Familial Colorectal Cancer
What's New
Last Posted: Nov 15, 2022
- The Roles of MTRR and MTHFR Gene Polymorphisms in Colorectal Cancer Survival.
Wang Yu et al. Nutrients 2022 14(21) - Familial component of early-onset colorectal cancer: opportunity for prevention.
Daca-Alvarez Maria et al. The British journal of surgery 2022 - Familial colorectal cancer.
Mangas-Sanjuan Carolina et al. Best practice & research. Clinical gastroenterology 2022 58-59101798 - Association between Dietary Fiber Intake and Mortality among Colorectal Cancer Survivors: Results from the Newfoundland Familial Colorectal Cancer Cohort Study and a Meta-Analysis of Prospective Studies.
Zhao Jing et al. Cancers 2022 14(15) - New insights on familial colorectal cancer type X syndrome.
Garcia Felipe Antonio de Oliveira et al. Scientific reports 2022 12(1) 2846 - Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer.
Miao Beiping et al. International journal of molecular sciences 2022 23(3) - Familial Colorectal Cancer and Genetic Susceptibility: Colorectal Risk Variants in First-Degree Relatives of Patients With Colorectal Cancer.
Gargallo-Puyuelo Carla J et al. Clinical and translational gastroenterology 2021 Feb 12(2) e00301 - New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients.
Djursby Malene et al. Frontiers in genetics 2020 11566266 - Spectrum of mutations in genes associated with familial colorectal cancer syndrome (MLH1, MSH2, PMS2, MSH6, and APC): A not so common hereditary cancer syndrome in Indian population.
Bhai Pratibha et al. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2020 Nov - BRIP1, a gene potentially implicated in Familial Colorectal Cancer Type X.
Martin-Morales Lorena et al. Cancer prevention research (Philadelphia, Pa.) 2020 Oct
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 01, 2024
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