BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

903 related articles for article (PubMed ID: 27120077)

  • 1. Exome Sequencing of Familial Bipolar Disorder.
    Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
    JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
    Jia X; Goes FS; Locke AE; Palmer D; Wang W; Cohen-Woods S; Genovese G; Jackson AU; Jiang C; Kvale M; Mullins N; Nguyen H; Pirooznia M; Rivera M; Ruderfer DM; Shen L; Thai K; Zawistowski M; Zhuang Y; Abecasis G; Akil H; Bergen S; Burmeister M; Chapman S; DelaBastide M; Juréus A; Kang HM; Kwok PY; Li JZ; Levy SE; Monson ET; Moran J; Sobell J; Watson S; Willour V; Zöllner S; Adolfsson R; Blackwood D; Boehnke M; Breen G; Corvin A; Craddock N; DiFlorio A; Hultman CM; Landen M; Lewis C; McCarroll SA; Richard McCombie W; McGuffin P; McIntosh A; McQuillin A; Morris D; Myers RM; O'Donovan M; Ophoff R; Boks M; Kahn R; Ouwehand W; Owen M; Pato C; Pato M; Posthuma D; Potash JB; Reif A; Sklar P; Smoller J; Sullivan PF; Vincent J; Walters J; Neale B; Purcell S; Risch N; Schaefer C; Stahl EA; Zandi PP; Scott LJ
    Mol Psychiatry; 2021 Sep; 26(9):5239-5250. PubMed ID: 33483695
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome sequencing in large, multiplex bipolar disorder families from Cuba.
    Maaser A; Forstner AJ; Strohmaier J; Hecker J; Ludwig KU; Sivalingam S; Streit F; Degenhardt F; Witt SH; Reinbold CS; Koller AC; Raff R; Heilmann-Heimbach S; Fischer SB; ; Herms S; Hoffmann P; Thiele H; Nürnberg P; Löhlein Fier H; Orozco-Díaz G; Carmenate-Naranjo D; Proenza-Barzaga N; Auburger GWJ; Andlauer TFM; Cichon S; Marcheco-Teruel B; Mors O; Rietschel M; Nöthen MM
    PLoS One; 2018; 13(10):e0205895. PubMed ID: 30379966
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.
    Forstner AJ; Fischer SB; Schenk LM; Strohmaier J; Maaser-Hecker A; Reinbold CS; Sivalingam S; Hecker J; Streit F; Degenhardt F; Witt SH; Schumacher J; Thiele H; Nürnberg P; Guzman-Parra J; Orozco Diaz G; Auburger G; Albus M; Borrmann-Hassenbach M; González MJ; Gil Flores S; Cabaleiro Fabeiro FJ; Del Río Noriega F; Perez Perez F; Haro González J; Rivas F; Mayoral F; Bauer M; Pfennig A; Reif A; Herms S; Hoffmann P; Pirooznia M; Goes FS; Rietschel M; Nöthen MM; Cichon S
    Transl Psychiatry; 2020 Feb; 10(1):57. PubMed ID: 32066727
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder.
    Salvoro C; Bortoluzzi S; Coppe A; Valle G; Feltrin E; Mostacciuolo ML; Vazza G
    Mol Neurobiol; 2018 Sep; 55(9):7366-7376. PubMed ID: 29411265
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
    Toma C; Shaw AD; Heath A; Pierce KD; Mitchell PB; Schofield PR; Fullerton JM
    J Psychiatry Neurosci; 2021 Mar; 46(2):E247-E257. PubMed ID: 33729739
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.
    Kataoka M; Matoba N; Sawada T; Kazuno AA; Ishiwata M; Fujii K; Matsuo K; Takata A; Kato T
    Mol Psychiatry; 2016 Jul; 21(7):885-93. PubMed ID: 27217147
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia.
    Palmer DS; Howrigan DP; Chapman SB; Adolfsson R; Bass N; Blackwood D; Boks MPM; Chen CY; Churchhouse C; Corvin AP; Craddock N; Curtis D; Di Florio A; Dickerson F; Freimer NB; Goes FS; Jia X; Jones I; Jones L; Jonsson L; Kahn RS; Landén M; Locke AE; McIntosh AM; McQuillin A; Morris DW; O'Donovan MC; Ophoff RA; Owen MJ; Pedersen NL; Posthuma D; Reif A; Risch N; Schaefer C; Scott L; Singh T; Smoller JW; Solomonson M; Clair DS; Stahl EA; Vreeker A; Walters JTR; Wang W; Watts NA; Yolken R; Zandi PP; Neale BM
    Nat Genet; 2022 May; 54(5):541-547. PubMed ID: 35410376
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome.
    Courtois E; Schmid M; Wajsbrot O; Barau C; Le Corvoisier P; Aouizerate B; Bellivier F; Belzeaux R; Dubertret C; Kahn JP; Leboyer M; Olie E; Passerieux C; Polosan M; Etain B; Jamain S;
    Transl Psychiatry; 2020 Apr; 10(1):124. PubMed ID: 32345981
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genetics of bipolar disorder].
    Budde M; Forstner AJ; Adorjan K; Schaupp SK; Nöthen MM; Schulze TG
    Nervenarzt; 2017 Jul; 88(7):755-759. PubMed ID: 28474173
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.
    Ganesh S; Ahmed P H; Nadella RK; More RP; Seshadri M; Viswanath B; Rao M; Jain S; ; Mukherjee O
    Psychiatry Clin Neurosci; 2019 Jan; 73(1):11-19. PubMed ID: 30367527
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.
    Andlauer TFM; Guzman-Parra J; Streit F; Strohmaier J; González MJ; Gil Flores S; Cabaleiro Fabeiro FJ; Del Río Noriega F; Perez FP; Haro González J; Orozco Diaz G; de Diego-Otero Y; Moreno-Küstner B; Auburger G; Degenhardt F; Heilmann-Heimbach S; Herms S; Hoffmann P; Frank J; Foo JC; Treutlein J; Witt SH; Cichon S; Kogevinas M; ; ; Rivas F; Mayoral F; Müller-Myhsok B; Forstner AJ; Nöthen MM; Rietschel M
    Mol Psychiatry; 2021 Apr; 26(4):1286-1298. PubMed ID: 31712721
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
    Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
    Mol Autism; 2017; 8():14. PubMed ID: 28344757
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An examination of multiple classes of rare variants in extended families with bipolar disorder.
    Toma C; Shaw AD; Allcock RJN; Heath A; Pierce KD; Mitchell PB; Schofield PR; Fullerton JM
    Transl Psychiatry; 2018 Mar; 8(1):65. PubMed ID: 29531218
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between ST8SIA2 and the Risk of Schizophrenia and Bipolar I Disorder across Diagnostic Boundaries.
    Yang SY; Huh IS; Baek JH; Cho EY; Choi MJ; Ryu S; Kim JS; Park T; Ha K; Hong KS
    PLoS One; 2015; 10(9):e0139413. PubMed ID: 26418860
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 46.