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 *

168 related articles for article (PubMed ID: 18349700)

  • 1. Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.
    Wassink TH; Vieland VJ; Sheffield VC; Bartlett CW; Goedken R; Childress D; Piven J
    Psychiatr Genet; 2008 Apr; 18(2):85-91. PubMed ID: 18349700
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
    Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
    Wassink TH; Piven J; Vieland VJ; Jenkins L; Frantz R; Bartlett CW; Goedken R; Childress D; Spence MA; Smith M; Sheffield VC
    Am J Med Genet B Neuropsychiatr Genet; 2005 Jul; 136B(1):36-44. PubMed ID: 15892143
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evidence for multiple loci from a genome scan of autism kindreds.
    Schellenberg GD; Dawson G; Sung YJ; Estes A; Munson J; Rosenthal E; Rothstein J; Flodman P; Smith M; Coon H; Leong L; Yu CE; Stodgell C; Rodier PM; Spence MA; Minshew N; McMahon WM; Wijsman EM
    Mol Psychiatry; 2006 Nov; 11(11):1049-60, 979. PubMed ID: 16880825
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.
    Auranen M; Nieminen T; Majuri S; Vanhala R; Peltonen L; Järvelä I
    Mol Psychiatry; 2000 May; 5(3):320-2. PubMed ID: 10889536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An autosomal genomic screen for autism.
    Collaborative Linkage Study of Autism
    Am J Med Genet; 2001 Dec; 105(8):609-15. PubMed ID: 11811142
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.
    McCauley JL; Li C; Jiang L; Olson LM; Crockett G; Gainer K; Folstein SE; Haines JL; Sutcliffe JS
    BMC Med Genet; 2005 Jan; 6():1. PubMed ID: 15647115
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ordered-subset analysis of savant skills in autism for 15q11-q13.
    Ma DQ; Jaworski J; Menold MM; Donnelly S; Abramson RK; Wright HH; Delong GR; Gilbert JR; Pericak-Vance MA; Cuccaro ML
    Am J Med Genet B Neuropsychiatr Genet; 2005 May; 135B(1):38-41. PubMed ID: 15756693
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Incorporating language phenotypes strengthens evidence of linkage to autism.
    Bradford Y; Haines J; Hutcheson H; Gardiner M; Braun T; Sheffield V; Cassavant T; Huang W; Wang K; Vieland V; Folstein S; Santangelo S; Piven J
    Am J Med Genet; 2001 Aug; 105(6):539-47. PubMed ID: 11496372
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Incorporating language phenotypes strengthens evidence of linkage to autism.
    Collaborative Linkage Study of Autism
    Am J Med Genet; 2001 Dec; 105(8):539-47. PubMed ID: 11811141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A genomewide screen for autism susceptibility loci.
    Liu J; Nyholt DR; Magnussen P; Parano E; Pavone P; Geschwind D; Lord C; Iversen P; Hoh J; Ott J; Gilliam TC;
    Am J Hum Genet; 2001 Aug; 69(2):327-40. PubMed ID: 11452361
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families.
    Alarcón M; Cantor RM; Liu J; Gilliam TC; Geschwind DH;
    Am J Hum Genet; 2002 Jan; 70(1):60-71. PubMed ID: 11741194
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.
    Asherson P; Zhou K; Anney RJ; Franke B; Buitelaar J; Ebstein R; Gill M; Altink M; Arnold R; Boer F; Brookes K; Buschgens C; Butler L; Cambell D; Chen W; Christiansen H; Feldman L; Fleischman K; Fliers E; Howe-Forbes R; Goldfarb A; Heise A; Gabriëls I; Johansson L; Lubetzki I; Marco R; Medad S; Minderaa R; Mulas F; Müller U; Mulligan A; Neale B; Rijsdijk F; Rabin K; Rommelse N; Sethna V; Sorohan J; Uebel H; Psychogiou L; Weeks A; Barrett R; Xu X; Banaschewski T; Sonuga-Barke E; Eisenberg J; Manor I; Miranda A; Oades RD; Roeyers H; Rothenberger A; Sergeant J; Steinhausen HC; Taylor E; Thompson M; Faraone SV
    Mol Psychiatry; 2008 May; 13(5):514-21. PubMed ID: 18180756
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.
    Schmidt S; Scott WK; Postel EA; Agarwal A; Hauser ER; De La Paz MA; Gilbert JR; Weeks DE; Gorin MB; Haines JL; Pericak-Vance MA
    BMC Genet; 2004 Jul; 5():18. PubMed ID: 15238159
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.
    Bartlett CW; Flax JF; Logue MW; Smith BJ; Vieland VJ; Tallal P; Brzustowicz LM
    Hum Hered; 2004; 57(1):10-20. PubMed ID: 15133308
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A posterior probability of linkage-based re-analysis of schizophrenia data yields evidence of linkage to chromosomes 1 and 17.
    Logue MW; Brzustowicz LM; Bassett AS; Chow EW; Vieland VJ
    Hum Hered; 2006; 62(1):47-54. PubMed ID: 17019084
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.
    Strom SP; Stone JL; Ten Bosch JR; Merriman B; Cantor RM; Geschwind DH; Nelson SF
    Mol Psychiatry; 2010 Oct; 15(10):996-1005. PubMed ID: 19455149
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
    International Molecular Genetic Study of Autism Consortium (IMGSAC)
    Am J Hum Genet; 2001 Sep; 69(3):570-81. PubMed ID: 11481586
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
    Levinson DF; Holmans P; Straub RE; Owen MJ; Wildenauer DB; Gejman PV; Pulver AE; Laurent C; Kendler KS; Walsh D; Norton N; Williams NM; Schwab SG; Lerer B; Mowry BJ; Sanders AR; Antonarakis SE; Blouin JL; DeLeuze JF; Mallet J
    Am J Hum Genet; 2000 Sep; 67(3):652-63. PubMed ID: 10924404
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.