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Ans MW van den Ouweland
Observed names:
A M van den Ouweland,
Ans MW Van den Ouweland,
Van Den Ouweland, Ans M. W.,
van den Ouweland, Ans Mw
Institutions:
Erasmus MC,
The Netherlands Cancer Institute
Observed institutions:
Erasmus MC,
The Netherlands Cancer Institute,
University Medical Center Utrecht,
Erasmus MC Cancer Institute
OpenAlex ID:
A5111493016
Mental status of females with an FMR1 gene full mutation.
1996
·
B B de Vries
, A M Wiegers
, et al.
·
PubMed
·
206
Somatic aberrations of mismatch repair genes as a cause of microsatellite‐unstable cancers
2014
·
Willemina RR Geurts‐Giele
, Celine HM Leenen
, et al.
·
The Journal of Pathology
·
146
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
2017
·
Setareh Moghadasi
, Huong D Meeks
, et al.
·
Journal of Medical Genetics
·
83
PDF
Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome
2011
·
Margot GF van Lier
, Celine HM Leenen
, et al.
·
The Journal of Pathology
·
72
Body mass index and breast cancer survival: a Mendelian randomization analysis
2017
·
Qi Guo
, Stephen Burgess
, et al.
·
International Journal of Epidemiology
·
64
PDF
Legius syndrome in fourteen families
2010
·
Ellen Denayer
, Magdalena Chmara
, et al.
·
Human Mutation
·
59
PDF
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11.
1995
·
W Wuyts
, S Ramlakhan
, et al.
·
PubMed
·
57
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
2015
·
Sophie Blein
, Claire Bardel
, et al.
·
Breast Cancer Research
·
34
PDF
Common germline polymorphisms associated with breast cancer-specific survival
2015
·
Ailith Pirie
, Qi Guo
, et al.
·
Breast Cancer Research
·
29
PDF
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2mutation carriers
2010
·
Logan C Walker
, Zachary S Fredericksen
, et al.
·
Breast Cancer Research
·
29
PDF
Apparently synonymous substitutions in FGFR2affect splicing and result in mild Crouzon syndrome
2014
·
Aimee L Fenwick
, Jacqueline AC Goos
, et al.
·
BMC Medical Genetics
·
19
PDF
Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repair
2014
·
Eva AL Wielders
, Jan Hettinger
, et al.
·
Journal of Medical Genetics
·
15
Clinical utility gene card for: Tuberous sclerosis complex (TSC1, TSC2)
2013
·
Karin Mayer
, Christa Fonatsch
, et al.
·
European Journal of Human Genetics
·
6
PDF
[From gene to disease; from defective chloride ion transport to cystic fibrosis].
2001
·
H Scheffer
, A M van den Ouweland
, et al.
·
PubMed
·
3
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Works count:
16
Citation count:
822
H-index:
12
I10-index:
12
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