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

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Publikationen

Suchbegriffe: HAPLOTYPES - GENETICS , . Treffer: 30

2019

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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2016

Pearce, KF; Balavarca, Y; Norden, J; Jackson, G; Holler, E; Dressel, R; Greinix, H; Toubert, A; Gluckman, E; Hromadnikova, I; Sedlacek, P; Wolff, D; Holtick, U; Bickeböller, H; Dickinson, AM Impact of genomic risk factors on survival after haematopoietic stem cell transplantation for patients with acute leukaemia.
Int J Immunogenet. 2016; 43(6):404-412
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2015

Ebner, S; Mangge, H; Langhof, H; Halle, M; Siegrist, M; Aigner, E; Paulmichl, K; Paulweber, B; Datz, C; Sperl, W; Kofler, B; Weghuber, D Mitochondrial Haplogroup T Is Associated with Obesity in Austrian Juveniles and Adults.
PLoS One. 2015; 10(8):e0135622-e0135622 [OPEN ACCESS]
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Niklas, N; Hafenscher, J; Barna, A; Wiesinger, K; Pröll, J; Dreiseitl, S; Preuner-Stix, S; Valent, P; Lion, T; Gabriel, C cFinder: definition and quantification of multiple haplotypes in a mixed sample.
BMC Res Notes. 2015; 8(9):422-422 [OPEN ACCESS]
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Rafiq, MA; Leblond, CS; Saqib, MA; Vincent, AK; Ambalavanan, A; Khan, FS; Ayaz, M; Shaheen, N; Spiegelman, D; Ali, G; Amin-ud-Din, M; Laurent, S; Mahmood, H; Christian, M; Ali, N; Fennell, A; Nanjiani, Z; Egger, G; Caron, C; Waqas, A; Ayub, M; Rasheed, S; Forgeot d'Arc, B; Johnson, A; So, J; Brohi, MQ; Mottron, L; Ansar, M; Vincent, JB; Xiong, L Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features.
BMC Med Genet. 2015; 16(7):41-41 (- Case Report) [OPEN ACCESS]
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2013

Nevado, B; Mautner, S; Sturmbauer, C; Verheyen, E Water-level fluctuations and metapopulation dynamics as drivers of genetic diversity in populations of three Tanganyikan cichlid fish species.
Mol Ecol. 2013; 22(15): 3933-3948. [OPEN ACCESS]
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2012

Barral, S; Fernández-Cadenas, I; Bis, JC; Montaner, J; Ikram, AM; Launer, LJ; Fornage, M; Schmidt, H; Brickman, AM; Seshadri, S; Mayeux, R No association of ALOX5AP polymorphisms with risk of MRI-defined brain infarcts.
Neurobiol Aging. 2012; 33(3):629.e1-629.e3 [OPEN ACCESS]
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2011

Graupp, M; Wehr, E; Schweighofer, N; Pieber, TR; Obermayer-Pietsch, B Association of genetic variants in the two isoforms of 5α-reductase, SRD5A1 and SRD5A2, in lean patients with polycystic ovary syndrome.
Eur J Obstet Gynecol Reprod Biol. 2011; 157(2):175-179 [OPEN ACCESS]
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Langsenlehner, T; Renner, W; Gerger, A; Hofmann, G; Thurner, EM; Kapp, KS; Langsenlehner, U Impact of VEGF gene polymorphisms and haplotypes on radiation-induced late toxicity in prostate cancer patients.
Strahlenther Onkol. 2011; 187(12):784-791
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Winder, T; Ning, Y; Yang, D; Zhang, W; Power, DG; Bohanes, P; Gerger, A; Wilson, PM; Lurje, G; Tang, LH; Shah, M; Lenz, HJ Germline polymorphisms in genes involved in the CD44 signaling pathway are associated with clinical outcome in localized gastric adenocarcinoma.
Int J Cancer. 2011; 129(5):1096-1104 [OPEN ACCESS]
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2010

Danzer, M; Polin, H; Stabentheiner, S; Hartmann, CC; Lennartz, K; Gabriel, C Comprehensive polymorphism analysis of ABO using allele-specific separation by bead technology and subsequent sequencing.
Vox Sang. 2010; 98(3 Pt 2): 451-454.
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2009

Ulrich, S; Sorantin, S; Posch, U; Helmberg, W; Lanzer, G A new HLA-A*26 variant, A*2637 identified by haplotype-specific extraction and sequencing-based typing.
TISSUE ANTIGEN. 2009; 73(3): 275-276.
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2008

Langsenlehner, T; Langsenlehner, U; Renner, W; Krippl, P; Mayer, R; Wascher, TC; Kapp, KS Single nucleotide polymorphisms and haplotypes in the gene for vascular endothelial growth factor and risk of prostate cancer.
Eur J Cancer. 2008; 44(11):1572-1576
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Ulrich, S; Posch, U; Helmberg, W; Lanzer, G A new HLA-B*44 variant, B*4453, identified by haplotype-specific extraction and sequencing-based typing.
Tissue Antigens. 2008; 71(1):91-92
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2007

Eder, T; Mayer, R; Langsenlehner, U; Renner, W; Krippl, P; Wascher, TC; Pummer, K; Kapp, KS Interleukin-10 [ATA] promoter haplotype and prostate cancer risk: a population-based study.
Eur J Cancer. 2007; 43(3):472-475
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2006

Laimer, M; Klausegger, A; Aberer, W; Oender, K; Steinhuber, M; Lanschuetzer, CM; Wally, V; Hintner, H; Bauer, JW Haploinsufficiency due to deletion within the 3'-UTR of C1-INH-gene associated with hereditary angioedema.
GENET MED. 2006; 8: 249-254. [OPEN ACCESS]
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Storch, MK; Bauer, J; Linington, C; Olsson, T; Weissert, R; Lassmann, H Cortical demyelination can be modeled in specific rat models of autoimmune encephalomyelitis and is major histocompatability complex (MHC) haplotype-related.
J Neuropathol Exp Neurol. 2006; 65(12):1137-1142 [OPEN ACCESS]
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2005

Auer-Grumbach, M; Schlotter-Weigel, B; Lochmüller, H; Strobl-Wildemann, G; Auer-Grumbach, P; Fischer, R; Offenbacher, H; Zwick, EB; Robl, T; Hartl, G; Hartung, HP; Wagner, K; Windpassinger, C; Austrian Peripheral Neuropathy Study Group Phenotypes of the N88S Berardinelli-Seip congenital lipodystrophy 2 mutation.
Ann Neurol. 2005; 57(3):415-424
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Langsenlehner, U; Krippl, P; Renner, W; Yazdani-Biuki, B; Eder, T; Köppel, H; Wascher, TC; Paulweber, B; Samonigg, H Interleukin-10 promoter polymorphism is associated with decreased breast cancer risk.
Breast Cancer Res Treat. 2005; 90(2):113-115
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Renner, W; Nauck, M; Winkelmann, BR; Hoffmann, MM; Scharnagl, H; Mayer, V; Boehm, BO; März, W; LURIC Study team Association of angiotensinogen haplotypes with angiotensinogen levels but not with blood pressure or coronary artery disease: the Ludwigshafen Risk and Cardiovascular Health Study.
J Mol Med (Berl). 2005; 83(3):235-239
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2004

Fröhlich, LF; Gensure, RC; Schipani, E; Jüppner, H; Bastepe, M Haplotype frequencies and linkage disequilibrium analysis of four frequent polymorphisms at the PTH/PTH-related peptide receptor gene locus.
Mol Cell Probes. 2004; 18(5): 353-357.
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Schmidt, H; Aulchenko, YS; Schweighofer, N; Schmidt, R; Frank, S; Kostner, GM; Ott, E; van Duijn, C Angiotensinogen promoter B-haplotype associated with cerebral small vessel disease enhances basal transcriptional activity.
STROKE. 2004; 35: 2592-2597. [OPEN ACCESS]
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2003

Petek, E; Jenne, DE; Smolle, J; Binder, B; Lasinger, W; Windpassinger, C; Wagner, K; Kroisel, PM; Kehrer-Sawatzki, H Mitotic recombination mediated by the JJAZF1 (KIAA0160) gene causing somatic mosaicism and a new type of constitutional NF1 microdeletion in two children of a mosaic female with only few manifestations.
J Med Genet. 2003; 40(7):520-525 (- Case Report) [OPEN ACCESS]
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Petek, E; Windpassinger, C; Simma, B; Mueller, T; Wagner, K; Kroisel, PM Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies.
J Hum Genet. 2003; 48(6):283-287 (- Case Report) [OPEN ACCESS]
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Windpassinger, C; Wagner, K; Petek, E; Fischer, R; Auer-Grumbach, M Refinement of the Silver syndrome locus on chromosome 11q12-q14 in four families and exclusion of eight candidate genes.
HUM GENET. 2003; 114(1): 99-109.
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Winkelmann, BR; Hoffmann, MM; Nauck, M; Kumar, AM; Nandabalan, K; Judson, RS; Boehm, BO; Tall, AR; Ruaño, G; März, W Haplotypes of the cholesteryl ester transfer protein gene predict lipid-modifying response to statin therapy.
PHARMACOGENOMICS J. 2003; 3(5): 284-296. [OPEN ACCESS]
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2002

De Jonghe, P; Auer-Grumbach, M; Irobi, J; Wagner, K; Plecko, B; Kennerson, M; Zhu, D; De Vriendt, E; Van Gerwen, V; Nicholson, G; Hartung, HP; Timmerman, V Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?
Brain. 2002; 125(Pt 6):1320-1325 [OPEN ACCESS]
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2001

Langer, S; Jentsch, I; Gangnus, R; Yan, H; Lengauer, C; Speicher, MR Facilitating haplotype analysis by fully automated analysis of all chromosomes in human-mouse hybrid cell lines.
Cytogenet Cell Genet. 2001; 93(1-2):11-15
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Schmidt, H; Fazekas, F; Kostner, GM; van Duijn , CM; Schmidt, R Angiotensinogen gene promoter haplotype and microangiopathy-related cerebral damage: results of the Austrian Stroke Prevention Study.
Stroke. 2001; 32(2):405-412 [OPEN ACCESS]
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1992

Wagner, K; Zach, M; Rosenkranz, W Frequency of delta F508 and haplotype association in Austrian cystic fibrosis families.
HUM GENET. 1992; 89(4): 437-438.
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