Similar articles for PMID: 29758293

Year	Number of Results
2005	1
2006	1
2007	1
2008	1
2009	6
2010	5
2011	4
2012	8
2013	4
2014	5
2015	8
2016	13
2017	18
2018	18
2019	11
2020	12
2021	13
2022	6
2023	3
2024	0

1

TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly.

Cavallin M, Maillard C, Hully M, Philbert M, Boddaert N, Reilly ML, Nitschké P, Bery A, Bahi-Buisson N. Cavallin M, et al. Eur J Med Genet. 2018 Dec;61(12):729-732. doi: 10.1016/j.ejmg.2018.05.002. Epub 2018 May 25. Eur J Med Genet. 2018. PMID: 29758293

2

14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.

Allou L, Lambert L, Amsallem D, Bieth E, Edery P, Destrée A, Rivier F, Amor D, Thompson E, Nicholl J, Harbord M, Nemos C, Saunier A, Moustaïne A, Vigouroux A, Jonveaux P, Philippe C. Allou L, et al. Eur J Hum Genet. 2012 Dec;20(12):1216-23. doi: 10.1038/ejhg.2012.127. Epub 2012 Jun 27. Eur J Hum Genet. 2012. PMID: 22739344 Free PMC article.

3

Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome.

Wilpert NM, Marguet F, Maillard C, Guimiot F, Martinovic J, Drunat S, Attié-Bitach T, Razavi F, Tessier A, Capri Y, Laquerrière A, Bahi-Buisson N. Wilpert NM, et al. Eur J Med Genet. 2021 Sep;64(9):104282. doi: 10.1016/j.ejmg.2021.104282. Epub 2021 Jul 17. Eur J Med Genet. 2021. PMID: 34284163

4

Transducin-like enhancer of Split-1 (TLE1) combines with Forkhead box protein G1 (FoxG1) to promote neuronal survival.

Dastidar SG, Narayanan S, Stifani S, D'Mello SR. Dastidar SG, et al. J Biol Chem. 2012 Apr 27;287(18):14749-59. doi: 10.1074/jbc.M111.328336. Epub 2012 Feb 21. J Biol Chem. 2012. PMID: 22354967 Free PMC article.

5

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.

Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, de Villemeur TB, Boespflug-Tanguy O, Burglen L, Del Giudice E, Guimiot F, Hyon C, Isidor B, Mégarbané A, Moog U, Odent S, Hernandez K, Pouvreau N, Scala I, Schaer M, Gressens P, Gerard B, Verloes A. Passemard S, et al. Neurology. 2009 Sep 22;73(12):962-9. doi: 10.1212/WNL.0b013e3181b8799a. Neurology. 2009. PMID: 19770472

6

A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family.

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. Waseem SS, et al. Genes (Basel). 2021 Sep 24;12(10):1494. doi: 10.3390/genes12101494. Genes (Basel). 2021. PMID: 34680889 Free PMC article.

7

Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features.

Ansar M, Ullah F, Paracha SA, Adams DJ, Lai A, Pais L, Iwaszkiewicz J, Millan F, Sarwar MT, Agha Z, Shah SF, Qaisar AA, Falconnet E, Zoete V, Ranza E, Makrythanasis P, Santoni FA, Ahmed J, Katsanis N, Walsh C, Davis EE, Antonarakis SE. Ansar M, et al. Am J Hum Genet. 2019 Jun 6;104(6):1073-1087. doi: 10.1016/j.ajhg.2019.04.002. Epub 2019 May 9. Am J Hum Genet. 2019. PMID: 31079899 Free PMC article.

8

Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from Iran.

Hozhabri H, Talebi M, Mehrjardi MYV, De Luca A, Dehghani M. Hozhabri H, et al. Am J Med Genet A. 2020 May;182(5):957-961. doi: 10.1002/ajmg.a.61543. Epub 2020 Mar 12. Am J Med Genet A. 2020. PMID: 32162791

9

WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.

Cavallin M, Rujano MA, Bednarek N, Medina-Cano D, Bernabe Gelot A, Drunat S, Maillard C, Garfa-Traore M, Bole C, Nitschké P, Beneteau C, Besnard T, Cogné B, Eveillard M, Kuster A, Poirier K, Verloes A, Martinovic J, Bidat L, Rio M, Lyonnet S, Reilly ML, Boddaert N, Jenneson-Liver M, Motte J, Doco-Fenzy M, Chelly J, Attie-Bitach T, Simons M, Cantagrel V, Passemard S, Baffet A, Thomas S, Bahi-Buisson N. Cavallin M, et al. Brain. 2017 Oct 1;140(10):2597-2609. doi: 10.1093/brain/awx218. Brain. 2017. PMID: 28969387

10

Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephaly.

Jang HN, Kim T, Jung AY, Lee BH, Yum MS, Ko TS. Jang HN, et al. Medicine (Baltimore). 2021 Nov 24;100(47):e27949. doi: 10.1097/MD.0000000000027949. Medicine (Baltimore). 2021. PMID: 34964776 Free PMC article.

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