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Prokisch H
Prokisch H
Institute of Human Genetics TU-Munich
Bestätigte E-Mail-Adresse bei helmholtz-muenchen.de
Titel
Zitiert von
Zitiert von
Jahr
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
11349*2021
Systematic identification of trans eQTLs as putative drivers of known disease associations
HJ Westra, MJ Peters, T Esko, H Yaghootkar, C Schurmann, J Kettunen, ...
Nature genetics 45 (10), 1238-1243, 2013
16982013
ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition
S Doll, B Proneth, YY Tyurina, E Panzilius, S Kobayashi, I Ingold, M Irmler, ...
Nature chemical biology 13 (1), 91-98, 2017
12522017
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
M Kolz, T Johnson, S Sanna, A Teumer, V Vitart, M Perola, M Mangino, ...
PLoS genetics 5 (6), e1000504, 2009
7092009
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
S Wahl, A Drong, B Lehne, M Loh, WR Scott, S Kunze, PC Tsai, JS Ried, ...
Nature 541 (7635), 81-86, 2017
6752017
Novel biomarkers for pre‐diabetes identified by metabolomics
R Wang‐Sattler, Z Yu, C Herder, AC Messias, A Floegel, Y He, K Heim, ...
Molecular systems biology 8 (1), 615, 2012
6522012
Systematic screen for human disease genes in yeast
LM Steinmetz, C Scharfe, AM Deutschbauer, D Mokranjac, ZS Herman, ...
Nature genetics 31 (4), 400-404, 2002
6392002
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
N Soranzo, TD Spector, M Mangino, B Kühnel, A Rendon, A Teumer, ...
Nature genetics 41 (11), 1182-1190, 2009
5752009
The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity
CJ Gloeckner, N Kinkl, A Schumacher, RJ Braun, E O'Neill, T Meitinger, ...
Human molecular genetics 15 (2), 223-232, 2006
5332006
SLC2A9 influences uric acid concentrations with pronounced sex-specific effects
A Döring, C Gieger, D Mehta, H Gohlke, H Prokisch, S Coassin, G Fischer, ...
Nature genetics 40 (4), 430-436, 2008
4802008
The transcriptional landscape of age in human peripheral blood
MJ Peters, R Joehanes, LC Pilling, C Schurmann, KN Conneely, J Powell, ...
Nature communications 6 (1), 1-14, 2015
4532015
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
A Xue, Y Wu, Z Zhu, F Zhang, KE Kemper, Z Zheng, L Yengo, ...
Nature communications 9 (1), 1-14, 2018
4412018
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
4342010
Differences between human plasma and serum metabolite profiles
Z Yu, G Kastenmüller, Y He, P Belcredi, G Möller, C Prehn, J Mendes, ...
PloS one 6 (7), e21230, 2011
4282011
Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene
R Horvath, G Hudson, G Ferrari, N Fütterer, S Ahola, E Lamantea, ...
Brain 129 (7), 1674-1684, 2006
4262006
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
U Võsa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ...
BioRxiv, 447367, 2018
4182018
Genetic diagnosis of Mendelian disorders via RNA sequencing
LS Kremer, DM Bader, C Mertes, R Kopajtich, G Pichler, A Iuso, TB Haack, ...
Nature communications 8 (1), 1-11, 2017
4062017
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
SF Heeringa, G Chernin, M Chaki, W Zhou, AJ Sloan, Z Ji, LX Xie, ...
The Journal of clinical investigation 121 (5), 2013-2024, 2011
3932011
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ...
Nature genetics 51 (2), 245-257, 2019
3902019
Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study
JC Chambers, M Loh, B Lehne, A Drong, J Kriebel, V Motta, S Wahl, ...
The lancet Diabetes & endocrinology 3 (7), 526-534, 2015
3722015
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