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 *

203 related articles for article (PubMed ID: 27725659)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Involvement of Rare Mutations of SCN9A, DPP4, ABCA13, and SYT14 in Schizophrenia and Bipolar Disorder.
    Chen CH; Huang YS; Fang TH
    Int J Mol Sci; 2021 Dec; 22(24):. PubMed ID: 34947986
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Support for the N-methyl-D-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.
    Timms AE; Dorschner MO; Wechsler J; Choi KY; Kirkwood R; Girirajan S; Baker C; Eichler EE; Korvatska O; Roche KW; Horwitz MS; Tsuang DW
    JAMA Psychiatry; 2013 Jun; 70(6):582-90. PubMed ID: 23553203
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole-exome sequencing in an Afrikaner family with bipolar disorder.
    Engelbrecht HR; Dalvie S; Agenbag G; Stein DJ; Ramesar RS
    J Affect Disord; 2020 Nov; 276():69-75. PubMed ID: 32697718
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors.
    Cruceanu C; Schmouth JF; Torres-Platas SG; Lopez JP; Ambalavanan A; Darcq E; Gross F; Breton B; Spiegelman D; Rochefort D; Hince P; Petite JM; Gauthier J; Lafrenière RG; Dion PA; Greenwood CM; Kieffer BL; Alda M; Turecki G; Rouleau GA
    Mol Psychiatry; 2018 Oct; 23(10):2050-2056. PubMed ID: 29158579
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani Families.
    Fatima A; Abdullah U; Farooq M; Mang Y; Mehrjouy MM; Asif M; Ali Z; Tommerup N; Baig SM
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946848
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Haplotype phasing of a bipolar disorder pedigree revealed rare multiple mutations of SPOCD1 gene in the 1p36-35 susceptibility locus.
    Takamatsu G; Yanagi K; Koganebuchi K; Yoshida F; Lee JS; Toyama K; Hattori K; Katagiri C; Kondo T; Kunugi H; Kimura R; Kaname T; Matsushita M
    J Affect Disord; 2022 Aug; 310():96-105. PubMed ID: 35504398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
    Harold D; Connolly S; Riley BP; Kendler KS; McCarthy SE; McCombie WR; Richards A; Owen MJ; O'Donovan MC; Walters J; ; ; Donohoe G; Gill M; Corvin A; Morris DW
    Am J Med Genet B Neuropsychiatr Genet; 2019 Apr; 180(3):223-231. PubMed ID: 30801977
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds.
    Boies S; Mérette C; Paccalet T; Maziade M; Bureau A
    Am J Med Genet B Neuropsychiatr Genet; 2018 Apr; 177(3):329-336. PubMed ID: 29193655
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.