Obesity and survival among women with ovarian cancer: results from the Ovarian Cancer Association Consortium von Nagle, C M, Dixon, S C, Jensen, A, Kjaer, S K, Modugno, F, deFazio, A, Fereday, S, Hung, J, Johnatty, S E, Fasching, P A, Beckmann, M W, Lambrechts, D, Vergote, I, Van Nieuwenhuysen, E, Lambrechts, S, Risch, H A, Rossing, M A, Doherty, J A, Wicklund, K G, Chang-Claude, J, Goodman, M T, Ness, R B, Moysich, K, Heitz, F, du Bois, A, Harter, P, Schwaab, I, Matsuo, K, Hosono, S, Goode, E L, Vierkant, R A, Larson, M C, Fridley, B L, Høgdall, C, Schildkraut, J M, Weber, R P, Cramer, D W, Terry, K L, Bandera, E V, Paddock, L, Rodriguez-Rodriguez, L, Wentzensen, N, Yang, H P, Brinton, L A, Lissowska, J, Høgdall, E, Lundvall, L, Whittemore, A, McGuire, V, Sieh, W, Rothstein, J, Sutphen, R, Anton-Culver, H, Ziogas, A, Pearce, C L, Wu, A H, Webb, P M

Volltext

National telephone genetic counseling service supports informed and timely decisions in reproductive medicine von Schuetzle, M, Steenblock, K, Trivedi, A, Sutphen, R

Volltext

The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome von Bamshad, M., Le, T., Watkins, W.S., Dixon, M.E., Kramer, B.E., Roeder, A.D., Carey, J.C., Root, S., Schinzel, A., Van Maldergem, L., Gardner, R.J.M., Lin, R.C., Seidman, C.E., Seidman, J.G., Wallerstein, R., Moran, E., Sutphen, R., Campbell, C.E., Jorde, L.B.

Volltext

Identification of genes associated with ovarian cancer metastasis using microarray expression analysis von LANCASTER, J.M., DRESSMAN, H.K., CLARKE, J.P., SAYER, R.A., MARTINO, M.A., CRAGUN, J.M., HENRIOTT, A.H., GRAY, J., SUTPHEN, R., ELAHI, A., WHITAKER, R.S., WEST, M., MARKS, J.R., NEVINS, J.R., BERCHUCK, A.

Volltext

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases von Pal, Tuya, Permuth‐Wey, Jenny, Betts, Judith A., Krischer, Jeffrey P., Fiorica, James, Arango, Hector, LaPolla, James, Hoffman, Mitchell, Martino, Martin A., Wakeley, Katie, Wilbanks, George, Nicosia, Santo, Cantor, Alan, Sutphen, Rebecca

Volltext

The presence of germ line mosaicism in cleidocranial dysplasia von Pal, T, Napierala, D, Becker, TA, Loscalzo, M, Baldridge, D, Lee, B, Sutphen, R

Volltext

Lysophospholipids Are Potential Biomarkers of Ovarian Cancer von SUTPHEN, Rebecca, YAN XU, GRIFFIN, David, BLANCO, Rafael W, CANTOR, Alan B, XIAO, Yi-Jin, KRISCHER, Jeffrey P, WILBANKS, George D, FIORICA, James, GRENDYS, Edward C, LAPOLLA, James P, ARANGO, Hector, HOFFMAN, Mitchell S, MARTINO, Martin, WAKELEY, Katie

Volltext

BRCA1 and BRCA2 Mutations in a Study of African American Breast Cancer Patients von PAL, Tuya, PERMUTH-WEY, Jenny, HOLTJE, Tricia, SUTPHEN, Rebecca

Volltext

Abstract P2-10-06: Identification and Referral of Appropriate Patients for Genetic Services in the Community Setting: An innovative Approach von Sutphen, R, Steenblock, K, Carmany, E, Trivedi, A, Lewis, K.

Volltext

Identification of genes associated with ovarian cancer metastasis using microarray expression analysis von Lancaster, J. M., Dressman, H. K., Clarke, J. P., Sayer, R. A., Martino, M. A., Cragun, J. M., Henriott, A. H., Gray, J., Sutphen, R., Elahi, A., Whitaker, R. S., West, M., Marks, J. R., Nevins, J. R., Berchuck, A.

Volltext

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy von Wilce, Matthew, Hübner, Christoph, Nowak, Kristen J, Laing, Nigel G, Wattanasirichaigoon, Duangrurdee, Pelin, Katarina, Oexle, Konrad, Müller, Clemens R, Nürnberg, Peter, Iannaccone, Susan T, Beggs, Alan H, Wallgren-Pettersson, Carina, Donner, Kati, Sutphen, Rebecca, Sewry, Caroline, Jacob, Rebecca L, Anderson, Janice R, Verity, Christopher M, Lacson, Atilano G, Swoboda, Kathryn J, Goebel, Hans H, North, Kathryn N, Muntoni, Francesco, Hughes, Imelda, Vigneron, Jaqueline

Volltext

Surface-enhanced Raman scattering detection of lysophosphatidic acid von Seballos, Leo, Zhang, Jin Z, Sutphen, Rebecca

Volltext

Examining Substance Abuse in Truant Youths and Their Caregivers: Implications for Truancy Intervention von Flaherty, Christopher W., Sutphen, Richard D., Ely, Gretchen E.

Volltext

Obesity and survival among women with ovarian cancer: results from the Ovarian Cancer Association Consortium von Nagle, C.M, Dixon, S.C, Jensen, A, Kjaer, S.K, Modugno, F, deFazio, A, Fereday, S, Hung, J, Johnatty, S.E, Fasching, P.A, Beckmann, M.W, Lambrechts, Diether, Vergote, Ignace, Van Nieuwenhuysen, Els, Lambrechts, S, Risch, H.A, Rossing, M.A, Doherty, J.A, Wicklund, K.G, Chang-Claude, J, Goodman, M.T, Ness, R.B, Moysich, K, Heitz, F, du Bois, A, Harter, P, Schwaab, I, Matsuo, K, Hosono, S, Goode, E.L, Vierkant, R.A, Larson, M.C, Fridley, B.L, Høgdall, C, Schildkraut, J.M, Weber, R.P, Cramer, D.W, Terry, K.L, Bandera, E.V, Paddock, L, Rodriguez-Rodriguez, L, Wentzensen, N, Yang, H.P, Brinton, L.A, Lissowska, J, Høgdall, E, Lundvall, L, Whittemore, A, McGuire, V, Sieh, W, Rothstein, Jonathan, Sutphen, R, Anton-Culver, H, Ziogas, A, Pearce, C.L, Wu, A.H, Webb, P.M

Volltext

Expanded phenotype of cranioectodermal dysplasia (Sensenbrenner syndrome) von Amar, M. J. A., Sutphen, R., Kousseff, B. G.

Volltext

Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium von Johnatty, S. E, Tyrer, J. P, Kar, S, Beesley, J, Lu, Y, Gao, B, Fasching, P. A, Hein, A, Ekici, A. B, Beckmann, M. W, Lambrechts, D, Van Nieuwenhuysen, E, Vergote, I, Lambrechts, S, Rossing, M. A, Doherty, J. A, Chang-Claude, J, Modugno, F, Ness, R. B, Moysich, K. B, Levine, D. A, Kiemeney, L. A, Massuger, L. F. A. G, Lubinski, J, Jakubowska, A, Cybulski, C, Brinton, L, Lissowska, J, Wentzensen, N, Song, H, Rhenius, V, Campbell, I, Eccles, D, Sieh, W, Whittemore, A. S, McGuire, V, Rothstein, J. H, Sutphen, R, Anton-Culver, H, Ziogas, A, Gayther, S. A, Gentry-Maharaj, A, Menon, U, Ramus, S. J, Pearce, C. L, Pike, M. C, Stram, D. O, Wu, A. H, Kupryjanczyk, J, Dansonka-Mieszkowska, A, Rzepecka, I. K, Spiewankiewicz, B, Goodman, M. T, Wilkens, L. R, Carney, M. E, Thompson, P. J, Heitz, F, du Bois, A, Schwaab, I, Harter, P, Pisterer, J, Hillemanns, P, Karlan, B. Y, Walsh, C, Lester, J, Orsulic, S, Winham, S. J, Earp, M, Larson, M. C, Fogarty, Z. C, Jensen, A, Kjaer, S. K, Fridley, B. L, Cunningham, J. M, Vierkant, R. A, Schildkraut, J. M, Iversen, E. S, Terry, Kathryn Lynne, Cramer, Daniel William, Bandera, E. V, Orlow, I, Pejovic, T, Bean, Y, Hogdall, C, Lundvall, L, McNeish, I, Paul, J, Carty, K, Siddiqui, N, Glasspool, R, Sellers, T, Kennedy, C, Chiew, Y.-E, Berchuck, A, MacGregor, S, Pharoah, P. D. P, Goode, E. L, deFazio, A, Webb, P. M, Chenevix-Trench, G

Volltext

Interobserver and interlaboratory variability of mismatch repair protein expression in ovarian tumors von Coppola, D., Nicosia, S., Lee, J., Kim, J., Schildkraut, J., Narod, S., Sutphen, R., Sellers, T., Pal, T.

Volltext

Genetic data from nearly 63,000 women of European descent predicts DNA methylation biomarkers and epithelial ovarian cancer risk von Yang, Y, Wu, L, Shu, X, Lu, Y, Shu, X-O, Cai, Q, Beeghly-Fadiel, A, Li, B, Ye, F, Berchuck, A, Anton-Culver, H, Banerjee, S, Benitez, J, Bjørge, L, Brenton, JD, Butzow, R, Campbell, IG, Chang-Claude, J, Chen, K, Cook, LS, Cramer, DW, DeFazio, A, Dennis, J, Doherty, JA, Dork, T, Eccles, DM, Velez Edwards, D, Fasching, PA, Fortner, RT, Gayther, SA, Giles, GG, Glasspool, RM, Goode, EL, Goodman, MT, Gronwald, J, Harris, HR, Heitz, F, Hildebrandt, MAT, Høgdall, E, Høgdall, CK, Huntsman, DG, Kar, SP, Karlan, BY, Kelemen, LE, Kiemeney, LA, Kjaer, SK, Koushik, A, Lambrechts, D, Le, ND, Levine, DA, Massuger, LFAG, Matsuo, K, May, T, McNeish, IA, Menon, U, Modugno, F, Monteiro, AN, Moorman, PG, Moysich, KB, Ness, RB, Nevanlinna, H, Olsson, H, Onland-Moret, NC, Park, SK, Paul, J, Pearce, CL, Pejovic, T, Phelan, CM, Pike, MC, Ramus, SJ, Riboli, E, Rodríguez-Antona, C, Romieu, I, Sandler, DP, Schildkraut, JM, Setiawan, VW, Shan, K, Siddiqui, N, Sieh, W, Stampfer, MJ, Sutphen, R, Swerdlow, AJ, Szafron, LM, Teo, SH, Tworoger, SS, Tyrer, JP, Webb, PM, Wentzensen, N, White, E, Willett, WC, Wolk, A, Woo, YL, Wu, AH, Yan, L, Yannoukakos, D, Chenevix-Trench, G, Sellers, TA, Pharoah, PDP, Zheng, W, Long, J

Volltext

Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome) von Herman, Gail E., Kelley, Richard I., Pureza, V., Smith, D., Kopacz, Kevin, Pitt, James, Sutphen, Rebecca, Sheffield, Leslie J., Metzenberg, Aida B.

Volltext

LIN28B Polymorphisms Influence Susceptibility to Epithelial Ovarian Cancer von Permuth-Wey, J, Kim, D, Tsai, Y.-Y, Lin, H.-Y, Chen, Y. A, Barnholtz-Sloan, J, Birrer, Michael James, Bloom, G, Chanock, S. J, Chen, Z, Cramer, Daniel William, Cunningham, J. M, Dagne, G, Ebbert-Syfrett, J, Fenstermacher, D, Fridley, B. L, Garcia-Closas, M, Gayther, S. A, Ge, W, Gentry-Maharaj, A, Gonzalez-Bosquet, J, Goode, E. L, Iversen, E, Jim, H, Kong, W, McLaughlin, J, Menon, U, Monteiro, A. N. A, Narod, S. A, Pharoah, P. D. P, Phelan, C. M, Qu, X, Ramus, S. J, Risch, H, Schildkraut, J. M, Song, H, Stockwell, H, Sutphen, R, Terry, Kathryn Lynne, Tyrer, J, Vierkant, R. A, Wentzensen, N, Lancaster, J. M, Cheng, J. Q, Sellers, T. A

Volltext