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Beike K. Leegte

Observed names: B Leegte, Beike Leegte, LEEGTE, B, Leegte, B.
OpenAlex ID: A5111643727
Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: high cancer incidence at older age
2010 · Dorina M. van der Kolk, Geertruida H. de Bock, et al. · Breast Cancer Research and Treatment · 190
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Time to stop ovarian cancer screening in BRCA1/2 mutation carriers?
2008 · Nienke M. van der Velde, Marian J.E. Mourits, et al. · International Journal of Cancer · 134
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Phenotypic variability of Cat-Eye syndrome.
2001 · M J Berends, G Tan-Sindhunata, et al. · PubMed · 103
Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)]
1993 · Rolf H. Sijmons, Beike Leegte, et al. · American Journal of Medical Genetics · 103
Bilateral split hand/foot malformation and inv(7)(p22q21.3).
1995 · J M Cobben, J B Verheij, et al. · Journal of Medical Genetics · 86
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Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype
2000 · Gita Tan-Sindhunata, S�rgio Castedo, et al. · American Journal of Medical Genetics · 85
Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations
2005 · B Leegte, A H van der Hout, et al. · Journal of Medical Genetics · 72
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Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype
1999 · Roel Hordijk, Henk Wierenga, et al. · Journal of Medical Genetics · 59
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Three cases of mosaicism for balanced reciprocal translocations
1998 · Beike Leegte, Birgit Sikkema-Raddatz, et al. · American Journal of Medical Genetics · 49
Trisomy 1q42→qter in a sister and brother: Further delineation of the “trisomy 1q42→qter Syndrome”
1995 · Corien C. Verschuuren‐Bemelmans, Beike Leegte, et al. · American Journal of Medical Genetics · 31
11q- syndrome: three cases and a review of the literature.
1999 · B Leegte, W S Kerstjens-Frederikse, et al. · PubMed · 29
Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22
1999 · Joke B.G.M. Verheij, Katel�ne Bouman, et al. · American Journal of Medical Genetics · 17
Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co‐occurring FANCC and CHEK2 mutations
2018 · Gerbrig Berger, Eva van den Berg, et al. · British Journal of Haematology · 10
Cytogenetic evidence that carcinoma in situ is the precursor lesion for invasive testicular germ cell tumors
1994 · Jannie van Echten, Marian Stoepker, et al. · Cancer Genetics and Cytogenetics · 3
Two unbalanced segregation products due to a maternal t(7;16)inv(16)
2001 · Beike Leegte, Birgit Sikkema‐Raddatz, et al. · Prenatal Diagnosis · 1
What if we would turn a diagnostic multi-cancer gene panel into a screening tool?
2019 · Johansson, L. F.; id_orcid 0000-0002-4914-3737, van Dijk-Bos, K. K.; id_orcid 0009-0007-8381-6492, et al. · University of Groningen research database (University of Groningen / Centre for Information Technology)
Fishing for a diagnosis.
2002 · Y C M Duijvestijn, J M Cobben, et al. · PubMed
A chromosomal rearrangement causing velopharyngeal and developmental delay.
2000 · WS Kerstjens‐Frederikse, Beike Leegte, et al. · University of Groningen research database (University of Groningen / Centre for Information Technology)
Jumping translocation in umbilical cord blood
1998 · Beike Leegte, K. Bouman, et al. · University of Groningen research database (University of Groningen / Centre for Information Technology)
Relatively Mild Phenotype of Partial Trisomy-13 (q21.2-q32), Due to Familial Insertion (3-13), in a 8-year-old Boy
1995 · SIJMONS, RH, LEEGTE, B, et al. · University of Groningen research database (University of Groningen / Centre for Information Technology)
Works count: 20
Citation count: 972
H-index: 12
I10-index: 13
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