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Cited by in F6Publishing
For: Jean F, Stuart A, Tarailo-Graovac M. Dissecting the Genetic and Etiological Causes of Primary Microcephaly. Front Neurol 2020;11:570830. [PMID: 33178111 DOI: 10.3389/fneur.2020.570830] [Cited by in Crossref: 10] [Cited by in F6Publishing: 23] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Wang L, Park JY, Liu F, Olesen KM, Hou S, Peng JC, Infield J, Levesque AC, Wang YD, Jin H, Fan Y, Connelly PJ, Pruett-Miller SM, Hu MG, Hinds PW, Han YG. A kinase-independent function of cyclin-dependent kinase 6 promotes outer radial glia expansion and neocortical folding. Proc Natl Acad Sci U S A 2022;119:e2206147119. [PMID: 36095192 DOI: 10.1073/pnas.2206147119] [Reference Citation Analysis]
2 Wang Y, Zong W, Sun W, Chen C, Wang Z, Li T. The Central Domain of MCPH1 Controls Development of the Cerebral Cortex and Gonads in Mice. Cells 2022;11:2715. [DOI: 10.3390/cells11172715] [Reference Citation Analysis]
3 Apridita Sebastian W, Shiraishi H, Shimizu N, Umeda R, Lai S, Ikeuchi M, Morisaki I, Yano S, Yoshimura A, Hanada R, Hanada T. Ankle2 deficiency-associated microcephaly and spermatogenesis defects in zebrafish are alleviated by heterozygous deletion of vrk1. Biochemical and Biophysical Research Communications 2022. [DOI: 10.1016/j.bbrc.2022.07.070] [Reference Citation Analysis]
4 Bolat H, Sağer SG, Türkyılmaz A, Çebi AH, Akın Y, Onay H, Özkınay F, Ünsel-bolat G. Autosomal Recessive Primary Microcephaly (MCPH) and Novel Pathogenic Variants in <b><i>ASPM</i></b> and <b><i>WDR62</i></b> Genes. Mol Syndromol. [DOI: 10.1159/000524391] [Reference Citation Analysis]
5 Yadav N, Kirola L, Geetha TS, Mittal K, Kadandale J, Yogev Y, Birk OS, Gupta N, Balakrishnan P, Jana M, Gupta M, Kabra M, Thelma BK. A novel leaky splice variant in centromere protein J (CENPJ)-associated Seckel syndrome. Ann Hum Genet 2022. [PMID: 35451063 DOI: 10.1111/ahg.12469] [Reference Citation Analysis]
6 Komarasamy TV, Adnan NAA, James W, Balasubramaniam VRMT. Zika Virus Neuropathogenesis: The Different Brain Cells, Host Factors and Mechanisms Involved. Front Immunol 2022;13:773191. [PMID: 35371036 DOI: 10.3389/fimmu.2022.773191] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Lafita-Navarro MC, Conacci-Sorrell M. Nucleolar stress: From development to cancer. Semin Cell Dev Biol 2022:S1084-9521(22)00126-4. [PMID: 35410715 DOI: 10.1016/j.semcdb.2022.04.001] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Schuler-Faccini L, Del Campo M, García-Alix A, Ventura LO, Boquett JA, van der Linden V, Pessoa A, van der Linden Júnior H, Ventura CV, Leal MC, Kowalski TW, Rodrigues Gerzson L, Skilhan de Almeida C, Santi L, Beys-da-Silva WO, Quincozes-Santos A, Guimarães JA, Garcez PP, Gomes JDA, Vianna FSL, Anjos da Silva A, Fraga LR, Vieira Sanseverino MT, Muotri AR, Lopes da Rosa R, Abeche AM, Marcolongo-Pereira C, Souza DO. Neurodevelopment in Children Exposed to Zika in utero: Clinical and Molecular Aspects. Front Genet 2022;13:758715. [PMID: 35350244 DOI: 10.3389/fgene.2022.758715] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
9 Biel A, Castanza AS, Rutherford R, Fair SR, Chifamba L, Wester JC, Hester ME, Hevner RF. AUTS2 Syndrome: Molecular Mechanisms and Model Systems. Front Mol Neurosci 2022;15:858582. [DOI: 10.3389/fnmol.2022.858582] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Naqvi SF, Shabbir RMK, Tolun A, Basit S, Malik S. A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family. Genet Test Mol Biomarkers 2022;26:37-42. [PMID: 35089071 DOI: 10.1089/gtmb.2021.0231] [Reference Citation Analysis]
11 Carvalhal S, Bader I, Rooimans MA, Oostra AB, Balk JA, Feichtinger RG, Beichler C, Speicher MR, van Hagen JM, Waisfisz Q, van Haelst M, Bruijn M, Tavares A, Mayr JA, Wolthuis RMF, Oliveira RA, de Lange J. Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation. Sci Adv 2022;8:eabk0114. [PMID: 35044816 DOI: 10.1126/sciadv.abk0114] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
12 Zaqout S, Kaindl AM. Autosomal Recessive Primary Microcephaly: Not Just a Small Brain. Front Cell Dev Biol 2022;9:784700. [DOI: 10.3389/fcell.2021.784700] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
13 Kristofova M, Ori A, Wang Z. Multifaceted Microcephaly-Related Gene MCPH1. Cells 2022;11:275. [DOI: 10.3390/cells11020275] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Buchwalter RA, Ogden SC, York SB, Sun L, Zheng C, Hammack C, Cheng Y, Chen JV, Cone AS, Meckes DG Jr, Tang H, Megraw TL. Coordination of Zika Virus Infection and Viroplasm Organization by Microtubules and Microtubule-Organizing Centers. Cells 2021;10:3335. [PMID: 34943843 DOI: 10.3390/cells10123335] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
15 Ben Ayed I, Bouchaala W, Bouzid A, Feki W, Souissi A, Ben Nsir S, Ben Said M, Sammouda T, Majdoub F, Kharrat I, Kamoun F, Elloumi I, Kamoun H, Tlili A, Masmoudi S, Triki C. Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly. Eur J Med Genet 2021;64:104373. [PMID: 34737153 DOI: 10.1016/j.ejmg.2021.104373] [Reference Citation Analysis]
16 Waseem SS, Moawia A, Budde B, Tariq M, Khan A, Ali Z, Khan S, Iqbal M, Malik NA, Haque SU, Altmüller J, Thiele H, Hussain MS, Cirak S, Baig SM, Nürnberg P. A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family. Genes (Basel) 2021;12:1494. [PMID: 34680889 DOI: 10.3390/genes12101494] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 Porciúncula LO, Goto-Silva L, Ledur PF, Rehen SK. The Age of Brain Organoids: Tailoring Cell Identity and Functionality for Normal Brain Development and Disease Modeling. Front Neurosci 2021;15:674563. [PMID: 34483818 DOI: 10.3389/fnins.2021.674563] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
18 Khan NM, Hussain B, Zheng C, Khan A, Masoud MS, Gu Q, Qiu L, Malik NA, Qasim M, Tariq M, Chang J. Updates on Clinical and Genetic Heterogeneity of ASPM in 12 Autosomal Recessive Primary Microcephaly Families in Pakistani Population. Front Pediatr 2021;9:695133. [PMID: 34295862 DOI: 10.3389/fped.2021.695133] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
19 Makhdoom EUH, Waseem SS, Iqbal M, Abdullah U, Hussain G, Asif M, Budde B, Höhne W, Tinschert S, Saadi SM, Yousaf H, Ali Z, Fatima A, Kaygusuz E, Khan A, Jameel M, Khan S, Tariq M, Anjum I, Altmüller J, Thiele H, Höning S, Baig SM, Nürnberg P, Hussain MS. Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ. Genes (Basel) 2021;12:731. [PMID: 34068194 DOI: 10.3390/genes12050731] [Reference Citation Analysis]
20 Xu S, Wu X, Wang P, Cao SL, Peng B, Xu X. ASPM promotes homologous recombination-mediated DNA repair by safeguarding BRCA1 stability. iScience 2021;24:102534. [PMID: 34142045 DOI: 10.1016/j.isci.2021.102534] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
21 Catusi I, Garzo M, Capra AP, Briuglia S, Baldo C, Canevini MP, Cantone R, Elia F, Forzano F, Galesi O, Grosso E, Malacarne M, Peron A, Romano C, Saccani M, Larizza L, Recalcati MP. 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature. Genes (Basel) 2021;12:652. [PMID: 33925474 DOI: 10.3390/genes12050652] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
22 Uehara DT, Mitsubuchi H, Inazawa J. A missense variant in NUF2, a component of the kinetochore NDC80 complex, causes impaired chromosome segregation and aneuploidy associated with microcephaly and short stature. Hum Genet 2021;140:1047-60. [PMID: 33721060 DOI: 10.1007/s00439-021-02273-4] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
23 Iegiani G, Gai M, Di Cunto F, Pallavicini G. CENPE Inhibition Leads to Mitotic Catastrophe and DNA Damage in Medulloblastoma Cells. Cancers (Basel) 2021;13:1028. [PMID: 33804489 DOI: 10.3390/cancers13051028] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]