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2006 1
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Page 1
Regulation of autism-relevant behaviors by cerebellar-prefrontal cortical circuits.
Kelly E, Meng F, Fujita H, Morgado F, Kazemi Y, Rice LC, Ren C, Escamilla CO, Gibson JM, Sajadi S, Pendry RJ, Tan T, Ellegood J, Basson MA, Blakely RD, Dindot SV, Golzio C, Hahn MK, Katsanis N, Robins DM, Silverman JL, Singh KK, Wevrick R, Taylor MJ, Hammill C, Anagnostou E, Pfeiffer BE, Stoodley CJ, Lerch JP, du Lac S, Tsai PT. Kelly E, et al. Among authors: golzio c. Nat Neurosci. 2020 Sep;23(9):1102-1110. doi: 10.1038/s41593-020-0665-z. Epub 2020 Jul 13. Nat Neurosci. 2020. PMID: 32661395 Free PMC article.
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.
Beunders G, Voorhoeve E, Golzio C, Pardo LM, Rosenfeld JA, Talkowski ME, Simonic I, Lionel AC, Vergult S, Pyatt RE, van de Kamp J, Nieuwint A, Weiss MM, Rizzu P, Verwer LE, van Spaendonk RM, Shen Y, Wu BL, Yu T, Yu Y, Chiang C, Gusella JF, Lindgren AM, Morton CC, van Binsbergen E, Bulk S, van Rossem E, Vanakker O, Armstrong R, Park SM, Greenhalgh L, Maye U, Neill NJ, Abbott KM, Sell S, Ladda R, Farber DM, Bader PI, Cushing T, Drautz JM, Konczal L, Nash P, de Los Reyes E, Carter MT, Hopkins E, Marshall CR, Osborne LR, Gripp KW, Thrush DL, Hashimoto S, Gastier-Foster JM, Astbury C, Ylstra B, Meijers-Heijboer H, Posthuma D, Menten B, Mortier G, Scherer SW, Eichler EE, Girirajan S, Katsanis N, Groffen AJ, Sistermans EA. Beunders G, et al. Among authors: golzio c. Am J Hum Genet. 2013 Feb 7;92(2):210-20. doi: 10.1016/j.ajhg.2012.12.011. Epub 2013 Jan 17. Am J Hum Genet. 2013. PMID: 23332918 Free PMC article.
Disruptive CHD8 mutations define a subtype of autism early in development.
Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT, Schuurs-Hoeijmakers JH, Fichera M, Bosco P, Buono S, Alberti A, Failla P, Peeters H, Steyaert J, Vissers LELM, Francescatto L, Mefford HC, Rosenfeld JA, Bakken T, O'Roak BJ, Pawlus M, Moon R, Shendure J, Amaral DG, Lein E, Rankin J, Romano C, de Vries BBA, Katsanis N, Eichler EE. Bernier R, et al. Among authors: golzio c. Cell. 2014 Jul 17;158(2):263-276. doi: 10.1016/j.cell.2014.06.017. Epub 2014 Jul 3. Cell. 2014. PMID: 24998929 Free PMC article.
A genetic-epigenetic interplay at 1q21.1 locus underlies CHD1L-mediated vulnerability to primary progressive multiple sclerosis.
Pahlevan Kakhki M, Giordano A, Starvaggi Cucuzza C, Venkata S Badam T, Samudyata S, Lemée MV, Stridh P, Gkogka A, Shchetynsky K, Harroud A, Gyllenberg A, Liu Y, Boddul S, James T, Sorosina M, Filippi M, Esposito F, Wermeling F, Gustafsson M, Casaccia P, Hillert J, Olsson T, Kockum I, Sellgren CM, Golzio C, Kular L, Jagodic M. Pahlevan Kakhki M, et al. Among authors: golzio c. Nat Commun. 2024 Jul 30;15(1):6419. doi: 10.1038/s41467-024-50794-z. Nat Commun. 2024. PMID: 39079955 Free PMC article.
Improving laboratory animal genetic reporting: LAG-R guidelines.
Teboul L, Amos-Landgraf J, Benavides FJ, Birling MC, Brown SDM, Bryda E, Bunton-Stasyshyn R, Chin HJ, Crispo M, Delerue F, Dobbie M, Franklin CL, Fuchtbauer EM, Gao X, Golzio C, Haffner R, Hérault Y, Hrabe de Angelis M, Lloyd KCK, Magnuson TR, Montoliu L, Murray SA, Nam KH, Nutter LMJ, Pailhoux E, Pardo Manuel de Villena F, Peterson K, Reinholdt L, Sedlacek R, Seong JK, Shiroishi T, Smith C, Takeo T, Tinsley L, Vilotte JL, Warming S, Wells S, Whitelaw CB, Yoshiki A; Asian Mouse Mutagenesis Resource Association; CELPHEDIA infrastructure; INFRAFRONTIER consortium; International Mammalian Genome Society; International Mouse Phenotyping Consortium; International Society for Transgenic Technologies; Mutant Mouse Resource and Research Centers; Phenomics Australia; RRRC- Rat Resource and Research Center; Pavlovic G. Teboul L, et al. Among authors: golzio c. Nat Commun. 2024 Jul 2;15(1):5574. doi: 10.1038/s41467-024-49439-y. Nat Commun. 2024. PMID: 38956430 Free PMC article. Review.
Endoglin interacts with VEGFR2 to promote angiogenesis.
Tian H, Huang JJ, Golzio C, Gao X, Hector-Greene M, Katsanis N, Blobe GC. Tian H, et al. Among authors: golzio c. FASEB J. 2018 Jun;32(6):2934-2949. doi: 10.1096/fj.201700867RR. Epub 2018 Jan 11. FASEB J. 2018. PMID: 29401587
SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems.
Di Leva F, Arnoldi M, Santarelli S, Massonot M, Lemée MV, Bon C, Pellegrini M, Castellini ME, Zarantonello G, Messina A, Bozzi Y, Bernier R, Zucchelli S, Casarosa S, Dassi E, Ronzitti G, Golzio C, Morandell J, Gustincich S, Espinoza S, Biagioli M. Di Leva F, et al. Among authors: golzio c. Mol Ther. 2025 Mar 5;33(3):1180-1196. doi: 10.1016/j.ymthe.2024.12.043. Epub 2024 Dec 30. Mol Ther. 2025. PMID: 39741407 Free article.
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders.
Ellegood J, Beauchamp A, Yee Y, Devenyi G, Ziolkowski J, Qiu L, Askalan R, Ayub M, Suetterlin P, Donovan A, Basson MA, Quesnel KM, Berube NG, Woo T, Beversdorf D, Bjornsson H, Blakely R, Crawley J, Crosbie J, Orr BO, Davis GW, Genestine M, DiCicco-Bloom E, Egan S, Fink KD, Asbury S, Lai J, Rilett K, Foster JA, Vincent JB, Frankland P, Georgiades S, Penagarikano O, Geschwind D, Giger RJ, Markx S, Gogos J, Golzio C, Pagani M, Gozzi A, Pacey LK, Hampson D, Huang TN, Yen TL, Hsueh YP, Iaboni A, Amar M, Iakoucheva LM, Jones JK, Kelly E, Kieffer B, Bae M, Jung H, Kim H, Park H, Roh JD, Kim E, Konopka G, Laliberte C, Lefebvre JL, Eagleson K, Levitt P, Bach AM, Cunningham TJ, Fisher E, Miller K, Mills A, Muotri A, Nicolson R, Noakes LS, Nieman BJ, Canales CP, Nord AS, Nutter LM, Tam E, Osborne LR, Clipperton-Allen A, Page D, Babineau B, Palmer TD, Yan K, Picketts D, Xia Q, Powell CM, Raznahan A, Robins DM, Rumbaugh G, Sengar AS, Salter MW, Schachar RJ, D'Abate L, Bradley CA, Scherer SW, Copping NW, Petkova SP, Silverman JL, Singh KK, Kim NS, Yoon KK, Ming GL, Song H, Spring S, Nakatani J, Nakai N, Nomura J, Takumi T, Taylor M, Tsai P, Bruce M, Jones KL, Van de Water J, Van Eede MC,… See abstract for full author list ➔ Ellegood J, et al. Among authors: golzio c. bioRxiv [Preprint]. 2025 Mar 8:2025.03.04.641443. doi: 10.1101/2025.03.04.641443. bioRxiv. 2025. PMID: 40568076 Free PMC article. Preprint.
The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domains.
Vitoria Gomes M, Landwerlin P, Diebold-Durand ML, Shaik TB, Durand A, Troesch E, Weber C, Brillet K, Lemée MV, Decroos C, Dulac L, Antony P, Watrin E, Ennifar E, Golzio C, Romier C. Vitoria Gomes M, et al. Among authors: golzio c. Cell Rep. 2024 Sep 24;43(9):114656. doi: 10.1016/j.celrep.2024.114656. Epub 2024 Sep 5. Cell Rep. 2024. PMID: 39240714 Free article.
Genetic architecture of reciprocal CNVs.
Golzio C, Katsanis N. Golzio C, et al. Curr Opin Genet Dev. 2013 Jun;23(3):240-8. doi: 10.1016/j.gde.2013.04.013. Epub 2013 Jun 5. Curr Opin Genet Dev. 2013. PMID: 23747035 Free PMC article. Review.
50 results