J. Dreesen

502 citations

14 papers · 361 · h-index 9

Impact in

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

Papers in

Pediatrics, Perinatology and Child Health 9
- Prenatal Screening and Diagnostics 9
- Assisted Reproductive Technology and Twin Pregnancy 2
- Ethics and Legal Issues in Pediatric Healthcare 1
Molecular Biology 5
- Mitochondrial Function and Pathology 4

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

In The Last Decade

J. Dreesen

14 papers receiving 337 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

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14 of 14 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, R. Prates, 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	136
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	63
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	38
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	33
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	17
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	16
7	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
8	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	15
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	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
12	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	3
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	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, Clinical Biochemistry, Genetics and Cancer Research, having authored 14 papers that have together received 361 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (9 papers), Metabolism and Genetic Disorders (4 papers), Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Cancer Genomics and Diagnostics (2 papers), Assisted Reproductive Technology and Twin Pregnancy (2 papers), Cystic Fibrosis Research Advances (1 paper) and Ethics and Legal Issues in Pediatric Healthcare (1 paper). The work is most often cited by research in Clinical Biochemistry (83 citations), Pediatrics, Perinatology and Child Health (213 citations), Genetics (143 citations), Molecular Biology (179 citations) and Reproductive Medicine (18 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, Christine de Die‐Smulders, Marion Drüsedau, Joep Geraedts, Servi J.C. Stevens, Suzanne C.E.H. Sallevelt, R. Prates and Sharyn Stock‐Myer. Their work appears in journals such as Human Reproduction, Journal of Medical Genetics, Molecular Human Reproduction, Reproductive BioMedicine Online and European Journal of Human 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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