J. B. Bijlsma

768 total citations
32 papers, 553 citations indexed

About

J. B. Bijlsma is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, J. B. Bijlsma has authored 32 papers receiving a total of 553 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 11 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in J. B. Bijlsma's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). J. B. Bijlsma is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). J. B. Bijlsma collaborates with scholars based in Netherlands, Germany and United States. J. B. Bijlsma's co-authors include H. F. de France, Martijn H. Breuning, E. M. Bleeker‐Wagemakers, Piet F. Dijkstra, J. Willemse, N. J. Leschot, Raoul C. M. Hennekam, C. A. F. Tulleken, Liesbeth M. Bleeker-Wagemakers and P.F. Ippel and has published in prestigious journals such as Nature, Brain and Neurosurgery.

In The Last Decade

J. B. Bijlsma

32 papers receiving 517 citations

Peers

J. B. Bijlsma

GENET

PPCH

NEURO

Hyon J. Kim South Korea

M D Crawfurd United Kingdom

Kouji Narahara Japan

Constance K. Stein United States

Alicia Delicado Spain

B. Rafael Elejalde United States

Federica Natacci Italy

Marie‐France Portnoï France

Leah W. Burke United States

B. G. A. ter Haar Netherlands

Hyon J. Kim South Korea

J. B. Bijlsma

292 ×0.9

GENET

191 ×0.9

112 ×0.7

PPCH

49 ×0.5

39 ×0.4

NEURO

Citations per year, relative to J. B. Bijlsma J. B. Bijlsma (= 1×) peers Hyon J. Kim

Countries citing papers authored by J. B. Bijlsma

Since Specialization

Citations

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

Fields of papers citing papers by J. B. Bijlsma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. B. Bijlsma

This figure shows the co-authorship network connecting the top 25 collaborators of J. B. Bijlsma. A scholar is included among the top collaborators of J. B. Bijlsma 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. B. Bijlsma. J. B. Bijlsma 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:

20 of 20 papers shown

Pater, Jennie M., Martin Poot, F. A. Beemer, et al.. (2005). Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18. European Journal of Medical Genetics. 49(1). 19–27. 8 indexed citations

Thomas, Gilles, et al.. (2005). Interstitial deletion in 3q in a patient with blepharophimosis‐ptosis‐epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: Clinical report and review of the literature. American Journal of Medical Genetics Part A. 137A(1). 81–87. 26 indexed citations

Ippel, P.F., et al.. (1998). Atelencephalic microcephaly: a case report and review of the literature. European Journal of Pediatrics. 157(6). 493–497. 8 indexed citations

Bijlsma, J. B., Dick Lindhout, Frits A. Beemer, et al.. (1997). The Dutch uniform multicenter registration system for genetic disorders and malformation syndromes. American Journal of Medical Genetics. 70(4). 444–447. 5 indexed citations

Pater, Jennie M., P.F. Ippel, J. B. Bijlsma, & Onno van Nieuwenhuizen. (1997). Interstitial deletion 11q. Case report and review of the literature.. PubMed. 8(4). 335–9. 7 indexed citations

Ausems, Margreet G.E.M., et al.. (1996). Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.. PubMed. 7(1). 61–5. 1 indexed citations

Ippel, P.F., D. Wittebol‐Post, Bernadette P. M. van Nesselrooij, & J. B. Bijlsma. (1994). Sutural cataract, retinitis pigmentosa, microcephaly and psychomotor retardation a new autosomal recessive disorder?. Ophthalmic Genetics. 15(3-4). 121–127. 3 indexed citations

Oosterwijk, Jan C., et al.. (1992). A differential diagnostic problem ?. Ophthalmic Paediatrics and Genetics. 13(3). 171–177. 22 indexed citations

Ippel, P.F., et al.. (1992). Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: Confirmation of the Gorlin–Chaudhry–Moss syndrome. American Journal of Medical Genetics. 44(4). 518–522. 22 indexed citations

10.

Berg, J.W.M. ter, et al.. (1989). Ophthalmological abnormalities in (relatives of) patients with familial intracranial aneurysms: A collagen deficiency?. Neuro-Ophthalmology. 9(4). 213–218. 1 indexed citations

11.

Gooskens, R. H. J. M., et al.. (1988). Megalencephaly: Definition and classification. Brain and Development. 10(1). 1–7. 22 indexed citations

12.

Hennekam, Raoul C. M., et al.. (1988). Martsolf syndrome in a brother and sister: clinical features and pattern of inheritance. European Journal of Pediatrics. 147(5). 539–543. 21 indexed citations

13.

Dippel, Diederik W.J., et al.. (1988). Treatment of Intact Familial Intracranial Aneurysms: A Decision-analytical Approach. Neurosurgery. 23(3). 329–334. 25 indexed citations

14.

Bijlsma, J. B., et al.. (1987). Familial Occurrence of Intracranial Aneurysms in Childhood:A Case Report and Review of the Literature. Neuropediatrics. 18(4). 227–230. 15 indexed citations

15.

Hennekam, Raoul C. M., J. B. Bijlsma, J. Spranger, & Giovanni Neri. (1987). Further delineation of the 3‐M syndrome with review of the literature. American Journal of Medical Genetics. 28(1). 195–209. 25 indexed citations

16.

France, H. F. de, et al.. (1985). Interstitial deletion of the long arm of chromosome 11.. Journal of Medical Genetics. 22(3). 224–226. 25 indexed citations

17.

Bijlsma, J. B., et al.. (1979). Two cases with different deletions of the long arm of chromosome 7.. Journal of Medical Genetics. 16(2). 151–154. 36 indexed citations

18.

France, H. F. de, et al.. (1974). Direct giemsa-banding pattern analysis of human chromosomes by means of a television microdensitometer: The Quantimet 720 D. PubMed. 22(2). 167–170. 2 indexed citations

19.

Hustinx, T. W. J., J. B. Bijlsma, & L. E. Nijenhuis. (1965). Localization of Haptoglobin and ABO. Nature. 207(4994). 327–328. 5 indexed citations

20.

Bijlsma, J. B., J. James, & W Drukker. (1964). TRIPLE MOSAICISM OF THE SEX CHROMOSOMES IN A PHENOTYPICAL FEMALE. European Journal of Endocrinology. 46(3). 336–340. 2 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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