Jurgen Del-Favero
#101,814
Most Influential Person Now
Scientist
Jurgen Del-Favero's AcademicInfluence.com Rankings
Jurgen Del-Faverocomputer-science Degrees
Computer Science
#11826
World Rank
#12582
Historical Rank
Machine Learning
#5437
World Rank
#5509
Historical Rank
Artificial Intelligence
#5870
World Rank
#5960
Historical Rank
Database
#8909
World Rank
#9365
Historical Rank
Download Badge
Computer Science
Why Is Jurgen Del-Favero Influential?
(Suggest an Edit or Addition)According to Wikipedia, Jurgen Del-Favero is a Belgian scientist working at the VIB Department of Molecular Genetics at the University of Antwerp. His research is directed towards the identification of susceptibility genes for psychiatric disorders and tools for DNA sequence research. His research, in collaboration with the Swedish research group under the direction of Rolf Adolfsson, indicated that the TPH2 protein is involved in the development of depression and manic depression.
Jurgen Del-Favero's Published Works
Published Works
- De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. (2001) (1076)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death (2003) (881)
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. (2003) (592)
- Meta-analyses of genetic studies on major depressive disorder (2008) (445)
- Thrombomodulin mutations in atypical hemolytic-uremic syndrome. (2009) (420)
- APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy. (2006) (355)
- Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1 (2008) (315)
- novoSNP, a novel computational tool for sequence variation discovery. (2005) (276)
- Mutations in SEPT9 cause hereditary neuralgic amyotrophy (2005) (217)
- Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing (2011) (210)
- Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis (2008) (203)
- De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy (2003) (195)
- Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease (2011) (182)
- Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study (2005) (176)
- Short Telomeres in Depression and the General Population Are Associated with a Hypocortisolemic State (2012) (171)
- Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations (2010) (161)
- Glucocorticoid Receptor Gene-Based SNP Analysis in Patients with Recurrent Major Depression (2006) (156)
- High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy. (2005) (154)
- BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation (2011) (129)
- Microdeletions involving the SCN1A gene may be common in SCN1A‐mutation‐negative SMEI patients (2006) (125)
- Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population. (2006) (124)
- A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression (2003) (104)
- Mutations in SACS cause atypical and late-onset forms of ARSACS (2010) (103)
- The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
- Comprehensive Profiling of the Androgen Receptor in Liquid Biopsies from Castration-resistant Prostate Cancer Reveals Novel Intra-AR Structural Variation and Splice Variant Expression Patterns. (2017) (99)
- SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles. (2010) (95)
- Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects (2009) (94)
- Progranulin locus deletion in frontotemporal dementia (2008) (93)
- Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study (2004) (92)
- Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion. (1998) (91)
- Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS (2009) (90)
- Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region. (2005) (88)
- Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression. (2000) (86)
- Non‐replication of the brain‐derived neurotrophic factor (BDNF) association in bipolar affective disorder: A Belgian patient‐control study (2004) (78)
- MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets (2014) (75)
- Expression profiling of endocrine-disrupting compounds using a customized Cyprinus carpio cDNA microarray. (2006) (74)
- Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study (2001) (73)
- Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population (2009) (71)
- miRNA genes and the brain: implications for psychiatric disorders a (2010) (66)
- Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population (2011) (66)
- Spinocerebellar ataxia type 7 (SCA7) – correlations between phenotype and genotype in one large Belgian family (1999) (65)
- Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR–based GS‐FLX sequencing (2009) (65)
- Familial occipitotemporal lobe epilepsy and migraine with visual aura (2007) (64)
- Effluent impact assessment using microarray-based analysis in common carp: a systems toxicology approach. (2007) (63)
- Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population. (2005) (63)
- The kynurenine pathway in major depression: Haplotype analysis of three related functional candidate genes (2011) (61)
- Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures (2004) (60)
- Gene expression analysis of estrogenic compounds in the liver of common carp (Cyprinus carpio) using a custom cDNA microarray (2007) (59)
- Excess of allele1 for α3 subunit GABA receptor gene (GABRA3) in bipolar patients: a multicentric association study (2002) (59)
- Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European Multicenter Association Study of affective disorders. (2002) (58)
- The corticotropin-releasing hormone binding protein is associated with major depression in a population from Northern Sweden (2003) (58)
- A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder. (2007) (58)
- Camelid Ig V genes reveal significant human homology not seen in therapeutic target genes, providing for a powerful therapeutic antibody platform (2015) (56)
- Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody. (1999) (55)
- De novo KCNQ2 mutations in patients with benign neonatal seizures (2004) (54)
- Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future (2009) (53)
- Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample. (2005) (51)
- Epistatic effect of genes from the dopamine and serotonin systems on the temperament traits of Novelty Seeking and Harm Avoidance (2002) (51)
- A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder (2002) (44)
- The Relationship between the Val158Met Catechol-o-Methyltransferase (COMT) Polymorphism and Irritable Bowel Syndrome (2011) (42)
- Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated population. (2009) (40)
- HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study (2007) (40)
- Gene-based SNP genetic association study of the corticotropin-releasing hormone receptor-2 (CRHR2) in major depression. (2002) (40)
- A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus (2005) (39)
- Response to Zhang et al. (2005) Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major Depression. Neuron 45, 11–16 (2005) (39)
- No implication of brain-derived neurotrophic factor (BDNF) gene in unipolar affective disorder: Evidence from Belgian first and replication patient–control studies (2005) (37)
- Multiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastoma (2010) (36)
- Associations between common arginine vasopressin 1b receptor and glucocorticoid receptor gene variants and HPA axis responses to psychosocial stress in a child psychiatric population (2010) (35)
- Evaluation of a multiplex-PCR detection in combination with an isolation method for STEC O26, O103, O111, O145 and sorbitol fermenting O157 in food. (2012) (33)
- Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not? (2012) (33)
- Sucrose synthase ofArabidopsis: Genomic cloning and sequence characterization (2004) (33)
- SNPbox: a modular software package for large-scale primer design (2005) (32)
- Targeted screening and validation of copy number variations. (2012) (31)
- A network of synaptic genes associated with schizophrenia and bipolar disorder (2016) (28)
- Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after “gamma”-fusion (1991) (28)
- SNPbox: web-based high-throughput primer design from gene to genome (2004) (27)
- Patient-control association study of substance P-related genes in unipolar and bipolar affective disorders. (2005) (27)
- Molecular Interpretation of Expanded RED Products in Bipolar Disorder by CAG/CTG Repeats Located at Chromosomes 17q and 18q (1999) (27)
- Identification of rare copy number variants in high burden schizophrenia families (2013) (27)
- Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families (2008) (26)
- Parametric and nonparametric genome scan analyses for human handedness (2003) (26)
- Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage‐dependent calcium channels in psychiatric disorders (2012) (25)
- Lack of association between the 5HT2A receptor polymorphism (T102C) and unipolar affective disorder in a multicentric European study (2003) (25)
- A qPCR Assay to Detect and Quantify Shiga Toxin-Producing E. coli (STEC) in Cattle and on Farms: A Potential Predictive Tool for STEC Culture-Positive Farms (2014) (24)
- European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder (2002) (23)
- A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes. (1999) (23)
- Genome-wide association study identifies 30 loci associated with bipolar disorder (2019) (22)
- Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation (2005) (22)
- Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case–control study (2003) (21)
- Chasing genes for mood disorders and schizophrenia in genetically isolated populations (2007) (20)
- Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration (1999) (20)
- Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness (2015) (19)
- Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population (2011) (19)
- Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population (2009) (19)
- Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder (1999) (19)
- Lack of association of an insertion/deletion polymorphism in the G protein-coupled receptor 50 with bipolar disorder in a Northern Swedish population. (2006) (19)
- Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior* (2016) (18)
- Trinucleotide repeat expansions: do they contribute to bipolar disorder? (2001) (17)
- Gene copy number variation in schizophrenia (2007) (17)
- Less Cognitive and Neurological Deficits in Schizophrenia Patients Carrying Risk Variant in ZNF804A (2012) (17)
- Major affective disorders and schizophrenia: a common molecular signature? (2006) (17)
- Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in recurrent major depressive disorder (2007) (16)
- NR4A2: effects of an "orphan" receptor on sustained attention in a schizophrenic population. (2013) (16)
- A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes. (1999) (15)
- Arginine vasopressin receptor gene-based single-nucleotide polymorphism analysis in attention deficit hyperactivity disorder (2009) (15)
- The genomics of major psychiatric disorders in a large pedigree from Northern Sweden (2019) (14)
- PCM1 and schizophrenia: A replication study in the Northern Swedish population (2010) (14)
- Co-occurrence of Marfan syndrome and schizophrenia: what can be learned? (2012) (13)
- Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa‐responsive dystonia (2012) (13)
- Lack of association between GABRA3 and unipolar affective disorder: a multicentre study. (2001) (12)
- No allelic association or interaction of three known functional polymorphisms with bipolar disorder in a northern Swedish isolated population (2006) (11)
- No association of the trace amine-associated receptor 6 with bipolar disorder in a northern Swedish population. (2006) (10)
- Lens-free imaging of magnetic particles in DNA assays. (2013) (9)
- Identification of a Drosophila presenilin homologue: evidence of alternatively spliced forms. (1998) (9)
- Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA (1999) (9)
- Dual association of a TRKA polymorphism with schizophrenia (2011) (9)
- No evidence for the involvement of CAG/CTG repeats from within 18q21.33–q23 in bipolar disorder (2000) (8)
- Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration. (1999) (8)
- A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families (2012) (8)
- Use of suppression subtractive hybridization PCR for the development of cDNA arrays for the detection of endocrine disruption in carp (Cyprinus carpio). (2007) (8)
- Manic depressive disorder and chromosome 18 (1998) (7)
- A catalog of hemizygous variation in 127 22q11 deletion patients (2016) (7)
- Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder. (2012) (7)
- Meta-analysis of genetic studies in major depressive disorder (2006) (7)
- YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14. (1999) (6)
- SSHSuite: an integrated software package for analysis of large-scale suppression subtractive hybridization data. (2004) (6)
- novoSNP3: variant detection and sequence annotation in resequencing projects. (2007) (6)
- Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation (1999) (5)
- The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease. (2001) (5)
- Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila (2016) (5)
- Reduced metallothionein expression in colonic Crohn's disease: evidence for it new disease-modifying gene (2008) (4)
- Expanded RED products and loci containing CAG/CTG repeats on chromosome 17 (ERDA1) and chromosome 18 (CTG18.1) in trans‐generational pairs with bipolar affective disorder (2004) (4)
- Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case–control study (2006) (4)
- Direct cloning of PCR products amplified with Pwo DNA polymerase. (1996) (3)
- Pharmacogenetics in Affective Disorders: A Drug Response Approach (2006) (3)
- Method for rapid restriction analysis of YAC clones. (1996) (3)
- Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalents (1994) (2)
- TheTNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease (2001) (2)
- SNPbox: web-based high-throughput primer design with an eye for repetitive sequences. (2007) (2)
- Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in bipolar disorder (2007) (2)
- FC05.05 A genome-wide scan in 10 multiplex families with bipolar disorder (2000) (1)
- The val158met Catechol-O-methyl-transferase (COMT) polymorphism is associated with irritable bowel syndrome-like symptoms (2008) (1)
- P.7.b.005 Arginine vasopressin receptor gene-based single nucleotide polymorphism (SNP) analysis in ADHD (2009) (1)
- M2045 Reduced Metallothionein Expression in Colonic Crohn's Disease: Evidence for a New Disease-Modifying Gene (2008) (1)
- P.1.051 A gene based SNP map analysis of the glucocorticoid receptor gene shows no evidence for association with major depression (2004) (1)
- ack of association between the 5 HT receptor polymorphism ( T 102 C ) 2 A and unipolar affective disorder in a multicentric European study (2016) (1)
- Developmental and social-contextual origins of depressive control-related beliefs and behavior (Cognitive Therapy and Research (August 2001) 25:4) (2001) (1)
- In situ hybridization to plant metaphase chromosomes using digoxigenin labeled nucleic acid sequences (1994) (1)
- Heritability and genetics of personality in healthy families and families with affective disorders from Sweden (2002) (1)
- Genetic association analysis of HPA axis related genes in major depression (2004) (0)
- Rare but Relevant Kidney Disorders (2009) (0)
- ARSACS cause atypical and late-onset forms of SACS Mutations in (2010) (0)
- Anti CD70 Llama glama Fab 27B3 (2015) (0)
- Genome-wide significant evidence for linkage on chromosome 10q in 10 multiplex BP families (2006) (0)
- KIF1B, the First Neuronally Expressed Gene Associated with Multiple Sclerosis (2009) (0)
- Simultaneous Detection and Isolation of Shiga Toxin Producing E. coli O157 (NSF and SF), O26, O103, O111, and O145 from food and cattle faeces; evaluation and validation (2012) (0)
- Triplet repeat expansions and psychiatric disorders (1998) (0)
- Structure of a Llama Glama Fab 48A2 against human cMet (2015) (0)
- Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila (2016) (0)
- Presenilins and Alzheimer's disease: identification of proteins that interact with presenilin I using the yeast two-hybrid system (1997) (0)
- 12th Annual Scientific Meeting of the Irish Society of Human Genetics, Friday 18th September 2009 (2010) (0)
- Microdeletions of the SCN1A gene may be common in "SCN1A-mutation-negative" SMEI patients (2006) (0)
- Microarray analysis of xeno-estrogen exposed MCF7 breast cancer cells as a tool to developing high-throughput toxicity tests (2004) (0)
- Detection of NRAS, KRAS and BRAF mutations in FFPE derived DNA with a novel targeted resequencing-based diagnostics assay (2016) (0)
- P123 A Functional Promoter Polymorphism in CARD15 Associated with Crohn's Disease (2007) (0)
- Genomic alterations on chromosome 3p21.1 and 17q21.31 in patients with schizophrenia and controls (2008) (0)
- A specific haplotype of the CRH binding protein (CRHBP) gene shows association with major depression in a Northern Swedish population (2002) (0)
- Accurate and precise targeted NGS with BRCA MASTR Plus Dx for BRCA1 and BRCA2 mutation detection in formalin-fixed paraffin-embedded tumor tissue-derived DNA. (2017) (0)
- P.1.231 The brain-derived neurotrophic factor (BDNF) in bipolar affective disorder: A case-control association study (2003) (0)
- P3-162 Increased variability of the tau gene MAPT due to genomic instability (2006) (0)
- Sequence based evaluation of the remaining allele in 22q11.2 deletion patients (2016) (0)
- Prevalence and heterogeneity of androgen receptor splice variants and intra-AR structural variation in patient with castration-resistant prostate cancer. (2017) (0)
- O2-02-08 Duplication of the APP locus in a Dutch family with early-onset Alzheimer dementia (2006) (0)
- P.1.a.004 Associations between AVPR1b and NR3C1 gene variants and HPA axis responses to psychosocial stress (2010) (0)
- Abstract 4328: New perspectives on the use of polo-like kinase 1 as a prognostic biomarker in non-small cell lung cancer (2015) (0)
- Lack of association between GABRA3 and unipolar affective disorder: a multicenter study (2001) (0)
- NBEA, SCAMP5 and AMISYN: three candidate genes for autism involved in regulated secretion (2008) (0)
- Polymorphisms in the 5 ' regulatory region of presenilin 1 associated with an increased risk for early-onset Alzheimers Disease (1999) (0)
- Evidence that not MASS1 but another gene is mutated in a Belgian FEB4 family (2005) (0)
- Complete Genome Sequencing of Monozygotic Twins with Discordant Schizophrenia Phenotypes (2010) (0)
- Genetic analysis of ovarian cancer progression using full genome sequencing (2010) (0)
- BioGraph: Knowledge Discovery and Exploration in the Biomedical Domain (2011) (0)
- A haplotype-based analysis of NF1 gene in bipolar disorder and schizophrenia (2006) (0)
- miRNA DYSFUNCTION IN SCHIZOPHRENIA: GENETIC AND FUNCTIONAL EVIDENCE (2008) (0)
- P.1.06 Brain-derived neurotrophic factor (BDNF) gene in unipolar affective disorder: a Belgian patient-control association study (2004) (0)
- Association between major depressive disorder and a specific haplotype of the CRH binding protein gene (2002) (0)
- Complete genome sequencing of discordant monozygotic twins: finding the differences (2010) (0)
- EXPRESSION IN COLONIC CROHN'S DISEASE: EVIDENCE FOR A NEW DISEASE-MODIFYING GENE STUDY OF MUCOSAL ANTIMICROBIAL PEPTIDES IN PATIENTS WITH INFLAMMATORY BOWEL DISEASE AND AFTER (2008) (0)
- IDENTIFYINGGENES FOR SCHIZOPHRENIA IN A LARGE PEDIGREE FROMA NORTHERN SWEDISH ISOLATED POPULATION (2008) (0)
- A genome-wide scan in extended families with bipolar disorder from an isolated region in North Sweden reveals candidate loci on chromosomes 2q and 9q (2002) (0)
- MAQ, A NOVEL METHOD FOR PCR BASED, HIGH-THROUGHPUT COPY NUMBER VARIATION ANALYSIS APPLIED TO THE 22q11 DELETION SYNDROME (2008) (0)
- Quality control of Complete Genomics sequences of germline and fresh tumor derived DNA samples (2010) (0)
- Lack of association between the 5HT 2A receptor polymorphisms ( T102C) and unipolar affective disorder in a multicentic European study (2003) (0)
- Stress Responsivity in Childhood and Adulthood: Role of the Glucocorticoid Receptor Gene (2009) (0)
- SU28 THE GENOMICS OF BIPOLAR AND SCHIZOPHRENIC DISORDERS IN A LARGE PEDIGREE FROM A NORTHERN SWEDISH ISOLATE (2019) (0)
- HPA axis dysfunction in psychiatry: Genetic background (2007) (0)
- Full genome sequencing of highly rearranged, contaminated tumor samples: a feasibility study (2010) (0)
- VEGF is a modifier gene of amyotrophic lateral sclerosis in humans (2003) (0)
- Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder (2018) (0)
This paper list is powered by the following services:
Other Resources About Jurgen Del-Favero
What Schools Are Affiliated With Jurgen Del-Favero?
Jurgen Del-Favero is affiliated with the following schools: