BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Alhamoudi KM, Bhat J, Nashabat M, Alharbi M, Alyafee Y, Asiri A, Umair M, Alfadhel M. A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Front Pediatr 2020;8:71. [PMID: 32175296 DOI: 10.3389/fped.2020.00071] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
Number Citing Articles
1 Alyafee Y, Al Tuwaijri A, Umair M, Alharbi M, Haddad S, Ballow M, Alayyar L, Alam Q, Althenayyan S, Al Ghilan N, Al Khaldi A, Faden MS, Al Sufyan H, Alfadhel M. Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach. Front Genet 2022;13. [DOI: 10.3389/fgene.2022.1047474] [Reference Citation Analysis]
2 Al Hawsawi K, Al Jabri M, Dajam MS, Almahdi B, Alhawsawi WK, Abbas S, Al Tuwaijri A, Umair M, Alfadhel M, Al-khenaizan S. Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles. Front Genet 2022;13:994509. [DOI: 10.3389/fgene.2022.994509] [Reference Citation Analysis]
3 Mackowetzky K, Dicipulo R, Fox SC, Philibert DA, Todesco H, Doshi JD, Kawakami K, Tierney K, Waskiewicz AJ. Retinoic acid signaling regulates late stages of semicircular canal morphogenesis and otolith maintenance in the zebrafish inner ear. Dev Dyn 2022. [PMID: 35710880 DOI: 10.1002/dvdy.510] [Reference Citation Analysis]
4 Duenser A, Singh P, Lecaudey LA, Sturmbauer C, Albertson C, Gessl W, Ahi EP. Parallel molecular mechanisms underlie convergent evolution of the exaggerated snout phenotype in East African cichlids.. [DOI: 10.1101/2022.01.13.476207] [Reference Citation Analysis]
5 Vymětal J, Jakubec D, Galgonek J, Vondrášek J. Amino Acid Interactions (INTAA) web server v2.0: a single service for computation of energetics and conservation in biomolecular 3D structures. Nucleic Acids Res 2021;49:W15-20. [PMID: 34019656 DOI: 10.1093/nar/gkab377] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
6 Anderson LM, Fox DB, Chesney KL, Coates JR, Torres BT, Lyons LA. Skeletal Manifestations of Heritable Disproportionate Dwarfism in Cats as Determined by Radiography and Magnetic Resonance Imaging. Vet Comp Orthop Traumatol 2021. [PMID: 34082456 DOI: 10.1055/s-0041-1730355] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Alfadhel M, Umair M, Almuzzaini B, Asiri A, Al Tuwaijri A, Alhamoudi K, Alyafee Y, Al-Owain M. Identification of the TTC26 Splice Variant in a Novel Complex Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations. Mol Syndromol 2021;12:133-40. [PMID: 34177428 DOI: 10.1159/000513829] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
8 Buckley RM, Davis BW, Brashear WA, Farias FHG, Kuroki K, Graves T, Hillier LW, Kremitzki M, Li G, Middleton RP, Minx P, Tomlinson C, Lyons LA, Murphy WJ, Warren WC. A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism. PLoS Genet 2020;16:e1008926. [PMID: 33090996 DOI: 10.1371/journal.pgen.1008926] [Cited by in Crossref: 39] [Cited by in F6Publishing: 44] [Article Influence: 19.5] [Reference Citation Analysis]
9 Zimmer BM, Barycki JJ, Simpson MA. Integration of Sugar Metabolism and Proteoglycan Synthesis by UDP-glucose Dehydrogenase. J Histochem Cytochem 2021;69:13-23. [PMID: 32749901 DOI: 10.1369/0022155420947500] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 5.5] [Reference Citation Analysis]