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Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections
45 auth.
A. Bertoli-Avella,
Elisabeth Gillis,
H. Morisaki,
J. Verhagen,
B. D. de Graaf,
Gerarda van de Beek,
E. Gallo,
B. Kruithof,
H. Venselaar,
Loretha A Myers,
S. Laga,
A. J. Doyle,
Gretchen L. Oswald,
G. V. van Cappellen,
I. Yamanaka,
...
R. van der Helm,
B. Beverloo,
A. de Klein,
L. Pardo,
M. Lammens,
C. Evers,
K. Devriendt,
Michiel Dumoulein,
J. Timmermans,
H. Bruggenwirth,
F. Verheijen,
I. Rodrigus,
G. Baynam,
M. Kempers,
J. Saenen,
E. V. Van Craenenbroeck,
K. Minatoya,
R. Matsukawa,
T. Tsukube,
Noriaki Kubo,
R. Hofstra,
M. Goumans,
J. Bekkers,
J. Roos‐Hesselink,
I. M. van de Laar,
H. Dietz,
L. Van Laer,
T. Morisaki,
M. Wessels,
B. Loeys
|
7 |
2015 |
7
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|
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Evidence of a new chimeric bcr/c-abl mRNA in patients with chronic myelocytic leukemia and the Philadelphia chromosome.
8 auth.
K. Stam,
N. Heisterkamp,
G. Grosveld,
A. de Klein,
R. Verma,
M. Coleman,
...
H. Dosik,
J. Groffen
|
7 |
1985 |
7
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|
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Uveal Melanomas with SF3B1 Mutations: A Distinct Subclass Associated with Late-Onset Metastases.
9 auth.
S. Yavuzyigitoglu,
Anna E. Koopmans,
R. Verdijk,
J. Vaarwater,
Bert Eussen,
Alice van Bodegom,
...
D. Paridaens,
E. Kiliç,
A. de Klein
|
7 |
2016 |
7
🐢
|
|
🐢
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Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma
13 auth.
Anna E. Koopmans,
R. Verdijk,
R. Brouwer,
T. V. D. van den Bosch,
M. M. van den Berg,
J. Vaarwater,
C. Kockx,
D. Paridaens,
N. Naus,
M. Nellist,
...
W. V. van Ijcken,
E. Kiliç,
A. de Klein
|
7 |
2014 |
7
🐢
|
|
🐜
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Early-onset parkinsonism associated with PINK1 mutations: Frequency, genotypes, and phenotypes
35 auth.
V. Bonifati,
C. Rohé,
G. Breedveld,
E. Fabrizio,
M. de Mari,
C. Tassorelli,
A. Tavella,
R. Marconi,
D. Nicholl,
H. F. Chien,
E. Fincati,
G. Abbruzzese,
P. Marini,
A. De Gaetano,
M. Horstink,
...
J. Maat-Kievit,
C. Sampaio,
A. Antonini,
F. Stocchi,
P. Montagna,
V. Toni,
M. Guidi,
A. D. Libera,
M. Tinazzi,
F. de Pandis,
G. Fabbrini,
S. Goldwurm,
A. de Klein,
E. Barbosa,
L. Lopiano,
E. Martignoni,
P. Lamberti,
N. Vanacore,
G. Meco,
B. Oostra
|
7 |
2005 |
7
🐜
|
|
🐜
|
Clinical and cytogenetic analyses in uveal melanoma.
9 auth.
E. Kiliç,
Walter van Gils,
Elisabeth M. Lodder,
H. Beverloo,
Marjan E van Til,
C. Mooy,
...
D. Paridaens,
A. de Klein,
G. Luyten
|
7 |
2006 |
7
🐜
|
|
🐢
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Concurrent loss of chromosome arm 1p and chromosome 3 predicts a decreased disease-free survival in uveal melanoma patients.
12 auth.
E. Kiliç,
N. Naus,
Walter van Gils,
C. Klaver,
Marjan E van Til,
Michael M. Verbiest,
...
T. Stijnen,
C. Mooy,
D. Paridaens,
H. Beverloo,
G. Luyten,
A. de Klein
|
7 |
2005 |
7
🐢
|
|
🐜
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Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder
29 auth.
P. Szafranski,
Avinash V Dharmadhikari,
E. Brosens,
Priyatansh Gurha,
K. Kołodziejska,
Z. Ou,
P. Dittwald,
Tadeusz Majewski,
K. N. Mohan,
Bo Chen,
R. Person,
D. Tibboel,
A. de Klein,
J. Pinner,
M. Chopra,
...
G. Malcolm,
G. Peters,
S. Arbuckle,
S. Guiang,
V. Hustead,
J. Jessurun,
R. Hirsch,
D. Witte,
I. Maystadt,
N. Sebire,
R. Fisher,
C. Langston,
P. Sen,
P. Stankiewicz
|
6 |
2013 |
6
🐜
|
|
🐜
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Prognostic parameters in uveal melanoma and their association with BAP1 expression
16 auth.
T. van Essen,
Sake I. van Pelt,
M. Versluis,
Inge H. G. Bronkhorst,
S. V. van Duinen,
M. Marinkovic,
W. Kroes,
C. Ruivenkamp,
S. Shukla,
A. de Klein,
...
E. Kiliç,
J. Harbour,
G. Luyten,
P. A. van der Velden,
R. Verdijk,
M. Jager
|
6 |
2014 |
6
🐜
|
|
🐜
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Higher percentage of FISH-determined monosomy 3 and 8q amplification in uveal melanoma cells relate to poor patient prognosis.
8 auth.
T. van den Bosch,
J. V. van Beek,
J. Vaarwater,
R. Verdijk,
N. Naus,
D. Paridaens,
...
A. de Klein,
E. Kiliç
|
6 |
2012 |
6
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