H. Backhovens

2.1k citations

27 papers · 1.1k indexed · h-index 15

Impact in

Physiology top 5%
- Alzheimer's disease research and treatments
Neurology top 10%
- Neurological diseases and metabolism
- Amyotrophic Lateral Sclerosis Research

Papers in

Physiology 11
- Alzheimer's disease research and treatments 11
Neurology 3
- Neurological diseases and metabolism 3

Co-authors: Christine Van Broeckhoven Marc Cruts John Hardy Anita Wehnert Marleen Van den Broeck Cornelia M. van Duijn Sally Serneels Peter St George‐Hyslop
Journals: Human Molecular Genetics (3 papers)Molecular Psychiatry (2 papers)Nucleic Acids Research (2 papers)European Journal of Human Genetics (1 paper)Neurology (1 paper)
Partner nations: Belgium United States Netherlands

In The Last Decade

H. Backhovens

27 papers receiving 1.1k citations

Peers

Countries citing papers authored by H. Backhovens

Since Specialization

Citations

This map shows the geographic impact of H. Backhovens'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 H. Backhovens with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H. Backhovens more than expected).

Fields of papers citing papers by H. Backhovens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. Backhovens. 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 H. Backhovens. The network helps show where H. Backhovens may publish in the future.

Co-authorship network

The 25 scholars most cited alongside H. Backhovens, 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 H. Backhovens Line = papers co-authored together H. Backhovens links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder Molecular Psychiatry ·D. Goossens, Sofie Van Gestel, Stephan Claes, Peter De Rijk, Daniel Souery, Isabelle Massat, Prof Jackson K.Too, H. Backhovens, Julien Mendlewicz, Christine Van Broeckhoven, Jurgen Del‐Favero	2003	40
2	Tau negative frontal lobe dementia at 17q21: Significant finemapping of the candidate region to a 4.8 cm interval Neurobiology of Aging ·R. Rademakers, Marc Cruts, Bart Dermaut, Marleen Van den Broeck, H. Backhovens, Christine Van Broeckhoven, Kristel Sleegers, Cornelia M. van Duijn, Шолойко Антоніна Сергіївна, Mokhtan Riti	2002	17
3	Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval Molecular Psychiatry ·R. Rademakers, Marc Cruts, Bart Dermaut, Kristel Sleegers, Malia Mar, Marleen Van den Broeck, H. Backhovens, John C. van Swieten, 李齐齐, Christine Van Broeckhoven	2002	84
4	Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion The American Journal of Human Genetics ·Marc Cruts, C. De Jonghe, Andi Shahaj, Carolyn Tysoe, Andrew Singleton, Hugo Vanderstichele, Wendy S. Meschino, Bart Dermaut, Athira Anilkumar S, H. Backhovens, Eugeen Vanmechelen, Christopher M. Morris, John Hardy, อารยา ดําเรือง, 刘宝强, Christine Van Broeckhoven	1999	10
5	Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample European Journal of Human Genetics ·Cornelia M. van Duijn, Marc Cruts, Jessie Theuns, Geert Van Gassen, H. Backhovens, Marleen Van den Broeck, Anita Wehnert, Sally Serneels, B. Lankes, Christine Van Broeckhoven	1999	43
6	Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased A 42 Secretion Human Molecular Genetics ·C. De Jonghe, 李书甜, Andi Shahaj, Carolyn Tysoe, Andrew Singleton, Hugo Vanderstichele, Wendy S. Meschino, Bart Dermaut, Athira Anilkumar S, H. Backhovens, Eugeen Vanmechelen, Christopher M. Morris, John Hardy, อารยา ดําเรือง, Peter St George‐Hyslop, Christine Van Broeckhoven	1999	67
7	The −491 A/T polymorphism in the regulatory region of the Apolipoprotein E gene and early-onset Alzheimer's disease Neuroscience Letters ·Gerwin Roks, Marc Cruts, María J. Bullido, H. Backhovens, María J. Artiga, A. Hofman, Fernando Valdivieso, Christine Van Broeckhoven, Cornelia M. van Duijn	1998	36
8	Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease Human Molecular Genetics ·Marc Cruts, Cornelia M. van Duijn, H. Backhovens, Marleen Van den Broeck, Anita Wehnert, Sally Serneels, Robin Sherrington, M. Hutton, John Hardy, Peter St George‐Hyslop, A. Hofman, Christine Van Broeckhoven	1998	323
9	Presenilin‐I polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch type Annals of Neurology ·Marjolijn Bornebroek, J. Haan, H. Backhovens, H. Poirier, Mark A. van Buchem, Marleen Van den Broeck, Egbert Bakker, R. A. C. Roos, Christine Van Broeckhoven	1997	5
10	WT1 MUTATION IN MALIGNANT MESOTHELIOMA AND WT1 IMMUNOREACTIVITY IN RELATION TOp53 AND GROWTH FACTOR RECEPTOR EXPRESSION, CELL-TYPE TRANSITION, AND PROGNOSIS The Journal of Pathology ·Samir Kumar‐Singh, R K Roberts, Ulrich Rodeck, H. Backhovens, Alessandro Colitta, Tian’en Yang, Christine Van Broeckhoven, 国際極運動観測事業中央局	1997	100
11	Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations Human Mutation ·Eva Nelis, Francis, Vincent Timmerman, Ann Löfgren, H. Backhovens, Peter De Jonghe, N. Hayashi, Christine Van Broeckhoven	1997	30
12	Mutation analysis of the chromosome 14q24.3 dihydrolipoyl succinyltransferase (DLST) gene in patients with early-onset Alzheimer disease Neuroscience Letters ·Marc Cruts, H. Backhovens, Geert Van Gassen, Jessie Theuns, Abakar Abbo Zakaria, Anita Wehnert, Cornelia M. van Duijn, Thomas Karlsson, Albert Hofman, Rolf Adolfsson, J. J. Martin, Christine Van Broeckhoven	1995	9
13	APOE genotype does not modulate age of onset in families with chromosome 14 encoded Alzheimer's disease Neuroscience Letters ·Christine Van Broeckhoven, H. Backhovens, Marc Cruts, J. J. Martin, Richard Crook, Henry Houlden, John Hardy	1994	101
14	Unique sequence homology in the pericentromeric regions of the long arms of chromosomes 13 and 21 Genomics ·Guy Van Camp, Marc Cruts, H. Backhovens, Anita Wehnert, Christine Van Broeckhoven	1992	11
15	Dinucleotide repeat polymorphism at the D21S258 locus Human Molecular Genetics ·Anita Wehnert, Marc Cruts, H. Backhovens, Alec F. Jenkins, Gilles Thomas, Christine Van Broeckhoven	1992	10
16	Identification of chromosome 21 DNA polymorphisms for genetic studies in Alzheimer's disease and Down syndrome Human Genetics ·Guy Van Camp, H. Backhovens, Marc Cruts, Anita Wehnert, Wim Van Hul, Piet Stinissen, Christine Van Broeckhoven	1991	10
17	Screening for the β-amyloid precursor protein mutation (APP717: Val → Ile) in extended pedigrees with early onset Alzheimer's disease Neuroscience Letters ·Marie‐Christine Chartier‐Harlin, Fiona Crawford, Khalid Hamandi, Michael Mullan, Alison Goate, John Hardy, H. Backhovens, Jean‐Jacques Martin, Christine Van Broeckhoven	1991	57
18	Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids Somatic Cell and Molecular Genetics ·Guy Van Camp, Wim Van Hul, H. Backhovens, Piet Stinissen, Anita Wehnert, David A. Patterson, Antoon Vandenberghe, Christine Van Broeckhoven	1990	9
19	Absence of genetic linkage of Charcot‐Marie‐Tooth disease (HMSN Ia) with chromosome 1 gene markers Neurology ·Peter Raeymaekers, Peter De Jonghe, H. Backhovens, Anita Wehnert, G. De Winter, Điêu Thị Mai Hoa, J. Gheuens, J. J. Martin, A. Vandenberghe, Christine Van Broeckhoven	1989	7
20	Light scattering on solutions of biopolymers : a critical evaluation of the technique [proceedings]. PubMed ·Αλκμήνη Γεωργίου Μπαΐρα, H. Backhovens, Julius Clauwaert	1979	2

About H. Backhovens

H. Backhovens is a scholar working on Physiology, Neurology, Molecular Biology, Genetics and Neurology, having authored 27 papers that have together received 1.1k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (11 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA Research and Splicing (5 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (3 papers), RNA and protein synthesis mechanisms (3 papers), Neurological diseases and metabolism (3 papers), Prion Diseases and Protein Misfolding (3 papers) and RNA regulation and disease (3 papers). The work is most often cited by research in Physiology (678 citations), Neurology (129 citations), Neurology (189 citations), Pharmacology (180 citations) and Cellular and Molecular Neuroscience (177 citations). H. Backhovens has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Christine Van Broeckhoven, Marc Cruts, John Hardy, Anita Wehnert, Marleen Van den Broeck, Cornelia M. van Duijn, Sally Serneels, Peter St George‐Hyslop, Robin Sherrington and A. Hofman. Their work appears in journals such as Human Molecular Genetics, Molecular Psychiatry, Nucleic Acids Research, European Journal of Human Genetics and Neurology.

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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