487 related articles for article (PubMed ID: 27240531)
1. Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.
Loviglio MN; Leleu M; Männik K; Passeggeri M; Giannuzzi G; van der Werf I; Waszak SM; Zazhytska M; Roberts-Caldeira I; Gheldof N; Migliavacca E; Alfaiz AA; Hippolyte L; Maillard AM; ; ; Van Dijck A; Kooy RF; Sanlaville D; Rosenfeld JA; Shaffer LG; Andrieux J; Marshall C; Scherer SW; Shen Y; Gusella JF; Thorsteinsdottir U; Thorleifsson G; Dermitzakis ET; Deplancke B; Beckmann JS; Rougemont J; Jacquemont S; Reymond A
Mol Psychiatry; 2017 Jun; 22(6):836-849. PubMed ID: 27240531
[TBL] [Abstract][Full Text] [Related]
2. The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs.
Loviglio MN; Arbogast T; Jønch AE; Collins SC; Popadin K; Bonnet CS; Giannuzzi G; Maillard AM; Jacquemont S; ; Yalcin B; Katsanis N; Golzio C; Reymond A
Am J Hum Genet; 2017 Oct; 101(4):564-577. PubMed ID: 28965845
[TBL] [Abstract][Full Text] [Related]
3. 16p11.2 Locus modulates response to satiety before the onset of obesity.
Maillard AM; Hippolyte L; Rodriguez-Herreros B; Chawner SJ; Dremmel D; Agüera Z; Fagundo AB; Pain A; Martin-Brevet S; Hilbert A; Kurz S; Etienne R; Draganski B; Jimenez-Murcia S; Männik K; Metspalu A; Reigo A; Isidor B; Le Caignec C; David A; Mignot C; Keren B; ; van den Bree MB; Munsch S; Fernandez-Aranda F; Beckmann JS; Reymond A; Jacquemont S
Int J Obes (Lond); 2016 May; 40(5):870-6. PubMed ID: 26620891
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Language characterization in 16p11.2 deletion and duplication syndromes.
Kim SH; Green-Snyder L; Lord C; Bishop S; Steinman KJ; Bernier R; Hanson E; Goin-Kochel RP; Chung WK
Am J Med Genet B Neuropsychiatr Genet; 2020 Sep; 183(6):380-391. PubMed ID: 32652891
[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. Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.
Blumenthal I; Ragavendran A; Erdin S; Klei L; Sugathan A; Guide JR; Manavalan P; Zhou JQ; Wheeler VC; Levin JZ; Ernst C; Roeder K; Devlin B; Gusella JF; Talkowski ME
Am J Hum Genet; 2014 Jun; 94(6):870-83. PubMed ID: 24906019
[TBL] [Abstract][Full Text] [Related]
9. Motor difficulties in 16p11.2 copy number variation.
Jutla A; Harvey L; Veenstra-VanderWeele J; Chung WK
Autism Res; 2024 May; 17(5):906-916. PubMed ID: 38660979
[TBL] [Abstract][Full Text] [Related]
10. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Jacquemont S; Reymond A; Zufferey F; Harewood L; Walters RG; Kutalik Z; Martinet D; Shen Y; Valsesia A; Beckmann ND; Thorleifsson G; Belfiore M; Bouquillon S; Campion D; de Leeuw N; de Vries BB; Esko T; Fernandez BA; Fernández-Aranda F; Fernández-Real JM; Gratacòs M; Guilmatre A; Hoyer J; Jarvelin MR; Kooy RF; Kurg A; Le Caignec C; Männik K; Platt OS; Sanlaville D; Van Haelst MM; Villatoro Gomez S; Walha F; Wu BL; Yu Y; Aboura A; Addor MC; Alembik Y; Antonarakis SE; Arveiler B; Barth M; Bednarek N; Béna F; Bergmann S; Beri M; Bernardini L; Blaumeiser B; Bonneau D; Bottani A; Boute O; Brunner HG; Cailley D; Callier P; Chiesa J; Chrast J; Coin L; Coutton C; Cuisset JM; Cuvellier JC; David A; de Freminville B; Delobel B; Delrue MA; Demeer B; Descamps D; Didelot G; Dieterich K; Disciglio V; Doco-Fenzy M; Drunat S; Duban-Bedu B; Dubourg C; El-Sayed Moustafa JS; Elliott P; Faas BH; Faivre L; Faudet A; Fellmann F; Ferrarini A; Fisher R; Flori E; Forer L; Gaillard D; Gerard M; Gieger C; Gimelli S; Gimelli G; Grabe HJ; Guichet A; Guillin O; Hartikainen AL; Heron D; Hippolyte L; Holder M; Homuth G; Isidor B; Jaillard S; Jaros Z; Jiménez-Murcia S; Helas GJ; Jonveaux P; Kaksonen S; Keren B; Kloss-Brandstätter A; Knoers NV; Koolen DA; Kroisel PM; Kronenberg F; Labalme A; Landais E; Lapi E; Layet V; Legallic S; Leheup B; Leube B; Lewis S; Lucas J; MacDermot KD; Magnusson P; Marshall C; Mathieu-Dramard M; McCarthy MI; Meitinger T; Mencarelli MA; Merla G; Moerman A; Mooser V; Morice-Picard F; Mucciolo M; Nauck M; Ndiaye NC; Nordgren A; Pasquier L; Petit F; Pfundt R; Plessis G; Rajcan-Separovic E; Ramelli GP; Rauch A; Ravazzolo R; Reis A; Renieri A; Richart C; Ried JS; Rieubland C; Roberts W; Roetzer KM; Rooryck C; Rossi M; Saemundsen E; Satre V; Schurmann C; Sigurdsson E; Stavropoulos DJ; Stefansson H; Tengström C; Thorsteinsdóttir U; Tinahones FJ; Touraine R; Vallée L; van Binsbergen E; Van der Aa N; Vincent-Delorme C; Visvikis-Siest S; Vollenweider P; Völzke H; Vulto-van Silfhout AT; Waeber G; Wallgren-Pettersson C; Witwicki RM; Zwolinksi S; Andrieux J; Estivill X; Gusella JF; Gustafsson O; Metspalu A; Scherer SW; Stefansson K; Blakemore AI; Beckmann JS; Froguel P
Nature; 2011 Aug; 478(7367):97-102. PubMed ID: 21881559
[TBL] [Abstract][Full Text] [Related]
11. Atypical neural variability in carriers of 16p11.2 copy number variants.
Al-Jawahiri R; Jones M; Milne E
Autism Res; 2019 Sep; 12(9):1322-1333. PubMed ID: 31260176
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
Giannuzzi G; Schmidt PJ; Porcu E; Willemin G; Munson KM; Nuttle X; Earl R; Chrast J; Hoekzema K; Risso D; Männik K; De Nittis P; Baratz ED; ; Herault Y; Gao X; Philpott CC; Bernier RA; Kutalik Z; Fleming MD; Eichler EE; Reymond A
Am J Hum Genet; 2019 Nov; 105(5):947-958. PubMed ID: 31668704
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
Vysotskiy M; Zhong X; Miller-Fleming TW; Zhou D; ; ; ; Cox NJ; Weiss LA
Genome Med; 2021 Oct; 13(1):172. PubMed ID: 34715901
[TBL] [Abstract][Full Text] [Related]
16. Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder.
Deshpande A; Yadav S; Dao DQ; Wu ZY; Hokanson KC; Cahill MK; Wiita AP; Jan YN; Ullian EM; Weiss LA
Cell Rep; 2017 Dec; 21(10):2678-2687. PubMed ID: 29212016
[TBL] [Abstract][Full Text] [Related]
17. 16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2.
Barber JC; Hall V; Maloney VK; Huang S; Roberts AM; Brady AF; Foulds N; Bewes B; Volleth M; Liehr T; Mehnert K; Bateman M; White H
Eur J Hum Genet; 2013 Feb; 21(2):182-9. PubMed ID: 22828807
[TBL] [Abstract][Full Text] [Related]
18. Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature.
Lengyel A; Pinti É; Pikó H; Jávorszky E; David D; Tihanyi M; Gönczi É; Kiss E; Tóth Z; Tory K; Fekete G; Haltrich I
Eur J Med Genet; 2020 Oct; 63(10):104027. PubMed ID: 32758661
[TBL] [Abstract][Full Text] [Related]
19. Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways.
Pettersson M; Viljakainen H; Loid P; Mustila T; Pekkinen M; Armenio M; Andersson-Assarsson JC; Mäkitie O; Lindstrand A
J Clin Endocrinol Metab; 2017 Aug; 102(8):3029-3039. PubMed ID: 28605459
[TBL] [Abstract][Full Text] [Related]
20. Characterizing Sleep Problems in 16p11.2 Deletion and Duplication.
Kamara D; De Boeck P; Lecavalier L; Neuhaus E; Beauchaine TP
J Autism Dev Disord; 2023 Apr; 53(4):1462-1475. PubMed ID: 34633643
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
