J. O. Van Hemel

1.8k total citations
38 papers, 1.1k citations indexed

About

J. O. Van Hemel is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, J. O. Van Hemel has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 17 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in J. O. Van Hemel's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). J. O. Van Hemel is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). J. O. Van Hemel collaborates with scholars based in Netherlands, Belgium and Australia. J. O. Van Hemel's co-authors include H. J. Eussen, Martinus F. Niermeijer, E. S. Sachs, M. G. J. Jahoda, Eveline Wesby–van Swaay, D. J. J. Halley, Jan C. den Hollander, Frans J. Los, Pieter In 'T Veld and M.H.E.C. Pieters and has published in prestigious journals such as The Lancet, The Journal of Urology and Human Reproduction.

In The Last Decade

J. O. Van Hemel

38 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. O. Van Hemel Netherlands	21	809	457	356	193	164	38	1.1k
Arabella Smith Australia	22	1.2k 1.4×	605 1.3×	591 1.7×	103 0.5×	95 0.6×	119	1.8k
R H Lindenbaum United Kingdom	20	960 1.2×	715 1.6×	529 1.5×	192 1.0×	157 1.0×	39	1.7k
Udo Trautmann Germany	23	1.1k 1.3×	930 2.0×	328 0.9×	331 1.7×	55 0.3×	65	1.7k
E. Boyd United Kingdom	22	804 1.0×	623 1.4×	233 0.7×	304 1.6×	28 0.2×	55	1.3k
Alina T. Midro Poland	16	575 0.7×	436 1.0×	244 0.7×	192 1.0×	72 0.4×	74	943
F. J. Dill Canada	16	579 0.7×	242 0.5×	486 1.4×	105 0.5×	39 0.2×	24	897
Jacques C. Giltay Netherlands	23	760 0.9×	665 1.5×	306 0.9×	130 0.7×	35 0.2×	65	1.3k
Marie‐France Portnoï France	19	574 0.7×	446 1.0×	166 0.5×	119 0.6×	22 0.1×	29	908
Peter Miny Germany	21	629 0.8×	437 1.0×	844 2.4×	65 0.3×	29 0.2×	88	1.5k
Brigitte Benzacken France	20	737 0.9×	462 1.0×	426 1.2×	156 0.8×	43 0.3×	61	1.3k

Countries citing papers authored by J. O. Van Hemel

Since Specialization

Citations

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

Fields of papers citing papers by J. O. Van Hemel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. O. Van Hemel

This figure shows the co-authorship network connecting the top 25 collaborators of J. O. Van Hemel. A scholar is included among the top collaborators of J. O. Van Hemel 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. O. Van Hemel. J. O. Van Hemel 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

Boehmer, Annemie L. M., Rien J.M. Nijman, J. O. Van Hemel, et al.. (2001). ETIOLOGICAL STUDIES OF SEVERE OR FAMILIAL HYPOSPADIAS. The Journal of Urology. 1246–1254. 4 indexed citations

Wouters, Carine, et al.. (2001). Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome. American Journal of Medical Genetics. 102(3). 261–265. 6 indexed citations

Vries, Bert B.A. de, Bert H.J. Eussen, Otto P. van Diggelen, et al.. (1999). Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14). American Journal of Medical Genetics. 87(2). 189–194. 1 indexed citations

Frohn-Mulder, Ingrid M.E., et al.. (1999). Chromosome 22q11 deletions in patients with selected outflow tract malformations.. PubMed. 10(1). 35–41. 24 indexed citations

Opstal, Diane Van, Frans J. Los, J. O. Van Hemel, et al.. (1997). Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection. Human Reproduction. 12(4). 682–686. 115 indexed citations

Veld, Pieter In 'T, R. F. A. Weber, Frans J. Los, et al.. (1997). Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection. Human Reproduction. 12(8). 1642–1644. 43 indexed citations

Duits, Annelien, Rob Willemsen, J. O. Van Hemel, et al.. (1996). Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family.. Journal of Medical Genetics. 33(12). 1007–1010. 62 indexed citations

Graaff, Esther de, et al.. (1996). The fragile X phenotype in a mosaic male with a deletion showing expression of theFMR1 protein in 28% of the cells. American Journal of Medical Genetics. 64(2). 302–308. 34 indexed citations

Opstal, Diane Van, J. O. Van Hemel, Bert H.J. Eussen, et al.. (1995). A chromosome 21‐specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei. Prenatal Diagnosis. 15(8). 705–711. 8 indexed citations

10.

Ouweland, Ans M.W. van den, Bert B.A. de Vries, Wout H. Deelen, et al.. (1994). DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR‐1 gene. American Journal of Medical Genetics. 51(4). 482–485. 43 indexed citations

11.

Vries, Bert Ba de, J. P. Fryns, Merlin G. Butler, et al.. (1993). Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.. Journal of Medical Genetics. 30(9). 761–766. 73 indexed citations

12.

Opstal, Diane Van, H. J. Eussen, J. O. Van Hemel, & E. S. Sachs. (1993). Application of fluorescent in situ hybridization for ‘de novo’ anomalies in prenatal diagnosis. Prenatal Diagnosis. 13(9). 825–832. 12 indexed citations

13.

Hemel, J. O. Van, Bert Eussen, Eveline Wesby–van Swaay, & B. A. Oostra. (1992). Molecular detection of a translocation (Y;11)(q11.2;q24) in a 45,X male with signs of Jacobsen syndrome. Human Genetics. 88(6). 661–667. 26 indexed citations

14.

Hazebroek, Frans W.J., et al.. (1992). Avoidance of emergency surgery in newborn infants with trisomy 18. The Lancet. 339(8798). 913–915. 52 indexed citations

15.

Verkerk, Annemieke J.M.H., Bert H.J. Eussen, J. O. Van Hemel, & Ben A. Oostra. (1992). Limited size of the fragile X site shown by fluorescence in situ hybridization. American Journal of Medical Genetics. 43(1-2). 187–191. 11 indexed citations

16.

Oostra, B. A., Daniëlle Majoor‐Krakauer, J. O. Van Hemel, et al.. (1991). Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27–q28. American Journal of Medical Genetics. 38(2-3). 332–335. 5 indexed citations

17.

Oostra, B. A., J.F. de Rijk-van Andel, H. J. Eussen, et al.. (1991). DNA analysis in patients with lissencephaly type I and other cortical dysplasias. American Journal of Medical Genetics. 40(3). 383–386. 5 indexed citations

18.

Andel, J.F. de Rijk-van, Coriene E. Catsman‐Berrevoets, J. O. Van Hemel, & A.J.H. Hamers. (1991). Clinical and Chromosome Studies of Three Patients with Smith‐Magenis Syndrome. Developmental Medicine & Child Neurology. 33(4). 343–347. 25 indexed citations

19.

Madan, K., M.H.E.C. Pieters, L. P. Kuyt, et al.. (1990). Paracentric inversion inv(11) (q21q23) in the Netherlands. Human Genetics. 85(1). 15–20. 11 indexed citations

20.

Kerkhofs, H., A Hagemeijer, C. H. W. Leeksma, et al.. (1982). The 5q‐ chromosome abnormality in haematological disorders:|a collaborative study of 34 cases from the Netheralands. British Journal of Haematology. 52(3). 365–381. 74 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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