J. Dreesen

502 total citations
14 papers, 361 citations indexed

About

J. Dreesen is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, J. Dreesen has authored 14 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 5 papers in Molecular Biology and 4 papers in Clinical Biochemistry. Recurrent topics in J. Dreesen's work include Prenatal Screening and Diagnostics (9 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). J. Dreesen is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (4 papers). J. Dreesen collaborates with scholars based in Netherlands, United States and United Kingdom. J. Dreesen's co-authors include Edith Coonen, Hubert J.M. Smeets, Aimée Paulussen, Christine de Die‐Smulders, Marion Drüsedau, Joep Geraedts, Suzanne C.E.H. Sallevelt, Servi J.C. Stevens, Serdar Coşkun and Dagan Wells and has published in prestigious journals such as Nucleic Acids Research, Human Reproduction and Journal of Medical Genetics.

In The Last Decade

J. Dreesen

14 papers receiving 337 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. Dreesen Netherlands	9	213	179	143	83	41	14	361
Alison Lashwood United Kingdom	10	268 1.3×	141 0.8×	168 1.2×	24 0.3×	52 1.3×	20	439
Maartje C. van Rij Netherlands	7	185 0.9×	84 0.5×	82 0.6×	15 0.2×	39 1.0×	8	266
Júlia Baptista United Kingdom	12	95 0.4×	254 1.4×	291 2.0×	12 0.1×	23 0.6×	22	496
J Boué France	7	98 0.5×	141 0.8×	163 1.1×	18 0.2×	59 1.4×	23	358
Pingyuan Xie China	13	196 0.9×	182 1.0×	151 1.1×	6 0.1×	93 2.3×	36	388
M. Pierluigi Italy	9	160 0.8×	129 0.7×	264 1.8×	9 0.1×	30 0.7×	18	349
Jia‐Chi Wang Canada	12	196 0.9×	118 0.7×	234 1.6×	5 0.1×	21 0.5×	28	385
Sue Ann Berend United States	15	336 1.6×	174 1.0×	432 3.0×	8 0.1×	47 1.1×	20	584
Julie Scuffins United States	5	126 0.6×	123 0.7×	215 1.5×	16 0.2×	5 0.1×	10	348
Prochi F. Madon India	7	163 0.8×	102 0.6×	190 1.3×	4 0.0×	72 1.8×	25	320

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-authorship network of co-authors of J. Dreesen

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

All Works

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

14 of 14 papers shown

Derks, Kasper, Marion Drüsedau, J. Dreesen, et al.. (2022). Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing. Human Reproduction. 37(11). 2700–2708. 3 indexed citations

Esteki, Masoud Zamani, Cindy Melotte, Edith Coonen, et al.. (2019). Agilent Technologies OnePGT solution: External verification on both blastomere and trophectoderm biopsies. Reproductive BioMedicine Online. 38. e11–e12. 1 indexed citations

Schoot, Vyne van der, Wybo Dondorp, J. Dreesen, et al.. (2019). Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas. Human Reproduction. 34(6). 1146–1154. 16 indexed citations

Otten, Auke B.C., Suzanne C.E.H. Sallevelt, Phillippa J. Carling, et al.. (2018). Mutation-specific effects in germline transmission of pathogenic mtDNA variants. Human Reproduction. 33(7). 1331–1341. 38 indexed citations

Sallevelt, Suzanne C.E.H., J. Dreesen, Edith Coonen, et al.. (2017). Preimplantation genetic diagnosis for mitochondrial DNA mutations: analysis of one blastomere suffices. Journal of Medical Genetics. 54(10). 693–697. 15 indexed citations

Sallevelt, Suzanne C.E.H., J. Dreesen, Marion Drüsedau, et al.. (2016). PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy. Human Reproduction. 32(3). 698–703. 16 indexed citations

Coşkun, Serdar, R. Prates, S. Munné, et al.. (2014). Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro. Genetics in Medicine. 16(11). 838–845. 136 indexed citations

Sallevelt, Suzanne C.E.H., J. Dreesen, Marion Drüsedau, et al.. (2013). Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success. Journal of Medical Genetics. 50(2). 125–132. 63 indexed citations

Stevens, Servi J.C., J. Dreesen, Marion Drüsedau, et al.. (2012). SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations. European Journal of Human Genetics. 20(9). 938–944. 33 indexed citations

10.

Dreesen, J., Marion Drüsedau, Hubert J.M. Smeets, et al.. (2008). Validation of preimplantation genetic diagnosis by PCR analysis: genotype comparison of the blastomere and corresponding embryo, implications for clinical practice. Molecular Human Reproduction. 14(10). 573–579. 17 indexed citations

11.

Dreesen, J., L.J.A.M. Jacobs, M. Bras, et al.. (1999). O-075. Multiplex PCR of polymorphic markers flanking the CFTR gene: a general approach for pre-implantation genetic diagnosis of cystic fibrosis. Human Reproduction. 14(Suppl_3). 41–42. 2 indexed citations

12.

Die‐Smulders, Christine de, Joep Geraedts, J. Dreesen, Edith Coonen, & J. A. Land. (1998). [Genetic diagnosis of IVF embryos: preliminary results from 'preimplantation genetic diagnoses' in the Netherlands].. PubMed. 142(45). 2441–4. 8 indexed citations

13.

Oost, Bernard A. van, Anne Smits, J. Dreesen, et al.. (1991). Multipoint linkage analysis of DXS369 and DXS304 in fragile X families. American Journal of Medical Genetics. 38(2-3). 328–331. 9 indexed citations

14.

Hurk, José A. J. M. van den, et al.. (1991). Two polymorphisms at the DXS539 locus. Nucleic Acids Research. 19(7). 1723–1723. 4 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.

Explore authors with similar magnitude of impact