BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

239 related articles for article (PubMed ID: 29411265)

  • 21. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
    Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
    Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia.
    Al Eissa MM; Fiorentino A; Sharp SI; O'Brien NL; Wolfe K; Giaroli G; Curtis D; Bass NJ; McQuillin A
    Ann Hum Genet; 2018 Mar; 82(2):88-92. PubMed ID: 29148569
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder.
    Cruceanu C; Ambalavanan A; Spiegelman D; Gauthier J; Lafrenière RG; Dion PA; Alda M; Turecki G; Rouleau GA
    Genome; 2013 Oct; 56(10):634-40. PubMed ID: 24237345
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Rare deleterious mutations are associated with disease in bipolar disorder families.
    Rao AR; Yourshaw M; Christensen B; Nelson SF; Kerner B
    Mol Psychiatry; 2017 Jul; 22(7):1009-1014. PubMed ID: 27725659
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGΒ4 gene in schizophrenia and bipolar disorder.
    O'Brien NL; Fiorentino A; Curtis D; Rayner C; Petrosellini C; Al Eissa M; Bass NJ; McQuillin A; Sharp SI
    Schizophr Res; 2018 Sep; 199():181-188. PubMed ID: 29526452
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Transcriptome analysis of cortical tissue reveals shared sets of downregulated genes in autism and schizophrenia.
    Ellis SE; Panitch R; West AB; Arking DE
    Transl Psychiatry; 2016 May; 6(5):e817. PubMed ID: 27219343
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of de novo mutations in prenatal neurodevelopment-associated genes in schizophrenia in two Han Chinese patient-sibling family-based cohorts.
    Jiang S; Zhou D; Wang YY; Jia P; Wan C; Li X; He G; Cao D; Jiang X; Kendler KS; Tsuang M; Mize T; Wu JS; Lu Y; He L; Chen J; Zhao Z; Chen X
    Transl Psychiatry; 2020 Sep; 10(1):307. PubMed ID: 32873781
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.
    John J; Sharma A; Kukshal P; Bhatia T; Nimgaonkar VL; Deshpande SN; Thelma BK
    Schizophr Bull; 2019 Jan; 45(1):256-263. PubMed ID: 29385606
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Commonality in dysregulated expression of gene sets in cortical brains of individuals with autism, schizophrenia, and bipolar disorder.
    Guan J; Cai JJ; Ji G; Sham PC
    Transl Psychiatry; 2019 May; 9(1):152. PubMed ID: 31127088
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity.
    Hall J; Trent S; Thomas KL; O'Donovan MC; Owen MJ
    Biol Psychiatry; 2015 Jan; 77(1):52-8. PubMed ID: 25152434
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.
    Leonenko G; Richards AL; Walters JT; Pocklington A; Chambert K; Al Eissa MM; Sharp SI; O'Brien NL; Curtis D; Bass NJ; McQuillin A; Hultman C; Moran JL; McCarroll SA; Sklar P; Neale BM; Holmans PA; Owen MJ; Sullivan PF; O'Donovan MC
    Am J Med Genet B Neuropsychiatr Genet; 2017 Oct; 174(7):724-731. PubMed ID: 28719003
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Assessment of somatic single-nucleotide variation in brain tissue of cases with schizophrenia.
    Fullard JF; Charney AW; Voloudakis G; Uzilov AV; Haroutunian V; Roussos P
    Transl Psychiatry; 2019 Jan; 9(1):21. PubMed ID: 30655504
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel relationship for schizophrenia, bipolar and major depressive disorder Part 3: Evidence from chromosome 3 high density association screen.
    Chen X; Long F; Cai B; Chen X; Chen G
    J Comp Neurol; 2018 Jan; 526(1):59-79. PubMed ID: 28856687
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
    Nguyen HT; Bryois J; Kim A; Dobbyn A; Huckins LM; Munoz-Manchado AB; Ruderfer DM; Genovese G; Fromer M; Xu X; Pinto D; Linnarsson S; Verhage M; Smit AB; Hjerling-Leffler J; Buxbaum JD; Hultman C; Sklar P; Purcell SM; Lage K; He X; Sullivan PF; Stahl EA
    Genome Med; 2017 Dec; 9(1):114. PubMed ID: 29262854
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A Multilevel Functional Study of a
    Houenou J; Boisgontier J; Henrion A; d'Albis MA; Dumaine A; Linke J; Wessa M; Daban C; Hamdani N; Delavest M; Llorca PM; Lançon C; Schürhoff F; Szöke A; Le Corvoisier P; Barau C; Poupon C; Etain B; Leboyer M; Jamain S
    J Neurosci; 2017 Oct; 37(43):10389-10397. PubMed ID: 28972123
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The genetic architecture of schizophrenia, bipolar disorder, obsessive-compulsive disorder and autism spectrum disorder.
    O'Connell KS; McGregor NW; Lochner C; Emsley R; Warnich L
    Mol Cell Neurosci; 2018 Apr; 88():300-307. PubMed ID: 29505902
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia.
    Al Eissa MM; Sharp SI; O'Brien NL; Fiorentino A; Bass NJ; Curtis D; McQuillin A
    Am J Med Genet B Neuropsychiatr Genet; 2019 Jun; 180(4):258-265. PubMed ID: 30859703
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
    Torrico B; Shaw AD; Mosca R; Vivó-Luque N; Hervás A; Fernàndez-Castillo N; Aloy P; Bayés M; Fullerton JM; Cormand B; Toma C
    J Psychiatry Neurosci; 2019 Sep; 44(5):350-359. PubMed ID: 31094488
    [TBL] [Abstract][Full Text] [Related]  

  • 39. De novo variation in bipolar disorder.
    Goes FS; Pirooznia M; Tehan M; Zandi PP; McGrath J; Wolyniec P; Nestadt G; Pulver AE
    Mol Psychiatry; 2021 Aug; 26(8):4127-4136. PubMed ID: 31776463
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis.
    Li M; Huang L; Grigoroiu-Serbanescu M; Bergen SE; Landén M; Hultman CM; Forstner AJ; Strohmaier J; Hecker J; Schulze TG; Müller-Myhsok B; Reif A; Mitchell PB; Martin NG; Cichon S; Nöthen MM; Alkelai A; Lerer B; Jamain S; Leboyer M; Bellivier F; Etain B; Kahn JP; Henry C; Rietschel M; ;
    Mol Neurobiol; 2016 Dec; 53(10):6608-6619. PubMed ID: 26637325
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.