Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

od Hilgert, Nele, Smith, Richard J.H., Van Camp, Guy
Izdano 2008

Function and expression pattern of nonsyndromic deafness genes

od Hilgert, Nele, Smith, Richard J.H., Van Camp, Guy
Izdano 2009

Apoptosis in acquired and genetic hearing impairment: The programmed death of the hair cell

od de Beeck, Ken Op, Schacht, Jochen, Van Camp, Guy
Izdano 2011

Role of DFNA5 in hearing loss and cancer – a comment on Rakusic et al

od Croes, Lieselot, Op de Beeck, Ken, Van Camp, Guy
izdano v Onco Targets Ther (2015)

A Pilot Genome-Wide Association Study Identifies Potential Metabolic Pathways Involved in Tinnitus

od Gilles, Annick, Van Camp, Guy, Van de Heyning, Paul, Fransen, Erik
izdano v Front Neurosci (2017)

pyAmpli: an amplicon-based variant filter pipeline for targeted resequencing data

od Beyens, Matthias, Boeckx, Nele, Van Camp, Guy, Op de Beeck, Ken, Vandeweyer, Geert
izdano v BMC Bioinformatics (2017)

The Gasdermin E Gene Has Potential as a Pan-Cancer Biomarker, While Discriminating between Different Tumor Types

od Ibrahim, Joe, Op de Beeck, Ken, Fransen, Erik, Peeters, Marc, Van Camp, Guy
izdano v Cancers (Basel) (2019)

The deafness gene DFNA5 induces programmed cell death through mitochondria and MAPK-related pathways

od Van Rossom, Sofie, Op de Beeck, Ken, Hristovska, Vesna, Winderickx, Joris, Van Camp, Guy
izdano v Front Cell Neurosci (2015)

Echinacea purpurea (L.) Moench treatment of monocytes promotes tonic interferon signaling, increased innate immunity gene expression and DNA repeat hypermethylated silencing of end...

od Declerck, Ken, Novo, Claudina Perez, Grielens, Lisa, Van Camp, Guy, Suter, Andreas, Vanden Berghe, Wim
izdano v BMC Complement Med Ther (2021)

Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study

od Weytjens Caroline, Droogmans Steven, Cosyns Bernard, Lahoutte Tony, Van Camp Guy, Schoors Danny, Franken Philippe R
Izdano 2007-10-01

Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study

od Cosyns, Bernard, Droogmans, Steven, Weytjens, Caroline, Lahoutte, Tony, Van Camp, Guy, Schoors, Danny, Franken, Philippe R
Izdano 2007

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

od Alasti, Fatemeh, Sadeghi, Abdorrahim, Sanati, Mohammad Hossein, Farhadi, Mohammad, Stollar, Elliot, Somers, Thomas, Van Camp, Guy
Izdano 2008

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

od Alasti, Fatemeh, Sadeghi, Abdorrahim, Sanati, Mohammad Hossein, Farhadi, Mohammad, Stollar, Elliot, Somers, Thomas, Van Camp, Guy
Izdano 2008

A large deletion in GPR98 causes type IIC Usher syndrome in male and female patients of an Iranian family

od Hilgert, Nele, Kahrizi, Kimia, Najmabadi, Hossein, Dieltjens, Nele, Bazazzadegan, Niloofar, Smith, Richard JH, Van Camp, Guy
izdano v J Med Genet (2009)

Disturbing effect of lockdown for COVID-19 on the incidence of infective endocarditis: a word of caution

od Van Camp, Guy, De Beenhouwer, Hans, Beles, Monika, Collet, Carlos, Nasser, Riwa, Schelfaut, Dan, Penicka, Martin
izdano v Clin Res Cardiol (2020)

Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment

od Hilgert, Nele, Monahan, Kelly, Kurima, Kiyoto, Li, Cindy, Friedman, Rick A, Griffith, Andrew J, Van Camp, Guy
Izdano 2009

A novel missense mutation in the C2C domain of otoferlin causes profound hearing impairment in an Omani family with auditory neuropathy

od Al-Wardy, Nadia M., Al-Kindi, Mohammed N., Al-Khabouri, Mazin J., Tamimi, Yahya, van Camp, Guy
izdano v Saudi Med J (2016)

Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling

od Ealy, Megan, Meyer, Nicole C., Corchado, Johnny Cruz, Schrauwen, Isabelle, Bress, Andreas, Pfister, Markus, Van Camp, Guy, Smith, Richard JH
Izdano 2014

Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment

od Schrauwen, Isabelle, Liaqat, Khurram, Schatteman, Isabelle, Bharadwaj, Thashi, Nasir, Abdul, Acharya, Anushree, Ahmad, Wasim, Van Camp, Guy, Leal, Suzanne M.
izdano v Genes (Basel) (2020)

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 ...

od Declerck, Ken, Remy, Sylvie, Wohlfahrt-Veje, Christine, Main, Katharina M., Van Camp, Guy, Schoeters, Greet, Vanden Berghe, Wim, Andersen, Helle R.
izdano v Clin Epigenetics (2017)