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J. Del-Favero · SciRah

Researcher profile · Semantic Scholar

J. Del-Favero

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J. Del-Favero — researcher profile on SciRah

h-index: 60
Works: 246
Citations: 23K

Most-cited papers

Biological Insights From 108 Schizophrenia-Associated Genetic Loci
S. Ripke, B. Neale, A. Corvin, J. Walters +296 more
2014Nature7,486 citations Open access
Semantic Scholar
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium
C. Marshall, D. Howrigan, D. Merico, B. Thiruvahindrapuram +265 more
2016bioRxiv1,294 citations Open access
Semantic Scholar
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
C. Marshall, D. Howrigan, D. Merico, B. Thiruvahindrapuram +259 more
2016Nature Genetics959 citations Open access
Semantic Scholar
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes
D. Ruderfer, S. Ripke, A. McQuillin, J. Boocock +496 more
2018Cell675 citations Open access
Semantic Scholar
Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
M. Delvaeye, M. Noris, A. de Vriese, C. Esmon +9 more
2009New England Journal of Medicine523 citations Open access
Semantic Scholar
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing
J. Reumers, P. De Rijk, Hui Zhao, A. Liekens +11 more
2011Nature Biotechnology236 citations
Semantic Scholar
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease
Y. Momozawa, M. Mni, Kayo Nakamura, W. Coppieters +25 more
2011Nature Genetics199 citations Open access
Semantic Scholar
Cell‐Free DNA: An Upcoming Biomarker in Transplantation
E. M. Gielis, K. Ledeganck, B. De Winter, J. Del-Favero +4 more
2015American Journal of Transplantation190 citations Open access
Semantic Scholar
Short telomeres in depression and the general population are associated with a hypocortisolemic state.
Mikael Wikgren, M. Maripuu, T. Karlsson, Katarina Nordfjall +7 more
2012Biological Psychiatry184 citations
Semantic Scholar
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations
L. Deprez, S. Weckhuysen, Philip Holmgren, A. Suls +13 more
2010Neurology171 citations
Semantic Scholar
TP53 outperforms other androgen receptor biomarkers to predict abiraterone or enzalutamide outcome in metastatic castration-resistant prostate cancer
B. De Laere, Steffi Oeyen, M. Mayrhofer, Thomas Whitington +33 more
2018Clinical Cancer Research159 citations Open access
Semantic Scholar
BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation
A. Liekens, J. De Knijf, Walter Daelemans, Bart Goethals +2 more
2011Genome Biology142 citations Open access
Semantic Scholar
Genetic variants in microRNA genes: impact on microRNA expression, function, and disease
Sophia Cammaerts, Mojca Strazisar, P. De Rijk, J. Del-Favero
2015Frontiers in Genetics135 citations Open access
Semantic Scholar
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.
B. De Laere, Pieter-Jan van Dam, Thomas Whitington, M. Mayrhofer +8 more
2017European Urology124 citations
Semantic Scholar
SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.
Dries Castermans, Karolien Volders, A. Crepel, L. Backx +12 more
2010Human Molecular Genetics109 citations Open access
Semantic Scholar
Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
E. Ashton, A. Legrand, V. Benoit, Isabelle Roncelin +16 more
2018Kidney International92 citations Open access
Semantic Scholar
Camelid Ig V genes reveal significant human homology not seen in therapeutic target genes, providing for a powerful therapeutic antibody platform
A. Klarenbeek, Khalil El Mazouari, A. Desmyter, C. Blanchetot +9 more
2015mAbs91 citations Open access
Semantic Scholar
The use of plasma donor-derived, cell-free DNA to monitor acute rejection after kidney transplantation.
E. Gielis, K. Ledeganck, A. Dendooven, P. Meysman +10 more
2019Nephrology, Dialysis and Transplantation89 citations Open access
Semantic Scholar
MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets
M. Strazisar, S. Cammaerts, K. van der Ven, D. Forero +10 more
2014Molecular Psychiatry83 citations Open access
Semantic Scholar
Caspase deficiency alters the murine gut microbiome
B. Brinkman, F. Hildebrand, Malgorzata Kubica, D. Goosens +4 more
2011Cell Death and Disease73 citations Open access
Semantic Scholar
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population
K. Nuytemans, Bram Meeus, D. Crosiers, N. Brouwers +11 more
2009Human Mutation71 citations
Semantic Scholar
Plasma donor-derived cell-free DNA kinetics after kidney transplantation using a single tube multiplex PCR assay
E. Gielis, C. Beirnaert, A. Dendooven, P. Meysman +10 more
2018PLoS ONE69 citations Open access
Semantic Scholar
The kynurenine pathway in major depression: haplotype analysis of three related functional candidate genes.
S. Claes, A. Myint, K. Domschke, J. Del-Favero +6 more
2011Psychiatry Research69 citations
Semantic Scholar
miRNA genes and the brain: implications for psychiatric disorders a
Diego A. Forero, K. van der Ven, P. Callaerts, J. Del-Favero
2010Human Mutation69 citations Open access
Semantic Scholar
Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR–based GS‐FLX sequencing
D. Goossens, L. Moens, E. Nelis, An-Sofie Lenaerts +7 more
2009Human Mutation69 citations
Semantic Scholar
Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population
L. Moens, P. De Rijk, J. Reumers, M. V. D. Van Den Bossche +11 more
2011PLoS ONE67 citations Open access
Semantic Scholar
Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future
M. Alaerts, J. Del-Favero
2009Human Mutation51 citations
Semantic Scholar
The Relationship between the Val158Met Catechol-o-Methyltransferase (COMT) Polymorphism and Irritable Bowel Syndrome
P. Karling, Å. Danielsson, Mikael Wikgren, I. Söderström +3 more
2011PLoS ONE49 citations Open access
Semantic Scholar
High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.
M. Hureaux, E. Ashton, K. Dahan, P. Houillier +15 more
2019Kidney International48 citations Open access
Semantic Scholar
Chronic Fatigue Syndrome and DNA Hypomethylation of the Glucocorticoid Receptor Gene Promoter 1F Region: Associations With HPA Axis Hypofunction and Childhood Trauma
E. Vangeel, F. Van Den Eede, T. Hompes, B. Izzi +5 more
2015Psychosomatic Medicine43 citations
Semantic Scholar
Associations between common arginine vasopressin 1b receptor and glucocorticoid receptor gene variants and HPA axis responses to psychosocial stress in a child psychiatric population.
D. van West, J. Del-Favero, D. Deboutte, C. van Broeckhoven +1 more
2010Psychiatry Research40 citations
Semantic Scholar
A network of synaptic genes associated with schizophrenia and bipolar disorder.
D. Forero, L. Herteleer, Sonia De Zutter, K. Norrback +4 more
2016Schizophrenia Research39 citations
Semantic Scholar
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Eduardo A. Maury, Maxwell A. Sherman, G. Genovese, Thomas G. Gilgenast +364 more
2023Cell Genomics36 citations Open access
Semantic Scholar
Targeted screening and validation of copy number variations.
S. Ceulemans, K. van der Ven, J. Del-Favero
2012Methods in molecular biology36 citations
Semantic Scholar
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
M. V. D. Van Den Bossche, M. Johnstone, Mojca Strazisar, B. Pickard +12 more
2012American Journal of Medical Genetics Part B: Neuropsychiatric Genetics36 citations
Semantic Scholar
Evaluation of a multiplex-PCR detection in combination with an isolation method for STEC O26, O103, O111, O145 and sorbitol fermenting O157 in food.
K. Verstraete, J. Robyn, J. Del-Favero, P. De Rijk +5 more
2012Food microbiology35 citations
Semantic Scholar
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage‐dependent calcium channels in psychiatric disorders
M. V. D. Van Den Bossche, Mojca Strazisar, S. De Bruyne, C. Bervoets +14 more
2012American Journal of Medical Genetics Part B: Neuropsychiatric Genetics31 citations
Semantic Scholar
Identification of rare copy number variants in high burden schizophrenia families
M. V. D. Van Den Bossche, Mojca Strazisar, Sophia Cammaerts, Anthony M. Liekens +8 more
2013American Journal of Medical Genetics Part B: Neuropsychiatric Genetics29 citations
Semantic Scholar
miRVaS: a tool to predict the impact of genetic variants on miRNAs
Sophia Cammaerts, Mojca Strazisar, Jenne Dierckx, J. Del-Favero +1 more
2015Nucleic Acids Research26 citations Open access
Semantic Scholar
Age at first birth in women is genetically associated with increased risk of schizophrenia
G. Ni, J. Gratten, N. Wray, Sang-Hong Lee +297 more
2017Scientific Reports25 citations Open access
Semantic Scholar
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
K. Verstraete, E. van Coillie, H. Werbrouck, S. Van Weyenberg +7 more
2014Toxins25 citations Open access
Semantic Scholar
The skin microbiome of caspase‐14‐deficient mice shows mild dysbiosis
M. Kubica, F. Hildebrand, B. Brinkman, D. Goossens +7 more
2014Experimental Dermatology23 citations
Semantic Scholar
Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior*
Daniel R. Dries, Yi Zhu, M. Brooks, D. Forero +13 more
2016Journal of Biological Chemistry21 citations Open access
Semantic Scholar
Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population
S. Ceulemans, Sonia De Zutter, L. Heyrman, K. Norrback +5 more
2011Bipolar Disorders21 citations
Semantic Scholar
Less Cognitive and Neurological Deficits in Schizophrenia Patients Carrying Risk Variant in ZNF804A
M. V. D. Van Den Bossche, L. Docx, M. Morrens, Sophia Cammaerts +8 more
2012Neuropsychobiology20 citations
Semantic Scholar
Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical Disease.
D. Proost, J. Saenen, G. Vandeweyer, A. Rotthier +9 more
2017Journal of Molecular Diagnostics19 citations Open access
Semantic Scholar
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability
E. Derks, M. Ayub, K. Chambert, J. Del-Favero +13 more
2013American Journal of Medical Genetics Part B: Neuropsychiatric Genetics18 citations Open access
Semantic Scholar
NR4A2: effects of an "orphan" receptor on sustained attention in a schizophrenic population.
I. Ancín, J. Cabranes, B. Vázquez-Álvarez, J. Santos +4 more
2013Schizophrenia bulletin18 citations Open access
Semantic Scholar
Co-occurrence of Marfan syndrome and schizophrenia: what can be learned?
M. V. D. Van Den Bossche, Kevin L. P. Van Wallendael, Mojca Strazisar, B. Sabbe +1 more
2012European Journal of Medical Genetics17 citations
Semantic Scholar
The genomics of major psychiatric disorders in a large pedigree from Northern Sweden
J. Szatkiewicz, J. Crowley, A. N. Adolfsson, K. Åberg +6 more
2019Translational Psychiatry16 citations Open access
Semantic Scholar

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