173 related articles for article (PubMed ID: 34112971)
1. Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome.
Chapman G; Alsaqati M; Lunn S; Singh T; Linden SC; Linden DEJ; van den Bree MBM; Ziller M; Owen MJ; Hall J; Harwood AJ; Syed YA
Mol Psychiatry; 2022 Feb; 27(2):819-830. PubMed ID: 34112971
[TBL] [Abstract][Full Text] [Related]
2. Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Bernier R; Steinman KJ; Reilly B; Wallace AS; Sherr EH; Pojman N; Mefford HC; Gerdts J; Earl R; Hanson E; Goin-Kochel RP; Berry L; Kanne S; Snyder LG; Spence S; Ramocki MB; Evans DW; Spiro JE; Martin CL; Ledbetter DH; Chung WK;
Genet Med; 2016 Apr; 18(4):341-9. PubMed ID: 26066539
[TBL] [Abstract][Full Text] [Related]
3. Duplication Versus Deletion Through the Lens of 15q13.3: Clinical and Research Implications of Studying Copy Number Variants Associated with Neuropsychiatric Disorders in Induced Pluripotent Stem Cell-Derived Neurons.
Antony I; Narasimhan M; Shen R; Prakasam R; Kaushik K; Chapman G; Kroll KL
Stem Cell Rev Rep; 2023 Apr; 19(3):639-650. PubMed ID: 36370261
[TBL] [Abstract][Full Text] [Related]
4. Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders.
Yoon J; Mao Y
Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34071723
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. An eight-case 1q21 region series: novel aberrations and clinical variability with new features.
Ceylan AC; Sahin I; Erdem HB; Kayhan G; Simsek-Kiper PO; Utine GE; Percin F; Boduroglu K; Alikasifoglu M
J Intellect Disabil Res; 2019 Jun; 63(6):548-557. PubMed ID: 30773728
[TBL] [Abstract][Full Text] [Related]
7. Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.
Busè M; Cuttaia HC; Palazzo D; Mazara MV; Lauricella SA; Malacarne M; Pierluigi M; Cavani S; Piccione M
Ital J Pediatr; 2017 Jul; 43(1):61. PubMed ID: 28724436
[TBL] [Abstract][Full Text] [Related]
8. Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literature.
Upadhyai P; Amiri EF; Guleria VS; Bielas SL; Girisha KM; Shukla A
Clin Dysmorphol; 2020 Jul; 29(3):127-131. PubMed ID: 32459673
[TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
Wang HD; Liu L; Wu D; Li T; Cui CY; Zhang LZ; Wang CZ
J Gene Med; 2017 Apr; 19(4):. PubMed ID: 28220983
[TBL] [Abstract][Full Text] [Related]
10. [Establishment of induced pluripotent stem cell lines from human amniotic fluid cells with 1q21.1 microdeletion].
Gong Y; Li Y; Song Y; Sun X; Song B; Sun W; Chen X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):175-9. PubMed ID: 25863080
[TBL] [Abstract][Full Text] [Related]
11. Altered neuronal physiology, development, and function associated with a common chromosome 15 duplication involving CHRNA7.
Meganathan K; Prakasam R; Baldridge D; Gontarz P; Zhang B; Urano F; Bonni A; Maloney SE; Turner TN; Huettner JE; Constantino JN; Kroll KL
BMC Biol; 2021 Jul; 19(1):147. PubMed ID: 34320968
[TBL] [Abstract][Full Text] [Related]
12. The psychiatric phenotypes of 1q21 distal deletion and duplication.
Linden SC; Watson CJ; Smith J; Chawner SJRA; Lancaster TM; Evans F; Williams N; Skuse D; Raymond FL; Hall J; Owen MJ; Linden DEJ; Green-Snyder L; Chung WK; Maillard AM; Jacquemont S; van den Bree MBM
Transl Psychiatry; 2021 Feb; 11(1):105. PubMed ID: 33542195
[TBL] [Abstract][Full Text] [Related]
13. Understanding the impact of 1q21.1 copy number variant.
Harvard C; Strong E; Mercier E; Colnaghi R; Alcantara D; Chow E; Martell S; Tyson C; Hrynchak M; McGillivray B; Hamilton S; Marles S; Mhanni A; Dawson AJ; Pavlidis P; Qiao Y; Holden JJ; Lewis SM; O'Driscoll M; Rajcan-Separovic E
Orphanet J Rare Dis; 2011 Aug; 6():54. PubMed ID: 21824431
[TBL] [Abstract][Full Text] [Related]
14. Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.
Rosenfeld JA; Traylor RN; Schaefer GB; McPherson EW; Ballif BC; Klopocki E; Mundlos S; Shaffer LG; Aylsworth AS;
Eur J Hum Genet; 2012 Jul; 20(7):754-61. PubMed ID: 22317977
[TBL] [Abstract][Full Text] [Related]
15. Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.
Boen R; Kaufmann T; van der Meer D; Frei O; Agartz I; Ames D; Andersson M; Armstrong NJ; Artiges E; Atkins JR; Bauer J; Benedetti F; Boomsma DI; Brodaty H; Brosch K; Buckner RL; Cairns MJ; Calhoun V; Caspers S; Cichon S; Corvin AP; Crespo-Facorro B; Dannlowski U; David FS; de Geus EJC; de Zubicaray GI; Desrivières S; Doherty JL; Donohoe G; Ehrlich S; Eising E; Espeseth T; Fisher SE; Forstner AJ; Fortaner-Uyà L; Frouin V; Fukunaga M; Ge T; Glahn DC; Goltermann J; Grabe HJ; Green MJ; Groenewold NA; Grotegerd D; Grøntvedt GR; Hahn T; Hashimoto R; Hehir-Kwa JY; Henskens FA; Holmes AJ; Håberg AK; Haavik J; Jacquemont S; Jansen A; Jockwitz C; Jönsson EG; Kikuchi M; Kircher T; Kumar K; Le Hellard S; Leu C; Linden DE; Liu J; Loughnan R; Mather KA; McMahon KL; McRae AF; Medland SE; Meinert S; Moreau CA; Morris DW; Mowry BJ; Mühleisen TW; Nenadić I; Nöthen MM; Nyberg L; Ophoff RA; Owen MJ; Pantelis C; Paolini M; Paus T; Pausova Z; Persson K; Quidé Y; Marques TR; Sachdev PS; Sando SB; Schall U; Scott RJ; Selbæk G; Shumskaya E; Silva AI; Sisodiya SM; Stein F; Stein DJ; Straube B; Streit F; Strike LT; Teumer A; Teutenberg L; Thalamuthu A; Tooney PA; Tordesillas-Gutierrez D; Trollor JN; van 't Ent D; van den Bree MBM; van Haren NEM; Vázquez-Bourgon J; Völzke H; Wen W; Wittfeld K; Ching CRK; Westlye LT; Thompson PM; Bearden CE; Selmer KK; Alnæs D; Andreassen OA; Sønderby IE;
Biol Psychiatry; 2024 Jan; 95(2):147-160. PubMed ID: 37661008
[TBL] [Abstract][Full Text] [Related]
16. DUF1220-domain copy number implicated in human brain-size pathology and evolution.
Dumas LJ; O'Bleness MS; Davis JM; Dickens CM; Anderson N; Keeney JG; Jackson J; Sikela M; Raznahan A; Giedd J; Rapoport J; Nagamani SS; Erez A; Brunetti-Pierri N; Sugalski R; Lupski JR; Fingerlin T; Cheung SW; Sikela JM
Am J Hum Genet; 2012 Sep; 91(3):444-54. PubMed ID: 22901949
[TBL] [Abstract][Full Text] [Related]
17. Discordance of cardiovascular abnormalities in a monozygotic twin pair carrying a class II 1q21.1 microdeletion.
Shi SS; Lin SB; Cai DL; Wen WR; Li RM
Taiwan J Obstet Gynecol; 2020 Jan; 59(1):123-126. PubMed ID: 32039779
[TBL] [Abstract][Full Text] [Related]
18. A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men.
Lacaria M; Saha P; Potocki L; Bi W; Yan J; Girirajan S; Burns B; Elsea S; Walz K; Chan L; Lupski JR; Gu W
PLoS Genet; 2012; 8(5):e1002713. PubMed ID: 22654670
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of clinical characteristics and molecular genetics in eighteen patients with 1q21.1 microdeletion syndrome].
Luo X; Niu H; Zhou F; Li S; Li Z; Guo Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Apr; 41(4):480-485. PubMed ID: 38565516
[TBL] [Abstract][Full Text] [Related]
20. Clinical characterization of individuals with the distal 1q21.1 microdeletion.
Edwards SD; Schulze KV; Rosenfeld JA; Westerfield LE; Gerard A; Yuan B; Grigorenko EL; Posey JE; Bi W; Liu P
Am J Med Genet A; 2021 May; 185(5):1388-1398. PubMed ID: 33576134
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
