106 related articles for article (PubMed ID: 34680999)
1. Autism Spectrum Disorders: Analysis of Mobile Elements at 7q11.23 Williams-Beuren Region by Comparative Genomics.
Cupaioli FA; Fallerini C; Mencarelli MA; Perticaroli V; Filippini V; Mari F; Renieri A; Mezzelani A
Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34680999
[TBL] [Abstract][Full Text] [Related]
2. Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome.
Codina-Sola M; Costa-Roger M; Pérez-García D; Flores R; Palacios-Verdú MG; Cusco I; Pérez-Jurado LA
J Med Genet; 2019 Dec; 56(12):801-808. PubMed ID: 31413120
[TBL] [Abstract][Full Text] [Related]
3. Consistent hypersocial behavior in mice carrying a deletion of
Martin LA; Iceberg E; Allaf G
Brain Behav; 2018 Jan; 8(1):e00895. PubMed ID: 29568691
[TBL] [Abstract][Full Text] [Related]
4. Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.
Kopp ND; Parrish PCR; Lugo M; Dougherty JD; Kozel BA
Mol Genet Genomic Med; 2018 Sep; 6(5):749-765. PubMed ID: 30008175
[TBL] [Abstract][Full Text] [Related]
5. Autistic disorder in patients with Williams-Beuren syndrome: a reconsideration of the Williams-Beuren syndrome phenotype.
Tordjman S; Anderson GM; Botbol M; Toutain A; Sarda P; Carlier M; Saugier-Veber P; Baumann C; Cohen D; Lagneaux C; Tabet AC; Verloes A
PLoS One; 2012; 7(3):e30778. PubMed ID: 22412832
[TBL] [Abstract][Full Text] [Related]
6. The genomic basis of the Williams-Beuren syndrome.
Schubert C
Cell Mol Life Sci; 2009 Apr; 66(7):1178-97. PubMed ID: 19039520
[TBL] [Abstract][Full Text] [Related]
7. Rearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development.
Osborne LR; Mervis CB
Expert Rev Mol Med; 2007 Jun; 9(15):1-16. PubMed ID: 17565757
[TBL] [Abstract][Full Text] [Related]
8. A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.
Osborne LR; Li M; Pober B; Chitayat D; Bodurtha J; Mandel A; Costa T; Grebe T; Cox S; Tsui LC; Scherer SW
Nat Genet; 2001 Nov; 29(3):321-5. PubMed ID: 11685205
[TBL] [Abstract][Full Text] [Related]
9. Activity of Genes with Functions in Human Williams-Beuren Syndrome Is Impacted by Mobile Element Insertions in the Gray Wolf Genome.
vonHoldt BM; Ji SS; Aardema ML; Stahler DR; Udell MAR; Sinsheimer JS
Genome Biol Evol; 2018 Jun; 10(6):1546-1553. PubMed ID: 29860323
[TBL] [Abstract][Full Text] [Related]
10. Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23.
Antonell A; de Luis O; Domingo-Roura X; Pérez-Jurado LA
Genome Res; 2005 Sep; 15(9):1179-88. PubMed ID: 16140988
[TBL] [Abstract][Full Text] [Related]
11. Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome.
Tordjman S; Anderson GM; Cohen D; Kermarrec S; Carlier M; Touitou Y; Saugier-Veber P; Lagneaux C; Chevreuil C; Verloes A
Mol Autism; 2013 Aug; 4(1):29. PubMed ID: 23972161
[TBL] [Abstract][Full Text] [Related]
12. A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome.
Porter MA; Dobson-Stone C; Kwok JB; Schofield PR; Beckett W; Tassabehji M
PLoS One; 2012; 7(10):e47457. PubMed ID: 23118870
[TBL] [Abstract][Full Text] [Related]
13.
López-Tobón A; Shyti R; Villa CE; Cheroni C; Fuentes-Bravo P; Trattaro S; Caporale N; Troglio F; Tenderini E; Mihailovich M; Skaros A; Gibson WT; Cuomo A; Bonaldi T; Mercurio C; Varasi M; Osborne L; Testa G
Sci Adv; 2023 Dec; 9(48):eadh2726. PubMed ID: 38019906
[TBL] [Abstract][Full Text] [Related]
14. Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Qaiser F; Yin Y; Mervis CB; Morris CA; Klein-Tasman BP; Tam E; Osborne LR; Yuen RKC
Orphanet J Rare Dis; 2021 Jan; 16(1):6. PubMed ID: 33407644
[TBL] [Abstract][Full Text] [Related]
15. Innate frequency-discrimination hyperacuity in Williams-Beuren syndrome mice.
Davenport CM; Teubner BJW; Han SB; Patton MH; Eom TY; Garic D; Lansdell BJ; Shirinifard A; Chang TC; Klein J; Pruett-Miller SM; Blundon JA; Zakharenko SS
Cell; 2022 Oct; 185(21):3877-3895.e21. PubMed ID: 36152627
[TBL] [Abstract][Full Text] [Related]
16. Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes.
Merla G; Howald C; Henrichsen CN; Lyle R; Wyss C; Zabot MT; Antonarakis SE; Reymond A
Am J Hum Genet; 2006 Aug; 79(2):332-41. PubMed ID: 16826523
[TBL] [Abstract][Full Text] [Related]
17. Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome).
Courdier C; Boudjarane J; Malan V; Muti C; Sperelakis-Beedham B; Odent S; Jaillard S; Quelin C; Le Caignec C; Patat O; Dubucs C; Julia S; Schluth-Bolard C; Goumy C; Redon S; Gaillard JB; Huynh MT; Dupont C; Tabet AC; Cogan G; Vialard F; Dard R; Jedraszak G; Jobic F; Lefebvre M; Quenum G; Inai S; Rama M; Sauvestre F; Coatleven F; Thomas J; Rooryck C
Prenat Diagn; 2023 Jun; 43(6):734-745. PubMed ID: 36914926
[TBL] [Abstract][Full Text] [Related]
18. Transposons in the Williams-Beuren Syndrome Critical Region are Associated with Social Behavior in Assistance Dogs.
Gnanadesikan GE; Tandon D; Bray EE; Kennedy BS; Tennenbaum SR; MacLean EL; vonHoldt BM
Behav Genet; 2024 Mar; 54(2):196-211. PubMed ID: 38091228
[TBL] [Abstract][Full Text] [Related]
19. A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion.
Kolaitis G; Bouwkamp CG; Papakonstantinou A; Otheiti I; Belivanaki M; Haritaki S; Korpa T; Albani Z; Terzioglou E; Apostola P; Skamnaki A; Xaidara A; Kosma K; Kitsiou-Tzeli S; Tzetis M
Child Adolesc Psychiatry Ment Health; 2016; 10():33. PubMed ID: 27651829
[TBL] [Abstract][Full Text] [Related]
20. Genomic strategies to untangle the etiology of autism: A primer.
Vashisth S; Chahrour MH
Autism Res; 2023 Jan; 16(1):31-39. PubMed ID: 36415077
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
