125 related articles for article (PubMed ID: 24664471)
1. Outfoxed by RBFOX1-a caution about ascertainment bias.
Kamien B; Lionel AC; Bain N; Scherer SW; Hunter M
Am J Med Genet A; 2014 Jun; 164A(6):1411-8. PubMed ID: 24664471
[TBL] [Abstract][Full Text] [Related]
2. Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder.
Bill BR; Lowe JK; Dybuncio CT; Fogel BL
Int Rev Neurobiol; 2013; 113():251-67. PubMed ID: 24290388
[TBL] [Abstract][Full Text] [Related]
3. Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs.
Prandini P; Zusi C; Malerba G; Itan ; Pignatti PF; Trabetti E
Mol Cell Probes; 2014; 28(5-6):242-5. PubMed ID: 24938762
[TBL] [Abstract][Full Text] [Related]
4. Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.
Mikhail FM; Lose EJ; Robin NH; Descartes MD; Rutledge KD; Rutledge SL; Korf BR; Carroll AJ
Am J Med Genet A; 2011 Oct; 155A(10):2386-96. PubMed ID: 22031302
[TBL] [Abstract][Full Text] [Related]
5. Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.
Lal D; Pernhorst K; Klein KM; Reif P; Tozzi R; Toliat MR; Winterer G; Neubauer B; Nürnberg P; Rosenow F; Becker F; Lerche H; Kunz WS; Kurki MI; Hoffmann P; Becker AJ; Perucca E; Zara F; Sander T; Weber YG
Epilepsia; 2015 Sep; 56(9):e129-33. PubMed ID: 26174448
[TBL] [Abstract][Full Text] [Related]
6. Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis.
Davis LK; Maltman N; Mosconi MW; Macmillan C; Schmitt L; Moore K; Francis SM; Jacob S; Sweeney JA; Cook EH
Am J Med Genet A; 2012 Jul; 158A(7):1654-61. PubMed ID: 22678932
[TBL] [Abstract][Full Text] [Related]
7. Neurodevelopmental disorders among individuals with duplication of 4p13 to 4p12 containing a GABAA receptor subunit gene cluster.
Polan MB; Pastore MT; Steingass K; Hashimoto S; Thrush DL; Pyatt R; Reshmi S; Gastier-Foster JM; Astbury C; McBride KL
Eur J Hum Genet; 2014 Jan; 22(1):105-9. PubMed ID: 23695283
[TBL] [Abstract][Full Text] [Related]
8. Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.
Martin CL; Duvall JA; Ilkin Y; Simon JS; Arreaza MG; Wilkes K; Alvarez-Retuerto A; Whichello A; Powell CM; Rao K; Cook E; Geschwind DH
Am J Med Genet B Neuropsychiatr Genet; 2007 Oct; 144B(7):869-76. PubMed ID: 17503474
[TBL] [Abstract][Full Text] [Related]
9. Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Girirajan S; Dennis MY; Baker C; Malig M; Coe BP; Campbell CD; Mark K; Vu TH; Alkan C; Cheng Z; Biesecker LG; Bernier R; Eichler EE
Am J Hum Genet; 2013 Feb; 92(2):221-37. PubMed ID: 23375656
[TBL] [Abstract][Full Text] [Related]
10. Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay.
Wiśniowiecka-Kowalnik B; Nesteruk M; Peters SU; Xia Z; Cooper ML; Savage S; Amato RS; Bader P; Browning MF; Haun CL; Duda AW; Cheung SW; Stankiewicz P
Am J Med Genet B Neuropsychiatr Genet; 2010 Jul; 153B(5):983-93. PubMed ID: 20162629
[TBL] [Abstract][Full Text] [Related]
11. Structural, genetic, and functional signatures of disordered neuro-immunological development in autism spectrum disorder.
Saxena V; Ramdas S; Ochoa CR; Wallace D; Bhide P; Kohane I
PLoS One; 2012; 7(12):e48835. PubMed ID: 23239965
[TBL] [Abstract][Full Text] [Related]
12. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
[TBL] [Abstract][Full Text] [Related]
13. A novel X-linked disorder with developmental delay and autistic features.
Kaya N; Colak D; Albakheet A; Al-Owain M; Abu-Dheim N; Al-Younes B; Al-Zahrani J; Mukaddes NM; Dervent A; Al-Dosari N; Al-Odaib A; Kayaalp IV; Al-Sayed M; Al-Hassnan Z; Nester MJ; Al-Dosari M; Al-Dhalaan H; Chedrawi A; Gunoz H; Karakas B; Sakati N; Alkuraya FS; Gascon GG; Ozand PT
Ann Neurol; 2012 Apr; 71(4):498-508. PubMed ID: 22213401
[TBL] [Abstract][Full Text] [Related]
14. Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.
Nagamani SC; Erez A; Ben-Zeev B; Frydman M; Winter S; Zeller R; El-Khechen D; Escobar L; Stankiewicz P; Patel A; Cheung SW
Eur J Hum Genet; 2013 Mar; 21(3):343-6. PubMed ID: 22872102
[TBL] [Abstract][Full Text] [Related]
15. Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy.
Lal D; Trucks H; Møller RS; Hjalgrim H; Koeleman BP; de Kovel CG; Visscher F; Weber YG; Lerche H; Becker F; Schankin CJ; Neubauer BA; Surges R; Kunz WS; Zimprich F; Franke A; Illig T; Ried JS; Leu C; Nürnberg P; Sander T; ;
Epilepsia; 2013 Feb; 54(2):265-71. PubMed ID: 23350840
[TBL] [Abstract][Full Text] [Related]
16. Special Report: Chromosomal Microarray for the Genetic Evaluation of Patients With Global Developmental Delay, Intellectual Disability, and Autism Spectrum Disorder.
Blue Cross Blue Shield Asssociation
Technol Eval Cent Assess Program Exec Summ; 2015 Aug; 30(2):1-4. PubMed ID: 26376503
[No Abstract] [Full Text] [Related]
17. Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy.
Li J; Fung I; Glessner JT; Pandey R; Wei Z; Bakay M; Mentch FD; Pellegrino R; Wang T; Kim C; Hou C; Wang F; Chiavacci RM; Thomas KA; Spergel JM; Hakonarson H; Sleiman PM
J Immunol; 2015 Aug; 195(4):1599-607. PubMed ID: 26188062
[TBL] [Abstract][Full Text] [Related]
18. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
[TBL] [Abstract][Full Text] [Related]
19. [Disease susceptibility genes and genome structural abnormalities associated with developmental disabilities].
Yamamoto T
No To Hattatsu; 2014 Mar; 46(2):131-5. PubMed ID: 24738191
[No Abstract] [Full Text] [Related]
20. PARK2 copy number aberrations in two children presenting with autism spectrum disorder: further support of an association and possible evidence for a new microdeletion/microduplication syndrome.
Scheuerle A; Wilson K
Am J Med Genet B Neuropsychiatr Genet; 2011 Jun; 156B(4):413-20. PubMed ID: 21360662
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
