T. W. J. Hustinx

1.3k total citations
26 papers, 784 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 26 papers receiving a total of 784 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in T. W. J. Hustinx's work include Genomic variations and chromosomal abnormalities (10 papers), DNA Repair Mechanisms (5 papers) and Prenatal Screening and Diagnostics (5 papers). T. W. J. Hustinx is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), DNA Repair Mechanisms (5 papers) and Prenatal Screening and Diagnostics (5 papers). T. W. J. Hustinx collaborates with scholars based in Netherlands. T. W. J. Hustinx's co-authors include J. M. J. C. Scheres, Corry M.R. Weemaes, P.J.J. Van Munster, J. A. J. M. Bakkeren, R. Taalman, J. M. J. C. Scheres, B. G. A. ter Haar, C. Haanen, G. B. A. Stoelinga and F.J.M. Gabreëls and has published in prestigious journals such as Blood, Experimental Cell Research and Acta Neuropathologica.

In The Last Decade

T. W. J. Hustinx

26 papers receiving 734 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	16	451	292	178	136	128	26	784
A.E. Retief South Africa	20	623 1.4×	592 2.0×	157 0.9×	25 0.2×	85 0.7×	48	1.3k
Becky Alhadeff United States	13	374 0.8×	183 0.6×	96 0.5×	30 0.2×	42 0.3×	17	538
R. Marzella Italy	15	923 2.0×	267 0.9×	55 0.3×	106 0.8×	39 0.3×	25	1.4k
Rocío Acuña‐Hidalgo United States	7	443 1.0×	340 1.2×	162 0.9×	115 0.8×	56 0.4×	8	824
Emilie Falconnet Switzerland	15	409 0.9×	251 0.9×	161 0.9×	67 0.5×	91 0.7×	16	672
Dvorah Abeliovich Israel	12	443 1.0×	557 1.9×	189 1.1×	104 0.8×	69 0.5×	15	965
G Russo Italy	15	684 1.5×	156 0.5×	35 0.2×	298 2.2×	128 1.0×	23	1.2k
Jörg Seidel Germany	8	505 1.1×	284 1.0×	93 0.5×	18 0.1×	52 0.4×	18	767
Merete Bugge Denmark	10	935 2.1×	584 2.0×	71 0.4×	31 0.2×	146 1.1×	15	1.2k
Nicole L. Hoppman United States	14	279 0.6×	279 1.0×	92 0.5×	173 1.3×	115 0.9×	62	704

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

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

Taalman, R., et al.. (1987). Chromosome studies in IgA‐deficient patients. Clinical Genetics. 32(2). 81–87. 15 indexed citations

Witte, T. de, J. Hoogenhout, Ben de Pauw, et al.. (1986). Depletion of donor lymphocytes by counterflow centrifugation successfully prevents acute graft-versus-host disease in matched allogeneic marrow transplantation. Blood. 67(5). 1302–1308. 76 indexed citations

Smeets, Dominique, J. M. J. C. Scheres, & T. W. J. Hustinx. (1986). The most common fragile site in man is 3p14. Human Genetics. 74(3). 5 indexed citations

Scheres, J. M. J. C., et al.. (1986). Specific translocation t(1;3) in acute myelomonocytic leukemia: A further case. Cancer Genetics and Cytogenetics. 22(1). 69–73. 9 indexed citations

Renier, W. O., et al.. (1983). THE MARTIN‐BELL SYNDROME: A PSYCHOLOGICAL, LOGOPAEDIC AND CYTOGENETIC STUDY OF TWO AFFECTED BROTHERS. Journal of Intellectual Disability Research. 27(1). 51–59. 7 indexed citations

Renier, W.O., T. W. J. Hustinx, J.H. Veerkamp, et al.. (1983). Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs. Clinical Genetics. 24(4). 243–251. 37 indexed citations

Scheres, J. M. J. C., Gerard Merkx, & T. W. J. Hustinx. (1982). Prometaphase banding of human chromosomes with basic fuchsin. Human Genetics. 61(1). 8–11. 15 indexed citations

Renier, W. O., et al.. (1982). AN X‐LINKED SYNDROME WITH MICROCEPHALY, SEVERE MENTAL RETARDATION, SPASTICITY, EPILEPSY AND DEAFNESS. Journal of Intellectual Disability Research. 26(1). 27–40. 13 indexed citations

10.

Renier, W.O., F.J.M. Gabreëls, T. W. J. Hustinx, et al.. (1981). Connatal Pelizaeus-Merzbacher Disease with congenital stridor in two maternal cousins. Acta Neuropathologica. 54(1). 11–17. 23 indexed citations

11.

Weemaes, Corry M.R., T. W. J. Hustinx, J. M. J. C. Scheres, et al.. (1981). A NEW CHROMOSOMAL INSTABILITY DISORDER: THE NIJMEGEN BREAKAGE SYNDROME. Acta Paediatrica. 70(4). 557–564. 255 indexed citations

12.

Scheres, J. M. J. C., T. W. J. Hustinx, & Gerard Merkx. (1980). Nomarski-optical studies of human chromosomes R-banded with barium hydroxide. Human Genetics. 53(2). 255–9. 2 indexed citations

13.

Hustinx, T. W. J., et al.. (1980). Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter. Clinical Genetics. 18(6). 456–461. 58 indexed citations

14.

Hustinx, T. W. J., et al.. (1979). Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6. American Journal of Medical Genetics. 3(4). 353–358. 21 indexed citations

15.

Weemaes, Corry M.R., J. A. J. M. Bakkeren, B. G. A. ter Haar, T. W. J. Hustinx, & P.J.J. Van Munster. (1979). Immune responses in four patients with Bloom syndrome. Clinical Immunology and Immunopathology. 12(1). 12–19. 28 indexed citations

16.

Scheres, J. M. J. C., et al.. (1978). 2:2 and 3:1 Meiotic disjunctions in a carrier of a reciprocal 10/14 translocation. Clinical Genetics. 13(6). 481–485. 1 indexed citations

17.

Hustinx, T. W. J., et al.. (1977). Bloom's syndrome in two Dutch families. Clinical Genetics. 12(2). 85–96. 17 indexed citations

18.

Hustinx, T. W. J., et al.. (1977). Monosomy 7 in Two Patients with a Myeloproliferative Disorder. British Journal of Haematology. 37(1). 101–109. 16 indexed citations

19.

Scheres, J. M. J. C., et al.. (1977). “Reverse” differential staining of sister chromatids. Experimental Cell Research. 109(2). 466–468. 20 indexed citations

20.

Hustinx, T. W. J., et al.. (1974). Trisomy‐9 in the Bone Marrow of a Patient with Acute Myelomonoblastic Leukaemia. British Journal of Haematology. 26(3). 391–394. 24 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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