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For: Deng H, Xia H, Deng S. Genetic basis of human left-right asymmetry disorders. Expert Rev Mol Med 2015;16:e19. [PMID: 26258520 DOI: 10.1017/erm.2014.22] [Cited by in Crossref: 33] [Cited by in F6Publishing: 27] [Article Influence: 4.7] [Reference Citation Analysis]
Number Citing Articles
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3 Sakamori R, Yamada R, Tahata Y, Kodama T, Hikita H, Tatsumi T, Yamada T, Takehara T. The absence of warfarin treatment and situs inversus are associated with the occurrence of hepatocellular carcinoma after Fontan surgery. J Gastroenterol. [DOI: 10.1007/s00535-021-01842-8] [Reference Citation Analysis]
4 Liu S, Chen W, Zhan Y, Li S, Ma X, Ma D, Sheng W, Huang G. DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome. Sci Rep 2019;9:6683. [PMID: 31040315 DOI: 10.1038/s41598-019-43109-6] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
5 Xiong Y, Xia H, Yuan L, Deng S, Ding Z, Deng H. Identification of compound heterozygous DNAH11 variants in a Han-Chinese family with primary ciliary dyskinesia. J Cell Mol Med 2021;25:9028-37. [PMID: 34405951 DOI: 10.1111/jcmm.16866] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Carrion-Castillo A, Van der Haegen L, Tzourio-Mazoyer N, Kavaklioglu T, Badillo S, Chavent M, Saracco J, Brysbaert M, Fisher SE, Mazoyer B, Francks C. Genome sequencing for rightward hemispheric language dominance. Genes Brain Behav 2019;18:e12572. [PMID: 30950222 DOI: 10.1111/gbb.12572] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.7] [Reference Citation Analysis]
7 Bolkier Y, Barel O, Marek-Yagel D, Atias-Varon D, Kagan M, Vardi A, Mishali D, Katz U, Salem Y, Tirosh-Wagner T, Jacobson JM, Raas-Rothschild A, Chorin O, Eliyahu A, Sarouf Y, Shlomovitz O, Veber A, Shalva N, Javasky E, Ben Moshe Y, Staretz-Chacham O, Rechavi G, Mane S, Anikster Y, Vivante A, Pode-Shakked B. Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects. J Med Genet 2021:jmedgenet-2021-107775. [PMID: 34215651 DOI: 10.1136/jmedgenet-2021-107775] [Reference Citation Analysis]
8 Alsafwani RS, Nasser KK, Shinawi T, Banaganapalli B, ElSokary HA, Zaher ZF, Shaik NA, Abdelmohsen G, Al-Aama JY, Shapiro AJ, O Al-Radi O, Elango R, Alahmadi T. Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects. Front Med (Lausanne) 2021;8:724826. [PMID: 34589502 DOI: 10.3389/fmed.2021.724826] [Reference Citation Analysis]
9 Le Fevre A, Baptista J, Ellard S, Overton T, Oliver A, Gradhand E, Scurr I. Compound heterozygous Pkd1l1 variants in a family with two fetuses affected by heterotaxy and complex Chd. Eur J Med Genet 2020;63:103657. [PMID: 31026592 DOI: 10.1016/j.ejmg.2019.04.014] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
10 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]
11 Pi S, Gong J, Xiao W, Xiao B, Mao X, Long H. The second DDOST-CDG patient with lactose intolerance, developmental delay, and situs inversus totalis. J Hum Genet 2021. [PMID: 34462534 DOI: 10.1038/s10038-021-00974-2] [Reference Citation Analysis]
12 Xia H, Huang X, Deng S, Xu H, Yang Y, Liu X, Yuan L, Deng H. DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease. PLoS One 2021;16:e0252786. [PMID: 34133440 DOI: 10.1371/journal.pone.0252786] [Reference Citation Analysis]
13 Soofi M, Alpert MA, Barbadora J, Mukerji B, Mukerji V. Human Laterality Disorders: Pathogenesis, Clinical Manifestations, Diagnosis, and Management. Am J Med Sci 2021:S0002-9629(21)00190-7. [PMID: 34052215 DOI: 10.1016/j.amjms.2021.05.020] [Reference Citation Analysis]
14 Kleipool RP, Vuurberg G, Stufkens SAS, van der Merwe AE, Oostra RJ. Bilateral symmetry of the subtalar joint facets and the relationship between the morphology and osteoarthritic changes. Clin Anat 2020;33:997-1006. [PMID: 31749217 DOI: 10.1002/ca.23525] [Reference Citation Analysis]
15 Hyland RM, Brody SL. Impact of Motile Ciliopathies on Human Development and Clinical Consequences in the Newborn. Cells 2021;11:125. [PMID: 35011687 DOI: 10.3390/cells11010125] [Reference Citation Analysis]
16 Malik A, Thanekar U, Mourya R, Shivakumar P. Recent developments in etiology and disease modeling of biliary atresia: a narrative review. Dig Med Res 2020;3:59. [PMID: 33615212 DOI: 10.21037/dmr-20-97] [Reference Citation Analysis]
17 Marek‐yagel D, Bolkier Y, Barel O, Vardi A, Mishali D, Katz U, Salem Y, Abudi S, Nayshool O, Kol N, Raas‐rothschild A, Rechavi G, Anikster Y, Pode‐shakked B. A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds. Am J Med Genet 2020;182:987-93. [DOI: 10.1002/ajmg.a.61509] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
18 Hafezi F, Javdani A, Naghibzadeh B, Ashtiani AK. Laterality and Left-sidedness in the Nose, Face, and Body: A New Finding. Plast Reconstr Surg Glob Open 2017;5:e1590. [PMID: 29632770 DOI: 10.1097/GOX.0000000000001590] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Deng S, Wu S, Xia H, Xiong W, Deng X, Liao J, Deng H, Yuan L. Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome. Biosci Rep 2020;40:BSR20192510. [PMID: 32490514 DOI: 10.1042/BSR20192510] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
20 Bieder A, Einarsdottir E, Matsson H, Nilsson HE, Eisfeldt J, Dragomir A, Paucar M, Granberg T, Li TQ, Lindstrand A, Kere J, Tapia-Páez I. Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report. BMC Med Genet 2020;21:87. [PMID: 32357925 DOI: 10.1186/s12881-020-01020-2] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Wang W, Zheng X, Song H, Yang J, Liu X, Wang Y, Zhang M, Zhang Z. Spatial and temporal deletion reveals a latent effect of Megf8 on the left-right patterning and heart development. Differentiation 2020;113:19-25. [PMID: 32203821 DOI: 10.1016/j.diff.2020.03.002] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Antony D, Brunner HG, Schmidts M. Ciliary Dyneins and Dynein Related Ciliopathies. Cells 2021;10:1885. [PMID: 34440654 DOI: 10.3390/cells10081885] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Cho YK, Cho EH, Choi HS, Kim SW. Novel deletion mutation in the glucokinase gene from a korean man with GCK-MODY phenotype and situs inversus. Diabetes Res Clin Pract 2018;143:263-6. [PMID: 30086370 DOI: 10.1016/j.diabres.2018.07.036] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
24 Berauer JP, Mezina AI, Okou DT, Sabo A, Muzny DM, Gibbs RA, Hegde MR, Chopra P, Cutler DJ, Perlmutter DH, Bull LN, Thompson RJ, Loomes KM, Spinner NB, Rajagopalan R, Guthery SL, Moore B, Yandell M, Harpavat S, Magee JC, Kamath BM, Molleston JP, Bezerra JA, Murray KF, Alonso EM, Rosenthal P, Squires RH, Wang KS, Finegold MJ, Russo P, Sherker AH, Sokol RJ, Karpen SJ; Childhood Liver Disease Research Network (ChiLDReN). Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome. Hepatology 2019;70:899-910. [PMID: 30664273 DOI: 10.1002/hep.30515] [Cited by in Crossref: 35] [Cited by in F6Publishing: 29] [Article Influence: 11.7] [Reference Citation Analysis]
25 Vingerhoets G, Gerrits R, Verhelst H. Atypical Brain Asymmetry in Human Situs Inversus: Gut Feeling or Real Evidence? Symmetry 2021;13:695. [DOI: 10.3390/sym13040695] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
26 Shi D, Motamed M, Mejía-Benítez A, Li L, Lin E, Budhram D, Kaur Y, Meyre D. Genetic syndromes with diabetes: A systematic review. Obes Rev 2021;22:e13303. [PMID: 34268868 DOI: 10.1111/obr.13303] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
27 Chen X, Deng S, Xia H, Yuan L, Xu H, Tang S, Deng H. Identification of a CCDC114 variant in a Han-Chinese patient with situs inversus. Exp Ther Med 2020;20:3336-42. [PMID: 32855706 DOI: 10.3892/etm.2020.9059] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
28 Catana A, Apostu AP. The determination factors of left-right asymmetry disorders- a short review. Clujul Med 2017;90:139-46. [PMID: 28559696 DOI: 10.15386/cjmed-701] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
29 Williams K, Carson J, Lo C. Genetics of Congenital Heart Disease. Biomolecules 2019;9:E879. [PMID: 31888141 DOI: 10.3390/biom9120879] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 6.0] [Reference Citation Analysis]
30 Postema MC, Carrion-Castillo A, Fisher SE, Vingerhoets G, Francks C. The genetics of situs inversus without primary ciliary dyskinesia. Sci Rep 2020;10:3677. [PMID: 32111882 DOI: 10.1038/s41598-020-60589-z] [Cited by in Crossref: 12] [Cited by in F6Publishing: 3] [Article Influence: 6.0] [Reference Citation Analysis]
31 Antony D, Gulec Yilmaz E, Gezdirici A, Slagter L, Bakey Z, Bornaun H, Tanidir IC, Van Dinh T, Brunner HG, Walentek P, Arnold SJ, Backofen R, Schmidts M. Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases. Front Genet 2022;13:861236. [DOI: 10.3389/fgene.2022.861236] [Reference Citation Analysis]
32 de Kovel CGF, Francks C. The molecular genetics of hand preference revisited. Sci Rep 2019;9:5986. [PMID: 30980028 DOI: 10.1038/s41598-019-42515-0] [Cited by in Crossref: 38] [Cited by in F6Publishing: 25] [Article Influence: 12.7] [Reference Citation Analysis]
33 Schmitz J, Güntürkün O, Ocklenburg S. Building an Asymmetrical Brain: The Molecular Perspective. Front Psychol 2019;10:982. [PMID: 31133928 DOI: 10.3389/fpsyg.2019.00982] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 4.3] [Reference Citation Analysis]
34 Abdali HA, Duddu JR, Mubarak MJ, Mohamed AS. Rare association of Klippel-Feil syndrome with situs inversus totalis and review of the genetic background. BMJ Case Rep 2021;14:e241906. [PMID: 33980560 DOI: 10.1136/bcr-2021-241906] [Reference Citation Analysis]