Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. [electronic resource] - Human molecular genetics Nov 2009 - 4442-56 p. digital
Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
1460-2083
10.1093/hmg/ddp372 doi
Adult
Aged
Aged, 80 and over
BRCA1 Protein--genetics
BRCA2 Protein--genetics
Breast Neoplasms--genetics
Chromosomes, Human, Pair 2--genetics
Chromosomes, Human, Pair 8--genetics
Female
Follow-Up Studies
Genetic Predisposition to Disease
Genetic Variation
Genetics, Population
Genome-Wide Association Study
Heterozygote
Humans
Microfilament Proteins--genetics
Middle Aged
Mutation
Polymorphism, Single Nucleotide
Young Adult
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
APA
Antoniou A. C., Sinilnikova O. M., McGuffog L., Healey S., Nevanlinna H., Heikkinen T., Simard J., Spurdle A. B., Beesley J., Chen X., Neuhausen S. L., Ding Y. C., Couch F. J., Wang X., Fredericksen Z., Peterlongo P., Peissel B., Bonanni B., Viel A., Bernard L., Radice P., Szabo C. I., Foretova L., Zikan M., Claes K., Greene M. H., Mai P. L., Rennert G., Lejbkowicz F., Andrulis I. L., Ozcelik H., Glendon G., Gerdes A., Thomassen M., Sunde L., Caligo M. A., Laitman Y., Kontorovich T., Cohen S., Kaufman B., Dagan E., Baruch R. G., Friedman E., Harbst K., Barbany-Bustinza G., Rantala J., Ehrencrona H., Karlsson P., Domchek S. M., Nathanson K. L., Osorio A., Blanco I., Lasa A., Benítez J., Hamann U., Hogervorst F. B. L., Rookus M. A., Collee J. M., Devilee P., Ligtenberg M. J., van der Luijt R. B., Aalfs C. M., Waisfisz Q., Wijnen J., van Roozendaal C. E. P., Peock S., Cook M., Frost D., Oliver C., Platte R., Evans D. G., Lalloo F., Eeles R., Izatt L., Davidson R., Chu C., Eccles D., Cole T., Hodgson S., Godwin A. K., Stoppa-Lyonnet D., Buecher B., Léoné M., Bressac-de Paillerets B., Remenieras A., Caron O., Lenoir G. M., Sevenet N., Longy M., Ferrer S. F., Prieur F., Goldgar D., Miron A., John E. M., Buys S. S., Daly M. B., Hopper J. L., Terry M. B., Yassin Y., Singer C., Gschwantler-Kaulich D., Staudigl C., Hansen T. v. O., Barkardottir R. B., Kirchhoff T., Pal P., Kosarin K., Offit K., Piedmonte M., Rodriguez G. C., Wakeley K., Boggess J. F., Basil J., Schwartz P. E., Blank S. V., Toland A. E., Montagna M., Casella C., Imyanitov E. N., Allavena A., Schmutzler R. K., Versmold B., Engel C., Meindl A., Ditsch N., Arnold N., Niederacher D., Deissler H., Fiebig B., Suttner C., Schönbuchner I., Gadzicki D., Caldes T., de la Hoya M., Pooley K. A., Easton D. F. & Chenevix-Trench G. (20100203). Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. : Human molecular genetics.
Chicago
Antoniou Antonis C, Sinilnikova Olga M, McGuffog Lesley, Healey Sue, Nevanlinna Heli, Heikkinen Tuomas, Simard Jacques, Spurdle Amanda B, Beesley Jonathan, Chen Xiaoqing, Neuhausen Susan L, Ding Yuan C, Couch Fergus J, Wang Xianshu, Fredericksen Zachary, Peterlongo Paolo, Peissel Bernard, Bonanni Bernardo, Viel Alessandra, Bernard Loris, Radice Paolo, Szabo Csilla I, Foretova Lenka, Zikan Michal, Claes Kathleen, Greene Mark H, Mai Phuong L, Rennert Gad, Lejbkowicz Flavio, Andrulis Irene L, Ozcelik Hilmi, Glendon Gord, Gerdes Anne-Marie, Thomassen Mads, Sunde Lone, Caligo Maria A, Laitman Yael, Kontorovich Tair, Cohen Shimrit, Kaufman Bella, Dagan Efrat, Baruch Ruth Gershoni, Friedman Eitan, Harbst Katja, Barbany-Bustinza Gisela, Rantala Johanna, Ehrencrona Hans, Karlsson Per, Domchek Susan M, Nathanson Katherine L, Osorio Ana, Blanco Ignacio, Lasa Adriana, Benítez Javier, Hamann Ute, Hogervorst Frans B L, Rookus Matti A, Collee J Margriet, Devilee Peter, Ligtenberg Marjolijn J, van der Luijt Rob B, Aalfs Cora M, Waisfisz Quinten, Wijnen Juul, van Roozendaal Cornelis E P, Peock Susan, Cook Margaret, Frost Debra, Oliver Clare, Platte Radka, Evans D Gareth, Lalloo Fiona, Eeles Rosalind, Izatt Louise, Davidson Rosemarie, Chu Carol, Eccles Diana, Cole Trevor, Hodgson Shirley, Godwin Andrew K, Stoppa-Lyonnet Dominique, Buecher Bruno, Léoné Mélanie, Bressac-de Paillerets Brigitte, Remenieras Audrey, Caron Olivier, Lenoir Gilbert M, Sevenet Nicolas, Longy Michel, Ferrer Sandra Fert, Prieur Fabienne, Goldgar David, Miron Alexander, John Esther M, Buys Saundra S, Daly Mary B, Hopper John L, Terry Mary Beth, Yassin Yosuf, Singer Christian, Gschwantler-Kaulich Daphne, Staudigl Christine, Hansen Thomas v O, Barkardottir Rosa Bjork, Kirchhoff Tomas, Pal Prodipto, Kosarin Kristi, Offit Kenneth, Piedmonte Marion, Rodriguez Gustavo C, Wakeley Katie, Boggess John F, Basil Jack, Schwartz Peter E, Blank Stephanie V, Toland Amanda E, Montagna Marco, Casella Cinzia, Imyanitov Evgeny N, Allavena Anna, Schmutzler Rita K, Versmold Beatrix, Engel Christoph, Meindl Alfons, Ditsch Nina, Arnold Norbert, Niederacher Dieter, Deissler Helmut, Fiebig Britta, Suttner Christian, Schönbuchner Ines, Gadzicki Dorothea, Caldes Trinidad, de la Hoya Miguel, Pooley Karen A, Easton Douglas F and Chenevix-Trench Georgia. 20100203. Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. : Human molecular genetics.
Harvard
Antoniou A. C., Sinilnikova O. M., McGuffog L., Healey S., Nevanlinna H., Heikkinen T., Simard J., Spurdle A. B., Beesley J., Chen X., Neuhausen S. L., Ding Y. C., Couch F. J., Wang X., Fredericksen Z., Peterlongo P., Peissel B., Bonanni B., Viel A., Bernard L., Radice P., Szabo C. I., Foretova L., Zikan M., Claes K., Greene M. H., Mai P. L., Rennert G., Lejbkowicz F., Andrulis I. L., Ozcelik H., Glendon G., Gerdes A., Thomassen M., Sunde L., Caligo M. A., Laitman Y., Kontorovich T., Cohen S., Kaufman B., Dagan E., Baruch R. G., Friedman E., Harbst K., Barbany-Bustinza G., Rantala J., Ehrencrona H., Karlsson P., Domchek S. M., Nathanson K. L., Osorio A., Blanco I., Lasa A., Benítez J., Hamann U., Hogervorst F. B. L., Rookus M. A., Collee J. M., Devilee P., Ligtenberg M. J., van der Luijt R. B., Aalfs C. M., Waisfisz Q., Wijnen J., van Roozendaal C. E. P., Peock S., Cook M., Frost D., Oliver C., Platte R., Evans D. G., Lalloo F., Eeles R., Izatt L., Davidson R., Chu C., Eccles D., Cole T., Hodgson S., Godwin A. K., Stoppa-Lyonnet D., Buecher B., Léoné M., Bressac-de Paillerets B., Remenieras A., Caron O., Lenoir G. M., Sevenet N., Longy M., Ferrer S. F., Prieur F., Goldgar D., Miron A., John E. M., Buys S. S., Daly M. B., Hopper J. L., Terry M. B., Yassin Y., Singer C., Gschwantler-Kaulich D., Staudigl C., Hansen T. v. O., Barkardottir R. B., Kirchhoff T., Pal P., Kosarin K., Offit K., Piedmonte M., Rodriguez G. C., Wakeley K., Boggess J. F., Basil J., Schwartz P. E., Blank S. V., Toland A. E., Montagna M., Casella C., Imyanitov E. N., Allavena A., Schmutzler R. K., Versmold B., Engel C., Meindl A., Ditsch N., Arnold N., Niederacher D., Deissler H., Fiebig B., Suttner C., Schönbuchner I., Gadzicki D., Caldes T., de la Hoya M., Pooley K. A., Easton D. F. and Chenevix-Trench G. (20100203). Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. : Human molecular genetics.
MLA
Antoniou Antonis C, Sinilnikova Olga M, McGuffog Lesley, Healey Sue, Nevanlinna Heli, Heikkinen Tuomas, Simard Jacques, Spurdle Amanda B, Beesley Jonathan, Chen Xiaoqing, Neuhausen Susan L, Ding Yuan C, Couch Fergus J, Wang Xianshu, Fredericksen Zachary, Peterlongo Paolo, Peissel Bernard, Bonanni Bernardo, Viel Alessandra, Bernard Loris, Radice Paolo, Szabo Csilla I, Foretova Lenka, Zikan Michal, Claes Kathleen, Greene Mark H, Mai Phuong L, Rennert Gad, Lejbkowicz Flavio, Andrulis Irene L, Ozcelik Hilmi, Glendon Gord, Gerdes Anne-Marie, Thomassen Mads, Sunde Lone, Caligo Maria A, Laitman Yael, Kontorovich Tair, Cohen Shimrit, Kaufman Bella, Dagan Efrat, Baruch Ruth Gershoni, Friedman Eitan, Harbst Katja, Barbany-Bustinza Gisela, Rantala Johanna, Ehrencrona Hans, Karlsson Per, Domchek Susan M, Nathanson Katherine L, Osorio Ana, Blanco Ignacio, Lasa Adriana, Benítez Javier, Hamann Ute, Hogervorst Frans B L, Rookus Matti A, Collee J Margriet, Devilee Peter, Ligtenberg Marjolijn J, van der Luijt Rob B, Aalfs Cora M, Waisfisz Quinten, Wijnen Juul, van Roozendaal Cornelis E P, Peock Susan, Cook Margaret, Frost Debra, Oliver Clare, Platte Radka, Evans D Gareth, Lalloo Fiona, Eeles Rosalind, Izatt Louise, Davidson Rosemarie, Chu Carol, Eccles Diana, Cole Trevor, Hodgson Shirley, Godwin Andrew K, Stoppa-Lyonnet Dominique, Buecher Bruno, Léoné Mélanie, Bressac-de Paillerets Brigitte, Remenieras Audrey, Caron Olivier, Lenoir Gilbert M, Sevenet Nicolas, Longy Michel, Ferrer Sandra Fert, Prieur Fabienne, Goldgar David, Miron Alexander, John Esther M, Buys Saundra S, Daly Mary B, Hopper John L, Terry Mary Beth, Yassin Yosuf, Singer Christian, Gschwantler-Kaulich Daphne, Staudigl Christine, Hansen Thomas v O, Barkardottir Rosa Bjork, Kirchhoff Tomas, Pal Prodipto, Kosarin Kristi, Offit Kenneth, Piedmonte Marion, Rodriguez Gustavo C, Wakeley Katie, Boggess John F, Basil Jack, Schwartz Peter E, Blank Stephanie V, Toland Amanda E, Montagna Marco, Casella Cinzia, Imyanitov Evgeny N, Allavena Anna, Schmutzler Rita K, Versmold Beatrix, Engel Christoph, Meindl Alfons, Ditsch Nina, Arnold Norbert, Niederacher Dieter, Deissler Helmut, Fiebig Britta, Suttner Christian, Schönbuchner Ines, Gadzicki Dorothea, Caldes Trinidad, de la Hoya Miguel, Pooley Karen A, Easton Douglas F and Chenevix-Trench Georgia. Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. : Human molecular genetics. 20100203.