316 related articles for article (PubMed ID: 27865048)
1. Neuroligin 2 nonsense variant associated with anxiety, autism, intellectual disability, hyperphagia, and obesity.
Parente DJ; Garriga C; Baskin B; Douglas G; Cho MT; Araujo GC; Shinawi M
Am J Med Genet A; 2017 Jan; 173(1):213-216. PubMed ID: 27865048
[TBL] [Abstract][Full Text] [Related]
2. Developmental delays and reduced pup ultrasonic vocalizations but normal sociability in mice lacking the postsynaptic cell adhesion protein neuroligin2.
Wöhr M; Silverman JL; Scattoni ML; Turner SM; Harris MJ; Saxena R; Crawley JN
Behav Brain Res; 2013 Aug; 251():50-64. PubMed ID: 22820233
[TBL] [Abstract][Full Text] [Related]
3. A novel nonsense homozygous variant in the NLGN1 gene found in a pair of monozygotic twin brothers with intellectual disability and autism.
Tejada MI; Elcoroaristizabal X; Ibarluzea N; Botella MP; de la Hoz AB; Ocio I
Clin Genet; 2019 Feb; 95(2):339-340. PubMed ID: 30460678
[No Abstract] [Full Text] [Related]
4. Two de novo novel mutations in one SHANK3 allele in a patient with autism and moderate intellectual disability.
Zhu W; Li J; Chen S; Zhang J; Vetrini F; Braxton A; Eng CM; Yang Y; Xia F; Keller KL; Okinaka-Hu L; Lee C; Holder JL; Bi W
Am J Med Genet A; 2018 Apr; 176(4):973-979. PubMed ID: 29423971
[TBL] [Abstract][Full Text] [Related]
5. Neuroligin 2 deletion alters inhibitory synapse function and anxiety-associated neuronal activation in the amygdala.
Babaev O; Botta P; Meyer E; Müller C; Ehrenreich H; Brose N; Lüthi A; Krueger-Burg D
Neuropharmacology; 2016 Jan; 100():56-65. PubMed ID: 26142252
[TBL] [Abstract][Full Text] [Related]
6. First de novo ANK3 nonsense mutation in a boy with intellectual disability, speech impairment and autistic features.
Kloth K; Denecke J; Hempel M; Johannsen J; Strom TM; Kubisch C; Lessel D
Eur J Med Genet; 2017 Sep; 60(9):494-498. PubMed ID: 28687526
[TBL] [Abstract][Full Text] [Related]
7. De novo duplication of 17p13.1-p13.2 in a patient with intellectual disability and obesity.
Kuroda Y; Ohashi I; Tominaga M; Saito T; Nagai J; Ida K; Naruto T; Masuno M; Kurosawa K
Am J Med Genet A; 2014 Jun; 164A(6):1550-4. PubMed ID: 24668897
[TBL] [Abstract][Full Text] [Related]
8. Analysis of four neuroligin genes as candidates for autism.
Ylisaukko-oja T; Rehnström K; Auranen M; Vanhala R; Alen R; Kempas E; Ellonen P; Turunen JA; Makkonen I; Riikonen R; Nieminen-von Wendt T; von Wendt L; Peltonen L; Järvelä I
Eur J Hum Genet; 2005 Dec; 13(12):1285-92. PubMed ID: 16077734
[TBL] [Abstract][Full Text] [Related]
9. Neuroligin-2 as a central organizer of inhibitory synapses in health and disease.
Ali H; Marth L; Krueger-Burg D
Sci Signal; 2020 Dec; 13(663):. PubMed ID: 33443230
[TBL] [Abstract][Full Text] [Related]
10. Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.
Kim HG; Rosenfeld JA; Scott DA; Bénédicte G; Labonne JD; Brown J; McGuire M; Mahida S; Naidu S; Gutierrez J; Lesca G; des Portes V; Bruel AL; Sorlin A; Xia F; Capri Y; Muller E; McKnight D; Torti E; Rüschendorf F; Hummel O; Islam Z; Kolatkar PR; Layman LC; Ryu D; Kong IK; Madan-Khetarpal S; Kim CH
Mol Autism; 2019; 10():35. PubMed ID: 31649809
[TBL] [Abstract][Full Text] [Related]
11. De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.
Schäfgen J; Cremer K; Becker J; Wieland T; Zink AM; Kim S; Windheuser IC; Kreiß M; Aretz S; Strom TM; Wieczorek D; Engels H
Eur J Hum Genet; 2016 Dec; 24(12):1739-1745. PubMed ID: 27436265
[TBL] [Abstract][Full Text] [Related]
12. DYRK1A mutations in two unrelated patients.
Ruaud L; Mignot C; Guët A; Ohl C; Nava C; Héron D; Keren B; Depienne C; Benoit V; Maystadt I; Lederer D; Amsallem D; Piard J
Eur J Med Genet; 2015 Mar; 58(3):168-74. PubMed ID: 25641759
[TBL] [Abstract][Full Text] [Related]
13. Distinct roles for extracellular and intracellular domains in neuroligin function at inhibitory synapses.
Nguyen QA; Horn ME; Nicoll RA
Elife; 2016 Nov; 5():. PubMed ID: 27805570
[TBL] [Abstract][Full Text] [Related]
14. Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
Xu X; Xiong Z; Zhang L; Liu Y; Lu L; Peng Y; Guo H; Zhao J; Xia K; Hu Z
Mol Biol Rep; 2014 Jun; 41(6):4133-40. PubMed ID: 24570023
[TBL] [Abstract][Full Text] [Related]
15. Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
Torrico B; Shaw AD; Mosca R; Vivó-Luque N; Hervás A; Fernàndez-Castillo N; Aloy P; Bayés M; Fullerton JM; Cormand B; Toma C
J Psychiatry Neurosci; 2019 Sep; 44(5):350-359. PubMed ID: 31094488
[TBL] [Abstract][Full Text] [Related]
16. Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3.
Hosie S; Ellis M; Swaminathan M; Ramalhosa F; Seger GO; Balasuriya GK; Gillberg C; Råstam M; Churilov L; McKeown SJ; Yalcinkaya N; Urvil P; Savidge T; Bell CA; Bodin O; Wood J; Franks AE; Bornstein JC; Hill-Yardin EL
Autism Res; 2019 Jul; 12(7):1043-1056. PubMed ID: 31119867
[TBL] [Abstract][Full Text] [Related]
17. A novel MYT1L mutation in a patient with severe early-onset obesity and intellectual disability.
Loid P; Mäkitie R; Costantini A; Viljakainen H; Pekkinen M; Mäkitie O
Am J Med Genet A; 2018 Sep; 176(9):1972-1975. PubMed ID: 30055078
[TBL] [Abstract][Full Text] [Related]
18. Hippocampal neuroligin-2 overexpression leads to reduced aggression and inhibited novelty reactivity in rats.
Kohl C; Riccio O; Grosse J; Zanoletti O; Fournier C; Schmidt MV; Sandi C
PLoS One; 2013; 8(2):e56871. PubMed ID: 23451101
[TBL] [Abstract][Full Text] [Related]
19. Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism.
Avdjieva-Tzavella DM; Todorov TP; Todorova AP; Kirov AV; Hadjidekova SP; Rukova BB; Litvinenko IO; Hristova-Naydenova DN; Tincheva RS; Toncheva DI
Genet Couns; 2012; 23(4):505-11. PubMed ID: 23431752
[TBL] [Abstract][Full Text] [Related]
20. KIAA2022 nonsense mutation in a symptomatic female.
Farach LS; Northrup H
Am J Med Genet A; 2016 Mar; 170(3):703-6. PubMed ID: 26576034
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
