190 related articles for article (PubMed ID: 35778412)
1. Association of mitochondrial DNA content, heteroplasmies and inter-generational transmission with autism.
Wang Y; Guo X; Hong X; Wang G; Pearson C; Zuckerman B; Clark AG; O'Brien KO; Wang X; Gu Z
Nat Commun; 2022 Jul; 13(1):3790. PubMed ID: 35778412
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
3. 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; 74(11):1161-1168. PubMed ID: 28832883
[TBL] [Abstract][Full Text] [Related]
4. Biomarkers of mitochondrial dysfunction in autism spectrum disorder: A systematic review and meta-analysis.
Frye RE; Rincon N; McCarty PJ; Brister D; Scheck AC; Rossignol DA
Neurobiol Dis; 2024 Jul; 197():106520. PubMed ID: 38703861
[TBL] [Abstract][Full Text] [Related]
5. 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; 118(30):. PubMed ID: 34301881
[TBL] [Abstract][Full Text] [Related]
6. 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; 18(2):151-156. PubMed ID: 27739340
[TBL] [Abstract][Full Text] [Related]
7. 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;
Mitochondrion; 2021 Sep; 60():33-42. PubMed ID: 34303007
[TBL] [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; 14(1):4. PubMed ID: 29458409
[TBL] [Abstract][Full Text] [Related]
9. 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; 10(2):. PubMed ID: 29439467
[TBL] [Abstract][Full Text] [Related]
10. An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes.
Yardeni T; Cristancho AG; McCoy AJ; Schaefer PM; McManus MJ; Marsh ED; Wallace DC
Proc Natl Acad Sci U S A; 2021 Feb; 118(6):. PubMed ID: 33536343
[TBL] [Abstract][Full Text] [Related]
11. The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives.
Citrigno L; Muglia M; Qualtieri A; Spadafora P; Cavalcanti F; Pioggia G; Cerasa A
Int J Mol Sci; 2020 Aug; 21(16):. PubMed ID: 32806635
[TBL] [Abstract][Full Text] [Related]
12. 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; 77(1):9-21. PubMed ID: 23130936
[TBL] [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; 27(5):891-900. PubMed ID: 29340697
[TBL] [Abstract][Full Text] [Related]
14. Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.
Patowary A; Nesbitt R; Archer M; Bernier R; Brkanac Z
Autism Res; 2017 Aug; 10(8):1338-1343. PubMed ID: 28419775
[TBL] [Abstract][Full Text] [Related]
15. Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder.
Caporali L; Fiorini C; Palombo F; Romagnoli M; Baccari F; Zenesini C; Visconti P; Posar A; Scaduto MC; Ormanbekova D; Battaglia A; Tancredi R; Cameli C; Viggiano M; Olivieri A; Torroni A; Maestrini E; Rochat MJ; Bacchelli E; Carelli V; Maresca A
Front Genet; 2022; 13():953762. PubMed ID: 36419830
[TBL] [Abstract][Full Text] [Related]
16. The Association Between Somatic Health, Autism Spectrum Disorder, and Autistic Traits.
Pan PY; Tammimies K; Bölte S
Behav Genet; 2020 Jul; 50(4):233-246. PubMed ID: 31811521
[TBL] [Abstract][Full Text] [Related]
17. 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;
J Neurodev Disord; 2020 Feb; 12(1):5. PubMed ID: 32024459
[TBL] [Abstract][Full Text] [Related]
18. 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; 2023 Dec; ():. PubMed ID: 38072244
[TBL] [Abstract][Full Text] [Related]
19. Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA.
Rebolledo-Jaramillo B; Su MS; Stoler N; McElhoe JA; Dickins B; Blankenberg D; Korneliussen TS; Chiaromonte F; Nielsen R; Holland MM; Paul IM; Nekrutenko A; Makova KD
Proc Natl Acad Sci U S A; 2014 Oct; 111(43):15474-9. PubMed ID: 25313049
[TBL] [Abstract][Full Text] [Related]
20. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
