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 *

997 related articles for article (PubMed ID: 19755429)

  • 21. Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder.
    Carter MT; Nikkel SM; Fernandez BA; Marshall CR; Noor A; Lionel AC; Prasad A; Pinto D; Joseph-George AM; Noakes C; Fairbrother-Davies C; Roberts W; Vincent J; Weksberg R; Scherer SW
    Clin Genet; 2011 Nov; 80(5):435-43. PubMed ID: 21114665
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Association of syndromic mental retardation and autism with 22q11.2 duplication.
    Lo-Castro A; Galasso C; Cerminara C; El-Malhany N; Benedetti S; Nardone AM; Curatolo P
    Neuropediatrics; 2009 Jun; 40(3):137-40. PubMed ID: 20020400
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Delineation of 15q13.3 microdeletions.
    Masurel-Paulet A; Andrieux J; Callier P; Cuisset JM; Le Caignec C; Holder M; Thauvin-Robinet C; Doray B; Flori E; Alex-Cordier MP; Beri M; Boute O; Delobel B; Dieux A; Vallee L; Jaillard S; Odent S; Isidor B; Beneteau C; Vigneron J; Bilan F; Gilbert-Dussardier B; Dubourg C; Labalme A; Bidon C; Gautier A; Pernes P; Pinoit JM; Huet F; Mugneret F; Aral B; Jonveaux P; Sanlaville D; Faivre L
    Clin Genet; 2010 Aug; 78(2):149-61. PubMed ID: 20236110
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
    Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
    Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Profiles of executive function in parents and siblings of individuals with autism spectrum disorders.
    Wong D; Maybery M; Bishop DV; Maley A; Hallmayer J
    Genes Brain Behav; 2006 Nov; 5(8):561-76. PubMed ID: 17081261
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class.
    Peters SU; Horowitz L; Barbieri-Welge R; Taylor JL; Hundley RJ
    J Child Psychol Psychiatry; 2012 Feb; 53(2):152-9. PubMed ID: 21831244
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Modeling clinical outcome of children with autistic spectrum disorders.
    Coplan J; Jawad AF
    Pediatrics; 2005 Jul; 116(1):117-22. PubMed ID: 15995041
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Major contribution of dominant inheritance to autism spectrum disorders (ASDs) in population-based families.
    Nishiyama T; Notohara M; Sumi S; Takami S; Kishino H
    J Hum Genet; 2009 Dec; 54(12):721-6. PubMed ID: 19893580
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Characteristics and concordance of autism spectrum disorders among 277 twin pairs.
    Rosenberg RE; Law JK; Yenokyan G; McGready J; Kaufmann WE; Law PA
    Arch Pediatr Adolesc Med; 2009 Oct; 163(10):907-14. PubMed ID: 19805709
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation.
    Yang Y; Wang C; Wang F; Zhu L; Liu H; He X
    Gene; 2012 Jul; 502(2):154-8. PubMed ID: 22555022
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.
    McBride KL; Varga EA; Pastore MT; Prior TW; Manickam K; Atkin JF; Herman GE
    Autism Res; 2010 Jun; 3(3):137-41. PubMed ID: 20533527
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Etiologic yield of autistic spectrum disorders: a prospective study.
    Battaglia A; Carey JC
    Am J Med Genet C Semin Med Genet; 2006 Feb; 142C(1):3-7. PubMed ID: 16419094
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.
    Munesue T; Yokoyama S; Nakamura K; Anitha A; Yamada K; Hayashi K; Asaka T; Liu HX; Jin D; Koizumi K; Islam MS; Huang JJ; Ma WJ; Kim UH; Kim SJ; Park K; Kim D; Kikuchi M; Ono Y; Nakatani H; Suda S; Miyachi T; Hirai H; Salmina A; Pichugina YA; Soumarokov AA; Takei N; Mori N; Tsujii M; Sugiyama T; Yagi K; Yamagishi M; Sasaki T; Yamasue H; Kato N; Hashimoto R; Taniike M; Hayashi Y; Hamada J; Suzuki S; Ooi A; Noda M; Kamiyama Y; Kido MA; Lopatina O; Hashii M; Amina S; Malavasi F; Huang EJ; Zhang J; Shimizu N; Yoshikawa T; Matsushima A; Minabe Y; Higashida H
    Neurosci Res; 2010 Jun; 67(2):181-91. PubMed ID: 20435366
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?
    Sporn AL; Addington AM; Gogtay N; Ordoñez AE; Gornick M; Clasen L; Greenstein D; Tossell JW; Gochman P; Lenane M; Sharp WS; Straub RE; Rapoport JL
    Biol Psychiatry; 2004 May; 55(10):989-94. PubMed ID: 15121482
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms.
    Lespinasse J; Gimelli S; Béna F; Antonarakis SE; Ansermet F; Paoloni-Giacobino A
    Eur J Med Genet; 2009; 52(1):49-52. PubMed ID: 18992376
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Psychotic symptoms in 16p11.2 copy-number variant carriers.
    Jutla A; Turner JB; Green Snyder L; Chung WK; Veenstra-VanderWeele J
    Autism Res; 2020 Feb; 13(2):187-198. PubMed ID: 31724820
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardation.
    Raedle J; Friedl W; Engels H; Koenig R; Trojan J; Zeuzem S
    Am J Gastroenterol; 2001 Oct; 96(10):3016-20. PubMed ID: 11693343
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Siblings of individuals with autism or Down syndrome: effects on adult lives.
    Orsmond GI; Seltzer MM
    J Intellect Disabil Res; 2007 Sep; 51(Pt 9):682-96. PubMed ID: 17845237
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 50.