J.J.M. Engelen

3.1k total citations
92 papers, 1.7k citations indexed

About

J.J.M. Engelen is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, J.J.M. Engelen has authored 92 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Genetics, 35 papers in Plant Science and 32 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in J.J.M. Engelen's work include Genomic variations and chromosomal abnormalities (60 papers), Chromosomal and Genetic Variations (35 papers) and Prenatal Screening and Diagnostics (31 papers). J.J.M. Engelen is often cited by papers focused on Genomic variations and chromosomal abnormalities (60 papers), Chromosomal and Genetic Variations (35 papers) and Prenatal Screening and Diagnostics (31 papers). J.J.M. Engelen collaborates with scholars based in Netherlands, United States and Belgium. J.J.M. Engelen's co-authors include A.J.H. Hamers, C. T. R. M. Schrander‐Stumpel, Christine de Die‐Smulders, Wim A. Buurman, Paul Borm, Dominique Smeets, Ron Hochstenbach, Ute Moog, Joep Geraedts and Pino J. Poddighe and has published in prestigious journals such as Environmental Health Perspectives, Human Molecular Genetics and Genomics.

In The Last Decade

J.J.M. Engelen

90 papers receiving 1.6k citations

Peers

Countries citing papers authored by J.J.M. Engelen

Since Specialization

Citations

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

Fields of papers citing papers by J.J.M. Engelen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J.J.M. Engelen

This figure shows the co-authorship network connecting the top 25 collaborators of J.J.M. Engelen. A scholar is included among the top collaborators of J.J.M. Engelen 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.J.M. Engelen. J.J.M. Engelen 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	Perinatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014 2018 ·Journal of Assisted Reproduction and Genetics ·(unknown), Aafke P.A. van Montfoort, M. Meijer‐Hoogeveen, Frank J. Broekmans, Katelijne Bouman, Irene Homminga, Jos Dreesen, Aimée Paulussen, J.J.M. Engelen, Edith Coonen, Vyne van der Schoot, (unknown), N. D. Muntjewerff, Andrea Peeters, Ron van Golde, (unknown), Yvonne Arens, Christine de Die‐Smulders	17
2	A new syndrome of microtia with unilateral renal agenesis and short stature 2012 ·American Journal of Medical Genetics Part A ·Ahmet Okay Çağlayan, Servi J.C. Stevens, (unknown), Munis Dündar, J.J.M. Engelen	1
3	What academic publishing can do for science?* 2011 ·Information Services & Use ·J.J.M. Engelen	1
4	Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986-2007 in the Netherlands 2011 ·Journal of Intellectual Disability Research ·Gert de Graaf, Meindert Haveman, Ron Hochstenbach, J.J.M. Engelen, (unknown), Pino J. Poddighe, Dominique Smeets, Geert Van Hove	35
5	Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Geert Poelmans, J.J.M. Engelen, (unknown), Hubert J.M. Smeets, Eric Schoenmakers, Barbara Franke, Jan K. Buitelaar, (unknown), (unknown), Jean Steyaert, C. T. R. M. Schrander‐Stumpel	63
6	Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH 2006 ·European Journal of Medical Genetics ·(unknown), (unknown), (unknown), Jan Derks, (unknown), J.J.M. Engelen	5
7	XX male with sex reversal and a de novo 11;22 translocation 2006 ·American Journal of Medical Genetics Part A ·Merryn Macville, (unknown), (unknown), Erik Huys, Eric Schoenmakers, (unknown), Beverly S. Emanuel, J.J.M. Engelen	3
8	Sonographic genital ambiguity in a fetus due to a mosaic 45,X/46,X,idic(Y)(qter-p11.32::p11.32-qter) karyotype 2005 ·Prenatal Diagnosis ·(unknown), Guus Hamers, Antonius Mulder, (unknown), J. Offermans, J.J.M. Engelen, (unknown), Simon G. F. Robben, S de Muinck Keizer‐Schrama, Katja P. Wolffenbuttel, Leendert H. J. Looijenga, J. Wolter Oosterhuis, Connie Schrander‐Stumpel, J.G. Nijhuis	7
9	Kabuki syndrome is not caused by an 8p duplication: A cytogenetic study in 20 patients 2004 ·American Journal of Medical Genetics Part A ·J.J.M. Engelen, (unknown), (unknown), C. T. R. M. Schrander‐Stumpel	19
10	Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes 2003 ·American Journal of Medical Genetics Part A ·(unknown), Guus Hamers, (unknown), J.G. Nijhuis, (unknown), J. Herbergs, Christine de Die‐Smulders, C. T. R. M. Schrander‐Stumpel, J.J.M. Engelen	11
11	Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques 2003 ·Prenatal Diagnosis ·Jennie M. Pater, L. Govaerts, de Man, (unknown), G. C. M. L. Christiaens, (unknown), (unknown), J.J.M. Engelen	2
12	Velo‐cardio‐facial syndrome: Clinical report of a 70‐year‐old woman 2002 ·American Journal of Medical Genetics ·W.M.A. Verhoeven, S. Tuinier, J.J.M. Engelen, (unknown), Leopold Curfs	5
13	Familial dup(8)(p12p21.1): Mild phenotypic effect and review of partial 8p duplications 2000 ·American Journal of Medical Genetics ·Ute Moog, J.J.M. Engelen, (unknown), (unknown), Christine de Die‐Smulders	10
14	22q11 deletion: the Maastricht experience focussing on some unusual presentations 1999 ·C. T. R. M. Schrander‐Stumpel, Guus Hamers, J.J.M. Engelen, Suzanna G.M. Frints, J. Offermans, Jean‐Pierre Fryns	2
15	Assignment of the Human Gene for Smoothelin (SMTN) to Chromosome 22q12 by Fluorescence in Situ Hybridization and Radiation Hybrid Mapping 1997 ·Genomics ·J.J.M. Engelen, Lisa E. Esterling, (unknown), Sevilla D. Detera‐Wadleigh, (unknown)	12
16	Clinical features in patients with duplications of chromosome 18 1996 ·(unknown), J.J.M. Engelen, J.H.A.M. Tuerlings, (unknown), Ute Moog, Jean‐Pierre Fryns	1
17	Application of micro-FISH to delineate deletions 1996 ·Cytogenetic and Genome Research ·J.J.M. Engelen, (unknown), (unknown), (unknown), A.J.H. Hamers, Joep Geraedts	12
18	A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome 1994 ·Human Molecular Genetics ·(unknown), Esther de Graaff, (unknown), R. J. E. Jongbloed, Christine de Die‐Smulders, J.J.M. Engelen, Jean‐Pierre Fryns, (unknown), Ben A. Oostra	97
19	Mosaic tetrasomy 8p in two patients: Clinical data and review of the literature 1994 ·American Journal of Medical Genetics ·(unknown), (unknown), J.J.M. Engelen, (unknown), Martine Borghgraef, (unknown), J. Peters, (unknown), Dominique Smeets, Jean‐Pierre Fryns	16
20	Serum Type III Procollagen N-Terminal Peptide in Coal Miners 1992 ·Experimental Lung Research ·Yvonne M. W. Janssen, J.J.M. Engelen, M S Giancola, Robert B. Low, Pamela M. Vacek, Paul J. A. Borm	11

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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