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3. Mouse Model of Chromosome 15q13.3 Microdeletion Syndrome Demonstrates Features Related to Autism Spectrum Disorder. Kogan JH; Gross AK; Featherstone RE; Shin R; Chen Q; Heusner CL; Adachi M; Lin A; Walton NM; Miyoshi S; Miyake S; Tajinda K; Ito H; Siegel SJ; Matsumoto M J Neurosci; 2015 Dec; 35(49):16282-94. PubMed ID: 26658876 [TBL] [Abstract][Full Text] [Related]
4. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. Miller DT; Shen Y; Weiss LA; Korn J; Anselm I; Bridgemohan C; Cox GF; Dickinson H; Gentile J; Harris DJ; Hegde V; Hundley R; Khwaja O; Kothare S; Luedke C; Nasir R; Poduri A; Prasad K; Raffalli P; Reinhard A; Smith SE; Sobeih MM; Soul JS; Stoler J; Takeoka M; Tan WH; Thakuria J; Wolff R; Yusupov R; Gusella JF; Daly MJ; Wu BL J Med Genet; 2009 Apr; 46(4):242-8. PubMed ID: 18805830 [TBL] [Abstract][Full Text] [Related]
5. Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders. Ben-Shachar S; Lanpher B; German JR; Qasaymeh M; Potocki L; Nagamani SC; Franco LM; Malphrus A; Bottenfield GW; Spence JE; Amato S; Rousseau JA; Moghaddam B; Skinner C; Skinner SA; Bernes S; Armstrong N; Shinawi M; Stankiewicz P; Patel A; Cheung SW; Lupski JR; Beaudet AL; Sahoo T J Med Genet; 2009 Jun; 46(6):382-8. PubMed ID: 19289393 [TBL] [Abstract][Full Text] [Related]
6. OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome. Uddin M; Unda BK; Kwan V; Holzapfel NT; White SH; Chalil L; Woodbury-Smith M; Ho KS; Harward E; Murtaza N; Dave B; Pellecchia G; D'Abate L; Nalpathamkalam T; Lamoureux S; Wei J; Speevak M; Stavropoulos J; Hope KJ; Doble BW; Nielsen J; Wassman ER; Scherer SW; Singh KK Am J Hum Genet; 2018 Feb; 102(2):278-295. PubMed ID: 29395074 [TBL] [Abstract][Full Text] [Related]
7. Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons. Zhang S; Zhang X; Purmann C; Ma S; Shrestha A; Davis KN; Ho M; Huang Y; Pattni R; Wong WH; Bernstein JA; Hallmayer J; Urban AE Biol Psychiatry; 2021 Mar; 89(5):497-509. PubMed ID: 32919612 [TBL] [Abstract][Full Text] [Related]
8. Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature. Lowther C; Costain G; Stavropoulos DJ; Melvin R; Silversides CK; Andrade DM; So J; Faghfoury H; Lionel AC; Marshall CR; Scherer SW; Bassett AS Genet Med; 2015 Feb; 17(2):149-57. PubMed ID: 25077648 [TBL] [Abstract][Full Text] [Related]
9. The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Ziats MN; Goin-Kochel RP; Berry LN; Ali M; Ge J; Guffey D; Rosenfeld JA; Bader P; Gambello MJ; Wolf V; Penney LS; Miller R; Lebel RR; Kane J; Bachman K; Troxell R; Clark G; Minard CG; Stankiewicz P; Beaudet A; Schaaf CP Genet Med; 2016 Nov; 18(11):1111-1118. PubMed ID: 26963284 [TBL] [Abstract][Full Text] [Related]
10. Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype. Hoppman-Chaney N; Wain K; Seger PR; Superneau DW; Hodge JC Clin Genet; 2013 Apr; 83(4):345-51. PubMed ID: 22775350 [TBL] [Abstract][Full Text] [Related]
11. R-Baclofen Reverses Cognitive Deficits and Improves Social Interactions in Two Lines of 16p11.2 Deletion Mice. Stoppel LJ; Kazdoba TM; Schaffler MD; Preza AR; Heynen A; Crawley JN; Bear MF Neuropsychopharmacology; 2018 Feb; 43(3):513-524. PubMed ID: 28984295 [TBL] [Abstract][Full Text] [Related]
12. Following the Trail From Genotype to Phenotypes. Lord C; Veenstra-VanderWeele J JAMA Psychiatry; 2016 Jan; 73(1):7-8. PubMed ID: 26630619 [No Abstract] [Full Text] [Related]
13. 3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients. Città S; Buono S; Greco D; Barone C; Alfei E; Bulgheroni S; Usilla A; Pantaleoni C; Romano C Am J Med Genet A; 2013 Dec; 161A(12):3018-22. PubMed ID: 24214349 [TBL] [Abstract][Full Text] [Related]
14. An acetylcholine alpha7 positive allosteric modulator rescues a schizophrenia-associated brain endophenotype in the 15q13.3 microdeletion, encompassing CHRNA7. Gass N; Weber-Fahr W; Sartorius A; Becker R; Didriksen M; Stensbøl TB; Bastlund JF; Meyer-Lindenberg A; Schwarz AJ Eur Neuropsychopharmacol; 2016 Jul; 26(7):1150-60. PubMed ID: 27061851 [TBL] [Abstract][Full Text] [Related]
15. Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies. Jähn JA; von Spiczak S; Muhle H; Obermeier T; Franke A; Mefford HC; Stephani U; Helbig I Epilepsy Res; 2014 Jan; 108(1):109-16. PubMed ID: 24246141 [TBL] [Abstract][Full Text] [Related]
16. Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. Yin J; Chen W; Chao ES; Soriano S; Wang L; Wang W; Cummock SE; Tao H; Pang K; Liu Z; Pereira FA; Samaco RC; Zoghbi HY; Xue M; Schaaf CP Am J Hum Genet; 2018 Feb; 102(2):296-308. PubMed ID: 29395075 [TBL] [Abstract][Full Text] [Related]
17. Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome. Murphy MM; Lindsey Burrell T; Cubells JF; España RA; Gambello MJ; Goines KCB; Klaiman C; Li L; Novacek DM; Papetti A; Sanchez Russo RL; Saulnier CA; Shultz S; Walker E; Mulle JG BMC Psychiatry; 2018 Jun; 18(1):183. PubMed ID: 29884173 [TBL] [Abstract][Full Text] [Related]
18. Interactive effects between hemizygous 15q13.3 microdeletion and peripubertal stress on adult behavioral functions. Giovanoli S; Werge TM; Mortensen PB; Didriksen M; Meyer U Neuropsychopharmacology; 2019 Mar; 44(4):703-710. PubMed ID: 30188511 [TBL] [Abstract][Full Text] [Related]
19. Characterizing cognitive control abilities in children with 16p11.2 deletion using adaptive 'video game' technology: a pilot study. Anguera JA; Brandes-Aitken AN; Rolle CE; Skinner SN; Desai SS; Bower JD; Martucci WE; Chung WK; Sherr EH; Marco EJ Transl Psychiatry; 2016 Sep; 6(9):e893. PubMed ID: 27648915 [TBL] [Abstract][Full Text] [Related]
20. A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterations. Fejgin K; Nielsen J; Birknow MR; Bastlund JF; Nielsen V; Lauridsen JB; Stefansson H; Steinberg S; Sorensen HB; Mortensen TE; Larsen PH; Klewe IV; Rasmussen SV; Stefansson K; Werge TM; Kallunki P; Christensen KV; Didriksen M Biol Psychiatry; 2014 Jul; 76(2):128-37. PubMed ID: 24090792 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]