SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Eline C. Soer, Laura W. Leicher, Alexandra M. J. Langers, Paul C. van de Meeberg, Egbert-Jan van der Wouden, Jan Jakob Koornstra, Marloes Bigirwamungu-Bargeman, Hans F. A. Vasen, Wouter H. de Vos tot Nederveen Cappel, Equivalent Helicobacter pylori infection rates in Lynch syndrome mutation carriers with and without a first-degree relative with gastric cancer, International Journal of Colorectal Disease, 2016,

    CrossRef

  2. 2
    J.M. Helder-Woolderink, E.A. Blok, H.F.A. Vasen, H. Hollema, M.J. Mourits, G.H. De Bock, Ovarian cancer in Lynch syndrome; a systematic review, European Journal of Cancer, 2016, 55, 65

    CrossRef

  3. 3
    McKinsey L. Goodenberger, Brittany C. Thomas, Douglas Riegert-Johnson, C. Richard Boland, Sharon E. Plon, Mark Clendenning, Aung Ko Win, Leigha Senter, Steven M. Lipkin, Zsofia K. Stadler, Finlay A. Macrae, Henry T. Lynch, Jeffrey N. Weitzel, Albert de la Chapelle, Sapna Syngal, Patrick Lynch, Susan Parry, Mark A. Jenkins, Steven Gallinger, Spring Holter, Melyssa Aronson, Polly A. Newcomb, Terrilea Burnett, Loïc Le Marchand, Pavel Pichurin, Heather Hampel, Jonathan P. Terdiman, Karen H. Lu, Stephen Thibodeau, Noralane M. Lindor, PMS2 monoallelic mutation carriers: the known unknown, Genetics in Medicine, 2016, 18, 1, 13

    CrossRef

  4. 4
    Rolf H. Sijmons, Robert M.W. Hofstra, Review: Clinical aspects of hereditary DNA Mismatch repair gene mutations, DNA Repair, 2016, 38, 155

    CrossRef

  5. 5
    G. Möslein, Risikogruppen mit einer erblichen Disposition für familiäre (polygene) kolorektale Karzinome, Der Onkologe, 2016, 22, 2, 84

    CrossRef

  6. 6
    John A. Sandoval, Israel Fernandez-Pineda, Alpin D. Malkan, Risk-Reduction Surgery in Pediatric Surgical Oncology: A Perspective, Journal of Pediatric Surgery, 2016,

    CrossRef

  7. 7
    L.H. Katz, A.M. Burton-Chase, S. Advani, B. Fellman, K.M. Polivka, Y. Yuan, P.M. Lynch, S.K. Peterson, Screening adherence and cancer risk perceptions in colorectal cancer survivors with Lynch-like syndrome, Clinical Genetics, 2016, 89, 2
  8. 8
    Sapna Syngal, Randall E Brand, James M Church, Francis M Giardiello, Heather L Hampel, Randall W Burt, ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes, The American Journal of Gastroenterology, 2015, 110, 2, 223

    CrossRef

  9. 9
    Deborah Cragun, Rita D. DeBate, Tuya Pal, Applying Public Health Screening Criteria: How Does Universal Newborn Screening Compare to Universal Tumor Screening for Lynch Syndrome in Adults with Colorectal Cancer?, Journal of Genetic Counseling, 2015, 24, 3, 409

    CrossRef

  10. 10
    Yusuke Kobayashi, Kanako Nakamura, Hiroyuki Nomura, Kouji Banno, Haruko Irie, Masataka Adachi, Miho Iida, Kiyoko Umene, Yuya Nogami, Kenta Masuda, Iori Kisu, Arisa Ueki, Wataru Yamagami, Fumio Kataoka, Akira Hirasawa, Eiichiro Tominaga, Nobuyuki Susumu, Daisuke Aoki, Clinicopathologic Analysis With Immunohistochemistry for DNA Mismatch Repair Protein Expression in Synchronous Primary Endometrial and Ovarian Cancers, International Journal of Gynecological Cancer, 2015, 25, 3, 440

    CrossRef

  11. 11
    David Liska, Matthew F. Kalady, Colorectal Surgery in Lynch Syndrome Patients: When and How?, Current Colorectal Cancer Reports, 2015, 11, 2, 45

    CrossRef

  12. 12
    A. Barzi, S. Sadeghi, M. W. Kattan, N. J. Meropol, Comparative Effectiveness of Screening Strategies for Lynch Syndrome, JNCI Journal of the National Cancer Institute, 2015, 107, 4, djv005

    CrossRef

  13. 13
    Sarah Mange, Cecelia Bellcross, Deborah Cragun, Deb Duquette, Lisa Gorman, Heather Hampel, Kory Jasperson, Creation of a Network to Promote Universal Screening for Lynch Syndrome: The Lynch Syndrome Screening Network, Journal of Genetic Counseling, 2015, 24, 3, 421

    CrossRef

  14. 14
    Holly Etchegary, Elizabeth Dicks, Kathy Watkins, Sabrina Alani, Lesa Dawson, Decisions about prophylactic gynecologic surgery: a qualitative study of the experience of female Lynch syndrome mutation carriers, Hereditary Cancer in Clinical Practice, 2015, 13, 1

    CrossRef

  15. 15
    Susan Richman, Deficient mismatch repair: Read all about it (Review), International Journal of Oncology, 2015,

    CrossRef

  16. 16
    M. S. Lung, A. H. Trainer, I. Campbell, L. Lipton, Familial colorectal cancer, Internal Medicine Journal, 2015, 45, 5
  17. 17
    Jessica L. Profato, Banu K. Arun, Genetic risk assessment for breast and gynecological malignancies, Current Opinion in Obstetrics and Gynecology, 2015, 27, 1, 1

    CrossRef

  18. 18
    Michael D. Lehrer, Henry Lynch, David J. Glembocki, Neel B. Patel, Glioblastoma multiforme as initial internal malignancy in Muir-Torre syndrome (MTS), JAAD Case Reports, 2015, 1, 6, 381

    CrossRef

  19. 19
    C. Therkildsen, S. Ladelund, E. Rambech, A. Persson, A. Petersen, M. Nilbert, Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome, European Journal of Neurology, 2015, 22, 4
  20. 20
    Georgia A. McCann, Eric L. Eisenhauer, Hereditary cancer syndromes with high risk of endometrial and ovarian cancer: Surgical options for personalized care, Journal of Surgical Oncology, 2015, 111, 1
  21. 21
    Angela Toss, Chiara Tomasello, Elisabetta Razzaboni, Giannina Contu, Giovanni Grandi, Angelo Cagnacci, Russell J. Schilder, Laura Cortesi, Hereditary Ovarian Cancer: Not OnlyBRCA1 and 2 Genes, BioMed Research International, 2015, 2015, 1

    CrossRef

  22. 22
    Ashton A. Connor, Hagit Katzov-Eckert, Thomas Whelan, Melyssa Aronson, Lynette Lau, Christian Marshall, George S. Charames, Aaron Pollett, Steven Gallinger, Jordan Lerner-Ellis, Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing, Familial Cancer, 2015, 14, 1, 69

    CrossRef

  23. 23
    Katherine M. Dempsey, Russell Broaddus, Y. Nancy You, Sarah Jane Noblin, Maureen Mork, Bryan Fellman, Diana Urbauer, Molly Daniels, Karen Lu, Is it all Lynch syndrome?: An assessment of family history in individuals with mismatch repair–deficient tumors, Genetics in Medicine, 2015, 17, 6, 476

    CrossRef

  24. 24
    Maureen Mork, Scott G. Hubosky, Morgan Rouprêt, Vitaly Margulis, Jay Raman, Yair Lotan, Timothy O’Brien, Nancy You, Shahrokh F. Shariat, Surena F. Matin, Lynch Syndrome: A Primer for Urologists and Panel Recommendations, The Journal of Urology, 2015, 194, 1, 21

    CrossRef

  25. 25
    Tadeusz Dębniak, Tomasz Gromowski, Rodney J Scott, Jacek Gronwald, Tomasz Huzarski, Tomasz Byrski, Grzegorz Kurzawski, Dagmara Dymerska, Bohdan Górski, Katarzyna Paszkowska-Szczur, Cezary Cybulski, Pablo Serrano-Fernandez, Jan Lubiński, Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families, Hereditary Cancer in Clinical Practice, 2015, 13, 1

    CrossRef

  26. 26
    Hisato Kawakami, Aziz Zaanan, Frank A. Sinicrope, Microsatellite Instability Testing and Its Role in the Management of Colorectal Cancer, Current Treatment Options in Oncology, 2015, 16, 7

    CrossRef

  27. 27
    Henry T. Lynch, Carrie L. Snyder, Trudy G. Shaw, Christopher D. Heinen, Megan P. Hitchins, Milestones of Lynch syndrome: 1895–2015, Nature Reviews Cancer, 2015, 15, 3, 181

    CrossRef

  28. 28
    Mehrdad Zeinalian, Mohammad Hassan Emami, Rasoul Salehi, Azar Naimi, Mohammad Kazemi, Morteza Hashemzadeh-Chaleshtori, Molecular Analysis of Iranian Colorectal Cancer Patients at Risk for Lynch Syndrome: a New Molecular, Clinicopathological Feature, Journal of Gastrointestinal Cancer, 2015, 46, 2, 118

    CrossRef

  29. 29
    N. J. P. Engbang, H. Essome, E. Dina Bell, C. Fonkwa, O. J. L. Essame, Profil épidémiologique et histologique des cancers ovariens à Douala (Cameroun) : à propos de 91 cas, Journal Africain du Cancer / African Journal of Cancer, 2015, 7, 4, 190

    CrossRef

  30. 30
    T. Woods, N. B. Jennings, H. T. Fernandez, N. Onaca, B. K. Carlile, M. F. Levy, D. L. Gould, R. Ruiz, Renal Autotransplantation in Lynch Syndrome: A Viable Option in a Patient With Contralateral Metachronous Ureteral Cancer, American Journal of Transplantation, 2015, 15, 9
  31. 31
    Jacqueline Duffour, Audrey Combes, Evelyne Crapez, Florence Boissière-Michot, Frédéric Bibeau, Pierre Senesse, Marc Ychou, Julie Courraud, Hélène de Forges, Lise Roca, Reproductive Decision-Making in MMR Mutation Carriers After Results Disclosure: Impact of Psychological Status in Childbearing Options, Journal of Genetic Counseling, 2015,

    CrossRef

  32. 32
    Siriwan Tangjitgamol, Jakkapan Khunnarong, Sunamchok Srijaipracharoen, Synchronous and metachronous malignancy in endometrial cancer patients treated in a tertiary care center of Thailand, Journal of Gynecologic Oncology, 2015, 26, 4, 293

    CrossRef

  33. 33
    Yang Yu, Li Dong, Dapeng Li, Shaokun Chuai, Zhigang Wu, Xiangqian Zheng, Yanan Cheng, Lei Han, Jinpu Yu, Ming Gao, Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary Thyroid Cancer, Scientific Reports, 2015, 5, 16129

    CrossRef

  34. 34
    James P Beirne, Gareth W Irwin, Stuart A McIntosh, Ian JG Harley, D Paul Harkin, The molecular and genetic basis of inherited cancer risk in gynaecology, The Obstetrician & Gynaecologist, 2015, 17, 4
  35. 35
    Patrick Joost, Christina Therkildsen, Mev Dominguez-Valentin, Mats Jönsson, Mef Nilbert, Urinary Tract Cancer in Lynch Syndrome; Increased Risk in Carriers of MSH2 Mutations, Urology, 2015, 86, 6, 1212

    CrossRef

  36. 36
    Ralph Schneider, Claudia Schneider, Gabriela Möslein, Allgemein- und Viszeralchirurgie II - Spezielle Operative Techniken, 2015,

    CrossRef

  37. 37
    S. G. Barreto, A. Dutt, A. Chaudhary, A genetic model for gallbladder carcinogenesis and its dissemination, Annals of Oncology, 2014, 25, 6, 1086

    CrossRef

  38. 38
    Su Young Lee, Aesun Shin, Byung Chang Kim, Jeong Hee Lee, Kyung Su Han, Chang Won Hong, Dae Kyung Sohn, Sung Chan Park, Hee Jin Chang, Jae Hwan Oh, Association between family history of malignant neoplasm with colorectal adenomatous polyp in 40s aged relative person, Cancer Epidemiology, 2014, 38, 5, 623

    CrossRef

  39. 39
    Ellen T. Matloff, Danielle C. Bonadies, Anne Moyer, Karina L. Brierley, Changes in Specialists’ Perspectives on Cancer Genetic Testing, Prophylactic Surgery and Insurance Discrimination: Then and Now, Journal of Genetic Counseling, 2014, 23, 2, 164

    CrossRef

  40. 40
    Fangqi Liu, Li Yang, Xiaoyan Zhou, Weiqi Sheng, Sanjun Cai, Lei Liu, Peng Nan, Ye Xu, Clinicopathological and genetic features of Chinese hereditary nonpolyposis colorectal cancer (HNPCC), Medical Oncology, 2014, 31, 10

    CrossRef

  41. 41
    Denise R. Nebgen, Karen H. Lu, Sue Rimes, Elizabeth Keeler, Russell Broaddus, Mark F. Munsell, Patrick M. Lynch, Combined colonoscopy and endometrial biopsy cancer screening results in women with Lynch syndrome, Gynecologic Oncology, 2014, 135, 1, 85

    CrossRef

  42. 42
    Deborah Cragun, Rita D. DeBate, Susan T. Vadaparampil, Julie Baldwin, Heather Hampel, Tuya Pal, Comparing universal Lynch syndrome tumor-screening programs to evaluate associations between implementation strategies and patient follow-through, Genetics in Medicine, 2014, 16, 10, 773

    CrossRef

  43. 43
    Jenny-Maria Jönsson, Katarina Bartuma, Mev Dominguez-Valentin, Katja Harbst, Zohreh Ketabi, Susanne Malander, Mats Jönsson, Ana Carneiro, Anna Måsbäck, Göran Jönsson, Mef Nilbert, Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome, Familial Cancer, 2014, 13, 4, 537

    CrossRef

  44. 44
    A. Ouzzane, M. Rouprêt, P. Leon, D.R. Yates, P. Colin, Épidémiologie et facteurs de risque des tumeurs de la voie excrétrice urinaire supérieure : revue de la littérature pour le rapport annuel de l’Association française d’urologie, Progrès en Urologie, 2014, 24, 15, 966

    CrossRef

  45. 45
    Verena Steinke, Stefanie Holzapfel, Markus Loeffler, Elke Holinski-Feder, Monika Morak, Hans K. Schackert, Heike Görgens, Christian Pox, Brigitte Royer-Pokora, Magnus Knebel-Doeberitz, Reinhard Büttner, Peter Propping, Christoph Engel, Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families, International Journal of Cancer, 2014, 135, 1
  46. 46
    Mairi H. McLean, Emad M. El-Omar, Genetics of gastric cancer, Nature Reviews Gastroenterology & Hepatology, 2014, 11, 11, 664

    CrossRef

  47. 47
    Henry T. Lynch, Kristen Drescher, Joseph Knezetic, Stephen Lanspa, Genetics, Biomarkers, Hereditary Cancer Syndrome Diagnosis, Heterogeneity and Treatment: A Review, Current Treatment Options in Oncology, 2014, 15, 3, 429

    CrossRef

  48. 48
    U. Andersson, C. Wibom, K. Cederquist, S. Aradottir, A. Borg, G. N. Armstrong, S. Shete, C. C. Lau, M. N. Bainbridge, E. B. Claus, J. Barnholtz-Sloan, R. Lai, D. Il'yasova, R. S. Houlston, J. Schildkraut, J. L. Bernstein, S. H. Olson, R. B. Jenkins, D. H. Lachance, M. Wrensch, F. G. Davis, R. Merrell, C. Johansen, S. Sadetzki, M. L. Bondy, B. S. Melin, P. Adatto, F. Morice, S. Payen, L. McQuinn, R. McGaha, S. Guerra, L. Paith, K. Roth, D. Zeng, H. Zhang, A. Yung, K. Aldape, M. Gilbert, J. Weinberger, H. Colman, C. Conrad, J. de Groot, A. Forman, M. Groves, V. Levin, M. Loghin, V. Puduvalli, R. Sawaya, A. Heimberger, F. Lang, N. Levine, L. Tolentino, K. Saunders, T.-T. Thach, D. D. Iacono, A. Sloan, S. Gerson, W. Selman, N. Bambakidis, D. Hart, J. Miller, A. Hoffer, M. Cohen, L. Rogers, C. J. Nock, Y. Wolinsky, K. Devine, J. Fulop, W. Barrett, K. Shimmel, Q. Ostrom, G. Barnett, S. Rosenfeld, M. Vogelbaum, R. Weil, M. Ahluwalia, D. Peereboom, S. Staugaitis, C. Schilero, C. Brewer, K. Smolenski, M. McGraw, T. Naska, S. Rosenfeld, Z. Ram, D. T. Blumenthal, F. Bokstein, F. Umansky, M. Zaaroor, A. Cohen, T. Tzuk-Shina, B. Voldby, R. Laursen, C. Andersen, J. Brennum, M. B. Henriksen, M. Marzouk, M. E. Davis, E. Boland, M. Smith, O. Eze, M. Way, P. Lada, N. Miedzianowski, M. Frechette, N. Paleologos, G. Bystrom, E. Svedberg, S. Huggert, M. Kimdal, M. Sandstrom, N. Brannstrom, A. Hayat, T. Tihan, S. Zheng, M. Berger, N. Butowski, S. Chang, J. Clarke, M. Prados, T. Rice, J. Sison, V. Kivett, X. Duo, H. Hansen, G. Hsuang, R. Lamela, C. Ramos, J. Patoka, K. Wagenman, M. Zhou, A. Klein, N. McGee, J. Pfefferle, C. Wilson, P. Morris, M. Hughes, M. Britt-Williams, J. Foft, J. Madsen, C. Polony, B. McCarthy, C. Zahora, J. Villano, H. Engelhard, A. Borg, S. K. Chanock, P. Collins, R. Elston, P. Kleihues, C. Kruchko, G. Petersen, S. Plon, P. Thompson, C. Johansen, S. Sadetzki, B. Melin, M. L. Bondy, C. C. Lau, M. E. Scheurer, G. N. Armstrong, Y. Liu, S. Shete, R. K. Yu, K. D. Aldape, M. R. Gilbert, J. Weinberg, R. S. Houlston, F. J. Hosking, L. Robertson, E. Papaemmanuil, E. B. Claus, E. B. Claus, J. Barnholtz-Sloan, A. E. Sloan, G. Barnett, K. Devine, Y. Wolinsky, R. Lai, R. McKean-Cowdin, D. Il'yasova, J. Schildkraut, S. Sadetzki, G. H. Yechezkel, R. B.-S. Bruchim, L. Aslanov, S. Sadetzki, C. Johansen, M. Kosteljanetz, H. Broholm, J. L. Bernstein, S. H. Olson, E. Schubert, L. DeAngelis, R. B. Jenkins, P. Yang, A. Rynearson, U. Andersson, C. Wibom, R. Henriksson, B. S. Melin, K. Cederquist, S. Aradottir, A. Borg, R. Merrell, P. Lada, M. Wrensch, J. Wiencke, J. Wiemels, L. McCoy, B. J. McCarthy, F. G. Davis, Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer, Neuro-Oncology, 2014, 16, 10, 1333

    CrossRef

  49. 49
    Francis M. Giardiello, John I. Allen, Jennifer E. Axilbund, C. Richard Boland, Carol A. Burke, Randall W. Burt, James M. Church, Jason A. Dominitz, David A. Johnson, Tonya Kaltenbach, Theodore R. Levin, David A. Lieberman, Douglas J. Robertson, Sapna Syngal, Douglas K. Rex, Guidelines on genetic evaluation and management of Lynch syndrome: A consensus statement by the U.S. Multi-Society Task Force on Colorectal Cancer, Gastrointestinal Endoscopy, 2014, 80, 2, 197

    CrossRef

  50. 50
    Francis M Giardiello, John I Allen, Jennifer E Axilbund, C Richard Boland, Carol A Burke, Randall W Burt, James M Church, Jason A Dominitz, David A Johnson, Tonya Kaltenbach, Theodore R Levin, David A Lieberman, Douglas J Robertson, Sapna Syngal, Douglas K Rex, Guidelines on Genetic Evaluation and Management of Lynch Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer, The American Journal of Gastroenterology, 2014, 109, 8, 1159

    CrossRef

  51. 51
    Francis M. Giardiello, John I. Allen, Jennifer E. Axilbund, C. Richard Boland, Carol A. Burke, Randall W. Burt, James M. Church, Jason A. Dominitz, David A. Johnson, Tonya Kaltenbach, Theodore R. Levin, David A. Lieberman, Douglas J. Robertson, Sapna Syngal, Douglas K. Rex, Guidelines on Genetic Evaluation and Management of Lynch Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer, Gastroenterology, 2014, 147, 2, 502

    CrossRef

  52. 52
    Jesper A.B. Strickertsson, Claus Desler, Lene Juel Rasmussen, Impact of bacterial infections on aging and cancer: Impairment of DNA repair and mitochondrial function of host cells, Experimental Gerontology, 2014, 56, 164

    CrossRef

  53. 53
    Christopher M. J. Conklin, Teri A. Longacre, Lynch Syndrome in Endometrial Carcinoma, Pathology Case Reviews, 2014, 19, 2, 78

    CrossRef

  54. 54
    Koah R. Vierkoetter, Asia R. Ayabe, Maya VanDrunen, Hyeong Jun Ahn, David M. Shimizu, Keith Y. Terada, Lynch Syndrome in patients with clear cell and endometrioid cancers of the ovary, Gynecologic Oncology, 2014, 135, 1, 81

    CrossRef

  55. 55
    Arjen R. Mensenkamp, Ingrid P. Vogelaar, Wendy A.G. van Zelst–Stams, Monique Goossens, Hicham Ouchene, Sandra J.B. Hendriks–Cornelissen, Michael P. Kwint, Nicoline Hoogerbrugge, Iris D. Nagtegaal, Marjolijn J.L. Ligtenberg, Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors, Gastroenterology, 2014, 146, 3, 643

    CrossRef

  56. 56
    Michael Herman Chui, Paul Ryan, Jordan Radigan, Sarah E. Ferguson, Aaron Pollett, Melyssa Aronson, Kara Semotiuk, Spring Holter, Keiyan Sy, Janice S. Kwon, Anita Soma, Naveena Singh, Steven Gallinger, Patricia Shaw, Jocelyne Arseneau, William D. Foulkes, C. Blake Gilks, Blaise A. Clarke, The Histomorphology of Lynch Syndrome–associated Ovarian Carcinomas, The American Journal of Surgical Pathology, 2014, 38, 9, 1173

    CrossRef

  57. 57
    Zohreh Ketabi, Anne-Marie Gerdes, Berit Mosgaard, Steen Ladelund, Inge Bernstein, The results of gynecologic surveillance in families with hereditary nonpolyposis colorectal cancer, Gynecologic Oncology, 2014, 133, 3, 526

    CrossRef

  58. 58
    John A. Heath, Jessica Ng, Victoria Beshay, Lee Coleman, Patrick Lo, David J. Amor, Anaplastic oligodendroglioma in an adolescent with Lynch syndrome, Pediatric Blood & Cancer, 2013, 60, 6
  59. 59
    Emma Barrow, James Hill, D. Gareth Evans, Cancer risk in Lynch Syndrome, Familial Cancer, 2013, 12, 2, 229

    CrossRef

  60. You have free access to this content60
    Keita Wada, Kyoichi Takaori, L. William Traverso, Ralph H. Hruban, Toru Furukawa, Teresa A. Brentnall, Takashi Hatori, Keiji Sano, Tadahiro Takada, Yoshiyuki Majima, Tooru Shimosegawa, Clinical importance of Familial Pancreatic Cancer Registry in Japan: a report from kick-off meeting at International Symposium on Pancreas Cancer 2012, Journal of Hepato-Biliary-Pancreatic Sciences, 2013, 20, 6
  61. You have free access to this content61
    Akke Botma, Hans F. A. Vasen, Fränzel J. B. van Duijnhoven, Jan H. Kleibeuker, Fokko M. Nagengast, Ellen Kampman, Dietary patterns and colorectal adenomas in Lynch syndrome, Cancer, 2013, 119, 3
  62. 62
    Anni Niskakoski, Sippy Kaur, Laura Renkonen-Sinisalo, Heini Lassus, Heikki J. Järvinen, Jukka-Pekka Mecklin, Ralf Bützow, Päivi Peltomäki, Distinct molecular profiles in Lynch syndrome-associated and sporadic ovarian carcinomas, International Journal of Cancer, 2013, 133, 11
  63. 63
    Karen H. Lu, Molly Daniels, Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention, Familial Cancer, 2013, 12, 2, 273

    CrossRef

  64. 64
    Kevin M. Lin-Hurtubise, Christopher G. Yheulon, Ronald A. Gagliano, Henry T. Lynch, Excess of extracolonic non-endometrial multiple primary cancers in MSH2 germline mutation carriers over MLH1, Journal of Surgical Oncology, 2013, 108, 7
  65. 65
    Andrew I. Wolf, Adam H. Buchanan, Linda M. Farkas, Historical review of Lynch syndrome, Journal of Coloproctology, 2013, 33, 2, 95

    CrossRef

  66. 66
    C. Adaniel, T. Kirchhoff, Introduction to epidemiology of breast and ovarian cancers, Annals of Oncology, 2013, 24, suppl 8, viii61

    CrossRef

  67. 67
    Paul J Barrow, Tara Clancy, D Gareth Evans, Key genetic considerations in the management of suspected hereditary colorectal cancer, Colorectal Cancer, 2013, 2, 1, 31

    CrossRef

  68. 68
    Andrew D Beggs, George Kousparos, Shirley V Hodgson, Loss of Mismatch Repair Protein Expression in Breast Carcinoma in Patients with Lynch Syndrome: Report of Two Cases, The Breast Journal, 2013, 19, 2
  69. 69
    Yiying Wang, Yue Wang, Jie Li, Janiel Cragun, Kenneth Hatch, Setsuko K Chambers, Wenxin Zheng, Lynch syndrome related endometrial cancer: clinical significance beyond the endometrium, Journal of Hematology & Oncology, 2013, 6, 1, 22

    CrossRef

  70. 70
    Peter A Ongom, Michael Odida, Robert L Lukande, Josephat Jombwe, Emmanuel Elobu, Metastatic colorectal carcinoma mimicking primary ovarian carcinoma presenting as ‘giant’ ovarian tumors in an individual with probable Lynch syndrome: a case report, Journal of Medical Case Reports, 2013, 7, 1, 158

    CrossRef

  71. 71
    Shuting Bai, Amberly L. Nunez, Shi Wei, Amy Ziober, Yuan Yao, John E. Tomaszewski, Zhanyong Bing, Microsatellite Instability andTARBP2Mutation Study in Upper Urinary Tract Urothelial Carcinoma, American Journal of Clinical Pathology, 2013, 139, 6, 765

    CrossRef

  72. 72
    Vivek Verma, Kalyani Patel, Irene Peregrin, Steven Brandes, Israel Zighelboim, Occult transitional cell carcinoma and Lynch syndrome incidentally revealed after laparoscopic hysterectomy and cystoscopy during staging for endometrial cancer, Gynecologic Oncology Case Reports, 2013, 4, 26

    CrossRef

  73. 73
    Murray Joseph Casey, Chhanda Bewtra, Henry T. Lynch, Carrie Snyder, Mark Stacy, Patrice Watson, Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry, Familial Cancer, 2013, 12, 4, 719

    CrossRef

  74. 74
    Fabio Ghezzi, Stefano Uccella, Antonella Cromi, Giorgio Bogani, Nicoletta Donadello, Cristina Riva, Primary Peritoneal Cancer in Lynch Syndrome, International Journal of Gynecological Pathology, 2013, 32, 2, 163

    CrossRef

  75. 75
    Aung Win, Noralane M Lindor, Mark A Jenkins, Risk of breast cancer in Lynch syndrome: a systematic review, Breast Cancer Research, 2013, 15, 2, R27

    CrossRef

  76. 76
    Inge Thomsen Bernstein, Torben Myrhøj, Surveillance for urinary tract cancer in Lynch syndrome, Familial Cancer, 2013, 12, 2, 279

    CrossRef

  77. 77
    Andrew S. Williams, Weei-Yuarn Huang, The analysis of microsatellite instability in extracolonic gastrointestinal malignancy, Pathology, 2013, 45, 6, 540

    CrossRef

  78. 78
    P. J. Barrow, S. Ingham, C. O’Hara, K. Green, I. McIntyre, F. Lalloo, J. Hill, D. G. Evans, The spectrum of urological malignancy in Lynch syndrome, Familial Cancer, 2013, 12, 1, 57

    CrossRef

  79. 79
    Scott G. Hubosky, Bruce M. Boman, Sarah Charles, Marluce Bibbo, Demetrius H. Bagley, Ureteroscopic management of upper tract urothelial carcinoma (UTUC) in patients with Lynch Syndrome (hereditary nonpolyposis colorectal cancer syndrome), BJU International, 2013, 112, 6
  80. You have free access to this content80
    François Audenet, Pierre Colin, David R. Yates, Adil Ouzzane, Géraldine Pignot, Jean-Alexandre Long, Michel Soulie, Véronique Phé, Henri Bensadoun, Laurent Guy, Alain Ruffion, Antoine Valeri, Luc Cormier, Stéphane Droupy, Alexandre de La Taille, Fabien Saint, Pierre-Olivier Faïs, Alain Houlgatte, Olivier Cussenot, Morgan Rouprêt, A proportion of hereditary upper urinary tract urothelial carcinomas are misclassified as sporadic according to a multi-institutional database analysis: proposal of patient-specific risk identification tool, BJU International, 2012, 110, 11b
  81. 81
    Johanna E Lotsari, Annette Gylling, Wael M Abdel-Rahman, Taina T Nieminen, Kristiina Aittomäki, Marjukka Friman, Reino Pitkänen, Markku Aarnio, Heikki J Järvinen, Jukka-Pekka Mecklin, Teijo Kuopio, Päivi Peltomäki, Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases, Breast Cancer Research, 2012, 14, 3, R90

    CrossRef

  82. 82
    Nadia Hindi Muñiz, Ángela Lamarca Lete, Jaime Feliú Batlle, Cáncer de colon hereditario, Medicina Clínica, 2012, 138, 5, 220

    CrossRef

  83. 83
    Christina Therkildsen, Anna Isinger-Ekstrand, Steen Ladelund, Anja Nissen, Eva Rambech, Inge Bernstein, Mef Nilbert, Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation, Familial Cancer, 2012, 11, 4, 579

    CrossRef

  84. 84
    Kirsi Pylvänäinen, Tuula Lehtinen, Ilmo Kellokumpu, Heikki Järvinen, Jukka-Pekka Mecklin, Causes of death of mutation carriers in Finnish Lynch syndrome families, Familial Cancer, 2012, 11, 3, 467

    CrossRef

  85. 85
    Markku Aarnio, Clinicopathological Features and Management of Cancers in Lynch Syndrome, Pathology Research International, 2012, 2012, 1

    CrossRef

  86. 86
    R. Schneider, C. Schneider, M. Kloor, A. Fürst, G. Möslein, Das Lynch-Syndrom, coloproctology, 2012, 34, 5, 329

    CrossRef

  87. 87
    Yong H. Wen, Edi Brogi, Zhaoshi Zeng, Muzaffar Akram, Jeff Catalano, Philip B. Paty, Larry Norton, Jinru Shia, DNA Mismatch Repair Deficiency in Breast Carcinoma, The American Journal of Surgical Pathology, 2012, 36, 11, 1700

    CrossRef

  88. 88
    Jennifer L. Maranki, Oleh Haluszka, Endoscopic therapy of small-bowel neoplasms, Techniques in Gastrointestinal Endoscopy, 2012, 14, 2, 112

    CrossRef

  89. 89
    Ricardo Marcos-Pinto, Mário Dinis-Ribeiro, Fátima Carneiro, José Carlos Machado, Ceu Figueiredo, Celso A. Reis, José Ferreira, Jorge Areias, First degree relatives and familial aggregation of gastric cancer: who to choose for control in case–control studies?, Familial Cancer, 2012, 11, 1, 137

    CrossRef

  90. 90
    Carmen Guillén-Ponce, Maria-José Molina-Garrido, Alfredo Carrato, Follow-up recommendations and risk-reduction initiatives for Lynch syndrome, Expert Review of Anticancer Therapy, 2012, 12, 10, 1359

    CrossRef

  91. 91
    Laura L. Holman, Karen H. Lu, Genetic Risk and Gynecologic Cancers, Hematology/Oncology Clinics of North America, 2012, 26, 1, 13

    CrossRef

  92. 92
    Nicki Chun, James M. Ford, Genetic Testing by Cancer Site, The Cancer Journal, 2012, 18, 4, 355

    CrossRef

  93. 93
    Scott M. Weissman, Shelly M. Weiss, Anna C. Newlin, Genetic Testing by Cancer Site, The Cancer Journal, 2012, 18, 4, 320

    CrossRef

  94. 94
    Kristen Mahoney Shannon, Anu Chittenden, Genetic Testing by Cancer Site, The Cancer Journal, 2012, 18, 4, 310

    CrossRef

  95. 95
    Karin Kast, Teresa M Neuhann, Heike Görgens, Kerstin Becker, Katja Keller, Barbara Klink, Daniela Aust, Wolfgang Distler, Evelin Schröck, Hans K Schackert, Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancer, BMC Cancer, 2012, 12, 1, 531

    CrossRef

  96. 96
    Benjamin E. Northrup, Clinton E. Jokerst, Robert L. Grubb, Christine O. Menias, Geetika Khanna, Cary Lynn Siegel, Hereditary Renal Tumor Syndromes: Imaging Findings and Management Strategies, American Journal of Roentgenology, 2012, 199, 6, 1294

    CrossRef

  97. 97
    Scott M. Weissman, Randall Burt, James Church, Steve Erdman, Heather Hampel, Spring Holter, Kory Jasperson, Matt F. Kalady, Joy Larsen Haidle, Henry T. Lynch, Selvi Palaniappan, Paul E. Wise, Leigha Senter, Identification of Individuals at Risk for Lynch Syndrome Using Targeted Evaluations and Genetic Testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer Joint Practice Guideline, Journal of Genetic Counseling, 2012, 21, 4, 484

    CrossRef

  98. 98
    Cecelia A. Bellcross, Sara R. Bedrosian, Elvan Daniels, Debra Duquette, Heather Hampel, Kory Jasperson, Djenaba A. Joseph, Celia Kaye, Ira Lubin, Laurence J. Meyer, Michele Reyes, Maren T. Scheuner, Sheri D. Schully, Leigha Senter, Sherri L. Stewart, Jeanette St. Pierre, Judith Westman, Paul Wise, Vincent W. Yang, Muin J. Khoury, Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting, Genetics in Medicine, 2012, 14, 1, 152

    CrossRef

  99. 99
    Simon A. Gayther, Inherited Risk of Ovarian Cancer and the Implications for Screening, International Journal of Gynecological Cancer, 2012, 22, S12

    CrossRef

  100. 100
    Ralph Schneider, Claudia Schneider, Matthias Kloor, Alois Fürst, Gabriela Möslein, Lynch syndrome: clinical, pathological, and genetic insights, Langenbeck's Archives of Surgery, 2012, 397, 4, 513

    CrossRef

  101. 101
    M. Dinis-Ribeiro, M. Areia, A. C. de Vries, R. Marcos-Pinto, M. Monteiro-Soares, A. O’Connor, C. Pereira, P. Pimentel-Nunes, R. Correia, A. Ensari, J. M. Dumonceau, J. C. Machado, G. Macedo, P. Malfertheiner, T. Matysiak-Budnik, F. Megraud, K. Miki, C. O’Morain, R. M. Peek, T. Ponchon, A. Ristimaki, B. Rembacken, F. Carneiro, E. J. Kuipers, Management of precancerous conditions and lesions in the stomach (MAPS): guideline from the European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter Study Group (EHSG), European Society of Pathology (ESP), and the Sociedade Portuguesa de Endoscopia Digestiva (SPED), Virchows Archiv, 2012, 460, 1, 19

    CrossRef

  102. 102
    Ramunas Janavicius, Pavel Elsakov, Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers, Hereditary Cancer in Clinical Practice, 2012, 10, 1, 1

    CrossRef

  103. 103
    Anil Aysal, Anthony Karnezis, Irum Medhi, James P. Grenert, Charles J. Zaloudek, Joseph T. Rabban, Ovarian Endometrioid Adenocarcinoma, The American Journal of Surgical Pathology, 2012, 36, 2, 163

    CrossRef

  104. 104
    K. L. Bolton, C. Ganda, A. Berchuck, P. D. P. Pharaoh, S. A. Gayther, Role of common genetic variants in ovarian cancer susceptibility and outcome: progress to date from the ovarian cancer association consortium (OCAC), Journal of Internal Medicine, 2012, 271, 4
  105. 105
    Christian Adonizio, Michelle Gazzillo, Joseph Knezetic, Carrie Snyder, Henry T. Lynch, Christina Rybak, Michael J. Hall, Kristina Lowstuter, Julie Eggington, Gloria J. Morris, Thirty-Nine-Year-Old With Familial Colon Cancer, and Variant of Undetermined Significance in MSH6, Seminars in Oncology, 2012, 39, 2, 125

    CrossRef

  106. 106
    Yevgeniy Karamurzin, Zhaoshi Zeng, Zsofia K. Stadler, Liying Zhang, Ihsane Ouansafi, Hikmat A. Al-Ahmadie, Christine Sempoux, Leonard B. Saltz, Robert A. Soslow, Eileen M. O'Reilly, Philip B. Paty, Daniel G. Coit, Jinru Shia, David S. Klimstra, Unusual DNA mismatch repair–deficient tumors in Lynch syndrome: a report of new cases and review of the literature, Human Pathology, 2012, 43, 10, 1677

    CrossRef

  107. 107
    Peter Zachhau, Steen Walter, Urinary tract cancer in patients with hereditary non-polyposis colorectal cancer, Scandinavian Journal of Urology and Nephrology, 2012, 46, 1, 5

    CrossRef

  108. 108
    Chrystelle Colas, Florence Coulet, Magali Svrcek, Ada Collura, Jean-François Fléjou, Alex Duval, Richard Hamelin, 2012,

    CrossRef

  109. 109
    Lindsay Dohany, Whitney Ducaine, Dana Zakalik, A patient with four metachronous cancers and multiple adenomatous colon polyps harboring the American Founder Lynch syndrome mutation: a case report, Hereditary Cancer in Clinical Practice, 2011, 9, Suppl 1, P8

    CrossRef

  110. 110
    ANNIKA AURANEN, TITTA JOUTSINIEMI, A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families, Acta Obstetricia et Gynecologica Scandinavica, 2011, 90, 5
  111. 111
    V. Medina-Arana, L. Delgado, L. González, A. Bravo, H. Díaz, E. Salido, D. Riverol, J. J. González-Aguilera, A. M. Fernández-Peralta, Adrenocortical carcinoma, an unusual extracolonic tumor associated with Lynch II syndrome, Familial Cancer, 2011, 10, 2, 265

    CrossRef

  112. 112
    J. -C. Saurin, B. Filoche, A. de Leusse, V. Maunoury, D. Heresbach, Consensus en endoscopie digestive. Indications de la vidéocapsule du grêle selon et hors indications validées en 2008 par la Haute Autorité de santé (HAS), Acta Endoscopica, 2011, 41, 4, 230

    CrossRef

  113. 113
    Dae Young Cheung, Myung-Gyu Choi, Current Advance in Small Bowel Tumors, Clinical Endoscopy, 2011, 44, 1, 13

    CrossRef

  114. 114
    Bernard Bonaïti, Valérie Bonadona, Hervé Perdry, Nadine Andrieu, Catherine Bonaïti-Pellié, Estimating penetrance from multiple case families with predisposing mutations: extension of the ‘genotype-restricted likelihood’ (GRL) method, European Journal of Human Genetics, 2011, 19, 2, 173

    CrossRef

  115. 115
    María Sereno, Cristina Aguayo, Carmen Guillén Ponce, César Gómez-Raposo, Francisco Zambrana, Miriam Gómez-López, Enrique Casado, Gastric tumours in hereditary cancer syndromes: clinical features, molecular biology and strategies for prevention, Clinical and Translational Oncology, 2011, 13, 9, 599

    CrossRef

  116. 116
    Scott M. Weissman, Cecelia Bellcross, Christina Chimera Bittner, Mary E. Freivogel, Joy Larsen Haidle, Pardeep Kaurah, Anna Leininger, Selvi Palaniappan, Kelle Steenblock, Thuy M. Vu, Molly S. Daniels, Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review, Journal of Genetic Counseling, 2011, 20, 1, 5

    CrossRef

  117. 117
    Manish Gala, Daniel C. Chung, Hereditary Colon Cancer Syndromes, Seminars in Oncology, 2011, 38, 4, 490

    CrossRef

  118. 118
    Karsten Schulmann, Wolff Schmiegel, Indexläsionen: Awareness-Alarm für Kliniker – gibt es Precursor-Läsionen?, Viszeralmedizin, 2011, 27, 4, 316

    CrossRef

  119. 119
    Haig Dudukgian, Jose R. Cintron, Indication and Extent of Surgery in Hereditary Nonpolyposis Colorectal Cancer, Seminars in Colon and Rectal Surgery, 2011, 22, 2, 118

    CrossRef

  120. 120
    Aziz Zaanan, Katy Meunier, Fatiha Sangar, Jean-François Fléjou, Françoise Praz, Microsatellite instability in colorectal cancer: from molecular oncogenic mechanisms to clinical implications, Cellular Oncology, 2011, 34, 3, 155

    CrossRef

  121. 121
    Zohreh Ketabi, Katarina Bartuma, Inge Bernstein, Susanne Malander, Henrik Grönberg, Erik Björck, Susanne Holck, Mef Nilbert, Ovarian cancer linked to lynch syndrome typically presents as early-onset, non-serous epithelial tumors, Gynecologic Oncology, 2011, 121, 3, 462

    CrossRef

  122. 122
    Noralane M. Lindor, Gloria M. Petersen, Amanda B. Spurdle, Bryony Thompson, David E. Goldgar, Stephen N. Thibodeau, Pancreatic Cancer and a Novel MSH2 Germline Alteration, Pancreas, 2011, 40, 7, 1138

    CrossRef

  123. 123
    Melissa W. Taggart, Asif Rashid, Pathology and Immunohistochemistry of Hereditary Colorectal Cancer, Seminars in Colon and Rectal Surgery, 2011, 22, 2, 71

    CrossRef

  124. 124
    V. Celentano, G. Luglio, G. Antonelli, R. Tarquini, L. Bucci, Prophylactic surgery in Lynch syndrome, Techniques in Coloproctology, 2011, 15, 2, 129

    CrossRef

  125. 125
    Roland P. Kuiper, Lisenka E.L.M. Vissers, Ramprasath Venkatachalam, Danielle Bodmer, Eveline Hoenselaar, Monique Goossens, Aline Haufe, Eveline Kamping, Renée C. Niessen, Frans B.L. Hogervorst, Johan J.P. Gille, Bert Redeker, Carli M.J. Tops, Marielle E. van Gijn, Ans M.W. van den Ouweland, Nils Rahner, Verena Steinke, Philip Kahl, Elke Holinski-Feder, Monika Morak, Matthias Kloor, Susanne Stemmler, Beate Betz, Pierre Hutter, David J. Bunyan, Sapna Syngal, Julie O. Culver, Tracy Graham, Tsun L. Chan, Iris D. Nagtegaal, J. Han J.M van Krieken, Hans K. Schackert, Nicoline Hoogerbrugge, Ad Geurts van Kessel, Marjolijn J.L. Ligtenberg, Recurrence and variability of germline EPCAM deletions in Lynch syndrome, Human Mutation, 2011, 32, 4
  126. 126
    Marlies JE Kempers, Roland P Kuiper, Charlotte W Ockeloen, Pierre O Chappuis, Pierre Hutter, Nils Rahner, Hans K Schackert, Verena Steinke, Elke Holinski-Feder, Monika Morak, Matthias Kloor, Reinhard Büttner, Eugene TP Verwiel, J Han van Krieken, Iris D Nagtegaal, Monique Goossens, Rachel S van der Post, Renée C Niessen, Rolf H Sijmons, Irma Kluijt, Frans BL Hogervorst, Edward M Leter, Johan JP Gille, Cora M Aalfs, Egbert JW Redeker, Frederik J Hes, Carli MJ Tops, Bernadette PM van Nesselrooij, Marielle E van Gijn, Encarna B Gómez García, Diana M Eccles, David J Bunyan, Sapna Syngal, Elena M Stoffel, Julie O Culver, Melanie R Palomares, Tracy Graham, Lea Velsher, Janos Papp, Edith Oláh, Tsun L Chan, Suet Y Leung, Ad Geurts van Kessel, Lambertus ALM Kiemeney, Nicoline Hoogerbrugge, Marjolijn JL Ligtenberg, Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study, The Lancet Oncology, 2011, 12, 1, 49

    CrossRef

  127. 127
    Lillias Holmes, Liliana Bordeianou, Screening and Prevention of Extracolonic Cancers in Patients with Hereditary Nonpolyposis Colon Cancer, Seminars in Colon and Rectal Surgery, 2011, 22, 2, 123

    CrossRef

  128. 128
    Dominique Béchade, Stratégies de dépistage de l’adénocarcinome pancréatique chez les patients à haut risque : la place de l’écho-endoscopie, La Presse Médicale, 2011, 40, 3, 230

    CrossRef

  129. 129
    David G. Crockett, David G. Wagner, Sten Holmäng, Sonny L. Johansson, Henry T. Lynch, Upper Urinary Tract Carcinoma in Lynch Syndrome Cases, The Journal of Urology, 2011, 185, 5, 1627

    CrossRef

  130. 130
    D. E. McIlvried, R. E. Birhiray, J. Z. Lu, Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma, Familial Cancer, 2010, 9, 3, 377

    CrossRef

  131. 131
    David Cunningham, Wendy Atkin, Heinz-Josef Lenz, Henry T Lynch, Bruce Minsky, Bernard Nordlinger, Naureen Starling, Colorectal cancer, The Lancet, 2010, 375, 9719, 1030

    CrossRef

  132. 132
    Kristen M. Drescher, Poonam Sharma, Henry T. Lynch, Current Hypotheses on How Microsatellite Instability Leads to Enhanced Survival of Lynch Syndrome Patients, Clinical and Developmental Immunology, 2010, 2010, 1

    CrossRef

  133. 133
    David J. Gallagher, James D. Smith, Kenneth Offit, Zsofia K. Stadler, Diagnosing Hereditary Colorectal Cancer, Clinical Colorectal Cancer, 2010, 9, 4, 205

    CrossRef

  134. 134
    Christoph Engel, Nils Rahner, Karsten Schulmann, Elke Holinski–Feder, Timm O. Goecke, Hans K. Schackert, Matthias Kloor, Verena Steinke, Holger Vogelsang, Gabriela Möslein, Heike Görgens, Stefan Dechant, Magnus von Knebel Doeberitz, Josef Rüschoff, Nicolaus Friedrichs, Reinhard Büttner, Markus Loeffler, Peter Propping, Wolff Schmiegel, Efficacy of Annual Colonoscopic Surveillance in Individuals With Hereditary Nonpolyposis Colorectal Cancer, Clinical Gastroenterology and Hepatology, 2010, 8, 2, 174

    CrossRef

  135. 135
    Marco Del Chiaro, Alessandro Zerbi, Gabriele Capurso, Giuseppe Zamboni, Patrick Maisonneuve, Silvano Presciuttini, Paolo Giorgio Arcidiacono, Lucia Calculli, Massimo Falconi, Familial pancreatic cancer in Italy. Risk assessment, screening programs and clinical approach: A position paper from the Italian Registry, Digestive and Liver Disease, 2010, 42, 9, 597

    CrossRef

  136. 136
    Katharina Wimmer, Stefanie Kalb, Peter Schütz, Johannes Zschocke, Familiäre Tumorerkrankungen, Wiener klinische Wochenschrift Education, 2010, 5, 2, 73

    CrossRef

  137. 137
    K. Schulmann, W. Schmiegel, Hereditäres nichtpolypöses kolorektales Karzinom, Der Gastroenterologe, 2010, 5, 1, 16

    CrossRef

  138. 138
    Lee P. Shulman, Hereditary Breast and Ovarian Cancer (HBOC): Clinical Features and Counseling for BRCA1 and BRCA2, Lynch Syndrome, Cowden Syndrome, and Li-Fraumeni Syndrome, Obstetrics and Gynecology Clinics of North America, 2010, 37, 1, 109

    CrossRef

  139. 139
    Eunjeong Jang, Daniel C. Chung, Hereditary Colon Cancer: Lynch Syndrome, Gut and Liver, 2010, 4, 2, 151

    CrossRef

  140. 140
    V. Steinke, S. Vogt, S. Aretz, Klinik und Genetik des familiären Darmkrebses, medizinische genetik, 2010, 22, 2, 265

    CrossRef

  141. 141
    C. Richard Boland, Ajay Goel, Microsatellite Instability in Colorectal Cancer, Gastroenterology, 2010, 138, 6, 2073

    CrossRef

  142. 142
    Uffe Birk Jensen, Lone Sunde, Susanne Timshel, Britta Halvarsson, Anja Nissen, Inge Bernstein, Mef Nilbert, Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome, Breast Cancer Research and Treatment, 2010, 120, 3, 777

    CrossRef

  143. 143
    Fei Bao, Nicole C. Panarelli, Hanna Rennert, David L. Sherr, Rhonda K. Yantiss, Neoadjuvant Therapy Induces Loss of MSH6 Expression in Colorectal Carcinoma, The American Journal of Surgical Pathology, 2010, 34, 12, 1798

    CrossRef

  144. 144
    J. -C. Saurin, Prédispositions génétiques à l’adénocarcinome du grêle: polypose adénomateuse familiale, syndrome de Peutz-Jeghers, syndrome de Lynch, Acta Endoscopica, 2010, 40, 3, 173

    CrossRef

  145. 145
    Kathleen M. Schmeler, Molly S. Daniels, Pamela T. Soliman, Russell R. Broaddus, Michael T. Deavers, Thuy M. Vu, George J. Chang, Karen H. Lu, Primary Peritoneal Cancer After Bilateral Salpingo-Oophorectomy in Two Patients With Lynch Syndrome, Obstetrics & Gynecology, 2010, 115, Supplement, 432

    CrossRef

  146. 146
    C. Richard Boland, Moshe Shike, Report From the Jerusalem Workshop on Lynch Syndrome-Hereditary Nonpolyposis Colorectal Cancer, Gastroenterology, 2010, 138, 7, 2197.e1

    CrossRef

  147. 147
    Lisette G. Capelle, Nicole C.T. Van Grieken, Hester F. Lingsma, Ewout W. Steyerberg, Willem J. Klokman, Marco J. Bruno, Hans F.A. Vasen, Ernst J. Kuipers, Risk and Epidemiological Time Trends of Gastric Cancer in Lynch Syndrome Carriers in The Netherlands, Gastroenterology, 2010, 138, 2, 487

    CrossRef

  148. 148
    Andreas Obermair, Danny R. Youlden, Joanne P. Young, Noralane M. Lindor, John A. Baron, Polly Newcomb, Susan Parry, John L. Hopper, Robert Haile, Mark A. Jenkins, Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinoma, International Journal of Cancer, 2010, 127, 11
  149. 149
    Andrejs Vanags, Ilze Strumfa, Arnis Abolins, Andris Gardovskis, Inga Melbarde-Gorkusa, Genadijs Trofimovics, Janis Gardovskis, The Concept, Diagnostics, Surgical Prevention and Treatment of Hereditary Colorectal Cancer in Nowadays Medicine, Acta Chirurgica Latviensis, 2010, 10, 2

    CrossRef

  150. 150
    Simon A Gayther, Paul DP Pharoah, The inherited genetics of ovarian and endometrial cancer, Current Opinion in Genetics & Development, 2010, 20, 3, 231

    CrossRef

  151. 151
    Andrejs Vanags, Ilze Strumfa, Andris Gardovskis, Inga Melbarde-Gorkusa, Arnis Abolins, Genadijs Trofimovics, Janis Gardovskis, The Upgrade of Hereditary Cancer Surveillance Schedule by Valka District Population Screening Data, Acta Chirurgica Latviensis, 2010, 10, 2

    CrossRef

  152. 152
    Peter Acher, Geraldine Kiela, Kay Thomas, Timothy O’Brien, TOWARDS A RATIONAL STRATEGY FOR THE SURVEILLANCE OF PATIENTS WITH LYNCH SYNDROME (HEREDITARY NON-POLYPOSIS COLON CANCER) FOR UPPER TRACT TRANSITIONAL CELL CARCINOMA, BJU International, 2010, 106, 3
  153. 153
    D. JOSEPH JERRY, NICHOLAS B. GRINER, LUWEI TAO, TUMOR SUPPRESSOR PATHWAYS AND CELLULAR ORIGINS OF BREAST CANCER: NEW COMPLEXITIES AND NEW HOPES, Nano LIFE, 2010, 01, 01n02, 1

    CrossRef

  154. 154
    Benjamin Purow, David Schiff, Advances in the genetics of glioblastoma: are we reaching critical mass?, Nature Reviews Neurology, 2009, 5, 8, 419

    CrossRef

  155. 155
    J. -C. Saurin, Besoins de clarification des modalités de surveillance des cancers extracoliques de la maladie de Lynch, Côlon & Rectum, 2009, 3, 3, 177

    CrossRef

  156. 156
    Tim Ripperger, Dorothea Gadzicki, Alfons Meindl, Brigitte Schlegelberger, Breast cancer susceptibility: current knowledge and implications for genetic counselling, European Journal of Human Genetics, 2009, 17, 6, 722

    CrossRef

  157. 157
    Glenn E Palomaki, Monica R McClain, Stephanie Melillo, Heather L Hampel, Stephen N Thibodeau, EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome, Genetics in Medicine, 2009, 11, 1, 42

    CrossRef

  158. 158
    Henry T. Lynch, Murray Joseph Casey, Carrie L. Snyder, Chhanda Bewtra, Jane F. Lynch, Matthew Butts, Andrew K. Godwin, Hereditary ovarian carcinoma: Heterogeneity, molecular genetics, pathology, and management, Molecular Oncology, 2009, 3, 2, 97

    CrossRef

  159. 159
    Jennifer A. Sparr, Prathap Bandipalliam, Mark S. Redston, Sapna Syngal, Intraductal Papillary Mucinous Neoplasm of the Pancreas With Loss of Mismatch Repair in a Patient With Lynch Syndrome, The American Journal of Surgical Pathology, 2009, 33, 2, 309

    CrossRef

  160. 160
    Awad M. Jarrar, James M. Church, Susan Fay, Matthew F. Kalady, Is the Phenotype Mixed or Mistaken? Hereditary Nonpolyposis Colorectal Cancer and Hyperplastic Polyposis Syndrome, Diseases of the Colon & Rectum, 2009, 52, 12, 1949

    CrossRef

  161. 161
    Jan J Koornstra, Marian JE Mourits, Rolf H Sijmons, Annemarie M Leliveld, Harry Hollema, Jan H Kleibeuker, Management of extracolonic tumours in patients with Lynch syndrome, The Lancet Oncology, 2009, 10, 4, 400

    CrossRef

  162. 162
    HT Lynch, PM Lynch, SJ Lanspa, CL Snyder, JF Lynch, CR Boland, Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications, Clinical Genetics, 2009, 76, 1
  163. 163
    Kerrington D. Smith, Miguel A. Rodriguez-Bigas, Role of Surgery in Familial Adenomatous Polyposis and Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome), Surgical Oncology Clinics of North America, 2009, 18, 4, 705

    CrossRef

  164. 164
    Mef Nilbert, Christina Therkildsen, Anja Nissen, Måns Åkerman, Inge Bernstein, Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum, Familial Cancer, 2009, 8, 3, 209

    CrossRef

  165. 165
    Familial Myeloma, New England Journal of Medicine, 2008, 359, 16, 1734

    CrossRef

  166. 166
    Gillian Crawford, Genetic Susceptibility to Female Cancers,
  167. 167
    David Shapiro, Joshua Melson, Abhitabh Patil, The Role of Endoscopy in Small Bowel Malignancies,