460 related articles for article (PubMed ID: 30258228)
1. Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Niemi MEK; Martin HC; Rice DL; Gallone G; Gordon S; Kelemen M; McAloney K; McRae J; Radford EJ; Yu S; Gecz J; Martin NG; Wright CF; Fitzpatrick DR; Firth HV; Hurles ME; Barrett JC
Nature; 2018 Oct; 562(7726):268-271. PubMed ID: 30258228
[TBL] [Abstract][Full Text] [Related]
2. Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk.
McKenna B; Koomar T; Vervier K; Kremsreiter J; Michaelson JJ
Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30559312
[TBL] [Abstract][Full Text] [Related]
3. Genetic modifiers of rare variants in monogenic developmental disorder loci.
Kingdom R; Beaumont RN; Wood AR; Weedon MN; Wright CF
Nat Genet; 2024 May; 56(5):861-868. PubMed ID: 38637616
[TBL] [Abstract][Full Text] [Related]
4. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations.
Rees E; Creeth HDJ; Hwu HG; Chen WJ; Tsuang M; Glatt SJ; Rey R; Kirov G; Walters JTR; Holmans P; Owen MJ; O'Donovan MC
Nat Commun; 2021 Sep; 12(1):5353. PubMed ID: 34504065
[TBL] [Abstract][Full Text] [Related]
5. Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.
Devanna P; Chen XS; Ho J; Gajewski D; Smith SD; Gialluisi A; Francks C; Fisher SE; Newbury DF; Vernes SC
Mol Psychiatry; 2018 May; 23(5):1375-1384. PubMed ID: 28289279
[TBL] [Abstract][Full Text] [Related]
6. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Singh T; Kurki MI; Curtis D; Purcell SM; Crooks L; McRae J; Suvisaari J; Chheda H; Blackwood D; Breen G; Pietiläinen O; Gerety SS; Ayub M; Blyth M; Cole T; Collier D; Coomber EL; Craddock N; Daly MJ; Danesh J; DiForti M; Foster A; Freimer NB; Geschwind D; Johnstone M; Joss S; Kirov G; Körkkö J; Kuismin O; Holmans P; Hultman CM; Iyegbe C; Lönnqvist J; Männikkö M; McCarroll SA; McGuffin P; McIntosh AM; McQuillin A; Moilanen JS; Moore C; Murray RM; Newbury-Ecob R; Ouwehand W; Paunio T; Prigmore E; Rees E; Roberts D; Sambrook J; Sklar P; St Clair D; Veijola J; Walters JT; Williams H; ; ; ; ; Sullivan PF; Hurles ME; O'Donovan MC; Palotie A; Owen MJ; Barrett JC
Nat Neurosci; 2016 Apr; 19(4):571-7. PubMed ID: 26974950
[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. Genetic and phenotypic heterogeneity in early neurodevelopmental traits in the Norwegian Mother, Father and Child Cohort Study.
Hegemann L; Corfield EC; Askelund AD; Allegrini AG; Askeland RB; Ronald A; Ask H; St Pourcain B; Andreassen OA; Hannigan LJ; Havdahl A
Mol Autism; 2024 Jun; 15(1):25. PubMed ID: 38849897
[TBL] [Abstract][Full Text] [Related]
9. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.
Singh T; Walters JTR; Johnstone M; Curtis D; Suvisaari J; Torniainen M; Rees E; Iyegbe C; Blackwood D; McIntosh AM; Kirov G; Geschwind D; Murray RM; Di Forti M; Bramon E; Gandal M; Hultman CM; Sklar P; ; ; Palotie A; Sullivan PF; O'Donovan MC; Owen MJ; Barrett JC
Nat Genet; 2017 Aug; 49(8):1167-1173. PubMed ID: 28650482
[TBL] [Abstract][Full Text] [Related]
10. A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants.
López-Rivera JA; Pérez-Palma E; Symonds J; Lindy AS; McKnight DA; Leu C; Zuberi S; Brunklaus A; Møller RS; Lal D
Brain; 2020 Apr; 143(4):1099-1105. PubMed ID: 32168371
[TBL] [Abstract][Full Text] [Related]
11. The genetics of autism.
Muhle R; Trentacoste SV; Rapin I
Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
[TBL] [Abstract][Full Text] [Related]
12. All for one and one for all: heterogeneity of genetic etiologies in neurodevelopmental psychiatric disorders.
Moreno-De-Luca D; Martin CL
Curr Opin Genet Dev; 2021 Jun; 68():71-78. PubMed ID: 33773394
[TBL] [Abstract][Full Text] [Related]
13. Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia.
John J; Kukshal P; Bhatia T; Nimgaonkar VL; Deshpande SN; Thelma BK
Schizophr Res; 2019 Aug; 210():296-298. PubMed ID: 30612842
[No Abstract] [Full Text] [Related]
14. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Weiner DJ; Wigdor EM; Ripke S; Walters RK; Kosmicki JA; Grove J; Samocha KE; Goldstein JI; Okbay A; Bybjerg-Grauholm J; Werge T; Hougaard DM; Taylor J; ; ; Skuse D; Devlin B; Anney R; Sanders SJ; Bishop S; Mortensen PB; Børglum AD; Smith GD; Daly MJ; Robinson EB
Nat Genet; 2017 Jul; 49(7):978-985. PubMed ID: 28504703
[TBL] [Abstract][Full Text] [Related]
15. Common genetic variants with fetal effects on birth weight are enriched for proximity to genes implicated in rare developmental disorders.
Beaumont RN; Mayne IK; Freathy RM; Wright CF
Hum Mol Genet; 2021 May; 30(11):1057-1066. PubMed ID: 33682876
[TBL] [Abstract][Full Text] [Related]
16. Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia.
Mojarad BA; Yin Y; Manshaei R; Backstrom I; Costain G; Heung T; Merico D; Marshall CR; Bassett AS; Yuen RKC
Transl Psychiatry; 2021 Feb; 11(1):84. PubMed ID: 33526774
[TBL] [Abstract][Full Text] [Related]
17. No evidence that common genetic risk variation is shared between schizophrenia and autism.
Vorstman JA; Anney RJ; Derks EM; Gallagher L; Gill M; de Jonge MV; van Engeland H; Kahn RS; Ophoff RA;
Am J Med Genet B Neuropsychiatr Genet; 2013 Jan; 162B(1):55-60. PubMed ID: 23193033
[TBL] [Abstract][Full Text] [Related]
18. Polygenic risk for autism spectrum disorder associates with anger recognition in a neurodevelopment-focused phenome-wide scan of unaffected youths from a population-based cohort.
Wendt FR; Carvalho CM; Pathak GA; Gelernter J; Polimanti R
PLoS Genet; 2020 Sep; 16(9):e1009036. PubMed ID: 32941431
[TBL] [Abstract][Full Text] [Related]
19. Utilizing population controls in rare-variant case-parent association tests.
Jiang Y; Satten GA; Han Y; Epstein MP; Heinzen EL; Goldstein DB; Allen AS
Am J Hum Genet; 2014 Jun; 94(6):845-53. PubMed ID: 24836453
[TBL] [Abstract][Full Text] [Related]
20. A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.
Antaki D; Guevara J; Maihofer AX; Klein M; Gujral M; Grove J; Carey CE; Hong O; Arranz MJ; Hervas A; Corsello C; Vaux KK; Muotri AR; Iakoucheva LM; Courchesne E; Pierce K; Gleeson JG; Robinson EB; Nievergelt CM; Sebat J
Nat Genet; 2022 Sep; 54(9):1284-1292. PubMed ID: 35654974
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
