Genotype and phenotype of patients with both familial adenomatous polyposis and thyroid carcinoma by Truta, Brindusa, Allen, Brian A, Conrad, Peggy G, Kim, Young S, Berk, Terri, Gallinger, Steven, Bapat, Bharati, Terdiman, Jonathan P, Sleisenger, Marvin H

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Tumor histology helps to identify Lynch syndrome among colorectal cancer patients by Truta, Brindusa, Chen, Yunn-Yi, Blanco, Amie M., Deng, Guoren, Conrad, Peggy G., Kim, Yong Ho, Park, Eun Taek, Kakar, Sanjay, Kim, Young S., Velayos, Fernando, Sleisenger, Marvin H., Terdiman, Jonathan P.

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A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history by Truta, Brindusa, Allen, Brian A, Conrad, Peggy G, Weinberg, Vivian, Miller, Glenn A, Pomponio, Rob, Lipton, Lara R, Guerra, Germano, Tomlinson, Ian P M, Sleisenger, Marvin H, Kim, Young S, Terdiman, Jonathan P

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Predictors of Enteral Autonomy in Children with Intestinal Failure: A Multicenter Cohort Study by Khan, Faraz A., MD, Squires, Robert H., MD, Litman, Heather J., PhD, Balint, Jane, MD, Carter, Beth A., MD, Fisher, Jeremy G., MD, Horslen, Simon P., MB, ChB, Jaksic, Tom, MD, PhD, Kocoshis, Samuel, MD, Martinez, J. Andres, MD, Mercer, David, MD, Rhee, Susan, MD, Rudolph, Jeffrey A., MD, Soden, Jason, MD, Sudan, Debra, MD, Superina, Riccardo A., MD, Teitelbaum, Daniel H., MD, Venick, Robert, MD, Wales, Paul W., MD, MSc, Duggan, Christopher, MD, MPH

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Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency: Familial Colorectal Cancer Type X by Lindor, Noralane M, Rabe, Kari, Petersen, Gloria M, Haile, Robert, Casey, Graham, Baron, John, Gallinger, Steve, Bapat, Bharati, Aronson, Melyssa, Hopper, John, Jass, Jeremy, LeMarchand, Loic, Grove, John, Potter, John, Newcomb, Polly, Terdiman, Jonathan P, Conrad, Peggy, Moslein, Gabriella, Goldberg, Richard, Ziogas, Argyrios, Anton-Culver, Hoda, de Andrade, Mariza, Siegmund, Kim, Thibodeau, Stephen N, Boardman, Lisa A, Seminara, Daniela

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Pathologic features of endometrial carcinoma associated with HNPCC : A comparison with sporadic endometrial carcinoma by BROADDUS, Russell R, LYNCH, Henry T, CHEN, Lee-May, DANIELS, Molly S, CONRAD, Peggy, MUNSELL, Mark F, WHITE, Kristin G, LUTHRA, Rajyalakshmi, LU, Karen H

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Standardization of analysis sets for reporting results from ADNI MRI data by Wyman, Bradley T, Harvey, Danielle J, Crawford, Karen, Bernstein, Matt A, Carmichael, Owen, Cole, Patricia E, Crane, Paul K, DeCarli, Charles, Fox, Nick C, Gunter, Jeffrey L, Hill, Derek, Killiany, Ronald J, Pachai, Chahin, Schwarz, Adam J, Schuff, Norbert, Senjem, Matthew L, Suhy, Joyce, Thompson, Paul M, Weiner, Michael, Jack, Clifford R

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Longitudinal measurement and hierarchical classification framework for the prediction of Alzheimer's disease by Huang, Meiyan, Yang, Wei, Feng, Qianjin, Chen, Wufan

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Genome-wide association analysis of hippocampal volume identifies enrichment of neurogenesis-related pathways by Horgusluoglu-Moloch, Emrin, Risacher, Shannon L, Crane, Paul K, Hibar, Derrek, Thompson, Paul M, Saykin, Andrew J, Nho, Kwangsik

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Mining Outcome-relevant Brain Imaging Genetic Associations via Three-way Sparse Canonical Correlation Analysis in Alzheimer's Disease by Hao, Xiaoke, Li, Chanxiu, Du, Lei, Yao, Xiaohui, Yan, Jingwen, Risacher, Shannon L, Saykin, Andrew J, Shen, Li, Zhang, Daoqiang

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Effect of CLU genetic variants on cerebrospinal fluid and neuroimaging markers in healthy, mild cognitive impairment and Alzheimer's disease cohorts by Tan, Lin, Wang, Hui-Fu, Tan, Meng-Shan, Tan, Chen-Chen, Zhu, Xi-Chen, Miao, Dan, Yu, Wan-Jiang, Jiang, Teng, Tan, Lan, Yu, Jin-Tai

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Regional Amyloid-β Load and White Matter Abnormalities Contribute to Hypometabolism in Alzheimer’s Dementia by Schilling, Lucas Porcello, Pascoal, Tharick A., Zimmer, Eduardo R., Mathotaarachchi, Sulantha, Shin, Monica, de Mello Rieder, Carlos Roberto, Gauthier, Serge, Palmini, André, Rosa-Neto, Pedro

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An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers by Blein, Sophie, Danjean, Vincent, Goldgar, David E, Janavicius, Ramunas, Dorfling, Cecilia M, van Rensburg, Elizabeth J, Neuhausen, Susan L, Ding, Yuan Chun, Ejlertsen, Bent, Conejero, Raquel Andrés, Segota, Ena, Weitzel, Jeffrey N, Thelander, Margo, Peissel, Bernard, Zaffaroni, Daniela, Manoukian, Siranoush, Varesco, Liliana, Konstantopoulou, Irene, Brewer, Carole, Evans, D Gareth, Frost, Debra, Douglas, Fiona, Cook, Jackie, Walker, Lisa, Side, Lucy E, Kennedy, M John, Porteous, Mary E, Eeles, Ros, Davidson, Rosemarie, Hodgson, Shirley, Cole, Trevor, Isaacs, Claudine, De Leeneer, Kim, Meindl, Alfons, Kast, Karin, Rhiem, Kerstin, Ditsch, Nina, Varon-Mateeva, Raymonda, Schmutzler, Rita K, Wang-Gohrke, Shan, de Pauw, Antoine, Lefol, Cédrick, Rouleau, Etienne, Damiola, Francesca, Barjhoux, Laure, Uhrhammer, Nancy, Bonadona, Valérie, Carter, Jonathan, Van Le, Linda, Piedmonte, Marion, DiSilvestro, Paul A, Caldes, Trinidad, Jager, Agnes, van den Ouweland, Ans Mw, Aalfs, Cora M, van Leeuwen, Flora E, Oosterwijk, Jan C, van Roozendaal, Kees Ep, van der Luijt, Rob B, Olah, Edith, Diez, Orland, Teulé, Alex, Gronwald, Jacek, Lubinski, Jan, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Agnarsson, Bjarni A, Maugard, Christine, Montagna, Marco, Teixeira, Manuel R, Olswold, Curtis, Lindor, Noralane M, Jacobs, Lauren, Corines, Marina, Berger, Andreas, Fink-Retter, Anneliese, Singer, Christian F, Kaulich, Daphne Geschwantler, Pfeiler, Georg, Mai, Phuong L, Rennert, Gad, Imyanitov, Evgeny N, Mulligan, Anna Marie, Glendon, Gord, Tchatchou, Sandrine, Toland, Amanda Ewart, Kruse, Torben A, Jensen, Uffe Birk, Friedman, Eitan, Zidan, Jamal, Lindblom, Annika, Olopade, Olufunmilayo I, Mitchell, Gillian, Karlan, Beth Y, Orsulic, Sandra, Simard, Jacques, Easton, Douglas F, Chenevix-Trench, Georgia, Mazoyer, Sylvie, Cox, David G

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The impact of PICALM genetic variations on reserve capacity of posterior cingulate in AD continuum by Xu, Wei, Wang, Hui-Fu, Tan, Lin, Tan, Meng-Shan, Tan, Chen-Chen, Zhu, Xi-Chen, Miao, Dan, Yu, Wan-Jiang, Jiang, Teng, Tan, Lan, Yu, Jin-Tai

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Haploinsufficiency in tumor predisposition syndromes: altered genomic transcription in morphologically normal cells heterozygous for VHL or TSC mutation by Peri, Suraj, Caretti, Elena, Tricarico, Rossella, Devarajan, Karthik, Cheung, Mitchell, Sementino, Eleonora, Menges, Craig W, Nicolas, Emmanuelle, Vanderveer, Lisa A, Howard, Sharon, Conrad, Peggy, Crowell, James A, Campbell, Kerry S, Ross, Eric A, Godwin, Andrew K, Yeung, Anthony T, Clapper, Margie L, Uzzo, Robert G, Henske, Elizabeth P, Ricketts, Christopher J, Vocke, Cathy D, Linehan, W Marston, Testa, Joseph R, Bellacosa, Alfonso, Kopelovich, Levy, Knudson, Alfred G

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Pathologic features of endometrial carcinoma associated with HNPCC by Broaddus, Russell R., Lynch, Henry T., Chen, Lee‐may, Daniels, Molly S., Conrad, Peggy, Munsell, Mark F., White, Kristin G., Luthra, Rajyalakshmi, Lu, Karen H.

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