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 *

218 related articles for article (PubMed ID: 35898556)

  • 41. Strong association of de novo copy number mutations with autism.
    Sebat J; Lakshmi B; Malhotra D; Troge J; Lese-Martin C; Walsh T; Yamrom B; Yoon S; Krasnitz A; Kendall J; Leotta A; Pai D; Zhang R; Lee YH; Hicks J; Spence SJ; Lee AT; Puura K; Lehtimäki T; Ledbetter D; Gregersen PK; Bregman J; Sutcliffe JS; Jobanputra V; Chung W; Warburton D; King MC; Skuse D; Geschwind DH; Gilliam TC; Ye K; Wigler M
    Science; 2007 Apr; 316(5823):445-9. PubMed ID: 17363630
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Identification of Copy Number Variation by Array-CGH in Portuguese Children and Adolescents Diagnosed with Autism Spectrum Disorders.
    Monteiro S; Pinto J; Mira Coelho A; Leão M; Dória S
    Neuropediatrics; 2019 Dec; 50(6):367-377. PubMed ID: 31398764
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Epigenetics of autism-related impairment: copy number variation and maternal infection.
    Mazina V; Gerdts J; Trinh S; Ankenman K; Ward T; Dennis MY; Girirajan S; Eichler EE; Bernier R
    J Dev Behav Pediatr; 2015; 36(2):61-7. PubMed ID: 25629966
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
    Kushima I; Aleksic B; Nakatochi M; Shimamura T; Okada T; Uno Y; Morikawa M; Ishizuka K; Shiino T; Kimura H; Arioka Y; Yoshimi A; Takasaki Y; Yu Y; Nakamura Y; Yamamoto M; Iidaka T; Iritani S; Inada T; Ogawa N; Shishido E; Torii Y; Kawano N; Omura Y; Yoshikawa T; Uchiyama T; Yamamoto T; Ikeda M; Hashimoto R; Yamamori H; Yasuda Y; Someya T; Watanabe Y; Egawa J; Nunokawa A; Itokawa M; Arai M; Miyashita M; Kobori A; Suzuki M; Takahashi T; Usami M; Kodaira M; Watanabe K; Sasaki T; Kuwabara H; Tochigi M; Nishimura F; Yamasue H; Eriguchi Y; Benner S; Kojima M; Yassin W; Munesue T; Yokoyama S; Kimura R; Funabiki Y; Kosaka H; Ishitobi M; Ohmori T; Numata S; Yoshikawa T; Toyota T; Yamakawa K; Suzuki T; Inoue Y; Nakaoka K; Goto YI; Inagaki M; Hashimoto N; Kusumi I; Son S; Murai T; Ikegame T; Okada N; Kasai K; Kunimoto S; Mori D; Iwata N; Ozaki N
    Cell Rep; 2018 Sep; 24(11):2838-2856. PubMed ID: 30208311
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Structure and function of neonatal social communication in a genetic mouse model of autism.
    Takahashi T; Okabe S; Broin PÓ; Nishi A; Ye K; Beckert MV; Izumi T; Machida A; Kang G; Abe S; Pena JL; Golden A; Kikusui T; Hiroi N
    Mol Psychiatry; 2016 Sep; 21(9):1208-14. PubMed ID: 26666205
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
    da Silva Montenegro EM; Costa CS; Campos G; Scliar M; de Almeida TF; Zachi EC; Silva IMW; Chan AJS; Zarrei M; Lourenço NCV; Yamamoto GL; Scherer S; Passos-Bueno MR
    Autism Res; 2020 Feb; 13(2):199-206. PubMed ID: 31696658
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Cell Adhesion Molecules Involved in Neurodevelopmental Pathways Implicated in 3p-Deletion Syndrome and Autism Spectrum Disorder.
    Gandawijaya J; Bamford RA; Burbach JPH; Oguro-Ando A
    Front Cell Neurosci; 2020; 14():611379. PubMed ID: 33519384
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Ohnologs are overrepresented in pathogenic copy number mutations.
    McLysaght A; Makino T; Grayton HM; Tropeano M; Mitchell KJ; Vassos E; Collier DA
    Proc Natl Acad Sci U S A; 2014 Jan; 111(1):361-6. PubMed ID: 24368850
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications.
    Oikonomakis V; Kosma K; Mitrakos A; Sofocleous C; Pervanidou P; Syrmou A; Pampanos A; Psoni S; Fryssira H; Kanavakis E; Kitsiou-Tzeli S; Tzetis M
    Clin Genet; 2016 Jun; 89(6):708-18. PubMed ID: 26777411
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Autism and duplication of 17q12q21.2 by array-CGH: a case report.
    Weingartner A; Pegoraro NB; Maglioni RT; Moreira ICFN; Rodrigues GE; Kunz AC; Piai CB; Milano AS; Raskin S; Ferrari LP; Mikami LR
    Rev Paul Pediatr; 2023; 41():e2021387. PubMed ID: 36700567
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.
    Blumenthal I; Ragavendran A; Erdin S; Klei L; Sugathan A; Guide JR; Manavalan P; Zhou JQ; Wheeler VC; Levin JZ; Ernst C; Roeder K; Devlin B; Gusella JF; Talkowski ME
    Am J Hum Genet; 2014 Jun; 94(6):870-83. PubMed ID: 24906019
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Evaluation of Chromosome Microarray Analysis in a Large Cohort of Females with Autism Spectrum Disorders: A Single Center Italian Study.
    Calderoni S; Ricca I; Balboni G; Cagiano R; Cassandrini D; Doccini S; Cosenza A; Tolomeo D; Tancredi R; Santorelli FM; Muratori F
    J Pers Med; 2020 Oct; 10(4):. PubMed ID: 33050239
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model.
    Hiramoto T; Kang G; Suzuki G; Satoh Y; Kucherlapati R; Watanabe Y; Hiroi N
    Hum Mol Genet; 2011 Dec; 20(24):4775-85. PubMed ID: 21908517
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.
    Moreno-De-Luca D; Sanders SJ; Willsey AJ; Mulle JG; Lowe JK; Geschwind DH; State MW; Martin CL; Ledbetter DH
    Mol Psychiatry; 2013 Oct; 18(10):1090-5. PubMed ID: 23044707
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Performance of case-control rare copy number variation annotation in classification of autism.
    Engchuan W; Dhindsa K; Lionel AC; Scherer SW; Chan JH; Merico D
    BMC Med Genomics; 2015; 8 Suppl 1(Suppl 1):S7. PubMed ID: 25783485
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
    Merikangas AK; Segurado R; Heron EA; Anney RJ; Paterson AD; Cook EH; Pinto D; Scherer SW; Szatmari P; Gill M; Corvin AP; Gallagher L
    Mol Psychiatry; 2015 Nov; 20(11):1366-72. PubMed ID: 25421404
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A critical review of the impact of candidate copy number variants on autism spectrum disorder.
    Abedini SS; Akhavantabasi S; Liang Y; Heng JI; Alizadehsani R; Dehzangi I; Bauer DC; Alinejad-Rokny H
    Mutat Res Rev Mutat Res; 2024; 794():108509. PubMed ID: 38977176
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Autism spectrum disorder and genes for synaptic proteins].
    Shishido E
    Brain Nerve; 2012 Jan; 64(1):65-70. PubMed ID: 22223503
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.