Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Publikationen
Suchbegriffe: GENOTYPING, . Treffer: 150
2023
Magarbeh, L; Hassel, C; Choi, M; Islam, F; Marshe, VS; Zai, CC; Zuberi, R; Gammal, RS; Men, X; Scherf-Clavel, M; Enko, D; Frey, BN; Milev, R; Soares, CN; Parikh, SV; Placenza, F; Strother, SC; Hassel, S; Taylor, VH; Leri, F; Blier, P; Farzan, F; Lam, RW; Turecki, G; Foster, JA; Rotzinger, S; Kloiber, S; Kennedy, JL; Kennedy, SH; Bousman, CA; Müller, DJ
ABCB1 Gene Variants and Antidepressant Treatment Outcomes: A Systematic Review and Meta-Analysis Including Results from the CAN-BIND-1 Study.
Clin Pharmacol Ther. 2023;
Doi: 10.1002/cpt.2854
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2022
Knoll, MA; Lackner, N; Ulmer, H; Samardzic, E; Steinmann, J; Krause, R; Verhasselt, HL; Rath, PM; Fuchs, F; Koehler, P; Denis, B; Hamane, S; Alanio, A; Lass-Flörl, C
Multiple colony antifungal susceptibility testing detects polyresistance in clinical Candida cultures: a European Confederation of Medical Mycology excellence centers study.
Clin Microbiol Infect. 2022; 28(9):1288.e1-1288.e7
Doi: 10.1016/j.cmi.2022.04.014
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König, T; Wurm, R; Parvizi, T; Silvaieh, S; Hotzy, C; Cetin, H; Klotz, S; Gelpi, E; Bancher, C; Benke, T; Dal-Bianco, P; Defrancesco, M; Fischer, P; Marksteiner, J; Sutterlüty, H; Ransmayr, G; Schmidt, R; Zimprich, A; Stögmann, E
C9orf72 repeat length might influence clinical sub-phenotypes in dementia patients.
Neurobiol Dis. 2022; 175: 105927
Doi: 10.1016/j.nbd.2022.105927
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Mishra, A; Duplaà, C; Vojinovic, D; Suzuki, H; Sargurupremraj, M; Zilhão, NR; Li, S; Bartz, TM; Jian, X; Zhao, W; Hofer, E; Wittfeld, K; Harris, SE; van, der, Auwera-Palitschka, S; Luciano, M; Bis, JC; Adams, HHH; Satizabal, CL; Gottesman, RF; Gampawar, PG; Bülow, R; Weiss, S; Yu, M; Bastin, ME; Lopez, OL; Vernooij, MW; Beiser, AS; Völker, U; Kacprowski, T; Soumare, A; Smith, JA; Knopman, DS; Morris, Z; Zhu, Y; Rotter, JI; Dufouil, C; Valdés, Hernández, M; Muñoz, Maniega, S; Lathrop, M; Boerwinkle, E; Schmidt, R; Ihara, M; Mazoyer, B; Yang, Q; Joutel, A; Tournier-Lasserve, E; Launer, LJ; Deary, IJ; Mosley, TH; Amouyel, P; DeCarli, CS; Psaty, BM; Tzourio, C; Kardia, SLR; Grabe, HJ; Teumer, A; van, Duijn, CM; Schmidt, H; Wardlaw, JM; Ikram, MA; Fornage, M; Gudnason, V; Seshadri, S; Matthews, PM; Longstreth, WT; Couffinhal, T; Debette, S
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.
Brain. 2022; 145(6): 1992-2007.
Doi: 10.1093/brain/awab432
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Muzammal, M; Ali, MZ; Brugger, B; Blatterer, J; Ahmad, S; Taj, S; Shah, SK; Khan, S; Enzinger, C; Petek, E; Wagner, K; Khan, MA; Windpassinger, C
A novel protein truncating mutation in L2HGDH causes L-2-hydroxyglutaric aciduria in a consanguineous Pakistani family.
Metab Brain Dis. 2022; 37(1):243-252
Doi: 10.1007/s11011-021-00832-2
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2021
Bressler, J; Davies, G; Smith, AV; Saba, Y; Bis, JC; Jian, X; Hayward, C; Yanek, L; Smith, JA; Mirza, SS; Wang, R; Adams, HHH; Becker, D; Boerwinkle, E; Campbell, A; Cox, SR; Eiriksdottir, G; Fawns-Ritchie, C; Gottesman, RF; Grove, ML; Guo, X; Hofer, E; Kardia, SLR; Knol, MJ; Koini, M; Lopez, OL; Marioni, RE; Nyquist, P; Pattie, A; Polasek, O; Porteous, DJ; Rudan, I; Satizabal, CL; Schmidt, H; Schmidt, R; Sidney, S; Simino, J; Smith, BH; Turner, ST; van, der, Lee, SJ; Ware, EB; Whitmer, RA; Yaffe, K; Yang, Q; Zhao, W; Gudnason, V; Launer, LJ; Fitzpatrick, AL; Psaty, BM; Fornage, M; Arfan, Ikram, M; van, Duijn, CM; Seshadri, S; Mosley, TH; Deary, IJ
Association of low-frequency and rare coding variants with information processing speed.
Transl Psychiatry. 2021; 11(1):613
Doi: 10.1038/s41398-021-01736-6
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Harun, A; Kan, AL; Schwabenbauer, K; Gilgado, F; Perdomo, H; Firacative, C; Losert, H; Abdullah, S; Giraud, S; Kaltseis, J; Fraser, M; Buzina, W; Lackner, M; Blyth, CC; Arthur, I; Rainer, J; Lira, JFC; Artigas, JG; Tintelnot, K; Slavin, MA; Heath, CH; Bouchara, JP; Chen, SCA; Meyer, W
Multilocus Sequence Typing Reveals Extensive Genetic Diversity of the Emerging Fungal Pathogen Scedosporium aurantiacum
FRONT CELL INFECT MI. 2021; 11: 761596
Doi: 10.3389/fcimb.2021.761596
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Pastuschek, J; Nonn, O; Gutiérrez-Samudio, RN; Murrieta-Coxca, JM; Müller, J; Sanft, J; Huppertz, B; Markert, UR; Groten, T; Morales-Prieto, DM
Molecular characteristics of established trophoblast-derived cell lines.
Placenta. 2021; 108(6): 122-133.
Doi: 10.1016/j.placenta.2021.02.022
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Van, Keer, S; van, Splunter, AP; Pattyn, J; De, Smet, A; Herzog, SA; Van, Ostade, X; Tjalma, WAA; Ieven, M; Van, Damme, P; Steenbergen, RDM; Vorsters, A
Triage of human papillomavirus infected women by methylation analysis in first-void urine.
Sci Rep. 2021; 11(1): 7862
Doi: 10.1038/s41598-021-87329-1
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2020
Bis, JC; Jian, X; Kunkle, BW; Chen, Y; Hamilton-Nelson, KL; Bush, WS; Salerno, WJ; Lancour, D; Ma, Y; Renton, AE; Marcora, E; Farrell, JJ; Zhao, Y; Qu, L; Ahmad, S; Amin, N; Amouyel, P; Beecham, GW; Below, JE; Campion, D; Cantwell, L; Charbonnier, C; Chung, J; Crane, PK; Cruchaga, C; Cupples, LA; Dartigues, JF; Debette, S; Deleuze, JF; Fulton, L; Gabriel, SB; Genin, E; Gibbs, RA; Goate, A; Grenier-Boley, B; Gupta, N; Haines, JL; Havulinna, AS; Helisalmi, S; Hiltunen, M; Howrigan, DP; Ikram, MA; Kaprio, J; Konrad, J; Kuzma, A; Lander, ES; Lathrop, M; Lehtimäki, T; Lin, H; Mattila, K; Mayeux, R; Muzny, DM; Nasser, W; Neale, B; Nho, K; Nicolas, G; Patel, D; Pericak-Vance, MA; Perola, M; Psaty, BM; Quenez, O; Rajabli, F; Redon, R; Reitz, C; Remes, AM; Salomaa, V; Sarnowski, C; Schmidt, H; Schmidt, M; Schmidt, R; Soininen, H; Thornton, TA; Tosto, G; Tzourio, C; van der Lee, SJ; van Duijn, CM; Valladares, O; Vardarajan, B; Wang, LS; Wang, W; Wijsman, E; Wilson, RK; Witten, D; Worley, KC; Zhang, X; Alzheimer’s Disease Sequencing Project; Bellenguez, C; Lambert, JC; Kurki, MI; Palotie, A; Daly, M; Boerwinkle, E; Lunetta, KL; Destefano, AL; Dupuis, J; Martin, ER; Schellenberg, GD; Seshadri, S; Naj, AC; Fornage, M; Farrer, LA
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
Mol Psychiatry. 2020; 25(8):1859-1875
Doi: 10.1038/s41380-018-0112-7
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D'Onofrio, V; Conzemius, R; Varda-Brkić, D; Bogdan, M; Grisold, A; Gyssens, IC; Bedenić, B; Barišić, I
Epidemiology of colistin-resistant, carbapenemase-producing Enterobacteriaceae and Acinetobacter baumannii in Croatia.
Infect Genet Evol. 2020; 81(10):104263-104263
Doi: 10.1016/j.meegid.2020.104263
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Matzhold, EM; Drexler, C; Wagner, A; Bernecker, C; Pessentheiner, A; Bogner-Strauß, JG; Helmberg, W; Wagner, T
A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O.
Transfusion. 2020; 60(7):1564-1572
Doi: 10.1111/trf.15907
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Meinitzer, S; Baranyi, A; Holasek, S; Schnedl, WJ; Zelzer, S; Mangge, H; Herrmann, M; Meinitzer, A; Enko, D
Sex-Specific Associations of Trimethylamine-N-Oxide and Zonulin with Signs of Depression in Carbohydrate Malabsorbers and Nonmalabsorbers.
Dis Markers. 2020; 2020(2):7897240-7897240
Doi: 10.1155/2020/7897240
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Reich, O; Regauer, S; Kashofer, K
Possibly carcinogenic HPV subtypes are a cause of HSIL and negative clinical HPV tests - A European prospective single center study.
Gynecol Oncol. 2020; 158(1):112-116
Doi: 10.1016/j.ygyno.2020.04.685
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2019
Ahmed, J; Windpassinger, C; Salim, M; Wiener, M; Petek, E; Schaflinger, E; Taj, S; Hussain, S; Abbas, S; Abbas, M; Younis, I; Muhammad, N; Khan, S; Khan, MA
Genetic study of Khyber-Pukhtunkhwa resident Pakistani families presenting primary microcephaly with intellectual disability.
J Pak Med Assoc. 2019; 69(12): 1812-1816.
Doi: 10.5455/JPMA.300681
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Allerkamp, H; Lehner, S; Ekhlasi-Hundrieser, M; Detering, C; von, Depka, Prondzinski, M; Pfarrer, C
Expression of angiogenic factors in the uteroplacental unit is altered at time of placentation in a porcine model of von Willebrand disease type 1.
Reprod Biol. 2019; 19(4): 412-420.
Doi: 10.1016/j.repbio.2019.09.007
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Binder, E; Rohrer, T; Denzer, C; Marg, W; Ohlenschläger, U; Schenk-Huber, H; Schierloh, U; Skopnik, H; Fröhlich-Reiterer, EE; Holl, RW; Prinz, N
Screening for coeliac disease in 1624 mainly asymptomatic children with type 1 diabetes: is genotyping for coeliac-specific human leucocyte antigen the right approach?
Arch Dis Child. 2019; 104(4):354-359
Doi: 10.1136/archdischild-2018-315549
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Borghini, L; Png, E; Binder, A; Wright, VJ; Pinnock, E; de Groot, R; Hazelzet, J; Emonts, M; Van der Flier, M; Schlapbach, LJ; Anderson, S; Secka, F; Salas, A; Fink, C; Carrol, ED; Pollard, AJ; Coin, LJ; Kuijpers, TW; Martinon-Torres, F; Zenz, W; Levin, M; Hibberd, ML; Davila, S; EUCLIDS consortium
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease.
Sci Rep. 2019; 9(1):6966-6966
Doi: 10.1038/s41598-019-43292-6
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Gallon, R; Mühlegger, B; Wenzel, SS; Sheth, H; Hayes, C; Aretz, S; Dahan, K; Foulkes, W; Kratz, CP; Ripperger, T; Azizi, AA; Baris Feldman, H; Chong, AL; Demirsoy, U; Florkin, B; Imschweiler, T; Januszkiewicz-Lewandowska, D; Lobitz, S; Nathrath, M; Pander, HJ; Perez-Alonso, V; Perne, C; Ragab, I; Rosenbaum, T; Rueda, D; Seidel, MG; Suerink, M; Taeubner, J; Zimmermann, SY; Zschocke, J; Borthwick, GM; Burn, J; Jackson, MS; Santibanez-Koref, M; Wimmer, K
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.
Hum Mutat. 2019; 40(5):649-655
Doi: 10.1002/humu.23721
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Lilly, E; Bunick, CG; Maley, AM; Zhang, S; Spraker, MK; Theos, AJ; Vivar, KL; Seminario-Vidal, L; Bennett, AE; Sidbury, R; Ogawa, Y; Akiyama, M; Binder, B; Hadj-Rabia, S; Morotti, RA; Glusac, EJ; Choate, KA; Richard, G; Milstone, LM
More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations.
J AM ACAD DERMATOL. 2019; 80(3): 617-625.
Doi: 10.1016/j.jaad.2018.09.042
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Lukić-Grlić, A; Kos, M; Žižek, M; Luxner, J; Grisold, A; Zarfel, G; Bedenić, B
Emergence of Carbapenem-Hydrolyzing Oxacillinases in Acinetobacter baumannii in Children from Croatia.
Chemotherapy. 2019; 64(4):167-172
Doi: 10.1159/000503746
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Regauer, S; Reich, O; Kashofer, K
Thin variant of high-grade squamous intraepithelial lesion - relationship with high-risk and possibly carcinogenic human papilloma virus subtypes and somatic cancer gene mutations.
HISTOPATHOLOGY. 2019; 75(3): 405-412.
Doi: 10.1111/his.13869
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Rhodes, CJ; Batai, K; Bleda, M; Haimel, M; Southgate, L; Germain, M; Pauciulo, MW; Hadinnapola, C; Aman, J; Girerd, B; Arora, A; Knight, J; Hanscombe, KB; Karnes, JH; Kaakinen, M; Gall, H; Ulrich, A; Harbaum, L; Cebola, I; Ferrer, J; Lutz, K; Swietlik, EM; Ahmad, F; Amouyel, P; Archer, SL; Argula, R; Austin, ED; Badesch, D; Bakshi, S; Barnett, C; Benza, R; Bhatt, N; Bogaard, HJ; Burger, CD; Chakinala, M; Church, C; Coghlan, JG; Condliffe, R; Corris, PA; Danesino, C; Debette, S; Elliott, CG; Elwing, J; Eyries, M; Fortin, T; Franke, A; Frantz, RP; Frost, A; Garcia, JGN; Ghio, S; Ghofrani, HA; Gibbs, JSR; Harley, J; He, H; Hill, NS; Hirsch, R; Houweling, AC; Howard, LS; Ivy, D; Kiely, DG; Klinger, J; Kovacs, G; Lahm, T; Laudes, M; Machado, RD; MacKenzie Ross, RV; Marsolo, K; Martin, LJ; Moledina, S; Montani, D; Nathan, SD; Newnham, M; Olschewski, A; Olschewski, H; Oudiz, RJ; Ouwehand, WH; Peacock, AJ; Pepke-Zaba, J; Rehman, Z; Robbins, I; Roden, DM; Rosenzweig, EB; Saydain, G; Scelsi, L; Schilz, R; Seeger, W; Shaffer, CM; Simms, RW; Simon, M; Sitbon, O; Suntharalingam, J; Tang, H; Tchourbanov, AY; Thenappan, T; Torres, F; Toshner, MR; Treacy, CM; Vonk Noordegraaf, A; Waisfisz, Q; Walsworth, AK; Walter, RE; Wharton, J; White, RJ; Wilt, J; Wort, SJ; Yung, D; Lawrie, A; Humbert, M; Soubrier, F; Trégouët, DA; Prokopenko, I; Kittles, R; Gräf, S; Nichols, WC; Trembath, RC; Desai, AA; Morrell, NW; Wilkins, MR; UK NIHR BioResource Rare Diseases Consortium; UK PAH Cohort Study Consortium; US PAH Biobank Consortium
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
Lancet Respir Med. 2019; 7(3):227-238
Doi: 10.1016/S2213-2600(18)30409-0
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Schmitz, B; Kleber, ME; Lenders, M; Delgado, GE; Engelbertz, C; Huang, J; Pavenstädt, H; Breithardt, G; Brand, SM; März, W; Brand, E
Genome-wide association study suggests impact of chromosome 10 rs139401390 on kidney function in patients with coronary artery disease.
SCI REP-UK. 2019; 9(1): 2750-2750.
Doi: 10.1038/s41598-019-39055-y
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2018
Buder, A; Hochmair, MJ; Schwab, S; Bundalo, T; Schenk, P; Errhalt, P; Mikes, RE; Absenger, G; Patocka, K; Baumgartner, B; Setinek, U; Burghuber, OC; Prosch, H; Pirker, R; Filipits, M
Cell-Free Plasma DNA-Guided Treatment With Osimertinib in Patients With Advanced EGFR-Mutated NSCLC.
J Thorac Oncol. 2018; 13(6):821-830
Doi: 10.1016/j.jtho.2018.02.014
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Enko, D; Harringer, S; Oberkanins, C; Pühringer, H; Halwachs-Baumann, G; Kriegshäuser, G
SLCO1B1 c.521T>C Genotyping in the Austrian Population Using 2 Commercial Real-Time Polymerase Chain Reaction Assays: An Implementation Study.
Pharmacology. 2018; 102(1-2): 88-90.
Doi: 10.1159/000490619
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Enko, D; Wagner, H; Kriegshäuser, G; Brandmayr, W; Halwachs-Baumann, G; Schnedl, WJ; Zelzer, S; Mangge, H; Meinitzer, A
Assessment of tryptophan metabolism and signs of depression in individuals with carbohydrate malabsorption.
Psychiatry Res. 2018; 262(1):595-599
Doi: 10.1016/j.psychres.2017.09.049
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Harripaul, R; Vasli, N; Mikhailov, A; Rafiq, MA; Mittal, K; Windpassinger, C; Sheikh, TI; Noor, A; Mahmood, H; Downey, S; Johnson, M; Vleuten, K; Bell, L; Ilyas, M; Khan, FS; Khan, V; Moradi, M; Ayaz, M; Naeem, F; Heidari, A; Ahmed, I; Ghadami, S; Agha, Z; Zeinali, S; Qamar, R; Mozhdehipanah, H; John, P; Mir, A; Ansar, M; French, L; Ayub, M; Vincent, JB
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
Mol Psychiatry. 2018; 23(4):973-984
Doi: 10.1038/mp.2017.60
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Heits, N; Brosch, M; Herrmann, A; Behrens, R; Röcken, C; Schrem, H; Kaltenborn, A; Klempnauer, J; Kreipe, HH; Reichert, B; Lenschow, C; Wilms, C; Vogel, T; Wolters, H; Wardelmann, E; Seehofer, D; Buch, S; Zeissig, S; Pannach, S; Raschzok, N; Dietel, M; von Schoenfels, W; Hinz, S; Teufel, A; Evert, M; Franke, A; Becker, T; Braun, F; Hampe, J; Schafmayer, C
Evolutionary Distance Predicts Recurrence After Liver Transplantation in Multifocal Hepatocellular Carcinoma.
Transplantation. 2018; 102(10): e424-e430-e424-e430.
Doi: 10.1097/TP.0000000000002356
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Kimbacher, C; Paar, C; Freystetter, A; Berg, J
Cell Line Controls for the Genotyping of a Spectrum of Human Single Nucleotide Polymorphisms in the Clinical Laboratory.
Clin Lab. 2018; 64(5):823-834
Doi: 10.7754/Clin.Lab.2018.171212
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2017
Binder, E; Loinger, M; Mühlbacher, A; Edlinger, M; Steichen, E; Meraner, D; Loacker, L; Weigel, G; Müller, T; Fröhlich-Reiterer, E; Hofer, SE
Genotyping of coeliac-specific human leucocyte antigen in children with type 1 diabetes: does this screening method make sense?
Arch Dis Child. 2017; 102(7):603-606
Doi: 10.1136/archdischild-2016-311610
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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
Doi: 10.1212/NXG.0000000000000180
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Jajić, I; Benčić, A; Siroglavić, M; Zarfel, G; Ružić, B; Pezelj, I; Bedenić, B
Klebsiella Pneumoniaeoxa-48 in a Urology Patient: Case Report
Acta Clin Croat. 2017; 56(1):166-171
Doi: 10.20471/acc.2017.56.01.23
(- Case Report)
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Kessler, HH; Stelzl, E
Profile of Roche's cobas® HCV tests.
Expert Rev Mol Diagn. 2017; 17(4):311-319
Doi: 10.1080/14737159.2017.1293526
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Lucas, JS; Barbato, A; Collins, SA; Goutaki, M; Behan, L; Caudri, D; Dell, S; Eber, E; Escudier, E; Hirst, RA; Hogg, C; Jorissen, M; Latzin, P; Legendre, M; Leigh, MW; Midulla, F; Nielsen, KG; Omran, H; Papon, JF; Pohunek, P; Redfern, B; Rigau, D; Rindlisbacher, B; Santamaria, F; Shoemark, A; Snijders, D; Tonia, T; Titieni, A; Walker, WT; Werner, C; Bush, A; Kuehni, CE
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia.
Eur Respir J. 2017; 49(1):
Doi: 10.1183/13993003.01090-2016
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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
Doi: 10.1093/brain/awx220
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Sims, R; van der Lee, SJ; Naj, AC; Bellenguez, C; Badarinarayan, N; Jakobsdottir, J; Kunkle, BW; Boland, A; Raybould, R; Bis, JC; Martin, ER; Grenier-Boley, B; Heilmann-Heimbach, S; Chouraki, V; Kuzma, AB; Sleegers, K; Vronskaya, M; Ruiz, A; Graham, RR; Olaso, R; Hoffmann, P; Grove, ML; Vardarajan, BN; Hiltunen, M; Nöthen, MM; White, CC; Hamilton-Nelson, KL; Epelbaum, J; Maier, W; Choi, SH; Beecham, GW; Dulary, C; Herms, S; Smith, AV; Funk, CC; Derbois, C; Forstner, AJ; Ahmad, S; Li, H; Bacq, D; Harold, D; Satizabal, CL; Valladares, O; Squassina, A; Thomas, R; Brody, JA; Qu, L; Sánchez-Juan, P; Morgan, T; Wolters, FJ; Zhao, Y; Garcia, FS; Denning, N; Fornage, M; Malamon, J; Naranjo, MCD; Majounie, E; Mosley, TH; Dombroski, B; Wallon, D; Lupton, MK; Dupuis, J; Whitehead, P; Fratiglioni, L; Medway, C; Jian, X; Mukherjee, S; Keller, L; Brown, K; Lin, H; Cantwell, LB; Panza, F; McGuinness, B; Moreno-Grau, S; Burgess, JD; Solfrizzi, V; Proitsi, P; Adams, HH; Allen, M; Seripa, D; Pastor, P; Cupples, LA; Price, ND; Hannequin, D; Frank-García, A; Levy, D; Chakrabarty, P; Caffarra, P; Giegling, I; Beiser, AS; Giedraitis, V; Hampel, H; Garcia, ME; Wang, X; Lannfelt, L; Mecocci, P; Eiriksdottir, G; Crane, PK; Pasquier, F; Boccardi, V; Henández, I; Barber, RC; Scherer, M; Tarraga, L; Adams, PM; Leber, M; Chen, Y; Albert, MS; Riedel-Heller, S; Emilsson, V; Beekly, D; Braae, A; Schmidt, R; Blacker, D; Masullo, C; Schmidt, H; Doody, RS; Spalletta, G; Longstreth, WT; Fairchild, TJ; Bossù, P; Lopez, OL; Frosch, MP; Sacchinelli, E; Ghetti, B; Yang, Q; Huebinger, RM; Jessen, F; Li, S; Kamboh, MI; Morris, J; Sotolongo-Grau, O; Katz, MJ; Corcoran, C; Dunstan, M; Braddel, A; Thomas, C; Meggy, A; Marshall, R; Gerrish, A; Chapman, J; Aguilar, M; Taylor, S; Hill, M; Fairén, MD; Hodges, A; Vellas, B; Soininen, H; Kloszewska, I; Daniilidou, M; Uphill, J; Patel, Y; Hughes, JT; Lord, J; Turton, J; Hartmann, AM; Cecchetti, R; Fenoglio, C; Serpente, M; Arcaro, M; Caltagirone, C; Orfei, MD; Ciaramella, A; Pichler, S; Mayhaus, M; Gu, W; Lleó, A; Fortea, J; Blesa, R; Barber, IS; Brookes, K; Cupidi, C; Maletta, RG; Carrell, D; Sorbi, S; Moebus, S; Urbano, M; Pilotto, A; Kornhuber, J; Bosco, P; Todd, S; Craig, D; Johnston, J; Gill, M; Lawlor, B; Lynch, A; Fox, NC; Hardy, J; ARUK Consortium; Albin, RL; Apostolova, LG; Arnold, SE; Asthana, S; Atwood, CS; Baldwin, CT; Barnes, LL; Barral, S; Beach, TG; Becker, JT; Bigio, EH; Bird, TD; Boeve, BF; Bowen, JD; Boxer, A; Burke, JR; Burns, JM; Buxbaum, JD; Cairns, NJ; Cao, C; Carlson, CS; Carlsson, CM; Carney, RM; Carrasquillo, MM; Carroll, SL; Diaz, CC; Chui, HC; Clark, DG; Cribbs, DH; Crocco, EA; DeCarli, C; Dick, M; Duara, R; Evans, DA; Faber, KM; Fallon, KB; Fardo, DW; Farlow, MR; Ferris, S; Foroud, TM; Galasko, DR; Gearing, M; Geschwind, DH; Gilbert, JR; Graff-Radford, NR; Green, RC; Growdon, JH; Hamilton, RL; Harrell, LE; Honig, LS; Huentelman, MJ; Hulette, CM; Hyman, BT; Jarvik, GP; Abner, E; Jin, LW; Jun, G; Karydas, A; Kaye, JA; Kim, R; Kowall, NW; Kramer, JH; LaFerla, FM; Lah, JJ; Leverenz, JB; Levey, AI; Li, G; Lieberman, AP; Lunetta, KL; Lyketsos, CG; Marson, DC; Martiniuk, F; Mash, DC; Masliah, E; McCormick, WC; McCurry, SM; McDavid, AN; McKee, AC; Mesulam, M; Miller, BL; Miller, CA; Miller, JW; Morris, JC; Murrell, JR; Myers, AJ; O'Bryant, S; Olichney, JM; Pankratz, VS; Parisi, JE; Paulson, HL; Perry, W; Peskind, E; Pierce, A; Poon, WW; Potter, H; Quinn, JF; Raj, A; Raskind, M; Reisberg, B; Reitz, C; Ringman, JM; Robe ...
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Nat Genet. 2017; 49(9):1373-1384
Doi: 10.1038/ng.3916
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Skrabl-Baumgartner, A; Christine Hauer, A; Erwa, W; Jahnel, J
HLA genotyping as first-line screening tool for coeliac disease in children with juvenile idiopathic arthritis.
Arch Dis Child. 2017; 102(7):607-611
Doi: 10.1136/archdischild-2016-311544
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Stelzl, E; Appel, HM; Mehta, R; Marins, EG; Berg, J; Paar, C; Zurl, H; Santner, BI; Kessler, HH
Evaluation of the new cobas® HCV genotyping test based on real-time PCRs of three different HCV genome regions.
Clin Chem Lab Med. 2017; 55(4):517-521
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Stelzl, E; Haas, B; Bauer, B; Zhang, S; Fiss, EH; Hillman, G; Hamilton, AT; Mehta, R; Heil, ML; Marins, EG; Santner, BI; Kessler, HH
First identification of a recombinant form of hepatitis C virus in Austrian patients by full-genome next generation sequencing.
PLoS One. 2017; 12(7):e0181273-e0181273
Doi: 10.1371/journal.pone.0181273
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Zeller, T; Seiffert, M; Müller, C; Scholz, M; Schäffer, A; Ojeda, F; Drexel, H; Mündlein, A; Kleber, ME; März, 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(12):57-57
Doi: 10.3389/fcvm.2017.00057
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2016
Bedenić, B; Firis, N; Elveđi-Gašparović, V; Krilanović, M; Matanović, K; Štimac, I; Luxner, J; Vraneš, J; Meštrović, T; Zarfel, G; Grisold, A
Emergence of multidrug-resistant Proteus mirabilis in a long-term care facility in Croatia.
Wien Klin Wochenschr. 2016; 128(11-12):404-413
Doi: 10.1007/s00508-016-1005-x
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Bedenić, B; Sardelić, S; Luxner, J; Bošnjak, Z; Varda-Brkić, D; Lukić-Grlić, A; Mareković, I; Frančula-Zaninović, S; Krilanović, M; Šijak, D; Grisold, A; Zarfel, G
Molecular characterization of class b carbapenemases in advanced stage of dissemination and emergence of class d carbapenemases in Enterobacteriaceae from Croatia.
Infect Genet Evol. 2016; 43(3):74-82
Doi: 10.1016/j.meegid.2016.05.011
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Endris, V; Stenzinger, A; Pfarr, N; Penzel, R; Möbs, M; Lenze, D; Darb-Esfahani, S; Hummel, M; Sabine-Merkelbach-Bruse, M; Jung, A; Lehmann, U; Kreipe, H; Kirchner, T; Büttner, R; Jochum, W; Höfler, G; Dietel, M; Weichert, W; Schirmacher, P
NGS-based BRCA1/2 mutation testing of high-grade serous ovarian cancer tissue: results and conclusions of the first international round robin trial.
Virchows Arch. 2016; 468(6):697-705
Doi: 10.1007/s00428-016-1919-8
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Enko, D; Kriegshäuser, G; Stolba, R; Mangge, H; Brandstetter, D; Mayr, N; Forstner, T; Halwachs-Baumann, G
Assessment of vitamin D status and serum CrossLaps levels in adults with primary lactose malabsorption.
Eur J Clin Nutr. 2016; 70(9):1000-1003
Doi: 10.1038/ejcn.2016.66
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Enko, D; Pollheimer, V; Németh, S; Pühringer, H; Stolba, R; Halwachs-Baumann, G; Kriegshäuser, G
Lactase Non-Persistence Genotyping: Comparison of Two Real-Time PCR Assays and Assessment of Concomitant Fructose/Sorbitol Malabsorption Rates.
Clin Lab. 2016; 62(4):727-730
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Holtfreter, S; Grumann, D; Balau, V; Barwich, A; Kolata, J; Goehler, A; Weiss, S; Holtfreter, B; Bauerfeind, SS; Döring, P; Friebe, E; Haasler, N; Henselin, K; Kühn, K; Nowotny, S; Radke, D; Schulz, K; Schulz, SR; Trübe, P; Vu, CH; Walther, B; Westphal, S; Cuny, C; Witte, W; Völzke, H; Grabe, HJ; Kocher, T; Steinmetz, I; Bröker, BM
Molecular Epidemiology of Staphylococcus aureus in the General Population in Northeast Germany: Results of the Study of Health in Pomerania (SHIP-TREND-0).
J Clin Microbiol. 2016; 54(11): 2774-2785.
Doi: 10.1128/JCM.00312-16
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Khan, MA; Mohan, S; Zubair, M; Windpassinger, C
Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome.
BMC Med Genet. 2016; 17(6): 10-10.
Doi: 10.1186/s12881-016-0271-9
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Lin, H; Mueller-Nurasyid, M; Smith, AV; Arking, DE; Barnard, J; Bartz, TM; Lunetta, KL; Lohman, K; Kleber, ME; Lubitz, SA; Geelhoed, B; Trompet, S; Niemeijer, MN; Kacprowski, T; Chasman, DI; Klarin, D; Sinner, MF; Waldenberger, M; Meitinger, T; Harris, TB; Launer, LJ; Soliman, EZ; Chen, LY; Smith, JD; Van Wagoner, DR; Rotter, JI; Psaty, BM; Xie, Z; Hendricks, AE; Ding, J; Delgado, GE; Verweij, N; van der Harst, P; Macfarlane, PW; Ford, I; Hofman, A; Uitterlinden, A; Heeringa, J; Franco, OH; Kors, JA; Weiss, S; Völzke, H; Rose, LM; Natarajan, P; Kathiresan, S; Kääb, S; Gudnason, V; Alonso, A; Chung, MK; Heckbert, SR; Benjamin, EJ; Liu, Y; März, W; Rienstra, M; Jukema, JW; Stricker, BH; Dörr, M; Albert, CM; Ellinor, PT
Gene-gene Interaction Analyses for Atrial Fibrillation.
Sci Rep. 2016; 6(24):35371-35371
Doi: 10.1038/srep35371
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Paar, C; Hammerl, V; Blessberger, H; Stekel, H; Steinwender, C; Berg, J
Conditions of High Resolution Melting Analysis on the Cobas z480 Instrument for the Genotyping of VKORC1 in the Clinical Routine Laboratory.
Clin Lab. 2016; 62(12):2461-2467
Doi: 10.7754/Clin.Lab.2016.160616
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