lee, SJ; Amlie-Wolf, A; Bellenguez, C; Frizatti, A; Chouraki, V; Martin, ER; Sleegers, K; Badarinarayan, N; Jakobsdottir, J; Hamilton-Nelson, KL; Moreno-Grau, S; Olaso, R; Raybould, R; Chen, Y; Kuzma, AB; Hiltunen, M; Morgan, T; Ahmad, S; Vardarajan, BN; Epelbaum, J; Hoffmann, P; Boada, M; Beecham, GW; Garnier, JG; Harold, D; Fitzpatrick, AL; Valladares, O; Moutet, ML; Gerrish, A; Smith, AV; Qu, L; Bacq, D; Denning, N; Jian, X; Zhao, Y; Del Zompo, M; Fox, NC; Choi, SH; Mateo, I; Hughes, JT; Adams, HH; Malamon, J; Sanchez-Garcia, F; Patel, Y; Brody, JA; Dombroski, BA; Naranjo, MCD; Daniilidou, M; Eiriksdottir, G; Mukherjee, S; Wallon, D; Uphill, J; Aspelund, T; Cantwell, LB; Garzia, F; Galimberti, D; Hofer, E; Butkiewicz, M; Fin, B; Scarpini, E; Sarnowski, C; Bush, WS; Meslage, S; Kornhuber, J; White, CC; Song, Y; Barber, RC; Engelborghs, S; Sordon, S; Voijnovic, D; Adams, PM; Vandenberghe, R; Mayhaus, M; Cupples, LA; Albert, MS; De Deyn, PP; Gu, W; Himali, JJ; Beekly, D; Squassina, A; Hartmann, AM; Orellana, A; Blacker, D; Rodriguez-Rodriguez, E; Lovestone, S; Garcia, ME; Doody, RS; Munoz-Fernadez, C; Sussams, R; Lin, H; Fairchild, TJ; Benito, YA; Holmes, C; Karamujić-Čomić, H; Frosch, MP; Thonberg, H; Maier, W; Roschupkin, G; Ghetti, B; Giedraitis, V; Kawalia, A; Li, S; Huebinger, RM; Kilander, L; Moebus, S; Hernández, I; Kamboh, MI; Brundin, R; Turton, J; Yang, Q; Katz, MJ; Concari, L; Lord, J; Beiser, AS; Keene, CD; Helisalmi, S; Kloszewska, I; Kukull, WA; Koivisto, AM; Lynch, A; Tarraga, L; Larson, EB; Haapasalo, A; Lawlor, B; Mosley, TH; Lipton, RB; Solfrizzi, V; Gill, M; Longstreth, WT; Montine, TJ; Frisardi, V; Diez-Fairen, M; Rivadeneira, F; Petersen, RC; Deramecourt, V; Alvarez, I; Salani, F; Ciaramella, A; Boerwinkle, E; Reiman, EM; Fievet, N; Rotter, JI; Reisch, JS; Hanon, O; Cupidi, C; Andre Uitterlinden, AG; Royall, DR; Dufouil, C; Maletta, RG; de Rojas, I; Sano, M; Brice, A; Cecchetti, R; George-Hyslop, PS; Ritchie, K; Tsolaki, M; Tsuang, DW; Dubois, B; Craig, D; Wu, CK; Soininen, H; Avramidou, D; Albin, RL; Fratiglioni, L; Germanou, A; Apostolova, LG; Keller, L; Koutroumani, M; Arnold, SE; Panza, F; Gkatzima, O; Asthana, S; Hannequin, D; Whitehead, P; Atwood, CS; Caffarra, P; Hampel, H; Quintela, I; Carracedo, Á; Lannfelt, L; Rubinsztein, DC; Barnes, LL; Pasquier, F; Frölich, L; Barral, S; McGuinness, B; Beach, TG; Johnston, JA; Becker, JT; Passmore, P; Bigio, EH; Schott, JM; Bird, TD; Warren, JD; Boeve, BF; Lupton, MK; Bowen, JD; Proitsi, P; Boxer, A; Powell, JF; Burke, JR; Kauwe, JSK; Burns, JM; Mancuso, M; Buxbaum, JD; Bonuccelli, U; Cairns, NJ; McQuillin, A; Cao, C; Livingston, G; Carlson, CS; Bass, NJ; Carlsson, CM; Hardy, J; Carney, RM; Bras, J; Carrasquillo, MM; Guerreiro, R; Allen, M; Chui, HC; Fisher, E; Masullo, C; Crocco, EA; DeCarli, C; Bisceglio, G; Dick, M; Ma, L; Duara, R; Graff-Radford, NR; Evans, DA; Hodges, A; Faber, KM; Scherer, M; Fallon, KB; Riemenschneider, M; Fardo, DW; Heun, R; Farlow, MR; Kölsch, H; Ferris, S; Leber, M; Foroud, TM; Heuser, I; Galasko, DR; Giegling, I; Gearing, M; Hüll, M; Geschwind, DH; Gilbert, JR; Morris, J; Green, RC; Mayo, K; Growdon, JH; Feulner, T; Hamilton, RL; Harrell, LE; Drichel, D; Honig, LS; Cushion, TD; Huentelman, MJ; Hollingworth, P; Hulette, CM; Hyman, BT; Marshall, R; Jarvik, GP; Meggy, A; Abner, E; Menzies, GE; Jin, LW; Leonenko, G; Real, LM; Jun, GR; Baldwin, CT ... Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
Nat Genet. 2019; 51(3):414-430 [OPEN ACCESS]
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Kuret, T; Burja, B; Feichtinger, J; Thallinger, GG; Frank-Bertoncelj, M; Lakota, K; Žigon, P; Sodin-Semrl, S; Čučnik, S; Tomšič, M; Hočevar, A Gene and miRNA expression in giant cell arteritis-a concise systematic review of significantly modified studies.
Clin Rheumatol. 2019; 38(2):307-316
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Marini, S; Crawford, K; Morotti, A; Lee, MJ; Pezzini, A; Moomaw, CJ; Flaherty, ML; Montaner, J; Roquer, J; Jimenez-Conde, J; Giralt-Steinhauer, E; Elosua, R; Cuadrado-Godia, E; Soriano-Tarraga, C; Slowik, A; Jagiella, JM; Pera, J; Urbanik, A; Pichler, A; Hansen, BM; McCauley, JL; Tirschwell, DL; Selim, M; Brown, DL; Silliman, SL; Worrall, BB; Meschia, JF; Kidwell, CS; Testai, FD; Kittner, SJ; Schmidt, H; Enzinger, C; Deary, IJ; Rannikmae, K; Samarasekera, N; Al-Shahi Salman, R; Sudlow, CL; Klijn, CJM; van Nieuwenhuizen, KM; Fernandez-Cadenas, I; Delgado, P; Norrving, B; Lindgren, A; Goldstein, JN; Viswanathan, A; Greenberg, SM; Falcone, GJ; Biffi, A; Langefeld, CD; Woo, D; Rosand, J; Anderson, CD; International Stroke Genetics Consortium Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity: A Meta-analysis.
JAMA Neurol. 2019; 140(1): [OPEN ACCESS]
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Rath, M; Spiegler, S; Strom, TM; Trenkler, J; Kroisel, PM; Felbor, U Identification of pathogenic YY1AP1 splice variants in siblings with Grange syndrome by whole exome sequencing.
Am J Med Genet A. 2019; 179(2): 295-299. (- Case Report) [OPEN ACCESS]
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Sabater-Lleal, M; Huffman, JE; de Vries, PS; Marten, J; Mastrangelo, MA; Song, C; Pankratz, N; Ward-Caviness, CK; Yanek, LR; Trompet, S; Delgado, GE; Guo, X; Bartz, TM; Martinez-Perez, A; Germain, M; de Haan, HG; Ozel, AB; Polasek, O; Smith, AV; Eicher, JD; Reiner, AP; Tang, W; Davies, NM; Stott, DJ; Rotter, JI; Tofler, GH; Boerwinkle, E; de Maat, MPM; Kleber, ME; Welsh, P; Brody, JA; Chen, MH; Vaidya, D; Soria, JM; Suchon, P; van Hylckama Vlieg, A; Desch, KC; Kolcic, I; Joshi, PK; Launer, LJ; Harris, TB; Campbell, H; Rudan, I; Becker, DM; Li, JZ; Rivadeneira, F; Uitterlinden, AG; Hofman, A; Franco, OH; Cushman, M; Psaty, BM; Morange, PE; McKnight, B; Chong, MR; Fernandez-Cadenas, I; Rosand, J; Lindgren, A; Gudnason, V; Wilson, JF; Hayward, C; Ginsburg, D; Fornage, M; Rosendaal, FR; Souto, JC; Becker, LC; Jenny, NS; Marz, W; Jukema, JW; Dehghan, A; Tregouet, DA; Morrison, AC; Johnson, AD; O'Donnell, CJ; Strachan, DP; Lowenstein, CJ; Smith, NL Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
CIRCULATION. 2019; 139(5): 620-635. [OPEN ACCESS]
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Seidel, MG; Kindle, G; Gathmann, B; Quinti, I; Buckland, M; van Montfrans, J; Scheible, R; Rusch, S; Gasteiger, LM; Grimbacher, B; Mahlaoui, N; Ehl, S; ESID Registry Working Party Mario Abinun The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity.
J Allergy Clin Immunol Pract. 2019;
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Spasic, S; Brcic, I; Freire, R; Garcia-Buitrago, MT; Rosenberg, AE Epithelioid Hemangioendothelioma of the Bowel in Crohn's Disease: The First Reported Case.
Int J Surg Pathol. 2019; 27(4):423-426
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Wadsack, D; Sattler, H; Kleber, ME; Eirich, K; Scharnagl, H; Fauler, G; März, W; Grammer, TB Recurrent tendosynovitis as a rare manifestation of a lipid disorder.
J Clin Lipidol. 2019; 13(1): 54-61.
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Wu, O; Winzeck, S; Giese, AK; Hancock, BL; Etherton, MR; Bouts, MJRJ; Donahue, K; Schirmer, MD; Irie, RE; Mocking, SJT; McIntosh, EC; Bezerra, R; Kamnitsas, K; Frid, P; Wasselius, J; Cole, JW; Xu, H; Holmegaard, L; Jiménez-Conde, J; Lemmens, R; Lorentzen, E; McArdle, PF; Meschia, JF; Roquer, J; Rundek, T; Sacco, RL; Schmidt, R; Sharma, P; Slowik, A; Stanne, TM; Thijs, V; Vagal, A; Woo, D; Bevan, S; Kittner, SJ; Mitchell, BD; Rosand, J; Worrall, BB; Jern, C; Lindgren, AG; Maguire, J; Rost, NS Big Data Approaches to Phenotyping Acute Ischemic Stroke Using Automated Lesion Segmentation of Multi-Center Magnetic Resonance Imaging Data.
Stroke. 2019; 50(7):1734-1741
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2018

Berger, AW; Raedler, K; Langner, C; Ludwig, L; Dikopoulos, N; Becker, KF; Slotta-Huspenina, J; Quante, M; Schwerdel, D; Perkhofer, L; Kleger, A; Zizer, E; Oswald, F; Seufferlein, T; Meining, A Genetic Biopsy for Prediction of Surveillance Intervals after Endoscopic Resection of Colonic Polyps: Results of the GENESIS Study.
United European Gastroenterol J. 2018; 6(2): 290-299. [OPEN ACCESS]
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Day, F; Karaderi, T; Jones, MR; Meun, C; He, C; Drong, A; Kraft, P; Lin, N; Huang, H; Broer, L; Magi, R; Saxena, R; Laisk, T; Urbanek, M; Hayes, MG; Thorleifsson, G; Fernandez-Tajes, J; Mahajan, A; Mullin, BH; Stuckey, BGA; Spector, TD; Wilson, SG; Goodarzi, MO; Davis, L; Obermayer-Pietsch, B; Uitterlinden, AG; Anttila, V; Neale, BM; Jarvelin, MR; Fauser, B; Kowalska, I; Visser, JA; Andersen, M; Ong, K; Stener-Victorin, E; Ehrmann, D; Legro, RS; Salumets, A; McCarthy, MI; Morin-Papunen, L; Thorsteinsdottir, U; Stefansson, K; 23andMe Research Team; Styrkarsdottir, U; Perry, JRB; Dunaif, A; Laven, J; Franks, S; Lindgren, CM; Welt, CK Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
PLoS Genet. 2018; 14(12):e1007813-e1007813 [OPEN ACCESS]
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Emons, G; Steiner, E; Vordermark, D; Uleer, C; Bock, N; Paradies, K; Ortmann, O; Aretz, S; Mallmann, P; Kurzeder, C; Hagen, V; van Oorschot, B; Höcht, S; Feyer, P; Egerer, G; Friedrich, M; Cremer, W; Prott, FJ; Horn, LC; Prömpeler, H; Langrehr, J; Leinung, S; Beckmann, MW; Kimmig, R; Letsch, A; Reinhardt, M; Alt-Epping, B; Kiesel, L; Menke, J; Gebhardt, M; Steinke-Lange, V; Rahner, N; Lichtenegger, W; Zeimet, A; Hanf, V; Weis, J; Mueller, M; Henscher, U; Schmutzler, RK; Meindl, A; Hilpert, F; Panke, JE; Strnad, V; Niehues, C; Dauelsberg, T; Niehoff, P; Mayr, D; Grab, D; Kreißl, M; Witteler, R; Schorsch, A; Mustea, A; Petru, E; Hübner, J; Rose, AD; Wight, E; Tholen, R; Bauerschmitz, GJ; Fleisch, M; Juhasz-Boess, I; Sigurd, L; Runnebaum, I; Tempfer, C; Nothacker, MJ; Blödt, S; Follmann, M; Langer, T; Raatz, H; Wesselmann, S; Erdogan, S Interdisciplinary Diagnosis, Therapy and Follow-up of Patients with Endometrial Cancer. Guideline (S3-Level, AWMF Registry Nummer 032/034-OL, April 2018) - Part 1 with Recommendations on the Epidemiology, Screening, Diagnosis and Hereditary Factors of Endometrial Cancer.
Geburtshilfe Frauenheilkd. 2018; 78(10):949-971 [OPEN ACCESS]
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Griewank, KG; Wiesner, T; Murali, R; Pischler, C; Müller, H; Koelsche, C; Möller, I; Franklin, C; Cosgarea, I; Sucker, A; Schadendorf, D; Schaller, J; Horn, S; Brenn, T; Mentzel, T Atypical fibroxanthoma and pleomorphic dermal sarcoma harbor frequent NOTCH1/2 and FAT1 mutations and similar DNA copy number alteration profiles.
Mod Pathol. 2018; 31(3): 418-428. [OPEN ACCESS]
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International Consortium on Lithium Genetics (ConLi+Gen); Amare, AT; Schubert, KO; Hou, L; Clark, SR; Papiol, S; Heilbronner, U; Degenhardt, F; Tekola-Ayele, F; Hsu, YH; Shekhtman, T; Adli, M; Akula, N; Akiyama, K; Ardau, R; Arias, B; Aubry, JM; Backlund, L; Bhattacharjee, AK; Bellivier, F; Benabarre, A; Bengesser, S; Biernacka, JM; Birner, A; Brichant-Petitjean, C; Cervantes, P; Chen, HC; Chillotti, C; Cichon, S; Cruceanu, C; Czerski, PM; Dalkner, N; Dayer, A; Del Zompo, M; DePaulo, JR; Étain, B; Falkai, P; Forstner, AJ; Frisen, L; Frye, MA; Fullerton, JM; Gard, S; Garnham, JS; Goes, FS; Grigoroiu-Serbanescu, M; Grof, P; Hashimoto, R; Hauser, J; Herms, S; Hoffmann, P; Hofmann, A; Jamain, S; Jiménez, E; Kahn, JP; Kassem, L; Kuo, PH; Kato, T; Kelsoe, J; Kittel-Schneider, S; Kliwicki, S; König, B; Kusumi, I; Laje, G; Landén, M; Lavebratt, C; Leboyer, M; Leckband, SG; Tortorella, A; Manchia, M; Martinsson, L; McCarthy, MJ; McElroy, S; Colom, F; Mitjans, M; Mondimore, FM; Monteleone, P; Nievergelt, CM; Nöthen, MM; Novák, T; O'Donovan, C; Ozaki, N; Ösby, U; Pfennig, A; Potash, JB; Reif, A; Reininghaus, E; Rouleau, GA; Rybakowski, JK; Schalling, M; Schofield, PR; Schweizer, BW; Severino, G; Shilling, PD; Shimoda, K; Simhandl, C; Slaney, CM; Squassina, A; Stamm, T; Stopkova, P; Maj, M; Turecki, G; Vieta, E; Volkert, J; Witt, S; Wright, A; Zandi, PP; Mitchell, PB; Bauer, M; Alda, M; Rietschel, M; McMahon, FJ; Schulze, TG; Baune, BT Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study.
JAMA Psychiatry. 2018; 75(1):65-74 [OPEN ACCESS]
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Kriegshäuser, G; Enko, D; Hayrapetyan, H; Atoyan, S; Oberkanins, C; Sarkisian, T Clinical and genetic heterogeneity in a large cohort of Armenian patients with late-onset familial Mediterranean fever.
Genet Med. 2018; [OPEN ACCESS]
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Lahousen, T; Kapfhammer, HP [Anxiety disorders - clinical and neurobiological aspects].
Psychiatr Danub. 2018; 30(4):479-490 [OPEN ACCESS]
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Ligthart, S; Vaez, A; Võsa, U; Stathopoulou, MG; de Vries, PS; Prins, BP; Van der Most, PJ; Tanaka, T; Naderi, E; Rose, LM; Wu, Y; Karlsson, R; Barbalic, M; Lin, H; Pool, R; Zhu, G; Macé, A; Sidore, C; Trompet, S; Mangino, M; Sabater-Lleal, M; Kemp, JP; Abbasi, A; Kacprowski, T; Verweij, N; Smith, AV; Huang, T; Marzi, C; Feitosa, MF; Lohman, KK; Kleber, ME; Milaneschi, Y; Mueller, C; Huq, M; Vlachopoulou, E; Lyytikäinen, LP; Oldmeadow, C; Deelen, J; Perola, M; Zhao, JH; Feenstra, B; LifeLines Cohort Study; Amini, M; CHARGE Inflammation Working Group; Lahti, J; Schraut, KE; Fornage, M; Suktitipat, B; Chen, WM; Li, X; Nutile, T; Malerba, G; Luan, J; Bak, T; Schork, N; Del Greco M, F; Thiering, E; Mahajan, A; Marioni, RE; Mihailov, E; Eriksson, J; Ozel, AB; Zhang, W; Nethander, M; Cheng, YC; Aslibekyan, S; Ang, W; Gandin, I; Yengo, L; Portas, L; Kooperberg, C; Hofer, E; Rajan, KB; Schurmann, C; den Hollander, W; Ahluwalia, TS; Zhao, J; Draisma, HHM; Ford, I; Timpson, N; Teumer, A; Huang, H; Wahl, S; Liu, Y; Huang, J; Uh, HW; Geller, F; Joshi, PK; Yanek, LR; Trabetti, E; Lehne, B; Vozzi, D; Verbanck, M; Biino, G; Saba, Y; Meulenbelt, I; O'Connell, JR; Laakso, M; Giulianini, F; Magnusson, PKE; Ballantyne, CM; Hottenga, JJ; Montgomery, GW; Rivadineira, F; Rueedi, R; Steri, M; Herzig, KH; Stott, DJ; Menni, C; Frånberg, M; St Pourcain, B; Felix, SB; Pers, TH; Bakker, SJL; Kraft, P; Peters, A; Vaidya, D; Delgado, G; Smit, JH; Großmann, V; Sinisalo, J; Seppälä, I; Williams, SR; Holliday, EG; Moed, M; Langenberg, C; Räikkönen, K; Ding, J; Campbell, H; Sale, MM; Chen, YI; James, AL; Ruggiero, D; Soranzo, N; Hartman, CA; Smith, EN; Berenson, GS; Fuchsberger, C; Hernandez, D; Tiesler, CMT; Giedraitis, V; Liewald, D; Fischer, K; Mellström, D; Larsson, A; Wang, Y; Scott, WR; Lorentzon, M; Beilby, J; Ryan, KA; Pennell, CE; Vuckovic, D; Balkau, B; Concas, MP; Schmidt, R; Mendes de Leon, CF; Bottinger, EP; Kloppenburg, M; Paternoster, L; Boehnke, M; Musk, AW; Willemsen, G; Evans, DM; Madden, PAF; Kähönen, M; Kutalik, Z; Zoledziewska, M; Karhunen, V; Kritchevsky, SB; Sattar, N; Lachance, G; Clarke, R; Harris, TB; Raitakari, OT; Attia, JR; van Heemst, D; Kajantie, E; Sorice, R; Gambaro, G; Scott, RA; Hicks, AA; Ferrucci, L; Standl, M; Lindgren, CM; Starr, JM; Karlsson, M; Lind, L; Li, JZ; Chambers, JC; Mori, TA; de Geus, EJCN; Heath, AC; Martin, NG; Auvinen, J; Buckley, BM; de Craen, AJM; Waldenberger, M; Strauch, K; Meitinger, T; Scott, RJ; McEvoy, M; Beekman, M; Bombieri, C; Ridker, PM; Mohlke, KL; Pedersen, NL; Morrison, AC; Boomsma, DI; Whitfield, JB; Strachan, DP; Hofman, A; Vollenweider, P; Cucca, F; Jarvelin, MR; Jukema, JW; Spector, TD; Hamsten, A; Zeller, T; Uitterlinden, AG; Nauck, M; Gudnason, V; Qi, L; Grallert, H; Borecki, IB; Rotter, JI; März, W; Wild, PS; Lokki, ML; Boyle, M; Salomaa, V; Melbye, M; Eriksson, JG; Wilson, JF; Penninx, BWJH; Becker, DM; Worrall, BB; Gibson, G; Krauss, RM; Ciullo, M; Zaza, G; Wareham, NJ; Oldehinkel, AJ; Palmer, LJ; Murray, SS; Pramstaller, PP; Bandinelli, S; Heinrich, J; Ingelsson, E; Deary, IJ; Mägi, R; Vandenput, L; van der Harst, P; Desch, KC; Kooner, JS; Ohlsson, C; Hayward, C; Lehtimäki, T; Shuldiner, AR; Arnett, DK; Beilin, LJ; Robino, A; Froguel, P; Pirastu, M; Jess, T; Koenig, W; Loos, RJF; Evans, DA; Schmidt, H; Smith, GD; Slagboom, PE; Eiriksdottir, G; Morris, AP; Psaty, BM; Tracy, RP; Nolte, IM; Boerwinkle, E; Visvikis-Siest, S; Reiner, AP; Gross, M; Bis, JC; Franke, L; Franco, OH; Benjamin, EJ; Chasm Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
Am J Hum Genet. 2018; 103(5): 691-706. [OPEN ACCESS]
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Löscher, WN; Huemer, M; Stulnig, TM; Simschitz, P; Iglseder, S; Eggers, C; Moser, H; Möslinger, D; Freilinger, M; Lagler, F; Grinzinger, S; Reichhardt, M; Bittner, RE; Schmidt, WM; Lex, U; Brunner-Krainz, M; Quasthoff, S; Wanschitz, JV Pompe disease in Austria: clinical, genetic and epidemiological aspects.
J Neurol. 2018; 265(1):159-164 [OPEN ACCESS]
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Mayr, C; Helm, K; Jakab, M; Ritter, M; Shrestha, R; Makaju, R; Wagner, A; Pichler, M; Beyreis, M; Staettner, S; Jaeger, T; Klieser, E; Kiesslich, T; Neureiter, D The histone methyltransferase G9a: a new therapeutic target in biliary tract cancer.
Hum Pathol. 2018; 72:117-126
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Mörkl, S; Wagner-Skacel, J; Lahousen, T; Lackner, S; Holasek, SJ; Bengesser, SA; Painold, A; Holl, AK; Reininghaus, E The Role of Nutrition and the Gut-Brain Axis in Psychiatry: A Review of the Literature.
Neuropsychobiology. 2018; 1-9 [OPEN ACCESS]
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Olschewski, A; Berghausen, EM; Eichstaedt, CA; Fleischmann, BK; Grünig, E; Grünig, G; Hansmann, G; Harbaum, L; Hennigs, JK; Jonigk, D; Kuebler, WM; Kwapiszewska, G; Pullamsetti, SS; Stacher, E; Weissmann, N; Wenzel, D; Schermuly, RT Pathobiology, pathology and genetics of pulmonary hypertension: Update from the Cologne Consensus Conference 2018.
Int J Cardiol. 2018; 272S(10): 4-10.
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Pfeifer, B; Lercher, MJ BlockFeST: Bayesian calculation of region-specific FST to detect local adaptation.
Bioinformatics. 2018; 34(18): 3205-3207.
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Reinbold, CS; Forstner, AJ; Hecker, J; Fullerton, JM; Hoffmann, P; Hou, L; Heilbronner, U; Degenhardt, F; Adli, M; Akiyama, K; Akula, N; Ardau, R; Arias, B; Backlund, L; Benabarre, A; Bengesser, S; Bhattacharjee, AK; Biernacka, JM; Birner, A; Marie-Claire, C; Cervantes, P; Chen, GB; Chen, HC; Chillotti, C; Clark, SR; Colom, F; Cousins, DA; Cruceanu, C; Czerski, PM; Dayer, A; Étain, B; Falkai, P; Frisén, L; Gard, S; Garnham, JS; Goes, FS; Grof, P; Gruber, O; Hashimoto, R; Hauser, J; Herms, S; Jamain, S; Jiménez, E; Kahn, JP; Kassem, L; Kittel-Schneider, S; Kliwicki, S; König, B; Kusumi, I; Lackner, N; Laje, G; Landén, M; Lavebratt, C; Leboyer, M; Leckband, SG; López Jaramillo, CA; MacQueen, G; Manchia, M; Martinsson, L; Mattheisen, M; McCarthy, MJ; McElroy, SL; Mitjans, M; Mondimore, FM; Monteleone, P; Nievergelt, CM; Ösby, U; Ozaki, N; Perlis, RH; Pfennig, A; Reich-Erkelenz, D; Rouleau, GA; Schofield, PR; Schubert, KO; Schweizer, BW; Seemüller, F; Severino, G; Shekhtman, T; Shilling, PD; Shimoda, K; Simhandl, C; Slaney, CM; Smoller, JW; Squassina, A; Stamm, TJ; Stopkova, P; Tighe, SK; Tortorella, A; Turecki, G; Volkert, J; Witt, SH; Wright, AJ; Young, LT; Zandi, PP; Potash, JB; DePaulo, JR; Bauer, M; Reininghaus, E; Novák, T; Aubry, JM; Maj, M; Baune, BT; Mitchell, PB; Vieta, E; Frye, MA; Rybakowski, JK; Kuo, PH; Kato, T; Grigoroiu-Serbanescu, M; Reif, A; Del Zompo, M; Bellivier, F; Schalling, M; Wray, NR; Kelsoe, JR; Alda, M; McMahon, FJ; Schulze, TG; Rietschel, M; Nöthen, MM; Cichon, S Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder.
Front Psychiatry. 2018; 9: 207-207. [OPEN ACCESS]
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Weerakkody, R; Ross, D; Parry, DA; Ziganshin, B; Vandrovcova, J; Gampawar, P; Abdullah, A; Biggs, J; Dumfarth, J; Ibrahim, Y; Yale Aortic Institute Data and Repository Team; Bicknell, C; Field, M; Elefteriades, J; Cheshire, N; Aitman, TJ Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta.
Genet Med. 2018; 20(11): 1414-1422. [OPEN ACCESS]
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2017

Diomede, F; Thangavelu, SR; Merciaro, I; D'Orazio, M; Bramanti, P; Mazzon, E; Trubiani, O Porphyromonas gingivalis lipopolysaccharide stimulation in human periodontal ligament stem cells: role of epigenetic modifications to the inflammation.
Eur J Histochem. 2017; 61(3):2826-2826 [OPEN ACCESS]
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Giese, AK; Schirmer, MD; Donahue, KL; Cloonan, L; Irie, R; Winzeck, S; Bouts, MJRJ; McIntosh, EC; Mocking, SJ; Dalca, AV; Sridharan, R; Xu, H; Frid, P; Giralt-Steinhauer, E; Holmegaard, L; Roquer, J; Wasselius, J; Cole, JW; McArdle, PF; Broderick, JP; Jimenez-Conde, J; Jern, C; Kissela, BM; Kleindorfer, DO; Lemmens, R; Lindgren, A; Meschia, JF; Rundek, T; Sacco, RL; Schmidt, R; Sharma, P; Slowik, A; Thijs, V; Woo, D; Worrall, BB; Kittner, SJ; Mitchell, BD; Rosand, J; Golland, P; Wu, O; Rost, NS Design and rationale for examining neuroimaging genetics in ischemic stroke: The MRI-GENIE study.
Neurol Genet. 2017; 3(5):e180-e180 [OPEN ACCESS]
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Ikram, MA; Bersano, A; Manso-Calderón, R; Jia, JP; Schmidt, H; Middleton, L; Nacmias, B; Siddiqi, S; Adams, HH Genetics of vascular dementia - review from the ICVD working group.
BMC Med. 2017; 15(1):48-48 [OPEN ACCESS]
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Kostner, KM; Kostner, GM Lipoprotein (a): a historical appraisal.
J Lipid Res. 2017; 58(1):1-14 [OPEN ACCESS]
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Phuah, CL; Dave, T; Malik, R; Raffeld, MR; Ayres, AM; Goldstein, JN; Viswanathan, A; Greenberg, SM; Jagiella, JM; Hansen, BM; Norrving, B; Jimenez-Conde, J; Roquer, J; Pichler, A; Enzinger, C; Montaner, J; Fernandez-Cadenas, I; Lindgren, A; Slowik, A; Schmidt, R; Biffi, A; Rost, N; Langefeld, CD; Markus, HS; Mitchell, BD; Worrall, BB; Kittner, SJ; Woo, D; Dichgans, M; Rosand, J; Anderson, CD; METASTROKE; NINDS-SiGN Consortium; International Stroke Genetics Consortium Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke.
Brain. 2017; 140(10):2663-2672 [OPEN ACCESS]
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Rainer, BM; Kang, S; Chien, AL Rosacea: Epidemiology, pathogenesis, and treatment.
Dermatoendocrinol. 2017; 9(1):e1361574-e1361574 [OPEN ACCESS]
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Reismüller, B; Steiner, M; Pichler, H; Dworzak, M; Urban, C; Meister, B; Schmitt, K; Pötschger, U; König, M; Mann, G; Haas, OA; Attarbaschi, A; Austrian ALL-BFM (Berlin-Frankfurt-Münster) Study Group High hyperdiploid acute lymphoblastic leukemia (ALL)-A 25-year population-based survey of the Austrian ALL-BFM (Berlin-Frankfurt-Münster) Study Group.
Pediatr Blood Cancer. 2017; 64(6):
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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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van der Lee, SJ; Roshchupkin, GV; Adams, HH; Schmidt, H; Hofer, E; Saba, Y; Schmidt, R; Hofman, A; Amin, N; van Duijn, CM; Vernooij, MW; Ikram, MA; Niessen, WJ Gray matter heritability in family-based and population-based studies using voxel-based morphometry.
Hum Brain Mapp. 2017; 38(5):2408-2423
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van Rooij, FJ; Qayyum, R; Smith, AV; Zhou, Y; Trompet, S; Tanaka, T; Keller, MF; Chang, LC; Schmidt, H; Yang, ML; Chen, MH; Hayes, J; Johnson, AD; Yanek, LR; Mueller, C; Lange, L; Floyd, JS; Ghanbari, M; Zonderman, AB; Jukema, JW; Hofman, A; van Duijn, CM; Desch, KC; Saba, Y; Ozel, AB; Snively, BM; Wu, JY; Schmidt, R; Fornage, M; Klein, RJ; Fox, CS; Matsuda, K; Kamatani, N; Wild, PS; Stott, DJ; Ford, I; Slagboom, PE; Yang, J; Chu, AY; Lambert, AJ; Uitterlinden, AG; Franco, OH; Hofer, E; Ginsburg, D; Hu, B; Keating, B; Schick, UM; Brody, JA; Li, JZ; Chen, Z; Zeller, T; Guralnik, JM; Chasman, DI; Peters, LL; Kubo, M; Becker, DM; Li, J; Eiriksdottir, G; Rotter, JI; Levy, D; Grossmann, V; Patel, KV; Chen, CH; BioBank Japan Project; Ridker, PM; Tang, H; Launer, LJ; Rice, KM; Li-Gao, R; Ferrucci, L; Evans, MK; Choudhuri, A; Trompouki, E; Abraham, BJ; Yang, S; Takahashi, A; Kamatani, Y; Kooperberg, C; Harris, TB; Jee, SH; Coresh, J; Tsai, FJ; Longo, DL; Chen, YT; Felix, JF; Yang, Q; Psaty, BM; Boerwinkle, E; Becker, LC; Mook-Kanamori, DO; Wilson, JG; Gudnason, V; O'Donnell, CJ; Dehghan, A; Cupples, LA; Nalls, MA; Morris, AP; Okada, Y; Reiner, AP; Zon, LI; Ganesh, SK Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
Am J Hum Genet. 2017; 100(1): 51-63. [OPEN ACCESS]
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Windpassinger, C; Piard, J; Bonnard, C; Alfadhel, M; Lim, S; Bisteau, X; Blouin, S; Ali, NB; Ng, AYJ; Lu, H; Tohari, S; Talib, SZA; van Hul, N; Caldez, MJ; Van Maldergem, L; Yigit, G; Kayserili, H; Youssef, SA; Coppola, V; de Bruin, A; Tessarollo, L; Choi, H; Rupp, V; Roetzer, K; Roschger, P; Klaushofer, K; Altmüller, J; Roy, S; Venkatesh, B; Ganger, R; Grill, F; Ben Chehida, F; Wollnik, B; Altunoglu, U; Al Kaissi, A; Reversade, B; Kaldis, P CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.
Am J Hum Genet. 2017; 101(3):391-403 [OPEN ACCESS]
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Zadora, J; Singh, M; Herse, F; Przybyl, L; Haase, N; Golic, M; Yung, HW; Huppertz, B; Cartwright, JE; Whitley, G; Johnsen, GM; Levi, G; Isbruch, A; Schulz, H; Luft, FC; Müller, DN; Staff, AC; Hurst, LD; Dechend, R; Izsvák, Z Disturbed Placental Imprinting in Preeclampsia Leads to Altered Expression of DLX5, a Human-Specific Early Trophoblast Marker.
CIRCULATION. 2017; 136(19): 1824-1839. [OPEN ACCESS]
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Zeitelhofer, M; Adzemovic, MZ; Gomez-Cabrero, D; Bergman, P; Hochmeister, S; N'diaye, M; Paulson, A; Ruhrmann, S; Almgren, M; Tegnér, JN; Ekström, TJ; Guerreiro-Cacais, AO; Jagodic, M Functional genomics analysis of vitamin D effects on CD4+ T cells in vivo in experimental autoimmune encephalomyelitis ‬.
Proc Natl Acad Sci U S A. 2017; 114(9):E1678-E1687 [OPEN ACCESS]
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Zeller, T; Seiffert, M; Muller, C; Scholz, M; Schaffer, A; Ojeda, F; Drexel, H; Mundlein, A; Kleber, ME; Marz, W; Sinning, C; Brunner, FJ; Waldeyer, C; Keller, T; Saely, CH; Sydow, K; Thiery, J; Teupser, D; Blankenberg, S; Schnabel, R Genome-Wide Association Analysis for Severity of Coronary Artery Disease Using the Gensini Scoring System
FRONT CARDIOVASC MED. 2017; 4: UNSP 57 [OPEN ACCESS]
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2016

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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Auer-Grumbach, M; Toegel, S; Schabhüttl, M; Weinmann, D; Chiari, C; Bennett, DLH; Beetz, C; Klein, D; Andersen, PM; Böhme, I; Fink-Puches, R; Gonzalez, M; Harms, MB; Motley, W; Reilly, MM; Renner, W; Rudnik-Schöneborn, S; Schlotter-Weigel, B; Themistocleous, AC; Weishaupt, JH; Ludolph, AC; Wieland, T; Tao, F; Abreu, L; Windhager, R; Zitzelsberger, M; Strom, TM; Walther, T; Scherer, SS; Züchner, S; Martini, R; Senderek, J Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
Am J Hum Genet. 2016; 99(3):607-623 [OPEN ACCESS]
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Fan, P; Liu, L; Yin, Y; Zhao, Z; Zhang, Y; Amponsah, PS; Xiao, X; Bauer, N; Abukiwan, A; Nwaeburu, CC; Gladkich, J; Gao, C; Schemmer, P; Gross, W; Herr, I MicroRNA-101-3p reverses gemcitabine resistance by inhibition of ribonucleotide reductase M1 in pancreatic cancer.
Cancer Lett. 2016; 373(1):130-137
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Graziadei, I; Zoller, H; Fickert, P; Schneeberger, S; Finkenstedt, A; Peck-Radosavljevic, M; Müller, H; Kohl, C; Sperner-Unterweger, B; Eschertzhuber, S; Hofer, H; Öfner, D; Tilg, H; Vogel, W; Trauner, M; Berlakovich, G Indications for liver transplantation in adults : Recommendations of the Austrian Society for Gastroenterology and Hepatology (ÖGGH) in cooperation with the Austrian Society for Transplantation, Transfusion and Genetics (ATX).
Wien Klin Wochenschr. 2016; 128(19-20):679-690 [OPEN ACCESS]
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Hou, L; Bergen, SE; Akula, N; Song, J; Hultman, CM; Landén, M; Adli, M; Alda, M; Ardau, R; Arias, B; Aubry, JM; Backlund, L; Badner, JA; Barrett, TB; Bauer, M; Baune, BT; Bellivier, F; Benabarre, A; Bengesser, S; Berrettini, WH; Bhattacharjee, AK; Biernacka, JM; Birner, A; Bloss, CS; Brichant-Petitjean, C; Bui, ET; Byerley, W; Cervantes, P; Chillotti, C; Cichon, S; Colom, F; Coryell, W; Craig, DW; Cruceanu, C; Czerski, PM; Davis, T; Dayer, A; Degenhardt, F; Del Zompo, M; DePaulo, JR; Edenberg, HJ; Étain, B; Falkai, P; Foroud, T; Forstner, AJ; Frisén, L; Frye, MA; Fullerton, JM; Gard, S; Garnham, JS; Gershon, ES; Goes, FS; Greenwood, TA; Grigoroiu-Serbanescu, M; Hauser, J; Heilbronner, U; Heilmann-Heimbach, S; Herms, S; Hipolito, M; Hitturlingappa, S; Hoffmann, P; Hofmann, A; Jamain, S; Jiménez, E; Kahn, JP; Kassem, L; Kelsoe, JR; Kittel-Schneider, S; Kliwicki, S; Koller, DL; König, B; Lackner, N; Laje, G; Lang, M; Lavebratt, C; Lawson, WB; Leboyer, M; Leckband, SG; Liu, C; Maaser, A; Mahon, PB; Maier, W; Maj, M; Manchia, M; Martinsson, L; McCarthy, MJ; McElroy, SL; McInnis, MG; McKinney, R; Mitchell, PB; Mitjans, M; Mondimore, FM; Monteleone, P; Mühleisen, TW; Nievergelt, CM; Nöthen, MM; Novák, T; Nurnberger, JI; Nwulia, EA; Ösby, U; Pfennig, A; Potash, JB; Propping, P; Reif, A; Reininghaus, E; Rice, J; Rietschel, M; Rouleau, GA; Rybakowski, JK; Schalling, M; Scheftner, WA; Schofield, PR; Schork, NJ; Schulze, TG; Schumacher, J; Schweizer, BW; Severino, G; Shekhtman, T; Shilling, PD; Simhandl, C; Slaney, CM; Smith, EN; Squassina, A; Stamm, T; Stopkova, P; Streit, F; Strohmaier, J; Szelinger, S; Tighe, SK; Tortorella, A; Turecki, G; Vieta, E; Volkert, J; Witt, SH; Wright, A; Zandi, PP; Zhang, P; Zollner, S; McMahon, FJ Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Hum Mol Genet. 2016; 25(15):3383-3394 [OPEN ACCESS]
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Hrzenjak, A JAZF1/SUZ12 gene fusion in endometrial stromal sarcomas.
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