251 related articles for article (PubMed ID: 31353025)
1. Phenome-wide Burden of Copy-Number Variation in the UK Biobank.
Aguirre M; Rivas MA; Priest J
Am J Hum Genet; 2019 Aug; 105(2):373-383. PubMed ID: 31353025
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Bassett AS; Lowther C; Merico D; Costain G; Chow EWC; van Amelsvoort T; McDonald-McGinn D; Gur RE; Swillen A; Van den Bree M; Murphy K; Gothelf D; Bearden CE; Eliez S; Kates W; Philip N; Sashi V; Campbell L; Vorstman J; Cubells J; Repetto GM; Simon T; Boot E; Heung T; Evers R; Vingerhoets C; van Duin E; Zackai E; Vergaelen E; Devriendt K; Vermeesch JR; Owen M; Murphy C; Michaelovosky E; Kushan L; Schneider M; Fremont W; Busa T; Hooper S; McCabe K; Duijff S; Isaev K; Pellecchia G; Wei J; Gazzellone MJ; Scherer SW; Emanuel BS; Guo T; Morrow BE; Marshall CR;
Am J Psychiatry; 2017 Nov; 174(11):1054-1063. PubMed ID: 28750581
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.
Qiu Y; Arbogast T; Lorenzo SM; Li H; Tang SC; Richardson E; Hong O; Cho S; Shanta O; Pang T; Corsello C; Deutsch CK; Chevalier C; Davis EE; Iakoucheva LM; Herault Y; Katsanis N; Messer K; Sebat J
Cell Rep; 2019 Sep; 28(13):3320-3328.e4. PubMed ID: 31553903
[TBL] [Abstract][Full Text] [Related]
6. An Update on Common Chromosome Microdeletion and Microduplication Syndromes.
Goldenberg P
Pediatr Ann; 2018 May; 47(5):e198-e203. PubMed ID: 29750287
[TBL] [Abstract][Full Text] [Related]
7. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
Yap CX; Alvares GA; Henders AK; Lin T; Wallace L; Farrelly A; McLaren T; Berry J; Vinkhuyzen AAE; Trzaskowski M; Zeng J; Yang Y; Cleary D; Grove R; Hafekost C; Harun A; Holdsworth H; Jellett R; Khan F; Lawson L; Leslie J; Levis Frenk M; Masi A; Mathew NE; Muniandy M; Nothard M; Visscher PM; Dawson PA; Dissanayake C; Eapen V; Heussler HS; Whitehouse AJO; Wray NR; Gratten J
Mol Autism; 2021 Feb; 12(1):12. PubMed ID: 33568206
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
Rees E; Kendall K; Pardiñas AF; Legge SE; Pocklington A; Escott-Price V; MacCabe JH; Collier DA; Holmans P; O'Donovan MC; Owen MJ; Walters JTR; Kirov G
JAMA Psychiatry; 2016 Sep; 73(9):963-969. PubMed ID: 27602560
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM
Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457
[TBL] [Abstract][Full Text] [Related]
13. Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children.
Fetit R; Price DJ; Lawrie SM; Johnstone M
Psychiatr Genet; 2020 Oct; 30(5):136-140. PubMed ID: 32732550
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank.
Owen D; Bracher-Smith M; Kendall KM; Rees E; Einon M; Escott-Price V; Owen MJ; O'Donovan MC; Kirov G
BMC Genomics; 2018 Dec; 19(1):867. PubMed ID: 30509170
[TBL] [Abstract][Full Text] [Related]
18. Clinical and Genetic Study of Three Inherited Microdeletions of Chromosome 16p11.2.
Liu F; Liu R; Yu C; Duan J; Hu Y; Luo L
Altern Ther Health Med; 2024 Mar; 30(3):190-192. PubMed ID: 37856819
[TBL] [Abstract][Full Text] [Related]
19. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
[TBL] [Abstract][Full Text] [Related]
20. Who ever heard of 16p11.2 deletion syndrome? Parents' perspectives on a susceptibility copy number variation syndrome.
Kleinendorst L; van den Heuvel LM; Henneman L; van Haelst MM
Eur J Hum Genet; 2020 Sep; 28(9):1196-1204. PubMed ID: 32415274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]