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For: Chitty LS, Friedman JM, Langlois S. Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus? Prenat Diagn 2016;36:15-9. [PMID: 26525746 DOI: 10.1002/pd.4718] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 1.9] [Reference Citation Analysis]
Number Citing Articles
1 Pangalos C, Hagnefelt B, Lilakos K, Konialis C. First applications of a targeted exome sequencing approach in fetuses with ultrasound abnormalities reveals an important fraction of cases with associated gene defects. PeerJ 2016;4:e1955. [PMID: 27168972 DOI: 10.7717/peerj.1955] [Cited by in Crossref: 45] [Cited by in F6Publishing: 34] [Article Influence: 7.5] [Reference Citation Analysis]
2 Westerfield LE, Braxton AA, Walkiewicz M. Prenatal Diagnostic Exome Sequencing: a Review. Curr Genet Med Rep 2017;5:75-83. [DOI: 10.1007/s40142-017-0120-y] [Cited by in Crossref: 3] [Article Influence: 0.6] [Reference Citation Analysis]
3 Feingold-zadok M, Chitayat D, Chong K, Injeyan M, Shannon P, Chapmann D, Maymon R, Pillar N, Reish O. Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita: Mutated NEB causes severe fetal nemaline myopathy. Prenat Diagn 2017;37:144-50. [DOI: 10.1002/pd.4977] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 1.6] [Reference Citation Analysis]
4 Lamont RE, Xi Y, Popko C, Lazier J, Bernier FP, Lauzon JL, Innes AM, Parboosingh JS, Thomas MA. Next-Generation Sequencing Using a Cardiac Gene Panel in Prenatally Diagnosed Cardiac Anomalies. J Obstet Gynaecol Can 2018;40:1417-23. [PMID: 30473118 DOI: 10.1016/j.jogc.2018.02.002] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
5 Harel T, Hacohen N, Shaag A, Gomori M, Singer A, Elpeleg O, Meiner V. Homozygous null variant in CRADD , encoding an adaptor protein that mediates apoptosis, is associated with lissencephaly. Am J Med Genet 2017;173:2539-44. [DOI: 10.1002/ajmg.a.38347] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
6 Wou K, Chung WK, Wapner RJ. Laboratory considerations for prenatal genetic testing. Semin Perinatol 2018;42:307-13. [PMID: 30206017 DOI: 10.1053/j.semperi.2018.07.020] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
7 Kehrer C, Hoischen A, Menkhaus R, Schwab E, Müller A, Kim S, Kreiß M, Weitensteiner V, Hilger A, Berg C, Geipel A, Reutter H, Gembruch U. Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome. Prenat Diagn 2016;36:961-5. [PMID: 27589329 DOI: 10.1002/pd.4920] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 2.3] [Reference Citation Analysis]
8 Konialis C, Assimakopoulos E, Hagnefelt B, Karapanou S, Sotiriadis A, Pangalos C. Prenatal diagnosis of X-linked myopathy associated with a VMA21 gene mutation afforded through a novel targeted exome sequencing strategy applied in fetuses with abnormal ultrasound findings. Clin Case Rep 2017;5:308-11. [PMID: 28265396 DOI: 10.1002/ccr3.822] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
9 Guo Y, Zhang H, Fan L, Chen J, Zhang X, Yang H, Sun Y. Simpson-Golabi-Behmel syndrome in one of the Dichorionic-diamniotic twin: a case report and literature review. BMC Pregnancy Childbirth 2022;22:42. [PMID: 35038998 DOI: 10.1186/s12884-021-04309-z] [Reference Citation Analysis]
10 Wou K, DeBie I, Carroll J, Brock JA, Douglas Wilson R. Fetal Exome Sequencing on the Horizon. J Obstet Gynaecol Can 2019;41:64-7. [PMID: 30580830 DOI: 10.1016/j.jogc.2018.06.016] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]