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 *

119 related articles for article (PubMed ID: 24591081)

  • 1. Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia.
    Veerappa AM; Saldanha M; Padakannaya P; Ramachandra NB
    Am J Med Genet B Neuropsychiatr Genet; 2013 Dec; 162B(8):889-97. PubMed ID: 24591081
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics.
    Veerappa AM; Saldanha M; Padakannaya P; Ramachandra NB
    Am J Med Genet B Neuropsychiatr Genet; 2014 Oct; 165B(7):572-80. PubMed ID: 25139666
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity.
    Veerappa AM; Saldanha M; Padakannaya P; Ramachandra NB
    J Hum Genet; 2013 Aug; 58(8):539-47. PubMed ID: 23677055
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a human X-chromosome-transposed region (XTR) in the Y chromosome.
    Veerappa AM; Padakannaya P; Ramachandra NB
    Funct Integr Genomics; 2013 Aug; 13(3):285-93. PubMed ID: 23708688
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.
    Kaminen N; Hannula-Jouppi K; Kestilä M; Lahermo P; Muller K; Kaaranen M; Myllyluoma B; Voutilainen A; Lyytinen H; Nopola-Hemmi J; Kere J
    J Med Genet; 2003 May; 40(5):340-5. PubMed ID: 12746395
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
    Grimm T; Garshasbi M; Puettmann L; Chen W; Ullmann R; Müller-Myhsok B; Klopocki E; Herbst L; Haug J; Jensen LR; Fischer C; Nöthen M; Ludwig K; Warnke A; Ott J; Schulte-Körne G; Ropers HH; Kuss AW
    Z Kinder Jugendpsychiatr Psychother; 2020 Nov; 48(6):478-489. PubMed ID: 33172359
    [No Abstract]   [Full Text] [Related]  

  • 7. Familial dyslexia in a large Swedish family: a whole genome linkage scan.
    Svensson I; Nilsson S; Wahlström J; Jernås M; Carlsson LM; Hjelmquist E
    Behav Genet; 2011 Jan; 41(1):43-9. PubMed ID: 20862559
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
    Pagnamenta AT; Khan H; Walker S; Gerrelli D; Wing K; Bonaglia MC; Giorda R; Berney T; Mani E; Molteni M; Pinto D; Le Couteur A; Hallmayer J; Sutcliffe JS; Szatmari P; Paterson AD; Scherer SW; Vieland VJ; Monaco AP
    J Med Genet; 2011 Jan; 48(1):48-54. PubMed ID: 20972252
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion.
    Poelmans G; Engelen JJ; Van Lent-Albrechts J; Smeets HJ; Schoenmakers E; Franke B; Buitelaar JK; Wuisman-Frerker M; Erens W; Steyaert J; Schrander-Stumpel C
    Am J Med Genet B Neuropsychiatr Genet; 2009 Jan; 150B(1):140-7. PubMed ID: 18521840
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A dominant gene for developmental dyslexia on chromosome 3.
    Nopola-Hemmi J; Myllyluoma B; Haltia T; Taipale M; Ollikainen V; Ahonen T; Voutilainen A; Kere J; Widén E
    J Med Genet; 2001 Oct; 38(10):658-64. PubMed ID: 11584043
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.
    de Kovel CG; Hol FA; Heister JG; Willemen JJ; Sandkuijl LA; Franke B; Padberg GW
    J Med Genet; 2004 Sep; 41(9):652-7. PubMed ID: 15342694
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia.
    Naseer MI; Faheem M; Chaudhary AG; Kumosani TA; Al-Quaiti MM; Jan MM; Saleh Jamal H; Al-Qahtani MH
    BMC Genomics; 2015; 16 Suppl 1(Suppl 1):S10. PubMed ID: 25923336
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Replication profile of PCDH11X and PCDH11Y, a gene pair located in the non-pseudoautosomal homologous region Xq21.3/Yp11.2.
    Wilson ND; Ross LJ; Close J; Mott R; Crow TJ; Volpi EV
    Chromosome Res; 2007; 15(4):485-98. PubMed ID: 17671842
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.
    Field LL; Shumansky K; Ryan J; Truong D; Swiergala E; Kaplan BJ
    Genes Brain Behav; 2013 Feb; 12(1):56-69. PubMed ID: 23190410
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Case history and genome-wide scans for copy number variants in a family with patient having 15q11.1-q11.2 duplication and 22q11.2 deletion, and schizophrenia.
    Takahashi S; Suzuki T; Nakamura-Tomizuka S; Osaki K; Sotome Y; Sagawa T; Uchiyama M
    Am J Med Genet B Neuropsychiatr Genet; 2015 Jun; 168B(4):229-35. PubMed ID: 25776014
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
    Hippolyte L; Maillard AM; Rodriguez-Herreros B; Pain A; Martin-Brevet S; Ferrari C; Conus P; Macé A; Hadjikhani N; Metspalu A; Reigo A; Kolk A; Männik K; Barker M; Isidor B; Le Caignec C; Mignot C; Schneider L; Mottron L; Keren B; David A; Doco-Fenzy M; Gérard M; Bernier R; Goin-Kochel RP; Hanson E; Green Snyder L; ; Ramus F; Beckmann JS; Draganski B; Reymond A; Jacquemont S
    Biol Psychiatry; 2016 Jul; 80(2):129-139. PubMed ID: 26742926
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music.
    Ukkola-Vuoti L; Kanduri C; Oikkonen J; Buck G; Blancher C; Raijas P; Karma K; Lähdesmäki H; Järvelä I
    PLoS One; 2013; 8(2):e56356. PubMed ID: 23460800
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of two inherited copy number variants in a male with autism supports two-hit and compound heterozygosity models of autism.
    Gau SS; Liao HM; Hong CC; Chien WH; Chen CH
    Am J Med Genet B Neuropsychiatr Genet; 2012 Sep; 159B(6):710-7. PubMed ID: 22778016
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.
    Veerappa AM; Suresh RV; Vishweswaraiah S; Lingaiah K; Murthy M; Manjegowda DS; Padakannaya P; Ramachandra NB
    Genet Res (Camb); 2015 Sep; 97():e18. PubMed ID: 26390810
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.
    Ulfarsson MO; Walters GB; Gustafsson O; Steinberg S; Silva A; Doyle OM; Brammer M; Gudbjartsson DF; Arnarsdottir S; Jonsdottir GA; Gisladottir RS; Bjornsdottir G; Helgason H; Ellingsen LM; Halldorsson JG; Saemundsen E; Stefansdottir B; Jonsson L; Eiriksdottir VK; Eiriksdottir GR; Johannesdottir GH; Unnsteinsdottir U; Jonsdottir B; Magnusdottir BB; Sulem P; Thorsteinsdottir U; Sigurdsson E; Brandeis D; Meyer-Lindenberg A; Stefansson H; Stefansson K
    Transl Psychiatry; 2017 Apr; 7(4):e1109. PubMed ID: 28440815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.