Guy Van Camp

Research interests

Publications

• Nano-targeted induction of dual ferroptotic mechanisms eradicates high-risk neuroblastoma

  Journal of Clinical Investigation · 2018 · https://doi.org/10.1172/jci99032

• Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studies

  Annals of Oncology · 2017 · 10.1093/annonc/mdx119

• Congenital hearing loss

  Nature Reviews Disease Primers · 2017 · https://doi.org/10.1038/nrdp.2016.94

• GRM7 variants confer susceptibility to age-related hearing impairment

  Human Molecular Genetics · 2008 · 10.1093/hmg/ddn402

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

  Mutation Research/Reviews in Mutation Research · 2008 · https://doi.org/10.1016/j.mrrev.2008.08.002

• 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

  Journal of the Association for Research in Otolaryngology · 2008 · https://doi.org/10.1007/s10162-008-0123-1

• The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors

  Audiology and Neurotology · 2007 · 10.1159/000106478

• Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

  Nature Genetics · 2006 · 10.1038/ng1829

• A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene

  The American Journal of Human Genetics · 2006 · 10.1086/506478

• GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

  The American Journal of Human Genetics · 2005 · https://doi.org/10.1086/497996

• 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

  Journal of Medical Genetics · 2005 · 10.1136/jmg.2004.028324

• Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

  The American Journal of Human Genetics · 2004 · 10.1086/383285

• Recommendations for the Description of Genetic and Audiological Data for Families with Nonsyndromic Hereditary Hearing Impairment

  Hearing Balance and Communication · 2003 · 10.1080/16513860301713

• Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease

  Human Mutation · 2003 · 10.1002/humu.10258

• Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

  The American Journal of Human Genetics · 2003 · 10.1086/380205

• Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

  Human Genetics · 1999 · 10.1007/s004390050933

• Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

  Nature Genetics · 1999 · 10.1038/70516

• Mutations in the Connexin 26 Gene ( GJB2 ) among Ashkenazi Jews with Nonsyndromic Recessive Deafness

  New England Journal of Medicine · 1998 · https://doi.org/10.1056/nejm199811193392103

• Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

  Human Mutation · 1998 · 10.1002/(sici)1098-1004(1998)11:5<387::aid-humu6>3.0.co;2-8

• Nonsyndromic hearing impairment is associated with a mutation in DFNA5

  Nature Genetics · 1998 · 10.1038/2503

• Two Frequent Missense Mutations in Pendred Syndrome

  Human Molecular Genetics · 1998 · 10.1093/hmg/7.7.1099

• Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

  Nature Genetics · 1998 · 10.1038/ng0598-60

• Nonsyndromic hearing impairment: unparalleled heterogeneity.

  PubMed · 1997

• The hereditary hearing loss homepage

  · 1997

• CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1

  European Journal of Human Genetics · 1995 · 10.1159/000472311

Current projects

No projects listed.