Jos Dreesen

1.4k total citations
32 papers, 898 citations indexed

About

Jos Dreesen is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Jos Dreesen has authored 32 papers receiving a total of 898 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Pediatrics, Perinatology and Child Health, 13 papers in Genetics and 12 papers in Molecular Biology. Recurrent topics in Jos Dreesen's work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Jos Dreesen is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Jos Dreesen collaborates with scholars based in Netherlands, Belgium and France. Jos Dreesen's co-authors include Joep Geraedts, J.L.H. Evers, John C.M. Dumoulin, Bernard A. van Oost, M. Bras, Nine Knoers, Marian Verdijk, Ans M.W. van den Ouweland, L.A.H. Monnens and Mariano Rocchi and has published in prestigious journals such as Nature Genetics, Annals of the New York Academy of Sciences and Human Reproduction.

In The Last Decade

Jos Dreesen

31 papers receiving 864 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jos Dreesen Netherlands 17 382 372 314 127 114 32 898
Susan H. Black United States 20 632 1.7× 275 0.7× 505 1.6× 146 1.1× 35 0.3× 41 1.2k
Arabella Smith Australia 22 591 1.5× 605 1.6× 1.2k 3.7× 132 1.0× 75 0.7× 119 1.8k
J G Lesko United States 12 308 0.8× 383 1.0× 274 0.9× 62 0.5× 63 0.6× 15 805
Julie Steffann France 23 346 0.9× 809 2.2× 445 1.4× 111 0.9× 32 0.3× 67 1.4k
Ilse Feenstra Netherlands 19 377 1.0× 479 1.3× 731 2.3× 74 0.6× 49 0.4× 45 1.3k
J.J.M. Engelen Netherlands 23 464 1.2× 680 1.8× 1.1k 3.6× 118 0.9× 169 1.5× 92 1.7k
J. O. Van Hemel Netherlands 21 356 0.9× 457 1.2× 809 2.6× 107 0.8× 57 0.5× 38 1.1k
Ayala Aviram‐Goldring Israel 17 244 0.6× 411 1.1× 429 1.4× 115 0.9× 94 0.8× 31 872
Rena E. Falk United States 19 174 0.5× 408 1.1× 447 1.4× 23 0.2× 75 0.7× 39 1.0k
Arie P.T. Smits Netherlands 21 283 0.7× 612 1.6× 858 2.7× 119 0.9× 39 0.3× 43 1.2k

Countries citing papers authored by Jos Dreesen

Since Specialization
Citations

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

Fields of papers citing papers by Jos Dreesen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jos Dreesen

This figure shows the co-authorship network connecting the top 25 collaborators of Jos Dreesen. A scholar is included among the top collaborators of Jos Dreesen 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 Jos Dreesen. Jos Dreesen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Carvalho, Filipa, Céline Moutou, Eftychia Dimitriadou, et al.. (2020). ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders†. Human Reproduction Open. 2020(3). hoaa018–hoaa018. 99 indexed citations
2.
Montfoort, Aafke P.A. van, M. Meijer‐Hoogeveen, Frank J. Broekmans, et al.. (2018). Perinatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014. Journal of Assisted Reproduction and Genetics. 35(11). 1995–2002. 17 indexed citations
3.
Derks-Smeets, I. A. P., Theodora C van Tilborg, Aafke P.A. van Montfoort, et al.. (2017). BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD. Journal of Assisted Reproduction and Genetics. 34(11). 1475–1482. 37 indexed citations
4.
Derks-Smeets, I. A. P., Christine de Die‐Smulders, Shari Mackens, et al.. (2014). Hereditary breast and ovarian cancer and reproduction: an observational study on the suitability of preimplantation genetic diagnosis for both asymptomatic carriers and breast cancer survivors. Breast Cancer Research and Treatment. 145(3). 673–681. 35 indexed citations
5.
Drüsedau, Marion, Jos Dreesen, I. A. P. Derks-Smeets, et al.. (2013). PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers. European Journal of Human Genetics. 21(12). 1361–1368. 16 indexed citations
6.
Dreesen, Jos, Aspasia Destouni, Georgia Kourlaba, et al.. (2013). Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study. European Journal of Human Genetics. 22(8). 1012–1018. 48 indexed citations
7.
Rij, Maartje C. van, Marjan De Rademaeker, Céline Moutou, et al.. (2011). Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres. European Journal of Human Genetics. 20(4). 368–375. 36 indexed citations
8.
Berking, Matthias, et al.. (2004). Was wollen Patienten wann und wo erreichen? Die Veränderungen von Therapiezielen während und nach einer stationären Verhaltenstherapie. Verhaltenstherapie. 14(4). 245–252. 4 indexed citations
9.
Dreesen, Jos, L.J.A.M. Jacobs, M. Bras, et al.. (2000). Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis*. Molecular Human Reproduction. 6(5). 391–396. 69 indexed citations
10.
Dumoulin, John C.M., M. Bras, Edith Coonen, et al.. (1998). Effect of Ca2+/Mg2+-free medium on the biopsy procedure for preimplantation genetic diagnosis and further development of human embryos. Human Reproduction. 13(10). 2880–2883. 54 indexed citations
11.
Dreesen, Jos. (1998). Preimplantation genetic diagnosis of spinal muscular atrophy. Molecular Human Reproduction. 4(9). 881–885. 45 indexed citations
12.
Coonen, Edith, John C.M. Dumoulin, Jos Dreesen, et al.. (1996). Clinical application of FISH for sex determination of embryos in preimplantation diagnosis of X-linked diseases. Journal of Assisted Reproduction and Genetics. 13(2). 133–136. 13 indexed citations
13.
Dreesen, Jos, John C.M. Dumoulin, J.L.H. Evers, Joep Geraedts, & M.H.E.C. Pieters. (1995). Diagnosing and preventing inherited disease: Multiplex polymerase chain reaction for sex determination of single mouse blastomeres. Human Reproduction. 10(3). 743–748. 8 indexed citations
14.
Smits, Arie P.T., et al.. (1994). Prediction of mental status in carriers of the fragile X mutation using CGG repeat length. American Journal of Medical Genetics. 51(4). 497–500. 24 indexed citations
15.
Dreesen, Jos, et al.. (1993). DXS539, a polymorphic DNA marker proximal of the fragile-X gene. Human Genetics. 91(1). 80–82. 1 indexed citations
16.
Knoers, Nine, et al.. (1993). Nephrogenic diabetes insipidus: identification of the genetic defect. Pediatric Nephrology. 7(5). 685–688. 11 indexed citations
17.
Oost, Bernard A. van, Arie P.T. Smits, Jos Dreesen, Ans M.W. van den Ouweland, & Ben A. Oostra. (1992). Validation of linkage‐based DNA‐diagnosis of fragile X gene carriers with the CGG repeat probe. American Journal of Medical Genetics. 43(1-2). 320–327. 4 indexed citations
18.
Smits, Arie P.T., Bernard A. van Oost, Anton F. J. de Haan, et al.. (1992). Penetrance of Fra(X) gene: Influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male. American Journal of Medical Genetics. 43(1-2). 365–372. 7 indexed citations
19.
Smits, Arie P.T., et al.. (1992). High prevalence of the Fra(X) syndrome cannot be explained by a high mutation rate. American Journal of Medical Genetics. 43(1-2). 345–352. 12 indexed citations
20.
Bröcker-Vriends, A, E Briët, H. H. H. Kanhai, et al.. (1988). First trimester prenatal diagnosis of haemophilia A: Two years' experience. Prenatal Diagnosis. 8(6). 411–421. 8 indexed citations

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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