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 *

106 related articles for article (PubMed ID: 8911221)

  • 1. Autism and the X chromosome. Multipoint sib-pair analysis.
    Hallmayer J; Hebert JM; Spiker D; Lotspeich L; McMahon WM; Petersen PB; Nicholas P; Pingree C; Lin AA; Cavalli-Sforza LL; Risch N; Ciaranello RD
    Arch Gen Psychiatry; 1996 Nov; 53(11):985-9. PubMed ID: 8911221
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Autism and the X chromosome: no linkage to microsatellite loci detected using the affected sibling pair method.
    Schutz CK; Polley D; Robinson PD; Chalifoux M; Macciardi F; White BN; Holden JJ
    Am J Med Genet; 2002 Apr; 109(1):36-41. PubMed ID: 11932990
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The genetics of autism.
    Muhle R; Trentacoste SV; Rapin I
    Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome. International Consortium for the Genetics of Autoimmune Thyroid Disease.
    Barbesino G; Tomer Y; Concepcion ES; Davies TF; Greenberg DA
    J Clin Endocrinol Metab; 1998 Sep; 83(9):3290-5. PubMed ID: 9745443
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B; Hallmayer J; Rogers T; Kalaydjieva L; Petersen PB; Nicholas P; Pingree C; McMahon W; Spiker D; Lotspeich L; Kraemer H; McCague P; Dimiceli S; Nouri N; Pitts T; Yang J; Hinds D; Myers RM; Risch N
    Am J Med Genet; 1999 Oct; 88(5):551-6. PubMed ID: 10490715
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An autosomal genomic screen for autism. Collaborative linkage study of autism.
    Barrett S; Beck JC; Bernier R; Bisson E; Braun TA; Casavant TL; Childress D; Folstein SE; Garcia M; Gardiner MB; Gilman S; Haines JL; Hopkins K; Landa R; Meyer NH; Mullane JA; Nishimura DY; Palmer P; Piven J; Purdy J; Santangelo SL; Searby C; Sheffield V; Singleton J; Slager S
    Am J Med Genet; 1999 Dec; 88(6):609-15. PubMed ID: 10581478
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genomic screen and follow-up analysis for autistic disorder.
    Shao Y; Wolpert CM; Raiford KL; Menold MM; Donnelly SL; Ravan SA; Bass MP; McClain C; von Wendt L; Vance JM; Abramson RH; Wright HH; Ashley-Koch A; Gilbert JR; DeLong RG; Cuccaro ML; Pericak-Vance MA
    Am J Med Genet; 2002 Jan; 114(1):99-105. PubMed ID: 11840513
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
    Hum Mol Genet; 1998 Mar; 7(3):571-8. PubMed ID: 9546821
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.
    Molloy CA; Keddache M; Martin LJ
    Mol Psychiatry; 2005 Aug; 10(8):741-6. PubMed ID: 15940295
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Evidence for inflammatory bowel disease of a susceptibility locus on the X chromosome.
    Vermeire S; Satsangi J; Peeters M; Parkes M; Jewell DP; Vlietinck R; Rutgeerts P
    Gastroenterology; 2001 Mar; 120(4):834-40. PubMed ID: 11231937
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.
    Stine OC; McMahon FJ; Chen L; Xu J; Meyers DA; MacKinnon DF; Simpson S; McInnis MG; Rice JP; Goate A; Reich T; Edenberg HJ; Foroud T; Nurnberger JI; Detera-Wadleigh SD; Goldin LR; Guroff J; Gershon ES; Blehar MC; DePaulo JR
    Am J Med Genet; 1997 May; 74(3):263-9. PubMed ID: 9184308
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A genomic screen of autism: evidence for a multilocus etiology.
    Risch N; Spiker D; Lotspeich L; Nouri N; Hinds D; Hallmayer J; Kalaydjieva L; McCague P; Dimiceli S; Pitts T; Nguyen L; Yang J; Harper C; Thorpe D; Vermeer S; Young H; Hebert J; Lin A; Ferguson J; Chiotti C; Wiese-Slater S; Rogers T; Salmon B; Nicholas P; Petersen PB; Pingree C; McMahon W; Wong DL; Cavalli-Sforza LL; Kraemer HC; Myers RM
    Am J Hum Genet; 1999 Aug; 65(2):493-507. PubMed ID: 10417292
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.
    Villard L; des Portes V; Levy N; Louboutin JP; Recan D; Coquet M; Chabrol B; Figarella-Branger D; Chelly J; Pellissier JF; Fontes M
    Eur J Hum Genet; 2000 Feb; 8(2):125-9. PubMed ID: 10757644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.