These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 27021940)

  • 1. Rare genetic variants and schizophrenia.
    Flint J
    Nat Neurosci; 2016 Apr; 19(4):525-7. PubMed ID: 27021940
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene.
    Takata A; Xu B; Ionita-Laza I; Roos JL; Gogos JA; Karayiorgou M
    Neuron; 2014 May; 82(4):773-80. PubMed ID: 24853937
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
    Zhang Y; Wang T; Wang Y; Xia K; Li J; Sun Z
    Mol Neurobiol; 2021 Aug; 58(8):3863-3873. PubMed ID: 33860439
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype correlation at codon 1740 of SETD2.
    Rabin R; Radmanesh A; Glass IA; Dobyns WB; Aldinger KA; Shieh JT; Romoser S; Bombei H; Dowsett L; Trapane P; Bernat JA; Baker J; Mendelsohn NJ; Popp B; Siekmeyer M; Sorge I; Sansbury FH; Watts P; Foulds NC; Burton J; Hoganson G; Hurst JA; Menzies L; Osio D; Kerecuk L; Cobben JM; Jizi K; Jacquemont S; Bélanger SA; Löhner K; Veenstra-Knol HE; Lemmink HH; Keller-Ramey J; Wentzensen IM; Punj S; McWalter K; Lenberg J; Ellsworth KA; Radtke K; Akbarian S; Pappas J
    Am J Med Genet A; 2020 Sep; 182(9):2037-2048. PubMed ID: 32710489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Setd1a Insufficiency in Mice Attenuates Excitatory Synaptic Function and Recapitulates Schizophrenia-Related Behavioral Abnormalities.
    Nagahama K; Sakoori K; Watanabe T; Kishi Y; Kawaji K; Koebis M; Nakao K; Gotoh Y; Aiba A; Uesaka N; Kano M
    Cell Rep; 2020 Sep; 32(11):108126. PubMed ID: 32937141
    [TBL] [Abstract][Full Text] [Related]  

  • 11.
    Roston A; Evans D; Gill H; McKinnon M; Isidor B; Cogné B; Mwenifumbo J; van Karnebeek C; An J; Jones SJM; Farrer M; Demos M; Connolly M; Gibson WT; ;
    J Med Genet; 2021 Mar; 58(3):196-204. PubMed ID: 32546566
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder.
    Gregor A; Sadleir LG; Asadollahi R; Azzarello-Burri S; Battaglia A; Ousager LB; Boonsawat P; Bruel AL; Buchert R; Calpena E; Cogné B; Dallapiccola B; Distelmaier F; Elmslie F; Faivre L; Haack TB; Harrison V; Henderson A; Hunt D; Isidor B; Joset P; Kumada S; Lachmeijer AMA; Lees M; Lynch SA; Martinez F; Matsumoto N; McDougall C; Mefford HC; Miyake N; Myers CT; Moutton S; Nesbitt A; Novelli A; Orellana C; Rauch A; Rosello M; Saida K; Santani AB; Sarkar A; Scheffer IE; Shinawi M; Steindl K; Symonds JD; Zackai EH; ; ; Reis A; Sticht H; Zweier C
    Am J Hum Genet; 2018 Aug; 103(2):305-316. PubMed ID: 30057029
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation pattern and genotype-phenotype correlations of SETD2 in neurodevelopmental disorders.
    Chen M; Quan Y; Duan G; Wu H; Bai T; Wang Y; Zhou S; Ou J; Shen Y; Hu Z; Xia K; Guo H
    Eur J Med Genet; 2021 May; 64(5):104200. PubMed ID: 33766796
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing.
    Hu X; Zhang B; Liu W; Paciga S; He W; Lanz TA; Kleiman R; Dougherty B; Hall SK; McIntosh AM; Lawrie SM; Power A; John SL; Blackwood D; St Clair D; Brandon NJ
    Mol Psychiatry; 2014 Aug; 19(8):857-8. PubMed ID: 24126932
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetics of Childhood-onset Schizophrenia 2019 Update.
    Forsyth JK; Asarnow RF
    Child Adolesc Psychiatr Clin N Am; 2020 Jan; 29(1):157-170. PubMed ID: 31708045
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.
    Stolerman ES; Francisco E; Stallworth JL; Jones JR; Monaghan KG; Keller-Ramey J; Person R; Wentzensen IM; McWalter K; Keren B; Heron B; Nava C; Heron D; Kim K; Burton B; Al-Musafri F; O'Grady L; Sahai I; Escobar LF; Meuwissen M; Reyniers E; Kooy F; Lacassie Y; Gunay-Aygun M; Schatz KS; Hochstenbach R; Zwijnenburg PJG; Waisfisz Q; van Slegtenhorst M; Mancini GMS; Louie RJ
    Am J Med Genet A; 2019 Jul; 179(7):1276-1286. PubMed ID: 31124279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mini-review: Update on the genetics of schizophrenia.
    Coelewij L; Curtis D
    Ann Hum Genet; 2018 Sep; 82(5):239-243. PubMed ID: 29923609
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Revisiting Schizophrenia from an Evolutionary Perspective: An Association Study of Recent Evolutionary Markers and Schizophrenia.
    Bhattacharyya U; Deshpande SN; Bhatia T; Thelma BK
    Schizophr Bull; 2021 Apr; 47(3):827-836. PubMed ID: 33350444
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.