J. Dreesen

509 citations

15 papers · 384 · h-index 9

Impact in

Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders

Papers in

Pediatrics, Perinatology and Child Health 7
- Prenatal Screening and Diagnostics 7
Molecular Biology 6
- Mitochondrial Function and Pathology 5
- Ubiquitin and proteasome pathways 1

Co-authors: Edith Coonen (10 shared papers)Hubert J.M. Smeets (8 shared papers)Aimée Paulussen (7 shared papers)Marion Drüsedau (7 shared papers)Christine de Die‐Smulders (9 shared papers)Suzanne C.E.H. Sallevelt (5 shared papers)Joep Geraedts (4 shared papers)Servi J.C. Stevens (3 shared papers)
Journals: Human Reproduction (5 papers)Journal of Medical Genetics (2 papers)European Journal of Human Genetics (1 paper)Molecular Human Reproduction (1 paper)Reproductive BioMedicine Online (1 paper)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

J. Dreesen

15 papers receiving 355 citations

Peers

Countries citing papers authored by J. Dreesen

Since Specialization

Citations

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

Fields of papers citing papers by J. Dreesen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

#	Work
1	Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro Genetics in Medicine ·Senthilkumar A. Natesan, Alex J. Bladon, Serdar Coşkun, Wafa Qubbaj, (unknown), S. Munné, Edith Coonen, J. Dreesen, Servi J.C. Stevens, Aimée Paulussen, Sharyn Stock‐Myer, L. Wilton, Souraya Jaroudi, Dagan Wells, Anthony P. Brown, Alan H. Handyside	2014	140
2	Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success Journal of Medical Genetics ·Suzanne C.E.H. Sallevelt, J. Dreesen, Marion Drüsedau, Sabine Spierts, Edith Coonen, Florence H. J. van Tienen, Ronald J T van Golde, I.F.M. de Coo, Joep Geraedts, Christine de Die‐Smulders, Hubert J.M. Smeets	2013	70
3	Mutation-specific effects in germline transmission of pathogenic mtDNA variants Human Reproduction ·Auke B.C. Otten, Suzanne C.E.H. Sallevelt, Phillippa J. Carling, J. Dreesen, Marion Drüsedau, Sabine Spierts, Aimée Paulussen, Christine de Die‐Smulders, Mary Herbert, Patrick F. Chinnery, David C. Samuels, Patrick Lindsey, Hubert J.M. Smeets	2018	40
4	SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations European Journal of Human Genetics ·Chris MJ van Uum, Servi J.C. Stevens, J. Dreesen, Marion Drüsedau, Hubert J.M. Smeets, B.H.T.M. Hollanders-Crombach, Christine EM de Die-Smulders, Joep Geraedts, J.J.M. Engelen, Edith Coonen	2012	37
5	Validation of preimplantation genetic diagnosis by PCR analysis: genotype comparison of the blastomere and corresponding embryo, implications for clinical practice Molecular Human Reproduction ·J. Dreesen, Marion Drüsedau, Hubert J.M. Smeets, C. de Die-Smulders, Edith Coonen, John C.M. Dumoulin, Marij Gielen, J.L.H. Evers, J. Herbergs, J.P.M. Geraedts	2008	18
6	PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy Human Reproduction ·Suzanne C.E.H. Sallevelt, J. Dreesen, Marion Drüsedau, Debby M.E.I. Hellebrekers, Aimée Paulussen, Edith Coonen, Ronald J T van Golde, Joep Geraedts, Luca Gianaroli, Maria Cristina Magli, Massimo Zeviani, Hubert J.M. Smeets, Christine de Die‐Smulders	2016	17
7	Preimplantation genetic diagnosis for mitochondrial DNA mutations: analysis of one blastomere suffices Journal of Medical Genetics ·Suzanne C.E.H. Sallevelt, J. Dreesen, Edith Coonen, Aimée Paulussen, Debby M.E.I. Hellebrekers, Christine de Die‐Smulders, Hubert J.M. Smeets, Patrick Lindsey	2017	16
8	Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas Human Reproduction ·Vyne van der Schoot, Wybo Dondorp, J. Dreesen, Edith Coonen, Aimée Paulussen, Guido de Wert, Christine de Die‐Smulders	2019	16
9	Multipoint linkage analysis of DXS369 and DXS304 in fragile X families American Journal of Medical Genetics ·Bernard A. van Oost, Anne Smits, J. Dreesen, Dominique Smeets, L.F. Perdon, Coen A. M. van Bennekom, Niklas Dahl, Egbert Bakker, B. A. Oostra	1991	9
10	[Genetic diagnosis of IVF embryos: preliminary results from 'preimplantation genetic diagnoses' in the Netherlands]. PubMed ·Christine de Die‐Smulders, Joep Geraedts, J. Dreesen, Edith Coonen, J. A. Land	1998	8
11	Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing Human Reproduction ·Wanwisa van Dijk, Kasper Derks, Marion Drüsedau, Jeroen Meekels, Rebekka M. Koeck, Rick Essers, J. Dreesen, Edith Coonen, Christine de Die‐Smulders, Servi J.C. Stevens, Han G. Brunner, Arthur van den Wijngaard, Aimée Paulussen, Masoud Zamani Esteki	2022	4
12	Two polymorphisms at the DXS539 locus Nucleic Acids Research ·José A. J. M. van den Hurk, J. Dreesen, Harold van den Berg, Coen A. M. van Bennekom, Ans M. W. van den Ouweland, Bernard A. van Oost	1991	4
13	O-075. Multiplex PCR of polymorphic markers flanking the CFTR gene: a general approach for pre-implantation genetic diagnosis of cystic fibrosis Human Reproduction ·J. Dreesen, L.J.A.M. Jacobs, M. Bras, Hubert J.M. Smeets, J. Herbergs, John C.M. Dumoulin, J.L.H. Evers, J.P.M. Geraedts	1999	2
14	Selecting the Right Embryo in Mitochondrial Disorders Data Archiving and Networked Services (DANS) ·Suzanne C.E.H. Sallevelt, J. Dreesen, I.F.M. de Coo, Christine de Die‐Smulders, Hubert J.M. Smeets	2015	2
15	Agilent Technologies OnePGT solution: External verification on both blastomere and trophectoderm biopsies Reproductive BioMedicine Online ·Masoud Zamani Esteki, Cindy Melotte, Edith Coonen, J. Dreesen, Aimée Paulussen, John C.M. Dumoulin, Christian Van Uum, Marion Drüsedau, J.J.M. Engelen, Kasper Derks, R. van Golde, Eftychia Dimitriadou, Heleen Masset, Katrien O. François, Joke Allemeersch, Rebecca Richards, Sara Moeys, Jessie Theuns, Christine de Die‐Smulders, Joris Vermeesch	2019	1

About J. Dreesen

J. Dreesen is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics, Clinical Biochemistry and Genetics, having authored 15 papers that have together received 384 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Mitochondrial Function and Pathology (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Metabolism and Genetic Disorders (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Ubiquitin and proteasome pathways (1 paper), Genomics and Rare Diseases (1 paper) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (201 citations), Clinical Biochemistry (73 citations), Genetics (112 citations), Molecular Biology (176 citations) and Reproductive Medicine (15 citations). J. Dreesen has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Edith Coonen, Hubert J.M. Smeets, Aimée Paulussen, Marion Drüsedau, Christine de Die‐Smulders, Suzanne C.E.H. Sallevelt, Joep Geraedts, Servi J.C. Stevens, Serdar Coşkun and Souraya Jaroudi. Their work appears in journals such as Human Reproduction, Journal of Medical Genetics, European Journal of Human Genetics, Molecular Human Reproduction and Reproductive BioMedicine Online.

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.

Explore authors with similar magnitude of impact

J. Dreesen

Impact in

Papers in i

In The Last Decade

J. Dreesen

Peers

Countries citing papers authored by J. Dreesen

Fields of papers citing papers by J. Dreesen

All Works

About J. Dreesen

Explore authors with similar magnitude of impact

Papers in