Guy Van Camp

Q: What Schools Are Affiliated With Guy Van Camp

Guy Van Camp is affiliated with the following schools: Vrije Universiteit Brussel, University of Antwerp, University of California, Berkeley, Stanford University

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Guy Van Camp

Computer Science

#5837

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#6160

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Computational Linguistics

#896

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#909

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Machine Learning

#1697

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#1719

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Artificial Intelligence

#1934

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#1967

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Computer Science

Guy Van Camp's Degrees

PhD Computer Science Stanford University
Masters Computer Science University of California, Berkeley
Bachelors Computer Science University of California, Berkeley

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Guy Van Camp'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

2015 ESC Guidelines for the diagnosis and management of pericardial diseases (2015) (1246)
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. (1998) (559)
GJB2 mutations and degree of hearing loss: a multicenter study. (2005) (479)
The hereditary hearing loss homepage (1997) (464)
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics? (2009) (450)
Nonsyndromic hearing impairment: unparalleled heterogeneity. (1997) (358)
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment (2005) (314)
Treatment of Parkinson's disease with pergolide and relation to restrictive valvular heart disease (2004) (304)
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment (1998) (298)
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. (2003) (296)
Nonsyndromic hearing impairment is associated with a mutation in DFNA5 (1998) (295)
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations (1999) (291)
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. (2001) (289)
Nano-targeted induction of dual ferroptotic mechanisms eradicates high-risk neuroblastoma (2018) (273)
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss (1998) (265)
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy (2006) (261)
L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns. (1998) (254)
Occupational Noise, Smoking, and a High Body Mass Index are Risk Factors for Age-related Hearing Impairment and Moderate Alcohol Consumption is Protective: A European Population-based Multicenter Study (2008) (250)
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13) (1999) (249)
CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1 (1995) (233)
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. (2001) (229)
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus. (2001) (216)
A genotype-phenotype correlation for GJB2 (connexin 26) deafness (2004) (212)
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment (2001) (206)
Congenital hearing loss (2017) (202)
L1-associated diseases: clinical geneticists divide, molecular geneticists unite. (1997) (196)
Importance of left ventricular longitudinal function and functional reserve in patients with degenerative mitral regurgitation: assessment by two-dimensional speckle tracking. (2008) (193)
GRM7 variants confer susceptibility to age-related hearing impairment. (2009) (193)
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease (2003) (183)
Two frequent missense mutations in Pendred syndrome. (1998) (179)
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation (2003) (165)
Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studies (2017) (159)
The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors (2007) (156)
Deafness and Hereditary Hearing Loss Overview (2014) (155)
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM (1994) (153)
Recommendations for the Description of Genetic and Audiological Data for Families with Nonsyndromic Hereditary Hearing Impairment (2003) (150)
The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors (2007) (150)
Destruction of Contrast Microbubbles by Ultrasound: Effects on Myocardial Function, Coronary Perfusion Pressure, and Microvascular Integrity (2001) (148)
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. (2006) (148)
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families. (1999) (148)
Function and expression pattern of nonsyndromic deafness genes. (2009) (147)
Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21. (1998) (146)
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. (1999) (146)
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4). (2004) (140)
A dominant-negative GFI1B mutation in the gray platelet syndrome. (2013) (138)
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. (1994) (137)
Second harmonic transthoracic echocardiography: the new reference screening method for the detection of patent foramen ovale. (2004) (134)
The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. (2008) (134)
A deafness mutation isolates a second role for the tectorial membrane in hearing (2005) (130)
Apoptosis in acquired and genetic hearing impairment: The programmed death of the hair cell (2011) (129)
Genetic Studies on Noise-Induced Hearing Loss: A Review (2009) (127)
Connexin-26 mutations in sporadic non-syndromal sensorineural deafness (1998) (126)
Heart valvular disease in patients with Parkinson’s disease treated with high-dose pergolide (2003) (124)
Localization of a gene for otosclerosis to chromosome 15q25-q26. (1998) (120)
Genetics of microtia and associated syndromes (2009) (118)
The contribution of genes involved in potassium‐recycling in the inner ear to noise‐induced hearing loss (2006) (114)
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment. (1998) (114)
KCNQ4: a gene for age‐related hearing impairment? (2006) (113)
Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia (2016) (108)
Determination of the carrier frequency of the common GJB2 (connexin‐26) 35delG mutation in the Belgian population using an easy and reliable screening method (1999) (107)
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome. (1998) (104)
Genotype-phenotype correlation in L1 associated diseases. (1998) (101)
Association between variations in CAT and noise-induced hearing loss in two independent noise-exposed populations. (2007) (100)
Endothelin-3 Gene Mutations in Isolated and Syndromic Hirschsprung Disease (1997) (99)
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36. (2001) (99)
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74. (2011) (97)
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 (2015) (96)
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease (2003) (95)
The influence of genetic variation in oxidative stress genes on human noise susceptibility (2005) (94)
A genome-wide association study for age-related hearing impairment in the Saami (2010) (94)
A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment. (2012) (91)
A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family. (2008) (91)
A duplication in the L1CAM gene associated with X–linked hydrocephalus (1993) (90)
Prognostic Implications of Magnetic Resonance–Derived Quantification in Asymptomatic Patients With Organic Mitral Regurgitation: Comparison With Doppler Echocardiography–Derived Integrative Approach (2017) (90)
Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15. (1995) (89)
Relation between patent foramen ovale and unexplained stroke. (1993) (89)
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells (2003) (88)
Hearing Disability Measured by the Speech, Spatial, and Qualities of Hearing Scale in Clinically Normal-Hearing and Hearing-Impaired Middle-Aged Persons, and Disability Screening by Means of a Reduced SSQ (the SSQ5) (2012) (88)
The DFNA5 gene, responsible for hearing loss and involved in cancer, encodes a novel apoptosis-inducing protein (2011) (88)
Discrimination among thermophilic Campylobacter species by polymerase chain reaction amplification of 23S rRNA gene fragments (1994) (87)
Age-related hearing impairment (ARHI): environmental risk factors and genetic prospects (2003) (87)
GJB2: The spectrum of deafness‐causing allele variants and their phenotype (2004) (86)
The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populations. (2007) (85)
Maternally inherited hearing impairment (2000) (85)
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment (2014) (84)
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment (2007) (84)
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations (2002) (83)
The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule. (1996) (83)
Mitral regurgitation in patients with aortic stenosis undergoing valve replacement (2009) (83)
Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3 (2002) (83)
Targeting of vascular cell adhesion molecule-1 by 18F-labelled nanobodies for PET/CT imaging of inflamed atherosclerotic plaques. (2016) (81)
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus (2005) (80)
Audiometric shape and presbycusis (2009) (78)
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. (2009) (77)
Whole-exome characterization of pancreatic neuroendocrine tumor cell lines BON-1 and QGP-1. (2015) (76)
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene (1999) (76)
Possible association between 3,4-methylenedioxymethamphetamine abuse and valvular heart disease. (2007) (76)
Branchio‐oto‐renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR (2008) (75)
A novel DFNB1 deletion allele supports the existence of a distant cis‐regulatory region that controls GJB2 and GJB6 expression (2010) (74)
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22–24 (2004) (74)
Candidate Gene Association Study for Noise‐induced Hearing Loss in Two Independent Noise‐exposed Populations (2009) (74)
DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System (2016) (73)
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss (2011) (72)
Variations in HSP70 genes associated with noise-induced hearing loss in two independent populations (2009) (72)
Nonsyndromic Hearing Loss (2003) (71)
Pharmacological Levels of Withaferin A (Withania somnifera) Trigger Clinically Relevant Anticancer Effects Specific to Triple Negative Breast Cancer Cells (2014) (71)
Association of Bone Morphogenetic Proteins With Otosclerosis (2007) (71)
Short course radiotherapy with simultaneous integrated boost for stage I-II breast cancer, early toxicities of a randomized clinical trial (2012) (69)
Mutation analysis of the GJB2 (Connexin 26) gene in Egypt (2005) (68)
The etiology of otosclerosis: A combination of genes and environment (2010) (68)
Cardiovascular disease prevention (2014) (67)
The Genetic Landscape of Malignant Pleural Mesothelioma: Results from Massively Parallel Sequencing (2016) (67)
In vivo model of drug-induced valvular heart disease in rats: pergolide-induced valvular heart disease demonstrated with echocardiography and correlation with pathology. (2007) (66)
Effects of valve replacement for aortic stenosis on mitral regurgitation. (2008) (66)
A sensitive and specific diagnostic test for hearing loss using a microdroplet PCR‐based approach and next generation sequencing (2013) (66)
Discrimination among thermophilic Campylobacter species by polymerase chain reaction amplification of 23S rRNA gene fragments (1993) (65)
Pendred syndrome and DFNB4‐mutation screening of SLC26A4 by denaturing high‐performance liquid chromatography and the identification of eleven novel mutations (2004) (65)
Large-scale analysis of DFNA5 methylation reveals its potential as biomarker for breast cancer (2018) (65)
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24. (1997) (64)
Analysis of Gene Polymorphisms Associated with K+ Ion Circulation in the Inner Ear of Patients Susceptible and Resistant to Noise‐induced Hearing Loss (2009) (64)
Long-term acquired everolimus resistance in pancreatic neuroendocrine tumours can be overcome with novel PI3K-AKT-mTOR inhibitors (2016) (64)
In vivo visualization of 111In labeled CD133+ peripheral blood stem cells after intracoronary administration in patients with chronic ischemic heart disease. (2007) (64)
Thoracic Aortic Aneurysm in Infancy in Aneurysms–Osteoarthritis Syndrome Due to a Novel SMAD3 Mutation: Further Delineation of the Phenotype (2013) (63)
Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q. (1995) (62)
Comparison of transthoracic echocardiography with second harmonic imaging with transesophageal echocardiography in the detection of right to left shunts. (2000) (62)
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6. (1996) (62)
Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findings. (1999) (61)
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p. (1997) (61)
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. (2008) (61)
A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1 (2007) (61)
Pericardial effusion in atrial fibrillation ablation: a comparison between cryoballoon and radiofrequency pulmonary vein isolation. (2010) (60)
A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9 (2008) (59)
The Role of Connexins in Human Disease (2003) (59)
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region. (2000) (59)
The risk of new onset heart failure associated with dopamine agonist use in Parkinson's disease. (2012) (57)
The Contribution of GJB2 (Connexin 26) 35delG to Age-Related Hearing Impairment and Noise-Induced Hearing Loss (2007) (57)
Withaferin A induces heme oxygenase (HO-1) expression in endothelial cells via activation of the Keap1/Nrf2 pathway. (2016) (57)
Aortic Valve Replacement Versus Conservative Treatment in Asymptomatic Severe Aortic Stenosis: The AVATAR Trial (2021) (57)
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform (2012) (57)
Molecular characterization of WFS1 in patients with Wolfram syndrome. (2003) (57)
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6. (1995) (56)
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11 (2008) (56)
The M34T allele variant of connexin 26. (2000) (56)
Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31. (1998) (56)
A Genotype-Phenotype Correlation with Gender-Effect for Hearing Impairment Caused by TECTA Mutations (2004) (56)
Rationale and design of the Aortic Valve replAcemenT versus conservative treatment in Asymptomatic seveRe aortic stenosis (AVATAR trial): A randomized multicenter controlled event-driven trial. (2016) (55)
A locus‐specific mutation database for the neural cell adhesion molecule L1CAM (Xq28) (1996) (55)
Deafness Genes and Their Diagnostic Applications (2003) (55)
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells (2005) (55)
Overcoming cetuximab resistance in HNSCC: the role of AURKB and DUSP proteins. (2014) (54)
Longitudinal and Cross-Sectional Phenotype Analysis in a New, Large Dutch DFNA2/KCNQ4 Family (2002) (54)
A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p. (1997) (53)
DFNA5: hearing impairment exon instead of hearing impairment gene? (2004) (53)
Alpha-tectorin involvement in hearing disabilities: one gene – two phenotypes (1999) (53)
Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss (1999) (53)
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene (2009) (52)
X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM gene. (1994) (52)
Otosclerosis: a genetically heterogeneous disease involving at least three different genes. (2002) (52)
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome (1999) (51)
Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing. (1997) (50)
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus (2007) (50)
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe (2002) (50)
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p. (1997) (50)
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families. (2008) (49)
Risk of Cardiac Valve Regurgitation with Dopamine Agonist use in Parkinson’s Disease and Hyperprolactinaemia (2012) (49)
Mutations in the KCNQ 4 gene are responsible for autosomal dominant deafness in four DFNA 2 families (1999) (49)
Prevalence of mechanical dyssynchrony in patients with heart failure and preserved left ventricular function (a report from the Belgian Multicenter Registry on dyssynchrony). (2005) (49)
The deafness gene DFNA5 induces programmed cell death through mitochondria and MAPK-related pathways (2015) (46)
A comprehensive catalogue of the coding and non-coding transcripts of the human inner ear (2016) (46)
Risk of valvular heart disease associated with the use of dopamine agonists in Parkinson’s disease: a systematic review (2009) (46)
Quantification of myocardial blood flow and assessment of its transmural distribution with real-time power modulation myocardial contrast echocardiography. (2003) (46)
A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment (2002) (46)
Mutation in the COCH gene is associated with superior semicircular canal dehiscence (2009) (46)
Prevalence of tinnitus and audiometric shape. (2007) (46)
Punching Holes in Cellular Membranes: Biology and Evolution of Gasdermins. (2021) (46)
Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families (2017) (45)
Methylation analysis of Gasdermin E shows great promise as a biomarker for colorectal cancer (2019) (45)
Amplification and sequencing of variable regions in bacterial 23S ribosomal RNA genes with conserved primer sequences (1993) (45)
Deafness linked to DFNA2: one locus but how many genes? (1999) (45)
Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2. (1997) (44)
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus (1999) (44)
A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3. (1999) (44)
Cardiac troponin T and malondialdehyde modified plasma lipids in haemodialysis patients. (2003) (44)
Whole-Genome Saliva and Blood DNA Methylation Profiling in Individuals with a Respiratory Allergy (2016) (43)
Hereditary Otovestibular Dysfunction and Ménière's Disease in a Large Belgian Family Is Caused by a Missense Mutation in the COCH Gene (2001) (43)
Autosomal recessive Stickler syndrome in two families is caused by mutations in the COL9A1 gene. (2011) (42)
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome (2014) (42)
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH. (2001) (42)
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway (2018) (42)
A yeast model for the study of human DFNA5, a gene mutated in nonsyndromic hearing impairment. (2003) (41)
High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects. (2010) (41)
Structure of 16S and 23S Ribosomal RNA Genes in Campylobacter Species: Phylogenetic Analysis of the Genus Campylobacter and Presence of Internal Transcribed Spacers (1993) (41)
A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome (2015) (40)
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation (2001) (40)
First experience with real-time three-dimensional transoesophageal echocardiography-guided transseptal in patients undergoing atrial fibrillation ablation. (2008) (39)
The predictive value of primary tumor location in patients with metastatic colorectal cancer: A systematic review. (2018) (39)
Effect of Primary Tumor Location on Second‐ or Later‐line Treatment Outcomes in Patients With RAS Wild‐type Metastatic Colorectal Cancer and All Treatment Lines in Patients With RAS Mutations in Four Randomized Panitumumab Studies (2018) (39)
Cardiovascular disease prevention (2014) (39)
Identification of Enteropathogenic Campylobacter Species by Oligonucleotide Probes and Polymerase Chain Reaction Based on 16S rRNA Genes. (1993) (39)
Global and regional parameters of dyssynchrony in ischemic and nonischemic cardiomyopathy. (2005) (38)
A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss (2008) (37)
Non-smoke spontaneous contrast in left atrium intensified by respiratory manoeuvres: a new transoesophageal echocardiographic observation. (1994) (37)
Evidence that intracoronary-injected CD133+ peripheral blood progenitor cells home to the myocardium in chronic postinfarction heart failure. (2007) (37)
A Pilot Genome-Wide Association Study Identifies Potential Metabolic Pathways Involved in Tinnitus (2017) (36)
Ectopic MicroRNA-150-5p Transcription Sensitizes Glucocorticoid Therapy Response in MM1S Multiple Myeloma Cells but Fails to Overcome Hormone Therapy Resistance in MM1R Cells (2014) (36)
A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family (2009) (36)
Doppler myocardial imaging in adult male rats: reference values and reproducibility of velocity and deformation parameters. (2006) (36)
Are MYO1C and MYO1F associated with hearing loss? (2009) (35)
Mutation and Methylation Analysis of Circulating Tumor DNA Can Be Used for Follow‐up of Metastatic Colorectal Cancer Patients (2018) (35)
Audiometric Analyses Confirm a Cochlear Component, Disproportional to Age, in Stapedial Otosclerosis (2006) (35)
Complementary deoxyribonucleic acid cloning and characterization of a putative human axonemal dynein light chain gene. (1997) (35)
Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1). (2003) (35)
Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients. (2008) (34)
Progressive Late-Onset Sensorineural Hearing Loss and Vestibular Impairment with Vertigo (DFNA9/COCH): Longitudinal Analyses in a Belgian Family (2003) (34)
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing (2010) (34)
DFNA5 promoter methylation a marker for breast tumorigenesis (2017) (34)
Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q. (1995) (34)
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). (1998) (33)
The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment. (2000) (33)
A new perspective on the genetics of keratoconus: why have we not been more successful? (2018) (33)
Effect of streptozotocin-induced diabetes on myocardial blood flow reserve assessed by myocardial contrast echocardiography in rats (2008) (32)
The splicing mutant of the human tumor suppressor protein DFNA5 induces programmed cell death when expressed in the yeast Saccharomyces cerevisiae (2012) (32)
DFNA5, a gene involved in hearing loss and cancer: a review. (2012) (31)
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations (2010) (31)
Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population (2011) (31)
A Novel Z-Score–Based Method to Analyze Candidate Genes for Age-Related Hearing Impairment (2004) (31)
Is DFNA5 a susceptibility gene for age-related hearing impairment? (2002) (30)
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss. (1998) (30)
Detection of Rare Nonsynonymous Variants in TGFB1 in Otosclerosis Patients (2009) (30)
Circling behavior in the Ecl mouse is caused by lateral semicircular canal defects (2004) (30)
No Evidence for Association Between the Renin-Angiotensin-Aldosterone System and Otosclerosis in a Large Belgian-Dutch Population (2009) (30)
MYO1F as a candidate gene for nonsyndromic deafness, DFNB15. (2001) (30)
Impact of prosthesis–patient mismatch on mitral regurgitation after aortic valve replacement (2010) (30)
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family. (1994) (30)
Subsidies on low-skilled workers’ social security contributions: the case of Belgium (2011) (29)
Autosomal recessive nonsyndromic hearing loss. (1999) (29)
A new locus for otosclerosis, OTSC10, maps to chromosome 1q41–44 (2011) (29)
Cyproheptadine prevents pergolide-induced valvulopathy in rats: an echocardiographic and histopathological study. (2009) (29)
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment (2019) (28)
GSDME and its role in cancer: From behind the scenes to the front of the stage (2020) (28)
Dose Dependency and Reversibility of Serotonin-Induced Valvular Heart Disease in Rats (2009) (28)
Ca2+-binding protein 2 inhibits Ca2+-channel inactivation in mouse inner hair cells (2017) (28)
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9). (2000) (28)
Autosomal dominant non-syndromal low-frequency sensorineural hearing impairment linked to chromosome 4p16 (DFNA14): statistical analysis of hearing threshold in relation to age and evaluation of vestibulo-ocular functions. (1999) (28)
Familial aggregation of tinnitus: a European multicentre study. (2007) (28)
Interaction between prenatal pesticide exposure and a common polymorphism in the PON1 gene on DNA methylation in genes associated with cardio-metabolic disease risk—an exploratory study (2017) (27)
COL1A1 association and otosclerosis: A meta‐analysis (2012) (27)
Determination of the Potential Tumor-Suppressive Effects of Gsdme in a Chemically Induced and in a Genetically Modified Intestinal Cancer Mouse Model (2019) (27)
Interpretation of pure-tone thresholds in sensorineural hearing loss (SNHL): a review of measurement variability and age-specific references. (2002) (27)
Role of echocardiography in toxic heart valvulopathy. (2009) (27)
Sex-Related Hearing Impairment in Wolfram Syndrome Patients Identified by Inactivating WFS1 Mutations (2003) (26)
DFNB93, a novel locus for autosomal recessive moderate‐to‐severe hearing impairment (2011) (26)
Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia (2010) (26)
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q. (1997) (26)
Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES. (2000) (26)
Expression profiling of migrated and invaded breast cancer cells predicts early metastatic relapse and reveals Krüppel-like factor 9 as a potential suppressor of invasive growth in breast cancer (2013) (26)
Autosomal dominant nonsyndromic hearing impairment. (1999) (26)
Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome (2006) (26)
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3 (2004) (25)
Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study (2007) (25)
Superior vena cava syndrome associated with Nocardia farcinica infection. (1997) (24)
Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population (2008) (24)
High resolution imaging of the mouse inner ear by microtomography: A new tool in inner ear research (2000) (24)
DFNA5, a Gene Involved in Hearing Loss and Cancer: A Review (2012) (24)
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family. (2001) (24)
Cell-Free DNA From Metastatic Pancreatic Neuroendocrine Tumor Patients Contains Tumor-Specific Mutations and Copy Number Variations (2018) (24)
Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649) (2014) (24)
Establishment and characterization of cetuximab resistant head and neck squamous cell carcinoma cell lines: focus on the contribution of the AP-1 transcription factor. (2015) (24)
Intracardiac thrombi associated with antiphospholipid antibodies. (1996) (24)
Nonsyndromic Autosomal Dominant Progressive Sensorineural Hearing Loss: Audiologic Analysis of a Pedigree Linked to DFNA2 (1998) (24)
Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment (2018) (23)
Doppler myocardial imaging in the diagnosis of early systolic left ventricular dysfunction in diabetic rats. (2008) (23)
Transesophageal echocardiography of right atrial metastasis of a hepatocellular carcinoma. (1994) (23)
Redistributive effects of the shift from personal income taxes to indirect taxes: Belgium 1988-93 (2005) (23)
Refined Genetic and Physical Mapping of BPES Type II (1996) (22)
Refined Mapping of a Gene for Autosomal Dominant Progressive Sensorineural Hearing Loss (DFNA5) to a 2-cM Region, and Exclusion of a Candidate Gene That Is Expressed in the Cochlea (1997) (22)
Analysis of inner ear potassium recycling genes as potential factors associated with tinnitus (2012) (22)
Resistance to targeted treatment of gastroenteropancreatic neuroendocrine tumors (2019) (21)
Genetics of Otosclerosis (2009) (21)
A novel DFNA5 mutation does not cause hearing loss in an Iranian family (2007) (21)
Human hereditary hearing impairment: mouse models can help to solve the puzzle (2008) (21)
Fluctuant, progressive hearing loss associated with Menière like vertigo in three patients with the Pendred syndrome. (2001) (21)
Genetic Association Analysis in a Clinically and Histologically Confirmed Otosclerosis Population Confirms Association With the TGFB1 Gene but Suggests an Association of the RELN Gene With a Clinically Indistinguishable Otosclerosis-Like Phenotype (2014) (21)
Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction (2001) (21)
DFNA2/KCNQ4 and its manifestations. (2002) (20)
Effects of surgery on ischaemic mitral regurgitation: a prospective multicentre registry (SIMRAM registry). (2007) (20)
The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction? (1999) (20)
Heritability of audiometric shape parameters and familial aggregation of presbycusis in an elderly Flemish population (2010) (20)
Impact of anesthesia on valvular function in normal rats during echocardiography. (2008) (20)
Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasms. (2019) (20)
A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies (2011) (20)
A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene (2019) (19)
Primary tumor sidedness impacts on prognosis and treatment outcome: results from three randomized studies of panitumumab plus chemotherapy versus chemotherapy or chemotherapy plus bevacizumab in 1st and 2nd line RAS/BRAF WT mCRC (2016) (19)
Deep sequencing of the TP53 gene reveals a potential risk allele for non–small cell lung cancer and supports the negative prognostic value of TP53 variants (2017) (19)
The Gasdermin E Gene Has Potential as a Pan-Cancer Biomarker, While Discriminating between Different Tumor Types (2019) (19)
PDX1 DNA Methylation Distinguishes Two Subtypes of Pancreatic Neuroendocrine Neoplasms with a Different Prognosis (2020) (18)
Focal Sclerosis of Semicircular Canals With Severe DFNA9 Hearing Impairment Caused by a P51S COCH-Mutation: Is There a Link? (2014) (18)
Evaluation of host genetic and viral factors as surrogate markers for HTLV‐1‐associated myelopathy/tropical spastic paraparesis in Peruvian HTLV‐1‐infected patients (2010) (18)
Animal models of organic heart valve disease. (2013) (18)
Molecular characterization and peptide specificity of two Vasoactive Intestinal Peptide (VIP) binding sites in the chicken pineal (1991) (18)
Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization. (1996) (18)
GJB2 (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population (2005) (18)
Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression (1998) (18)
GLI2 promoter hypermethylation in saliva of children with a respiratory allergy (2018) (18)
Autosomal Dominant Low-Frequency Hearing Impairment (DFNA6/14): A Clinical and Genetic Family Study (2002) (17)
Mitochondrial inherited hearing loss. (1998) (17)
Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis (2018) (17)
Is redistribution through indirect taxes equitable (1997) (17)
Bio-effects of ultrasound contrast agents in daily clinical practice: fact or fiction? (2007) (17)
Audiometric analysis of a Belgian family linked to the DFNA10 locus. (2000) (17)
Echocardiographic integrated backscatter for detecting progression and regression of aortic valve calcifications in rats (2013) (17)
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472. (1998) (16)
Genotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MYO6 Mutations (2009) (16)
Aging of preleukemic thymocytes drives CpG island hypermethylation in T-cell acute lymphoblastic leukemia. (2020) (16)
Occurrence of cardiovascular calcifications in normal, aging rats (2012) (16)
Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment (2020) (16)
Molecular diagnostics for hereditary hearing loss in children (2017) (16)
Horizontal neutrality and vertical redistribution with indirect taxes (1997) (16)
Evidence for somatic and germline mosaicism in CRASH syndrome (1998) (16)
Large-scale copy number analysis reveals variations in genes not previously associated with malignant pleural mesothelioma (2017) (15)
The gene for human gap junction protein connexin37 (GJA4) maps to chromosome 1p35.1, in the vicinity of D1S195. (1995) (15)
Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population. (2011) (15)
Prolonged right ventricular ejection delay identifies high risk patients and gender differences in Brugada syndrome. (2015) (15)
Linkage Designer and Linkage Reporter software for automated gene localization studies (1996) (15)
Alpha-tectorin involvement in hearing disabilities: one gene--two phenotypes. (1999) (15)
Native valve endocarditis with aorta-to-left atrial fistula due to Corynebacterium amycolatum. (2003) (15)
Use of potentiometric sensors to study (bio)molecular interactions. (2012) (15)
Impact of second harmonic imaging on the determination of the global and regional left ventricular function by 2D echocardiography: a comparison with MIBI gated SPECT. (2000) (15)
Republished review: Mitral regurgitation in patients with aortic stenosis undergoing valve replacement (2009) (15)
How to monitor cardiac toxicity of chemotherapy: time is muscle! (2013) (15)
Prevalence of potential cardiac resynchronization therapy candidates and actual use of cardiac resynchronization therapy in patients hospitalized for heart failure (2011) (14)
Evaluation of contractile function and inotropic reserve with tissue velocity, strain and strain rate imaging in streptozotocin-induced diabetes. (2010) (14)
A new method for real-time co-registration of 3D coronary angiography and intravascular ultrasound or optical coherence tomography. (2014) (14)
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment (2009) (14)
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21. (1997) (14)
ABSENCE OF TRANSPLACENTAL TRANSFER OF ATRIAL NATRIURETIC PEPTIDE IN THE RAT: DIRECT EXPERIMENTAL EVIDENCE (1995) (14)
Next generation exome sequencing of pancreatic neuroendocrine tumor cell lines BON-1 and QGP-1 reveals different lineages. (2015) (14)
Cardiac and autonomic evaluation in a pediatric population with human immunodeficiency virus (1999) (14)
Familial Aggregation of Pure Tone Hearing Thresholds in an Aging European Population (2013) (14)
Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes. (2002) (13)
What makes personal income taxes progressive? The case of Belgium (2000) (13)
Potentiometric sensors doped with biomolecules as a new approach to small molecule/biomolecule binding kinetics analysis. (2014) (13)
Integrated Backscatter for the In Vivo Quantification of Supraphysiological Vitamin D3-Induced Cardiovascular Calcifications in Rats (2011) (13)
Minimally invasive mitral valve repair for functional mitral regurgitation in severe heart failure: MitraClip versus minimally invasive surgical approach. (2016) (13)
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment (2000) (13)
The unit of analysis in microsimulation models for personal income taxes: fiscal unit or household? (1998) (12)
Clinical presentation of the DFNA loci where causative genes have not yet been cloned. DFNA4, DFNA6/14, DFNA7, DFNA16, DFNA20 and DFNA21. (2002) (12)
Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2 (2010) (12)
A prospective non-randomized open label multi-center study to evaluate the effect of an iliofemoral arteriovenous fistula on blood pressure in patients with therapy-resistant hypertension (2013) (12)
Adult onset Kawasaki disease diagnosed by the echocardiographic demonstration of coronary aneurysms. (1995) (12)
A Review of Progressive Phenotypes in Nonsyndromic Autosomal Dominant Hearing Impairment (2003) (12)
A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region (2000) (12)
Further Delineation of the DFNA5 Phenotype: Results of Speech Recognition Tests (2002) (12)
The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner ear. (1999) (12)
DFNA10/EYA4--the clinical picture. (2002) (12)
Influence of heart rate reduction on Doppler myocardial imaging parameters in a small animal model. (2009) (12)
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13E. (1993) (12)
Clinical and genetic analysis of two Tunisian otosclerosis families (2007) (12)
Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration (2016) (12)
Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21. (1992) (12)
Prevalence, Determinants, and Prognostic Significance of Pulmonary Hypertension in Elderly Patients Admitted with Acute Decompensated Heart Failure: A Report from the BIO‐HF Registry (2015) (12)
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss (2011) (12)
Quantification of mitral regurgitation by the automated cardiac output method: an in vitro and in vivo study. (1998) (11)
Concentration-related response potentiometric titrations to study the interaction of small molecules with large biomolecules. (2014) (11)
Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research. (1998) (11)
Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11. (1997) (11)
Contrast harmonic imaging improves the evaluation of left ventricular function in ventilated patients: comparison with transesophageal echocardiography. (2004) (11)
Clinical applications of (epi)genetics in gastroenteropancreatic neuroendocrine neoplasms: Moving towards liquid biopsies (2019) (11)
Imaging of Myocardial Fibrosis and Its Functional Correlates in Aortic Stenosis: A Review and Clinical Potential (2018) (11)
Recognition of pacemaker lead infection by transoesophageal echocardiography (1991) (11)
Pulmonary stenosis caused by extrinsic compression of an aortic pseudoaneurysm of a composite aortic graft. (1999) (11)
Cardiac Resynchronization Therapy Optimization: A Comprehensive Approach (2019) (11)
Ophthalmologic complications in primary pulmonary hypertension. (1990) (10)
A novel missense mutation in the C2C domain of otoferlin causes profound hearing impairment in an Omani family with auditory neuropathy (2016) (10)
Disturbing effect of lockdown for COVID-19 on the incidence of infective endocarditis: a word of caution (2020) (10)
On the pathophysiology of DFNA9: Effect of pathogenic variants in the COCH gene on inner ear functioning in human and transgenic mice (2020) (10)
Pendred Syndrome/DFNB4 (2014) (10)
Echocardiographic and histological assessment of age-related valvular changes in normal rats. (2009) (10)
A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame (2011) (10)
Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigree. (2006) (10)
Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping. (1998) (10)
Ruptured aortic dissection into the left atrium which presented as congestive heart failure and was diagnosed by transoesophageal echocardiography. (1994) (10)
Marine Seagrass Extract of Thalassia testudinum Suppresses Colorectal Tumor Growth, Motility and Angiogenesis by Autophagic Stress and Immunogenic Cell Death Pathways (2021) (10)
A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13. (2001) (10)
Pendred syndrome redefined. Report of a new family with fluctuating and progressive hearing loss. (2002) (9)
Clinical features of DFNA5. (2002) (9)
Effect of high-intensity ultrasound-targeted microbubble destruction on perfusion and function of the rat heart assessed by pinhole-gated SPECT. (2010) (9)
Tumor-specific genetic variants can be detected in circulating cell-free DNA of malignant pleural mesothelioma patients. (2018) (9)
Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss (2021) (9)
Rare Variants in BMP2 and BMP4 Found in Otosclerosis Patients Reduce Smad Signaling (2014) (9)
Non-syndromic hearing impairment: gene linkage and cloning. (1999) (9)
Regional quantitative analysis of small animal myocardial sympathetic innervation and initial application in streptozotocin induced diabetes. (2009) (9)
Tricuspid stenosis: a rare complication of pacemaker-related endocarditis. (2000) (9)
Genetic Linkage Analysis in Two Large Belgian Alzheimer Families with Chromosome 21 DNA Markers (1988) (9)
Insufficient evidence for a role of SERPINF1 in otosclerosis (2019) (9)
Mitral Valve Repair of Atrial Functional Mitral Regurgitation in Heart Failure with Preserved Ejection Fraction (2020) (9)
Phenotype of the first otosclerosis family linked to OTSC10 (2011) (8)
Characterization of the murine Dfna5 promoter and regulatory regions. (2009) (8)
Aortic valve aneurysm after acute endocarditis (1997) (8)
Potentiometric detection in UPLC as an easy alternative to determine cocaine in biological samples. (2015) (8)
Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children. (2018) (8)
Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution. (2011) (8)
Tissue Doppler imaging does not show infraclinical alteration of myocardial function after contrast echocardiography. (2005) (8)
The Aortic Valve replAcemenT versus conservative treatment in Asymptomatic seveRe aortic stenosis (AVATAR trial): A protocol update (2018) (8)
[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease]. (1997) (8)
Clinical characteristics and short-term outcome of patients admitted with heart failure in Belgium: results from the BIO-HF registry (2015) (8)
Use of potentiometric detection in (ultra) high performance liquid chromatography and modelling with adsorption/desorption binding kinetics. (2013) (8)
Longitudinal Copy-Number Alteration Analysis in Plasma Cell-Free DNA of Neuroendocrine Neoplasms is a Novel Specific Biomarker for Diagnosis, Prognosis, and Follow-up (2021) (8)
[Essential thrombocytosis]. (1989) (7)
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids (1990) (7)
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island. (1990) (7)
Heart failure with preserved ejection fraction or non-cardiac dyspnea in paroxysmal atrial fibrillation: The role of left atrial strain. (2020) (7)
The Phenotype of the First Otosclerosis Family Linked to OTSC5 (2006) (7)
Possible implication of NFKB1A and NKG2D genes in susceptibility to HTLV‐1‐associated myelopathy/tropical spastic paraparesis in Peruvian patients infected with HTLV‐1 (2012) (7)
Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami (2010) (7)
Gender differences in the management and outcome of atrial fibrillation complicating acute heart failure. (2014) (7)
Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21 (2012) (7)
pyAmpli: an amplicon-based variant filter pipeline for targeted resequencing data (2017) (7)
Genotype-Phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9) Part II: A Prospective Cross-Sectional Study of the Vestibular Phenotype in 111 Carriers (2021) (6)
Safety of ultrasound contrast agents: “Primum non nocere”? (2009) (6)
Benfluorex: the last chapter of drug-induced valvular heart disease? (2011) (6)
Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant　- Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping. (2017) (6)
A polymorphic locus [D21S144] is detected by probe pVC12 on chromosome 21. (1989) (6)
Characteristic ERK1/2 signaling dynamics distinguishes necroptosis from apoptosis (2021) (6)
The genetics of hearing impairment (2003) (6)
Genetic Linkage Analysis in Early-Onset Familial Alzheimer’s Dementia (1990) (6)
Prognostic and Predictive Value of RAS Gene Mutations in Colorectal Cancer: Moving Beyond KRAS Exon 2 (2015) (6)
Pergolide and valvular heart disease: the lower the better? (2008) (6)
Chromosome 13 q deletion with Waardenburg syndrome : further evidence for a gene involved in neural crest function on 13 q (6)
Genetic testing for hearing impairment. (2005) (6)
Genome wide analysis in a family with sensorineural hearing loss, autism and mental retardation. (2012) (5)
Genome‐wide DNA methylation profiling and identification of potential pan‐cancer and tumor‐specific biomarkers (2021) (5)
Echocardiographic integrated backscatter for assessing reduction of aortic valve calcifications by R-568 in a rat model of chronic kidney disease. (2013) (5)
Double transseptal puncture guided by real-time three-dimensional transoesophageal echocardiography during atrial fibrillation ablation. (2008) (5)
Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7 (2007) (5)
Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15 (1997) (5)
Abnormal response to inotropic stimulation in young asymptomatic type I diabetic patients demonstrated by serial gated myocardial perfusion SPECT imaging (2005) (5)
Silent coronary artery disease in asymptomatic patients with severe aortic stenosis and normal exercise testing (2020) (5)
Users' guide for ASTER: A microsimulation model for indirect taxes. Version 2 (1996) (5)
Genes in the ear: what have we learned over the last years? (2001) (5)
A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis (2021) (5)
Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genes (2021) (5)
The FAS‐670 AA genotype is associated with high proviral load in peruvian HAM/TSP patients (2017) (5)
Performance of non‐invasive myocardial work to predict the first hospitalization for de novo heart failure with preserved ejection fraction (2021) (5)
Erratum: Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F (Human Molecular Genetics (2001) vol. 10 (1709-1718)) (2001) (5)
Summary 2015 ESC guidelines. (2016) (5)
Non-invasive evaluation of left ventricular power output by simultaneous recordings of applanation tonometry and echocardiographic Doppler signals (1997) (5)
Involvement of T cell receptor Beta alterations in the development of otosclerosis linked to OTSC 2 Running title : T cell receptor Beta alterations in otosclerosis (2010) (5)
MYO 1 F as a Candidate Gene for Nonsyndromic Deafness , DFNB 15 (2001) (5)
Echocardiographic diagnosis of right and left sinus of Valsalva aneurysms dissecting into the ventricular septum. (1996) (5)
Correction: Whole-Genome Saliva and Blood DNA Methylation Profiling in Individuals with a Respiratory Allergy (2017) (5)
Phenotype-genotype correlations in otosclerosis: clinical features of OTSC2. (2007) (5)
[Influence of exogenic factors on age-related hearing impairment]. (2009) (5)
A new, easy, and rapid high-throughput detection method for the common GJB2 (CX26), 35delG mutation. (2007) (4)
Deep sequencing of the TP 53 gene reveals a potential risk allele for non – small cell lung cancer and supports the negative prognostic value of TP 53 variants (2017) (4)
Substantial variations in clinical outcome following hospitalization for heart failure. (2002) (4)
A Pilot Study for Left Atrial Appendage Occlusion Guided by 3-Dimensional Rotational Angiography Alone. (2018) (4)
Role of killer cell immunoglobulin-like receptor gene content and human leukocyte antigen-C group in susceptibility to human T-lymphotropic virus 1-associated myelopathy/tropical spastic paraparesis in Peru. (2010) (4)
DNA methylation as a diagnostic biomarker for malignant mesothelioma: a systematic review and meta-analysis. (2021) (4)
Screening for silent myocardial ischaemia in patients with type 2 diabetes mellitus: a quest to improve selection of the target screening population (2011) (4)
Antiproliferative, Antiangiogenic, and Antimetastatic Therapy Response by Mangiferin in a Syngeneic Immunocompetent Colorectal Cancer Mouse Model Involves Changes in Mitochondrial Energy Metabolism (2021) (4)
Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms. (2005) (4)
A European multicenter study into age-related hearing impairment: Occupational noise, smoking and high BMI are risk factors and moderate akcohol consumption is protective. (2008) (4)
Genetic and clinical diagnosis in non-syndromic hearing loss (2013) (4)
Connexins and Deafness: From Molecules to Disease (2006) (4)
MDM2 SNP309 and SNP285 Act as Negative Prognostic Markers for Non-small Cell Lung Cancer Adenocarcinoma Patients (2017) (4)
Acute heart failure due to fulminant myocardial infiltration by a diffuse large B-cell lymphoma. (2012) (4)
Etiological Work-up in Referrals From Neonatal Hearing Screening: 20 Years of Experience (2020) (4)
Age-related hearing impairment: ensemble playing of environmental and genetic factors (2007) (4)
Homozygosity mapping applied to hereditary hearing impairment: localizing recessive deafness genes (1998) (4)
Evaluation of simultaneous reforms in personal income taxes and indirect taxes: Belgium 1988-1993 (1998) (3)
Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13. (2000) (3)
Genetic diagnostics of early childhood hearing loss: better testing with next-generation DNA sequencing. (2013) (3)
Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1‐22.3 (2005) (3)
Ketanserin and syncope. (1989) (3)
Methylation biomarkers for early cancer detection and diagnosis: Current and future perspectives. (2022) (3)
Minimally invasive mitral valve annuloplasty confers a long-term survival benefit compared with state-of-the-art treatment in heart failure with functional mitral regurgitation. (2017) (3)
Head to head comparison of transesophageal and transthoracic contrast-enhanced echocardiography during dobutamine administration for the detection of coronary artery disease. (2008) (3)
Anti-EGFR Resistance in Colorectal Cancer: Current Knowledge and Future Perspectives (2014) (3)
Genotype-phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9): Part I—A Cross-sectional Study of Hearing Function in 111 Carriers (2021) (3)
Echinacea purpurea (L.) Moench treatment of monocytes promotes tonic interferon signaling, increased innate immunity gene expression and DNA repeat hypermethylated silencing of endogenous retroviral sequences (2021) (3)
Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome (1989) (3)
Valorisation of Microsimulation Model for Social Security Mimosis (2008) (3)
Acute heart failure due to fulminant myocardial by a diffuse large B-cell lymphoma (2012) (3)
Summary 2014 ESC guidelines (2014) (3)
Age influence on clinical features in hospitalized thyroid patients: dissimilarity between clinical and laboratory findings in adulthood. A retrospective study. (1992) (3)
Low frequency of the GJB6 342 Kb deletion in the belgian deaf population. (2002) (3)
Transduction Efficiency and Immunogenicity of Viral Vectors for Cochlear Gene Therapy: A Systematic Review of Preclinical Animal Studies (2021) (3)
Outcomes in patients with moderate and asymptomatic severe aortic stenosis followed up in heart valve clinics (2022) (3)
Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome. (2010) (3)
Pharmacotherapy: Valvulopathy in patients treated for hyperprolactinemia? (2010) (3)
Genetics of otosclerosis: finally catching up with other complex traits? (2021) (3)
Poster session Friday 13 December - PM: 13/12/2013, 14:00-18:00 * Location: Poster area (2013) (2)
FINAL REPORT PROJECT AG/01/116 VALORISATION OF THE MICROSIMULATION MODEL FOR SOCIAL SECURITY MIMOSIS Part 2 (2008) (2)
Summary of 2017 ESC guidelines on valvular heart disease, peripheral artery disease, STEMI and on dual antiplatelet therapy (2018) (2)
Poster Session: Right ventricular systolic function (2012) (2)
Response: Asymptomatic severe aortic stenosis: Cardiopulmonary exercise testing in "the world of AVATAR". (2016) (2)
Hemangioma of the mitral valve as a rare, incidental finding in an adult female (2019) (2)
Cochlin Deficiency Protects Aged Mice from Noise-Induced Hearing Loss (2021) (2)
Early onset maternal inherited hearing loss with late onset neurological symptoms present in a three generation Dutch family. (1996) (2)
Molecular diagnosis of neurosensory deafness: the gap between basic research and diagnostic application is increasing. (2002) (2)
Role of DFNA5 in hearing loss and cancer – a comment on Rakusic et al (2015) (2)
Molecular analysis of an asbestos-exposed Belgian family with a high prevalence of mesothelioma (2018) (2)
Genes in the ear: what have we learned over the last years? (2001) (2)
Autosomal Dominant Nonsyndromic Hearing Impairment: an Overview (2003) (2)
An informative MspI polymorphism detected at the D21S16 locus (1990) (2)
Attitudes of Potential Participants Towards Potential Gene Therapy Trials in Autosomal Dominant Progressive Sensorineural Hearing Loss (2020) (2)
Aortic valve replacement improves survival in severe aortic stenosis with gradient–area mismatch (2018) (2)
Practical recommendations on the use of echocardiography to assess pulmonary arterial hypertension - a Belgian expert consensus endorsed by the Working Group on Non-Invasive Cardiac Imaging (2013) (2)
Localisation of the gene for Van Buchem disease to a candidate region of less than 1 cM on chromosome 17. (1997) (2)
Clinical presentation of DFNA8-DFNA12. (2002) (2)
Matching of income and expenditure data by means of nonparametric estimation of Engel curves (2004) (2)
Echocardiographic integrated backscatter for the differentiation between aortic valve calcification and valvular myxoid degeneration in rats. (2014) (2)
An unique case of “Atypical Ebstein’s Anomaly” with only isolated displacement of the inferior tricuspid leaflet (2013) (2)
Nonsyndromic hearing loss: cracking the cochlear code (2007) (2)
Lactococcus garviae Prosthetic Mitral Valve Endocarditis: a Case Report and Literature Review (2017) (2)
Acquisition of raw intracoronary Doppler signal for better characterization of flows (1996) (2)
TOXIC CARDIOPATHIES (2005) (2)
Novel human pathological mutations. Gene symbol: SLC26A4. Disease: deafness, non-syndromic, autosomal recessive. (2010) (1)
Genome-Wide Analysis of Biobanked Blood, Saliva and Cord Blood Identifies DNA Methylation Marks Related to Environmental Programming of Respiratory Allergy (2016) (1)
Host genetic factors associated to proviral load in Peruvian HTLV-1 infected (2011) (1)
Paradoxical embolism in a patient with a large tricuspid myxoma and patent foramen ovale. (2011) (1)
Genetics of auditory and vestibular disorders (2003) (1)
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform (2012) (1)
A gene for autosomal dominant hearing loss on the short arm of chromosome 1 (1994) (1)
Identification of a new connexin gene GJA11 (Cx59) using degenerate PCR primers (2000) (1)
Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome (1991) (1)
Belgian Society of Cardiology Position Paper on Heart Centres in Belgium (2009) (1)
Ummary 2013 ESC guidelines. (2014) (1)
Cloning genes for non-syndromal hearing impairment. (1999) (1)
Effects of catheter ablation on left atrial performance in different types of atrial fibrillation: a strain study (2020) (1)
Diagnosis of heart failure with preserved ejection fraction in patients with dyspnea and paroxysmal atrial fibrillation: a role of left atrial strain (2020) (1)
Outcomes benefit in asymptomatic patients with moderate aortic valve stenosis followed up in heart valve clinics (2022) (1)
Social family allowances in Belgium. The impact of potential reforms on child poverty (2010) (1)
FINAL REPORT PROJECT AG/01/116 VALORISATION OF THE MICROSIMULATION MODEL FOR SOCIAL SECURITY MIMOSIS Part 3 (2008) (1)
Strategies for identification of disease genes (1999) (1)
Summary 2013 ESC guidelines (2014) (1)
Cardiac resynchronisation therapy reduces the incidence of permanent atrial fibrillation in heart failure patients (2006) (1)
Clinical Features of (2002) (1)
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment (2019) (1)
Effect of respiration on Doppler parameters of normal tricuspid porcine bioprosthetic valves (1995) (1)
Dependence of the ligation efficiency of large DNA fragments isolated from agarose gels on the purification method. (1998) (1)
Review paper. Recent developments in genetic hearing impairment. (1998) (1)
Commentary on “Otosclerosis: Thirty-Year Follow-Up After Surgery” (2011) (1)
Giant pseudoaneurysm of the left ventricle (2019) (1)
Molecular diagnosis of neurosensory deafness: the gap between basic research and diagnostic application is increasing. (2002) (1)
Molecular forms of atrial natriuretic peptide in atria and plasma from fetal and adult female rats. (1995) (1)
DFNA 2, 5, 8, 12. (2000) (1)
Abstract 2066: Does Mitral Regurgitation Regress After Aortic Valve Replacement For Aortic Stenosis ? A Prospective Multicenter Study (2007) (1)
Quantification of low-gradient severe aortic stenosis using a hybrid approach combining Doppler echocardiography and thermodilution. (2014) (1)
Impact of non-invasive anatomical testing on optimal medical prescription in patients with suspected coronary artery disease. (2019) (1)
Pathogenic Variants in the COCH Gene That Lead to Hearing Loss and Vestibular Deficit: Update on DFNA9 and Introducing DFNB110 (2022) (1)
Labour Market Responses of Survival Pensioners: Estimating a Labour Supply Model and Predicting the Effect of the Reform (2007) (1)
Stop the grief and back to work!: An evaluation of the government's plan to activate widows and widowers (2006) (1)
Mapping and Cloning of Genes for Inherited Hearing Impairment (2002) (1)
Importance of In-Hospital Prospective Registry and Infectious Endocarditis Heart Team to Monitor and Improve Quality of Care in Patients with Infectious Endocarditis (2021) (1)
Standardized Echinacea purpurea extract primes an IFN specific innate immune monocyte response via JAK1-STAT1 dependent gene expression and epigenetic control of endogenous retroviral sequences (2020) (1)
Comparing survival in left-sided and right-sided colorectal carcinoma: A Belgian population-based study. (2018) (1)
Unique autosomal recessive variant of palmoplantar keratoderma associated with hearing loss not caused by known mutations* (2017) (1)
Poster Session 1: Thursday 8 December 2011, 08:30-12:30 * Location: Poster Area (2011) (1)
HLA-G 14 bp insertion/deletion polymorphism is not associated to proviral load levels and presence of HAM/TSP in Peruvian HTLV-1 infected individuals (2011) (1)
Multi-modality imaging in an exceptional case of aborted sudden cardiac death. (2014) (1)
Modelling labour supply and policy reform in the Belgian tax benefit model MIMOSIS (2010) (1)
Abstract 3236: Prosthesis-Patient Mismatch and Mitral Regurgitation After Aortic Valve Replacement: A Prospective Quantitative Study (2009) (1)
The Belgian Society of Cardiology: challenges for the next years (2013) (0)
Abstract 5628: Overcoming cetuximab resistance in HNSCC: the role of AURKB and DUSP6. (2013) (0)
The Impact of Radiofrequency Wide Circumferential Pulmonary Vein Isolation on Left Atrial Geometry in Patients with Recurrent Atrial Fibrillation (2020) (0)
Preface (2003) (0)
Echocardiography Markers Of Myocardial Deformation as Independent predictors of Sinus Rhythm Maintenance after Catheter Ablation for Paroxysmal Atrial Fibrillation (2021) (0)
Introduction of a heart failure nurse for the support of in-hospital management of mainly elderly patients with acute HF results in a shorter hospitalisation duration, a higher prescription of evidence based medication and a better outcome after 1 year follow-up (2014) (0)
Same Day Discharge Strategy by Default in a Tertiary Catheterization Laboratory. Value Based Healthcare-Change in Practice. (2023) (0)
Abstract P4-01-14: Whole exome sequencing of circulating and disseminated tumour cells in patients with metastatic breast cancer (2015) (0)
Belgian Society of Cardiology 29th Annual Scientific Meeting (2010) (0)
977 Quantitative assessment of myocardial contractile reserve during exercise in patients with mitral valve prolapse (2006) (0)
Contents Vol. 12, 2007 (2007) (0)
Large-scale analysis of DFNA5 methylation reveals its potential as biomarker for breast cancer (2018) (0)
MICROSIMULATION MODEL FOR SOCIAL SECURITY MIMOSIS AND EUROMOD (2009) (0)
Genotype-phenotype correlation in Li associated diseases (0)
DNA methylation patterns in respiratory allergy cases: comparability of saliva vs. blood (2014) (0)
Quantitative assessment of myocardial contractile reserve during exercise in patients with mitral valve prolapse (2006) (0)
FINAL REPORT PROJECT AG/01/116 VALORISATION OF THE MICROSIMULATION MODEL FOR SOCIAL SECURITY MIMOSIS Part 1 (2008) (0)
Long-term outcome of minimally invasive mitral valve annuloplasty in disproportionate mitral regurgitation (2020) (0)
Syddansk Universitet Interaction between prenatal pesticide exposure and a common polymorphism in the PON 1 gene on DNA methylation in genes associated with cardio-metabolic disease risk an exploratory study (2017) (0)
748 Quantitative assessment of perfusion of healthy and LAD-occluded rats with myocardial contrast echocardiography and 99mTc-sestamibi SPECT (2005) (0)
Table 2. [Percent Hearing Impairment]. (2014) (0)
P6469Catheter ablation during sinus rhythm is associated with acute loss of left atrial contractile function in paroxysmal atrial fibrillation: a strain study (2018) (0)
Mutation screening of SLC26A4 by DHPLC. (2002) (0)
Exclusion of the beta '-COP gene and identification of a novel candidate gene for the blepharophimosis syndrome (BPES) (1999) (0)
Poster session III * Friday 10 December 2010, 08:30-12:30 (2010) (0)
Treasury bill auctions with non-competitive bids (1995) (0)
Endoscopic repair of atrial functional mitral regurgitation in heart failure: long-term effects (2020) (0)
P2451Patterns of left atrial structural and functional remodeling after catheter ablation in paroxysmal and long-standing persistent atrial fibrillation (2019) (0)
Abstract 14907: Minimally Invasive Mitral Valve Annuloplasty Confers a Long-Term Survival Benefit Compared With State-Of-The-Art Treatment in Heart Failure Patients With Functional Mitral Regurgitation (2016) (0)
Table 4. [Clinical Manifestations and Molecular Genetics...]. (2014) (0)
7 – Hearing Impairment (2017) (0)
Relationship between late potentials and myocardial viability assessed by dobutamine echocardiography in the early postinfarction period (2002) (0)
26PWhole exome sequencing of circulating and disseminated tumour cells in patients with metastatic breast cancer (2015) (0)
Potentiometric methods to study biomolecular interactions (2014) (0)
Mitral valve annuloplasty ring dehiscence (2021) (0)
472 Can we use echocardiography to assess dyssynchrony in heart failure patients with atrial fibrillation (2005) (0)
1102 Effect of recent onset diabetes on myocardial blood flow reserve assessed by myocardial contrast echocardiography in rats (2006) (0)
Predictive Sensitivity and Concordance of Machine-learning Tools for Diagnosing DFNA9 in a Large Series of p.Pro51Ser Variant Carriers in the COCH-gene. (2021) (0)
Tissue Doppler imaging in normal and ischaemic rat models. (2005) (0)
177P Dissecting the molecular landscape of resistance to ROS1 tyrosine kinase inhibitors with improved NSCLC pre-clinical models (2023) (0)
Pre-clinical modelling of ROS1+ non-small cell lung cancer. (2023) (0)
P660The effect of hypertension and metabolic syndrome on left atrial function in patients with paroxysmal atrial fibrillation undergoing catheter ablation (2019) (0)
Table 3. [Clinical Manifestations and Molecular Genetics...]. (2014) (0)
Taxation of non-alcoholic beverages in Belgium: A critical appraisal (1999) (0)
Large deletion in VLGR1 causes Usher syndrome type IIC in male and female patients of an Iranian family (2009) (0)
Figure 2. [Causes of prelingual hearing loss ≥40 dB in children]. (2014) (0)
Early onset inherited hearing loss and late onset neurological complaints with maternal inheritance (1997) (0)
489 Dynamic left ventricular dyssynchrony contributes to exercise symptoms and dynamic mitral regurgitation in heart failure patients (2005) (0)
Twiddler’s syndrome (2000) (0)
An aptamer-based Potentiometric sensor for Dopamine (2012) (0)
Determination of the Association Constant Between Small Target Molecules and Large Biomolecules by Potentiometric Titration (2015) (0)
Interaction between prenatal pesticide exposure and a common polymorphism in the PON1 gene on DNA methylation in genes associated with cardio-metabolic disease risk—an exploratory study (2017) (0)
4105Magnetic resonance derived quantification of organic mitral regurgitation provides superior prognostic information to doppler echocardiography based integrative approach (2017) (0)
Early diastolic mitral insufficiency due to asynchrony of left ventricular contraction (1994) (0)
pyAmpli: an amplicon-based variant filter pipeline for targeted resequencing data (2017) (0)
Apparent high prevalence of mitochondrial DNA mutations in congenital/childhood non-syndromic sensorineural hearing impairment (2000) (0)
Control of Dyspnea in Advanced Cancer Patients (2017) (0)
Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive. (2010) (0)
Effective average and marginal tax rates in the Belgian tax benefit system (2010) (0)
Copy number alterations in plasma cell-free DNA from metastatic gastroenteropancreatic neuroendocrine neoplasms. (2021) (0)
Myocardial Work Predicts Outcome in Asymptomatic Severe Aortic Stenosis: Subanalysis of the Randomized AVATAR Trial. (2022) (0)
Table 2. [Selected SLC26A4 Pathogenic Variants Discussed in This GeneReview]. (2014) (0)
Dyspnoea in a 36-year-old woman (2016) (0)
Serial Non-Invasive Myocardial Work Measurements for Patient Risk Stratification and Early Detection of Cancer Therapeutics-Related Cardiac Dysfunction in Breast Cancer Patients: A Single-Centre Observational Study (2023) (0)
896 Restrictive valvular heart disease in patients with Parkinson's disease treated with pergolide (2003) (0)
Discrimination amongThermophilic Campylobacter Species byPolymerase ChainReaction Amplification of23SrRNAGeneFragments (1993) (0)
Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (2019) (0)
In vitro validation of absolute myocardial blood flow measurements with myocardial contrast echocardiography (1998) (0)
Atrial strain performance in patients with paroxysmal atrial fibrillation undergoing successful radio-frequency catheter ablation (2021) (0)
P038 Early detection of breast cancer in liquid biopsies using DNA methylation markers (2023) (0)
Corrigendum to ’ Same Day Discharge Strategy by Default in a Tertiary Catheterization Laboratory. Value Based Healthcare-Change in Practice.’ [Health Policy, Volume 132, June 2023, 104826, ISSN 0168-8510] (2023) (0)
270 How interpret exercise induced changes in E/Ea in patients with systolic heart failure (2005) (0)
Oligonucleotide and aptamer derivatized surfaces in potentiometric sensors: preliminary results (2011) (0)
A genome-wide association study for age-related hearing impairment in the Saami 1 2 (2009) (0)
Intra-aortic thrombi as a source of embolism in a middle-aged patient with protein C deficiency (1993) (0)
Volume reviewers (2011) (0)
NPY methylated ctDNA is a promising biomarker for treatment response monitoring in metastatic colorectal cancer. (2023) (0)
Erratum to: CRASH syndrome: Clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1 (1996) (0)
Aptamer-based Potentiometric Methods to detect specific Biomolecular Interactions (2014) (0)
GLI2 promoter hypermethylation in saliva of children with a respiratory allergy (2018) (0)
Abstract 1898: Potential molecular mechanisms of intrinsic resistance to EGFR-targeting monoclonal antibodies in HNSCC (2012) (0)
Table 6. [Mitochondrial Nonsyndromic Hearing Impairment]. (2014) (0)
Otosclerosis (2003) (0)
Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment (2018) (0)
Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia (2022) (0)
[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)]. (2003) (0)
Blood transcriptomics to facilitate diagnosis and stratification in pediatric rheumatic diseases – a proof of concept study (2022) (0)
Resolving Apparent Inconsistencies Between Area, Flow, and Gradient Measurements in Patients With Aortic Valve Stenosis and Preserved Left Ventricular Ejection Fraction. (2017) (0)
Table 5. [Clinical Manifestations and Molecular Genetics of X-Linked Nonsyndromic Hearing Impairment]. (2014) (0)
46PDFNA5 METHYLATION: A POTENTIAL BIOMARKER FOR BREAST CANCER? (2014) (0)
Illustration by transesophageal echocardiography of rapid and important pannus formation during infective endocarditis of a prosthetic valve. (1991) (0)
Impact of aortic regurgitation on long-term outcomes in heart failure with preserved ejection fraction (2022) (0)
Molecular analysis of an asbestos-exposed Belgian family with a high prevalence of mesothelioma (2018) (0)
A child’s spit epigenome can reveal its respiratory allergy risk (2016) (0)
A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis (2021) (0)
Volume reviewers (2014) (0)
Generation and characterization of a DFNA5 knockout mouse (2003) (0)
Cardiac abnormalities in an adults and pediatric population with human immunodificiency virus infection: an echocardiographic study (1995) (0)
Abstract 15567: Global Longitudinal Strain at Rest and During Exercise Accurately Predicts Extensive Diffuse Myocardial Fibrosis at Histology and T1 Mapping in Aortic Stenosis (2016) (0)
Figure 1. [Audioprofile]. (2014) (0)
MIMOSIS: MIcrosimulation MOdel for Belgian Social Insurance Systems: modelling rules for the sickness and disability benefits module (2007) (0)
Analysis of regional wall motion during contrast-enhanced dobutamine stress echocardiography: effect of contrast imaging settings. (2009) (0)
DNA methylation analysis in respiratory allergy cases: is saliva a good alternative for blood? (2014) (0)
R037: Genotype-Phenotype Correlation in a New Family with TECTA Mutation (2003) (0)
Performance of non-invasive myocardial work to predict the first hospitalization for de novo heart failure with preserved ejection fraction (HFpEF) (2022) (0)
Abstract 12828: Minimally Invasive Surgical Mitral Valve Repair of Secondary Mitral Regurgitation Improves Outcome in Non-Ischemic Heart Failure With Preserved Ejection Fraction (2019) (0)
Subject Index Vol. 12, 2007 (2007) (0)
Table 1. [Summary of Molecular Genetic Testing Used in Nonsyndromic Hearing Loss and Deafness, DFNA3]. (2014) (0)
Potentiometric sensors as a new tool to study biomolecular interactions (2013) (0)
PO-367 DFNA5 methylation: a potential biomarker for breast cancer, on the basis of a large scale analysis in TCGA (2018) (0)
THE ETIOLOGY OF HEARING IMPAIRMENT IN CHILDREN AND ADULTS WITH AN ASSOCIATED MENTAL HANDICAP AT AN INSTITUTE FOR THE DEAF (0)
Non-syndromal autosomal dominant hearing loss (1996) (0)
Selling treasury bills in Belgium: The role of non-competitive bids (1994) (0)
Genetics of otosclerosis: finally catching up with other complex traits? (2021) (0)
A Belgian Population-Based Study Reveals Subgroups of Right-Sided Colorectal Cancer with a Better Prognosis Compared to Left-sided Cancer. (2023) (0)
Incidence, severity, dose-dependency and evolution of valvular heart disease induced by pergolide in patients with Parkinsons disease. (2004) (0)
A dream comes true: Noninvasive delineation of endocardial blood flow and endocardial/epicardial flow ratio quantitation by myocardial contrast echocardiography (2001) (0)
The prognostic value of KRAS, NRAS, BRAF and DNA mismatch repair (MMR) status in left- and right-sided metastatic colorectal cancer (mCRC): A Belgian population-based study. (2018) (0)
18F-anti-VCAM-1 nanobody for PET/CT imaging of inflamed atherosclerotic plaque (2014) (0)
The state of the art in the genetics of hearing impairment (2002) (0)
Introduction of a heart failure nurse for the support of in-hospital management of mainly elderly patients with acute HF results in a better outcome after 1 year follow-up (2013) (0)
[Comparison of the effects of intravenous diltiazem and a placebo on hemodynamics and blood gases in the acute phase of myocardial infarction]. (1987) (0)
56-27: 3D rotation angiography to guide LAA closure (2016) (0)
Acute change in left atrial performance in patients with atrial fibrillation undergoing catheter ablation using AutoStrain (2021) (0)
Potentiometric detection in flow systems: an HPLC and FIA study for plant alkaloids (2011) (0)
A child's spit epigenome can reveal its respiratory allergy risk (2016) (0)
LEFT ATRIAL APPENDAGE OCCLUSION FACILITATED BY THREE DIMENSIONAL ROTATIONAL ANGIOGRAPHY ALONE IS SAFE AND ANATOMICALLY SUPERIOR TO TRASOESOPHAGEAL ECHOCARDIOGRAPHY (2017) (0)
Risk of cardiac valve fibrosis and other fibroses with dopamine agonist use in Parkinson's disease (2010) (0)
1039 Time course of left atrial performance in patients with paroxysmal atrial fibrillation undergoing radio-frequency catheter isolation of pulmonary veins (2020) (0)
Combining data from healthcare databases in Europe: A study of dopamine agonists (2010) (0)
Comprar Drug-induced valvular heart disease | S. Droogmans | 9781616689780 | Nova Science (2011) (0)
ESO-ESSO-ESTRO Multidisciplinary Course in Oncology for Medical Students: 4 Years of Experience (2016–2019) (2021) (0)
Large scale DFNA5 methylation and expression analysis in primary breast adenocarcinoma using data from the Cancer Genome Atlas (2016) (0)
Abstract 2633: Gene signatures derived from in vitro isolated migratory and invasive breast cancer cells indicate early metastatic relapse. (2013) (0)
Abstract 15605: Aortic Valve Replacement Improves Survival in Moderate to Severe Aortic Stenosis and Preserved Left Ventricular Ejection Fraction Regardless of the Gradient or Flow Pattern: a Role for Early Aortic Valve Replacement? (2016) (0)
Echocardiography in small animals (2005) (0)
Assessment of autonomic nervous system in a HIV infected population (1997) (0)
Table 1. [Summary of Molecular Genetic Testing Used in Pendred Syndrome/DFNB4]. (2014) (0)
NEW: An electrochemical alternative to SPR for (bio)molecule interaction studies (2012) (0)
Usefulness and Feasibility of Pocket-size Echocardiography in the Emergency Department (2012) (0)
Detection of mutations and copy number alterations in circulating DNA from pancreatic neuroendocrine tumor patients. (2018) (0)
438 Valvular heart disease associated with ecstasy abuse (2006) (0)
Table 1. [Severity of Hearing Loss in Decibels (dB)]. (2014) (0)
Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniques (1991) (0)
Mutations of the EDN3 gene in isolated and syndromic Hirschsprung's disease. (1997) (0)
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability (2021) (0)
Simultaneous exposure of isolated hearts to ultrasonic contrast and high energy ultrasound depresses left ventricular function irrespective of the contrast agent used (2000) (0)
Volume Reviewers (2013) (0)
554 Atrial mechanical dispersion in patients with atrial fibrillation undergoing catheter ablation: a strain study (2020) (0)
Targeted Next-Generation Sequencing in Children With Bilateral Sensorineural Hearing Loss: Diagnostic Yield and Predictors of a Genetic Cause (2023) (0)
Universitet Interaction between prenatal pesticide exposure and a common polymorphism in the PON 1 gene on DNA methylation in genes associated with cardio-metabolic disease risk (2017) (0)
Pilot Study to Compare DNA Methylation Patterns in Blood and Saliva in Respiratory Allergy Cases and Healthy Controls (2014) (0)
ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (2019) (0)
Evaluation of intraventricular dyssynchrony in heart failure patients: A direct comparison between pulsed wave and color tissue Doppler imaging (2005) (0)
Targeted Resequencing of Otosclerosis Patients from Different Populations Replicates Results from a Previous Genome-Wide Association Study (2022) (0)
Volume Reviewers (2009) (0)
783 Evolution of left ventricular diastolic parameters during exercise in heart failure patients (2006) (0)
598 Normal values and reproducibility of Doppler myocardial imaging in adult male rats (2005) (0)
Electrophysiology and Pathophysiology of the Autonomic Nervous System of the Heart (2015) (0)
Abstract 3331: Quantitative Assessment of Myocardial Contractile Reserve During Exercise in Patients with Mitral Valve Prolapse (2006) (0)
Risk of Heart Failure with Dopamine Agonist Use in Parkinson's Disease (2010) (0)
468P PANIB 20139173: Randomized, multicentre phase II trial comparing fluorouracil, leucovorin and oxaliplatin (FOLFOX) plus panitumumab versus FOLFOX plus bevacizumab in patients with previously untreated, RAS wild-type (WT) metastatic colorectal cancer (mCRC) (2020) (0)
Malignancy-driven hypercoagulability: a fatal combination. (2023) (0)
Response to: Correspondence on “Outcomes in patients with moderate and asymptomatic severe aortic stenosis followed up in heart valve clinics” by José Alberto San Román (2023) (0)
Cases of restrictive valve disease and ergot-derived drugs. (2006) (0)
436 Prevalence of mechanical inter- and intraventricular dyssynchrony in patients with heart failure and relatively preserved left ventricular function (2005) (0)
Insufficient evidence for a role of SERPINF1 in otosclerosis (2019) (0)
Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis (2018) (0)
Genetic mapping of the gene for van Buchem disease to chromosome 17q12-q21 (1998) (0)
Detection of organic ionics by Ion Selective Electrodes used as an HPLC detector: applications to alkaloids in plant extracts (2011) (0)
Physical mapping of the deafness gene DFNA 10 (1999) (0)
177 Impact of atrial fibrillation on response to cardiac resynchronisation therapy in patients with chronic heart failure (2006) (0)
Evidence for Somatic and Germhe Mosaicism in ynarome (1998) (0)
180 Contrast or transoesophageal dobutamine echo for the detection of ischaemia in poorly echogenic patients (2003) (0)
The Belgian Society of Cardiology: challenges for the next years (2013) (0)
268 IMPACT OF AORTIC REGURGITATION ON LONG TERM OUTCOME IN HEART FAILURE AND PRESERVED EJECTION FRACTION (2022) (0)
A mitochondrial point mutation at position 7472 causes early onset hearing impairment and late onset neurological symptoms: report of a Dutch family and a comparison with a Sicilian family (1998) (0)
Applications in audiological medicine (2008) (0)
Right coronary artery to coronary sinus fistula repair with the use of robotic-enhanced thoracoscopy (2016) (0)
Summary 2015 ESC guidelines (2016) (0)
1009 VV interval optimization in cardiac resynchronization therapy improves both left ventricular synchronicity and hemodynamics (2005) (0)
Increased low shear rate erythrocyte viscosity in insulin dependent diabetes mellitus (2016) (0)
Abstract 4319: Gene expression profiling of isolated small migratory and invasive breast cancer cells at different times during chemotaxis (2012) (0)
Determinants of exercise-induced changes in e/ea in patients with chronic systolic left ventricular dysfunction (2006) (0)
The political adequacy of quantitative impact assessment in the social field by means of micro-simulation models (2014) (0)

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