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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

207 related items for PubMed ID: 35778412

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder.
    Wang Y, Picard M, Gu Z.
    PLoS Genet; 2016 Oct; 12(10):e1006391. PubMed ID: 27792786
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial DNA Haplogroup K Is Protective Against Autism Spectrum Disorder Risk in Populations of European Ancestry.
    Chang X, Qu HQ, Liu Y, Glessner JT, Hakonarson H.
    J Am Acad Child Adolesc Psychiatry; 2024 Aug; 63(8):835-844. PubMed ID: 38072244
    [Abstract] [Full Text] [Related]

  • 4. Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders.
    Chalkia D, Singh LN, Leipzig J, Lvova M, Derbeneva O, Lakatos A, Hadley D, Hakonarson H, Wallace DC.
    JAMA Psychiatry; 2017 Nov 01; 74(11):1161-1168. PubMed ID: 28832883
    [Abstract] [Full Text] [Related]

  • 5. Difference in mitochondrial DNA copy number in peripheral blood cells between probands with autism spectrum disorders and their unaffected siblings.
    Yoo HJ, Park M, Kim SA.
    World J Biol Psychiatry; 2017 Mar 01; 18(2):151-156. PubMed ID: 27739340
    [Abstract] [Full Text] [Related]

  • 6. Accelerated expansion of pathogenic mitochondrial DNA heteroplasmies in Huntington's disease.
    Wang Y, Guo X, Ye K, Orth M, Gu Z.
    Proc Natl Acad Sci U S A; 2021 Jul 27; 118(30):. PubMed ID: 34301881
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion.
    Varga NÁ, Pentelényi K, Balicza P, Gézsi A, Reményi V, Hársfalvi V, Bencsik R, Illés A, Prekop C, Molnár MJ.
    Behav Brain Funct; 2018 Feb 20; 14(1):4. PubMed ID: 29458409
    [Abstract] [Full Text] [Related]

  • 9. Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestry.
    Liu C, Fetterman JL, Qian Y, Sun X, Blackwell TW, Pitsillides A, Cade BE, Wang H, Raffield LM, Lange LA, Anugu P, Abecasis G, Adrienne Cupples L, Redline S, Correa A, Vasan RS, Wilson JG, Ding J, Levy D, NHLBI Trans-Omics for Precision Medicine TOPMed Consortium.
    Mitochondrion; 2021 Sep 20; 60():33-42. PubMed ID: 34303007
    [Abstract] [Full Text] [Related]

  • 10. Blood Mitochondrial DNA Content in HIV-Exposed Uninfected Children with Autism Spectrum Disorder.
    Budd MA, Calli K, Samson L, Bowes J, Hsieh AYY, Forbes JC, Bitnun A, Singer J, Kakkar F, Alimenti A, Maan EJ, Lewis MES, Gentile C, Côté HCF, Brophy JC.
    Viruses; 2018 Feb 11; 10(2):. PubMed ID: 29439467
    [Abstract] [Full Text] [Related]

  • 11. The mitochondrial genome as a modifier of autism versus cancer phenotypes in PTEN hamartoma tumor syndrome.
    Wei R, Yehia L, Ni Y, Eng C.
    HGG Adv; 2023 Jul 13; 4(3):100199. PubMed ID: 37216009
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Genetic and clinical evidence of mitochondrial dysfunction in autism spectrum disorder and intellectual disability.
    Valiente-Pallejà A, Torrell H, Muntané G, Cortés MJ, Martínez-Leal R, Abasolo N, Alonso Y, Vilella E, Martorell L.
    Hum Mol Genet; 2018 Mar 01; 27(5):891-900. PubMed ID: 29340697
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.
    Patowary A, Nesbitt R, Archer M, Bernier R, Brkanac Z.
    Autism Res; 2017 Aug 01; 10(8):1338-1343. PubMed ID: 28419775
    [Abstract] [Full Text] [Related]

  • 18. Evaluating mitochondrial DNA variation in autism spectrum disorders.
    Hadjixenofontos A, Schmidt MA, Whitehead PL, Konidari I, Hedges DJ, Wright HH, Abramson RK, Menon R, Williams SM, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA, Martin ER, McCauley JL.
    Ann Hum Genet; 2013 Jan 01; 77(1):9-21. PubMed ID: 23130936
    [Abstract] [Full Text] [Related]

  • 19. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
    Yap CX, Alvares GA, Henders AK, Lin T, Wallace L, Farrelly A, McLaren T, Berry J, Vinkhuyzen AAE, Trzaskowski M, Zeng J, Yang Y, Cleary D, Grove R, Hafekost C, Harun A, Holdsworth H, Jellett R, Khan F, Lawson L, Leslie J, Levis Frenk M, Masi A, Mathew NE, Muniandy M, Nothard M, Visscher PM, Dawson PA, Dissanayake C, Eapen V, Heussler HS, Whitehouse AJO, Wray NR, Gratten J.
    Mol Autism; 2021 Feb 10; 12(1):12. PubMed ID: 33568206
    [Abstract] [Full Text] [Related]

  • 20. Quantitative trait variation in ASD probands and toddler sibling outcomes at 24 months.
    Girault JB, Swanson MR, Meera SS, Grzadzinski RL, Shen MD, Burrows CA, Wolff JJ, Pandey J, John TS, Estes A, Zwaigenbaum L, Botteron KN, Hazlett HC, Dager SR, Schultz RT, Constantino JN, Piven J, IBIS Network.
    J Neurodev Disord; 2020 Feb 05; 12(1):5. PubMed ID: 32024459
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.