These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
330 related articles for article (PubMed ID: 26872257)
21. Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2). Walz K; Paylor R; Yan J; Bi W; Lupski JR J Clin Invest; 2006 Nov; 116(11):3035-41. PubMed ID: 17024248 [TBL] [Abstract][Full Text] [Related]
22. Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder. Brunner D; Kabitzke P; He D; Cox K; Thiede L; Hanania T; Sabath E; Alexandrov V; Saxe M; Peles E; Mills A; Spooren W; Ghosh A; Feliciano P; Benedetti M; Luo Clayton A; Biemans B PLoS One; 2015; 10(8):e0134572. PubMed ID: 26273832 [TBL] [Abstract][Full Text] [Related]
23. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. D'Angelo D; Lebon S; Chen Q; Martin-Brevet S; Snyder LG; Hippolyte L; Hanson E; Maillard AM; Faucett WA; Macé A; Pain A; Bernier R; Chawner SJ; David A; Andrieux J; Aylward E; Baujat G; Caldeira I; Conus P; Ferrari C; Forzano F; Gérard M; Goin-Kochel RP; Grant E; Hunter JV; Isidor B; Jacquette A; Jønch AE; Keren B; Lacombe D; Le Caignec C; Martin CL; Männik K; Metspalu A; Mignot C; Mukherjee P; Owen MJ; Passeggeri M; Rooryck-Thambo C; Rosenfeld JA; Spence SJ; Steinman KJ; Tjernagel J; Van Haelst M; Shen Y; Draganski B; Sherr EH; Ledbetter DH; van den Bree MB; Beckmann JS; Spiro JE; Reymond A; Jacquemont S; Chung WK; ; ; JAMA Psychiatry; 2016 Jan; 73(1):20-30. PubMed ID: 26629640 [TBL] [Abstract][Full Text] [Related]
24. Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders. Martin Lorenzo S; Muniz Moreno MDM; Atas H; Pellen M; Nalesso V; Raffelsberger W; Prevost G; Lindner L; Birling MC; Menoret S; Tesson L; Negroni L; Concordet JP; Anegon I; Herault Y Front Neurosci; 2023; 17():1148683. PubMed ID: 37465586 [TBL] [Abstract][Full Text] [Related]
25. Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Bi W; Yan J; Shi X; Yuva-Paylor LA; Antalffy BA; Goldman A; Yoo JW; Noebels JL; Armstrong DL; Paylor R; Lupski JR Hum Mol Genet; 2007 Aug; 16(15):1802-13. PubMed ID: 17517686 [TBL] [Abstract][Full Text] [Related]
26. Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome. Blackmon K; Thesen T; Green S; Ben-Avi E; Wang X; Fuchs B; Kuzniecky R; Devinsky O Cereb Cortex; 2018 Jul; 28(7):2422-2430. PubMed ID: 28591836 [TBL] [Abstract][Full Text] [Related]
27. 16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort. Steinman KJ; Spence SJ; Ramocki MB; Proud MB; Kessler SK; Marco EJ; Green Snyder L; D'Angelo D; Chen Q; Chung WK; Sherr EH; Am J Med Genet A; 2016 Nov; 170(11):2943-2955. PubMed ID: 27410714 [TBL] [Abstract][Full Text] [Related]
28. Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub. Forrest MP; Dos Santos M; Piguel NH; Wang YZ; Hawkins NA; Bagchi VA; Dionisio LE; Yoon S; Simkin D; Martin-de-Saavedra MD; Gao R; Horan KE; George AL; LeDoux MS; Kearney JA; Savas JN; Penzes P Nat Commun; 2023 Feb; 14(1):825. PubMed ID: 36808153 [TBL] [Abstract][Full Text] [Related]
29. Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication. Jenkins J; Chow V; Blaskey L; Kuschner E; Qasmieh S; Gaetz L; Edgar JC; Mukherjee P; Buckner R; Nagarajan SS; Chung WK; Spiro JE; Sherr EH; Berman JI; Roberts TP Cereb Cortex; 2016 May; 26(5):1957-64. PubMed ID: 25678630 [TBL] [Abstract][Full Text] [Related]
30. Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome. Yan J; Keener VW; Bi W; Walz K; Bradley A; Justice MJ; Lupski JR Hum Mol Genet; 2004 Nov; 13(21):2613-24. PubMed ID: 15459175 [TBL] [Abstract][Full Text] [Related]
31. Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q). Shim SH; Shim JS; Min K; Lee HS; Park JE; Park SH; Hwang E; Kim M Gene; 2014 Jan; 534(1):100-6. PubMed ID: 24095776 [TBL] [Abstract][Full Text] [Related]
32. Phenotypes Associated with 16p11.2 Copy Number Gains and Losses at a Single Institution. Chu C; Wu H; Xu F; Ray JW; Britt A; Robinson SS; Lupo PJ; Murphy CRC; Dreyer CF; Lee PDK; Hu PC; Dong J Lab Med; 2020 Nov; 51(6):642-648. PubMed ID: 32537635 [TBL] [Abstract][Full Text] [Related]
33. Rock2 heterozygosity improves recognition memory and endothelial function in a mouse model of 16p11.2 deletion autism syndrome. Ouellette J; Lacoste B Neurosci Lett; 2024 Aug; 837():137904. PubMed ID: 39029613 [TBL] [Abstract][Full Text] [Related]
34. The 16p11.2 deletion mouse model of autism exhibits altered cortical progenitor proliferation and brain cytoarchitecture linked to the ERK MAPK pathway. Pucilowska J; Vithayathil J; Tavares EJ; Kelly C; Karlo JC; Landreth GE J Neurosci; 2015 Feb; 35(7):3190-200. PubMed ID: 25698753 [TBL] [Abstract][Full Text] [Related]
35. Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse model. Rusu A; Chevalier C; de Chaumont F; Nalesso V; Brault V; Hérault Y; Ey E Front Behav Neurosci; 2023; 17():1294558. PubMed ID: 38173978 [TBL] [Abstract][Full Text] [Related]
37. Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub. Blizinsky KD; Diaz-Castro B; Forrest MP; Schürmann B; Bach AP; Martin-de-Saavedra MD; Wang L; Csernansky JG; Duan J; Penzes P Proc Natl Acad Sci U S A; 2016 Jul; 113(30):8520-5. PubMed ID: 27402753 [TBL] [Abstract][Full Text] [Related]
38. Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication. Kishimoto K; Nomura J; Ellegood J; Fukumoto K; Lerch JP; Moreno-De-Luca D; Bourgeron T; Tamada K; Takumi T Genes Cells; 2017 May; 22(5):436-451. PubMed ID: 28370817 [TBL] [Abstract][Full Text] [Related]
39. Chemogenetic Activation of Prefrontal Cortex Rescues Synaptic and Behavioral Deficits in a Mouse Model of 16p11.2 Deletion Syndrome. Wang W; Rein B; Zhang F; Tan T; Zhong P; Qin L; Yan Z J Neurosci; 2018 Jun; 38(26):5939-5948. PubMed ID: 29853627 [TBL] [Abstract][Full Text] [Related]
40. Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders. Saito R; Miyoshi C; Koebis M; Kushima I; Nakao K; Mori D; Ozaki N; Funato H; Yanagisawa M; Aiba A Mol Brain; 2021 Apr; 14(1):68. PubMed ID: 33845872 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]