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

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Publikationen

Suchbegriffe: GENETICS, . Treffer: 364

2023

Alonso, N; Albagha, OME; Azfer, A; Larraz-Prieto, B; Berg, K; Riches, PL; Ostanek, B; Kocjan, T; Marc, J; Langdahl, BL; Ralston, SH Genome-wide association study identifies genetic variants which predict the response of bone mineral density to teriparatide therapy.
Ann Rheum Dis. 2023; Doi: 10.1136/ard-2022-223618
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Amare, A; Thalamuthu, A; Schubert, KO; Fullerton, J; Ahmed, M; Hartmann, S; Papiol, S; Heilbronner, U; Degenhardt, F; Tekola-Ayele, F; Hou, L; 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, J; Birner, A; Marie-Claire, C; Cervantes, P; Chen, HC; Chillotti, C; Cichon, S; Cruceanu, C; Czerski, P; Dalkner, N; Zompo, MD; DePaulo, JR; Etain, B; Jamain, S; Falkai, P; Forstner, AJ; Frisén, L; Frye, M; Gard, S; Garnham, J; Goes, F; Grigoroiu-Serbanescu, M; Fallgatter, A; Stegmaier, S; Ethofer, T; Biere, S; Petrova, K; Schuster, C; Adorjan, K; Budde, M; Heilbronner, M; Kalman, J; Kohshour, MO; Reich-Erkelenz, D; Schaupp, S; Schulte, E; Senner, F; Vogl, T; Anghelescu, IG; Arolt, V; Dannlowski, U; Dietrich, DE; Figge, C; Jäger, M; Lang, F; Juckel, G; Spitzer, C; Reimer, J; Schmauß, M; Schmitt, A; Konrad, C; von, Hagen, M; Wiltfang, J; Zimmermann, J; Andlauer, T; Fischer, A; Bermpohl, F; Kraft, V; Matura, S; Gryaznova, A; Falkenberg, I; Yildiz, C; Kircher, T; Schmidt, J; Koch, M; Gade, K; Trost, S; Haußleiter, I; Lambert, M; Rohenkohl, AC; Kraft, V; Grof, P; Hashimoto, R; Hauser, J; Herms, S; Hoffmann, P; Jiménez, E; Kahn, JP; Kassem, L; Kuo, PH; Kato, T; Kelsoe, J; Kittel-Schneider, S; Ferensztajn-Rochowiak, E; König, B; Kusumi, I; Laje, G; Landén, M; Lavebratt, C; Leboyer, M; Leckband, SG; Tortorella, A; Manchia, M; Martinsson, L; McCarthy, M; McElroy, SL; Colom, F; Mitjans, M; Mondimore, F; Monteleone, P; Nievergelt, C; Nöthen, M; Novak, T; O'Donovan, C; Ozaki, N; Pfennig, A; Pisanu, C; Potash, J; Reif, A; Reininghaus, E; Rouleau, G; Rybakowski, JK; Schalling, M; Schofield, P; Schweizer, BW; Severino, G; Shilling, PD; Shimoda, K; Simhandl, C; Slaney, C; Squassina, A; Stamm, T; Stopkova, P; Maj, M; Turecki, G; Vieta, E; Veeh, J; Witt, S; Wright, A; Zandi, P; Mitchell, P; Bauer, M; Alda, M; Rietschel, M; McMahon, F; Schulze, TG; Millischer, V; Clark, S; Baune, B Association of Polygenic Score and the involvement of Cholinergic and Glutamatergic Pathways with Lithium Treatment Response in Patients with Bipolar Disorder.
Res Sq. 2023; Doi: 10.21203/rs.3.rs-2580252/v1 [OPEN ACCESS]
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Andreu-Sánchez, S; Bourgonje, AR; Vogl, T; Kurilshikov, A; Leviatan, S; Ruiz-Moreno, AJ; Hu, S; Sinha, T; Vich, Vila, A; Klompus, S; Kalka, IN; de, Leeuw, K; Arends, S; Jonkers, I; Withoff, S; Brouwer, E; Weinberger, A; Wijmenga, C; Segal, E; Weersma, RK; Fu, J; Zhernakova, A, , Lifelines, Cohort, Study Phage display sequencing reveals that genetic, environmental, and intrinsic factors influence variation of human antibody epitope repertoire.
Immunity. 2023; Doi: 10.1016/j.immuni.2023.04.003
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Bölte, S; Neufeld, J; Marschik, PB; Williams, ZJ; Gallagher, L; Lai, MC Sex and gender in neurodevelopmental conditions.
Nat Rev Neurol. 2023; 19(3):136-159 Doi: 10.1038/s41582-023-00774-6 [OPEN ACCESS]
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Herrera-Rivero, M; Hofer, E; Maceski, A; Leppert, D; Benkert, P; Kuhle, J; Schmidt, R; Khalil, M; Wiendl, H; Stoll, M; Berger, K Evidence of polygenic regulation of the physiological presence of neurofilament light chain in human serum.
Front Neurol. 2023; 14:1145737 Doi: 10.3389/fneur.2023.1145737 [OPEN ACCESS]
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Schließleder, G; Kalitzeos, A; Kasilian, M; Singh, N; Wang, Z; Hu, Z; Großpötzl, M; Sadda, S; Wedrich, A; Michaelides, M; Strauss, RW Deep phenotyping of PROM1-associated retinal degeneration.
Br J Ophthalmol. 2023; Doi: 10.1136/bjo-2022-322036
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2022

Bonkhoff, AK; Hong, S; Bretzner, M; Schirmer, MD; Regenhardt, RW; Arsava, EM; Donahue, K; Nardin, M; Dalca, A; Giese, AK; Etherton, MR; Hancock, BL; Mocking, SJT; McIntosh, E; Attia, J; Benavente, O; Cole, JW; Donatti, A; Griessenauer, C; Heitsch, L; Holmegaard, L; Jood, K; Jimenez-Conde, J; Kittner, S; Lemmens, R; Levi, C; McDonough, CW; Meschia, J; Phuah, CL; Rolfs, A; Ropele, S; Rosand, J; Roquer, J; Rundek, T; Sacco, RL; Schmidt, R; Sharma, P; Slowik, A; Soederholm, M; Sousa, A; Stanne, TM; Strbian, D; Tatlisumak, T; Thijs, V; Vagal, A; Wasselius, J; Woo, D; Zand, R; McArdle, P; Worrall, BB; Jern, C; Lindgren, AG; Maguire, J; Golland, P; Bzdok, D; Wu, O; Rost, NS Association of Stroke Lesion Pattern and White Matter Hyperintensity Burden With Stroke Severity and Outcome.
Neurology. 2022; 99(13): e1364-e1379. Doi: 10.1212/WNL.0000000000200926 [OPEN ACCESS]
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Cearns, M; Amare, AT; Schubert, KO; Thalamuthu, A; Frank, J; Streit, F; 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; Degenhardt, F; Zompo, MD; 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; Heilbronner, U; Herms, S; Hoffmann, P; Hofmann, A; Hou, L; Hsu, YH; 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; Maj, M; 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; Millischer, V; Papiol, S; Pfennig, A; Pisanu, C; Potash, JB; Reif, A; Reininghaus, E; Rouleau, GA; Rybakowski, JK; Schalling, M; Schofield, PR; Schweizer, BW; Severino, G; Shekhtman, T; Shilling, PD; Shimoda, K; Simhandl, C; Slaney, CM; Squassina, A; Stamm, T; Stopkova, P; Tekola-Ayele, F; Tortorella, A; Turecki, G; Veeh, J; Vieta, E; Witt, SH; Roberts, G; Zandi, PP; Alda, M; Bauer, M; McMahon, FJ; Mitchell, PB; Schulze, TG; Rietschel, M; Clark, SR; Baune, BT, , Major, Depressive, Disorder, Working, Group, of, the, Psychiatric, Genomics, Consortium Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach.
Br J Psychiatry. 2022; 1-10 Doi: 10.1192/bjp.2022.28
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Gorski, M; Rasheed, H; Teumer, A; Thomas, LF; Graham, SE; Sveinbjornsson, G; Winkler, TW; Günther, F; Stark, KJ; Chai, JF; Tayo, BO; Wuttke, M; Li, Y; Tin, A; Ahluwalia, TS; Ärnlöv, J; Åsvold, BO; Bakker, SJL; Banas, B; Bansal, N; Biggs, ML; Biino, G; Böhnke, M; Boerwinkle, E; Bottinger, EP; Brenner, H; Brumpton, B; Carroll, RJ; Chaker, L; Chalmers, J; Chee, ML; Chee, ML; Cheng, CY; Chu, AY; Ciullo, M; Cocca, M; Cook, JP; Coresh, J; Cusi, D; de, Borst, MH; Degenhardt, F; Eckardt, KU; Endlich, K; Evans, MK; Feitosa, MF; Franke, A; Freitag-Wolf, S; Fuchsberger, C; Gampawar, P; Gansevoort, RT; Ghanbari, M; Ghasemi, S; Giedraitis, V; Gieger, C; Gudbjartsson, DF; Hallan, S; Hamet, P; Hishida, A; Ho, K; Hofer, E; Holleczek, B; Holm, H; Hoppmann, A; Horn, K; Hutri-Kähönen, N; Hveem, K; Hwang, SJ; Ikram, MA; Josyula, NS; Jung, B; Kähönen, M; Karabegović, I; Khor, CC; Koenig, W; Kramer, H; Krämer, BK; Kühnel, B; Kuusisto, J; Laakso, M; Lange, LA; Lehtimäki, T; Li, M; Lieb, W; Lind, L; Lindgren, CM; Loos, RJF; Lukas, MA; Lyytikäinen, LP; Mahajan, A; Matias-Garcia, PR; Meisinger, C; Meitinger, T; Melander, O; Milaneschi, Y; Mishra, PP; Mononen, N; Morris, AP; Mychaleckyj, JC; Nadkarni, GN; Naito, M; Nakatochi, M; Nalls, MA; Nauck, M; Nikus, K; Ning, B; Nolte, IM; Nutile, T; O'Donoghue, ML; O'Connell, J; Olafsson, I; Orho-Melander, M; Parsa, A; Pendergrass, SA; Penninx, BWJH; Pirastu, M; Preuss, MH; Psaty, BM; Raffield, LM; Raitakari, OT; Rheinberger, M; Rice, KM; Rizzi, F; Rosenkranz, AR; Rossing, P; Rotter, JI; Ruggiero, D; Ryan, KA; Sabanayagam, C; Salvi, E; Schmidt, H; Schmidt, R; Scholz, M; Schöttker, B; Schulz, CA; Sedaghat, S; Shaffer, CM; Sieber, KB; Sim, X; Sims, M; Snieder, H; Stanzick, KJ; Thorsteinsdottir, U; Stocker, H; Strauch, K; Stringham, HM; Sulem, P; Szymczak, S; Taylor, KD; Thio, CHL; Tremblay, J; Vaccargiu, S; van, der, Harst, P; van, der, Most, PJ; Verweij, N; Völker, U; Wakai, K; Waldenberger, M; Wallentin, L; Wallner, S; Wang, J; Waterworth, DM; White, HD; Willer, CJ; Wong, TY; Woodward, M; Yang, Q; Yerges-Armstrong, LM; Zimmermann, M; Zonderman, AB; Bergler, T; Stefansson, K; Böger, CA; Pattaro, C; Köttgen, A; Kronenberg, F; Heid, IM, , Lifelines, Cohort, Study Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.
Kidney Int. 2022; 102(3): 624-639. Doi: 10.1016/j.kint.2022.05.021 [OPEN ACCESS]
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Horvaticek, M; Peric, M; Beceheli, I; Klasic, M; Autic, M; Kesic, M; Desoye, G; Rados, SN; Ivanisevic, M; Hranilovic, D; Stefulj, J Maternal Metabolic State and Fetal Sex and Genotype Modulate Methylation of the Serotonin Receptor Type 2A Gene (HTR2A) in the Human Placenta
BIOMEDICINES. 2022; 10(2): 467 Doi: 10.3390/biomedicines10020467 [OPEN ACCESS]
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Keeling, IM; Aschauer, MA; Yates, AE Cardiogenic shock and tumor resection due to cardiac synovial sarcoma: a case report.
Egypt Heart J. 2022; 74(1): 54 Doi: 10.1186/s43044-022-00293-7 [OPEN ACCESS]
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Kerbs, P; Vosberg, S; Krebs, S; Graf, A; Blum, H; Swoboda, A; Batcha, AMN; Mansmann, U; Metzler, D; Heckman, CA; Herold, T; Greif, PA Fusion gene detection by RNA-sequencing complements diagnostics of acute myeloid leukemia and identifies recurring NRIP1-MIR99AHG rearrangements.
Haematologica. 2022; 107(1): 100-111. Doi: 10.3324/haematol.2021.278436 [OPEN ACCESS]
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Kieninger, S; Xiao, T; Weisschuh, N; Kohl, S; Rüther, K; Kroisel, PM; Brockmann, T; Knappe, S; Kellner, U; Lagrèze, W; Mazzola, P; Haack, TB; Wissinger, B; Tonagel, F DNAJC30 disease-causing gene variants in a large Central European cohort of patients with suspected Leber's hereditary optic neuropathy and optic atrophy.
J Med Genet. 2022; Doi: 10.1136/jmedgenet-2021-108235 [OPEN ACCESS]
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Li, H; Perino, A; Huang, Q; Von, Alvensleben, GVG; Banaei-Esfahani, A; Velazquez-Villegas, LA; Gariani, K; Korbelius, M; Bou, Sleiman, M; Imbach, J; Sun, Y; Li, X; Bachmann, A; Goeminne, LJE; Gallart-Ayala, H; Williams, EG; Ivanisevic, J; Auwerx, J; Schoonjans, K Integrative systems analysis identifies genetic and dietary modulators of bile acid homeostasis.
Cell Metab. 2022; 34(10): 1594-1610.e4. Doi: 10.1016/j.cmet.2022.08.015 [OPEN ACCESS]
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Maruszczak, K; Radzikowski, K; Schütz, S; Mangge, H; Bergsten, P; Forslund, A; Manell, H; Pixner, T; Ahlström, H; Kullberg, J; Mörwald, K; Weghuber, D Determinants of hyperglucagonemia in pediatric non-alcoholic fatty liver disease.
Front Endocrinol (Lausanne). 2022; 13: 1004128 Doi: 10.3389/fendo.2022.1004128 [OPEN ACCESS]
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Mathey, CM; Maj, C; Scheer, AB; Fazaal, J; Wedi, B; Wieczorek, D; Amann, PM; Löffler, H; Koch, L; Schöffl, C; Dickel, H; Ganjuur, N; Hornung, T; Forkel, S; Greve, J; Wurpts, G; Hallberg, P; Bygum, A; Von, Buchwald, C; Karawajczyk, M; Steffens, M; Stingl, J; Hoffmann, P; Heilmann-Heimbach, S; Mangold, E; Ludwig, KU; Rasmussen, ER; Wadelius, M; Sachs, B; Nöthen, MM; Forstner, AJ Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes.
Front Genet. 2022; 13: 914376 Doi: 10.3389/fgene.2022.914376 [OPEN ACCESS]
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Palles, C; Martin, L; Domingo, E; Chegwidden, L; McGuire, J; Cuthill, V; Heitzer, E; Kerr, R; Kerr, D; Kearsey, S; Clark, SK; Tomlinson, I; Latchford, A, , CORGI, Consortium The clinical features of polymerase proof-reading associated polyposis (PPAP) and recommendations for patient management.
Fam Cancer. 2022; Doi: 10.1007/s10689-021-00256-y [OPEN ACCESS]
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Reichmann, F; Pilic, J; Trajanoski, S; Norton, WHJ Transcriptomic underpinnings of high and low mirror aggression zebrafish behaviours.
BMC Biol. 2022; 20(1): 97 Doi: 10.1186/s12915-022-01298-z [OPEN ACCESS]
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Schaflinger, E; Enko, D [The Impact of Next-Generation Sequencing on Medical Genetic Diagnostics and Counseling].
Dtsch Med Wochenschr. 2022; 147(20): 1336-1341. Doi: 10.1055/a-1924-6646
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Verheyen, S; Blatterer, J; Speicher, MR; Bhavani, GS; Boons, GJ; Ilse, MB; Andrae, D; Sproß, J; Vaz, FM; Kircher, SG; Posch-Pertl, L; Baumgartner, D; Lübke, T; Shah, H; Al, Kaissi, A; Girisha, KM; Plecko, B Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency.
J Med Genet. 2022; 59(10):957-964 Doi: 10.1136/jmedgenet-2021-108061 [OPEN ACCESS]
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Vogt, G; Verheyen, S; Schwartzmann, S; Ehmke, N; Potratz, C; Schwerin-Nagel, A; Plecko, B; Holtgrewe, M; Seelow, D; Blatterer, J; Speicher, MR; Kornak, U; Horn, D; Mundlos, S; Fischer-Zirnsak, B; Boschann, F Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive.
J Med Genet. 2022; 59(7):662-668 Doi: 10.1136/jmedgenet-2021-107843 [OPEN ACCESS]
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Winkler, TW; Rasheed, H; Teumer, A; Gorski, M; Rowan, BX; Stanzick, KJ; Thomas, LF; Tin, A; Hoppmann, A; Chu, AY; Tayo, B; Thio, CHL; Cusi, D; Chai, JF; Sieber, KB; Horn, K; Li, M; Scholz, M; Cocca, M; Wuttke, M; van, der, Most, PJ; Yang, Q; Ghasemi, S; Nutile, T; Li, Y; Pontali, G; Günther, F; Dehghan, A; Correa, A; Parsa, A; Feresin, A; de, Vries, APJ; Zonderman, AB; Smith, AV; Oldehinkel, AJ; De, Grandi, A; Rosenkranz, AR; Franke, A; Teren, A; Metspalu, A; Hicks, AA; Morris, AP; Tönjes, A; Morgan, A; Podgornaia, AI; Peters, A; Körner, A; Mahajan, A; Campbell, A; Freedman, BI; Spedicati, B; Ponte, B; Schöttker, B; Brumpton, B; Banas, B; Krämer, BK; Jung, B; Åsvold, BO; Smith, BH; Ning, B; Penninx, BWJH; Vanderwerff, BR; Psaty, BM; Kammerer, CM; Langefeld, CD; Hayward, C; Spracklen, CN; Robinson-Cohen, C; Hartman, CA; Lindgren, CM; Wang, C; Sabanayagam, C; Heng, CK; Lanzani, C; Khor, CC; Cheng, CY; Fuchsberger, C; Gieger, C; Shaffer, CM; Schulz, CA; Willer, CJ; Chasman, DI; Gudbjartsson, DF; Ruggiero, D; Toniolo, D; Czamara, D; Porteous, DJ; Waterworth, DM; Mascalzoni, D; Mook-Kanamori, DO; Reilly, DF; Daw, EW; Hofer, E; Boerwinkle, E; Salvi, E; Bottinger, EP; Tai, ES; Catamo, E; Rizzi, F; Guo, F; Rivadeneira, F; Guilianini, F; Sveinbjornsson, G; Ehret, G; Waeber, G; Biino, G; Girotto, G; Pistis, G; Nadkarni, GN; Delgado, GE; Montgomery, GW; Snieder, H; Campbell, H; White, HD; Gao, H; Stringham, HM; Schmidt, H; Li, H; Brenner, H; Holm, H; Kirsten, H; Kramer, H; Rudan, I; Nolte, IM; Tzoulaki, I; Olafsson, I; Martins, J; Cook, JP; Wilson, JF; Halbritter, J; Felix, JF; Divers, J; Kooner, JS; Lee, JJ; O'Connell, J; Rotter, JI; Liu, J; Xu, J; Thiery, J; Ärnlöv, J; Kuusisto, J; Jakobsdottir, J; Tremblay, J; Chambers, JC; Whitfield, JB; Gaziano, JM; Marten, J; Coresh, J; Jonas, JB; Mychaleckyj, JC; Christensen, K; Eckardt, KU; Mohlke, KL; Endlich, K; Dittrich, K; Ryan, KA; Rice, KM; Taylor, KD; Ho, K; Nikus, K; Matsuda, K; Strauch, K; Miliku, K; Hveem, K; Lind, L; Wallentin, L; Yerges-Armstrong, LM; Raffield, LM; Phillips, LS; Launer, LJ; Lyytikäinen, LP; Lange, LA; Citterio, L; Klaric, L; Ikram, MA; Ising, M; Kleber, ME; Francescatto, M; Concas, MP; Ciullo, M; Piratsu, M; Orho-Melander, M; Laakso, M; Loeffler, M; Perola, M; de, Borst, MH; Gögele, M; Bianca, M; Lukas, MA; Feitosa, MF; Biggs, ML; Wojczynski, MK; Kavousi, M; Kanai, M; Akiyama, M; Yasuda, M; Nauck, M; Waldenberger, M; Chee, ML; Chee, ML; Boehnke, M; Preuss, MH; Stumvoll, M; Province, MA; Evans, MK; O'Donoghue, ML; Kubo, M; Kähönen, M; Kastarinen, M; Nalls, MA; Kuokkanen, M; Ghanbari, M; Bochud, M; Josyula, NS; Martin, NG; Tan, NYQ; Palmer, ND; Pirastu, N; Schupf, N; Verweij, N; Hutri-Kähönen, N; Mononen, N; Bansal, N; Devuyst, O; Melander, O; Raitakari, OT; Polasek, O; Manunta, P; Gasparini, P; Mishra, PP; Sulem, P; Magnusson, PKE; Elliott, P; Ridker, PM; Hamet, P; Svensson, PO; Joshi, PK; Kovacs, P; Pramstaller, PP; Rossing, P; Vollenweider, P; van, der, Harst, P; Dorajoo, R; Sim, RZH; Burkhardt, R; Tao, R; Noordam, R; Mägi, R; Schmidt, R; de, Mutsert, R; Rueedi, R; van, Dam, RM; Carroll, RJ; Gansevoort, RT; Loos, RJF; Felicita, SC; Sedaghat, S; Padmanabhan, S; Freitag-Wolf, S; Pendergrass, SA; Graham, SE; Gordon, SD; Hwang, SJ; Kerr, SM; Vaccargiu, S; Patil, SB; Hallan, S; Bakker, SJL; Lim, SC; Lucae, S; Vogelezang, S; Bergmann, S; Corre, T; Ahluwalia, TS; Lehtimäki, T; Boutin, TS; Meitinger, T; Wong, TY; Bergler, T; Rabelink, TJ; Esko, T; Haller, T; Thorsteinsdottir, U; Völke ... Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
COMMUN BIOL. 2022; 5(1): 580 Doi: 10.1038/s42003-022-03448-z [OPEN ACCESS]
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Winnicki, W; Fichtenbaum, A; Herkner, H; Regele, F; Baier, M; Zelzer, S; Wagner, L; Sengoelge, G Individualization of Mycophenolic Acid Therapy through Pharmacogenetic, Pharmacokinetic and Pharmacodynamic Testing
BIOMEDICINES. 2022; 10(11): 2882 Doi: 10.3390/biomedicines10112882 [OPEN ACCESS]
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2021

Amare, AT; Schubert, KO; Hou, L; Clark, SR; Papiol, S; Cearns, M; 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; Jamain, S; 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; Jiménez, E; Kahn, JP; Kassem, L; Kuo, PH; Kato, T; Kelsoe, JR; 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, SL; 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; Veeh, J; Witt, SH; Wright, A; Zandi, PP; Mitchell, PB; Bauer, M; Alda, M; Rietschel, M; McMahon, FJ; Schulze, TG; Baune, BT, , Major, Depressive, Disorder, Working, Group, of, the, Psychiatric, Genomics, Consortium Association of polygenic score for major depression with response to lithium in patients with bipolar disorder.
Mol Psychiatry. 2021; 26(6):2457-2470 Doi: 10.1038/s41380-020-0689-5 [OPEN ACCESS]
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Bousman, CA; Bengesser, SA; Aitchison, KJ; Amare, AT; Aschauer, H; Baune, BT; Asl, BB; Bishop, JR; Burmeister, M; Chaumette, B; Chen, LS; Cordner, ZA; Deckert, J; Degenhardt, F; DeLisi, LE; Folkersen, L; Kennedy, JL; Klein, TE; McClay, JL; McMahon, FJ; Musil, R; Saccone, NL; Sangkuhl, K; Stowe, RM; Tan, EC; Tiwari, AK; Zai, CC; Zai, G; Zhang, J; Gaedigk, A; Müller, DJ Review and Consensus on Pharmacogenomic Testing in Psychiatry.
Pharmacopsychiatry. 2021; 54(1):5-17 Doi: 10.1055/a-1288-1061
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Coombes, BJ; Millischer, V; Batzler, A; Larrabee, B; Hou, L; Papiol, S; Heilbronner, U; Adli, M; Akiyama, K; Akula, N; Amare, AT; Ardau, R; Arias, B; Aubry, JM; Backlund, L; Bauer, M; Baune, BT; Bellivier, F; Benabarre, A; Bengesser, S; Bhattacharjee, AK; Cervantes, P; Chen, HC; Chillotti, C; Cichon, S; Clark, SR; Colom, F; Cruceanu, C; Czerski, PM; Dalkner, N; Degenhardt, F; Del, Zompo, M; DePaulo, JR; Étain, B; Falkai, P; Ferensztajn-Rochowiak, E; Forstner, AJ; Frisen, L; Gard, S; Garnham, JS; Goes, FS; Grigoroiu-Serbanescu, M; Grof, P; Hashimoto, R; Hauser, J; Herms, S; Hoffmann, P; Jamain, S; Jiménez, E; Kahn, JP; Kassem, L; Kato, T; Kelsoe, JR; Kittel-Schneider, S; König, B; Kuo, PH; Kusumi, I; Laje, G; Landén, M; Lavebratt, C; Leboyer, M; Leckband, SG; Maj, M; Manchia, M; Martinsson, L; McCarthy, MJ; McElroy, SL; Mitchell, PB; Mitjans, M; Mondimore, FM; Monteleone, P; Nievergelt, CM; Nöthen, MM; Novák, T; O'Donovan, C; Osby, U; Ozaki, N; Pfennig, A; Pisanu, C; Potash, JB; Reif, A; Reininghaus, E; Rietschel, M; Rouleau, GA; Rybakowski, JK; Schalling, M; Schofield, PR; Schubert, KO; Schweizer, BW; Severino, G; Shekhtman, T; Shilling, PD; Shimoda, K; Simhandl, C; Slaney, CM; Squassina, A; Stamm, T; Stopkova, P; Tortorella, A; Turecki, G; Vieta, E; Witt, SH; Zandi, PP; Fullerton, JM; Alda, M; Frye, MA; Schulze, TG; McMahon, FJ; Biernacka, JM Association of Attention-Deficit/Hyperactivity Disorder and Depression Polygenic Scores with Lithium Response: A Consortium for Lithium Genetics Study.
Complex Psychiatry. 2021; 7(3-4):80-89 Doi: 10.1159/000519707 [OPEN ACCESS]
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Geier, A; Tiniakos, D; Denk, H; Trauner, M From the origin of NASH to the future of metabolic fatty liver disease
GUT. 2021; 70(8): 1570-1579. Doi: 10.1136/gutjnl-2020-323202 [OPEN ACCESS]
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Gorski, M; Jung, B; Li, Y; Matias-Garcia, PR; Wuttke, M; Coassin, S; Thio, CHL; Kleber, ME; Winkler, TW; Wanner, V; Chai, JF; Chu, AY; Cocca, M; Feitosa, MF; Ghasemi, S; Hoppmann, A; Horn, K; Li, M; Nutile, T; Scholz, M; Sieber, KB; Teumer, A; Tin, A; Wang, J; Tayo, BO; Ahluwalia, TS; Almgren, P; Bakker, SJL; Banas, B; Bansal, N; Biggs, ML; Boerwinkle, E; Bottinger, EP; Brenner, H; Carroll, RJ; Chalmers, J; Chee, ML; Chee, ML; Cheng, CY; Coresh, J; de Borst, MH; Degenhardt, F; Eckardt, KU; Endlich, K; Franke, A; Freitag-Wolf, S; Gampawar, P; Gansevoort, RT; Ghanbari, M; Gieger, C; Hamet, P; Ho, K; Hofer, E; Holleczek, B; Xian Foo, VH; Hutri-Kähönen, N; Hwang, SJ; Ikram, MA; Josyula, NS; Kähönen, M; Khor, CC; Koenig, W; Kramer, H; Krämer, BK; Kühnel, B; Lange, LA; Lehtimäki, T; Lieb, W; Lifelines Cohort Study; Regeneron Genetics Center; Loos, RJF; Lukas, MA; Lyytikäinen, LP; Meisinger, C; Meitinger, T; Melander, O; Milaneschi, Y; Mishra, PP; Mononen, N; Mychaleckyj, JC; Nadkarni, GN; Nauck, M; Nikus, K; Ning, B; Nolte, IM; O'Donoghue, ML; Orho-Melander, M; Pendergrass, SA; Penninx, BWJH; Preuss, MH; Psaty, BM; Raffield, LM; Raitakari, OT; Rettig, R; Rheinberger, M; Rice, KM; Rosenkranz, AR; Rossing, P; Rotter, JI; Sabanayagam, C; Schmidt, H; Schmidt, R; Schöttker, B; Schulz, CA; Sedaghat, S; Shaffer, CM; Strauch, K; Szymczak, S; Taylor, KD; Tremblay, J; Chaker, L; van der Harst, P; van der Most, PJ; Verweij, N; Völker, U; Waldenberger, M; Wallentin, L; Waterworth, DM; White, HD; Wilson, JG; Wong, TY; Woodward, M; Yang, Q; Yasuda, M; Yerges-Armstrong, LM; Zhang, Y; Snieder, H; Wanner, C; Böger, CA; Köttgen, A; Kronenberg, F; Pattaro, C; Heid, IM Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney Int. 2021; 99(4):926-939 Doi: 10.1016/j.kint.2020.09.030 [OPEN ACCESS]
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Guelly, C; Abilova, Z; Nuralinov, O; Panzitt, K; Akhmetova, A; Rakhimova, S; Kozhamkulov, U; Kairov, U; Molkenov, A; Seisenova, A; Trajanoski, S; Abildinova Rashbayeva, G; Kaussova, G; Windpassinger, C; Lee, JH; Zhumadilov, Z; Bekbossynova, M; Akilzhanova, A Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes.
PeerJ. 2021; 9: e10711-e10711. Doi: 10.7717/peerj.10711 [OPEN ACCESS]
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Hall, IF; Climent, M; Anselmi, CV; Papa, L; Tragante, V; Lambroia, L; Farina, FM; Kleber, ME; Marz, W; Biguori, C; Condorelli, G; Elia, L rs41291957 controls miR-143 and miR-145 expression and impacts coronary artery disease risk
EMBO MOL MED. 2021; e14060 Doi: 10.15252/emmm.202114060 [OPEN ACCESS]
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Heilbronner, U; Streit, F; Vogl, T; Senner, F; Schaupp, SK; Reich-Erkelenz, D; Papiol, S; Oraki, Kohshour, M; Klöhn-Saghatolislam, F; Kalman, JL; Heilbronner, M; Gade, K; Comes, AL; Budde, M; Andlauer, TFM; Anderson-Schmidt, H; Adorjan, K; Stürmer, T; Loerbroks, A; Amelang, M; Poisel, E; Foo, J; Heilmann-Heimbach, S; Forstner, AJ; Degenhardt, F; Zimmermann, J; Wiltfang, J; von, Hagen, M; Spitzer, C; Schmauss, M; Reininghaus, E; Reimer, J; Konrad, C; Juckel, G; Lang, FU; Jäger, M; Figge, C; Fallgatter, AJ; Dietrich, DE; Dannlowski, U; Baune, BT; Arolt, V; Anghelescu, IG; Nöthen, MM; Witt, SH; Andreassen, OA; Chen, CH; Falkai, P; Rietschel, M; Schulze, TG; Schulte, EC Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection.
BJPSYCH OPEN. 2021; 7(6): e188 Doi: 10.1192/bjo.2021.1030 [OPEN ACCESS]
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Hong, S; Giese, AK; Schirmer, MD; Bonkhoff, AK; Bretzner, M; Rist, P; Dalca, AV; Regenhardt, RW; Etherton, MR; Donahue, KL; Nardin, M; Mocking, SJT; McIntosh, EC; Attia, J; Benavente, OR; Cole, JW; Donatti, A; Griessenauer, CJ; Heitsch, L; Holmegaard, L; Jood, K; Jimenez-Conde, J; Roquer, J; Kittner, SJ; Lemmens, R; Levi, CR; McDonough, CW; Meschia, JF; Phuah, CL; Rolfs, A; Ropele, S; Rosand, J; Rundek, T; Sacco, RL; Schmidt, R; Enzinger, C; Sharma, P; Slowik, A; Sousa, A; Stanne, TM; Strbian, D; Tatlisumak, T; Thijs, V; Vagal, A; Wasselius, J; Woo, D; Zand, R; McArdle, PF; Worrall, BB; Wu, O; Jern, C; Lindgren, AG; Maguire, J; Tomppo, L; Golland, P; Rost, NS, , MRI-GENIE, and, GISCOME, Investigators, and, the, International, Stroke, Genetics, Consortium Excessive White Matter Hyperintensity Increases Susceptibility to Poor Functional Outcomes After Acute Ischemic Stroke.
Front Neurol. 2021; 12: 700616 Doi: 10.3389/fneur.2021.700616 [OPEN ACCESS]
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Kapfhammer, HP [Comorbidity of posttraumatic stress disorder and addiction from a biopsychosocial perspective].
Neuropsychiatr. 2021; 18(1): Doi: 10.1007/s40211-020-00384-4 [OPEN ACCESS]
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Kessing, LV; González-Pinto, A; Fagiolini, A; Bechdolf, A; Reif, A; Yildiz, A; Etain, B; Henry, C; Severus, E; Reininghaus, EZ; Morken, G; Goodwin, GM; Scott, J; Geddes, JR; Rietschel, M; Landén, M; Manchia, M; Bauer, M; Martinez-Cengotitabengoa, M; Andreassen, OA; Ritter, P; Kupka, R; Licht, RW; Nielsen, RE; Schulze, TG; Hajek, T; Lagerberg, TV; Bergink, V; Vieta, E DSM-5 and ICD-11 criteria for bipolar disorder: Implications for the prevalence of bipolar disorder and validity of the diagnosis - A narrative review from the ECNP bipolar disorders network.
Eur Neuropsychopharmacol. 2021; 47:54-61 Doi: 10.1016/j.euroneuro.2021.01.097
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Kluin-Nelemans, HC; Jawhar, M; Reiter, A; van Anrooij, B; Gotlib, J; Hartmann, K; Illerhaus, A; Elberink, HNGO; Gorska, A; Niedoszytko, M; Lange, M; Scaffidi, L; Zanotti, R; Bonadonna, P; Perkins, C; Elena, C; Malcovati, L; Shoumariyeh, K; von Bubnoff, N; Muller, S; Triggiani, M; Parente, R; Schwaab, J; Kundi, M; Fortina, AB; Caroppo, F; Brockow, K; Zink, A; Fuchs, D; Angelova-Fischer, I; Yavuz, AS; Doubek, M; Mattsson, M; Hagglund, H; Panse, J; Simonowski, A; Sabato, V; Schug, T; Jentzsch, M; Breynaert, C; Varkonyi, J; Kennedy, V; Hermine, O; Rossignol, J; Arock, M; Valent, P; Sperr, WR Cytogenetic and molecular aberrations and worse outcome for male patients in systemic mastocytosis
THERANOSTICS. 2021; 11(1): 292-303. Doi: 10.7150/thno.51872 [OPEN ACCESS]
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Kumpitsch, C; Fischmeister, FPS; Mahnert, A; Lackner, S; Wilding, M; Sturm, C; Springer, A; Madl, T; Holasek, S; Högenauer, C; Berg, IA; Schoepf, V; Moissl-Eichinger, C Reduced B12 uptake and increased gastrointestinal formate are associated with archaeome-mediated breath methane emission in humans.
Microbiome. 2021; 9(1):193 Doi: 10.1186/s40168-021-01130-w [OPEN ACCESS]
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Le, Clerc, S; Lombardi, L; Baune, BT; Amare, AT; Schubert, KO; Hou, L; Clark, SR; Papiol, S; Cearns, M; 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; Jamain, S; 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; Jiménez, E; Kahn, JP; Kassem, L; Kuo, PH; Kato, T; Kelsoe, JR; Kittel-Schneider, S; Ferensztajn-Rochowiak, E; König, B; Kusumi, I; Laje, G; Landén, M; Lavebratt, C; Leckband, SG; Tortorella, A; Manchia, M; Martinsson, L; McCarthy, MJ; McElroy, SL; Colom, F; Millischer, V; 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; Pisanu, C; Squassina, A; Stamm, T; Stopkova, P; Maj, M; Turecki, G; Vieta, E; Veeh, J; Witt, SH; Wright, A; Zandi, PP; Mitchell, PB; Bauer, M; Alda, M; Rietschel, M; McMahon, FJ; Schulze, TG; Spadoni, JL; Boukouaci, W; Richard, JR; Le, Corvoisier, P; Barrau, C; Zagury, JF; Leboyer, M; Tamouza, R HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders.
Sci Rep. 2021; 11(1): 17823 Doi: 10.1038/s41598-021-97140-7 [OPEN ACCESS]
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Luan, W; Hao, CZ; Li, JQ; Wei, Q; Gong, JY; Qiu, YL; Lu, Y; Shen, CH; Xia, Q; Xie, XB; Zhang, MH; Abuduxikuer, K; Li, ZD; Wang, L; Xing, QH; Knisely, AS; Wang, JS Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis.
J Med Genet. 2021; 58(8):514-525 Doi: 10.1136/jmedgenet-2019-106706
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Lumbers, RT; Shah, S; Lin, HH; Czuba, T; Henry, A; Swerdlow, DI; Malarstig, A; Andersson, C; Verweij, N; Holmes, MV; Arnlov, J; Svensson, P; Hemingway, H; Sallah, N; Almgren, P; Aragam, KG; Asselin, G; Backman, JD; Biggs, ML; Bloom, HL; Boersma, E; Brandimarto, J; Brown, MR; Brunner-La Rocca, HP; Carey, DJ; Chaffin, MD; Chasman, DI; Chazara, O; Chen, X; Chen, X; Chung, JH; Chutkow, W; Cleland, JGF; Cook, JP; de Denus, S; Dehghan, A; Delgado, GE; Denaxas, S; Doney, AS; Dorr, M; Dudley, SC; Engstrom, G; Esko, T; Fatemifar, G; Felix, SB; Finan, C; Ford, I; Fougerousse, F; Fouodjio, R; Ghanbari, M; Ghasemi, S; Giedraitis, V; Giulianini, F; Gottdiener, JS; Gross, S; Gudbjartsson, DF; Gui, HS; Gutmann, R; Haggerty, CM; van der Harst, P; Helgadottir, A; Hillege, H; Hyde, CL; Jacob, J; Jukema, JW; Kamanu, F; Kardys, I; Kavousi, M; Khaw, KT; Kleber, ME; Kober, L; Koekemoer, A; Kraus, B; Kuchenbaecker, K; Langenberg, C; Lind, L; Lindgren, CM; London, B; Lotta, LA; Lovering, RC; Luan, JA; Magnusson, P; Mahajan, A; Mann, D; Margulies, KB; Marston, NA; Marz, W; McMurray, JJV; Melander, O; Melloni, G; Mordi, IR; Morley, MP; Morris, AD; Morris, AP; Morrison, AC; Nagle, MW; Nelson, CP; Newton-Cheh, C; Niessner, A; Niiranen, T; Nowak, C; O'Donoghue, ML; Owens, AT; Palmer, CNA; Pare, G; Perola, M; Perreault, LPL; Portilla-Fernandez, E; Psaty, BM; Rice, KM; Ridker, PM; Romaine, SPR; Roselli, C; Rotter, JI; Ruff, CT; Sabatine, MS; Salo, P; Salomaa, V; van Setten, J; Shalaby, AA; Smelser, DT; Smith, NL; Stefansson, K; Stender, S; Stott, DJ; Sveinbjornsson, G; Tammesoo, ML; Tardif, JC; Taylor, KD; Teder-Laving, M; Teumer, A; Thorgeirsson, G; Thorsteinsdottir, U; Torp-Pedersen, C; Trompet, S; Tuckwell, D; Tyl, B; Uitterlinden, AG; Vaura, F; Veluchamy, A; Visscher, PM; Volker, U; Voors, AA; Wang, XS; Wareham, NJ; Weeke, PE; Weiss, R; White, HD; Wiggins, KL; Xing, HM; Yang, J; Yang, YF; Yerges-Armstrong, LM; Yu, B; Zannad, F; Zhao, FY; Wilk, JB; Holm, H; Sattar, N; Lubitz, SA; Lanfear, DE; Shah, S; Dunn, ME; Wells, QS; Asselbergs, FW; Hingorani, AD; Dube, MP; Samani, NJ; Lang, CC; Cappola, TP; Ellinor, PT; Vasan, RS; Smith, JG The genomics of heart failure: design and rationale of the HERMES consortium
ESC HEART FAIL. 2021; Doi: 10.1002/ehf2.13517 [OPEN ACCESS]
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Machherndl-Spandl, S; Jäger, E; Barna, A; Gurbisz, M; Marschon, R; Graf, T; Graf, E; Geissler, C; Hoermann, G; Nösslinger, T; Pfeilstöcker, M; Bettelheim, P; Zach, O; Weltermann, A; Heibl, S; Thaler, J; Zebisch, A; Sill, H; Stauder, R; Webersinke, G; Kusec, R; Ulsperger, E; Schneeweiss, B; Öhler, L; Germing, U; Valent, P; Tüchler, H; Geissler, K Impact of age on the cumulative risk of transformation in patients with chronic myelomonocytic leukaemia.
Eur J Haematol. 2021; 107(2):265-274 Doi: 10.1111/ejh.13647 [OPEN ACCESS]
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Merle, DA; Provenzano, F; Jarboui, MA; Kilger, E; Clark, SJ; Deleidi, M; Armento, A; Ueffing, M mTOR Inhibition via Rapamycin Treatment Partially Reverts the Deficit in Energy Metabolism Caused by FH Loss in RPE Cells.
Antioxidants (Basel). 2021; 10(12): Doi: 10.3390/antiox10121944 [OPEN ACCESS]
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Muin, DA; Kollmann, M; Blatterer, J; Hoermann, G; Husslein, PW; Lafer, I; Petek, E; Schwarzbraun, T Cardio-pathogenic variants in unexplained intrauterine fetal death: a retrospective pilot study.
Sci Rep. 2021; 11(1): 6737-6737. Doi: 10.1038/s41598-021-85893-0 [OPEN ACCESS]
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Nemes, K; Bens, S; Kachanov, D; Teleshova, M; Hauser, P; Simon, T; Tippelt, S; Woessmann, W; Beck, O; Flotho, C; Grigull, L; Driever, PH; Schlegel, PG; Khurana, C; Hering, K; Kolb, R; Leipold, A; Abbink, F; Gil-Da-Costa, MJ; Benesch, M; Kerl, K; Lowis, S; Marques, CH; Graf, N; Nysom, K; Vokuhl, C; Melchior, P; Kröncke, T; Schneppenheim, R; Kordes, U; Gerss, J; Siebert, R; Furtwängler, R; Frühwald, MC Clinical and genetic risk factors define two risk groups of extracranial malignant rhabdoid tumours (eMRT/RTK).
Eur J Cancer. 2020; 142: 112-122. Doi: 10.1016/j.ejca.2020.10.004
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Nkeh-Chungag, BN; Engwa, GA; Businge, C; Mdondolo, M; Pajaro, Medina, M; Goswami, N Assessment of the impact of HIV infection and anti-retroviral treatment on the cardiometabolic health of pregnant mothers and their offspring (ARTMOMSBABES).
BMC Cardiovasc Disord. 2021; 21(1): 322 Doi: 10.1186/s12872-021-02130-2 [OPEN ACCESS]
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Sallmon, H; Weber, SC; Berger, F; Will, JC Unexpected ventricular tachycardia following acoustic provocation during electroencephalography.
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Schubert, KO; Thalamuthu, A; Amare, AT; Frank, J; Streit, F; Adl, 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; Marie-Claire, C; Cearns, M; Cervantes, P; Chen, HC; Chillotti, C; Cichon, S; Clark, SR; Cruceanu, C; Czerski, PM; Dalkner, N; Dayer, A; Degenhardt, F; 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; Heilbronner, U; Herms, S; Hoffmann, P; Hou, L; Hsu, YH; Jamain, S; Jiménez, E; Kahn, JP; Kassem, L; Kuo, PH; Kato, T; Kelsoe, J; Kittel-Schneider, S; Ferensztajn-Rochowiak, E; König, B; Kusumi, I; Laje, G; Landén, M; Lavebratt, C; Leboyer, M; Leckband, SG; Maj, M; 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; Papiol, S; Pfennig, A; Pisanu, C; Potash, JB; Reif, A; Reininghaus, E; Rouleau, GA; Rybakowski, JK; Schalling, M; Schofield, PR; Schweizer, BW; Severino, G; Shekhtman, T; Shilling, PD; Shimoda, K; Simhandl, C; Slaney, CM; Squassina, A; Stamm, T; Stopkova, P; Tekola-Ayele, F; Tortorella, A; Turecki, G; Veeh, J; Vieta, E; Witt, SH; Roberts, G; Zandi, PP; Alda, M; Bauer, M; McMahon, FJ; Mitchell, PB; Schulze, TG; Rietschel, M; Baune, BT, , Major, Depressive, Disorder, Working, Group, of, the, Psychiatric, Genomics, Consortium Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients.
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Uhlig, HH; Charbit-Henrion, F; Kotlarz, D; Shouval, DS; Schwerd, T; Strisciuglio, C; de, Ridder, L; van, Limbergen, J; Macchi, M; Snapper, SB; Ruemmele, FM; Wilson, DC; Travis, SPL; Griffiths, AM; Turner, D; Klein, C; Muise, AM; Russell, RK, , Paediatric, IBD, Porto, group, of, ESPGHAN Clinical Genomics for the Diagnosis of Monogenic Forms of Inflammatory Bowel Disease: A Position Paper From the Paediatric IBD Porto Group of European Society of Paediatric Gastroenterology, Hepatology and Nutrition.
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J Allergy Clin Immunol. 2020; 146(5):1045-1055 Doi: 10.1016/j.jaci.2020.05.038
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Armstrong, NJ; Mather, KA; Sargurupremraj, M; Knol, MJ; Malik, R; Satizabal, CL; Yanek, LR; Wen, W; Gudnason, VG; Dueker, ND; Elliott, LT; Hofer, E; Bis, J; Jahanshad, N; Li, S; Logue, MA; Luciano, M; Scholz, M; Smith, AV; Trompet, S; Vojinovic, D; Xia, R; Alfaro-Almagro, F; Ames, D; Amin, N; Amouyel, P; Beiser, AS; Brodaty, H; Deary, IJ; Fennema-Notestine, C; Gampawar, PG; Gottesman, R; Griffanti, L; Jack, CR; Jenkinson, M; Jiang, J; Kral, BG; Kwok, JB; Lampe, L; C M Liewald, D; Maillard, P; Marchini, J; Bastin, ME; Mazoyer, B; Pirpamer, L; Rafael Romero, J; Roshchupkin, GV; Schofield, PR; Schroeter, ML; Stott, DJ; Thalamuthu, A; Trollor, J; Tzourio, C; van der Grond, J; Vernooij, MW; Witte, VA; Wright, MJ; Yang, Q; Morris, Z; Siggurdsson, S; Psaty, B; Villringer, A; Schmidt, H; Haberg, AK; van Duijn, CM; Jukema, JW; Dichgans, M; Sacco, RL; Wright, CB; Kremen, WS; Becker, LC; Thompson, PM; Mosley, TH; Wardlaw, JM; Ikram, MA; Adams, HHH; Seshadri, S; Sachdev, PS; Smith, SM; Launer, L; Longstreth, W; DeCarli, C; Schmidt, R; Fornage, M; Debette, S; Nyquist, PA Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
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