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For: García-Acero M, Acosta J. Whole-Exome Sequencing Identifies a de novo AHDC1 Mutation in a Colombian Patient with Xia-Gibbs Syndrome. Mol Syndromol 2017;8:308-12. [PMID: 29230160 DOI: 10.1159/000479357] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Gumus E. Extending the phenotype of Xia-Gibbs syndrome in a two-year-old patient with craniosynostosis with a novel de novo AHDC1 missense mutation. European Journal of Medical Genetics 2020;63:103637. [DOI: 10.1016/j.ejmg.2019.03.001] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
2 Wang Q, Huang X, Liu Y, Peng Q, Zhang Y, Liu J, Yuan H. Microdeletion and microduplication of 1p36.11p35.3 involving AHDC1 contribute to neurodevelopmental disorder. European Journal of Medical Genetics 2020;63:103611. [DOI: 10.1016/j.ejmg.2019.01.001] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
3 Cardoso-Dos-Santos AC, Oliveira Silva T, Silveira Faccini A, Woycinck Kowalski T, Bertoli-Avella A, Morales Saute JA, Schuler-Faccini L, de Oliveira Poswar F. Novel AHDC1 Gene Mutation in a Brazilian Individual: Implications of Xia-Gibbs Syndrome. Mol Syndromol 2020;11:24-9. [PMID: 32256298 DOI: 10.1159/000505843] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 Faergeman SL, Bojesen AB, Rasmussen M, Becher N, Andreasen L, Andersen BN, Erbs E, Lildballe DL, Nielsen JEK, Zilmer M, Hammer TB, Andersen MØ, Brasch-Andersen C, Fagerberg CR, Illum NO, Thorup MB, Gregersen PA. Phenotypic heterogeneity and mosaicism in Xia-Gibbs syndrome: Five Danish patients with novel variants in AHDC1. Eur J Med Genet 2021;64:104280. [PMID: 34229113 DOI: 10.1016/j.ejmg.2021.104280] [Reference Citation Analysis]
5 Khayat MM, Hu J, Jiang Y, Li H, Chander V, Dawood M, Hansen AW, Li S, Friedman J, Cross L, Bijlsma EK, Ruivenkamp CAL, Sansbury FH, Innis JW, O'Shea JO, Meng Q, Rosenfeld JA, McWalter K, Wangler MF, Lupski JR, Posey JE, Murdock D, Gibbs RA. AHDC1 missense mutations in Xia-Gibbs syndrome. HGG Adv 2021;2:100049. [PMID: 34950897 DOI: 10.1016/j.xhgg.2021.100049] [Reference Citation Analysis]
6 Khayat MM, Li H, Chander V, Hu J, Hansen AW, Li S, Traynelis J, Shen H, Weissenberger G, Stossi F, Johnson HL, Lupski JR, Posey JE, Sabo A, Meng Q, Murdock DR, Wangler M, Gibbs RA. Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia-Gibbs syndrome. Hum Mutat 2021;42:577-91. [PMID: 33644933 DOI: 10.1002/humu.24190] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
7 Jiang Y, Wangler MF, McGuire AL, Lupski JR, Posey JE, Khayat MM, Murdock DR, Sanchez-Pulido L, Ponting CP, Xia F, Hunter JV, Meng Q, Murugan M, Gibbs RA. The phenotypic spectrum of Xia-Gibbs syndrome. Am J Med Genet A 2018;176:1315-26. [PMID: 29696776 DOI: 10.1002/ajmg.a.38699] [Cited by in Crossref: 23] [Cited by in F6Publishing: 20] [Article Influence: 5.8] [Reference Citation Analysis]
8 Della Vecchia S, Milone R, Cagiano R, Calderoni S, Santocchi E, Pasquariello R, Battini R, Muratori F. Focusing on Autism Spectrum Disorder in Xia-Gibbs Syndrome: Description of a Female with High Functioning Autism and Literature Review. Children (Basel) 2021;8:450. [PMID: 34073322 DOI: 10.3390/children8060450] [Reference Citation Analysis]
9 Cheng X, Tang F, Hu X, Li H, Li M, Fu Y, Yan L, Li Z, Gou P, Su N, Gong C, He W, Xiang R, Bu D, Shen Y. Two Chinese Xia-Gibbs syndrome patients with partial growth hormone deficiency. Mol Genet Genomic Med 2019;7:e00596. [PMID: 30729726 DOI: 10.1002/mgg3.596] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
10 Galliou JM, Kiser JN, Oliver KF, Seabury CM, Moraes JGN, Burns GW, Spencer TE, Dalton J, Neibergs HL. Identification of Loci and Pathways Associated with Heifer Conception Rate in U.S. Holsteins. Genes (Basel) 2020;11:E767. [PMID: 32650431 DOI: 10.3390/genes11070767] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
11 Collier A, Liu A, Torkelson J, Pattison J, Gaddam S, Zhen H, Patel T, McCarthy K, Ghanim H, Oro AE. Gibbin mesodermal regulation patterns epithelial development. Nature 2022. [PMID: 35585237 DOI: 10.1038/s41586-022-04727-9] [Reference Citation Analysis]
12 Murdock DR, Jiang Y, Wangler M, Khayat MM, Sabo A, Juusola J, McWalter K, Schatz KS, Gunay-Aygun M, Gibbs RA. Xia-Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition. Cold Spring Harb Mol Case Stud 2019;5:a003608. [PMID: 30622101 DOI: 10.1101/mcs.a003608] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
13 Goyal C, Naqvi WM, Sahu A, Aujla AS. Xia-Gibbs Syndrome: A Review of Literature. Cureus 2020;12:e12352. [PMID: 33520547 DOI: 10.7759/cureus.12352] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]