Prokisch H
Prokisch H
Institute of Human Genetics TU-Munich
Verified email at helmholtz-muenchen.de
Title
Cited by
Cited by
Year
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
75832021
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
15132013
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
6632017
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 Genet 5 (6), e1000504, 2009
6562009
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
6122002
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
5792012
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
5472009
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
5152017
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
5002006
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
4422008
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 Genet 6 (2), e1000841, 2010
4052010
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
4002006
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
3482011
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
3442011
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
3412015
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus
S Weidinger, C Gieger, E Rodriguez, H Baurecht, M Mempel, N Klopp, ...
PLoS Genet 4 (8), e1000166, 2008
3172008
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis
L Paternoster, M Standl, CM Chen, A Ramasamy, K Bønnelykke, L Duijts, ...
Nature genetics 44 (2), 187-192, 2012
3112012
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene
K Gempel, H Topaloglu, B Talim, P Schneiderat, BGH Schoser, VH Hans, ...
Brain 130 (8), 2037-2044, 2007
3002007
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
2912015
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA
TB Haack, P Hogarth, MC Kruer, A Gregory, T Wieland, T Schwarzmayr, ...
The American journal of human genetics 91 (6), 1144-1149, 2012
2832012
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