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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1984 1
1990 1
1993 4
1994 9
1995 9
1996 8
1997 7
1998 11
1999 7
2000 14
2001 13
2002 10
2003 7
2004 8
2005 9
2006 11
2007 14
2008 10
2009 10
2010 9
2011 9
2012 22
2013 11
2014 14
2015 15
2016 32
2017 27
2018 13
2019 19
2020 23
2021 21
2022 15
2023 15
2024 2

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376 results

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Page 1
Hereditary breast and ovarian cancer (HBOC): review of its molecular characteristics, screening, treatment, and prognosis.
Yoshida R. Yoshida R. Breast Cancer. 2021 Nov;28(6):1167-1180. doi: 10.1007/s12282-020-01148-2. Epub 2020 Aug 29. Breast Cancer. 2021. PMID: 32862296 Free PMC article. Review.
Breast cancer is a common cancer affecting a large number of patients. ...Studies on hereditary breast and ovarian cancer (HBOC) involve not only determining the predisposition to developing cancer, but also considering the
Breast cancer is a common cancer affecting a large number of patients. ...Studies on hereditary breast an
Hereditary Breast and Ovarian Cancer: An Updated Primer for OB/GYNs.
Bellcross CA. Bellcross CA. Obstet Gynecol Clin North Am. 2022 Mar;49(1):117-147. doi: 10.1016/j.ogc.2021.11.005. Obstet Gynecol Clin North Am. 2022. PMID: 35168766 Review.
This article provides an update on hereditary breast and ovarian cancer syndrome (HBOC) associated with pathogenic variants (PVs) in BRCA1/2. ...Obstetricians and gynecologists familiar with these concepts can identify and improve the quality of …
This article provides an update on hereditary breast and ovarian cancer syndrome (HBOC) associated with p …
Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe.
Marmolejo DH, Wong MYZ, Bajalica-Lagercrantz S, Tischkowitz M, Balmaña J; extended ERN-GENTURIS Thematic Group 3. Marmolejo DH, et al. Eur J Med Genet. 2021 Dec;64(12):104350. doi: 10.1016/j.ejmg.2021.104350. Epub 2021 Oct 1. Eur J Med Genet. 2021. PMID: 34606975 Review.
Hereditary breast and ovarian cancer (HBOC) is a syndrome defined by an increased risk of developing breast and/or ovarian cancer most commonly due to germline disease-causing variants in the BRCA1 and BRCA2 genes, but also
Hereditary breast and ovarian cancer (HBOC) is a syndrome defined by an increased risk of developing b
Hereditary Prostate Cancer: Genes Related, Target Therapy and Prevention.
Vietri MT, D'Elia G, Caliendo G, Resse M, Casamassimi A, Passariello L, Albanese L, Cioffi M, Molinari AM. Vietri MT, et al. Int J Mol Sci. 2021 Apr 4;22(7):3753. doi: 10.3390/ijms22073753. Int J Mol Sci. 2021. PMID: 33916521 Free PMC article. Review.
Family history of PCa, hereditary breast and ovarian cancer (HBOC) and Lynch syndromes (LS), are among the most important risk factors compared to age, race, ethnicity and environmental factors for PCa development. Hereditary prostate …
Family history of PCa, hereditary breast and ovarian cancer (HBOC) and Lynch syndromes (LS), are among th …
Hereditary Ovarian Carcinoma: Cancer Pathogenesis Looking beyond BRCA1 and BRCA2.
Samuel D, Diaz-Barbe A, Pinto A, Schlumbrecht M, George S. Samuel D, et al. Cells. 2022 Feb 4;11(3):539. doi: 10.3390/cells11030539. Cells. 2022. PMID: 35159349 Free PMC article. Review.
Besides BRCA1 and BRCA2, several other inheritable mutations have been identified that increase ovarian cancer risk. Surgical excision of the fallopian tubes and ovaries reduces ovarian cancer risk, but for some non-BRCA hereditary ovarian
Besides BRCA1 and BRCA2, several other inheritable mutations have been identified that increase ovarian cancer risk. Surgical …
Cancer genetics and breast cancer.
Huber-Keener KJ. Huber-Keener KJ. Best Pract Res Clin Obstet Gynaecol. 2022 Jun;82:3-11. doi: 10.1016/j.bpobgyn.2022.01.007. Epub 2022 Jan 31. Best Pract Res Clin Obstet Gynaecol. 2022. PMID: 35272929 Review.
This chapter focuses on how genes play a role in breast cancer risk, why certain genes are commonly involved in hereditary breast cancer, and what are the specific genes and genetic syndromes that put patients at risk for breast
This chapter focuses on how genes play a role in breast cancer risk, why certain genes are commonly involved in hereditary
Hereditary breast cancer; Genetic penetrance and current status with BRCA.
Mahdavi M, Nassiri M, Kooshyar MM, Vakili-Azghandi M, Avan A, Sandry R, Pillai S, Lam AK, Gopalan V. Mahdavi M, et al. J Cell Physiol. 2019 May;234(5):5741-5750. doi: 10.1002/jcp.27464. Epub 2018 Dec 14. J Cell Physiol. 2019. PMID: 30552672 Review.
The most important cause of developing hereditary breast cancer is germline mutations occurring in breast cancer (BCs) susceptibility genes, for example, BRCA1, BRCA2, TP53, CHEK2, PTEN, ATM, and PPM1D. ...Germline mutations in BRCA1 and BRCA2 g …
The most important cause of developing hereditary breast cancer is germline mutations occurring in breast can
Hereditary pancreatic cancer.
Abe K, Kitago M, Kitagawa Y, Hirasawa A. Abe K, et al. Int J Clin Oncol. 2021 Oct;26(10):1784-1792. doi: 10.1007/s10147-021-02015-6. Epub 2021 Sep 2. Int J Clin Oncol. 2021. PMID: 34476650 Free PMC article. Review.
Pancreatic cancer is associated with both family and hereditary cancer syndromes. ...Since poly-ADP-ribose polymerase (PARP) inhibitor has been shown to be effective in improving the prognosis of BRCA-positive pancreatic cancer as well as her
Pancreatic cancer is associated with both family and hereditary cancer syndromes. ...Since poly-ADP-ribose polym …
Familial and hereditary gastric cancer, an overview.
Carneiro F. Carneiro F. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101800. doi: 10.1016/j.bpg.2022.101800. Epub 2022 May 4. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988963 Review.
There are three major hereditable syndromes that affect primarily the stomach: hereditary diffuse gastric cancer (HDGC), gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) and familial intestinal gastric cancer (FIGC). ...GAPPS is cau …
There are three major hereditable syndromes that affect primarily the stomach: hereditary diffuse gastric cancer (HDGC) …
Peutz-Jeghers syndrome.
Tacheci I, Kopacova M, Bures J. Tacheci I, et al. Curr Opin Gastroenterol. 2021 May 1;37(3):245-254. doi: 10.1097/MOG.0000000000000718. Curr Opin Gastroenterol. 2021. PMID: 33591027 Review.
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 …
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastr …
376 results