|
🐜
|
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
55 auth.
Judith E. Grolleman,
R. D. Voer,
F. A. Elsayed,
M. Nielsen,
Robbert D. A. Weren,
C. Palles,
M. Ligtenberg,
J. Vos,
S. T. Broeke,
N. Miranda,
Renske A. Kuiper,
E. Kamping,
Erik A. M. Jansen,
M. E. Vink-Börger,
Isabell Popp,
...
A. Lang,
I. Spier,
R. Hüneburg,
P. James,
Na Li,
N. Li,
Marija Staninova,
H. Lindsay,
D. Cockburn,
O. Spasic-Boskovic,
M. Clendenning,
K. Sweet,
G. Capellá,
W. Sjursen,
Hildegunn Høberg-Vetti,
M. Jongmans,
K. Neveling,
A. G. Kessel,
H. Morreau,
F. Hes,
R. Sijmons,
H. Schackert,
C. Ruíz-Ponte,
D. Dymerska,
J. Lubiński,
B. Rivera,
W. Foulkes,
I. Tomlinson,
L. Valle,
D. Buchanan,
S. Kenwrick,
J. Adlard,
A. Dimovski,
I. Campbell,
I. Campbell,
S. Aretz,
D. Schindler,
T. Wezel,
N. Hoogerbrugge,
R. Kuiper
|
7 |
2019 |
7
🐜
|
|
🐜
|
Update on genetic predisposition to colorectal cancer and polyposis.
12 auth.
L. Valle,
R. D. de Voer,
Y. Goldberg,
W. Sjursen,
A. Försti,
C. Ruíz-Ponte,
...
T. Caldés,
P. Garre,
M. F. Olsen,
M. Nordling,
S. Castellví-Bel,
K. Hemminki
|
7 |
2019 |
7
🐜
|
|
🐜
|
Selective inhibitors of cytosolic or secretory phospholipase A2 block TNF-induced activation of transcription factor nuclear factor-kappa B and expression of ICAM-1.
10 auth.
L. Thommesen,
W. Sjursen,
K. Gåsvik,
W. Hanssen,
O. Brekke,
L. Skattebol,
...
A. K. Holmeide,
T. Espevik,
B. Johansen,
A. Laegreid
|
6 |
1998 |
6
🐜
|
|
🦁
|
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers
15 auth.
W. Sjursen,
B. Haukanes,
E. Grindedal,
H. Aarset,
A. Stormorken,
L. Engebretsen,
C. Jonsrud,
Inga Bjørnevoll,
P. A. Andresen,
S. Ariansen,
...
L. A. Lavik,
Bodil Gilde,
I. M. Bowitz-Lothe,
L. Mæhle,
P. Møller
|
6 |
2010 |
6
🦁
|
|
🐜
|
Identification of serum microRNA profiles in colon cancer
9 auth.
E. Hofsli,
W. Sjursen,
W. S. Prestvik,
Jostein Johansen,
M. Rye,
G. Tranø,
...
H. Wasmuth,
I. Hatlevoll,
L. Thommesen
|
6 |
2013 |
6
🐜
|
|
🐢
|
A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine
9 auth.
Maren F Hansen,
Jostein Johansen,
Inga Bjørnevoll,
Anna E. Sylvander,
Kristin S. Steinsbekk,
Pål Sætrom,
...
Arne K. Sandvik,
F. Drabløs,
W. Sjursen
|
6 |
2015 |
6
🐢
|
|
🐢
|
Detecting copy number variation in next generation sequencing data from diagnostic gene panels
A. Singh,
M. F. Olsen,
L. A. Lavik,
Trine Vold,
F. Drabløs,
W. Sjursen
|
5 |
2021 |
5
🐢
|
|
🐢
|
Use of multigene‐panel identifies pathogenic variants in several CRC‐predisposing genes in patients previously tested for Lynch Syndrome
11 auth.
Maren F Hansen,
Jostein Johansen,
Anna E. Sylvander,
Inga Bjørnevoll,
B. Talseth-Palmer,
L. A. Lavik,
...
A. Xavier,
L. Engebretsen,
R. Scott,
F. Drabløs,
W. Sjursen
|
5 |
2017 |
5
🐢
|
|
🐬
|
Awareness of heredity in colorectal cancer patients is insufficient among clinicians: a Norwegian population‐based study
G. Tranø,
Hans H. Wasmuth,
W. Sjursen,
E. Hofsli,
Lars J. Vatten
|
5 |
2009 |
5
🐬
|
