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For: Reches A, Hiersch L, Simchoni S, Barel D, Greenberg R, Ben Sira L, Malinger G, Yaron Y. Whole-exome sequencing in fetuses with central nervous system abnormalities. J Perinatol 2018;38:1301-8. [PMID: 30108342 DOI: 10.1038/s41372-018-0199-3] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
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2 Tan H, Xie Y, Chen F, Chen M, Yu L, Chen D, Chen J. Novel and recurrent variants identified in fetuses with central nervous system abnormalities by trios-medical exome sequencing. Clin Chim Acta 2020;510:599-604. [PMID: 32798513 DOI: 10.1016/j.cca.2020.08.018] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Greenbaum L, Barel O, Nikitin V, Hersalis-Eldar A, Kol N, Reznik-Wolf H, Dominissini D, Pras E, Dori A. Identification of a homozygous VRK1 mutation in two patients with adult-onset distal hereditary motor neuropathy. Muscle Nerve 2020;61:395-400. [PMID: 31837156 DOI: 10.1002/mus.26779] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 Demaegd K, Brilstra EH, Hoogendijk JE, de Bie CI, de Pagter MS, van Hecke W, Mühlebner A, van Es MA, Milone M, van Rheenen W. Distal spinal muscular atrophy featured by predominant calf muscle involvement in VRK1 associated disease – case series and review. Neuromuscular Disorders 2022. [DOI: 10.1016/j.nmd.2022.04.007] [Reference Citation Analysis]
5 Martín-Doncel E, Rojas AM, Cantarero L, Lazo PA. VRK1 functional insufficiency due to alterations in protein stability or kinase activity of human VRK1 pathogenic variants implicated in neuromotor syndromes. Sci Rep 2019;9:13381. [PMID: 31527692 DOI: 10.1038/s41598-019-49821-7] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
6 Birnbaum R, Markovitch O, Biron-Shental T, Kidron D, Ben-Sira L, Litz Philipsborn S, Reinstein E. Prenatal diagnosis of a likely pathogenic variant in ZBTB18: Natural evolution of fetal phenotype including the long bones and corpus callosum. Am J Med Genet A 2021. [PMID: 34907638 DOI: 10.1002/ajmg.a.62599] [Reference Citation Analysis]
7 De Robertis V, Sen C, Timor-Tritsch I, Chaoui R, Volpe P, Galindo A, Achiron R, Pooh R, Khalil A, Volpe N, D'Antonio F, Birnbaum R. WAPM-World Association of Perinatal Medicine practice guidelines: fetal central nervous system examination. J Perinat Med 2021. [PMID: 34087958 DOI: 10.1515/jpm-2021-0183] [Reference Citation Analysis]
8 Zhang Q, Qin Z, Yi S, Wei H, Zhou XZ, Su J. Clinical application of whole-exome sequencing: A retrospective, single-center study. Exp Ther Med 2021;22:753. [PMID: 34035850 DOI: 10.3892/etm.2021.10185] [Reference Citation Analysis]
9 de Koning MA, Hoffer MJV, Nibbeling EAR, Bijlsma EK, Toirkens MJP, Adama-Scheltema PN, Verweij EJ, Veenhof MB, Santen GWE, Peeters-Scholte CMPCD. Prenatal exome sequencing: A useful tool for the fetal neurologist. Clin Genet 2022;101:65-77. [PMID: 34611884 DOI: 10.1111/cge.14070] [Reference Citation Analysis]
10 Pratt M, Garritty C, Thuku M, Esmaeilisaraji L, Hamel C, Hartley T, Millar K, Skidmore B, Dougan S, Armour CM. Application of exome sequencing for prenatal diagnosis: a rapid scoping review. Genet Med 2020;22:1925-34. [PMID: 32747765 DOI: 10.1038/s41436-020-0918-y] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
11 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]
12 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]
13 Moradi B, Taherian R, Tahmasebpour AR, Sanei Taheri M, Kazemi MA, Pak N, Shirazi M, Radmanesh A, Oztekin O, Arab-Ahmadi M. Fetal corpus callosum abnormalities: Ultrasound and magnetic resonance imaging role. J Clin Ultrasound 2022. [PMID: 35488776 DOI: 10.1002/jcu.23212] [Reference Citation Analysis]
14 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]
15 Sung A, Moretti P, Shaibani A. Adult-Onset Spinal Muscular Atrophy due to Mutations in the VRK1 Gene. Neurol Genet 2021;7:e599. [PMID: 34169149 DOI: 10.1212/NXG.0000000000000599] [Reference Citation Analysis]
16 Blumkin L, Leibovitz Z, Krajden-Haratz K, Arad A, Yosovich K, Gindes L, Zerem A, Ben-Sira L, Lev D, Nissenkorn A, Kidron D, Dobyns WB, Malinger G, Bahi-Buisson N, Leventer RJ, Lerman-Sagie T. Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features. Eur J Paediatr Neurol 2020;26:46-60. [PMID: 32169460 DOI: 10.1016/j.ejpn.2020.03.001] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
17 Leombroni M, Khalil A, Liberati M, D'Antonio F. Fetal midline anomalies: Diagnosis and counselling Part 1: Corpus callosum anomalies. Eur J Paediatr Neurol 2018;22:951-62. [PMID: 30448279 DOI: 10.1016/j.ejpn.2018.08.007] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
18 Stutterd CA, Brock S, Stouffs K, Fanjul-Fernandez M, Lockhart PJ, McGillivray G, Mandelstam S, Pope K, Delatycki MB, Jansen A, Leventer RJ. Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing. Brain Commun 2021;3:fcaa221. [PMID: 33604570 DOI: 10.1093/braincomms/fcaa221] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]