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Delineating genotype and parent‐of‐origin effect on the phenotype in MSH6‐associated Lynch syndrome.
- Published in:
- Genes, Chromosomes & Cancer, 2024, v. 63, n. 5, p. 1, doi. 10.1002/gcc.23237
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- Publication type:
- Article
Evaluation of <italic>MLH1</italic> variants of unclear significance.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 7, p. 350, doi. 10.1002/gcc.22536
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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
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
Actualización en cáncer colorrectal hereditario y su impacto en salud pública.
- Published in:
- Revista Facultad de Medicina de la Universidad Nacional de Colombia, 2020, v. 68, n. 4, p. 597, doi. 10.15446/revfacmed.v68n4.77829
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- Publication type:
- Article
Identification of genetic variants for clinical management of familial colorectal tumors.
- Published in:
- BMC Medical Genetics, 2018, v. 19, p. 1, doi. 10.1186/s12881-018-0533-9
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- Publication type:
- Article
MLH1 Ile219Val polymorphism in Argentinean Families with Suspected Lynch Syndrome.
- Published in:
- Frontiers in Oncology, 2016, p. 1, doi. 10.3389/fonc.2016.00189
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- Publication type:
- Article
Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
- Published in:
- Familial Cancer, 2023, v. 22, n. 4, p. 437, doi. 10.1007/s10689-023-00341-4
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- Publication type:
- Article
Correction to: Letter to the Editor—Recent advances in Lynch syndrome.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Letter to the Editor-Recent advances in Lynch syndrome.
- Published in:
- 2021
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- Publication type:
- Letter
Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD).
- Published in:
- Familial Cancer, 2021, v. 20, n. 1, p. 35, doi. 10.1007/s10689-020-00193-2
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- Publication type:
- Article
MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing.
- Published in:
- Familial Cancer, 2020, v. 19, n. 4, p. 323, doi. 10.1007/s10689-020-00182-5
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- Publication type:
- Article
Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort.
- Published in:
- Familial Cancer, 2018, v. 17, n. 3, p. 395, doi. 10.1007/s10689-017-0052-4
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- Publication type:
- Article
Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 141, doi. 10.1007/s10689-017-0011-0
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- Publication type:
- Article
Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome.
- Published in:
- Familial Cancer, 2014, v. 13, n. 4, p. 537, doi. 10.1007/s10689-014-9728-1
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- Publication type:
- Article
Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice survey.
- Published in:
- Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1141810
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- Publication type:
- Article
Molecular Subtyping of Serous Ovarian Tumors Reveals Multiple Connections to Intrinsic Breast Cancer Subtypes.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107643
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- Publication type:
- Article
Distinct Gene Expression Signatures in Lynch Syndrome and Familial Colorectal Cancer Type X.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071755
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- Publication type:
- Article
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome.
- Published in:
- 2016
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- Publication type:
- journal article
A Breast Cancer Polygenic Risk Score Is Feasible for Risk Stratification in the Norwegian Population.
- Published in:
- Cancers, 2023, v. 15, n. 16, p. 4124, doi. 10.3390/cancers15164124
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- Publication type:
- Article
Genetic Characterization in High-Risk Individuals from a Low-Resource City of Peru.
- Published in:
- Cancers, 2022, v. 14, n. 22, p. 5603, doi. 10.3390/cancers14225603
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- Publication type:
- Article
Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift.
- Published in:
- Cancers, 2019, v. 11, n. 2, p. 132, doi. 10.3390/cancers11020132
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- Publication type:
- Article
Challenges to Bringing Personalized Medicine to a Low-Resource Setting in Peru.
- Published in:
- International Journal of Environmental Research & Public Health, 2021, v. 18, n. 4, p. 1470, doi. 10.3390/ijerph18041470
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- Publication type:
- Article
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2 : A Prospective Lynch Syndrome Database Study.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 13, p. 2856, doi. 10.3390/jcm10132856
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- Publication type:
- Article
Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 7, p. 2290, doi. 10.3390/jcm9072290
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- Publication type:
- Article
Spectrum and Frequency of Tumors, Cancer Risk and Survival in Chilean Families with Lynch Syndrome: Experience of the Implementation of a Registry.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1861, doi. 10.3390/jcm9061861
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- Publication type:
- Article
Is HLA type a possible cancer risk modifier in Lynch syndrome?
- Published in:
- International Journal of Cancer, 2023, v. 152, n. 10, p. 2024, doi. 10.1002/ijc.34312
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- Publication type:
- Article
The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance.
- Published in:
- International Journal of Cancer, 2021, v. 148, n. 4, p. 800, doi. 10.1002/ijc.33224
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- Publication type:
- Article
Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum.
- Published in:
- International Journal of Cancer, 2021, v. 148, n. 2, p. 512, doi. 10.1002/ijc.33214
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- Publication type:
- Article
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
- Published in:
- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00241-1
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- Publication type:
- Article
Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein.
- Published in:
- Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 4, p. 352, doi. 10.1002/mgg3.80
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- Publication type:
- Article
Editorial: Advances in genetics and molecular diagnosis in colorectal, stomach, and pancreatic cancer vol II.
- Published in:
- Frontiers in Oncology, 2024, p. 01, doi. 10.3389/fonc.2024.1448183
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- Publication type:
- Article
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.
- Published in:
- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0127-3
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- Publication type:
- Article
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.
- Published in:
- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0106-8
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- Publication type:
- Article
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.
- Published in:
- Hereditary Cancer in Clinical Practice, 2018, v. 16, p. 1, doi. 10.1186/s13053-018-0086-0
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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