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 *

150 related articles for article (PubMed ID: 29325625)

  • 1. Evolving views of human genetic variation and its relationship to neurologic and psychiatric disease.
    Geschwind DH
    Handb Clin Neurol; 2018; 147():37-42. PubMed ID: 29325625
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The genetics of neuropsychiatric diseases: looking in and beyond the exome.
    Heinzen EL; Neale BM; Traynelis SF; Allen AS; Goldstein DB
    Annu Rev Neurosci; 2015 Jul; 38():47-68. PubMed ID: 25840007
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Genetic and genomic testing for neurologic disease in clinical practice.
    Fogel BL
    Handb Clin Neurol; 2018; 147():11-22. PubMed ID: 29325607
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exome sequencing to find rare variants causing neurologic diseases.
    Doherty D; Bamshad MJ
    Neurology; 2012 Jul; 79(5):396-7. PubMed ID: 22744653
    [No Abstract]   [Full Text] [Related]  

  • 6. Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations.
    Guerreiro R; Brás J; Hardy J; Singleton A
    Hum Mol Genet; 2014 Sep; 23(R1):R47-53. PubMed ID: 24794858
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
    Petrovski S; Todd JL; Durheim MT; Wang Q; Chien JW; Kelly FL; Frankel C; Mebane CM; Ren Z; Bridgers J; Urban TJ; Malone CD; Finlen Copeland A; Brinkley C; Allen AS; O'Riordan T; McHutchison JG; Palmer SM; Goldstein DB
    Am J Respir Crit Care Med; 2017 Jul; 196(1):82-93. PubMed ID: 28099038
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity.
    Petrovski S; Gussow AB; Wang Q; Halvorsen M; Han Y; Weir WH; Allen AS; Goldstein DB
    PLoS Genet; 2015 Sep; 11(9):e1005492. PubMed ID: 26332131
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.
    Karaca E; Harel T; Pehlivan D; Jhangiani SN; Gambin T; Coban Akdemir Z; Gonzaga-Jauregui C; Erdin S; Bayram Y; Campbell IM; Hunter JV; Atik MM; Van Esch H; Yuan B; Wiszniewski W; Isikay S; Yesil G; Yuregir OO; Tug Bozdogan S; Aslan H; Aydin H; Tos T; Aksoy A; De Vivo DC; Jain P; Geckinli BB; Sezer O; Gul D; Durmaz B; Cogulu O; Ozkinay F; Topcu V; Candan S; Cebi AH; Ikbal M; Yilmaz Gulec E; Gezdirici A; Koparir E; Ekici F; Coskun S; Cicek S; Karaer K; Koparir A; Duz MB; Kirat E; Fenercioglu E; Ulucan H; Seven M; Guran T; Elcioglu N; Yildirim MS; Aktas D; Alikaşifoğlu M; Ture M; Yakut T; Overton JD; Yuksel A; Ozen M; Muzny DM; Adams DR; Boerwinkle E; Chung WK; Gibbs RA; Lupski JR
    Neuron; 2015 Nov; 88(3):499-513. PubMed ID: 26539891
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical exome sequencing in neurogenetic and neuropsychiatric disorders.
    Fogel BL; Lee H; Strom SP; Deignan JL; Nelson SF
    Ann N Y Acad Sci; 2016 Feb; 1366(1):49-60. PubMed ID: 26250888
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.
    Visscher PM; Goddard ME; Derks EM; Wray NR
    Mol Psychiatry; 2012 May; 17(5):474-85. PubMed ID: 21670730
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exome versus transcriptome sequencing in identifying coding region variants.
    Ku CS; Wu M; Cooper DN; Naidoo N; Pawitan Y; Pang B; Iacopetta B; Soong R
    Expert Rev Mol Diagn; 2012 Apr; 12(3):241-51. PubMed ID: 22468815
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome and genome analysis as a tool for disease identification and treatment: the 2011 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2012 Mar; 33(3):586-90. PubMed ID: 22213110
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
    Rudan I
    Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study.
    Cardinale CJ; Li D; Tian L; Connolly JJ; March ME; Hou C; Wang F; Snyder J; Kim CE; Chiavacci RM; Sleiman PM; Burnham JM; Hakonarson H
    BMC Musculoskelet Disord; 2016 Nov; 17(1):462. PubMed ID: 27829420
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A genetic model for neurodevelopmental disease.
    Coe BP; Girirajan S; Eichler EE
    Curr Opin Neurobiol; 2012 Oct; 22(5):829-36. PubMed ID: 22560351
    [TBL] [Abstract][Full Text] [Related]  

  • 17. What can exome sequencing do for you?
    Majewski J; Schwartzentruber J; Lalonde E; Montpetit A; Jabado N
    J Med Genet; 2011 Sep; 48(9):580-9. PubMed ID: 21730106
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic screening and diagnosis in epilepsy?
    Sisodiya SM
    Curr Opin Neurol; 2015 Apr; 28(2):136-42. PubMed ID: 25692410
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Introduction to Neurogenetics.
    Vgontzas A; Renthal W
    Am J Med; 2019 Feb; 132(2):142-152. PubMed ID: 30098310
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Large-scale genomics unveils the genetic architecture of psychiatric disorders.
    Gratten J; Wray NR; Keller MC; Visscher PM
    Nat Neurosci; 2014 Jun; 17(6):782-90. PubMed ID: 24866044
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.