BetterScholar BetterScholar
13
Role
Title
Level Year L/R
🐜 Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
23 auth. A. Umar, C. Boland, J. Terdiman, S. Syngal, A. de la Chapelle, J. Rüschoff, R. Fishel, N. Lindor, L. Burgart, R. Hamelin, ... S. Hamilton, R. Hiatt, J. Jass, A. Lindblom, H. Lynch, P. Peltomaki, S. Ramsey, M. Rodriguez-Bigas, H. Vasen, E. Hawk, J. Barrett, A. Freedman, S. Srivastava
11 2004
11
🐜
🦁 Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors.
18 auth. N. Lindor, L. Burgart, Olga N Leontovich, R. Goldberg, J. Cunningham, D. Sargent, C. Walsh-Vockley, G. Petersen, M. Walsh, B. Leggett, ... Joanne P Young, M. Barker, J. Jass, J. Hopper, S. Gallinger, B. Bapat, M. Redston, S. Thibodeau
9 2002
9
🦁
🐢 American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility.
10 auth. M. Robson, A. Bradbury, B. Arun, S. Domchek, J. Ford, H. Hampel, ... Stephen M. Lipkin, S. Syngal, D. Wollins, N. Lindor
9 2010
9
🐢
🦁 Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.
9 auth. N. Lindor, G. Petersen, D. Hadley, A. Kinney, S. Miesfeldt, K. Lu, ... P. Lynch, W. Burke, N. Press
9 2006
9
🦁
🐜 Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
7 auth. S. Kitao, A. Shimamoto, M. Goto, Robert W. Miller, W. A. Smithson, N. Lindor, ... Y. Furuichi
9 1999
9
🐜
🐜 Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond.
35 auth. Samantha E Hansford, P. Kaurah, H. Li-Chang, M. Woo, J. Senz, H. Pinheiro, K. Schrader, D. Schaeffer, K. Shumansky, G. Zogopoulos, T. A. Santos, I. Claro, J. Carvalho, C. Nielsen, Sarah Padilla, ... A. Lum, A. Talhouk, Katie Baker-Lange, S. Richardson, Ivy Lewis, N. Lindor, Erin Pennell, A. MacMillan, B. Fernandez, G. Keller, H. Lynch, Sohrab P. Shah, P. Guilford, S. Gallinger, G. Corso, F. Roviello, C. Caldas, Carla Oliveira, P. Pharoah, D. Huntsman
9 2015
9
🐜
🦁 Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X.
26 auth. N. Lindor, K. Rabe, G. Petersen, R. Haile, G. Casey, J. Baron, S. Gallinger, B. Bapat, M. Aronson, J. Hopper, J. Jass, L. LeMarchand, J. Grove, J. Potter, P. Newcomb, ... J. Terdiman, P. Conrad, Gabriella Moslein, R. Goldberg, A. Ziogas, H. Anton-Culver, M. de Andrade, K. Siegmund, S. Thibodeau, L. Boardman, D. Seminara
9 2005
9
🦁
🐜 The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
18 auth. L. Senter, M. Clendenning, Kaisa Sotamaa, H. Hampel, Jane S Green, J. Potter, A. Lindblom, K. Lagerstedt, S. Thibodeau, N. Lindor, ... Joanne P Young, I. Winship, J. Dowty, Darren M White, J. Hopper, L. Baglietto, M. Jenkins, A. de la Chapelle
9 2008
9
🐜
🐜 Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
133 auth. N. Mavaddat, D. Barrowdale, I. Andrulis, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, A. Spurdle, M. Robson, M. Sherman, A. Mulligan, F. Couch, C. Engel, L. McGuffog, S. Healey, ... O. Sinilnikova, M. Southey, M. Terry, D. Goldgar, F. O'Malley, E. John, R. Janavicius, L. Tihomirova, T. V. Hansen, F. Nielsen, A. Osorio, A. Stavropoulou, J. Benítez, S. Manoukian, B. Peissel, M. Barile, S. Volorio, B. Pasini, R. Dolcetti, A. L. Putignano, L. Ottini, P. Radice, U. Hamann, M. Rashid, F. Hogervorst, M. Kriege, R. B. van der Luijt, S. Peock, D. Frost, D. Evans, C. Brewer, L. Walker, M. Rogers, L. Side, C. Houghton, J. Weaver, A. Godwin, R. Schmutzler, B. Wappenschmidt, A. Meindl, K. Kast, N. Arnold, D. Niederacher, C. Sutter, H. Deissler, D. Gadzicki, S. Preisler‐Adams, R. Varon‐Mateeva, Ines Schönbuchner, H. Gevensleben, D. Stoppa-Lyonnet, Muriel Belotti, L. Barjhoux, C. Isaacs, B. Peshkin, T. Caldés, M. de la Hoya, C. Cañadas, T. Heikkinen, P. Heikkilä, K. Aittomäki, I. Blanco, C. Lázaro, J. Brunet, B. Agnarsson, A. Arason, R. Barkardottir, M. Dumont, J. Simard, M. Montagna, S. Agata, E. D'andrea, M. Yan, S. Fox, T. Rebbeck, W. Rubinstein, N. Tung, J. Garber, Xianshu Wang, Z. Fredericksen, V. Pankratz, N. Lindor, C. Szabo, K. Offit, R. Sakr, M. Gaudet, C. Singer, M. Tea, C. Rappaport, P. Mai, M. Greene, A. Sokolenko, E. Imyanitov, A. Toland, L. Senter, K. Sweet, M. Thomassen, A. Gerdes, T. Kruse, M. Caligo, P. Aretini, Johanna Rantala, Anna von Wachenfeld, K. Henriksson, L. Steele, S. Neuhausen, R. Nussbaum, M. Beattie, K. Odunsi, Lara E. Sucheston, S. Gayther, K. Nathanson, J. Gross, C. Walsh, B. Karlan, G. Chenevix-Trench, D. Easton, A. Antoniou
9 2011
9
🐜
🐜 Identification of Lynch syndrome among patients with colorectal cancer.
23 auth. L. Moreira, F. Balaguer, N. Lindor, A. de la Chapelle, H. Hampel, L. Aaltonen, J. Hopper, L. Le Marchand, S. Gallinger, P. Newcomb, ... R. Haile, S. Thibodeau, Shanaka R. Gunawardena, M. Jenkins, D. Buchanan, J. Potter, J. Baron, D. Ahnen, V. Moreno, M. Andreu, M. Ponz de Leòn, A. Rustgi, A. Castells
8 2012
8
🐜
🐜 Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes.
13 auth. S. Thibodeau, A. French, P. Roche, J. Cunningham, D. Tester, N. Lindor, G. Möslein, S. Baker, R. Liskay, L. Burgart, ... R. Honchel, R. Honchel, K. Halling
8 1996
8
🐜
🐜 Increased Risk for Cancer in Patients with the Peutz-Jeghers Syndrome
10 auth. L. Boardman, S. Thibodeau, D. Schaid, N. Lindor, S. McDonnell, L. Burgart, ... D. Ahlquist, K. Podratz, M. Pittelkow, L. Hartmann
8 1998
8
🐜
🐜 Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder.
7 auth. C. Wise, J. Gillum, C. Seidman, N. Lindor, Rose A. Veile, S. Bashiardes, ... M. Lovett
8 2002
8
🐜