136 related articles for article (PubMed ID: 27179170)
1. Genetic Studies in Intellectual Disability and Behavioral Impairment.
Mehregan H; Najmabadi H; Kahrizi K
Arch Iran Med; 2016 May; 19(5):363-75. PubMed ID: 27179170
[TBL] [Abstract][Full Text] [Related]
2. Drosophila models of early onset cognitive disorders and their clinical applications.
van der Voet M; Nijhof B; Oortveld MA; Schenck A
Neurosci Biobehav Rev; 2014 Oct; 46 Pt 2():326-42. PubMed ID: 24661984
[TBL] [Abstract][Full Text] [Related]
3. Gene networks associated with non-syndromic intellectual disability.
Lee S; Rudd S; Gratten J; Visscher PM; Prins JB; Dawson PA
J Neurogenet; 2018 Mar; 32(1):6-14. PubMed ID: 29199528
[TBL] [Abstract][Full Text] [Related]
4. PDZD8 Disruption Causes Cognitive Impairment in Humans, Mice, and Fruit Flies.
Al-Amri AH; Armstrong P; Amici M; Ligneul C; Rouse J; El-Asrag ME; Pantiru A; Vancollie VE; Ng HWY; Ogbeta JA; Goodchild K; Ellegood J; Lelliott CJ; Mullins JGL; Bretman A; Al-Ali R; Beetz C; Al-Gazali L; Al Shamsi A; Lerch JP; Mellor JR; Al Sayegh A; Ali M; Inglehearn CF; Clapcote SJ
Biol Psychiatry; 2022 Aug; 92(4):323-334. PubMed ID: 35227461
[TBL] [Abstract][Full Text] [Related]
5. Fruit flies and intellectual disability.
Bolduc FV; Tully T
Fly (Austin); 2009; 3(1):91-104. PubMed ID: 19182539
[TBL] [Abstract][Full Text] [Related]
6. Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability.
Bhowmik AD; Chaudhury S; Dutta S; Shaw J; Chatterjee A; Choudhury A; Saha A; Sadhukhan D; Kar T; Sinha S; Mukhopadhyay K
Prog Neuropsychopharmacol Biol Psychiatry; 2011 Aug; 35(7):1714-22. PubMed ID: 21609749
[TBL] [Abstract][Full Text] [Related]
7. Animal models of mental retardation: from gene to cognitive function.
Branchi I; Bichler Z; Berger-Sweeney J; Ricceri L
Neurosci Biobehav Rev; 2003; 27(1-2):141-53. PubMed ID: 12732230
[TBL] [Abstract][Full Text] [Related]
8. The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.
Khan MA; Khan S; Windpassinger C; Badar M; Nawaz Z; Mohammad RM
Ann Hum Genet; 2016 Nov; 80(6):342-368. PubMed ID: 27870114
[TBL] [Abstract][Full Text] [Related]
9. Intellectual disability: dendritic anomalies and emerging genetic perspectives.
Quach TT; Stratton HJ; Khanna R; Kolattukudy PE; Honnorat J; Meyer K; Duchemin AM
Acta Neuropathol; 2021 Feb; 141(2):139-158. PubMed ID: 33226471
[TBL] [Abstract][Full Text] [Related]
10. [Behavioral disorders and substance abuse in adolescents with mental retardation].
Papachristou E; Anagnostopoulos D
Psychiatriki; 2014; 25(2):139-50. PubMed ID: 25035183
[TBL] [Abstract][Full Text] [Related]
11. Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems.
Vulto-van Silfhout AT; Rajamanickam S; Jensik PJ; Vergult S; de Rocker N; Newhall KJ; Raghavan R; Reardon SN; Jarrett K; McIntyre T; Bulinski J; Ownby SL; Huggenvik JI; McKnight GS; Rose GM; Cai X; Willaert A; Zweier C; Endele S; de Ligt J; van Bon BW; Lugtenberg D; de Vries PF; Veltman JA; van Bokhoven H; Brunner HG; Rauch A; de Brouwer AP; Carvill GL; Hoischen A; Mefford HC; Eichler EE; Vissers LE; Menten B; Collard MW; de Vries BB
Am J Hum Genet; 2014 May; 94(5):649-61. PubMed ID: 24726472
[TBL] [Abstract][Full Text] [Related]
12. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Battaglia A; Doccini V; Bernardini L; Novelli A; Loddo S; Capalbo A; Filippi T; Carey JC
Eur J Paediatr Neurol; 2013 Nov; 17(6):589-99. PubMed ID: 23711909
[TBL] [Abstract][Full Text] [Related]
13. Loss-of-function variants in HIVEP2 are a cause of intellectual disability.
Srivastava S; Engels H; Schanze I; Cremer K; Wieland T; Menzel M; Schubach M; Biskup S; Kreiß M; Endele S; Strom TM; Wieczorek D; Zenker M; Gupta S; Cohen J; Zink AM; Naidu S
Eur J Hum Genet; 2016 Apr; 24(4):556-61. PubMed ID: 26153216
[TBL] [Abstract][Full Text] [Related]
14. Exome sequencing identifies three novel candidate genes implicated in intellectual disability.
Agha Z; Iqbal Z; Azam M; Ayub H; Vissers LE; Gilissen C; Ali SH; Riaz M; Veltman JA; Pfundt R; van Bokhoven H; Qamar R
PLoS One; 2014; 9(11):e112687. PubMed ID: 25405613
[TBL] [Abstract][Full Text] [Related]
15. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Rauch A; Wieczorek D; Graf E; Wieland T; Endele S; Schwarzmayr T; Albrecht B; Bartholdi D; Beygo J; Di Donato N; Dufke A; Cremer K; Hempel M; Horn D; Hoyer J; Joset P; Röpke A; Moog U; Riess A; Thiel CT; Tzschach A; Wiesener A; Wohlleber E; Zweier C; Ekici AB; Zink AM; Rump A; Meisinger C; Grallert H; Sticht H; Schenck A; Engels H; Rappold G; Schröck E; Wieacker P; Riess O; Meitinger T; Reis A; Strom TM
Lancet; 2012 Nov; 380(9854):1674-82. PubMed ID: 23020937
[TBL] [Abstract][Full Text] [Related]
16. Modelling Learning and Memory in Drosophila to Understand Intellectual Disabilities.
Mariano V; Achsel T; Bagni C; Kanellopoulos AK
Neuroscience; 2020 Oct; 445():12-30. PubMed ID: 32730949
[TBL] [Abstract][Full Text] [Related]
17. Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci.
Chilian B; Abdollahpour H; Bierhals T; Haltrich I; Fekete G; Nagel I; Rosenberger G; Kutsche K
Clin Genet; 2013 Dec; 84(6):560-5. PubMed ID: 23350639
[TBL] [Abstract][Full Text] [Related]
18. Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25.
Rizzi TS; Beunders G; Rizzu P; Sistermans E; Twisk JW; van Mechelen W; Deijen JB; Meijers-Heijboer H; Verhage M; Heutink P; Posthuma D
Genes Brain Behav; 2012 Oct; 11(7):767-71. PubMed ID: 22762387
[TBL] [Abstract][Full Text] [Related]
19. Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits.
Ramakers GJ; Wolfer D; Rosenberger G; Kuchenbecker K; Kreienkamp HJ; Prange-Kiel J; Rune G; Richter K; Langnaese K; Masneuf S; Bösl MR; Fischer KD; Krugers HJ; Lipp HP; van Galen E; Kutsche K
Hum Mol Genet; 2012 Jan; 21(2):268-86. PubMed ID: 21989057
[TBL] [Abstract][Full Text] [Related]
20. Glutamate synapses in human cognitive disorders.
Volk L; Chiu SL; Sharma K; Huganir RL
Annu Rev Neurosci; 2015 Jul; 38():127-49. PubMed ID: 25897873
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
