Similar articles for PMID: 16825431

Year	Number of Results
1996	1
1997	1
2000	1
2001	1
2002	3
2003	15
2004	3
2005	10
2006	8
2007	3
2008	2
2009	2
2010	2
2011	5
2012	2
2013	2
2014	7
2015	7
2016	5
2017	2
2018	2
2019	1
2021	5
2022	2
2023	3
2024	0

1

Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.

Alter BP, Rosenberg PS, Brody LC. Alter BP, et al. J Med Genet. 2007 Jan;44(1):1-9. doi: 10.1136/jmg.2006.043257. Epub 2006 Jul 6. J Med Genet. 2007. PMID: 16825431 Free PMC article.

2

The clinical phenotype of children with Fanconi anemia caused by biallelic FANCD1/BRCA2 mutations.

Myers K, Davies SM, Harris RE, Spunt SL, Smolarek T, Zimmerman S, McMasters R, Wagner L, Mueller R, Auerbach AD, Mehta PA. Myers K, et al. Pediatr Blood Cancer. 2012 Mar;58(3):462-5. doi: 10.1002/pbc.23168. Epub 2011 May 5. Pediatr Blood Cancer. 2012. PMID: 21548014

3

Development of primary early-onset colorectal cancers due to biallelic mutations of the FANCD1/BRCA2 gene.

Degrolard-Courcet E, Sokolowska J, Padeano MM, Guiu S, Bronner M, Chery C, Coron F, Lepage C, Chapusot C, Loustalot C, Jouve JL, Hatem C, Ferrant E, Martin L, Coutant C, Baurand A, Couillault G, Delignette A, El Chehadeh S, Lizard S, Arnould L, Fumoleau P, Callier P, Mugneret F, Philippe C, Frebourg T, Jonveaux P, Faivre L. Degrolard-Courcet E, et al. Eur J Hum Genet. 2014 Aug;22(8):979-87. doi: 10.1038/ejhg.2013.278. Epub 2013 Dec 4. Eur J Hum Genet. 2014. PMID: 24301060 Free PMC article. Review.

4

Biallelic inactivation of BRCA2 in Fanconi anemia.

Howlett NG, Taniguchi T, Olson S, Cox B, Waisfisz Q, De Die-Smulders C, Persky N, Grompe M, Joenje H, Pals G, Ikeda H, Fox EA, D'Andrea AD. Howlett NG, et al. Science. 2002 Jul 26;297(5581):606-9. doi: 10.1126/science.1073834. Epub 2002 Jun 13. Science. 2002. PMID: 12065746

5

Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.

Feben C, Spencer C, Lochan A, Laing N, Fieggen K, Honey E, Wainstein T, Krause A. Feben C, et al. Fam Cancer. 2017 Jul;16(3):441-446. doi: 10.1007/s10689-017-9968-y. Fam Cancer. 2017. PMID: 28185119

6

The association between FANCD1/BRCA2 mutations and leukaemia.

Alter BP. Alter BP. Br J Haematol. 2006 May;133(4):446-8; author reply 448. doi: 10.1111/j.1365-2141.2006.06049.x. Br J Haematol. 2006. PMID: 16643458 Free article. No abstract available.

7

Hepatoblastoma in a 4-year-old girl with Fanconi anaemia.

Kopic S, Eirich K, Schuster B, Hanenberg H, Varon-Mateeva R, Rittinger O, Schimpl G, Schindler D, Jones N. Kopic S, et al. Acta Paediatr. 2011 May;100(5):780-3. doi: 10.1111/j.1651-2227.2010.02116.x. Epub 2011 Jan 12. Acta Paediatr. 2011. PMID: 21138478

8

A homozygous nonsense mutation early in exon 5 of BRCA2 is associated with very severe Fanconi anemia.

Radulovic I, Kuechler A, Schündeln MM, Paulussen M, von Neuhoff N, Reinhardt D, Hanenberg H. Radulovic I, et al. Eur J Med Genet. 2021 Aug;64(8):104260. doi: 10.1016/j.ejmg.2021.104260. Epub 2021 Jun 10. Eur J Med Genet. 2021. PMID: 34118472

9

Biallelic FANCD1/BRCA2 mutations predisposing to glioblastoma multiforme with multiple oncogenic amplifications.

Dodgshun AJ, Sexton-Oates A, Saffery R, Sullivan MJ. Dodgshun AJ, et al. Cancer Genet. 2016 Jan-Feb;209(1-2):53-6. doi: 10.1016/j.cancergen.2015.11.005. Epub 2015 Dec 9. Cancer Genet. 2016. PMID: 26740091

10

Genotype-cancer association in patients with Fanconi anemia due to pathogenic variants in FANCD1 (BRCA2) or FANCN (PALB2).

McReynolds LJ, Biswas K, Giri N, Sharan SK, Alter BP. McReynolds LJ, et al. Cancer Genet. 2021 Nov;258-259:101-109. doi: 10.1016/j.cancergen.2021.10.001. Epub 2021 Oct 4. Cancer Genet. 2021. PMID: 34687993 Free PMC article.

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