PubMed (OMIM) for id: 154288

Year	Number of Results
2002	1
2007	1
2008	1
2009	2
2011	2
2012	2
2013	2
2014	1
2015	1
2024	0

1

Identification of a human subcortical maternal complex.

Zhu K, Yan L, Zhang X, Lu X, Wang T, Yan J, Liu X, Qiao J, Li L. Zhu K, et al. Mol Hum Reprod. 2015 Apr;21(4):320-9. doi: 10.1093/molehr/gau116. Epub 2014 Dec 26. Mol Hum Reprod. 2015. PMID: 25542835

2

Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7.

Reddy R, Akoury E, Phuong Nguyen NM, Abdul-Rahman OA, Dery C, Gupta N, Daley WP, Ao A, Landolsi H, Ann Fisher R, Touitou I, Slim R. Reddy R, et al. Eur J Hum Genet. 2013 Sep;21(9):957-64. doi: 10.1038/ejhg.2012.274. Epub 2012 Dec 12. Eur J Hum Genet. 2013. PMID: 23232697 Free PMC article.

3

Mutations in NLRP7 and KHDC3L confer a complete hydatidiform mole phenotype on digynic triploid conceptions.

Fallahian M, Sebire NJ, Savage PM, Seckl MJ, Fisher RA. Fallahian M, et al. Hum Mutat. 2013 Feb;34(2):301-8. doi: 10.1002/humu.22228. Epub 2012 Nov 2. Hum Mutat. 2013. PMID: 23125094

4

Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.

Parry DA, Logan CV, Hayward BE, Shires M, Landolsi H, Diggle C, Carr I, Rittore C, Touitou I, Philibert L, Fisher RA, Fallahian M, Huntriss JD, Picton HM, Malik S, Taylor GR, Johnson CA, Bonthron DT, Sheridan EG. Parry DA, et al. Am J Hum Genet. 2011 Sep 9;89(3):451-8. doi: 10.1016/j.ajhg.2011.08.002. Epub 2011 Sep 1. Am J Hum Genet. 2011. PMID: 21885028 Free PMC article.

5

Screening for NLRP7 mutations in familial and sporadic recurrent hydatidiform moles: report of 2 Tunisian families.

Landolsi H, Rittore C, Philibert L, Missaoui N, Hmissa S, Touitou I, Gribaa M, Yacoubi MT. Landolsi H, et al. Int J Gynecol Pathol. 2011 Jul;30(4):348-53. doi: 10.1097/PGP.0b013e31820dc3b0. Int J Gynecol Pathol. 2011. PMID: 21623199

6

Role of Filia, a maternal effect gene, in maintaining euploidy during cleavage-stage mouse embryogenesis.

Zheng P, Dean J. Zheng P, et al. Proc Natl Acad Sci U S A. 2009 May 5;106(18):7473-8. doi: 10.1073/pnas.0900519106. Epub 2009 Apr 17. Proc Natl Acad Sci U S A. 2009. PMID: 19376971 Free PMC article.

7

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region.

Wang CM, Dixon PH, Decordova S, Hodges MD, Sebire NJ, Ozalp S, Fallahian M, Sensi A, Ashrafi F, Repiska V, Zhao J, Xiang Y, Savage PM, Seckl MJ, Fisher RA. Wang CM, et al. J Med Genet. 2009 Aug;46(8):569-75. doi: 10.1136/jmg.2008.064196. Epub 2009 Feb 25. J Med Genet. 2009. PMID: 19246479

8

A subcortical maternal complex essential for preimplantation mouse embryogenesis.

Li L, Baibakov B, Dean J. Li L, et al. Dev Cell. 2008 Sep;15(3):416-425. doi: 10.1016/j.devcel.2008.07.010. Dev Cell. 2008. PMID: 18804437 Free PMC article.

9

Atypical structure and phylogenomic evolution of the new eutherian oocyte- and embryo-expressed KHDC1/DPPA5/ECAT1/OOEP gene family.

Pierre A, Gautier M, Callebaut I, Bontoux M, Jeanpierre E, Pontarotti P, Monget P. Pierre A, et al. Genomics. 2007 Nov;90(5):583-94. doi: 10.1016/j.ygeno.2007.06.003. Epub 2007 Oct 3. Genomics. 2007. PMID: 17913455 Free article.

10

A global disorder of imprinting in the human female germ line.

Judson H, Hayward BE, Sheridan E, Bonthron DT. Judson H, et al. Nature. 2002 Apr 4;416(6880):539-42. doi: 10.1038/416539a. Nature. 2002. PMID: 11932746 Free article.

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