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Colorectal Adenocarcinoma: A Pediatric Case Review with a Focus on Mismatch Repair Gene Mutations and E-Cadherin Expression.
- Published in:
- Pediatric & Developmental Pathology, 2012, v. 15, n. 3, p. 192, doi. 10.2350/11-04-1015-OA.1
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- Publication type:
- Article
Annual outpatient hysteroscopy and endometrial sampling (OHES) in HNPCC/Lynch syndrome (LS).
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- Archives of Gynecology & Obstetrics, 2012, v. 286, n. 6, p. 1555, doi. 10.1007/s00404-012-2492-2
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- Publication type:
- Article
Knowledge, Attitudes and Referral Patterns of Lynch Syndrome: A Survey of Clinicians in Australia.
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- Journal of Personalized Medicine, 2014, v. 4, n. 2, p. 218, doi. 10.3390/jpm4020218
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- Publication type:
- Article
Barriers and Motivators for Referral of Patients with Suspected Lynch Syndrome to Cancer Genetic Services: A Qualitative Study.
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- Journal of Personalized Medicine, 2014, v. 4, n. 1, p. 20, doi. 10.3390/jpm4010020
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- Publication type:
- Article
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.
- Published in:
- BJU International, 2012, v. 110, n. 11b, p. E583, doi. 10.1111/j.1464-410X.2012.11298.x
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- Publication type:
- Article
Partial duplication of MSH2 spanning exons 7 through 14 in Lynch syndrome.
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- Journal of Gastroenterology, 2013, v. 48, n. 6, p. 770, doi. 10.1007/s00535-013-0804-3
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- Publication type:
- Article
Lynch syndrome in a 15-year-old boy.
- Published in:
- 2008
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- Publication type:
- journal article
Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2016, v. 14, p. 1, doi. 10.1186/s13053-016-0054-5
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- Publication type:
- Article
Familial cancer among consecutive uterine cancer patients in Sweden.
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- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-14
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- Publication type:
- Article
Patient-reported disease knowledge and educational needs in Lynch syndrome: findings of an interactive multidisciplinary patient conference.
- Published in:
- 2014
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- Publication type:
- Proceeding
Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-9
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- Publication type:
- Article
Mutation spectrum in South American Lynch syndrome families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-18
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- Publication type:
- Article
Sense of coherence and self-concept in Lynch syndrome.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-7
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- Publication type:
- Article
Dawning of the epigenetic era in hereditary cancer.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 5, p. 413, doi. 10.1111/cge.12369
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- Publication type:
- Article
Epigenetic mechanisms in the pathogenesis of Lynch syndrome.
- Published in:
- Clinical Genetics, 2014, v. 85, n. 5, p. 403, doi. 10.1111/cge.12349
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- Publication type:
- Article
A population-based study of hereditary non-polyposis colorectal cancer: evidence of pathologic and genetic heterogeneity.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 6, p. 522, doi. 10.1111/cge.12080
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- Publication type:
- Article
The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families.
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- Clinical Genetics, 2013, v. 84, n. 3, p. 244, doi. 10.1111/cge.12062
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- Publication type:
- Article
First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 1, p. 70, doi. 10.1111/cge.12025
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- Publication type:
- Article
Absence of PMS2 mutations in colon- CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression.
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- Clinical Genetics, 2013, v. 83, n. 6, p. 591, doi. 10.1111/cge.12011
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- Publication type:
- Article
Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation.
- Published in:
- Clinical Genetics, 2013, v. 83, n. 4, p. 359, doi. 10.1111/j.1399-0004.2012.01929.x
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- Publication type:
- Article
Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families.
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- Clinical Genetics, 2013, v. 83, n. 3, p. 215, doi. 10.1111/cge.12091
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- Publication type:
- Article
Recurrent and founder mutations in the PMS2 gene.
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- Clinical Genetics, 2013, v. 83, n. 3, p. 238, doi. 10.1111/j.1399-0004.2012.01898.x
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- Publication type:
- Article
Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 5, p. 439, doi. 10.1111/j.1399-0004.2011.01802.x
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- Publication type:
- Article
Colon-specific phenotype in Lynch syndrome associated with EPCAM deletion.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 1, p. 97, doi. 10.1111/j.1399-0004.2011.01826.x
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- Publication type:
- Article
Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome.
- Published in:
- Clinical Genetics, 2011, v. 79, n. 6, p. 512, doi. 10.1111/j.1399-0004.2010.01594.x
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- Publication type:
- Article
Mismatch Repair Deficiency Screening via Immunohistochemical Staining in Young Asians with Colorectal Cancers.
- Published in:
- World Journal of Surgery, 2013, v. 37, n. 10, p. 2468, doi. 10.1007/s00268-013-2134-2
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- Publication type:
- Article
Prenatal genetic counseling practices regarding recommendations for cancer genetic counseling: A retrospective chart review from two academic institutions.
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- Journal of Genetic Counseling, 2022, v. 31, n. 5, p. 1062, doi. 10.1002/jgc4.1577
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- Publication type:
- Article
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 4, p. 949, doi. 10.1002/jgc4.1567
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- Publication type:
- Article
Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 3, p. 568, doi. 10.1002/jgc4.1546
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- Publication type:
- Article
Genetic counselors' perspectives on population‐based screening for BRCA‐related hereditary breast and ovarian cancer and Lynch syndrome.
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- Journal of Genetic Counseling, 2021, v. 30, n. 1, p. 158, doi. 10.1002/jgc4.1305
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- Publication type:
- Article
Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices.
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- Journal of Genetic Counseling, 2020, v. 29, n. 5, p. 728, doi. 10.1002/jgc4.1198
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- Publication type:
- Article
Daily aspirin protects against colorectal cancer.
- Published in:
- 2009
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- Publication type:
- Proceeding
A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families.
- Published in:
- Acta Obstetricia et Gynecologica Scandinavica, 2011, v. 90, n. 5, p. 437, doi. 10.1111/j.1600-0412.2011.01091.x
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- Publication type:
- Article
Lynch Syndrome from a surgeon perspective: retrospective study of clinical impact of mismatch repair protein expression analysis in colorectal cancer patients less than 50 years old.
- Published in:
- BMC Surgery, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2482-14-9
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- Publication type:
- Article
Clinical significance of microsatellite instability in colorectal cancer.
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- Langenbeck's Archives of Surgery, 2014, v. 399, n. 1, p. 23, doi. 10.1007/s00423-013-1112-3
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- Publication type:
- Article
Lynch syndrome: clinical, pathological, and genetic insights.
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- Langenbeck's Archives of Surgery, 2012, v. 397, n. 4, p. 513, doi. 10.1007/s00423-012-0918-8
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- Publication type:
- Article
Asymptomatic Synchronous Quintuple Primary Cancers.
- Published in:
- Gynecologic & Obstetric Investigation, 2012, v. 74, n. 4, p. 324, doi. 10.1159/000339135
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- Publication type:
- Article
Identificación de cáncer colorrectal hereditario: Síndrome de Lynch.
- Published in:
- Revista del Cuerpo Médico del Hospital Nacional Almanzor Aguinaga Asenjo, 2014, v. 7, n. 1, p. 40
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- Publication type:
- Article
Genetic anticipation in Swedish Lynch syndrome families.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 11, p. 1, doi. 10.1371/journal.pgen.1007012
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- Publication type:
- Article
Clues to the origins of ovarian cancer: Family history assessment, genetic screening are key to prevention.
- Published in:
- Contemporary OB/GYN, 2022, v. 67, n. 4, p. 18
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- Publication type:
- Article
Mechanism of mismatch recognition revealed by human MutS? bound to unpaired DNA loops.
- Published in:
- Nature Structural & Molecular Biology, 2012, v. 19, n. 1, p. 72, doi. 10.1038/nsmb.2175
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- Publication type:
- Article
The 11TH Annual Scientific Meeting of the College of Pathologists, Academy of Medicine Malaysia was held at the Crowne Plaza Mutiara Hotel, Kuala Lumpur from 8-10 June 2012. Abstracts of papers presented follow.
- Published in:
- Malaysian Journal of Pathology, 2012, v. 34, n. 2, p. 171
- Publication type:
- Article
Genetics of Endometrial Cancers.
- Published in:
- Obstetrics & Gynecology International, 2010, v. 2010, p. 1, doi. 10.1155/2010/984013
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- Publication type:
- Article
The <i>MLH1</i> c.1852_1853delinsGC (p.K618A) Variant in Colorectal Cancer: Genetic Association Study in 18,723 Individuals.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0095022
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- Publication type:
- Article
Systematic Study on Genetic and Epimutational Profile of a Cohort of Amsterdam Criteria-Defined Lynch Syndrome in Singapore.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094170
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- Publication type:
- Article
Linkage Analysis in Familial Non-Lynch Syndrome Colorectal Cancer Families from Sweden.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083936
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- Publication type:
- Article
Prevalence of Lynch Syndrome among Patients with Newly Diagnosed Endometrial Cancers.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0079737
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- Publication type:
- Article
Functional Analysis in Mouse Embryonic Stem Cells Reveals Wild-Type Activity for Three <i>Msh6</i> Variants Found in Suspected Lynch Syndrome Patients.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0074766
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- Publication type:
- Article
Frequency and Variability of Genomic Rearrangements on <i>MSH2</i> in Spanish Lynch Syndrome Families.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0072195
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- Publication type:
- Article
Dietary Supplement Use and Colorectal Adenoma Risk in Individuals with Lynch Syndrome: The GEOLynch Cohort Study.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066819
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- Publication type:
- Article