Kristien Verhoeven

2.6k citations

27 papers · 1.9k indexed · h-index 17

Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics 9
Neurology top 2%
- Neurological diseases and metabolism 3
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders 11
- Genetic Neurodegenerative Diseases 4
Cell Biology top 2%
- Cellular transport and secretion 4
- Endoplasmic Reticulum Stress and Disease 3
Neurology top 5%
- Neurological diseases and metabolism 3
Cognitive Neuroscience
- Hearing Loss and Rehabilitation 7
Molecular Biology
- Mitochondrial Function and Pathology 4

Co-authors: Vincent Timmerman Peter De Jonghe Nathalie Verpoorten Michaela Auer‐Grumbach Guy Van Camp Klaus Wagner Hans‐Peter Hartung Veerle Van Gerwen
Cited by: Sensory Systems Neurology Cellular and Molecular Neuroscience
Journals: Proceedings of the National Academy of Sciences (1 paper)Nature Genetics (2 papers)Nature Neuroscience (1 paper)
Partner nations: Belgium United States Australia

In The Last Decade

Kristien Verhoeven

27 papers receiving 1.9k citations

Peers

Countries citing papers authored by Kristien Verhoeven

Since Specialization

Citations

This map shows the geographic impact of Kristien Verhoeven's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kristien Verhoeven with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kristien Verhoeven more than expected).

Fields of papers citing papers by Kristien Verhoeven

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kristien Verhoeven. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kristien Verhoeven. The network helps show where Kristien Verhoeven may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Kristien Verhoeven, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Kristien Verhoeven Line = papers co-authored together Kristien Verhoeven links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	An improved cochlear implant electrode array for use in experimental studies Hearing Research ·Robert K. Shepherd,Kristien Verhoeven,Jin Xu,Frank Risi,James B. Fallon,Andrew K. Wise	2011	35
2	Recent advances in hereditary sensory and autonomic neuropathies Current Opinion in Neurology ·Kristien Verhoeven,Vincent Timmerman,Barbara Mauko,Thomas R. Pieber,Peter De Jonghe,Michaela Auer‐Grumbach	2006	43
3	Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2 Annals of Neurology ·Stephan Züchner,Peter De Jonghe,Albena Jordanova,Kristl G. Claeys,Velina Guergueltcheva,Sylvia Cherninkova,Steven R. Hamilton,Greg Van Stavern,Karen Krajewski,Jeffery Stajich,I. Tournev,Kristien Verhoeven,C. T. Langerhorst,Marianne de Visser,Frank Baas,Thomas D. Bird,Vincent Timmerman,Michael E. Shy,Jeffery M. Vance	2006	268
4	A deafness mutation isolates a second role for the tectorial membrane in hearing Nature Neuroscience ·P. Kevin Legan,Victoria A. Lukashkina,Richard J. Goodyear,Andrei N. Lukashkin,Kristien Verhoeven,Guy Van Camp,Ian J. Russell,Guy P. Richardson	2005	97
5	Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease Nature Genetics ·Stephan Züchner,Maher Noureddine,Marina Kennerson,Kristien Verhoeven,Kristl G. Claeys,Peter De Jonghe,John Merory,Sofia A. Oliveira,Marcy C. Speer,Judith E. Stenger,Gina Walizada,Danqing Zhu,Margaret A. Pericak‐Vance,Garth A. Nicholson,Vincent Timmerman,Jeffery M. Vance	2005	263
6	Experimental Charcot–Marie–Tooth type 1A: A cDNA microarrays analysis Molecular and Cellular Neuroscience ·Tiziana Vigo,Lucilla Nobbio,Paul Van Hummelen,M. Abbruzzese,Gianluigi Mancardi,Nathalie Verpoorten,Kristien Verhoeven,Michael W. Sereda,Klaus‐Armin Nave,Vincent Timmerman,Angelo Schenone	2005	36
7	Synaptopodin and 4 novel genes identified in primary sensory neurons Molecular and Cellular Neuroscience ·Nathalie Verpoorten,Kristien Verhoeven,Stefan Weckx,An Jacobs,Sally Serneels,Jurgen Del‐Favero,C. Ceuterick,Dirk R. Van Bockstaele,Zwi Berneman,Ludo Van Den Bosch,Wim Robberecht,Lucilla Nobbio,Angelo Schenone,Éric Dessaud,Odile deLapeyrière,Danny Huylebroeck,An Zwijsen,Peter De Jonghe,Vincent Timmerman	2005	3
8	Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10 The American Journal of Human Genetics ·Kristien Verhoeven,Peter De Jonghe,Tom Van de Putte,Eva Nelis,An Zwijsen,Nathalie Verpoorten,Els De Vriendt,An Jacobs,Veerle Van Gerwen,Annick Francis,C. Ceuterick,Danny Huylebroeck,Vincent Timmerman	2003	90
9	Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations Archives of Neurology ·Michaela Auer‐Grumbach,Peter De Jonghe,Kristien Verhoeven,Vincent Timmerman,Klaus Wagner,Hans‐Peter Hartung,Garth A. Nicholson	2003	62
10	Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy The American Journal of Human Genetics ·Kristien Verhoeven,Peter De Jonghe,Katrien Coen,Nathalie Verpoorten,Michaela Auer‐Grumbach,Jennifer M. Kwon,David Fitzpatrick,Eric Schmedding,Els De Vriendt,An Jacobs,Veerle Van Gerwen,Klaus Wagner,Hans‐Peter Hartung,Vincent Timmerman	2003	351
11	Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathy Neuromuscular Disorders ·Jennifer L. Dawkins,Sonal Brahmbhatt,Michaela Auer‐Grumbach,Klaus Wagner,Hans-Peter Hartung,Kristien Verhoeven,Vincent Timmerman,Peter De Jonghe,Marina Kennerson,Éric Leguern,Garth A. Nicholson	2002	19
12	Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3 Journal of the Peripheral Nervous System ·Joy Irobi,Eva Nelis,Kristien Verhoeven,Els De Vriendt,Ines Dierick,Peter De Jonghe,Christine Van Broeckhoven,Vincent Timmerman	2002	3
13	Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1 The American Journal of Human Genetics ·Kristien Verhoeven,Marcello Villanova,Alessandro Rossi,Alessandro Malandrini,Peter De Jonghe,Vincent Timmerman	2001	42
14	Identification of BPESC1, a Novel Gene Disrupted by a Balanced Chromosomal Translocation, t(3;4)(q23;p15.2), in a Patient with BPES Genomics ·Elfride De Baere,Yoshimitsu Fukushima,Kent W. Small,Nitin Udar,Guy Van Camp,Kristien Verhoeven,Aarno Palotie,Anne De Paepe,Ludwine Messiaen	2000	19
15	Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment Human Genetics ·Kristien Verhoeven,Toril Fagerheim,Sai Prasad,Sigrid Wayne,Frank De Clau,Wendy Balemans,Margriet Verstreken,Isabelle Schatteman,Bjorn Solem,Paul Van de Heyning,Lisbeth Tranebjärg,Richard J. Smith,Guy Van Camp	2000	10
16	Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment Human Genetics ·Kristien Verhoeven,Toril Fagerheim,Sai Prasad,Sigrid Wayne,Frank De Clau,Wendy Balemans,Margriet Verstreken,Isabelle Schatteman,Bjorn Solem,Paul Van de Heyning,Lisbeth Tranebjärg,Richard J. Smith,Guy Van Camp	2000	4
17	Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene European Journal of Human Genetics ·Kristien Verhoeven,Robbert JH Ensink,Valeria Tiranti,P.L.M. Huygen,David Johnson,Isabelle Schatteman,Lut Van Laer,Margriet Verstreken,Paul Van de Heyning,Nathan Fischel‐Ghodsian,Massimo Zeviani,Cor W. R. J. Cremers,Patrick J. Willems,Guy Van Camp	1999	68
18	Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss European Journal of Human Genetics ·Nicole Alloisio,Laurette Morlé,Muriel Bozon,Jacqueline Godet,Kristien Verhoeven,Guy Van Camp,Henri Plauchu,Philippe Muller,Lionel Collet,Geneviève Lina‐Granade	1999	39
19	Presymptomatic Diagnosis of Nonsyndromic Hearing Loss by Genotyping Archives of Otolaryngology - Head and Neck Surgery ·Achih H. Chen,Robert F. Mueller,Sai Prasad,John H. Greinwald,José M. Manaligod,Ann Muilenburg,Kristien Verhoeven,Guy Van Camp,Richard J. Smith	1998	8
20	Early-Onset Sensorineural Hearing Loss and Late-Onset Neurologic Complaints Caused by a Mitochondrial Mutation at Position 7472 Archives of Otolaryngology - Head and Neck Surgery ·R.J.H. Ensink,Kristien Verhoeven,Henri A. M. Marres,P.L.M. Huygen,G.W. Padberg,H. ter Laak,Guy Van Camp,Patrick J. Willems,C. W. R. J. Cremers	1998	10

About Kristien Verhoeven

Kristien Verhoeven is a scholar working on Sensory Systems, Neurology and Cellular and Molecular Neuroscience, having authored 27 papers that have together received 1.9k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (11 papers), Hearing, Cochlea, Tinnitus, Genetics (9 papers), Hearing Loss and Rehabilitation (7 papers), Mitochondrial Function and Pathology (4 papers), Cellular transport and secretion (4 papers), Genetic Neurodegenerative Diseases (4 papers), Neurological diseases and metabolism (3 papers) and Endoplasmic Reticulum Stress and Disease (3 papers). The work is most often cited by research in Sensory Systems (439 citations), Neurology (472 citations) and Cellular and Molecular Neuroscience (737 citations). Kristien Verhoeven has collaborated with scholars based in Belgium, United States and Australia. Frequent co-authors include Vincent Timmerman, Peter De Jonghe, Nathalie Verpoorten, Michaela Auer‐Grumbach, Guy Van Camp, Klaus Wagner, Hans‐Peter Hartung, Veerle Van Gerwen, Els De Vriendt and An Jacobs. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Nature Neuroscience.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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