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Cited by in F6Publishing
For: Kibe T, Mori Y, Okanishi T, Shimojima K, Yokochi K, Yamamoto T. Two concurrent chromosomal aberrations involving interstitial deletion in 1q24.2q25.2 and inverted duplication and deletion in 10q26 in a patient with stroke associated with antithrombin deficiency and a patent foramen ovale. Am J Med Genet A. 2011;155A:215-220. [PMID: 21204235 DOI: 10.1002/ajmg.a.33786] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 1.2] [Reference Citation Analysis]
Number Citing Articles
1 Shimojima K, Okanishi T, Yamamoto T. Marfanoid hypermobility caused by an 862 kb deletion of Xq22.3 in a patient with Sotos syndrome. Am J Med Genet 2011;155:2293-7. [DOI: 10.1002/ajmg.a.34164] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
2 Al-Sarraj Y, Al-Khair HA, Taha RZ, Khattab N, El Sayed ZH, Elhusein B, El-Shanti H. Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 - qter, autism spectrum disorder and unusual features. Clin Case Rep 2014;2:201-5. [PMID: 25614812 DOI: 10.1002/ccr3.94] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 0.9] [Reference Citation Analysis]
3 Yamamoto T, Shimada S, Shimojima K. Fiber-fluorescence in situ hybridization analyses as a diagnostic application for orientation of microduplications. World J Med Genet 2013; 3(2): 5-8 [DOI: 10.5496/wjmg.v3.i2.5] [Reference Citation Analysis]
4 Lam F, Morris C. Nine year old boy with chromosome 1q23.3-q25.1 deletion. Am J Med Genet A 2016;170:3013-7. [PMID: 27416976 DOI: 10.1002/ajmg.a.37843] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
5 Takahashi I, Takahashi T, Sawada K, Shimojima K, Yamamoto T. Jacobsen syndrome due to an unbalanced translocation between 11q23 and 22q11.2 identified at age 40 years. Am J Med Genet 2012;158A:220-3. [DOI: 10.1002/ajmg.a.34382] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
6 Tucker T, Steinraths M, Oh T, Nelson TN, Van Allen MI, Brown L, Schlade-bartusiak K. Incidental finding of paternal UPD15 in a child with a deletion of 11q21–q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features. Clinical Dysmorphology 2016;25:77-81. [DOI: 10.1097/mcd.0000000000000108] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
7 Burkardt DD, Rosenfeld JA, Helgeson ML, Angle B, Banks V, Smith WE, Gripp KW, Moline J, Moran RT, Niyazov DM, Stevens CA, Zackai E, Lebel RR, Ashley DG, Kramer N, Lachman RS, Graham JM Jr. Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25. Am J Med Genet A 2011;155A:1336-51. [PMID: 21548129 DOI: 10.1002/ajmg.a.34049] [Cited by in Crossref: 31] [Cited by in F6Publishing: 29] [Article Influence: 2.8] [Reference Citation Analysis]
8 Shimada S, Okamoto N, Nomura S, Fukui M, Shimakawa S, Sangu N, Shimojima K, Osawa M, Yamamoto T. Microdeletions of 5.5 Mb (4q13.2-q13.3) and 4.1 Mb (7p15.3-p21.1) associated with a saethre-chotzen-like phenotype, severe intellectual disability, and autism. Am J Med Genet A 2013;161A:2078-83. [PMID: 23825006 DOI: 10.1002/ajmg.a.36027] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
9 Cole JW, Adigun T, Akinyemi R, Akpa OM, Bell S, Chen B, Jimenez Conde J, Lazcano Dobao U, Fernandez I, Fornage M, Gallego-Fabrega C, Jern C, Krawczak M, Lindgren A, Markus HS, Melander O, Owolabi M, Schlicht K, Söderholm M, Srinivasasainagendra V, Soriano Tárraga C, Stenman M, Tiwari H, Corasaniti M, Fecteau N, Guizzardi B, Lopez H, Nguyen K, Gaynor B, O'Connor T, Stine OC, Kittner SJ, McArdle P, Mitchell BD, Xu H, Grond-Ginsbach C. The copy number variation and stroke (CaNVAS) risk and outcome study. PLoS One 2021;16:e0248791. [PMID: 33872305 DOI: 10.1371/journal.pone.0248791] [Reference Citation Analysis]
10 Chen C, Chen M, Su Y, Huang J, Ma G, Chang S, Chern S, Chen Y, Su J, Lee C, Town D, Wang W. Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. Taiwanese Journal of Obstetrics and Gynecology 2012;51:245-52. [DOI: 10.1016/j.tjog.2012.04.015] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
11 Grond-Ginsbach C, Erhart P, Chen B, Kloss M, Engelter ST, Cole JW. Copy Number Variation and Risk of Stroke. Stroke 2018;49:2549-54. [PMID: 30355123 DOI: 10.1161/STROKEAHA.118.020371] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
12 Akopyan HR, Kushniruk VO, Mykytenko DO, Huleuk NL, Kremenskaya Y, Lukash LL. Chromosomal DNA balance in human stem cell line 4BL. Cytol Genet 2016;50:257-66. [DOI: 10.3103/s0095452716040022] [Reference Citation Analysis]
13 Fiorio P, Rosaia De Santis L, Cuoco C, Gimelli G, Gastaldi R, Bonatti F, Ravazzolo R, Bocciardi R. Hypogonadotropic hypogonadism in a trisomy X carrier: phenotype description and genotype correlation. Gynecol Endocrinol 2016;32:14-7. [PMID: 26572316 DOI: 10.3109/09513590.2015.1106472] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
14 Xiao B, Ji X, Xing Y, Jiang WT, Zhang JM, Tao J. Inverted Duplication and Deletion of 10q25q26 in a Patient without Any Obvious Skeletal Anomalies. Mol Syndromol 2012;3:185-9. [PMID: 23239961 DOI: 10.1159/000343047] [Reference Citation Analysis]
15 Wang J, Wang Y, Wang L, Chen WY, Sheng M. The diagnostic yield of intellectual disability: combined whole genome low-coverage sequencing and medical exome sequencing. BMC Med Genomics 2020;13:70. [PMID: 32429945 DOI: 10.1186/s12920-020-0726-x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]