Similar articles for PMID: 15235019

Year	Number of Results
1998	2
1999	6
2000	5
2001	6
2002	6
2003	6
2004	6
2005	7
2006	3
2007	4
2008	4
2009	6
2010	3
2011	7
2012	7
2013	4
2014	3
2015	3
2016	5
2017	7
2018	2
2019	3
2020	7
2021	1
2022	3
2023	1
2024	0

1

The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations.

Howe JR, Sayed MG, Ahmed AF, Ringold J, Larsen-Haidle J, Merg A, Mitros FA, Vaccaro CA, Petersen GM, Giardiello FM, Tinley ST, Aaltonen LA, Lynch HT. Howe JR, et al. J Med Genet. 2004 Jul;41(7):484-91. doi: 10.1136/jmg.2004.018598. J Med Genet. 2004. PMID: 15235019 Free PMC article.

2

Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis.

Howe JR, Bair JL, Sayed MG, Anderson ME, Mitros FA, Petersen GM, Velculescu VE, Traverso G, Vogelstein B. Howe JR, et al. Nat Genet. 2001 Jun;28(2):184-7. doi: 10.1038/88919. Nat Genet. 2001. PMID: 11381269

3

Identification of a novel BMPR1A germline mutation in a Korean juvenile polyposis patient without SMAD4 mutation.

Kim IJ, Park JH, Kang HC, Kim KH, Kim JH, Ku JL, Kang SB, Park SY, Lee JS, Park JG. Kim IJ, et al. Clin Genet. 2003 Feb;63(2):126-30. doi: 10.1034/j.1399-0004.2003.00008.x. Clin Genet. 2003. PMID: 12630959

4

Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis.

Sayed MG, Ahmed AF, Ringold JR, Anderson ME, Bair JL, Mitros FA, Lynch HT, Tinley ST, Petersen GM, Giardiello FM, Vogelstein B, Howe JR. Sayed MG, et al. Ann Surg Oncol. 2002 Nov;9(9):901-6. doi: 10.1007/BF02557528. Ann Surg Oncol. 2002. PMID: 12417513

5

Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers.

Friedl W, Uhlhaas S, Schulmann K, Stolte M, Loff S, Back W, Mangold E, Stern M, Knaebel HP, Sutter C, Weber RG, Pistorius S, Burger B, Propping P. Friedl W, et al. Hum Genet. 2002 Jul;111(1):108-11. doi: 10.1007/s00439-002-0748-9. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136244

6

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).

Gallione CJ, Repetto GM, Legius E, Rustgi AK, Schelley SL, Tejpar S, Mitchell G, Drouin E, Westermann CJ, Marchuk DA. Gallione CJ, et al. Lancet. 2004 Mar 13;363(9412):852-9. doi: 10.1016/S0140-6736(04)15732-2. Lancet. 2004. PMID: 15031030

7

Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients.

Friedl W, Kruse R, Uhlhaas S, Stolte M, Schartmann B, Keller KM, Jungck M, Stern M, Loff S, Back W, Propping P, Jenne DE. Friedl W, et al. Genes Chromosomes Cancer. 1999 Aug;25(4):403-6. Genes Chromosomes Cancer. 1999. PMID: 10398437

8

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.

Zhou XP, Woodford-Richens K, Lehtonen R, Kurose K, Aldred M, Hampel H, Launonen V, Virta S, Pilarski R, Salovaara R, Bodmer WF, Conrad BA, Dunlop M, Hodgson SV, Iwama T, Järvinen H, Kellokumpu I, Kim JC, Leggett B, Markie D, Mecklin JP, Neale K, Phillips R, Piris J, Rozen P, Houlston RS, Aaltonen LA, Tomlinson IP, Eng C. Zhou XP, et al. Am J Hum Genet. 2001 Oct;69(4):704-11. doi: 10.1086/323703. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536076 Free PMC article.

9

Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot.

Howe JR, Shellnut J, Wagner B, Ringold JC, Sayed MG, Ahmed AF, Lynch PM, Amos CI, Sistonen P, Aaltonen LA. Howe JR, et al. Am J Hum Genet. 2002 May;70(5):1357-62. doi: 10.1086/340258. Epub 2002 Mar 27. Am J Hum Genet. 2002. PMID: 11920286 Free PMC article.

10

Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis.

van Hattem WA, Brosens LA, de Leng WW, Morsink FH, Lens S, Carvalho R, Giardiello FM, Offerhaus GJ. van Hattem WA, et al. Gut. 2008 May;57(5):623-7. doi: 10.1136/gut.2007.142927. Epub 2008 Jan 4. Gut. 2008. PMID: 18178612

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