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dr. S.M.J. (Saskia) Hopman Assistant Professor - medical

  • Section Clinical Genetics

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Research Programs

Research Output (24)

Multiple tumors due to mosaic genome-wide paternal uniparental disomy

Postema Floor A.M., Bliek Jet, van Noesel Carel J.M., van Zutven Laura J.C.M., Oosterwijk Jan C., Hopman Saskia M.J., Merks Johannes H.M., Hennekam Raoul C. 1 jun 2019, In: Pediatric Blood and Cancer. 66 7 p.

Development, behaviour and autism in individuals with SMC1A variants

Mulder Paul A., Huisman Sylvia, Landlust Annemiek M., Moss Jo, Piening Sigrid, Hennekam Raoul C., van Balkom Ingrid D.C., Bader Ingrid, Bisgaard Anne Marie, Brooks Alice, Cereda Anna, Cinca Constanza, Clark Dinah, Cormier-Daire Valerie, Deardorff Matthew A., Diderich Karin, Elting Mariet, van Essen Anthonie, Fitzpatrick David, Gervasini Cristina, Gillessen-Kaesbach Gabriele, Girisha Katta M., Hilhorst-Hofstee Yvonne, Hopman Saskia, Horn Denise, Isrie Mala, Jansen Sandra, Jespersgaard Cathrine, Kaiser Frank J., Kaur Maninder, Kleefstra Tjitske, Krantz Ian D., Lakeman Phillis, Lessel Davor, Michot Caroline, Noon Sarah E., Oliver Chris, Parenti Ilaria, Pie-Juste Juan, Puisac Beatriz, Ramos Feliciano J., Redeker Egbert, Rieubland Claudine, Russo Silvia, Selicorni Angelo, Tümer Zeynep, Vorstenbosch Rieneke, de Vries Irene M., Wenger Tara L., Wierzba Jolanta, 1 mrt 2019, In: Journal of Child Psychology and Psychiatry and Allied Disciplines. 60 , p. 305-313 9 p.

High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer

Diets Illja J., Waanders Esme, Ligtenberg Marjolijn J., van Bladel Diede A.G., Kamping Eveline J., Hoogerbrugge Peter M., Hopman Saskia, Olderode-Berends Maran J., Gerkes Erica H., Koolen David A., Marcelis Carlo, Santen Gijs W., van Belzen Martine J., Mordaunt Dylan, McGregor Lesley, Thompson Elizabeth, Kattamis Antonis, Pastorczak Agata, Mlynarski Wojciech, Ilencikova Denisa, Vulto-Van Silfhout Anneke, Gardeitchik Thatjana, de Bont Eveline S., Loeffen Jan, Wagner Anja, Mensenkamp Arjen R., Kuiper Roland P., Hoogerbrugge Nicoline, Jongmans Marjolijn C. 1 apr 2018, In: Clinical Cancer Research. 24 , p. 1594-1603 10 p.

High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer

Diets Illja J., Waanders Esme, Ligtenberg Marjolijn J., van Bladel Diede A.G., Kamping Eveline J., Hoogerbrugge Peter M., Hopman Saskia, Olderode-Berends Maran J., Gerkes Erica H., Koolen David A., Marcelis Carlo, Santen Gijs W., van Belzen Martine J., Mordaunt Dylan, McGregor Lesley, Thompson Elizabeth, Kattamis Antonis, Pastorczak Agata, Mlynarski Wojciech, Ilencikova Denisa, Vulto-Van Silfhout Anneke, Gardeitchik Thatjana, de Bont Eveline S., Loeffen Jan, Wagner Anja, Mensenkamp Arjen R., Kuiper Roland P., Hoogerbrugge Nicoline, Jongmans Marjolijn C. 1 apr 2018, In: Clinical Cancer Research. 24 , p. 1594-1603 10 p.

Consequences of diagnosing a tumor predisposition syndrome in children with cancer:A literature review

Postema Floor A M, Hopman Saskia M.J., Hennekam Raoul C M, Merks Johannes H.M. 1 jan 2018, In: Pediatric Blood & Cancer. 65

Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS):Protocol for a prospective, observational, multicentre study

Postema Floor A M, Hopman Saskia M J, De Borgie Corianne A J M, Hammond Peter, Hennekam Raoul C., Merks Johannes H M, Aalfs Cora M., Anninga Jakob K., Berger Lieke P V, Bleeker Fonnet E., De Bont Eveline S J M, Dommering Charlotte J., Van Eijkelenburg Natasha K A, Van Den Heuvel-Eibrink Marry M., Jongmans Marjolijn C J, Kors Wijnanda A., Letteboer Tom G W, Loeffen Jan L C M, Olderode-Berends Maran J W, Wagner Anja 1 jan 2017, In: BMJ open [E]. 7

Childhood tumours with a high probability of being part of a tumour predisposition syndrome; reason for referral for genetic consultation

Postema Floor A M, Hopman Saskia M J, Aalfs Cora M, Berger Lieke P V, Bleeker Fonnet E, Dommering Charlotte J, Jongmans Marjolijn C J, Letteboer Tom G W, Olderode-Berends Maran J W, Wagner Anja, Hennekam Raoul C, Merks Johannes H M 2017, In: European Journal of Cancer. 80 , p. 48-54 7 p.

Childhood tumours with a high probability of being part of a tumour predisposition syndrome; reason for referral for genetic consultation

Postema Floor A M, Hopman Saskia M J, Aalfs Cora M, Berger Lieke P V, Bleeker Fonnet E, Dommering Charlotte J, Jongmans Marjolijn C J, Letteboer Tom G W, Olderode-Berends Maran J W, Wagner Anja, Hennekam Raoul C, Merks Johannes H M 2017, In: European Journal of Cancer. 80 , p. 48-54 7 p.

3D morphometry aids facial analysis of individuals with a childhood cancer

Hopman Saskia M J, Merks Johannes H M, Suttie Michael, Hennekam Raoul C M, Hammond Peter 17 okt 2016, In: American Journal of Medical Genetics. Part A. 170 , p. 2905–2915

Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups

Maas Saskia M, Vansenne Fleur, Kadouch Daniel J M, Ibrahim Abdulla, Bliek Jet, Hopman Saskia, Mannens Marcel M, Merks Johannes H M, Maher Eamonn R, Hennekam Raoul C sep 2016, In: American Journal of Medical Genetics. Part A. 170 , p. 2248–2260

All Research Output (24)
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