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Co-authors
(355)
Marjolijn J. L. Ligtenberg
13
Ad Geurts van Kessel
9
Marc J. Eleveld
8
Nicoline Hoogerbrugge
8
Marian A. J. Weterman
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CANCER GENET CYTOGENET
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Authors
Danielle Bodmer
Danielle Bodmer,University Medical Center St Radboud Nijmegen,Genetics & Genealogy,Oncology,Molecular Biology
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Danielle Bodmer
University Medical Center St Radboud Nijmegen
Publications:
24
|
Citations:
277
Fields:
Genetics & Genealogy
,
Oncology
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
355 co-authors
from 1998 to 2011
|
Cited by
880 authors
Cumulative
Annual
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Publications
(24)
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Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
S. J. Ramus
,
C. Kartsonaki
,
S. A. Gayther
,
P. D. P. Pharoah
,
O. Sinilnikova
,
J. Beesley
,
G. Chenevix-Trench
,
L. McGuffog
,
S. Healey
,
F. J. Couch
,
X. Wang
,
Z. Fredericksen
D. Bodmer
http://academic.research.microsoft.com/io.ashx?type=5&id=59392450&selfId1=5226899&selfId2=0&maxNumber=12&query=
Journal:
Journal of The National Cancer Institute - J NAT CANCER INST
, vol. 103, no. 2, pp. 105-116, 2011
Exploring the link between MORF4L1 and risk of breast cancer
Griselda Martrat
,
Christopher A Maxwell
,
Emiko Tominaga
,
Montserrat Porta-de-la-Riva
,
Núria Bonifaci
,
Laia Gómez-Baldó
,
Massimo Bogliolo
,
Conxi Lázaro
,
Ignacio Blanco
,
Joan Brunet
,
Helena Aguilar
,
Juana Fernández-Rodríguez
Danielle Bodmer
http://academic.research.microsoft.com/io.ashx?type=5&id=48392588&selfId1=5226899&selfId2=0&maxNumber=12&query=
Journal:
Breast Cancer Research - BREAST CANCER RES
, vol. 13, no. 2, pp. 1-14, 2011
Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome
(
Citations: 1
)
P. Manders
,
L. Spruijt
,
C. M. Kets
,
H. W. Willems
,
D. Bodmer
,
K. M. Hebeda
,
I. D. Nagtegaal
,
M. J. L. Ligtenberg
,
N. Hoogerbrugge
Journal:
European Journal of Cancer - EUR J CANCER
, vol. 47, no. 9, pp. 1407-1413, 2011
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
S. J. Ramus
,
C. Kartsonaki
,
S. A. Gayther
,
P. D. Pharoah
,
O. M. Sinilnikova
,
J. Beesley
,
X. Chen
,
L. McGuffog
,
S. Healey
,
F. J. Couch
,
X. Wang
,
Z. Fredericksen
D. Bodmer
http://academic.research.microsoft.com/io.ashx?type=5&id=59699157&selfId1=5226899&selfId2=0&maxNumber=12&query=
Journal:
Journal of The National Cancer Institute - J NAT CANCER INST
, pp. 105-116, 2011
Recurrence and variability of germline EPCAM deletions in Lynch syndrome
R. P. Kuiper
,
L. E. L. M. Vissers
,
R. Venkatachalam
,
D. Bodmer
,
E. Hoenselaar
,
M. Goossens
,
A. Haufe
,
E. J. Kamping
,
R. C. Niessen
,
F. B. L. Hogervorst
,
J. J. P. Gille
,
B. Redeker
http://academic.research.microsoft.com/io.ashx?type=5&id=59742524&selfId1=5226899&selfId2=0&maxNumber=12&query=
Journal:
Human Mutation - HUM MUTAT
, pp. 407-414, 2011
Sort by:
Citations
(277 times by 185 publications)
Understanding transgenerational epigenetic inheritance via the gametes in mammals
Lucia Daxinger
,
Emma Whitelaw
Journal:
Nature Reviews Genetics - NAT REV GENET
, vol. 13, no. 3, pp. 153-162, 2012
Large genomic rearrangements of the BRCA1 and BRCA2 genes: review of the literature and report of a novel BRCA1 mutation
(
Citations: 8
)
Michelle D. Sluiter
,
Elizabeth J. van Rensburg
Journal:
Breast Cancer Research and Treatment - BREAST CANCER RES TREAT
, vol. 125, no. 2, pp. 325-349, 2011
A decade of exploring the cancer epigenome — biological and translational implications
(
Citations: 2
)
Stephen B. Baylin
,
Peter A. Jones
Journal:
Nature Reviews Cancer - NAT REV CANCER
, vol. 11, no. 10, pp. 726-734, 2011
Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review
(
Citations: 2
)
Scott M. Weissman
,
Cecelia Bellcross
,
Christina Chimera Bittner
,
Mary E. Freivogel
,
Joy Larsen Haidle
,
Pardeep Kaurah
,
Anna Leininger
,
Selvi Palaniappan
,
Kelle Steenblock
,
Thuy M. Vu
,
Molly S. Daniels
Journal:
Journal of Genetic Counseling - J GENET COUNS
, vol. 20, no. 1, pp. 5-19, 2011
Methylation of MGMT in malignant pleural mesothelioma occurs in a subset of patients and is associated with the T allele of the rs16906252 MGMT promoter SNP
(
Citations: 1
)
Lasse Sommer Kristensen
,
Helene Myrtue Nielsen
,
Henrik Hager
,
Lise Lotte Hansen
Journal:
Lung Cancer
, vol. 71, no. 2, pp. 130-136, 2011
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