| Year |
Citation |
Score |
| 2022 |
Perrino PA, Chasse RY, Monaco AP, Molnár Z, Velayos-Baeza A, Fitch RH. Rapid auditory processing and medial geniculate nucleus anomalies in Kiaa0319 knockout mice. Genes, Brain, and Behavior. e12808. PMID 35419947 DOI: 10.1111/gbb.12808 |
0.421 |
|
| 2019 |
Yeshaw WM, van der Zwaag M, Pinto F, Lahaye LL, Faber AI, Gómez-Sánchez R, Dolga AM, Poland C, Monaco AP, van IJzendoorn S, Grzeschik NA, Velayos-Baeza A, Sibon OC. Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility. Elife. 8. PMID 30741634 DOI: 10.7554/Elife.43561 |
0.475 |
|
| 2019 |
Yeshaw WM, Zwaag Mvd, Pinto F, Lahaye LL, Faber AI, Gómez-Sánchez R, Dolga AM, Poland C, Monaco AP, IJzendoorn SCv, Grzeschik NA, Velayos-Baeza A, Sibon OC. Author response: Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility Elife. DOI: 10.7554/Elife.43561.038 |
0.431 |
|
| 2018 |
Guidi LG, Velayos-Baeza A, Martinez-Garay I, Monaco AP, Paracchini S, Bishop DVM, Molnár Z. The Neuronal Migration Hypothesis of Dyslexia: A Critical Evaluation Thirty Years On. The European Journal of Neuroscience. PMID 30218584 DOI: 10.1111/Ejn.14149 |
0.646 |
|
| 2018 |
Guidi LG, Holloway ZG, Arnoult C, Ray PF, Monaco AP, Molnár Z, Velayos-Baeza A. AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice. Scientific Reports. 8: 10379. PMID 29991750 DOI: 10.1038/S41598-018-28666-6 |
0.52 |
|
| 2017 |
Guidi LG, Mattley J, Martinez-Garay I, Monaco AP, Linden JF, Velayos-Baeza A, Molnár Z. Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing. Cerebral Cortex (New York, N.Y. : 1991). 1-15. PMID 29045729 DOI: 10.1093/Cercor/Bhx269 |
0.523 |
|
| 2017 |
Franquinho F, Nogueira-Rodrigues J, Duarte JM, Esteves SS, Carter-Su C, Monaco AP, Molnár Z, Velayos-Baeza A, Brites P, Sousa MM. The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling. Cerebral Cortex (New York, N.Y. : 1991). 1-16. PMID 28334068 DOI: 10.1093/Cercor/Bhx023 |
0.45 |
|
| 2017 |
Vonk JJ, Yeshaw WM, Pinto F, Faber AI, Lahaye LL, Kanon B, van der Zwaag M, Velayos-Baeza A, Freire R, van IJzendoorn SC, Grzeschik NA, Sibon OC. Drosophila Vps13 Is Required for Protein Homeostasis in the Brain. Plos One. 12: e0170106. PMID 28107480 DOI: 10.1371/Journal.Pone.0170106 |
0.439 |
|
| 2016 |
Martinez-Garay I, Guidi LG, Holloway ZG, Bailey MA, Lyngholm D, Schneider T, Donnison T, Butt SJ, Velayos-Baeza A, Molnár Z, Monaco AP. Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice. Brain Structure & Function. PMID 27510895 DOI: 10.1007/S00429-016-1282-1 |
0.569 |
|
| 2016 |
Mehta ZB, Fine N, Pullen TJ, Cane MC, Hu M, Chabosseau P, Meur G, Velayos-Baeza A, Monaco AP, Marselli L, Marchetti P, Rutter GA. Changes in the expression of the type 2 diabetes-associated gene VPS13C in the β cell are associated with glucose intolerance in humans and mice. American Journal of Physiology. Endocrinology and Metabolism. ajpendo.00074.2016. PMID 27329800 DOI: 10.1152/Ajpendo.00074.2016 |
0.453 |
|
| 2016 |
Yang RY, Xue H, Yu L, Velayos-Baeza A, Monaco AP, Liu FT. Identification of VPS13C as a Galectin-12-Binding Protein That Regulates Galectin-12 Protein Stability and Adipogenesis. Plos One. 11: e0153534. PMID 27073999 DOI: 10.1371/Journal.Pone.0153534 |
0.474 |
|
| 2013 |
Holloway ZG, Velayos-Baeza A, Howell GJ, Levecque C, Ponnambalam S, Sztul E, Monaco AP. Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2-, AP-1-, and Rab22-dependent steps. Molecular Biology of the Cell. 24: 1735-48, S1-8. PMID 23596324 DOI: 10.1091/Mbc.E12-08-0625 |
0.475 |
|
| 2011 |
Velayos-Baeza A, Holinski-Feder E, Neitzel B, Bader B, Critchley EM, Monaco AP, Danek A, Walker RH. Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindred. Archives of Neurology. 68: 1330-3. PMID 21987550 DOI: 10.1001/Archneurol.2011.239 |
0.474 |
|
| 2010 |
Velayos-Baeza A, Levecque C, Kobayashi K, Holloway ZG, Monaco AP. The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage. The Journal of Biological Chemistry. 285: 40148-62. PMID 20943657 DOI: 10.1074/Jbc.M110.145961 |
0.551 |
|
| 2009 |
Levecque C, Velayos-Baeza A, Holloway ZG, Monaco AP. The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway. American Journal of Physiology. Cell Physiology. 297: C160-8. PMID 19419997 DOI: 10.1152/Ajpcell.00630.2008 |
0.547 |
|
| 2008 |
Velayos-Baeza A, Toma C, Paracchini S, Monaco AP. The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. Human Molecular Genetics. 17: 859-71. PMID 18063668 DOI: 10.1093/Hmg/Ddm358 |
0.691 |
|
| 2008 |
Velayos-Baeza A, Lévecque C, Dobson-Stone C, Monaco AP. The function of chorein Neuroacanthocytosis Syndromes Ii. 87-105. DOI: 10.1007/978-3-540-71693-8_7 |
0.317 |
|
| 2007 |
Velayos-Baeza A, Toma C, da Roza S, Paracchini S, Monaco AP. Alternative splicing in the dyslexia-associated gene KIAA0319. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 627-34. PMID 17846832 DOI: 10.1007/S00335-007-9051-3 |
0.684 |
|
| 2007 |
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, et al. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Molecular Psychiatry. 12: 1129-39, 1057. PMID 17667961 DOI: 10.1038/Sj.Mp.4002053 |
0.61 |
|
| 2007 |
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, et al. LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells Molecular Psychiatry. 12: 1057. DOI: 10.1038/Sj.Mp.4002116 |
0.533 |
|
| 2005 |
Dobson-Stone C, Velayos-Baeza A, Jansen A, Andermann F, Dubeau F, Robert F, Summers A, Lang AE, Chouinard S, Danek A, Andermann E, Monaco AP. Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis. Neurogenetics. 6: 151-8. PMID 15918062 DOI: 10.1007/S10048-005-0220-9 |
0.462 |
|
| 2004 |
Velayos-Baeza A, Vettori A, Copley RR, Dobson-Stone C, Monaco AP. Analysis of the human VPS13 gene family. Genomics. 84: 536-49. PMID 15498460 DOI: 10.1016/J.Ygeno.2004.04.012 |
0.525 |
|
| 2004 |
Dobson-Stone C, Velayos-Baeza A, Filippone LA, Westbury S, Storch A, Erdmann T, Wroe SJ, Leenders KL, Lang AE, Dotti MT, Federico A, Mohiddin SA, Fananapazir L, Daniels G, Danek A, et al. Chorein detection for the diagnosis of chorea-acanthocytosis. Annals of Neurology. 56: 299-302. PMID 15293285 DOI: 10.1002/Ana.20200 |
0.474 |
|
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