141 related articles for article (PubMed ID: 35225680)
1. Identification of Chromosomal Regions Linked to Autism-Spectrum Disorders: A Meta-Analysis of Genome-Wide Linkage Scans.
Mpoulimari I; Zintzaras E
Genet Test Mol Biomarkers; 2022 Feb; 26(2):59-69. PubMed ID: 35225680
[No Abstract] [Full Text] [Related]
2. A heterogeneity-based genome search meta-analysis for autism-spectrum disorders.
Trikalinos TA; Karvouni A; Zintzaras E; Ylisaukko-oja T; Peltonen L; Järvelä I; Ioannidis JP
Mol Psychiatry; 2006 Jan; 11(1):29-36. PubMed ID: 16189507
[TBL] [Abstract][Full Text] [Related]
3. Identification of Chromosomal Regions Linked to Diabetic Nephropathy: A Meta-Analysis of Genome-Wide Linkage Scans.
Tziastoudi M; Stefanidis I; Stravodimos K; Zintzaras E
Genet Test Mol Biomarkers; 2019 Feb; 23(2):105-117. PubMed ID: 30694714
[TBL] [Abstract][Full Text] [Related]
4. Analysis of convergence of linkage and association studies in autism spectrum disorders.
Mpoulimari I; Zintzaras E
Psychiatr Genet; 2023 Jun; 33(3):113-124. PubMed ID: 37212558
[TBL] [Abstract][Full Text] [Related]
5. A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism.
Talebizadeh Z; Arking DE; Hu VW
PLoS One; 2013; 8(6):e67569. PubMed ID: 23840741
[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. Meta-analysis of genome-wide linkage studies of atopic dermatitis.
Cao Y; Liao M; Huang X; Mo Z; Gao F
Dermatitis; 2009; 20(4):193-9. PubMed ID: 19804695
[TBL] [Abstract][Full Text] [Related]
8. A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.
Woodbury-Smith M; Paterson AD; O'Connor I; Zarrei M; Yuen RKC; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Scherer SW; Vieland V; Szatmari P
J Neurodev Disord; 2018 Jun; 10(1):20. PubMed ID: 29890955
[TBL] [Abstract][Full Text] [Related]
9. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
Mol Autism; 2017; 8():21. PubMed ID: 28540026
[TBL] [Abstract][Full Text] [Related]
10. Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.
Tao Y; Gao H; Ackerman B; Guo W; Saffen D; Shugart YY
BMC Genomics; 2016 Mar; 17():163. PubMed ID: 26931105
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.
Al-Sarraj Y; Al-Dous E; Taha RZ; Ahram D; Alshaban F; Tolfat M; El-Shanti H; Albagha OME
Genes (Basel); 2021 May; 12(5):. PubMed ID: 34069769
[TBL] [Abstract][Full Text] [Related]
13. Genetic risk factors for autism-spectrum disorders: a systematic review based on systematic reviews and meta-analysis.
Wei H; Zhu Y; Wang T; Zhang X; Zhang K; Zhang Z
J Neural Transm (Vienna); 2021 Jun; 128(6):717-734. PubMed ID: 34115189
[TBL] [Abstract][Full Text] [Related]
14. A genome-wide linkage and association scan reveals novel loci for autism.
Weiss LA; Arking DE; ; Daly MJ; Chakravarti A
Nature; 2009 Oct; 461(7265):802-8. PubMed ID: 19812673
[TBL] [Abstract][Full Text] [Related]
15. Heterogeneity-based genome search meta-analysis for preeclampsia.
Zintzaras E; Kitsios G; Harrison GA; Laivuori H; Kivinen K; Kere J; Messinis I; Stefanidis I; Ioannidis JP
Hum Genet; 2006 Oct; 120(3):360-70. PubMed ID: 16868762
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide scans meta-analysis for pulse pressure.
Zintzaras E; Kitsios G; Kent D; Camp NJ; Atwood L; Hopkins PN; Hunt SC
Hypertension; 2007 Sep; 50(3):557-64. PubMed ID: 17635856
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.
Liu XQ; Paterson AD; Szatmari P;
Biol Psychiatry; 2008 Oct; 64(7):561-70. PubMed ID: 18632090
[TBL] [Abstract][Full Text] [Related]
18. Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.
Fradin D; Cheslack-Postava K; Ladd-Acosta C; Newschaffer C; Chakravarti A; Arking DE; Feinberg A; Fallin MD
PLoS One; 2010 Sep; 5(9):. PubMed ID: 20824079
[TBL] [Abstract][Full Text] [Related]
19. HEGESMA: genome search meta-analysis and heterogeneity testing.
Zintzaras E; Ioannidis JP
Bioinformatics; 2005 Sep; 21(18):3672-3. PubMed ID: 15955784
[TBL] [Abstract][Full Text] [Related]
20. Autism spectrum disorders and autistic traits share genetics and biology.
Bralten J; van Hulzen KJ; Martens MB; Galesloot TE; Arias Vasquez A; Kiemeney LA; Buitelaar JK; Muntjewerff JW; Franke B; Poelmans G
Mol Psychiatry; 2018 May; 23(5):1205-1212. PubMed ID: 28507316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]