316 related articles for article (PubMed ID: 25531260)
1. From Prader-Willi syndrome to psychosis: translating parent-of-origin effects into schizophrenia research.
Krefft M; Frydecka D; Adamowski T; Misiak B
Epigenomics; 2014; 6(6):677-88. PubMed ID: 25531260
[TBL] [Abstract][Full Text] [Related]
2. Mechanistic insights into the genetics of affective psychosis from Prader-Willi syndrome.
Aman LCS; Manning KE; Whittington JE; Holland AJ
Lancet Psychiatry; 2018 Apr; 5(4):370-378. PubMed ID: 29352661
[TBL] [Abstract][Full Text] [Related]
3. Psychotic illness in people with Prader-Willi syndrome: a systematic review of clinical presentation, course and phenomenology.
Aman LCS; Lester SD; Holland AJ; Fletcher PC
Orphanet J Rare Dis; 2024 Feb; 19(1):69. PubMed ID: 38360662
[TBL] [Abstract][Full Text] [Related]
4. Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.
Whittington JE; Butler JV; Holland AJ
Eur J Hum Genet; 2007 Jan; 15(1):127-30. PubMed ID: 16957680
[TBL] [Abstract][Full Text] [Related]
5. The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea.
Cho SY; Ki CS; Sohn YB; Maeng SH; Jung YJ; Kim SJ; Jin DK
J Hum Genet; 2013 Mar; 58(3):150-4. PubMed ID: 23303386
[TBL] [Abstract][Full Text] [Related]
6. Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome.
Vogels A; Matthijs G; Legius E; Devriendt K; Fryns JP
J Med Genet; 2003 Jan; 40(1):72-3. PubMed ID: 12525547
[No Abstract] [Full Text] [Related]
7. Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.
Zilina O; Kahre T; Talvik I; Oiglane-Shlik E; Tillmann V; Ounap K
Eur J Med Genet; 2014; 57(6):279-83. PubMed ID: 24704109
[TBL] [Abstract][Full Text] [Related]
8. Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.
Boer H; Holland A; Whittington J; Butler J; Webb T; Clarke D
Lancet; 2002 Jan; 359(9301):135-6. PubMed ID: 11809260
[TBL] [Abstract][Full Text] [Related]
9. Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD.
Muthusamy K; Macke EL; Klee EW; Tebben PJ; Hand JL; Hasadsri L; Marcou CA; Schimmenti LA
Am J Med Genet A; 2020 Oct; 182(10):2442-2449. PubMed ID: 32815268
[TBL] [Abstract][Full Text] [Related]
10. Prader-Willi syndrome: reflections on seminal studies and future therapies.
Chung MS; Langouët M; Chamberlain SJ; Carmichael GG
Open Biol; 2020 Sep; 10(9):200195. PubMed ID: 32961075
[TBL] [Abstract][Full Text] [Related]
11. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
Nicholls RD
Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
[TBL] [Abstract][Full Text] [Related]
12. Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.
Ingason A; Kirov G; Giegling I; Hansen T; Isles AR; Jakobsen KD; Kristinsson KT; le Roux L; Gustafsson O; Craddock N; Möller HJ; McQuillin A; Muglia P; Cichon S; Rietschel M; Ophoff RA; Djurovic S; Andreassen OA; Pietiläinen OP; Peltonen L; Dempster E; Collier DA; St Clair D; Rasmussen HB; Glenthøj BY; Kiemeney LA; Franke B; Tosato S; Bonetto C; Saemundsen E; Hreidarsson SJ; ; Nöthen MM; Gurling H; O'Donovan MC; Owen MJ; Sigurdsson E; Petursson H; Stefansson H; Rujescu D; Stefansson K; Werge T
Am J Psychiatry; 2011 Apr; 168(4):408-17. PubMed ID: 21324950
[TBL] [Abstract][Full Text] [Related]
13. Expressive and receptive language in Prader-Willi syndrome: report on genetic subtype differences.
Dimitropoulos A; Ferranti A; Lemler M
J Commun Disord; 2013; 46(2):193-201. PubMed ID: 23295077
[TBL] [Abstract][Full Text] [Related]
14. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
Hassan M; Butler MG
Eur J Med Genet; 2016 Nov; 59(11):584-589. PubMed ID: 27659713
[TBL] [Abstract][Full Text] [Related]
15. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N
Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
[TBL] [Abstract][Full Text] [Related]
16. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
Hartin SN; Hossain WA; Weisensel N; Butler MG
Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
[TBL] [Abstract][Full Text] [Related]
17. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Bittel DC; Butler MG
Expert Rev Mol Med; 2005 Jul; 7(14):1-20. PubMed ID: 16038620
[TBL] [Abstract][Full Text] [Related]
18. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
[TBL] [Abstract][Full Text] [Related]
19. Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis.
Heseding HM; Jahn K; Eberlein CK; Wieting J; Maier HB; Proskynitopoulos PJ; Glahn A; Bleich S; Frieling H; Deest M
Transl Psychiatry; 2022 Jun; 12(1):246. PubMed ID: 35688807
[TBL] [Abstract][Full Text] [Related]
20. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
Isles AR; Ingason A; Lowther C; Walters J; Gawlick M; Stöber G; Rees E; Martin J; Little RB; Potter H; Georgieva L; Pizzo L; Ozaki N; Aleksic B; Kushima I; Ikeda M; Iwata N; Levinson DF; Gejman PV; Shi J; Sanders AR; Duan J; Willis J; Sisodiya S; Costain G; Werge TM; Degenhardt F; Giegling I; Rujescu D; Hreidarsson SJ; Saemundsen E; Ahn JW; Ogilvie C; Girirajan SD; Stefansson H; Stefansson K; O'Donovan MC; Owen MJ; Bassett A; Kirov G
PLoS Genet; 2016 May; 12(5):e1005993. PubMed ID: 27153221
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
