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 *

160 related articles for article (PubMed ID: 24373520)

  • 61. Disentangling the heterogeneity of autism spectrum disorder through genetic findings.
    Jeste SS; Geschwind DH
    Nat Rev Neurol; 2014 Feb; 10(2):74-81. PubMed ID: 24468882
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Somatic overgrowth predisposes to seizures in autism spectrum disorders.
    Valvo G; Baldini S; Brachini F; Apicella F; Cosenza A; Ferrari AR; Guerrini R; Muratori F; Romano MF; Santorelli FM; Tancredi R; Sicca F
    PLoS One; 2013; 8(9):e75015. PubMed ID: 24086423
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Autism spectrum disorders--a genetics review.
    Miles JH
    Genet Med; 2011 Apr; 13(4):278-94. PubMed ID: 21358411
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Clustering by phenotype and genome-wide association study in autism.
    Narita A; Nagai M; Mizuno S; Ogishima S; Tamiya G; Ueki M; Sakurai R; Makino S; Obara T; Ishikuro M; Yamanaka C; Matsubara H; Kuniyoshi Y; Murakami K; Ueno F; Noda A; Kobayashi T; Kobayashi M; Usuzaki T; Ohseto H; Hozawa A; Kikuya M; Metoki H; Kure S; Kuriyama S
    Transl Psychiatry; 2020 Aug; 10(1):290. PubMed ID: 32807774
    [TBL] [Abstract][Full Text] [Related]  

  • 65. [One autism, several autisms. Phenotypical variability in autism spectrum disorders].
    Hervas A
    Rev Neurol; 2016; 62 Suppl 1():S9-14. PubMed ID: 26922965
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Applications of node-based resilience graph theoretic framework to clustering autism spectrum disorders phenotypes.
    Matta J; Zhao J; Ercal G; Obafemi-Ajayi T
    Appl Netw Sci; 2018; 3(1):38. PubMed ID: 30839816
    [TBL] [Abstract][Full Text] [Related]  

  • 67. From genes to environment: using integrative genomics to build a "systems-level" understanding of autism spectrum disorders.
    Hu VW
    Child Dev; 2013; 84(1):89-103. PubMed ID: 22497667
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Modeling the autism spectrum disorder phenotype.
    McCray AT; Trevvett P; Frost HR
    Neuroinformatics; 2014 Apr; 12(2):291-305. PubMed ID: 24163114
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Exploring the relationship between autism spectrum disorder and epilepsy using latent class cluster analysis.
    Cuccaro ML; Tuchman RF; Hamilton KL; Wright HH; Abramson RK; Haines JL; Gilbert JR; Pericak-Vance M
    J Autism Dev Disord; 2012 Aug; 42(8):1630-41. PubMed ID: 22105141
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Connecting phenotype to genotype: PheWAS-inspired analysis of autism spectrum disorder.
    Matta J; Dobrino D; Yeboah D; Howard S; El-Manzalawy Y; Obafemi-Ajayi T
    Front Hum Neurosci; 2022; 16():960991. PubMed ID: 36310845
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Behavioral signatures related to genetic disorders in autism.
    Bruining H; Eijkemans MJ; Kas MJ; Curran SR; Vorstman JA; Bolton PF
    Mol Autism; 2014 Feb; 5(1):11. PubMed ID: 24517317
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome.
    Campbell MG; Kohane IS; Kong SW
    BMC Med Genomics; 2013 Sep; 6():34. PubMed ID: 24063311
    [TBL] [Abstract][Full Text] [Related]  

  • 73. PUNCH: Population Characterization of Heterogeneity.
    Tunc B; Ghanbari Y; Smith AR; Pandey J; Browne A; Schultz RT; Verma R
    Neuroimage; 2014 Sep; 98():50-60. PubMed ID: 24799135
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Genes, brain, and behavior: development gone awry in autism? A report on the 23rd Annual International Symposium of the Center for the Study of Gene Structure and Function.
    Lewis MJ; Dictenberg JB
    Ann N Y Acad Sci; 2010 Sep; 1205 Suppl 1():E21-36. PubMed ID: 20860674
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Latent class model with familial dependence to address heterogeneity in complex diseases: adapting the approach to family-based association studies.
    Bureau A; Croteau J; Tayeb A; Mérette C; Labbe A
    Genet Epidemiol; 2011 Apr; 35(3):182-9. PubMed ID: 21308764
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
    Schaefer GB; Mendelsohn NJ;
    Genet Med; 2013 May; 15(5):399-407. PubMed ID: 23519317
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets.
    Ionita-Laza I; Makarov V; ; Buxbaum JD
    Am J Hum Genet; 2012 Jun; 90(6):1002-13. PubMed ID: 22578327
    [TBL] [Abstract][Full Text] [Related]  

  • 78. The relationship between social communication disorder (SCD) and broad autism phenotype (BAP).
    Tufan E
    J Am Acad Child Adolesc Psychiatry; 2014 Oct; 53(10):1130. PubMed ID: 25245357
    [No Abstract]   [Full Text] [Related]  

  • 79. The origin and natural history of autism spectrum disorders.
    Harris JC
    Nat Neurosci; 2016 Oct; 19(11):1390-1391. PubMed ID: 27786188
    [No Abstract]   [Full Text] [Related]  

  • 80. BAP: not-quite-autism in infants.
    Pruett JR
    J Am Acad Child Adolesc Psychiatry; 2014 Apr; 53(4):392-4. PubMed ID: 24655647
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.