Holger Prokisch

发表

Review Process File

Yixue Li, Ying He, Tao Xu, 2012 .

MitoP2, an integrated database on mitochondrial proteins in yeast and man

Thomas Meitinger, Jakob C. Mueller, Holger Prokisch, 2004, Nucleic Acids Res..

Network reconstruction for trans acting genetic loci using multi-omics data and prior information

Christian Gieger, Fabian J. Theis, Johann S. Hawe, 2020, bioRxiv.

Konzept für ein deutschlandweites Krankheitsnetz am Beispiel von mitoREGISTER

Claudia Eckert, Klaus A. Kuhn, Thomas Meitinger, 2010, GI Jahrestagung.

MitoP2: the mitochondrial proteome database—now including mouse data

Thomas Meitinger, Andreas Ruepp, Holger Prokisch, 2005, Nucleic Acids Res..

MITOP: database for mitochondria-related proteins, genes and diseases

Thomas Meitinger, Hans-Werner Mewes, Holger Prokisch, 1999, Nucleic Acids Res..

OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data.

Julien Gagneur, Christian Mertes, Holger Prokisch, 2018, American journal of human genetics.

The diagnosis of inborn errors of metabolism by an integrative “multi‐omics” approach: A perspective encompassing genomics, transcriptomics, and proteomics

Holger Prokisch, Christina Ludwig, Sarah L Stenton, 2020, Journal of inherited metabolic disease.

MITOP, the mitochondrial proteome database: 2000 update

Thomas Meitinger, Hans-Werner Mewes, Holger Prokisch, 2000, Nucleic Acids Res..

OUTRIDER: A statistical method for detecting aberrantly expressed genes in RNA sequencing data

Ziga Avsec, Julien Gagneur, Christian Mertes, 2018, bioRxiv.

Deficient methylation and formylation of mt-tRNAMet wobble cytosine in a patient carrying mutations in NSUN3

Michaela Frye, Richard Durbin, Holger Prokisch, 2016, Nature Communications.

META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES IDENTIFIES THREE NEW RISK LOCI FOR ATOPIC DERMATITIS

Christian Gieger, Nicholas J Timpson, Manuel A. R. Ferreira, 2011, Nature Genetics.

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

Katrien Stouffs, Melanie Bahlo, Holger Prokisch, 2016, American journal of human genetics.

Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood

Christian Gieger, Thomas Meitinger, Uwe Völker, 2012, European Journal of Human Genetics.

The transcriptional landscape of age in human peripheral blood

Andres Metspalu, Luigi Ferrucci, Alexander Teumer, 2015, Nature Communications.

Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy

Thomas Meitinger, Julien Gagneur, Holger Prokisch, 2015, American journal of human genetics.

Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency

Thomas Meitinger, Joanna Poulton, Hans-Werner Mewes, 2010, Nature Genetics.

Multiple Loci Are Associated with White Blood Cell Phenotypes

Christian Gieger, Yusuke Nakamura, Kazuhiko Yamamoto, 2011, PLoS genetics.

Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations

Christian Gieger, Thomas Meitinger, Uwe Völker, 2009, PLoS genetics.

Mechanisms for multiple intracellular localization of human mitochondrial proteins.

Thomas Meitinger, Holger Prokisch, Christophe Andreoli, 2004, Mitochondrion.

Novel biomarkers for pre-diabetes identified by metabolomics

Christian Gieger, Thomas Meitinger, Monica Campillos, 2012, Molecular systems biology.

Differences between Human Plasma and Serum Metabolite Profiles

Florian Kronenberg, Gabi Kastenmüller, Lu Xie, 2011, PloS one.

Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy.

Thomas Meitinger, Nathalie Boddaert, Robert Barouki, 2017, American journal of human genetics.

Association between DNA Methylation in Whole Blood and Measures of Glucose Metabolism: KORA F4 Study

Christian Gieger, Sophie Molnos, Simone Wahl, 2016, PloS one.

Risk gene variants for nicotine dependence in the CHRNA5–CHRNA3–CHRNB4 cluster are associated with cognitive performance

Christian Gieger, Thomas Meitinger, Jürgen Gallinat, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

Christian Gieger, Uwe Völker, Mario Falchi, 2009, Nature Genetics.

Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy.

Thomas Meitinger, Guy Lenaers, Patrizia Amati-Bonneau, 2016, American journal of human genetics.

High-density genotyping study identifies four new susceptibility loci for atopic dermatitis

Yusuke Nakamura, Sen Yang, Andre Franke, 2013, Nature Genetics.

Cell Specific eQTL Analysis without Sorting Cells

Jingyuan Fu, Thomas Meitinger, Uwe Völker, 2014, bioRxiv.

Genetic diagnosis of Mendelian disorders via RNA sequencing

Thomas Meitinger, Gabi Kastenmüller, Jerzy Adamski, 2017, Nature Communications.

The Human Blood Metabolome-Transcriptome Interface

Christian Gieger, Fabian J. Theis, Gabi Kastenmüller, 2015, PLoS genetics.

Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.

Marcella Attimonelli, Xiaowu Gai, Lishuang Shen, 2015, Molecular genetics and metabolism.

Guidelines for the use and interpretation of assays formonitoring autophagy (3rd edition)

Sangeeta Khare, Xin Qi, Ying Wang, 2016 .

A genome-wide association study identifies three loci associated with mean platelet volume.

Christian Gieger, Thomas Meitinger, Henry Völzke, 2009, American journal of human genetics.

Extensive alterations of the whole-blood transcriptome are associated with body mass index: results of an mRNA profiling study involving two large population-based cohorts

Christian Gieger, Thomas Meitinger, Uwe Völker, 2015, BMC Medical Genomics.

MITOP, THE MITOCHONDRIAL PROTEOME DATABASE

Thomas Meitinger, Hans-Werner Mewes, Holger Prokisch, 2000 .

Reconstituted TOM core complex and Tim9/Tim10 complex of mitochondria are sufficient for translocation of the ADP/ATP carrier across membranes.

Holger Prokisch, Walter Neupert, Irmgard Sinning, 2003, Molecular biology of the cell.

Assessing Systems Properties of Yeast Mitochondria through an Interaction Map of the Organelle

Peer Bork, Lars M Steinmetz, Lars J Jensen, 2006, PLoS genetics.

Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency

Holger Prokisch, Robert W. Taylor, Langping He, 2019, American journal of human genetics.