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 *

245 related articles for article (PubMed ID: 34615535)

  • 1. Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.
    Mahjani B; De Rubeis S; Gustavsson Mahjani C; Mulhern M; Xu X; Klei L; Satterstrom FK; Fu J; Talkowski ME; Reichenberg A; Sandin S; Hultman CM; Grice DE; Roeder K; Devlin B; Buxbaum JD
    Mol Autism; 2021 Oct; 12(1):65. PubMed ID: 34615535
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders.
    Mahjani B; Birnbaum R; Buxbaum Grice A; Cappi C; Jung S; Avila MN; Reichenberg A; Sandin S; Hultman CM; Buxbaum JD; Grice DE
    Genes (Basel); 2022 Oct; 13(10):. PubMed ID: 36292681
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 12(1):12. PubMed ID: 33568206
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.
    Vysotskiy M; Zhong X; Miller-Fleming TW; Zhou D; ; ; ; Cox NJ; Weiss LA
    Genome Med; 2021 Oct; 13(1):172. PubMed ID: 34715901
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neurogenetic analysis of childhood disintegrative disorder.
    Gupta AR; Westphal A; Yang DYJ; Sullivan CAW; Eilbott J; Zaidi S; Voos A; Vander Wyk BC; Ventola P; Waqar Z; Fernandez TV; Ercan-Sencicek AG; Walker MF; Choi M; Schneider A; Hedderly T; Baird G; Friedman H; Cordeaux C; Ristow A; Shic F; Volkmar FR; Pelphrey KA
    Mol Autism; 2017; 8():19. PubMed ID: 28392909
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD.
    Chaves TF; Ocampos M; Barbato IT; de Camargo Pinto LL; de Luca GR; Barbato Filho JH; Bernardi P; Costa Netto Muniz Y; Francesca Maris A
    Sci Rep; 2024 Feb; 14(1):3762. PubMed ID: 38355898
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.
    Stessman HAF; Willemsen MH; Fenckova M; Penn O; Hoischen A; Xiong B; Wang T; Hoekzema K; Vives L; Vogel I; Brunner HG; van der Burgt I; Ockeloen CW; Schuurs-Hoeijmakers JH; Klein Wassink-Ruiter JS; Stumpel C; Stevens SJC; Vles HS; Marcelis CM; van Bokhoven H; Cantagrel V; Colleaux L; Nicouleau M; Lyonnet S; Bernier RA; Gerdts J; Coe BP; Romano C; Alberti A; Grillo L; Scuderi C; Nordenskjöld M; Kvarnung M; Guo H; Xia K; Piton A; Gerard B; Genevieve D; Delobel B; Lehalle D; Perrin L; Prieur F; Thevenon J; Gecz J; Shaw M; Pfundt R; Keren B; Jacquette A; Schenck A; Eichler EE; Kleefstra T
    Am J Hum Genet; 2016 Mar; 98(3):541-552. PubMed ID: 26942287
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
    Hudac CM; Bove J; Barber S; Duyzend M; Wallace A; Martin CL; Ledbetter DH; Hanson E; Goin-Kochel RP; Green-Snyder L; Chung WK; Eichler EE; Bernier RA
    Autism Res; 2020 Aug; 13(8):1300-1310. PubMed ID: 32597026
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
    Callaghan DB; Rogic S; Tan PPC; Calli K; Qiao Y; Baldwin R; Jacobson M; Belmadani M; Holmes N; Yu C; Li Y; Li Y; Kurtzke FE; Kuzeljevic B; Yu AY; Hudson M; Mcaughton AJM; Xu Y; Dionne-Laporte A; Girard S; Liang P; Separovic ER; Liu X; Rouleau G; Pavlidis P; Lewis MES
    Clin Genet; 2019 Sep; 96(3):199-206. PubMed ID: 31038196
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing.
    Wu R; Li X; Meng Z; Li P; He Z; Liang L
    Orphanet J Rare Dis; 2024 May; 19(1):205. PubMed ID: 38764027
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
    Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM
    Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
    Torrico B; Shaw AD; Mosca R; Vivó-Luque N; Hervás A; Fernàndez-Castillo N; Aloy P; Bayés M; Fullerton JM; Cormand B; Toma C
    J Psychiatry Neurosci; 2019 Sep; 44(5):350-359. PubMed ID: 31094488
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
    Woodbury-Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Anagnostou E; Scherer SW; Vieland VJ; Szatmari P
    Am J Med Genet B Neuropsychiatr Genet; 2020 Jul; 183(5):268-276. PubMed ID: 32372567
    [TBL] [Abstract][Full Text] [Related]  

  • 17. How rare and common risk variation jointly affect liability for autism spectrum disorder.
    Klei L; McClain LL; Mahjani B; Panayidou K; De Rubeis S; Grahnat AS; Karlsson G; Lu Y; Melhem N; Xu X; Reichenberg A; Sandin S; Hultman CM; Buxbaum JD; Roeder K; Devlin B
    Mol Autism; 2021 Oct; 12(1):66. PubMed ID: 34615521
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Discovery and Validation of Novel Genes in a Large Chinese Autism Spectrum Disorder Cohort.
    Wang J; Yu J; Wang M; Zhang L; Yang K; Du X; Wu J; Wang X; Li F; Qiu Z
    Biol Psychiatry; 2023 Nov; 94(10):792-803. PubMed ID: 37393044
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders.
    Ashitha SNM; Ramachandra NB
    Neuroscience; 2020 Jul; 438():25-40. PubMed ID: 32407977
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications.
    Kalsner L; Twachtman-Bassett J; Tokarski K; Stanley C; Dumont-Mathieu T; Cotney J; Chamberlain S
    Mol Genet Genomic Med; 2018 Mar; 6(2):171-185. PubMed ID: 29271092
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.