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Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
86 auth.
A. Antoniou,
A. Spurdle,
O. Sinilnikova,
S. Healey,
K. Pooley,
R. Schmutzler,
B. Versmold,
C. Engel,
A. Meindl,
N. Arnold,
Wera Hofmann,
C. Sutter,
D. Niederacher,
H. Deissler,
T. Caldés,
...
Kati Kämpjärvi,
H. Nevanlinna,
J. Simard,
J. Beesley,
Xiaoqing Chen,
S. Neuhausen,
T. Rebbeck,
T. Wagner,
Henry T. Lynch,
C. Isaacs,
J. Weitzel,
Patricia A. Ganz,
M. Daly,
G. Tomlinson,
O. Olopade,
Joanne L. Blum,
F. Couch,
P. Peterlongo,
S. Manoukian,
M. Barile,
P. Radice,
C. Szabo,
Lutecia H. Mateus Pereira,
Mark H. Greene,
G. Rennert,
F. Lejbkowicz,
O. Barnett-Griness,
I. Andrulis,
H. Ozçelik,
A. Gerdes,
M. Caligo,
Y. Laitman,
B. Kaufman,
Roni Milgrom,
Eitan Friedman,
S. Domchek,
K. Nathanson,
A. Osorio,
G. Llort,
R. Milne,
J. Benítez,
U. Hamann,
Frans B. L. Hogervorst,
P. Manders,
M. Ligtenberg,
A. V. D. van den Ouweland,
S. Peock,
Margaret R. Cook,
Radka Platte,
D. Evans,
R. Eeles,
G. Pichert,
C. Chu,
D. Eccles,
R. Davidson,
F. Douglas,
Andrew K. Godwin,
L. Barjhoux,
S. Mazoyer,
H. Sobol,
V. Bourdon,
F. Eisinger,
A. Chompret,
C. Capoulade,
B. Bressac-de Paillerets,
Gilbert M. Lenoir,
M. Gauthier‐Villars,
C. Houdayer,
D. Stoppa-Lyonnet,
G. Chenevix-Trench,
D. Easton
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8 |
2008 |
8 🐜
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A descriptive study of BRCA1 testing and reactions to disclosure of test results
15 auth.
H. Lynch,
S. Lemon,
Carolyn Durham,
S. Tinley,
Chris L Connolly,
J. Lynch,
Jonathan Surdam,
Ernest Orinion,
Sue Slominski‐Caster,
P. Watson,
...
C. Lerman,
P. Tonin,
Gilbert M. Lenoir,
O. Serova,
S. Narod
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7 |
1997 |
7 🐜
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Effect of smoking on breast cancer in carriers of mutant BRCA1 or BRCA2 genes.
19 auth.
J. Brunet,
P. Ghadirian,
T. Rebbeck,
C. Lerman,
Judy Garber,
Patricia N. Tonin,
J. Abrahamson,
W. Foulkes,
M. Daly,
Josephine Wagner-Costalas,
...
A. Godwin,
O. Olopade,
R. Moslehi,
A. Liede,
P. Futreal,
Barbara L. Weber,
Gilbert M. Lenoir,
H. T. Lynch,
S. A. Narod
|
7 |
1998 |
7 🐜
|
🐢
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DNA screening for breast/ovarian cancer susceptibility based on linked markers. A family study.
8 auth.
H. T. Lynch,
P. Watson,
T. Conway,
J. Lynch,
Sue Slominski‐Caster,
S. Narod,
...
Jean Feunteun,
Gilbert M. Lenoir
|
6 |
1993 |
6 🐢
|
🐜
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An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer.
11 auth.
H. T. Lynch,
Patrice Watson,
S. Tinley,
C. Snyder,
Carolyn Durham,
J. Lynch,
...
Yulia Kirnarsky,
Olga Serova,
Gilbert M. Lenoir,
C. Lerman,
S. A. Narod
|
6 |
1999 |
6 🐜
|
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Nonlinkage of 16q markers to familial predisposition to Wilms' tumor.
11 auth.
Vicki D Huff,
A. Reeve,
Mark Leppert,
L. Strong,
Edwin C. Douglass,
Clementina F. Geiser,
...
Frederick P. Li,
Anna T. Meadows,
D. F. Callen,
Gilbert M. Lenoir,
Grady F. Saunders
|
6 |
1992 |
6 🐜
|
🐜
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Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12-21: exclusion of candidate genes EDH17B2 and RARA.
14 auth.
Jacques Simard,
Jean Feunteun,
Gilbert M. Lenoir,
Patricia N. Tonin,
Thlerry Normand,
Anne Vivler,
Dana Lasko,
Kenneth Morgan,
Kenneth Morgan,
Guy A. Rouleau,
...
Guy A. Rouleau,
H. T. Lynch,
Femand Labrie,
S. A. Narod
|
6 |
1993 |
6 🐜
|
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Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus.
13 auth.
Marc Sanson,
C. Marineau,
Chantale Desmaze,
M. Lutchman,
M. Ruttledge,
M. Ruttledge,
Chantal Baron,
S. A. Narod,
Olivier Delattre,
Gilbert M. Lenoir,
...
Gilles Thomas,
Alain Aurlas,
Guy A. Rouleau
|
5 |
1993 |
5 🐜
|
🐢
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Screening for multiple endocrine neoplasia type 2a with DNA-polymorphism analysis.
22 auth.
Hagay Sobol,
S. A. Narod,
Yusuke Nakamura,
Andrée Boneu,
Claude Calmettes,
Denis Chadenas,
Gilles Charpentier,
Jean François Chatal,
Nicole Delepine,
Marie Joëlle Delisle,
...
Jean Louis Dupond,
Paule Gardet,
Hélène Godefroy,
Pierre-Jean Guillausseau,
Claudine Guillausseau-Scholer,
Chantal Houdent,
Jean-Daniel Lalau,
Geneviève Mace,
Claude Parmentier,
Florent Soubrier,
Jacques Tourniaire,
Gilbert M. Lenoir
|
5 |
1989 |
5 🐢
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