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For: Splitt MP, Burn J, Goodship J. Defects in the determination of left-right asymmetry. J Med Genet 1996;33:498-503. [PMID: 8782051 DOI: 10.1136/jmg.33.6.498] [Cited by in Crossref: 58] [Cited by in F6Publishing: 41] [Article Influence: 2.3] [Reference Citation Analysis]
Number Citing Articles
1 Schlueter J, Brand T. Left-right axis development: examples of similar and divergent strategies to generate asymmetric morphogenesis in chick and mouse embryos. Cytogenet Genome Res 2007;117:256-67. [PMID: 17675867 DOI: 10.1159/000103187] [Cited by in Crossref: 31] [Cited by in F6Publishing: 23] [Article Influence: 2.2] [Reference Citation Analysis]
2 Gaba RC, Carlos RC, Weadock WJ, Reddy GP, Sneider MB, Cascade PN. Cardiovascular MR Imaging: Technique Optimization and Detection of Disease in Clinical Practice. RadioGraphics 2002;22:e6-e6. [DOI: 10.1148/rg.e6] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
3 Tubbs RS, Wellons JC 3rd, Oakes WJ. Split cord malformation and situs inversus totalis: case report and review of the literature. Childs Nerv Syst 2004;20:131-4. [PMID: 14648098 DOI: 10.1007/s00381-003-0857-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
4 Bader RS, Punn R, Silverman NH. Evaluation of Risk Factors for Prediction of Outcome in Fetal Spectrum of Atrioventricular Septal Defects: Atrioventricular Septal Defects in Fetuses. Congenit Heart Dis 2014;9:286-93. [DOI: 10.1111/chd.12136] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
5 Ryan AK, Blumberg B, Rodriguez-esteban C, Yonei-tamura S, Tamura K, Tsukui T, de la Peña J, Sabbagh W, Greenwald J, Choe S, Norris DP, Robertson EJ, Evans RM, Rosenfeld MG, Belmonte JCI. Pitx2 determines left–right asymmetry of internal organs in vertebrates. Nature 1998;394:545-51. [DOI: 10.1038/29004] [Cited by in Crossref: 375] [Cited by in F6Publishing: 348] [Article Influence: 16.3] [Reference Citation Analysis]
6 Morgan D, Turnpenny L, Goodship J, Dai W, Majumder K, Matthews L, Gardner A, Schuster G, Vien L, Harrison W, Elder FF, Penman-splitt M, Overbeek P, Strachan T. Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse. Nat Genet 1998;20:149-56. [DOI: 10.1038/2450] [Cited by in Crossref: 184] [Cited by in F6Publishing: 163] [Article Influence: 8.0] [Reference Citation Analysis]
7 Cramer N, Coombs C. Left-Sided Appendicitis: More Than Meets the Eye. Pediatr Emerg Care 2021;37:e275-6. [PMID: 30211839 DOI: 10.1097/PEC.0000000000001614] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Beltrami M, Fornaciari G, Conigliaro R, Sassatelli R, Garavelli L, Margini F. Biliary obstruction caused by portal cavernoma in a patient with laterality sequence. J Hepatol 1997;26:1427-8. [PMID: 9210636 DOI: 10.1016/s0168-8278(97)80484-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
9 Aylsworth AS. Clinical aspects of defects in the determination of laterality. Am J Med Genet 2001;101:345-55. [DOI: 10.1002/ajmg.1219] [Cited by in Crossref: 104] [Cited by in F6Publishing: 55] [Article Influence: 5.2] [Reference Citation Analysis]
10 Langford K, Sharland G, Simpson J. Relative risk of abnormal karyotype in fetuses found to have an atrioventricular septal defect (AVSD) on fetal echocardiography. Prenat Diagn 2005;25:137-9. [DOI: 10.1002/pd.1037] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 0.8] [Reference Citation Analysis]
11 Kamath B, Chatterjee AS, Chandorkar I. Splenic Injury in Situs Inversus Totalis - A Surgical Challenge. J Clin Diagn Res 2015;9:PD01-2. [PMID: 26155517 DOI: 10.7860/JCDR/2015/13376.5871] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
12 Seymour R, Sundberg JP, Hogenesch H. Abnormal lymphoid organ development in immunodeficient mutant mice. Vet Pathol. 2006;43:401-423. [PMID: 16846982 DOI: 10.1354/vp.43-4-401] [Cited by in Crossref: 37] [Cited by in F6Publishing: 32] [Article Influence: 2.5] [Reference Citation Analysis]
13 Brennan P, Young ID. Congenital heart malformations: aetiology and associations. Semin Neonatol 2001;6:17-25. [PMID: 11162282 DOI: 10.1053/siny.2000.0032] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 0.7] [Reference Citation Analysis]
14 Maclean K, Dunwoodie S. Breaking symmetry: a clinical overview of left-right patterning: Clinical overview of left-right patterning. Clinical Genetics 2004;65:441-57. [DOI: 10.1111/j.0009-9163.2004.00258.x] [Cited by in Crossref: 25] [Cited by in F6Publishing: 20] [Article Influence: 1.5] [Reference Citation Analysis]
15 Splitt M, Wright C, Sen D, Goodship J. Left-isomerism sequence and maternal type-1 diabetes. Lancet 1999;354:305-6. [PMID: 10440314 DOI: 10.1016/S0140-6736(99)01942-X] [Cited by in Crossref: 13] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
16 Tsung A, Feliz A, Kane TD. Laparoscopic Nissen fundoplication in an infant with situs inversus. J Laparoendosc Adv Surg Tech A 2007;17:698-700. [PMID: 17907992 DOI: 10.1089/lap.2006.0244] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.1] [Reference Citation Analysis]
17 Manning N, Archer N. A study to determine the incidence of structural congenital heart disease in monochorionic twins. Prenat Diagn 2006;26:1062-4. [PMID: 16958142 DOI: 10.1002/pd.1556] [Cited by in Crossref: 38] [Cited by in F6Publishing: 29] [Article Influence: 2.7] [Reference Citation Analysis]
18 Bittmann S, Ulus H, Springer A. Combined pentalogy of cantrell with tetralogy of fallot, gallbladder agenesis, and polysplenia: a case report. Journal of Pediatric Surgery 2004;39:107-9. [DOI: 10.1016/j.jpedsurg.2003.09.030] [Cited by in Crossref: 24] [Cited by in F6Publishing: 11] [Article Influence: 1.4] [Reference Citation Analysis]
19 Li-ling J. Connections between traditional Chinese medicine and congenital syndromes. Am J Med Genet 2001;103:257-62. [DOI: 10.1002/ajmg.1562] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
20 Macafee DA, Armstrong D, Hall RI, Dhingsa R, Zaitoun AM, Lobo DN. Pancreaticoduodenectomy with a "twist": the challenges of pancreatic resection in the presence of situs inversus totalis and situs ambiguus. Eur J Surg Oncol 2007;33:524-7. [PMID: 17081721 DOI: 10.1016/j.ejso.2006.09.029] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
21 Peeters H, Debeer P, Groenen P, Van Esch H, Vanderlinden G, Eyskens B, Mertens L, Gewillig M, Van de Ven W, Fryns J, Devriendt K. Recurrent involvement of chromosomal region 6q21 in heterotaxy. Am J Med Genet 2001;103:44-7. [DOI: 10.1002/ajmg.1499] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
22 Uemura S, Maeda H, Munekage M, Yoshioka R, Okabayashi T, Hanazaki K. Hepatic resection for metastatic colon cancer in patients with situs inversus totalis complicated by multiple anomalies of the hepatobiliary system: the first case report. J Gastrointest Surg 2009;13:1724-7. [PMID: 19415395 DOI: 10.1007/s11605-009-0909-4] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
23 Supp D, Brueckner M, Kuehn M, Witte D, Lowe L, Mcgrath J, Corrales J, Potter S. Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries. Development 1999;126:5495-504. [DOI: 10.1242/dev.126.23.5495] [Cited by in Crossref: 95] [Cited by in F6Publishing: 62] [Article Influence: 4.3] [Reference Citation Analysis]
24 Bonneau D, Mar�chaud M, Odent S, Piegay I, Godard A, Amati P. Heterotaxy-neural tube defect and holoprosencephaly occurring independently in two sib fetuses. Am J Med Genet 1999;84:373-6. [DOI: 10.1002/(sici)1096-8628(19990604)84:4<373::aid-ajmg13>3.0.co;2-8] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 0.3] [Reference Citation Analysis]
25 Han Y, Liu TT, Qiu XS, Li QC, Zhao Y, Pang XY, Wang EH. PEComa of the uterus with coexistence of situs inversus totalis, a case report and literature review. Diagn Pathol 2015;10:142. [PMID: 26268324 DOI: 10.1186/s13000-015-0351-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
26 Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B. Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2. Am J Med Genet A 2005;134A:158-64. [PMID: 15669097 DOI: 10.1002/ajmg.a.30587] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 0.8] [Reference Citation Analysis]
27 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: 3.9] [Reference Citation Analysis]
28 Tubbs RS, Wellons JC 3rd, Oakes WJ. Split cord malformation and situs inversus totalis: case report and review of the literature. Childs Nerv Syst 2005;21:161-4. [PMID: 14745579 DOI: 10.1007/s00381-003-0895-x] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
29 Meeks M, Walne A, Spiden S, Simpson H, Mussaffi-Georgy H, Hamam HD, Fehaid EL, Cheehab M, Al-Dabbagh M, Polak-Charcon S, Blau H, O'Rawe A, Mitchison HM, Gardiner RM, Chung E. A locus for primary ciliary dyskinesia maps to chromosome 19q. J Med Genet 2000;37:241-4. [PMID: 10745040 DOI: 10.1136/jmg.37.4.241] [Cited by in Crossref: 40] [Cited by in F6Publishing: 34] [Article Influence: 1.9] [Reference Citation Analysis]
30 Nelson MJ, Pesola GR. Left lower quadrant pain of unusual cause. J Emerg Med. 2001;20:241-245. [PMID: 11267811 DOI: 10.1016/s0736-4679(00)00316-4] [Cited by in Crossref: 30] [Cited by in F6Publishing: 10] [Article Influence: 1.5] [Reference Citation Analysis]
31 Bartram U, Wirbelauer J, Speer CP. Heterotaxy syndrome -- asplenia and polysplenia as indicators of visceral malposition and complex congenital heart disease. Biol Neonate 2005;88:278-90. [PMID: 16113522 DOI: 10.1159/000087625] [Cited by in Crossref: 77] [Cited by in F6Publishing: 47] [Article Influence: 4.8] [Reference Citation Analysis]
32 Springer S, Mlczoch E, Krampl-bettelheim E, Mailáth-pokorny M, Ulm B, Worda C, Worda K. Congenital heart disease in monochorionic twins with and without twin-to-twin transfusion syndrome: Congenital heart disease in twin pregnancies. Prenat Diagn 2014;34:994-9. [DOI: 10.1002/pd.4411] [Cited by in Crossref: 17] [Cited by in F6Publishing: 11] [Article Influence: 2.4] [Reference Citation Analysis]
33 Capdevila I, Izpisúa Belmonte JC. Knowing left from right: the molecular basis of laterality defects. Mol Med Today 2000;6:112-8. [PMID: 10689314 DOI: 10.1016/s1357-4310(00)01671-3] [Cited by in Crossref: 13] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
34 Lin AE, Ticho BS, Houde K, Westgate M, Holmes LB. Heterotaxy: Associated conditions and hospital-based prevalence in newborns. Genet Med 2000;2:157-72. [DOI: 10.1097/00125817-200005000-00002] [Cited by in Crossref: 106] [Cited by in F6Publishing: 83] [Article Influence: 5.0] [Reference Citation Analysis]
35 Li-ling J. The Jing-Mai connections of the Heart. International Journal of Cardiology 2003;89:1-11. [DOI: 10.1016/s0167-5273(02)00426-6] [Cited by in Crossref: 5] [Article Influence: 0.3] [Reference Citation Analysis]
36 Schidlow DV. Primary ciliary dyskinesia (the immotile cilia syndrome). Ann Allergy 1994;73:457-68; quiz 468-70. [PMID: 7998657 DOI: 10.1016/b978-0-323-01909-5.50015-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 10] [Article Influence: 0.0] [Reference Citation Analysis]
37 Wu CS, Lu YF, Liu YH, Huang CJ, Hwang SL. Zebrafish Cdx1b modulates epithalamic asymmetry by regulating ndr2 and lft1 expression. Dev Biol 2021;470:21-36. [PMID: 33197427 DOI: 10.1016/j.ydbio.2020.11.001] [Reference Citation Analysis]
38 Marino B, Digilio MC, Giannotti A, Dallapiccola B. Heterotaxia syndromes and 22q11 deletion. J Med Genet 1996;33:1052. [PMID: 9004146 DOI: 10.1136/jmg.33.12.1052] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.3] [Reference Citation Analysis]
39 Manning N. The influence of twinning on cardiac development. Early Human Development 2008;84:173-9. [DOI: 10.1016/j.earlhumdev.2008.01.009] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 1.9] [Reference Citation Analysis]
40 Ticho BS, Goldstein AM, Van Praagh R. Extracardiac anomalies in the heterotaxy syndromes with focus on anomalies of midline-associated structures. The American Journal of Cardiology 2000;85:729-34. [DOI: 10.1016/s0002-9149(99)00849-8] [Cited by in Crossref: 78] [Cited by in F6Publishing: 18] [Article Influence: 3.7] [Reference Citation Analysis]
41 Kayhan A, Lakadamyali H, Oommen J, Oto A. Polysplenia syndrome accompanied with situs inversus totalis and annular pancreas in an elderly patient. Clin Imaging 2010;34:472-5. [PMID: 21092879 DOI: 10.1016/j.clinimag.2009.11.011] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]