S. Hopman

PROFILE

Homepage
No homepage is listed.
ORCID
No ORCID is listed.
Affiliations
No affiliations are listed.
Aliases
Saskia Mj Hopman, S. M. J. Hopman, Saskia M.j. Hopman, Saskia Hopman, Saskia M Hopman, Saskia M J Hopman, Saskia M. J. Hopman
Publication record
24 papers · 533 citations · H-index 13

PAPERS

Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization
202245 citationsauthor #12
Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG)
202133 citationsauthor #6
Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study
20217 citationsauthor #2
RARE-21. CANCER SPECTRUM IN GERMLINE SUFU MUTATION CARRIERS: A COLLABORATIVE PROJECT OF THE SIOPE HOST GENOME WORKING GROUP
20200 citationsauthor #10
Consequences of diagnosing a tumor predisposition syndrome in children with cancer: A literature review
201821 citationsauthor #2
High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer
201856 citationsauthor #7
Facial asymmetry in head and neck rhabdomyosarcoma survivors
201727 citationsauthor #7
Childhood tumours with a high probability of being part of a tumour predisposition syndrome; reason for referral for genetic consultation.
201723 citationsauthor #2
Correspondence to Gripp et al. nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation
201710 citationsauthor #2
Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre study
201718 citationsauthor #18
High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome
201577 citationsauthor #10
Abstract 4934: Mosaic RNase IIIb domainDICER1mutations in children with multiple primary tumors
20150 citationsauthor #6
3D Morphometry enhances facial analysis of individuals with a childhood cancer
20140 citationsauthor #1
Co-occurrence in body site of malformations and cancer.
20146 citationsauthor #2
Brain Tumors and Syndromes in Children
201419 citationsauthor #2
Face shape differs in phylogenetically related populations
201445 citationsauthor #1
Cancer predisposition in children: genetics, phenotypes & screening
20140 citationsauthor #1
UvA-DARE ( Digital Academic Repository ) Cancer predisposition in children : genetics , phenotypes & screening
20140 citationsauthor #1
Structural genome variations in individuals with childhood cancer and tumour predisposition syndromes.
201312 citationsauthor #1
The development of a clinical screening tool for tumour predisposition syndromes in childhood cancer patients
20131 citationsauthor #1
Bloom syndrome in the Netherlands: Clinical review of a national cohort
20130 citationsauthor #1
PTEN hamartoma tumor syndrome and Gorham–Stout phenomenon
201225 citationsauthor #1
Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies
201050 citationsauthor #6
Dickkopf-1 is down-regulated by MYCN and inhibits neuroblastoma cell proliferation.
200757 citationsauthor #3

TIMELINE

2007 57 citations

2010 50 citations

2012 25 citations

2013 13 citations

2014 70 citations

2015 77 citations

2017 78 citations

2018 77 citations

2020 0 citations

2021 40 citations

2022 45 citations

S. Hopman

PROFILE

PAPERS

TIMELINE

COAUTHOR MAP

CONCEPT FOOTPRINT