BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Normand EA, Alaimo JT, Van den Veyver IB. Exome and genome sequencing in reproductive medicine. Fertil Steril 2018;109:213-20. [PMID: 29395096 DOI: 10.1016/j.fertnstert.2017.12.010] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Zheng H, Zeng Z, Wen H, Wang P, Huang C, Huang P, Chen Q, Gong D, Qiu X. Application of Genome-Wide Association Studies in Coronary Artery Disease. Curr Pharm Des 2019;25:4274-86. [PMID: 31692429 DOI: 10.2174/1381612825666191105125148] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
2 Lorenzi D, Fernández C, Bilinski M, Fabbro M, Galain M, Menazzi S, Miguens M, Perassi PN, Fulco MF, Kopelman S, Fiszbajn G, Nodar F, Papier S. First custom next-generation sequencing infertility panel in Latin America: design and first results. JBRA Assisted Reproduction. [DOI: 10.5935/1518-0557.20190065] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
3 Siristatidis C, Tzanakaki D, Simopoulou M, Vaitsopoulou C, Tsioulou P, Stavros S, Papapanou M, Drakakis P, Bakas P, Vlahos N. Empty Zona Pellucida Only Case: A Critical Review of the Literature. Int J Environ Res Public Health 2021;18:9409. [PMID: 34501995 DOI: 10.3390/ijerph18179409] [Reference Citation Analysis]
4 Sun Y, Liu F, Fan C, Wang Y, Song L, Fang Z, Han R, Wang Z, Wang X, Yang Z, Xu Z, Peng J, Shi C, Zhang H, Dong W, Huang H, Li Y, Le Y, Sun J, Peng Z. Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders. BMC Med Genomics 2021;14:102. [PMID: 33849535 DOI: 10.1186/s12920-021-00948-5] [Reference Citation Analysis]
5 Verma I, Lallar M, Arora V. Looking Back at Fetal Medicine in India in 2018, and Looking Forward to 2019. J Fetal Med 2019;6:47-50. [DOI: 10.1007/s40556-019-00201-1] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
6 Precone V, Cannarella R, Paolacci S, Busetto GM, Beccari T, Stuppia L, Tonini G, Zulian A, Marceddu G, Calogero AE, Bertelli M. Male Infertility Diagnosis: Improvement of Genetic Analysis Performance by the Introduction of Pre-Diagnostic Genes in a Next-Generation Sequencing Custom-Made Panel. Front Endocrinol (Lausanne) 2020;11:605237. [PMID: 33574797 DOI: 10.3389/fendo.2020.605237] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Kiani AK, Paolacci S, Scanzano P, Michelini S, Capodicasa N, D'Agruma L, Notarangelo A, Tonini G, Piccinelli D, Farshid KR, Petralia P, Fulcheri E, Chiurazzi P, Terranova C, Plotti F, Angioli R, Castori M, Bertelli M. Complications related to in vitro reproductive techniques support the implementation of natural procreative technologies. Acta Biomed 2020;91:e2020018. [PMID: 33170179 DOI: 10.23750/abm.v91i13-S.10525] [Reference Citation Analysis]
8 Merrick BA. Next generation sequencing data for use in risk assessment. Curr Opin Toxicol 2019;18:18-26. [PMID: 31058248 DOI: 10.1016/j.cotox.2019.02.010] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
9 Daum H, Meiner V, Elpeleg O, Harel T; collaborating authors. Fetal exome sequencing: yield and limitations in a tertiary referral center. Ultrasound Obstet Gynecol 2019;53:80-6. [PMID: 29947050 DOI: 10.1002/uog.19168] [Cited by in Crossref: 22] [Cited by in F6Publishing: 21] [Article Influence: 7.3] [Reference Citation Analysis]
10 Mollison L, O'Daniel JM, Henderson GE, Berg JS, Skinner D. Parents' perceptions of personal utility of exome sequencing results. Genet Med 2020;22:752-7. [PMID: 31857707 DOI: 10.1038/s41436-019-0730-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 3.7] [Reference Citation Analysis]
11 Sabbagh R, Van den Veyver IB. The current and future impact of genome-wide sequencing on fetal precision medicine. Hum Genet 2020;139:1121-30. [PMID: 31754893 DOI: 10.1007/s00439-019-02088-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]