D. Goossens

3.7k citations

73 papers · 2.0k · h-index 25

Impact in

Neurology top 5%
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases

Papers in

Molecular Biology 19
Genetics 18
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 6

Co-authors: Jurgen Del‐Favero (37 shared papers)Christine Van Broeckhoven (18 shared papers)Marc Cruts (5 shared papers)Ilse Gijselinck (4 shared papers)Cornelia M. van Duijn (2 shared papers)Jessie Theuns (5 shared papers)Kristel Sleegers (5 shared papers)J. Wauters (2 shared papers)
Journals: Blood (4 papers)Human Mutation (4 papers)Human Genetics (3 papers)Neurology (3 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (3 papers)
Partner nations: Belgium France Netherlands

In The Last Decade

D. Goossens

73 papers receiving 1.9k citations

Peers

Countries citing papers authored by D. Goossens

Since Specialization

Citations

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

Fields of papers citing papers by D. Goossens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy Brain ·Kristel Sleegers, Nathalie Brouwers, Ilse Gijselinck, Jessie Theuns, D. Goossens, J. Wauters, Jurgen Del‐Favero, Marc Cruts, Cornelia M. van Duijn, Christine Van Broeckhoven	2006	291
2	Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis Nature Genetics ·Yurii S. Aulchenko, Ilse A Hoppenbrouwers, Sreeram V. Ramagopalan, Linda Broer, Naghmeh Jafari, Jan Hillert, Jenny Link, Wangko Lundström, Eva Greiner, A. Dessa Sadovnick, D. Goossens, Christine Van Broeckhoven, Jurgen Del‐Favero, George C. Ebers, Ben A. Oostra, Cornelia M. van Duijn, Rogier Q. Hintzen	2008	130
3	Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations Neurology ·Liesbet Deprez, Sarah Weckhuysen, Philip Holmgren, Arvid Suls, Tom Van Dyck, D. Goossens, Jurgen Del‐Favero, Anna Jansen, Kristien Verhaert, Liesbet Lagae, Albena Jordanova, Rudy Van Coster, Simone C. Yendle, Samuel F. Berkovic, Ingrid E. Scheffer, Berten Ceulemans, Peter De Jonghe	2010	123
4	Microdeletions involving theSCN1A gene may be common inSCN1A-mutation-negative SMEI patients Human Mutation ·Arvid Suls, Kristl G. Claeys, D. Goossens, B Harding, Rob van Luijk, Stefaan Scheers, Liesbet Deprez, Dominique Audenaert, Tine Van Dyck, Sabine Beeckmans, Iris Smouts, Berten Ceulemans, Lieven Lagae, Gunnar Buyse, Nina Barišić, Jean‐Paul Misson, J. Wauters, Jurgen Del‐Favero, Peter De Jonghe, Lieve Claes	2006	90
5	Mutations in SACS cause atypical and late-onset forms of ARSACS Neurology ·Jonathan Baets, Tine Deconinck, Kaat Smets, D. Goossens, Peter Van den Bergh, Karine Dahan, Eric Schmedding, Patrick Santens, V. Milić Rašić, Philip Van Damme, Wim Robberecht, Linda De Meırleır, B. Michielsens, Jurgen Del‐Favero, Albena Jordanova, Peter De Jonghe	2010	86
6	Progranulin locus deletion in frontotemporal dementia Human Mutation ·Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, D. Goossens, Karin Peeters, Maria Mattheijssens, Ellen Corsmit, Jurgen Del‐Favero, Peter P. De Deyn, Christine Van Broeckhoven, Marc Cruts	2007	74
7	Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS Neurobiology of Aging ·Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, Wim Robberecht, Jean‐Jacques Martin, Rik Vandenberghe, Raf Sciot, Bart Dermaut, D. Goossens, Julie van der Zee, Tim De Pooter, Jurgen Del‐Favero, Patrick Santens, Peter De Jonghe, Peter P. De Deyn, Christine Van Broeckhoven, Marc Cruts	2008	72
8	Human monoclonal antibody against Rh(D) antigen: partial characterization of the Rh(D) polypeptide from human erythrocytes Blood ·C Bloy, Dominique Blanchard, P. Lambin, D. Goossens, P. Rouger, C Salmon, JP Cartron	1987	57
9	Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11 Clinical Genetics ·Nele Hilgert, Fatemeh Alasti, Nele Dieltjens, Barbara Pawlik, Bernd Wollnik, Zehra Oya Uyguner, Sedigheh Delmaghani, Dominique Weil, Christine Petit, Etienne Danis, Tao Yang, Effie Pandelia, MB Petersen, D. Goossens, JD Favero, Mohammad Hossein Sanati, (unknown), Guy Van Camp	2008	55
10	Familial occipitotemporal lobe epilepsy and migraine with visual aura Neurology ·Liesbet Deprez, Kristel Peeters, Wim Van Paesschen, Kristl G. Claeys, Laurence Claes, Arvid Suls, Dominique Audenaert, Tine Van Dyck, D. Goossens, Jurgen Del‐Favero, Peter De Jonghe	2007	55
11	Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population PLoS ONE ·Lotte Moens, Peter De Rijk, Joke Reumers, Maarten Van Den Bossche, Wim Glassee, Sonia De Zutter, An‐Sofie Lenaerts, Annelie Nordin, Lars‐Göran Nilsson, Ignacio Medina Castello, Karl‐Fredrik Norrback, D. Goossens, Kristel Van Steen, Rolf Adolfsson, Jurgen Del‐Favero	2011	51
12	Gene copy number variation in schizophrenia Schizophrenia Research ·Smitha R. Sutrala, D. Goossens, Noel N. Williams, Lien Heyrman, Rolf Adolfsson, Nadine Norton, Paul R. Buckland, Jurgen Del‐Favero	2007	50
13	Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing Human Mutation ·D. Goossens, Lotte Moens, Eva Nelis, An‐Sofie Lenaerts, Wim Glassee, Andreas Kalbe, Bruno S. Frey, Guido Kopal, Peter De Jonghe, Peter De Rijk, Jurgen Del‐Favero	2008	50
14	Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population Human Mutation ·Karen Nuytemans, Bram Meeus, David Crosiers, Nathalie Brouwers, D. Goossens, Sebastiaan Engelborghs, Philippe Pals, Barbara Pickut, Marleen Van den Broeck, Ellen Corsmit, Patrick Cras, Peter Paul De Deyn, Jurgen Del‐Favero, Christine Van Broeckhoven, Jessie Theuns	2009	46
15	Strong evidence that GNB1L is associated with schizophrenia Human Molecular Genetics ·Nigel Williams, Beate Glaser, Nadine Norton, Hywel Williams, Timothy Pierce, Valentina Moskvina, Stephen Monks, Jurgen Del‐Favero, D. Goossens, Dan Rujescu, Ina Giegling, George Kirov, Nicholas Craddock, Kieran C. Murphy, Michael O‘Donovan, Michael J. Owen	2007	44
16	Role of RhAG and AQP1 in NH3 and CO2 gas transport in red cell ghosts: a stopped-flow analysis Transfusion Clinique et Biologique ·Pierre Ripoche, D. Goossens, Olivier Devuyst, Pierre Gane, Yves Colin, A. S. Verkman, J.-P. Cartron	2006	44
17	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, Dirk Van den Bossche, H. Backhovens, Julien Mendlewicz, Christine Van Broeckhoven, Jurgen Del‐Favero	2003	40
18	A Soluble Recombinant Multimeric Anti-Rh(D) Single-Chain Fv/CR1 Molecule Restores the Immune Complex Binding Ability of CR1-Deficient Erythrocytes The Journal of Immunology ·S. Oudin, Marcelle Tonye Libyh, D. Goossens, Xavier Dervillez, F. Philbert, Brigitte Réveil, F. Bougy, Thierry Tabary, P. Rouger, David Klatzmann, J. Cohen	2000	35
19	A Recombinant Human scFv Anti-Rh(D) Antibody With Multiple Valences Using a C-Terminal Fragment of C4-Binding Protein Blood ·Marcelle Tonye Libyh, D. Goossens, S. Oudin, Nitika Gupta, Xavier Dervillez, Grzegorz R. Juszczak, Pascale Cornillet, F. Bougy, Brigitte Réveil, F. Philbert, Thierry Tabary, David Klatzmann, P. Rouger, J. Cohen	1997	35
20	A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder Brain ·Veerle Bogaerts, Sebastiaan Engelborghs, Samir Kumar‐Singh, D. Goossens, Barbara Pickut, Julie van der Zee, Kristel Sleegers, Karin Peeters, Jean‐Jacques Martin, Jurgen Del‐Favero, Thomas Gasser, Dennis W. Dickson, Zbigniew K. Wszołek, Peter Paul De Deyn, Jessie Theuns, Christine Van Broeckhoven	2007	34

About D. Goossens

D. Goossens is a scholar working on Molecular Biology, Genetics, Physiology, Hematology and Neurology, having authored 73 papers that have together received 2.0k indexed citations. Recurring topics across this work include Blood groups and transfusion (15 papers), Erythrocyte Function and Pathophysiology (12 papers), Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Monoclonal and Polyclonal Antibodies Research (6 papers), Genetic Neurodegenerative Diseases (6 papers), Genomics and Rare Diseases (6 papers) and Neonatal Health and Biochemistry (4 papers). The work is most often cited by research in Neurology (283 citations), Neurology (150 citations), Genetics (488 citations), Physiology (422 citations) and Hematology (177 citations). D. Goossens has collaborated with scholars based in Belgium, France and Netherlands. Frequent co-authors include Jurgen Del‐Favero, Christine Van Broeckhoven, Marc Cruts, Ilse Gijselinck, Cornelia M. van Duijn, Jessie Theuns, Kristel Sleegers, J. Wauters, Peter De Jonghe and Nathalie Brouwers. Their work appears in journals such as Blood, Human Mutation, Human Genetics, Neurology and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

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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D. Goossens

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