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For: Alkuraya FS. Primordial dwarfism: an update. Curr Opin Endocrinol Diabetes Obes. 2015;22:55-64. [PMID: 25490023 DOI: 10.1097/MED.0000000000000121] [Cited by in Crossref: 17] [Cited by in F6Publishing: 8] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Marakhonov AV, Konovalov FA, Makaov AK, Vasilyeva TA, Kadyshev VV, Galkina VA, Dadali EL, Kutsev SI, Zinchenko RA. Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders. BMC Med Genomics 2018;11:8. [PMID: 29504900 DOI: 10.1186/s12920-018-0326-1] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
2 Wang W, Sun H, Ye Y, Shao Z, Xiao Y. Influence and Effect of Acupoint Application of Chinese Medicine on Height and Bone Age of Children with Short Stature. Evid Based Complement Alternat Med 2021;2021:7459593. [PMID: 34745301 DOI: 10.1155/2021/7459593] [Reference Citation Analysis]
3 Shamseldin HE, Bennett AH, Alfadhel M, Gupta V, Alkuraya FS. GOLGA2, encoding a master regulator of golgi apparatus, is mutated in a patient with a neuromuscular disorder. Hum Genet 2016;135:245-51. [PMID: 26742501 DOI: 10.1007/s00439-015-1632-8] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 2.8] [Reference Citation Analysis]
4 Shaheen R, Abdel-Salam GM, Guy MP, Alomar R, Abdel-Hamid MS, Afifi HH, Ismail SI, Emam BA, Phizicky EM, Alkuraya FS. Mutation in WDR4 impairs tRNA m(7)G46 methylation and causes a distinct form of microcephalic primordial dwarfism. Genome Biol 2015;16:210. [PMID: 26416026 DOI: 10.1186/s13059-015-0779-x] [Cited by in Crossref: 69] [Cited by in F6Publishing: 60] [Article Influence: 9.9] [Reference Citation Analysis]
5 Shaheen R, Hashem A, Abdel-Salam GM, Al-Fadhli F, Ewida N, Alkuraya FS. Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans. Hum Genet 2016;135:1191-7. [PMID: 27503289 DOI: 10.1007/s00439-016-1722-2] [Cited by in Crossref: 23] [Cited by in F6Publishing: 18] [Article Influence: 3.8] [Reference Citation Analysis]
6 Shamseldin H, Alazami AM, Manning M, Hashem A, Caluseiu O, Tabarki B, Esplin E, Schelley S, Innes AM, Parboosingh JS, Lamont R, Majewski J, Bernier FP, Alkuraya FS; Care4Rare Canada Consortium. RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans. Am J Hum Genet 2015;97:862-8. [PMID: 26608784 DOI: 10.1016/j.ajhg.2015.10.012] [Cited by in Crossref: 29] [Cited by in F6Publishing: 27] [Article Influence: 4.1] [Reference Citation Analysis]
7 Bober MB, Jackson AP. Microcephalic Osteodysplastic Primordial Dwarfism, Type II: a Clinical Review. Curr Osteoporos Rep 2017;15:61-9. [PMID: 28409412 DOI: 10.1007/s11914-017-0348-1] [Cited by in Crossref: 32] [Cited by in F6Publishing: 26] [Article Influence: 8.0] [Reference Citation Analysis]
8 Yang LL, Liang SS. Study on pathogenic genes of dwarfism disease by next-generation sequencing. World J Clin Cases 2021; 9(7): 1600-1609 [PMID: 33728303 DOI: 10.12998/wjcc.v9.i7.1600] [Reference Citation Analysis]
9 García-de Teresa B, Hernández-Gómez M, Frías S. DNA Damage as a Driver for Growth Delay: Chromosome Instability Syndromes with Intrauterine Growth Retardation. Biomed Res Int 2017;2017:8193892. [PMID: 29238724 DOI: 10.1155/2017/8193892] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.8] [Reference Citation Analysis]