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4. 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]
5. The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition. Hippolyte L; Maillard AM; Rodriguez-Herreros B; Pain A; Martin-Brevet S; Ferrari C; Conus P; Macé A; Hadjikhani N; Metspalu A; Reigo A; Kolk A; Männik K; Barker M; Isidor B; Le Caignec C; Mignot C; Schneider L; Mottron L; Keren B; David A; Doco-Fenzy M; Gérard M; Bernier R; Goin-Kochel RP; Hanson E; Green Snyder L; ; Ramus F; Beckmann JS; Draganski B; Reymond A; Jacquemont S Biol Psychiatry; 2016 Jul; 80(2):129-139. PubMed ID: 26742926 [TBL] [Abstract][Full Text] [Related]
6. Sensorimotor Cortical Oscillations during Movement Preparation in 16p11.2 Deletion Carriers. Hinkley LBN; Dale CL; Luks TL; Findlay AM; Bukshpun P; Pojman N; Thieu T; Chung WK; Berman J; Roberts TPL; Mukherjee P; Sherr EH; Nagarajan SS J Neurosci; 2019 Sep; 39(37):7321-7331. PubMed ID: 31270155 [TBL] [Abstract][Full Text] [Related]
7. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. Shinawi M; Liu P; Kang SH; Shen J; Belmont JW; Scott DA; Probst FJ; Craigen WJ; Graham BH; Pursley A; Clark G; Lee J; Proud M; Stocco A; Rodriguez DL; Kozel BA; Sparagana S; Roeder ER; McGrew SG; Kurczynski TW; Allison LJ; Amato S; Savage S; Patel A; Stankiewicz P; Beaudet AL; Cheung SW; Lupski JR J Med Genet; 2010 May; 47(5):332-41. PubMed ID: 19914906 [TBL] [Abstract][Full Text] [Related]
8. Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion. Mei C; Fedorenko E; Amor DJ; Boys A; Hoeflin C; Carew P; Burgess T; Fisher SE; Morgan AT Eur J Hum Genet; 2018 May; 26(5):676-686. PubMed ID: 29445122 [TBL] [Abstract][Full Text] [Related]
9. Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication. Green Snyder L; D'Angelo D; Chen Q; Bernier R; Goin-Kochel RP; Wallace AS; Gerdts J; Kanne S; Berry L; Blaskey L; Kuschner E; Roberts T; Sherr E; Martin CL; Ledbetter DH; Spiro JE; Chung WK; Hanson E; J Autism Dev Disord; 2016 Aug; 46(8):2734-2748. PubMed ID: 27207092 [TBL] [Abstract][Full Text] [Related]
10. Developmental trajectories for young children with 16p11.2 copy number variation. Bernier R; Hudac CM; Chen Q; Zeng C; Wallace AS; Gerdts J; Earl R; Peterson J; Wolken A; Peters A; Hanson E; Goin-Kochel RP; Kanne S; Snyder LG; Chung WK; Am J Med Genet B Neuropsychiatr Genet; 2017 Jun; 174(4):367-380. PubMed ID: 28349640 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. The Phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples. Woodbury-Smith M; D'Abate L; Stavropoulos DJ; Howe J; Drmic I; Hoang N; Zarrei M; Trost B; Iaboni A; Anagnostou E; Scherer SW J Med Genet; 2023 Nov; 60(12):1153-1160. PubMed ID: 37290907 [TBL] [Abstract][Full Text] [Related]
13. Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism". Duyzend MH; Eichler EE Biol Psychiatry; 2015 May; 77(9):769-71. PubMed ID: 25843334 [No Abstract] [Full Text] [Related]
14. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions. Moreno-De-Luca A; Evans DW; Boomer KB; Hanson E; Bernier R; Goin-Kochel RP; Myers SM; Challman TD; Moreno-De-Luca D; Slane MM; Hare AE; Chung WK; Spiro JE; Faucett WA; Martin CL; Ledbetter DH JAMA Psychiatry; 2015 Feb; 72(2):119-26. PubMed ID: 25493922 [TBL] [Abstract][Full Text] [Related]