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Kristien Verhoeven | Researchclopedia

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Kristien Verhoeven

Cochlear (Australia)

28

Works

2,566

Citations

17

h-index

21

i10-index

Research Topics

Hereditary Neurological Disorders Hearing, Cochlea, Tinnitus, Genetics Hearing Loss and Rehabilitation

Affiliations

Cochlear (Australia)2021–2021

University of Sydney2003–2003

University of Wisconsin–Madison2016–2016

University of Antwerp1998–2007

University of Graz2003–2003

Top Works

Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy

Kristien Verhoeven,Peter De Jonghe,et al.

2003452 citations

Mitochondrial Function and Pathology

Cellular transport and secretion

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Stephan Züchner,Peter De Jonghe,et al.

2006358 citations

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

Stephan Züchner,Maher Noureddine,et al.

2005357 citations

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

Kristien Verhoeven,Lut Van Laer,et al.

1998339 citations

Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity

Philip Van Damme,Elke Bogaert,et al.

2007207 citations

A deafness mutation isolates a second role for the tectorial membrane in hearing

P. Kevin Legan,Victoria A. Lukashkina,et al.

2005138 citations

Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10

Kristien Verhoeven,Peter De Jonghe,et al.

2003118 citations

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

Kristien Verhoeven,Robbert JH Ensink,et al.

199988 citations

Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations

Michaela Auer‐Grumbach,Peter De Jonghe,et al.

200380 citations