D. Goossens

3.7k total citations
75 papers, 1.9k citations indexed

About

D. Goossens is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, D. Goossens has authored 75 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 20 papers in Genetics and 17 papers in Physiology. Recurrent topics in D. Goossens's work include Blood groups and transfusion (15 papers), Erythrocyte Function and Pathophysiology (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). D. Goossens is often cited by papers focused on Blood groups and transfusion (15 papers), Erythrocyte Function and Pathophysiology (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). D. Goossens collaborates with scholars based in Belgium, France and Netherlands. D. Goossens's co-authors include Jurgen Del‐Favero, Christine Van Broeckhoven, Marc Cruts, Ilse Gijselinck, Cornelia M. van Duijn, Kristel Sleegers, Jessie Theuns, J. Wauters, Peter De Jonghe and Nathalie Brouwers and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Blood.

In The Last Decade

D. Goossens

74 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-authorship network of co-authors of D. Goossens

This figure shows the co-authorship network connecting the top 25 collaborators of D. Goossens. A scholar is included among the top collaborators of D. Goossens based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with D. Goossens. D. Goossens is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Goat Milk‐Based Infant Formula and the Prevalence of Gastrointestinal Symptoms in Infants: A Real‐World‐Evidence Study From Brazil, Mexico, Russia, and the Netherlands 2025 ·Health Science Reports ·Karen Knipping, (unknown), D. Goossens, Linde van Lee, (unknown)	0
2	817P Response to olaparib monotherapy in relapsed ovarian cancer by HRR gene mutational status and HRD scarring analysis: Results from the randomized phase II CLIO trial 2020 ·Annals of Oncology ·Adriaan Vanderstichele, Liselore Loverix, (unknown), Lien Heyrman, Toon Van Gorp, Els Van Nieuwenhuysen, Sileny Han, Siel Olbrecht, Patrick Berteloot, Patrick Neven, Rogier Schepers, Pieter Busschaert, D. Goossens, Diether Lambrechts, Ignace Vergote	1
3	Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness 2015 ·PubMed ·Mandy Johnstone, Alan Maclean, Lien Heyrman, An‐Sofie Lenaerts, Annelie Nordin, Lars‐Göran Nilsson, Peter De Rijk, D. Goossens, Rolf Adolfsson, David M. St. Clair, Jérémy Hall, Stephen M. Lawrie, Andrew M. McIntosh, Jurgen Del‐Favero, Douglas Blackwood, Ben Pickard	14
4	Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population 2009 ·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	46
5	Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11 2008 ·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, (unknown), MB Petersen, D. Goossens, (unknown), Mohammad Hossein Sanati, Richard J. Smith, Guy Van Camp	55
6	Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS 2007 ·Ghent University Academic Bibliography (Ghent University) ·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	3
7	A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder 2007 ·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	34
8	Gene copy number variation in schizophrenia 2007 ·Schizophrenia Research ·(unknown), D. Goossens, Noel N. Williams, Lien Heyrman, Rolf Adolfsson, Nadine Norton, Paul R. Buckland, Jurgen Del‐Favero	50
9	Strong evidence that GNB1L is associated with schizophrenia 2007 ·Human Molecular Genetics ·Nigel Williams, Beate Glaser, Nadine Norton, Hywel Williams, (unknown), 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	44
10	Progranulin locus deletion in frontotemporal dementia 2007 ·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	73
11	Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families 2007 ·Molecular Psychiatry ·(unknown), Maaike Alaerts, Daniel Souery, D. Goossens, (unknown), Ruth Navon, Christine Van Broeckhoven, Julien Mendlewicz, Jurgen Del‐Favero, Stephan Claes	20
12	Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation 2005 ·Human Genetics ·Liesbet Deprez, Lieve Claes, Kristl G. Claeys, Dominique Audenaert, Tine Van Dyck, D. Goossens, Wim Van Paesschen, Jurgen Del‐Favero, Christine Van Broeckhoven, Peter De Jonghe	16
13	Trinucleotide repeat expansions: do they contribute to bipolar disorder? 2001 ·Brain Research Bulletin ·D. Goossens, Jurgen Del‐Favero, Christine Van Broeckhoven	15
14	No CAG or CCG repeats within 18Q2133-q23 involved in bipolar disorder 2000 ·American Journal of Medical Genetics Part A ·D. Goossens, S Villafuerte, Sofie Van Gestel, Fadel Tissir, Christine Van Broeckhoven, Jurgen Del‐Favero	1
15	A Soluble Recombinant Multimeric Anti-Rh(D) Single-Chain Fv/CR1 Molecule Restores the Immune Complex Binding Ability of CR1-Deficient Erythrocytes 2000 ·The Journal of Immunology ·(unknown), (unknown), D. Goossens, Xavier Dervillez, (unknown), Brigitte Réveil, (unknown), Thierry Tabary, P. Rouger, David Klatzmann, J. Cohen	35
16	Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation 1999 ·Human Genetics ·Jurgen Del‐Favero, D. Goossens, Peter De Jonghe, Kathleen F. Benson, Andrej Michalik, (unknown), Marshall S. Horwitz, Christine Van Broeckhoven	4
17	YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14 1999 ·Gene ·Jurgen Del‐Favero, D. Goossens, (unknown), Christine Van Broeckhoven	6
18	Amino acid sequence of the variable domains of a human anti-Rh(c) antibody: Presence of an unusually long CDR3 in the λ chain 1989 ·Molecular Immunology ·Lotfi Chouchane, (unknown), D. Goossens, P. Rouger, A. Donny Strosberg	1
19	Immunological characterization of 21 human anti-Rh (D) monoclonal antibodies 1988 ·Revue Fran&#xE7 aise de Transfusion et Immuno-h&#xE9 matologie ·(unknown), Michael T. Klein, (unknown), (unknown), (unknown), D. Goossens, Philippe Rouger	2
20	Characterization of the D, c, E and G antigens of the Rh blood group system with human monoclonal antibodies 1988 ·Molecular Immunology ·C Bloy, Dominique Blanchard, P. Lambin, D. Goossens, Philippe Rouger, Charles T. Salmon, S. P. Masouredis, Jean‐Pierre Cartron	19

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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