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For: Jelin AC, Vora N. Whole Exome Sequencing: Applications in Prenatal Genetics. Obstet Gynecol Clin North Am 2018;45:69-81. [PMID: 29428287 DOI: 10.1016/j.ogc.2017.10.003] [Cited by in Crossref: 24] [Cited by in F6Publishing: 21] [Article Influence: 6.0] [Reference Citation Analysis]
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5 Greenbaum L, Pode-Shakked B, Eisenberg-Barzilai S, Dicastro-Keidar M, Bar-Ziv A, Goldstein N, Reznik-Wolf H, Poran H, Rigbi A, Barel O, Bertoli-Avella AM, Bauer P, Regev M, Raas-Rothschild A, Pras E, Berkenstadt M. Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families. Front Genet 2019;10:425. [PMID: 31428121 DOI: 10.3389/fgene.2019.00425] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
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8 Gabriel H, Korinth D, Ritthaler M, Schulte B, Battke F, von Kaisenberg C, Wüstemann M, Schulze B, Friedrich-Freksa A, Pfeiffer L, Entezami M, Schröer A, Bürger J, Schwaibold EMC, Lebek H, Biskup S. Trio exome sequencing is highly relevant in prenatal diagnostics. Prenat Diagn 2021. [PMID: 34958143 DOI: 10.1002/pd.6081] [Reference Citation Analysis]
9 Robbins SM, Thimm MA, Valle D, Jelin AC. Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes. J Assist Reprod Genet 2019;36:1539-48. [PMID: 31273585 DOI: 10.1007/s10815-019-01499-6] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 4.7] [Reference Citation Analysis]
10 Guadagnolo D, Mastromoro G, Di Palma F, Pizzuti A, Marchionni E. Prenatal Exome Sequencing: Background, Current Practice and Future Perspectives-A Systematic Review. Diagnostics (Basel) 2021;11:224. [PMID: 33540854 DOI: 10.3390/diagnostics11020224] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
11 Jelin AC, Sagaser KG, Wilkins-Haug L. Prenatal Genetic Testing Options. Pediatr Clin North Am 2019;66:281-93. [PMID: 30819336 DOI: 10.1016/j.pcl.2018.12.016] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
12 Houdayer C, Ziegler A, Boussion F, Blesson S, Bris C, Toutain A, Biquard F, Guichet A, Bonneau D, Colin E. Prenatal diagnosis of Desbuquois dysplasia type 1 by whole exome sequencing before the occurrence of specific ultrasound signs. J Matern Fetal Neonatal Med 2021;34:2217-20. [PMID: 31510824 DOI: 10.1080/14767058.2019.1657084] [Reference Citation Analysis]
13 Su D, Nie M, Yue J. The G199X and V157fs mutations in the TP53 gene promote malignancy in serous ovarian cancer: an analysis using whole-exome sequencing. Ann Transl Med 2021;9:710. [PMID: 33987408 DOI: 10.21037/atm-21-583] [Reference Citation Analysis]
14 Felice V, Abhyankar A, Jobanputra V. Prenatal Diagnosis by Whole Exome Sequencing in Fetuses with Ultrasound Abnormalities. Methods Mol Biol 2019;1885:267-85. [PMID: 30506204 DOI: 10.1007/978-1-4939-8889-1_18] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Breuer M, Patten SA. A Great Catch for Investigating Inborn Errors of Metabolism-Insights Obtained from Zebrafish. Biomolecules 2020;10:E1352. [PMID: 32971894 DOI: 10.3390/biom10091352] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
16 Castleman JS, Wall E, Allen S, Williams D, Doyle S, Kilby MD. The prenatal exome - a door to prenatal diagnostics? Expert Rev Mol Diagn 2021;21:465-74. [PMID: 33877000 DOI: 10.1080/14737159.2021.1920398] [Reference Citation Analysis]
17 Pasternak Y, Daykan Y, Tenne T, Reinstein E, Miller N, Shechter-Maor G, Maya I, Biron-Shental T, Sukenik Halevy R. The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations. J Matern Fetal Neonatal Med 2020;:1-5. [PMID: 31973614 DOI: 10.1080/14767058.2020.1716722] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
18 Stevens BK, Nunley PB, Wagner C, Murphy L, Wittman T, Ramdaney A, Jones M, Choates MG. Utility of expanded carrier screening in pregnancies with ultrasound abnormalities. Prenat Diagn 2021. [PMID: 34792213 DOI: 10.1002/pd.6069] [Reference Citation Analysis]
19 Mastromoro G, Guadagnolo D, Khaleghi Hashemian N, Marchionni E, Traversa A, Pizzuti A. Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis. Diagnostics 2022;12:575. [DOI: 10.3390/diagnostics12030575] [Reference Citation Analysis]
20 Rajasekaran P, Gandhi P, Idhrees M, Velayudhan BV. Aortic complications in pregnancy: the less remembered chapter—a narrative review. Exploration of Medicine. [DOI: 10.37349/emed.2021.00060] [Reference Citation Analysis]
21 Kowalczyk K, Bartnik-Głaska M, Smyk M, Plaskota I, Bernaciak J, Kędzior M, Wiśniowiecka-Kowalnik B, Jakubów-Durska K, Braun-Walicka N, Barczyk A, Geremek M, Castañeda J, Kutkowska-Kaźmierczak A, Własienko P, Dębska M, Kucińska-Chahwan A, Roszkowski T, Kozłowski S, Mikulska B, Issat T, Obersztyn E, Nowakowska BA. Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities. Genes (Basel) 2021;12:2021. [PMID: 34946970 DOI: 10.3390/genes12122021] [Reference Citation Analysis]
22 Huang TX, Ma GC, Chen M, Li WF, Shaw SW. Difficulties of Prenatal Genetic Counseling for a Subsequent Child in a Family With Multiple Genetic Variations. Front Genet 2021;12:612100. [PMID: 34970295 DOI: 10.3389/fgene.2021.612100] [Reference Citation Analysis]
23 Vora NL, Hui L. Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development. Genet Med 2018;20:791-9. [PMID: 30032162 DOI: 10.1038/s41436-018-0087-4] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
24 Chau MHK, Choy KW. The role of chromosomal microarray and exome sequencing in prenatal diagnosis. Curr Opin Obstet Gynecol 2021;33:148-55. [PMID: 33620893 DOI: 10.1097/GCO.0000000000000692] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Brown JEH, Zamora AN, Outram S, Sparks TN, Lianoglou BR, Norstad M, Sahin Hodoglugil NN, Norton ME, Ackerman SL. “Let’s Just Wait Until She’s Born”: Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic Research. Front Genet 2022;13:882703. [DOI: 10.3389/fgene.2022.882703] [Reference Citation Analysis]
26 Evans MI, Britt DW, Evans SM, Devoe LD. Changing Perspectives of Electronic Fetal Monitoring. Reprod Sci 2021. [PMID: 34664218 DOI: 10.1007/s43032-021-00749-2] [Reference Citation Analysis]
27 Du Q, Zhang D, Zhuang Y, Xia Q, Wen T, Jia H. The Molecular Genetics of Marfan Syndrome. Int J Med Sci 2021;18:2752-66. [PMID: 34220303 DOI: 10.7150/ijms.60685] [Reference Citation Analysis]
28 Zhi X, Ai Q, Sheng W, Yu Y, Shu J, Yu C, Yu X, Li D, Cai C. Identification of a Novel Deep Intronic Variant by Whole Genome Sequencing Combined With RNA Sequencing in a Chinese Patient With Menkes Disease. Front Genet 2022;13:852764. [DOI: 10.3389/fgene.2022.852764] [Reference Citation Analysis]
29 Franks PW, Melén E, Friedman M, Sundström J, Kockum I, Klareskog L, Almqvist C, Bergen SE, Czene K, Hägg S, Hall P, Johnell K, Malarstig A, Catrina A, Hagström H, Benson M, Gustav Smith J, Gomez MF, Orho-Melander M, Jacobsson B, Halfvarson J, Repsilber D, Oresic M, Jern C, Melin B, Ohlsson C, Fall T, Rönnblom L, Wadelius M, Nordmark G, Johansson Å, Rosenquist R, Sullivan PF. Technological readiness and implementation of genomic-driven precision medicine for complex diseases. J Intern Med 2021;290:602-20. [PMID: 34213793 DOI: 10.1111/joim.13330] [Reference Citation Analysis]
30 Lei L, Zhou L, Xiong JJ. Whole-exome sequencing increases the diagnostic rate for prenatal fetal structural anomalies. Eur J Med Genet 2021;64:104288. [PMID: 34246755 DOI: 10.1016/j.ejmg.2021.104288] [Reference Citation Analysis]
31 Liang C, Wang YJ, Wei YX, Dong Y, Zhang ZC. Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole-Exome Sequencing. Orthop Surg 2020;12:990-6. [PMID: 32293802 DOI: 10.1111/os.12660] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
32 Yung NK, Maassel NL, Ullrich SJ, Ricciardi AS, Stitelman DH. A narrative review of in utero gene therapy: advances, challenges, and future considerations. Transl Pediatr 2021;10:1486-96. [PMID: 34189107 DOI: 10.21037/tp-20-89] [Reference Citation Analysis]
33 Rent S, Lemmon ME, Ellestad S, Bidegain M. The Role of Perinatal Palliative Care in Fetal Neurology. Am J Perinatol 2021. [PMID: 34710944 DOI: 10.1055/a-1682-2798] [Reference Citation Analysis]
34 Jin C, Qian H, Xu T, Chen J, Li X, Gu Z. Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability. Taiwan J Obstet Gynecol 2021;60:1094-7. [PMID: 34794744 DOI: 10.1016/j.tjog.2021.09.023] [Reference Citation Analysis]