Beike Leegte

949 total citations
15 papers, 531 citations indexed

About

Beike Leegte is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Beike Leegte has authored 15 papers receiving a total of 531 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Beike Leegte's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (4 papers). Beike Leegte is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (4 papers). Beike Leegte collaborates with scholars based in Netherlands, United Kingdom and Israel. Beike Leegte's co-authors include Jan C. Oosterwijk, Geertruida H. de Bock, Marian J.E. Mourits, Dorina M. van der Kolk, Jakob de Vries, Gita Tan-Sindhunata, Annemieke H. van der Hout, Michael Schaapveld, A.J. van Essen and Henriëtte J.G. Arts and has published in prestigious journals such as International Journal of Cancer, Journal of Medical Genetics and Breast Cancer Research and Treatment.

In The Last Decade

Beike Leegte

14 papers receiving 496 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Beike Leegte Netherlands	11	428	189	118	103	91	15	531
Izabela Brożek Poland	15	429 1.0×	353 1.9×	81 0.7×	82 0.8×	108 1.2×	23	583
Deborah M. Ketterer United States	6	242 0.6×	294 1.6×	50 0.4×	74 0.7×	120 1.3×	6	585
Colyn B. Cargile United States	7	204 0.5×	243 1.3×	35 0.3×	98 1.0×	56 0.6×	8	416
Sandra Bonache Spain	13	254 0.6×	293 1.6×	39 0.3×	106 1.0×	82 0.9×	24	493
Marie T. Mulcahy Australia	13	210 0.5×	193 1.0×	150 1.3×	24 0.2×	23 0.3×	25	472
B. A. J. Ponder United Kingdom	10	594 1.4×	275 1.5×	28 0.2×	146 1.4×	171 1.9×	15	822
C. B. van der Hagen Norway	12	259 0.6×	261 1.4×	70 0.6×	46 0.4×	27 0.3×	22	535
Ross Rowsey United States	11	131 0.3×	146 0.8×	66 0.6×	27 0.3×	68 0.7×	30	372
Bela Patel United States	15	146 0.3×	484 2.6×	89 0.8×	74 0.7×	68 0.7×	24	681
Marina Manvelyan Germany	13	228 0.5×	190 1.0×	93 0.8×	27 0.3×	43 0.5×	22	402

Countries citing papers authored by Beike Leegte

Since Specialization

Citations

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

Fields of papers citing papers by Beike Leegte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beike Leegte. 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 Beike Leegte. The network helps show where Beike Leegte may publish in the future.

Co-authorship network of co-authors of Beike Leegte

This figure shows the co-authorship network connecting the top 25 collaborators of Beike Leegte. A scholar is included among the top collaborators of Beike Leegte 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 Beike Leegte. Beike Leegte is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

1.

Kolk, Dorina M. van der, Geertruida H. de Bock, Beike Leegte, et al.. (2010). Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: high cancer incidence at older age. Breast Cancer Research and Treatment. 124(3). 643–651. 136 indexed citations

2.

Mourits, Marian J.E., Henriëtte J.G. Arts, J. de Vries, et al.. (2008). Time to stop ovarian cancer screening in BRCA1/2 mutation carriers?. International Journal of Cancer. 124(4). 919–923. 97 indexed citations

3.

Leegte, Beike, et al.. (2005). Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations. Journal of Medical Genetics. 42(3). e20–e20. 44 indexed citations

4.

Leegte, Beike, et al.. (2001). Two unbalanced segregation products due to a maternal t(7;16)inv(16). Prenatal Diagnosis. 21(7). 550–552.

5.

Tan-Sindhunata, Gita, et al.. (2001). Phenotypic variability of Cat-Eye syndrome.. PubMed. 12(1). 23–34. 57 indexed citations

6.

Tan-Sindhunata, Gita, et al.. (2000). Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype. American Journal of Medical Genetics. 92(2). 147–147. 3 indexed citations

7.

Tan-Sindhunata, Gita, et al.. (2000). Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype. American Journal of Medical Genetics. 92(2). 147–152. 17 indexed citations

8.

Verheij, Joanne, K. Bouman, Richard A. van Lingen, et al.. (1999). Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22. American Journal of Medical Genetics. 86(2). 168–173. 15 indexed citations

9.

Leegte, Beike, et al.. (1999). 11q- syndrome: three cases and a review of the literature.. PubMed. 10(3). 305–13. 21 indexed citations

10.

Hordijk, Roel, et al.. (1999). Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype. Journal of Medical Genetics. 36(10). 782–785. 48 indexed citations

11.

Leegte, Beike, Birgit Sikkema‐Raddatz, Roel Hordijk, et al.. (1998). Three cases of mosaicism for balanced reciprocal translocations. American Journal of Medical Genetics. 79(5). 362–365. 10 indexed citations

12.

Verschuuren‐Bemelmans, Corien C., et al.. (1995). Trisomy 1q42→qter in a sister and brother: Further delineation of the “trisomy 1q42→qter Syndrome”. American Journal of Medical Genetics. 58(1). 83–86. 19 indexed citations

13.

Cobben, Jan M., W. H. Eisma, P. H. Robinson, et al.. (1995). Bilateral split hand/foot malformation and inv(7)(p22q21.3).. Journal of Medical Genetics. 32(5). 375–378. 28 indexed citations

14.

Echten, Jannie van, et al.. (1994). Cytogenetic evidence that carcinoma in situ is the precursor lesion for invasive testicular germ cell tumors. Cancer Genetics and Cytogenetics. 77(2). 194–194. 2 indexed citations

15.

Sijmons, Rolf H., Beike Leegte, Richard A. van Lingen, et al.. (1993). Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)]. American Journal of Medical Genetics. 47(4). 559–562. 34 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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