Similar articles for PMID: 24115450

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

1

GALNT12 is not a major contributor of familial colorectal cancer type X.

Seguí N, Pineda M, Navarro M, Lázaro C, Brunet J, Infante M, Durán M, Soto JL, Blanco I, Capellá G, Valle L. Seguí N, et al. Hum Mutat. 2014 Jan;35(1):50-2. doi: 10.1002/humu.22454. Epub 2013 Oct 17. Hum Mutat. 2014. PMID: 24115450

2

Inherited deleterious variants in GALNT12 are associated with CRC susceptibility.

Clarke E, Green RC, Green JS, Mahoney K, Parfrey PS, Younghusband HB, Woods MO. Clarke E, et al. Hum Mutat. 2012 Jul;33(7):1056-8. doi: 10.1002/humu.22088. Epub 2012 Apr 9. Hum Mutat. 2012. PMID: 22461326

3

Evidence for GALNT12 as a moderate penetrance gene for colorectal cancer.

Evans DR, Venkitachalam S, Revoredo L, Dohey AT, Clarke E, Pennell JJ, Powell AE, Quinn E, Ravi L, Gerken TA, Green JS, Woods MO, Guda K. Evans DR, et al. Hum Mutat. 2018 Aug;39(8):1092-1101. doi: 10.1002/humu.23549. Epub 2018 May 28. Hum Mutat. 2018. PMID: 29749045 Free PMC article.

4

Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer.

Middeldorp A, Jagmohan-Changur SC, van der Klift HM, van Puijenbroek M, Houwing-Duistermaat JJ, Webb E, Houlston R, Tops C, Vasen HF, Devilee P, Morreau H, van Wezel T, Wijnen J. Middeldorp A, et al. Genes Chromosomes Cancer. 2010 Jun;49(6):539-48. doi: 10.1002/gcc.20763. Genes Chromosomes Cancer. 2010. PMID: 20222047

5

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer.

Jagmohan-Changur S, Poikonen T, Vilkki S, Launonen V, Wikman F, Orntoft TF, Møller P, Vasen H, Tops C, Kolodner RD, Mecklin JP, Järvinen H, Bevan S, Houlston RS, Aaltonen LA, Fodde R, Wijnen J, Karhu A. Jagmohan-Changur S, et al. Cancer Res. 2003 Jan 1;63(1):154-8. Cancer Res. 2003. PMID: 12517792

6

Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome.

Lorca V, Rueda D, Martín-Morales L, Poves C, Fernández-Aceñero MJ, Ruiz-Ponte C, Llovet P, Marrupe D, García-Barberán V, García-Paredes B, Pérez-Segura P, de la Hoya M, Díaz-Rubio E, Caldés T, Garre P. Lorca V, et al. PLoS One. 2017 Nov 2;12(11):e0187312. doi: 10.1371/journal.pone.0187312. eCollection 2017. PLoS One. 2017. PMID: 29095867 Free PMC article.

7

A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair.

Boardman LA, Schmidt S, Lindor NM, Burgart LJ, Cunningham JM, Price-Troska T, Snow K, Ahlquist DA, Thibodeau SN. Boardman LA, et al. Genes Chromosomes Cancer. 2001 Feb;30(2):181-6. Genes Chromosomes Cancer. 2001. PMID: 11135435

8

Increased frequency of 20q gain and copy-neutral loss of heterozygosity in mismatch repair proficient familial colorectal carcinomas.

Middeldorp A, van Eijk R, Oosting J, Forte GI, van Puijenbroek M, van Nieuwenhuizen M, Corver WE, Ruano D, Caldes T, Wijnen J, Morreau H, van Wezel T. Middeldorp A, et al. Int J Cancer. 2012 Feb 15;130(4):837-46. doi: 10.1002/ijc.26093. Epub 2011 Jul 15. Int J Cancer. 2012. PMID: 21445971 Free article.

9

A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy.

Baudi F, Fersini G, Lavecchia A, Terracciano R, Leone F, Quaresima B, Faniello MC, De Paola L, Doldo P, Cuda G, Costanzo F, Venuta S. Baudi F, et al. Cancer Lett. 2005 Jun 8;223(2):285-91. doi: 10.1016/j.canlet.2004.09.051. Epub 2004 Nov 25. Cancer Lett. 2005. PMID: 15896463

10

[Hereditary predisposition of colorectal cancer and prevalence of hereditary nonpolyposis colorectal cancer in general population of colorectal cancer patients in China].

Zhang YZ, Sheng JQ, Li SR, Wu ZT. Zhang YZ, et al. Zhonghua Yi Xue Za Zhi. 2005 Nov 9;85(42):2995-3000. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16324388 Chinese.

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