Rudi Balling | Academic Influence

Rudi Balling's AcademicInfluence.com Rankings

Rudi Balling

Biology

#2891

World Rank

#4517

Historical Rank

Biotechnology

#96

World Rank

#98

Historical Rank

Computational Biology

#219

World Rank

#220

Historical Rank

Genetics

#539

World Rank

#615

Historical Rank

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Biology

Rudi Balling's Degrees

PhD Genetics University of Cologne
Masters Biology University of Cologne

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Why Is Rudi Balling Influential?

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According to Wikipedia, Rudi Balling is a German geneticist. He is the founding director of the Luxembourg Centre for Systems Biomedicine at the University of Luxembourg He has served as president of the International Mammalian Genome Society and as co-editor of the Annual Review of Nutrition since 2018. In 2016 Balling received Luxembourg's Ordre de Mérite from Prime Minister Xavier Bettel.

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Rudi Balling's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. (1998) (840)
Immune-responsive gene 1 protein links metabolism to immunity by catalyzing itaconic acid production (2013) (707)
Genome-wide, large-scale production of mutant mice by ENU mutagenesis (2000) (696)
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene (1992) (684)
A family of octamer‐specific proteins present during mouse embryogenesis: evidence for germline‐specific expression of an Oct factor. (1989) (620)
Oct‐4: a germline‐specific transcription factor mapping to the mouse t‐complex. (1990) (615)
Antagonistic Interactions between FGF and BMP Signaling Pathways: A Mechanism for Positioning the Sites of Tooth Formation (1997) (607)
Pax: a murine multigene family of paired box-containing genes. (1991) (437)
Impaired insulin secretory capacity in mice lacking a functional vitamin D receptor (2003) (404)
Degree of methylation of transgenes is dependent on gamete of origin (1987) (403)
Pax genes and organogenesis (1997) (386)
Teeth. Where and how to make them. (1999) (375)
Variations of cervical vertebrate after expression of a Hox-1.1 transgene in mice (1990) (359)
The role of Pax-1 in axial skeleton development. (1994) (349)
Octamer binding proteins confer transcriptional activity in early mouse embryogenesis. (1989) (346)
undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1 (1988) (316)
Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1. (1995) (291)
A role for mel-18, a Polycomb group-related vertebrate gene, during theanteroposterior specification of the axial skeleton. (1996) (282)
Pax1 and Pax9 synergistically regulate vertebral column development. (1999) (272)
De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies. (2017) (272)
Deletion of deoxyribonucleic acid binding domain of the vitamin D receptor abrogates genomic and nongenomic functions of vitamin D. (2002) (271)
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36 (2002) (242)
Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice (1989) (239)
Pax1 is expressed during development of the thymus epithelium and is required for normal T-cell maturation. (1996) (232)
Systems medicine and integrated care to combat chronic noncommunicable diseases (2011) (230)
Integrating Pathways of Parkinson's Disease in a Molecular Interaction Map (2013) (230)
Revolutionizing medicine in the 21st century through systems approaches. (2012) (227)
1α,25-dihydroxyvitamin D3 is a potent suppressor of interferon-γ mediated macrophage activation (2005) (226)
Overexpression of activin A in the skin of transgenic mice reveals new activities of activin in epidermal morphogenesis, dermal fibrosis and wound repair (1999) (223)
Humanized mice for modeling human infectious disease: challenges, progress, and outlook. (2009) (221)
The Notch ligand Jagged1 is required for inner ear sensory development (2001) (214)
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy (2015) (211)
A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine. (1988) (207)
Making sense of big data in health research: Towards an EU action plan (2016) (205)
The hallmarks of Parkinson's disease (2013) (205)
From hype to reality: data science enabling personalized medicine (2018) (203)
Global implementation of genomic medicine: We are not alone (2015) (183)
Diseases as network perturbations. (2010) (182)
De novo mutations in HCN1 cause early infantile epileptic encephalopathy (2014) (182)
A role for Pax-1 as a mediator of notochordal signals during the dorsoventral specification of vertebrae. (1993) (180)
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes (2014) (170)
The P4 Health Spectrum – A Predictive, Preventive, Personalized and Participatory Continuum for Promoting Healthspan (2017) (170)
Neurodegeneration by Activation of the Microglial Complement–Phagosome Pathway (2014) (158)
A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36 (1995) (149)
Cloning and expression analysis of a novel mesodermally expressed cadherin. (1995) (146)
1alpha,25-Dihydroxyvitamin D3 is a potent suppressor of interferon gamma-mediated macrophage activation. (2005) (145)
Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures (2018) (144)
Analysis of the Pax-3 gene in the mouse mutant splotch. (1993) (138)
Targeted disruption of Pax1 defines its null phenotype and proves haploinsufficiency. (1998) (137)
Functional Annotation of Mouse Genome Sequences (2001) (136)
Characterization of Differentiated SH-SY5Y as Neuronal Screening Model Reveals Increased Oxidative Vulnerability (2016) (131)
ENU mutagenesis: analyzing gene function in mice. (2001) (130)
Pax1 and Pax9 activate Bapx1 to induce chondrogenic differentiation in the sclerotome (2003) (129)
The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor (1998) (127)
Large scale ENU screens in the mouse: genetics meets genomics. (1998) (126)
GARP: a key receptor controlling FOXP3 in human regulatory T cells (2009) (122)
A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51 (2015) (120)
Systems genomics evaluation of the SH-SY5Y neuroblastoma cell line as a model for Parkinson’s disease (2014) (119)
Systematic approaches to mouse mutagenesis. (2001) (114)
Expression of avian Pax1 and Pax9 is intrinsically regulated in the pharyngeal endoderm, but depends on environmental influences in the paraxial mesoderm. (1996) (113)
Conditional inactivation of Sox9: A mouse model for campomelic dysplasia (2002) (112)
Structure, expression and chromosomal location of the Oct-4 gene (1991) (110)
Separate elements cause lineage restriction and specify boundaries of Hox-1.1 expression. (1991) (109)
Targeted Disruption of the Peptide Transporter Pept2 Gene in Mice Defines Its Physiological Role in the Kidney (2003) (109)
COVID-19 Disease Map, building a computational repository of SARS-CoV-2 virus-host interaction mechanisms (2020) (107)
Notochord-dependent expression of MFH1 and PAX1 cooperates to maintain the proliferation of sclerotome cells during the vertebral column development. (1999) (103)
Mice, microbes and models of infection (2003) (95)
Erratum: Corrigendum: The European dimension for the mouse genome mutagenesis program (2004) (95)
Thymopoiesis requires Pax9 function in thymic epithelial cells (2002) (94)
Initial steps of myogenesis in somites are independent of influence from axial structures. (1994) (92)
Pax genes and organogenesis: Pax9 meets tooth development. (1998) (88)
Parkinson’s disease-associated alterations of the gut microbiome predict disease-relevant changes in metabolic functions (2020) (86)
An action plan for pan-European defence against new SARS-CoV-2 variants (2021) (86)
The ventralizing effect of the notochord on somite differentiation in chick embryos (1993) (84)
Critical transitions in chronic disease: transferring concepts from ecology to systems medicine. (2015) (82)
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia. (2015) (81)
Reverse engineering and verification of gene networks: principles, assumptions, and limitations of present methods and future perspectives. (2009) (79)
Systems medicine disease maps: community-driven comprehensive representation of disease mechanisms (2018) (78)
Zic1 regulates the patterning of vertebral arches in cooperation with Gli3 (1999) (78)
Position-specific activity of the Hox1.1 promoter in transgenic mice. (1990) (75)
Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice (1995) (75)
PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida. (1996) (74)
Expression and function of Pax 1 during development of the pectoral girdle. (1994) (73)
MINERVA—a platform for visualization and curation of molecular interaction networks (2016) (68)
Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse. (1999) (65)
Gene Regulatory Network Inference of Immunoresponsive Gene 1 (IRG1) Identifies Interferon Regulatory Factor 1 (IRF1) as Its Transcriptional Regulator in Mammalian Macrophages (2016) (65)
Systems medicine approaches for the definition of complex phenotypes in chronic diseases and ageing. From concept to implementation and policies. (2014) (64)
A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy. (2019) (64)
Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract. (2001) (63)
The large-scale Munich ENU-mouse-mutagenesis screen (2000) (63)
The clinical-chemical screen in the Munich ENU Mouse Mutagenesis Project: screening for clinically relevant phenotypes (2000) (61)
Progressive loss of PAX9 expression correlates with increasing malignancy of dysplastic and cancerous epithelium of the human oesophagus (2002) (61)
Parkinson’s disease mouse models in translational research (2011) (61)
A look into the future of the COVID-19 pandemic in Europe: an expert consultation (2021) (61)
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study (2018) (60)
Evaluating the Use of Circulating MicroRNA Profiles for Lung Cancer Detection in Symptomatic Patients. (2020) (60)
The battle of two genomes: genetics of bacterial host/pathogen interactions in mice (2001) (59)
Analysis of limb patterning in BMP-7-deficient mice. (1996) (59)
Pax-1, a regulator of sclerotome development is induced by notochord and floor plate signals in avian embryos (1995) (58)
PLAU inferred from a correlation network is critical for suppressor function of regulatory T cells (2012) (55)
The role of regulatory T cells in neurodegenerative diseases (2013) (55)
Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline. (2016) (52)
Community-driven roadmap for integrated disease maps (2018) (51)
Murine genes with homology to Drosophila segmentation genes. (1988) (51)
Reduced intragraft mRNA expression of matrix metalloproteinases Mmp3, Mmp12, Mmp13 and Adam8, and diminished transplant arteriosclerosis in Ccr5‐deficient mice (2004) (49)
Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene. (2001) (48)
A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease (2018) (45)
Tailchaser (Tlc): A new mouse mutation affecting hair bundle differentiation and hair cell survival (1999) (44)
Large‐Scale N‐Ethyl‐N‐Nitrosourea Mutagenesis of Mice – from Phenotypes to Genes (2000) (44)
Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse. (2001) (43)
The Luxembourg Parkinson’s Study: A Comprehensive Approach for Stratification and Early Diagnosis (2018) (43)
Similar α‐Synuclein staining in the colon mucosa in patients with Parkinson's disease and controls (2016) (42)
Influenza H3N2 infection of the collaborative cross founder strains reveals highly divergent host responses and identifies a unique phenotype in CAST/EiJ mice (2016) (42)
Tumorigenesis and eye abnormalities in transgenic mice expressing MSV-SV40 large T-antigen. (1990) (41)
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish (2019) (41)
Toward Omics-Based, Systems Biomedicine, and Path and Drug Discovery Methodologies for Depression-Inflammation Research (2016) (40)
Insertion of a bacterial gene into the mouse germ line using an infectious retrovirus vector. (1985) (39)
Integration and Visualization of Translational Medicine Data for Better Understanding of Human Diseases (2016) (38)
Emergence of the silicon human and network targeting drugs. (2012) (38)
Reliable recovery of inbred mouse lines using cryopreserved spermatozoa (1999) (38)
In Situ Gene Expression Analysis During BMP2-induced Ectopic Bone Formation in Mice Shows Simultaneous Endochondral and Intramembranous Ossification (2003) (37)
Screening for dysmorphological abnormalities—a powerful tool to isolate new mouse mutants (2000) (37)
A roadmap towards personalized immunology (2018) (37)
Commentaries on “Informatics and Medicine: From Molecules to Populations” (2008) (36)
A systems medicine clinical platform for understanding and managing non- communicable diseases. (2014) (36)
The biochemical metabolite screen in the Munich ENU Mouse Mutagenesis Project: determination of amino acids and acylcarnitines by tandem mass spectrometry (2000) (34)
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features (2017) (33)
A locus for radiation-induced gastroschisis on mouse Chromosome 7 (1998) (33)
MIC‐MAC: An automated pipeline for high‐throughput characterization and classification of three‐dimensional microglia morphologies in mouse and human postmortem brain samples (2019) (33)
Spatio‐temporal distribution of chondromodulin‐I mRNA in the chicken embryo: Expression during cartilage development and formation of the heart and eye (1999) (31)
Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH). (1992) (30)
V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice (2002) (30)
ROS networks: designs, aging, Parkinson’s disease and precision therapies (2020) (28)
Inhibitory action of BMPs on Pax1 expression and on shoulder girdle formation during limb development (1998) (28)
Finding and sharing: new approaches to registries of databases and services for the biomedical sciences (2010) (27)
Development of the skeletal system. (1992) (27)
Pax genes and sclerotome development (1996) (27)
The mouse brain metabolome: region-specific signatures and response to excitotoxic neuronal injury. (2015) (27)
From systems biology to systems biomedicine. (2012) (27)
Common diseases alter the physiological age-related blood microRNA profile (2020) (27)
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders (2020) (26)
Pax Genes and Skeletal Development (1996) (26)
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders (2017) (25)
COVID19 Disease Map, a computational knowledge repository of virus–host interaction mechanisms (2021) (24)
Fibroblast mitochondria in idiopathic Parkinson’s disease display morphological changes and enhanced resistance to depolarization (2020) (24)
Towards a European strategy to address the COVID-19 pandemic (2021) (24)
Identification of immunological relevant phenotypes in ENU mutagenized mice (2000) (22)
A new Pax gene, Pax-9, maps to mouse Chromosome 12 (2004) (22)
Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts. (2001) (21)
ENU Mouse Mutagenesis: Generation of Mouse Mutants with Aberrant Plasma IgE Levels (2001) (21)
Isolation of the PAX9 cDNA from adult human esophagus (2009) (21)
CRABP and the teratogenic effects of retinoids. (1991) (21)
PARK7/DJ-1 promotes pyruvate dehydrogenase activity and maintains Treg homeostasis during ageing (2019) (19)
Genetic and molecular control of folate-homocysteine metabolism in mutant mice (2002) (19)
Cadherin‐11 is highly expressed in rhabdomyosarcomas and during differentiation of myoblasts in vitro (1999) (19)
Structure, expression and chromosomal localization of Zfp-1, a murine zinc finger protein gene. (1989) (19)
Deep sequencing of sncRNAs reveals hallmarks and regulatory modules of the transcriptome during Parkinson’s disease progression (2021) (19)
Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013)) (2017) (19)
FOXP3: required but not sufficient. the role of GARP (LRRC32) as a safeguard of the regulatory phenotype. (2010) (17)
Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects (2017) (17)
Understanding complexity in neurodegenerative diseases: in silico reconstruction of emergence (2012) (17)
Neurodegeneration and neuroinflammation are linked, but independent of alpha‐synuclein inclusions, in a seeding/spreading mouse model of Parkinson's disease (2020) (17)
Comparative analysis of the genomic organization of Pax9 and its conserved physical association with Nkx2-9 in the human, mouse, and pufferfish genomes (2001) (17)
Embryonic development of selectively vulnerable neurons in Parkinson’s disease (2017) (16)
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy (2018) (15)
Platelet mitochondrial membrane potential in Parkinson's disease (2014) (14)
The undulated mouse and the development of the vertebral column. Is there a human PAX-1 homologue? (1994) (13)
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy (2020) (13)
Dynamic cumulative activity of transcription factors as a mechanism of quantitative gene regulation (2007) (13)
Functional Genomics, Proteomics, Metabolomics and Bioinformatics for Systems Biology (2013) (13)
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes (2020) (12)
Great times for mouse genetics: getting ready for large-scale ENU-mutagenesis (2000) (12)
Erratum to: Making sense of big data in health research: towards an EU action plan (2016) (12)
Identification of VIMP as a gene inhibiting cytokine production in human CD4+ effector T cells (2020) (12)
COVID-19 Disease Map, a computational knowledge repository of SARS-CoV-2 virus-host interaction mechanisms (2020) (11)
The molecular and genetic analysis of mouse development. (1992) (10)
Aey 2 , a New Mutation in the b B 2-Crystallin – Encoding Gene of the Mouse (2001) (10)
Viva Europa, a Land of Excellence in Research and Innovation for Health and Wellbeing (2017) (10)
Connecting environmental exposure and neurodegeneration using cheminformatics and high resolution mass spectrometry: potential and challenges. (2019) (9)
The genetics of skeletal development. (1993) (9)
A non‐functioning vitamin D receptor predisposes to leukaemoid reactions in mice (2010) (9)
Rare ABCA7 variants in 2 German families with Alzheimer disease (2018) (9)
COVID‐19 Disease Map, a computational knowledge repository of virus‐host interaction mechanisms (2021) (8)
Segment-specific expression of the gap junction gene connexin31 during hindbrain development (1997) (8)
Mitochondria interaction networks show altered topological patterns in Parkinson’s disease (2020) (7)
Accelerating the Development and Validation of New Value-Based Diagnostics by Leveraging Biobanks (2016) (7)
Molecular basis for skeletal variation: insights from developmental genetic studies in mice. (2007) (7)
Author Correction: COVID-19 Disease Map, building a computational repository of SARS-CoV-2 virus-host interaction mechanisms (2020) (7)
Systems Biology (2013) (7)
Pituitary Tumor Transforming Gene 1 Orchestrates Gene Regulatory Variation in Mouse Ventral Midbrain During Aging (2020) (6)
From parathyroid to thymus, via glial cells (2000) (6)
Rbt (rabo torcido), a new mouse skeletal mutation involved in anteroposterior patterning of the axial skeleton, maps close to the ts (tail-short) locus and distal to the sox9 locus on chromosome 11 (1996) (6)
On different aspects of network analysis in systems biology (2013) (5)
Chromosomal localization of the murine cadherin-11 (1995) (5)
COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight (2020) (4)
Maintaining your immune system--one method for enhanced longevity. (2004) (4)
Large-scale validation of miRNAs by disease association, evolutionary conservation and pathway activity (2019) (4)
DJ‐1 depletion prevents immunoaging in T‐cell compartments (2022) (4)
From mouse genetics to systems biology (2007) (4)
Computational Infrastructures for Data and Knowledge Management in Systems Biology (2013) (4)
We need more mutants: Plans for a large scale ENU mouse mutagenesis screen (1998) (4)
Neurological Diseases from a Systems Medicine Point of View. (2016) (4)
AsthmaMap: an interactive knowledge repository for mechanisms of asthma. (2020) (3)
Development of the vertebral column: Morphogenesis and genes (1996) (3)
"4D Biology for health and disease" workshop report. (2011) (3)
Genes associated with Parkinson's disease respond to increasing polychlorinated biphenyl levels in the blood of healthy females. (2019) (3)
Standard Peripheral Blood Mononuclear Cell Cryopreservation Selectively Decreases Detection of Nine Clinically Relevant T Cell Markers (2021) (3)
Genes associated with Parkinson's disease respond to increasing polychlorinated biphenyl levels in the blood of healthy females (2018) (3)
Deep sncRNA-seq of the PPMI cohort to study Parkinson’s disease progression (2020) (2)
Sudden and unexpected (2007) (2)
LSC Abstract – The AsthmaMap: Towards a community-driven reconstruction of asthma-relevant pathways and networks (2016) (2)
From Diagnosing Diseases to Predicting Diseases (2019) (2)
Quantitative trait locus mapping identifies a locus linked to striatal dopamine and points to collagen IV alpha‐6 chain as a novel regulator of striatal axonal branching in mice (2021) (2)
Staining for unphosphorylated alpha-synuclein in the colon mucosa. No difference between patients with Parkinson's disease and healthy controls (2015) (2)
Mapping of the Mod-1 locus on mouse Chromosome 9 (2004) (2)
DISCOVERY AND FUNCTIONAL CHARACTERIZATION OF NEW GENES BY LARGE SCALE ENU MUTAGENESIS IN MICE (1999) (2)
Mitochondria-mitochondria interaction networks show altered topological patterns in Parkinson’s disease (2020) (2)
Design principles of ROS dynamic networks relevant to precision therapies for age-related diseases (2019) (1)
Moratorium call (1988) (1)
The role of homeobox genes in mammalian development (1990) (1)
Standard PBMC cryopreservation selectively decreases detection of nine clinically-relevant T-cell markers (2021) (1)
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy (2018) (1)
Quantitative trait locus mapping identifies Col4a6 as a novel regulator of striatal dopamine level and axonal branching in mice (2020) (1)
The genetic map around the tail kinks (tk) locus on mouse Chromosome 9 (2004) (1)
Strain- and age-dependent features of the nigro-striatal circuit in three common laboratory mouse strains, C57BL/6J, A/J, and DBA/2J - Implications for Parkinson’s disease modeling (2020) (1)
EATRIS - Infrastructure bridges Basic Research and Medical Innovation (2009) (1)
ROS networks: designs, aging, Parkinson’s disease and precision therapies (2020) (1)
Systems medicine disease maps: community-driven comprehensive representation of disease mechanisms (2018) (1)
[Transgenic mice--biological fundamentals, practices and applications]. (1994) (1)
Fine genetic mapping of the proximal part of mouse Chromosome 2 excludes Pax-8 as a candidate gene for Danforth's short tail (Sd) (2004) (1)
A versatile and interoperable computational framework for the analysis and modeling of COVID-19 disease mechanisms (2022) (1)
Synaptopathies Heat Up: Mutations in STX1B in Fever-Associated Epilepsies (2015) (1)
UvA-DARE (Digital Academic Repository) Embryonic development of selectively vulnerable neurons in Parkinson's disease (2017) (0)
Search for downstream target genes of Pax1 and Pax9 (1999) (0)
Fighting the Diseases of the Future (2011) (0)
Oxidative stress and altered mitochondrial dynamics in neurodegenerative processes (2016) (0)
Development(s) in mouse genetics. (1990) (0)
Reborn for a new era (2000) (0)
Dynamic modelling of ROS management and ROS-induced mitophagy (2014) (0)
Mouse genetics and the development of vertebral column development (1994) (0)
Clinically Relevant T Cell Markers Cryopreservation Selectively Decreases Detection of Nine Standard Peripheral Blood Mononuclear Cell (2021) (0)
Neurodegeneration by a microglial complement-phagosome pathway (2015) (0)
Analysis of mitochondrial membrane potential in idiopathic Parkinson's disease: A case-control study (2014) (0)
Transcriptional activity of the octamer motif in embryonic stem cells and preimplantation embryos. (1989) (0)
Workshop Report: Systems Genetics of Neurodegenerative Disease, a Summer School in Systems Medicine, 25th August−1st September 2017 (2019) (0)
Influenza H3N2 infection of the collaborative cross founder strains reveals highly divergent host responses and identifies a unique phenotype in CAST/EiJ mice (2016) (0)
Publisher Correction: Age at onset as stratifier in idiopathic Parkinson’s disease – effect of ageing and polygenic risk score on clinical phenotypes (2022) (0)
ROS-activated signaling network: dynamic modelling and design principles study (2014) (0)
Toward Omics-Based, Systems Biomedicine, and Path and Drug Discovery Methodologies for Depression-Inflammation Research (2015) (0)
A network-based approach to identify hidden non-differentially-expressed key genes (2014) (0)
Constructing a comprehensive map of Parkinson’s disease to elucidate underlying mechanisms of its multifaceted molecular pathology (2012) (0)
Systems genomics evaluation of the SH-SY5Y neuroblastoma cell line as a model for Parkinson’s disease (2014) (0)
P04.01 Characterization of microglia/macrophage phenotypes in glioma patient-derived xenograft mouse models (2016) (0)
From Developmental Biology to Developmental Toxicology (2000) (0)
Modeling cellular ROS defense in mitochondrial-related diseases (2013) (0)
COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight [version 1; peer review: 3 approved with reservations] (2021) (0)
Mitochondria interaction networks show altered topological patterns in Parkinson’s disease (2020) (0)
Phenotyping of host-pathogen interactions in mice. In Standards of Mouse Model Phenotyping (2006) (0)
Celebrating 40 Years of the Annual Review of Nutrition. (2021) (0)
A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes (2020) (0)
Rare coding variants in GABAA receptor encoding genes in genetic generalized epilepsies: an exome-based case-control study (2018) (0)
Parkinson’s disease-associated alterations of the gut microbiome predict disease-relevant changes in metabolic functions (2020) (0)
Systems Biology of the Liver: Systems biology and clinics face à face (2013) (0)
Drug Toxicity in Embryonic Development; Chapter 4: Axial Skeleton (1996) (0)
Establishment of Inducible Expression Systems to Study the Role of STAT-Transcription Factors in AML (2003) (0)
ROS homeostasis in a dynamic model: How to save PD neuron? (2014) (0)
Addressing the Increased Expectations of Nutrition. (2019) (0)
A roadmap towards personalized immunology (2018) (0)
FAM13A regulates maturation and effector functions of natural killer cells (2020) (0)
inferred from a correlation network is critical for suppressor function of regulatory T cells (2013) (0)
Making sense of big data in health research: Towards an EU action plan (2016) (0)
4. Genetik-Workshop des Robert Koch-Instituts 2/99 in Berlin (1999) (0)
MIC-MAC: High-throughput analysis of three-dimensional microglia morphology in mammalian brains (2018) (0)
A kinetic model and design principles study of cellular ROS defence and its failure in Parkinson’s disease (2012) (0)
The Genetics of Vertebral Column Development (1997) (0)
eTRIKS Master Tree Package (2017) (0)
Author Correction: EMPReSS: standardized phenotype screens for functional annotation of the mouse genome (2022) (0)
Metabolic profile of normal and injured brain (2015) (0)
COVID-19 Disease Map, building a computational repository of SARS-CoV-2 virus-host interaction mechanisms (2020) (0)
15. Mainzer Allergie-Workshop 2003 (2003) (0)
Phenotyping of Host‐Pathogen Interactions in Mice (2008) (0)
COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight [version 1; peer review: awaiting peer review] (2020) (0)
Author Correction: COVID-19 Disease Map, building a computational repository of SARS-CoV-2 virus-host interaction mechanisms (2020) (0)
Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data (2017) (0)
New Probe for early detection of epithelial dysplasia of the stratified squamous epithelium and for tumor diagnosis and tumor therapy of squamous (1996) (0)
IDENTIFICATION OF A RARE GENE VARIANT THAT IS ASSOCIATED WITH FAMILIAL ALZHEIMER DISEASE AND REGULATES APP EXPRESSION (2017) (0)
Age at onset as stratifier in idiopathic Parkinson’s disease – effect of ageing and polygenic risk score on clinical phenotypes (2022) (0)
DJ-1 depletion slows down immunoaging in T-cell compartments (2021) (0)
Integrating Pathways of Parkinson's Disease in a Molecular Interaction Map (2013) (0)
Nutrition and the 2020 Pandemic. (2020) (0)
Identification of a New Mouse Mutation with Abnormalities of the Eye, AEY12 (2002) (0)
Transgenic technology as a tool (1997) (0)
A large scale mutagenesis in mice : Current status in Germany (1999) (0)
Design principles study of ROS management and ROS-induced mitophagy with a kinetic model (2013) (0)
P05.44 Single-cell transcriptomic analysis of microglia/macrophages in Glioblastoma (2018) (0)
Whose law for sharing research tools? (1998) (0)
Out of Curiosity from Blue Sky Research to Medical Innovation (2019) (0)
Pax genes and sclerotome induction (1996) (0)
Formation of paraxial muscles in vertebrate embryos depends upon interactions between early somites and the neural tube and notochord. Removal of both axial struc- (1994) (0)
Author and Subject Index (2002) (0)
COVID-19 and Beyond: A Call for Action and Audacious Solidarity to All the Citizens and Nations, It Is Humanity’s Fight (2020) (0)
Embryonic development of selectively vulnerable neurons in Parkinson’s disease (2017) (0)
Analysis of critical transitions in Parkinson's disease (2011) (0)
ENTERIC NERVOUS SYSTEM IN PARKINSON’S DISEASE: INCREASED MITOCHONDRIAL DENSITY BUT REDUCED GANGLIA VOLUME (2015) (0)
Erratum to: On Different Aspects of Network Analysis in Systems Biology (2013) (0)
Henning M. Beier (1940-2021): from discovering uteroglobin to shaping reproductive medicine in Germany. (2021) (0)
Scientific Board of the FMP (2007) (0)
ANALYSIS OF MITOCHONDRIAL MEMBRANE POTENTIAL IN THROMBOCYTES FROM PARKINSON’S DISEASE PATIENTS (2015) (0)
Differentiated SH-SY5Y Cells as PD Model for Mitochondrial Dysfunction: From Whole Genome Sequencing to an Educated Design of High-Throughput Experiments (2013) (0)
FAM13A Regulates KLRG1 Expression and Interferon Gamma Production of Natural Killer Cells (2020) (0)
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish (2019) (0)
Curation of complex molecular pathways of Parkinson's disease as a collaborative scientific community effort (2014) (0)
Functional analysis of genes involved in skeletal development. (2000) (0)
Candidate mutations for early-onset lung cancer by family genome sequencing (2011) (0)
Chapter 8: Phenotyping of Host-Pathogen Interactions in Mice (2006) (0)
1 (cid:1) ,25-dihydroxyvitamin D 3 is a potent suppressor of interferon (cid:2) –mediated macrophage activation (2005) (0)
Presenting and sharing clinical data using the eTRIKS Standards Master Tree for tranSMART (2018) (0)
Comparison of ODE-based models for reactive oxygen species regulation system (2014) (0)
ROS-induced regulation of mitophagy and its failure in Parkinson’s disease (2013) (0)
Expression Analysis In Vivo (2006) (0)
Erratum to: Making sense of big data in health research: towards an EU action plan (2016) (0)
Analysis of the spatial and temporal control of Hox 1.1 in transgenic mice (1990) (0)
EATRIS Infrastructure Accelerates Translation (2010) (0)
The bumpy road to personalized healthcare. (2010) (0)
Assignment of the paired box gene Pax1 to rat Chromosome 3 (1995) (0)
macrophage activation mediated γ ,25-dihydroxyvitamin D3 is a potent suppressor of interferon- α 1 (2013) (0)

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