Shama van Zelderen-Bhola

Research output

Research output per year 1997 2001 2004 2022

• 27 Article
• 1 Review article

Research output per year

Research output per year

Search results

• 2022

  Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study

  The Dutch NIPT Consortium & Dutch NIPT Consortium, 2 Jun 2022, In: American journal of human genetics. 109, 6, p. 1140-1152 13 p.

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
  37 Citations (Scopus)

• Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study (The American Journal of Human Genetics (2022) 109(6) (1140–1152), (S0002929722002051), (10.1016/j.ajhg.2022.04.018))

  Dutch NIPT Consortium, 7 Jul 2022, In: American journal of human genetics. 109, 7, p. 1344 1 p.

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
  4 Citations (Scopus)
• 2019

  TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands

  The Dutch NIPT Consortium & Dutch NIPT Consortium, 5 Dec 2019, In: American journal of human genetics. 105, 6, p. 1091-1101 11 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  201 Citations (Scopus)
• 2018

  A novel cryptic CBFB-MYH11 gene fusion present at birth leading to acute myeloid leukemia and allowing molecular monitoring for minimal residual disease

  Poddighe, P. J., Veening, M. A., Mansur, M. B., Loonen, A. H., Westers, T. M., Merle, P. A., Wessels, J. W., de Haas, V., Kors, W. A., Bhola, S. L., Wondergem, M. J., Ford, A. M. & Kaspers, G. J. L., 1 Mar 2018, In: Human Pathology: Case Reports. 11, p. 34-38 5 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  4 Citations (Scopus)

• A prenatal case of partial trisomy 21 (q22.2q22.3), resulting from a paternal insertion translocation ins(16;21) and uncovered by QF-PCR, and characterized by array CGH and FISH

  Bhola, S. L., Nieuwint, A. W. M. & Stuurman, K. E., 2018, In: Clinical Case Reports. 6, 7, p. 1313-1316

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
  2 Citations (Scopus)
• 2016

  Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects

  Jansen, F. A. R., Hoffer, M. J. V., van Velzen, C. L., Plati, S. K., Rijlaarsdam, M. E. B., Clur, S-A. B., Blom, N. A., Pajkrt, E., Bhola, S. L., Knegt, A. C., de Boer, M. A. & Haak, M. C., 2016, In: Prenatal diagnosis. 36, 2, p. 177-185 9 p.

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
  13 Citations (Scopus)
• 2014

  Evaluation of the introduction of the national Down syndrome screening program in the Netherlands: age-related uptake of prenatal screening and invasive diagnostic testing

  Engels, M. A. M. J., Bhola, S. L., Twisk, J. W. R., Blankenstein, M. A. & van Vugt, J. M. G., 2014, In: European Journal of Obstetrics and Gynecology and Reproductive Biology. 174, p. 59-63

  Research output: Contribution to journal › Article › Academic › peer-review
  17 Citations (Scopus)

• Genomic amplification of MYC as double minutes in a patient with APL-like leukemia

  Poddighe, P. J., Wessels, H., Merle, P., Westers, T. M., Bhola, S. L., Loonen, A., Zweegman, S., Ossenkoppele, G. J. & Wondergem, M. J., 2014, In: Molecular Cytogenetics. 7, 67.

  Research output: Contribution to journal › Article › Academic › peer-review
  8 Citations (Scopus)
• 2012

  Economic evaluation of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis: a cost-minimization analysis

  Boormans, E. M. A., Birnie, E., Hoffer, M. J. V., Macville, M. V. E., Galjaard, R-J., Schuring-Blom, G. H., Bhola, S. L., Huijsdens, K., Smits, A. & van Lith, J. M. M., 2012, In: Archives of gynecology and obstetrics. 285, 1, p. 67-75

  Research output: Contribution to journal › Article › Academic › peer-review
  2 Citations (Scopus)
• 2011

  Challenging diagnosis in a patient with clear lymphoid immunohistochemical features and myeloid morphology: Mixed phenotype acute leukemia with erythrophagocytosis

  de Leeuw, D. C., van den Ancker, W., Westers, T. M., Loonen, A. H., Bhola, S. L., Ossenkoppele, G. J. & van de Loosdrecht, A. A., 2011, In: Leukemia research. 35, 5, p. 693-696

  Research output: Contribution to journal › Article › Academic › peer-review
  3 Citations (Scopus)
• 2010

  Phenotypic and genomic analysis of an exceptional case of enteropathy associated T-cell lymphoma

  Tack, G. J., Verbeek, W. H. M., van de Water, J. M. W., von Blomberg, B. M. E., Bhola, S. L., Ylstra, B., Mulder, C. J. J. & Schreurs, M. W. J., 2010, In: Leukemia research. 34, 8, p. E183-E189

  Research output: Contribution to journal › Article › Academic › peer-review
  6 Citations (Scopus)
• 2008

  Monosomal karyotype in acute myeloid leukemia: A better indicator of poor prognosis than a complex karyotype: A better indicator of poor prognosis than a complex karyotype

  Breems, D. A., van Putten, W. L. J., de Greef, G. E., van Zelderen-Bhola, S. L., Gerssen-Schoorl, K. B. J., Mellink, C. H. M., Nieuwint, A., Jotterand, M., Hagemeijer, A., Beverloo, H. B., Lowenberg, B. & Löwenberg, B., 10 Oct 2008, In: Journal of clinical oncology. 26, 29, p. 4791-4797 7 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  494 Citations (Scopus)

• Multiplex ligation-dependent probe amplification versus karyotyping in prenatal diagnosis: the M.A.K.E. study: The M.A.K.E. study

  Boormans, E. M. A., Birnie, E., Wildschut, H. I., Schuring-Blom, H. G., Oepkes, D., van Oppen, C. A. C., Nijhuis, J. G., Macville, M. V. E., Kooper, A. J. A., Huijsdens, K., Hoffer, M. V. J., Go, A., Creemers, J., Bhola, S. L., Bilardo, K. M., Suijkerbuijk, R., Bouman, K., Galjaard, R-J. H., Bonsel, G. J. & van Lith, J. M. M., 2008, In: BMC pregnancy and childbirth. 8, 1, p. 18 18.

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
  25 Citations (Scopus)
• 2007

  The heterogeneous distribution of monosomy 3 in uveal melanomas - Implications for prognostication based on fine-needle aspiration biopsies: Implications for prognostication based on fine-needle aspiration biopsies

  Maat, W., Jordanova, E. S., van Zelderen-Bhola, S. L., Barthen, E. R., Wessels, H. W., Schalij-Delfos, N. E. & Jager, M. J., Jan 2007, In: Archives of Pathology & Laboratory Medicine. 131, 1, p. 91-96 6 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  86 Citations (Scopus)
• 2004

  Alpha-interferon with very-low-dose donor lymphocyte infusion for hematologic or cytogenetic relapse of chronic myeloid leukemia induces rapid and durable complete remissions and is associated with acceptable graft-versus-host disease

  Posthuma, E. F. M., Marijt, E. W. A. F., Barge, R. M. Y., van Soest, R. A., Baas, I. O., Starrenburg, C. W. J. I., van Zelderen-Bhola, S. L., Fibbe, W. E., Smit, W. M., Willemze, R. & Falkenburg, J. H. F., Mar 2004, In: Biology of blood and marrow transplantation. 10, 3, p. 204-212 9 p.

  Research output: Contribution to journal › Article › Academic › peer-review

  Open Access
  42 Citations (Scopus)

• A novel t(6;14)(q25∼q27;q32) in acute myelocytic leukemia involves the BCL11B gene

  Bezrookove, V., Van Zelderen-Bhola, S. L., Brink, A., Szuhai, K., Raap, A. K., Barge, R., Beverstock, G. C. & Rosenberg, C., Feb 2004, In: Cancer genetics and cytogenetics. 149, 1, p. 72-76 5 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  29 Citations (Scopus)

• Identification of a Novel RAS GTPpase-Activating Protein (RASGAP) Gene at 9q34 as an MLL Fusion Partner in a Patient with De Novo Acute Leukemia

  Von Bergh, A. R. M., Wijers, P. M., Groot, A. J., Van Zelderen-Bhola, S., Falkenburg, J. H. F., Kluin, P. M. & Schuuring, E., Apr 2004, In: Genes Chromosomes and Cancer. 39, 4, p. 324-334 11 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  25 Citations (Scopus)

• Interphase fluorescence in situ hybridization for detection of 8q24/MYC breakpoints on routine histologic sections: validation in Burkitt lymphomas from three geographic regions: Validation in Burkitt Lymphomas from Three Geographic Regions

  Haralambieva, E., Schuuring, E., Rosati, S., van Noesel, C., Jansen, P., Appel, I., Guikema, J., Wabinga, H., Bleggi-Torres, L. F., Lam, K., van den Berg, E., Mellink, C., van Zelderen-Bhola, S. & Kluin, P., May 2004, In: Genes, chromosomes & cancer. 40, 1, p. 10-18 9 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  58 Citations (Scopus)
• 2003

  Diabetes insipidus in a child with a monosomy-7 associated myelodysplastic syndrome and neurofibromatosis I

  Kollen, W. J. W., Ball, L. M., Snijder, P., Van Zelderen-Bhola, S. L. & Egeler, R. M., 1 Apr 2003, In: Medical and pediatric oncology. 40, 4, p. 257-259 3 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  5 Citations (Scopus)
• 2001

  A novel chromosomal translocation t(3;5)(q12;p15.3) and loss of heterozygosity on chromosome 22 in a multifocal follicular variant of papillary thyroid carcinoma presenting with skin metastases

  Smit, J. W. A., Van Zelderen-Bhola, S., Merx, R., De Leeuw, W., Wessels, H., Vink, R. & Morreau, H., 2001, In: Clinical endocrinology. 55, 4, p. 543-548 6 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  15 Citations (Scopus)

• Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: A cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes

  Bovée, J. V. M. G., Sciot, R., Cin, P. D., Debiec-Rychter, M., Van Zelderen-Bhola, S. L., Cornelisse, C. J. & Hogendoorn, P. C. W., 2001, In: Diagnostic molecular pathology. 10, 4, p. 228-235 8 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  37 Citations (Scopus)

• Monitoring of engraftment and progression of acute lymphoblastic leukemia in individual NOD/SCID mice

  Nijmeijer, B. A., Mollevanger, P., Van Zelderen-Bhola, S. L., Kluin-Nelemans, H. C., Willemze, R. & Falkenburg, J. H. F., 2001, In: Experimental Hematology. 29, 3, p. 322-329 8 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  43 Citations (Scopus)
• 2000

  A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias

  Von Bergh, A., Emanuel, B., Van Zelderen-Bhola, S., Smetsers, T., Van Soest, R., Stul, M., Vranckx, H., Schuuring, E., Hagemeijer, A. & Kluin, P., May 2000, In: Genes Chromosomes and Cancer. 28, 1, p. 14-22 9 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  52 Citations (Scopus)

• The generation of dendritic-like cells with increased allostimulatory function from acute myeloid leukemia cells of various FAB subclasses

  Brouwer, R. E., Van Der Hoorn, M., Kluin-Nelemans, H. C., Van Zelderen-Bhola, S., Willemze, R. & Falkenburg, J. H. F., Jun 2000, In: Human immunology. 61, 6, p. 565-574 10 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  63 Citations (Scopus)
• 1999

  Translocations (X;10)(p22;q24) and (1;10)(q21;q11) in a follicular adenoma of the thyroid without apparent involvement of the RET protooncogene

  Van Zelderen-Bhola, S., Vink, R., Smit, J., Wessels, H. & Morreau, H., 15 Jul 1999, In: Cancer genetics and cytogenetics. 112, 2, p. 178-180 3 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  3 Citations (Scopus)
• 1998

  Ring chromosome 4 as the sole cytogenetic anomaly in a chondroblastoma: A case report and review of the literature

  Van Zelderen-Bhola, S. L., Bovée, J. V. M. G., Wessels, H. W., Mollevanger, P., Nijhuis, J. V., Van Eendenburg, J. D. H., Taminiau, A. H. M. & Hogendoorn, P. C. W., Sept 1998, In: Cancer genetics and cytogenetics. 105, 2, p. 109-112 4 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  17 Citations (Scopus)
• 1997

  Prenatal and postnatal investigation of a case with Miller-Dieker syndrome due to a familial cryptic translocation t(17;20) (p13.3;q13.3) detected by fluorescence in situ hybridization

  Van Zelderen-Bhola, S. L., Breslau-Siderius, E. J., Beverstock, G. C., Stolte-Dijkstra, I., De Vries, L. S., Stoutenbeek, P. & De Pater, J. M., Feb 1997, In: Prenatal diagnosis. 17, 2, p. 173-179 7 p.

  Research output: Contribution to journal › Article › Academic › peer-review
  16 Citations (Scopus)