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For: Chung B, Shaffer LG, Keating S, Johnson J, Casey B, Chitayat D. From VACTERL-H to heterotaxy: Variable expressivity of ZIC3-related disorders. Am J Med Genet 2011;155:1123-8. [DOI: 10.1002/ajmg.a.33859] [Cited by in Crossref: 39] [Cited by in F6Publishing: 39] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Umaña LA, Magoulas P, Bi W, Bacino CA. A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH). Am J Med Genet A 2011;155A:3071-4. [PMID: 22052692 DOI: 10.1002/ajmg.a.34296] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
2 Mongerson CRL, Jaimes C, Zurakowski D, Jennings RW, Bajic D. Infant Corpus Callosum Size After Surgery and Critical Care for Long-Gap Esophageal Atresia: Qualitative and Quantitative MRI. Sci Rep 2020;10:6408. [PMID: 32286423 DOI: 10.1038/s41598-020-63212-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Puvabanditsin S, Van Gurp J, February M, Khalil M, Mayne J, Ai Mcconnell J, Mehta R. VATER/VACTERL Association and Caudal Regression with Xq25-q27.3 Microdeletion: A Case Report. Fetal and Pediatric Pathology 2016;35:133-41. [DOI: 10.3109/15513815.2016.1139019] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
4 Watanabe N, Tsutsumi S, Miyano Y, Sato H, Nagase S. X-linked VACTERL-H caused by deletion of exon 3 in FANCB: A case report. Congenit Anom (Kyoto) 2018;58:171-2. [PMID: 29232005 DOI: 10.1111/cga.12262] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
5 Cowan J, Tariq M, Ware SM. Genetic and functional analyses of ZIC3 variants in congenital heart disease. Hum Mutat 2014;35:66-75. [PMID: 24123890 DOI: 10.1002/humu.22457] [Cited by in Crossref: 37] [Cited by in F6Publishing: 34] [Article Influence: 4.6] [Reference Citation Analysis]
6 Houtmeyers R, Souopgui J, Tejpar S, Arkell R. The ZIC gene family encodes multi-functional proteins essential for patterning and morphogenesis. Cell Mol Life Sci 2013;70:3791-811. [DOI: 10.1007/s00018-013-1285-5] [Cited by in Crossref: 59] [Cited by in F6Publishing: 56] [Article Influence: 6.6] [Reference Citation Analysis]
7 Chen C, Chang T, Chen Y, Chern S, Su J, Wang W. VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer. Taiwanese Journal of Obstetrics and Gynecology 2013;52:575-9. [DOI: 10.1016/j.tjog.2013.10.022] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
8 Cast AE, Gao C, Amack JD, Ware SM. An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesis. Dev Biol 2012;364:22-31. [PMID: 22285814 DOI: 10.1016/j.ydbio.2012.01.011] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 2.2] [Reference Citation Analysis]
9 Salinas-torres V, Ramos-márquez M, Angulo-castellanos E. Asociación VACTERL-H con agenesia tibial. ¿Expansión del fenotipo clínico? Anales de Pediatría 2013;79:125-7. [DOI: 10.1016/j.anpedi.2012.11.003] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
10 Zeidler C, Woelfle J, Draaken M, Mughal SS, Große G, Hilger AC, Dworschak GC, Boemers TM, Jenetzky E, Zwink N, Lacher M, Schmidt D, Schmiedeke E, Grasshoff-Derr S, Märzheuser S, Holland-Cunz S, Schäfer M, Bartels E, Keppler K, Palta M, Leonhardt J, Kujath C, Rißmann A, Nöthen MM, Reutter H, Ludwig M. Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies. Birth Defects Res A Clin Mol Teratol 2014;100:750-9. [PMID: 25131394 DOI: 10.1002/bdra.23278] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 1.5] [Reference Citation Analysis]
11 Beauregard-Lacroix E, Tardif J, Lemyre E, Kibar Z, Faure C, Campeau PM. Genetic Testing in a Cohort of Complex Esophageal Atresia. Mol Syndromol 2017;8:236-43. [PMID: 28878607 DOI: 10.1159/000477429] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
12 Li S, Liu S, Chen W, Yuan Y, Gu R, Song Y, Li J, Cao Y, Lin Y, Xu J, Wang H, Ma D, Ma X, Sheng W, Huang G. A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease. Sci Rep 2018;8:12386. [PMID: 30120289 DOI: 10.1038/s41598-018-30204-3] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.8] [Reference Citation Analysis]
13 Saisawat P, Kohl S, Hilger AC, Hwang DY, Yung Gee H, Dworschak GC, Tasic V, Pennimpede T, Natarajan S, Sperry E, Matassa DS, Stajić N, Bogdanovic R, de Blaauw I, Marcelis CL, Wijers CH, Bartels E, Schmiedeke E, Schmidt D, Märzheuser S, Grasshoff-Derr S, Holland-Cunz S, Ludwig M, Nöthen MM, Draaken M, Brosens E, Heij H, Tibboel D, Herrmann BG, Solomon BD, de Klein A, van Rooij IA, Esposito F, Reutter HM, Hildebrandt F. Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association. Kidney Int 2014;85:1310-7. [PMID: 24152966 DOI: 10.1038/ki.2013.417] [Cited by in Crossref: 80] [Cited by in F6Publishing: 64] [Article Influence: 8.9] [Reference Citation Analysis]
14 Stevenson RE. Common pathogenesis for sirenomelia, OEIS complex, limb-body wall defect, and other malformations of caudal structures. Am J Med Genet A 2021;185:1379-87. [PMID: 33522143 DOI: 10.1002/ajmg.a.62103] [Reference Citation Analysis]
15 Solomon BD, Baker LA, Bear KA, Cunningham BK, Giampietro PF, Hadigan C, Hadley DW, Harrison S, Levitt MA, Niforatos N. An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association. J Pediatr. 2014;164:451-457.e1. [PMID: 24332453 DOI: 10.1016/j.jpeds.2013.10.086] [Cited by in Crossref: 46] [Cited by in F6Publishing: 31] [Article Influence: 5.1] [Reference Citation Analysis]
16 Odaka YS, Tohmonda T, Toyoda A, Aruga J. An Evolutionarily Conserved Mesodermal Enhancer in Vertebrate Zic3. Sci Rep 2018;8:14954. [PMID: 30297839 DOI: 10.1038/s41598-018-33235-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
17 Rudisill SS, Wang JT, Jaimes C, Mongerson CRL, Hansen AR, Jennings RW, Bajic D. Neurologic Injury and Brain Growth in the Setting of Long-Gap Esophageal Atresia Perioperative Critical Care: A Pilot Study. Brain Sci 2019;9:E383. [PMID: 31861169 DOI: 10.3390/brainsci9120383] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
18 Nakamura Y, Kikugawa S, Seki S, Takahata M, Iwasaki N, Terai H, Matsubara M, Fujioka F, Inagaki H, Kobayashi T, Kimura T, Kurahashi H, Kato H. PCSK5 mutation in a patient with the VACTERL association. BMC Res Notes 2015;8:228. [PMID: 26055999 DOI: 10.1186/s13104-015-1166-0] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 1.4] [Reference Citation Analysis]
19 Lubinsky M. The VACTERL Association as a disturbance of cell fate determination: Lubinsky VACTERL and Cell Fate. Am J Med Genet 2015;167:2582-8. [DOI: 10.1002/ajmg.a.37238] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
20 Winberg J, Gustavsson P, Papadogiannakis N, Sahlin E, Bradley F, Nordenskjöld E, Svensson PJ, Annerén G, Iwarsson E, Nordgren A, Nordenskjöld A. Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association. PLoS One 2014;9:e85313. [PMID: 24416387 DOI: 10.1371/journal.pone.0085313] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 2.6] [Reference Citation Analysis]
21 Ware SM, Jefferies JL. New Genetic Insights into Congenital Heart Disease. J Clin Exp Cardiolog 2012;S8:003. [PMID: 22822471 DOI: 10.4172/2155-9880.S8-003] [Cited by in Crossref: 7] [Cited by in F6Publishing: 18] [Article Influence: 0.7] [Reference Citation Analysis]
22 Sadler TW. Is VACTERL a laterality defect? Am J Med Genet 2015;167:2563-5. [DOI: 10.1002/ajmg.a.37234] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
23 Hilger AC, Halbritter J, Pennimpede T, van der Ven A, Sarma G, Braun DA, Porath JD, Kohl S, Hwang DY, Dworschak GC, Hermann BG, Pavlova A, El-Maarri O, Nöthen MM, Ludwig M, Reutter H, Hildebrandt F. Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association. Hum Mutat 2015;36:1150-4. [PMID: 26294094 DOI: 10.1002/humu.22859] [Cited by in Crossref: 34] [Cited by in F6Publishing: 28] [Article Influence: 4.9] [Reference Citation Analysis]
24 Galarreta CI, Vaida F, Bird LM. Patterns of malformation associated with esophageal atresia/tracheoesophageal fistula: A retrospective single center study. Am J Med Genet A 2020;182:1351-63. [PMID: 32250545 DOI: 10.1002/ajmg.a.61582] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
25 Haaning AM, Quinn ME, Ware SM. Heterotaxy-spectrum heart defects in Zic3 hypomorphic mice. Pediatr Res 2013;74:494-502. [PMID: 23999067 DOI: 10.1038/pr.2013.147] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.0] [Reference Citation Analysis]
26 Francis RJ, Christopher A, Devine WA, Ostrowski L, Lo C. Congenital heart disease and the specification of left-right asymmetry. Am J Physiol Heart Circ Physiol 2012;302:H2102-11. [PMID: 22408017 DOI: 10.1152/ajpheart.01118.2011] [Cited by in Crossref: 33] [Cited by in F6Publishing: 26] [Article Influence: 3.3] [Reference Citation Analysis]
27 Chen Y, Liu Z, Chen J, Zuo Y, Liu S, Chen W, Liu G, Qiu G, Giampietro PF, Wu N, Wu Z. The genetic landscape and clinical implications of vertebral anomalies in VACTERL association. J Med Genet 2016;53:431-7. [PMID: 27084730 DOI: 10.1136/jmedgenet-2015-103554] [Cited by in Crossref: 29] [Cited by in F6Publishing: 18] [Article Influence: 4.8] [Reference Citation Analysis]
28 Santos J, Nogueira R, Pinto R, Cerveira I, Pereira S. First Trimester Diagnosis of VACTERL Association. Clin Pract 2013;3:e5. [PMID: 24765498 DOI: 10.4081/cp.2013.e5] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
29 Xu G, Zhou Q, Zhang M, Pu D, Ouyang Z. TACRD and VACTERL associations in a fetus: Case report and review of the literature. International Journal of Pediatric Otorhinolaryngology 2013;77:2081-5. [DOI: 10.1016/j.ijporl.2013.09.016] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
30 Bellchambers HM, Ware SM. ZIC3 in Heterotaxy. Adv Exp Med Biol 2018;1046:301-27. [PMID: 29442328 DOI: 10.1007/978-981-10-7311-3_15] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
31 Pugnaloni F, Digilio MC, Putotto C, De Luca E, Marino B, Versacci P. Genetics of atrioventricular canal defects. Ital J Pediatr 2020;46:61. [PMID: 32404184 DOI: 10.1186/s13052-020-00825-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
32 Stevenson RE, Hunter AG. Considering the Embryopathogenesis of VACTERL Association. Mol Syndromol 2013;4:7-15. [PMID: 23653571 DOI: 10.1159/000346192] [Cited by in Crossref: 36] [Cited by in F6Publishing: 29] [Article Influence: 4.0] [Reference Citation Analysis]
33 Solomon BD, Bear KA, Kimonis V, de Klein A, Scott DA, Shaw-Smith C, Tibboel D, Reutter H, Giampietro PF. Clinical geneticists' views of VACTERL/VATER association. Am J Med Genet A 2012;158A:3087-100. [PMID: 23165726 DOI: 10.1002/ajmg.a.35638] [Cited by in Crossref: 50] [Cited by in F6Publishing: 40] [Article Influence: 5.0] [Reference Citation Analysis]
34 Brosens E, Eussen H, van Bever Y, van der Helm RM, Ijsselstijn H, Zaveri HP, Wijnen R, Scott DA, Tibboel D, de Klein A. VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations. Mol Syndromol 2013;4:20-6. [PMID: 23653573 DOI: 10.1159/000345577] [Cited by in Crossref: 1] [Cited by in F6Publishing: 12] [Article Influence: 0.1] [Reference Citation Analysis]
35 Reutter H, Ludwig M. VATER/VACTERL Association: Evidence for the Role of Genetic Factors. Mol Syndromol 2013;4:16-9. [PMID: 23653572 DOI: 10.1159/000345300] [Cited by in F6Publishing: 13] [Reference Citation Analysis]
36 Serra A, Eirich K, Winkler AK, Mrasek K, Göhring G, Barbi G, Cario H, Schlegelberger B, Pokora B, Liehr T, Leriche C, Henne-Bruns D, Barth TF, Schindler D. Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia. Mol Syndromol 2012;3:120-30. [PMID: 23112754 DOI: 10.1159/000341935] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 1.2] [Reference Citation Analysis]
37 Al-Qattan MM. The Classification of VACTERL Association into 3 Groups According to the Limb Defect. Plast Reconstr Surg Glob Open 2021;9:e3360. [PMID: 33680640 DOI: 10.1097/GOX.0000000000003360] [Reference Citation Analysis]
38 Solomon BD. The etiology of VACTERL association: Current knowledge and hypotheses. Am J Med Genet 2018;178:440-6. [DOI: 10.1002/ajmg.c.31664] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 5.3] [Reference Citation Analysis]
39 Chen CP, Shih JC, Huang MC, Liu YP, Su JW, Chern SR, Wang W. Prenatal ultrasound demonstration of scoliosis, absence of one rib, a radial club hand, congenital heart defects and absent stomach in a fetus with VACTERL association. Taiwan J Obstet Gynecol 2012;51:139-42. [PMID: 22482989 DOI: 10.1016/j.tjog.2012.01.031] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]