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Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history.
16 auth.
R. Lothe,
P. Peltomäki,
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L. Aaltonen,
M. Nyström-Lahti,
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Pal Mller,
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S. Fosså,
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F. Langmark,
Anton Br gger,
A. Chapelle,
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9 |
1993 |
9 🐜
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Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study
12 auth.
S. Narod,
J. Brunet,
P. Ghadirian,
M. Robson,
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9 |
2000 |
9 🐜
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Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.
29 auth.
J. Wijnen,
H. Vasen,
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H. Brunner,
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G. Griffioen,
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E. Bakker,
I. van Leeuwen‐Cornelisse,
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D. Lindhout,
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M. Bisgaard,
P. Goetz
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8 |
1998 |
8 🐜
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Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
38 auth.
S. Narod,
M. Dubé,
J. Klijn,
J. Lubiński,
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P. Ghadirian,
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2002 |
8 🐜
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Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.
16 auth.
E. Lynch,
E. A. Ostermeyer,
Ming K. Lee,
J. F. Arena,
Hanlee P. Ji,
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8 |
1997 |
8 🐜
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Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia
55 auth.
M. Faughnan,
J. Mager,
S. Hetts,
V. Palda,
Kelly Lang-Robertson,
E. Buscarini,
E. Deslandres,
R. Kasthuri,
A. Lausman,
David M. Poetker,
F. Ratjen,
M. Chesnutt,
Marianne Clancy,
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Hanny Al-Samkari,
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M. Chakinala,
M. Conrad,
D. Cortés,
Claudia Crocione,
J. Darling,
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U. Geisthoff,
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Kevin Korenblatt,
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J. McMahon,
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M. Meek,
M. Mei-Zahav,
S. Olitsky,
S. Palmer,
Rose Pantalone,
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Beth Plahn,
M. Porteous,
M. Post,
I. Radovanovic,
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J. Rodriguez-Lopez,
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R. Zarrabeitia
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8 |
2020 |
8 🐜
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Pathogenesis of the syndrome of hemolysis, elevated liver enzymes, and low platelet count (HELLP): a review.
U. Abildgaard,
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7 |
2013 |
7 🐢
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Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours
29 auth.
E. Rapley,
G. Crockford,
D. Teare,
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S. Seal,
R. Barfoot,
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K. Heimdal,
Sophie D. Fosså,
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Jenny Donald,
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Colin S. Cooper,
J. G. Bodmer,
Doug Easton,
Michael R. Stratton,
D. Bishop
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7 |
2000 |
7 🐜
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Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
93 auth.
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H. Sorte,
P. Samarakoon,
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Ivan K. Chinn,
Zeynep Coban Akdemir,
H. C. Erichsen,
L. Forbes,
Shen Gu,
Bo Yuan,
S. Jhangiani,
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O. Rødningen,
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W. Wiszniewski,
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T. Gedde-Dahl,
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I. Nordøy,
S. Jørgensen,
T. Abrahamsen,
Torstein Øverland,
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V. Skogen,
L. Osnes,
M. Kulseth,
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Nina Denisse Guerrero-Cursaru,
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A. Aiuti,
C. Cancrini,
E. Holmberg,
C. West,
Magnus Burstedt,
E. Karaca,
G. Yeşil,
H. Artaç,
Y. Bayram,
M. M. Atik,
M. Eldomery,
Mohammad S. Ehlayel,
S. Jolles,
B. Flatø,
A. Bertuch,
I. C. Hanson,
V. Zhang,
L. Wong,
Jianhong Hu,
M. Walkiewicz,
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C. Eng,
E. Boerwinkle,
R. Gibbs,
W. Shearer,
R. Lyle,
J. Orange,
J. Lupski
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7 |
2017 |
7 🐜
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The Y deletion gr/gr and susceptibility to testicular germ cell tumor.
49 auth.
K. Nathanson,
P. Kanetsky,
R. Hawes,
D. Vaughn,
R. Letrero,
K. Tucker,
M. Friedlander,
K. Phillips,
D. Hogg,
M. Jewett,
Radka Lohynska,
G. Daugaard,
S. Richard,
A. Chompret,
C. Bonaïti‐pellié,
...
A. Heidenreich,
E. Oláh,
L. Géczi,
I. Bodrogi,
W. Ormiston,
P. Daly,
J. Oosterhuis,
A. Gillis,
Leendert H. J. Looijenga,
P. Guilford,
S. Fosså,
K. Heimdal,
S. Tjulandin,
L. Liubchenko,
H. Stoll,
W. Weber,
M. Rudd,
R. Huddart,
G. Crockford,
D. Forman,
D. T. Oliver,
L. Einhorn,
B. Weber,
J. Kramer,
M. McMaster,
Mark H. Greene,
M. Pike,
V. Cortessis,
Chu Chen,
S. Schwartz,
D. Bishop,
D. Easton,
Michael R. Stratton,
E. Rapley
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7 |
2005 |
7 🐜
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Oestrogen receptor (ESR) polymorphisms and breast cancer susceptibility
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K. Heimdal,
M. Skrede,
K. Tveit,
K. Berg,
A. Børresen
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7 |
1994 |
7 🐬
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