Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gampawar Piyush Gajananrao |
** = Publikationen gelistet in SCI/SSCI/Pubmed
2025
Originalarbeit (Zeitschrift)
** Gampawar, P; Veeranki, SPK; Petrovic, KE; Schmidt, R; Schmidt, H
Epigenetic age acceleration is related to cognitive decline in the elderly: Results of the Austrian Stroke Prevention Study.
Psychiatry Clin Neurosci. 2025;
Doi: 10.1111/pcn.13793
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2023
Originalarbeit (Zeitschrift)
** Duperron, MG; Knol, MJ; Le, Grand, Q; Evans, TE; Mishra, A; Tsuchida, A; Roshchupkin, G; Konuma, T; Trégouët, DA; Romero, JR; Frenzel, S; Luciano, M; Hofer, E; Bourgey, M; Dueker, ND; Delgado, P; Hilal, S; Tankard, RM; Dubost, F; Shin, J; Saba, Y; Armstrong, NJ; Bordes, C; Bastin, ME; Beiser, A; Brodaty, H; Bülow, R; Carrera, C; Chen, C; Cheng, CY; Deary, IJ; Gampawar, PG; Himali, JJ; Jiang, J; Kawaguchi, T; Li, S; Macalli, M; Marquis, P; Morris, Z; Muñoz, Maniega, S; Miyamoto, S; Okawa, M; Paradise, M; Parva, P; Rundek, T; Sargurupremraj, M; Schilling, S; Setoh, K; Soukarieh, O; Tabara, Y; Teumer, A; Thalamuthu, A; Trollor, JN; Valdés, Hernández, MC; Vernooij, MW; Völker, U; Wittfeld, K; Wong, TY; Wright, MJ; Zhang, J; Zhao, W; Zhu, YC; Schmidt, H; Sachdev, PS; Wen, W; Yoshida, K; Joutel, A; Satizabal, CL; Sacco, RL; Bourque, G; Lathrop, M; Paus, T; Fernandez-Cadenas, I; Yang, Q; Mazoyer, B; Boutinaud, P; Okada, Y; Grabe, HJ; Mather, KA; Schmidt, R; Joliot, M; Ikram, MA; Matsuda, F; Tzourio, C; Wardlaw, JM; Seshadri, S; Adams, HHH; Debette, S, , CHARGE, consortium, , CHARGE, consortium, , CHARGE, consortium
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease.
Nat Med. 2023; 29(4):950-962
Doi: 10.1038/s41591-023-02268-w
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2022
Originalarbeit (Zeitschrift)
** Gampawar, P; Schmidt, R; Schmidt, H
Telomere length and brain aging: A systematic review and meta-analysis.
Ageing Res Rev. 2022; 80: 101679
Doi: 10.1016/j.arr.2022.101679
Web of Science
PubMed
FullText
FullText_MUG
** 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]
Web of Science
PubMed
FullText
FullText_MUG
** 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
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2021
Originalarbeit (Zeitschrift)
** 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]
Web of Science
PubMed
FullText
FullText_MUG
2020
Originalarbeit (Zeitschrift)
** 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.
Stroke. 2020; STROKEAHA119027544-STROKEAHA119027544.
Doi: 10.1161/STROKEAHA.119.027544
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
** Gampawar, P; Schmidt, R; Schmidt, H
Leukocyte Telomere Length Is Related to Brain Parenchymal Fraction and Attention/Speed in the Elderly: Results of the Austrian Stroke Prevention Study.
Front Psychiatry. 2020; 11: 100-100.
Doi: 10.3389/fpsyt.2020.00100
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Abstract (Zeitschrift)
** Gampawar, P; Schmidt, R; Schmidt, H
Leukocyte telomere length is related to brain parenchymal fraction and attention/speed in the elderly: Results of the Austrian Stroke Prevention Study.
EUR J HUM GENET. 2020; 28(SUPPL 1): 734-735.
[Poster]
Web of Science
2019
Originalarbeit (Zeitschrift)
** Gampawar, P; Saba, Y; Werner, U; Schmidt, R; Müller-Myhsok, B; Schmidt, H
Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton.
Front Genet. 2019; 10: 856-856.
Doi: 10.3389/fgene.2019.00856
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
** Tripolszki, K; Gampawar, P; Schmidt, H; Nagy, ZF; Nagy, D; Klivényi, P; Engelhardt, JI; Széll, M
Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort.
Front Genet. 2019; 10: 732-732.
Doi: 10.3389/fgene.2019.00732
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Abstract (Zeitschrift)
** Gampawar, P; Saba, Y; Werner, U; Schmidt, R; Muller-Myhsok, B; Schmidt, H
Establishing high sensitivity and specificity for exome sequencing on Ion Proton
EUR J HUM GENET. 2019; 27: 1636-1636.-52nd Conference of the European-Society-of-Human-Genetics (ESHG); JUN 15-18, 2019; Gothenburg, SWEDEN.
[Poster]
Web of Science
** Tripolszki, K; Gampawar, P; Schmidt, H; Nagy, ZF; Klivenyi, P; Engelhardt, JI; Szell, M
Comprehensive genetic analysis in a cohort of 107 Hungarian patients with amyotrophic lateral sclerosis
EUR J HUM GENET. 2019; 27: 1472-1473.-52nd Conference of the European-Society-of-Human-Genetics (ESHG); JUN 15-18, 2019; Gothenburg, SWEDEN.
[Poster]
Web of Science
2018
Originalarbeit (Zeitschrift)
** 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.
Doi: 10.1038/gim.2018.27
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
2016
Originalarbeit (Zeitschrift)
** Weerakkody, RA; Vandrovcova, J; Kanonidou, C; Mueller, M; Gampawar, P; Ibrahim, Y; Norsworthy, P; Biggs, J; Abdullah, A; Ross, D; Black, HA; Ferguson, D; Cheshire, NJ; Kazkaz, H; Grahame, R; Ghali, N; Vandersteen, A; Pope, FM; Aitman, TJ
Targeted next-generation sequencing makes new molecular diagnoses and expands genotype-phenotype relationship in Ehlers-Danlos syndrome.
Genet Med. 2016; 18(11):1119-1127
Doi: 10.1038/gim.2016.14
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG