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 *

219 related articles for article (PubMed ID: 25432440)

  • 1. Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
    Woodbury-Smith M; Paterson AD; Thiruvahindrapduram B; Lionel AC; Marshall CR; Merico D; Fernandez BA; Duku E; Sutcliffe JS; O'Conner I; Chrysler C; Thompson A; Kellam B; Tammimies K; Walker S; Yuen RK; Uddin M; Howe JL; Parlier M; Whitten K; Szatmari P; Vieland VJ; Piven J; Scherer SW
    Hum Genet; 2015 Feb; 134(2):191-201. PubMed ID: 25432440
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
    Woodbury-Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Anagnostou E; Scherer SW; Vieland VJ; Szatmari P
    Am J Med Genet B Neuropsychiatr Genet; 2020 Jul; 183(5):268-276. PubMed ID: 32372567
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.
    Woodbury-Smith M; Paterson AD; O'Connor I; Zarrei M; Yuen RKC; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Scherer SW; Vieland V; Szatmari P
    J Neurodev Disord; 2018 Jun; 10(1):20. PubMed ID: 29890955
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
    Leppa VM; Kravitz SN; Martin CL; Andrieux J; Le Caignec C; Martin-Coignard D; DyBuncio C; Sanders SJ; Lowe JK; Cantor RM; Geschwind DH
    Am J Hum Genet; 2016 Sep; 99(3):540-554. PubMed ID: 27569545
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
    J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
    Chaste P; Sanders SJ; Mohan KN; Klei L; Song Y; Murtha MT; Hus V; Lowe JK; Willsey AJ; Moreno-De-Luca D; Yu TW; Fombonne E; Geschwind D; Grice DE; Ledbetter DH; Lord C; Mane SM; Martin DM; Morrow EM; Walsh CA; Sutcliffe JS; State MW; Martin CL; Devlin B; Beaudet AL; Cook EH; Kim SJ
    Autism Res; 2014 Jun; 7(3):355-62. PubMed ID: 24821083
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
    Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
    Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
    Bacchelli E; Cameli C; Viggiano M; Igliozzi R; Mancini A; Tancredi R; Battaglia A; Maestrini E
    Sci Rep; 2020 Feb; 10(1):3198. PubMed ID: 32081867
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.
    Salyakina D; Cukier HN; Lee JM; Sacharow S; Nations LD; Ma D; Jaworski JM; Konidari I; Whitehead PL; Wright HH; Abramson RK; Williams SM; Menon R; Haines JL; Gilbert JR; Cuccaro ML; Pericak-Vance MA
    PLoS One; 2011; 6(10):e26049. PubMed ID: 22016809
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
    Lionel AC; Crosbie J; Barbosa N; Goodale T; Thiruvahindrapuram B; Rickaby J; Gazzellone M; Carson AR; Howe JL; Wang Z; Wei J; Stewart AF; Roberts R; McPherson R; Fiebig A; Franke A; Schreiber S; Zwaigenbaum L; Fernandez BA; Roberts W; Arnold PD; Szatmari P; Marshall CR; Schachar R; Scherer SW
    Sci Transl Med; 2011 Aug; 3(95):95ra75. PubMed ID: 21832240
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
    Sanders SJ; Ercan-Sencicek AG; Hus V; Luo R; Murtha MT; Moreno-De-Luca D; Chu SH; Moreau MP; Gupta AR; Thomson SA; Mason CE; Bilguvar K; Celestino-Soper PB; Choi M; Crawford EL; Davis L; Wright NR; Dhodapkar RM; DiCola M; DiLullo NM; Fernandez TV; Fielding-Singh V; Fishman DO; Frahm S; Garagaloyan R; Goh GS; Kammela S; Klei L; Lowe JK; Lund SC; McGrew AD; Meyer KA; Moffat WJ; Murdoch JD; O'Roak BJ; Ober GT; Pottenger RS; Raubeson MJ; Song Y; Wang Q; Yaspan BL; Yu TW; Yurkiewicz IR; Beaudet AL; Cantor RM; Curland M; Grice DE; Günel M; Lifton RP; Mane SM; Martin DM; Shaw CA; Sheldon M; Tischfield JA; Walsh CA; Morrow EM; Ledbetter DH; Fombonne E; Lord C; Martin CL; Brooks AI; Sutcliffe JS; Cook EH; Geschwind D; Roeder K; Devlin B; State MW
    Neuron; 2011 Jun; 70(5):863-85. PubMed ID: 21658581
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Autism spectrum disorder and genes for synaptic proteins].
    Shishido E
    Brain Nerve; 2012 Jan; 64(1):65-70. PubMed ID: 22223503
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autism genetics.
    Persico AM; Napolioni V
    Behav Brain Res; 2013 Aug; 251():95-112. PubMed ID: 23769996
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
    Matsunami N; Hadley D; Hensel CH; Christensen GB; Kim C; Frackelton E; Thomas K; da Silva RP; Stevens J; Baird L; Otterud B; Ho K; Varvil T; Leppert T; Lambert CG; Leppert M; Hakonarson H
    PLoS One; 2013; 8(1):e52239. PubMed ID: 23341896
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The landscape of copy number variations in Finnish families with autism spectrum disorders.
    Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I
    Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927
    [TBL] [Abstract][Full Text] [Related]  

  • 16. High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.
    Chen CH; Chen HI; Chien WH; Li LH; Wu YY; Chiu YN; Tsai WC; Gau SS
    Sci Rep; 2017 Sep; 7(1):11919. PubMed ID: 28931914
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural, genetic, and functional signatures of disordered neuro-immunological development in autism spectrum disorder.
    Saxena V; Ramdas S; Ochoa CR; Wallace D; Bhide P; Kohane I
    PLoS One; 2012; 7(12):e48835. PubMed ID: 23239965
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
    Casey JP; Magalhaes T; Conroy JM; Regan R; Shah N; Anney R; Shields DC; Abrahams BS; Almeida J; Bacchelli E; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bolton PF; Bourgeron T; Brennan S; Cali P; Correia C; Corsello C; Coutanche M; Dawson G; de Jonge M; Delorme R; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Foley S; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Green J; Guter SJ; Hakonarson H; Holt R; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Lamb JA; Leboyer M; Le Couteur A; Leventhal BL; Lord C; Lund SC; Maestrini E; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Merikangas A; Miller J; Minopoli F; Mirza GK; Munson J; Nelson SF; Nygren G; Oliveira G; Pagnamenta AT; Papanikolaou K; Parr JR; Parrini B; Pickles A; Pinto D; Piven J; Posey DJ; Poustka A; Poustka F; Ragoussis J; Roge B; Rutter ML; Sequeira AF; Soorya L; Sousa I; Sykes N; Stoppioni V; Tancredi R; Tauber M; Thompson AP; Thomson S; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Vorstman JA; Wallace S; Wang K; Wassink TH; White K; Wing K; Wittemeyer K; Yaspan BL; Zwaigenbaum L; Betancur C; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Geschwind DH; Haines JL; Hallmayer J; Monaco AP; Nurnberger JI; Pericak-Vance MA; Schellenberg GD; Scherer SW; Sutcliffe JS; Szatmari P; Vieland VJ; Wijsman EM; Green A; Gill M; Gallagher L; Vicente A; Ennis S
    Hum Genet; 2012 Apr; 131(4):565-79. PubMed ID: 21996756
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.
    Allen-Brady K; Cai G; Cannon D; Robison R; McMahon WM; Coon H; Buxbaum JD
    Autism Res; 2011 Aug; 4(4):293-6. PubMed ID: 21491612
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic architecture in autism spectrum disorder.
    Devlin B; Scherer SW
    Curr Opin Genet Dev; 2012 Jun; 22(3):229-37. PubMed ID: 22463983
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.