T. W. J. Hustinx

854 total citations
21 papers, 615 citations indexed

About

T. W. J. Hustinx is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, T. W. J. Hustinx has authored 21 papers receiving a total of 615 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in T. W. J. Hustinx's work include Genomic variations and chromosomal abnormalities (5 papers), Acute Myeloid Leukemia Research (4 papers) and DNA Repair Mechanisms (4 papers). T. W. J. Hustinx is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Acute Myeloid Leukemia Research (4 papers) and DNA Repair Mechanisms (4 papers). T. W. J. Hustinx collaborates with scholars based in Netherlands, United States and Germany. T. W. J. Hustinx's co-authors include J. M. J. C. Scheres, R. Taalman, Jan de Wit, N.G.J. Jaspers, Joep Geraedts, Corry M.R. Weemaes, G. A. M. de Vaan, J. M. J. C. Scheres, C. H. W. Leeksma and Paul S. Meltzer and has published in prestigious journals such as Nature, Cancer and The Journal of Pediatrics.

In The Last Decade

T. W. J. Hustinx

21 papers receiving 568 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. W. J. Hustinx Netherlands	14	328	209	169	108	81	21	615
T. W. J. Hustinx Netherlands	16	451 1.4×	292 1.4×	136 0.8×	178 1.6×	89 1.1×	26	784
Barbara K. Hecht United States	14	334 1.0×	323 1.5×	68 0.4×	102 0.9×	90 1.1×	23	693
Fiorella Shabtai Israel	17	229 0.7×	314 1.5×	116 0.7×	51 0.5×	63 0.8×	47	601
G.C. Beverstock Netherlands	14	318 1.0×	259 1.2×	198 1.2×	20 0.2×	51 0.6×	30	634
P. Mollevanger Netherlands	13	196 0.6×	189 0.9×	65 0.4×	32 0.3×	52 0.6×	19	428
M. Leversha United Kingdom	11	330 1.0×	330 1.6×	201 1.2×	44 0.4×	33 0.4×	23	732
Laëtitia Gressin France	8	438 1.3×	79 0.4×	224 1.3×	57 0.5×	87 1.1×	11	675
G.C. Beverstock Netherlands	15	337 1.0×	220 1.1×	340 2.0×	38 0.4×	131 1.6×	20	838
Hélia Neves Portugal	11	499 1.5×	86 0.4×	111 0.7×	38 0.4×	90 1.1×	23	729
Le Beau United States	9	279 0.9×	66 0.3×	155 0.9×	43 0.4×	73 0.9×	14	506

Countries citing papers authored by T. W. J. Hustinx

Since Specialization

Citations

This map shows the geographic impact of T. W. J. Hustinx'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 T. W. J. Hustinx with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. W. J. Hustinx more than expected).

Fields of papers citing papers by T. W. J. Hustinx

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T. W. J. Hustinx. 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 T. W. J. Hustinx. The network helps show where T. W. J. Hustinx may publish in the future.

Co-authorship network of co-authors of T. W. J. Hustinx

This figure shows the co-authorship network connecting the top 25 collaborators of T. W. J. Hustinx. A scholar is included among the top collaborators of T. W. J. Hustinx 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 T. W. J. Hustinx. T. W. J. Hustinx 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

Smeets, Dominique, et al.. (1989). Familial and individual variation in chromosome fragility. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 212(2). 223–229. 8 indexed citations

Taalman, R., T. W. J. Hustinx, Corry M.R. Weemaes, et al.. (1989). Further delineation of the Nijmegen breakage syndrome. American Journal of Medical Genetics. 32(3). 425–431. 67 indexed citations

Scherer, Gerd, M. Fraccaro, T. W. J. Hustinx, et al.. (1987). Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis. Human Genetics. 76(4). 332–336. 39 indexed citations

Scheres, J. M. J. C., et al.. (1986). Demonstration of X chromatin in drumstick-like nuclear appendages of leukocytes by in situ hybridization on blood smears. Histochemistry and Cell Biology. 84(4-6). 383–386. 7 indexed citations

Hustinx, T. W. J., et al.. (1986). Possible involvement of unstable sites on chromosomes 7 and 14 in human cancer. Cancer Genetics and Cytogenetics. 19(1-2). 151–158. 13 indexed citations

Smeets, Dominique, J. M. J. C. Scheres, & T. W. J. Hustinx. (1985). Heritable fragility at 11q13 and 12q13. Clinical Genetics. 28(2). 145–150. 9 indexed citations

Scheres, J. M. J. C., T. W. J. Hustinx, Joep Geraedts, C. H. W. Leeksma, & Paul S. Meltzer. (1985). Translocation 1;7 in hematologic disorders: A brief review of 22 cases. Cancer Genetics and Cytogenetics. 18(3). 207–213. 56 indexed citations

Renier, W.O., et al.. (1983). Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and a maternal uncle. Brain and Development. 5(1). 41–45. 19 indexed citations

Hustinx, T. W. J., et al.. (1983). Malignant histiocytosis. Clinical and cytogenetic studies in a newborn and a child. Cancer. 52(7). 1229–1236. 45 indexed citations

10.

Taalman, R., N.G.J. Jaspers, J. M. J. C. Scheres, Jan de Wit, & T. W. J. Hustinx. (1983). Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage syndrome. Mutation Research/DNA Repair Reports. 112(1). 23–32. 97 indexed citations

11.

Renier, W.O., B. G. A. ter Haar, J.L. Slooff, T. W. J. Hustinx, & F.J.M. Gabreëls. (1982). X-Linked congenital hydrocephalus. Clinical Neurology and Neurosurgery. 84(2). 113–123. 16 indexed citations

12.

Scheres, J. M. J. C., T. W. J. Hustinx, & Corry M.R. Weemaes. (1980). Chromosome 7 in ataxia-telangiectasia. The Journal of Pediatrics. 97(3). 440–441. 25 indexed citations

13.

Scheres, J. M. J. C. & T. W. J. Hustinx. (1980). Heritable fragile sites and lymphocyte culture medium containing BrdU.. PubMed. 32(4). 628–9. 30 indexed citations

14.

Hustinx, T. W. J., et al.. (1980). A case of AMMoL with 8/21 translocation and loss of the Y as probably secondary events. Cancer. 45(2). 285–288. 11 indexed citations

15.

Scheres, J. M. J. C., et al.. (1978). 15/17 Translocation in acute promyelocytic leukaemia. Human Genetics. 43(1). 115–117. 28 indexed citations

16.

Breed, W.P.M., et al.. (1977). A case of chronic myeloid leukemia with a translocation (12;22)(p13;q11). Human Genetics. 39(2). 229–231. 11 indexed citations

17.

Hustinx, T. W. J., et al.. (1974). Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.. PubMed. 17(4). 225–34. 6 indexed citations

18.

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

19.

Hustinx, T. W. J., et al.. (1964). An XYY chromosome pattern in a boy with Marfan's syndrome. Genetica. 34(1). 262–269. 28 indexed citations

20.

Hustinx, T. W. J., et al.. (1961). Mongoloid twins with 48 chromosomes (AA + A₂₁XXY). Annals of Human Genetics. 25(2). 111–115. 49 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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