BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

380 related articles for article (PubMed ID: 34715901)

  • 1. 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]  

  • 2. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
    Bassett AS; Lowther C; Merico D; Costain G; Chow EWC; van Amelsvoort T; McDonald-McGinn D; Gur RE; Swillen A; Van den Bree M; Murphy K; Gothelf D; Bearden CE; Eliez S; Kates W; Philip N; Sashi V; Campbell L; Vorstman J; Cubells J; Repetto GM; Simon T; Boot E; Heung T; Evers R; Vingerhoets C; van Duin E; Zackai E; Vergaelen E; Devriendt K; Vermeesch JR; Owen M; Murphy C; Michaelovosky E; Kushan L; Schneider M; Fremont W; Busa T; Hooper S; McCabe K; Duijff S; Isaev K; Pellecchia G; Wei J; Gazzellone MJ; Scherer SW; Emanuel BS; Guo T; Morrow BE; Marshall CR;
    Am J Psychiatry; 2017 Nov; 174(11):1054-1063. PubMed ID: 28750581
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Phenome-wide Burden of Copy-Number Variation in the UK Biobank.
    Aguirre M; Rivas MA; Priest J
    Am J Hum Genet; 2019 Aug; 105(2):373-383. PubMed ID: 31353025
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits.
    Vysotskiy M; ; ; ; Weiss LA
    PLoS Genet; 2023 Jun; 19(6):e1010780. PubMed ID: 37267418
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reciprocal Copy Number Variations at 22q11.2 Produce Distinct and Convergent Neurobehavioral Impairments Relevant for Schizophrenia and Autism Spectrum Disorder.
    Lin A; Vajdi A; Kushan-Wells L; Helleman G; Hansen LP; Jonas RK; Jalbrzikowski M; Kingsbury L; Raznahan A; Bearden CE
    Biol Psychiatry; 2020 Aug; 88(3):260-272. PubMed ID: 32143830
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
    Sønderby IE; Gústafsson Ó; Doan NT; Hibar DP; Martin-Brevet S; Abdellaoui A; Ames D; Amunts K; Andersson M; Armstrong NJ; Bernard M; Blackburn N; Blangero J; Boomsma DI; Bralten J; Brattbak HR; Brodaty H; Brouwer RM; Bülow R; Calhoun V; Caspers S; Cavalleri G; Chen CH; Cichon S; Ciufolini S; Corvin A; Crespo-Facorro B; Curran JE; Dale AM; Dalvie S; Dazzan P; de Geus EJC; de Zubicaray GI; de Zwarte SMC; Delanty N; den Braber A; Desrivières S; Donohoe G; Draganski B; Ehrlich S; Espeseth T; Fisher SE; Franke B; Frouin V; Fukunaga M; Gareau T; Glahn DC; Grabe H; Groenewold NA; Haavik J; Håberg A; Hashimoto R; Hehir-Kwa JY; Heinz A; Hillegers MHJ; Hoffmann P; Holleran L; Hottenga JJ; Hulshoff HE; Ikeda M; Jahanshad N; Jernigan T; Jockwitz C; Johansson S; Jonsdottir GA; Jönsson EG; Kahn R; Kaufmann T; Kelly S; Kikuchi M; Knowles EEM; Kolskår KK; Kwok JB; Hellard SL; Leu C; Liu J; Lundervold AJ; Lundervold A; Martin NG; Mather K; Mathias SR; McCormack M; McMahon KL; McRae A; Milaneschi Y; Moreau C; Morris D; Mothersill D; Mühleisen TW; Murray R; Nordvik JE; Nyberg L; Olde Loohuis LM; Ophoff R; Paus T; Pausova Z; Penninx B; Peralta JM; Pike B; Prieto C; Pudas S; Quinlan E; Quintana DS; Reinbold CS; Marques TR; Reymond A; Richard G; Rodriguez-Herreros B; Roiz-Santiañez R; Rokicki J; Rucker J; Sachdev P; Sanders AM; Sando SB; Schmaal L; Schofield PR; Schork AJ; Schumann G; Shin J; Shumskaya E; Sisodiya S; Steen VM; Stein DJ; Steinberg S; Strike L; Teumer A; Thalamuthu A; Tordesillas-Gutierrez D; Turner J; Ueland T; Uhlmann A; Ulfarsson MO; van 't Ent D; van der Meer D; van Haren NEM; Vaskinn A; Vassos E; Walters GB; Wang Y; Wen W; Whelan CD; Wittfeld K; Wright M; Yamamori H; Zayats T; Agartz I; Westlye LT; Jacquemont S; Djurovic S; Stefánsson H; Stefánsson K; Thompson P; Andreassen OA;
    Mol Psychiatry; 2020 Mar; 25(3):584-602. PubMed ID: 30283035
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
    D'Angelo D; Lebon S; Chen Q; Martin-Brevet S; Snyder LG; Hippolyte L; Hanson E; Maillard AM; Faucett WA; Macé A; Pain A; Bernier R; Chawner SJ; David A; Andrieux J; Aylward E; Baujat G; Caldeira I; Conus P; Ferrari C; Forzano F; Gérard M; Goin-Kochel RP; Grant E; Hunter JV; Isidor B; Jacquette A; Jønch AE; Keren B; Lacombe D; Le Caignec C; Martin CL; Männik K; Metspalu A; Mignot C; Mukherjee P; Owen MJ; Passeggeri M; Rooryck-Thambo C; Rosenfeld JA; Spence SJ; Steinman KJ; Tjernagel J; Van Haelst M; Shen Y; Draganski B; Sherr EH; Ledbetter DH; van den Bree MB; Beckmann JS; Spiro JE; Reymond A; Jacquemont S; Chung WK; ; ;
    JAMA Psychiatry; 2016 Jan; 73(1):20-30. PubMed ID: 26629640
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 16p11.2 Locus modulates response to satiety before the onset of obesity.
    Maillard AM; Hippolyte L; Rodriguez-Herreros B; Chawner SJ; Dremmel D; Agüera Z; Fagundo AB; Pain A; Martin-Brevet S; Hilbert A; Kurz S; Etienne R; Draganski B; Jimenez-Murcia S; Männik K; Metspalu A; Reigo A; Isidor B; Le Caignec C; David A; Mignot C; Keren B; ; van den Bree MB; Munsch S; Fernandez-Aranda F; Beckmann JS; Reymond A; Jacquemont S
    Int J Obes (Lond); 2016 May; 40(5):870-6. PubMed ID: 26620891
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways.
    Pettersson M; Viljakainen H; Loid P; Mustila T; Pekkinen M; Armenio M; Andersson-Assarsson JC; Mäkitie O; Lindstrand A
    J Clin Endocrinol Metab; 2017 Aug; 102(8):3029-3039. PubMed ID: 28605459
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Immune Signaling Adaptor LAT Contributes to the Neuroanatomical Phenotype of 16p11.2 BP2-BP3 CNVs.
    Loviglio MN; Arbogast T; Jønch AE; Collins SC; Popadin K; Bonnet CS; Giannuzzi G; Maillard AM; Jacquemont S; ; Yalcin B; Katsanis N; Golzio C; Reymond A
    Am J Hum Genet; 2017 Oct; 101(4):564-577. PubMed ID: 28965845
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children.
    Fetit R; Price DJ; Lawrie SM; Johnstone M
    Psychiatr Genet; 2020 Oct; 30(5):136-140. PubMed ID: 32732550
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
    Martin-Brevet S; Rodríguez-Herreros B; Nielsen JA; Moreau C; Modenato C; Maillard AM; Pain A; Richetin S; Jønch AE; Qureshi AY; Zürcher NR; Conus P; ; ; Chung WK; Sherr EH; Spiro JE; Kherif F; Beckmann JS; Hadjikhani N; Reymond A; Buckner RL; Draganski B; Jacquemont S
    Biol Psychiatry; 2018 Aug; 84(4):253-264. PubMed ID: 29778275
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Motor difficulties in 16p11.2 copy number variation.
    Jutla A; Harvey L; Veenstra-VanderWeele J; Chung WK
    Autism Res; 2024 May; 17(5):906-916. PubMed ID: 38660979
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
    Hippolyte L; Maillard AM; Rodriguez-Herreros B; Pain A; Martin-Brevet S; Ferrari C; Conus P; Macé A; Hadjikhani N; Metspalu A; Reigo A; Kolk A; Männik K; Barker M; Isidor B; Le Caignec C; Mignot C; Schneider L; Mottron L; Keren B; David A; Doco-Fenzy M; Gérard M; Bernier R; Goin-Kochel RP; Hanson E; Green Snyder L; ; Ramus F; Beckmann JS; Draganski B; Reymond A; Jacquemont S
    Biol Psychiatry; 2016 Jul; 80(2):129-139. PubMed ID: 26742926
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
    Moreno-De-Luca A; Evans DW; Boomer KB; Hanson E; Bernier R; Goin-Kochel RP; Myers SM; Challman TD; Moreno-De-Luca D; Slane MM; Hare AE; Chung WK; Spiro JE; Faucett WA; Martin CL; Ledbetter DH
    JAMA Psychiatry; 2015 Feb; 72(2):119-26. PubMed ID: 25493922
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Language characterization in 16p11.2 deletion and duplication syndromes.
    Kim SH; Green-Snyder L; Lord C; Bishop S; Steinman KJ; Bernier R; Hanson E; Goin-Kochel RP; Chung WK
    Am J Med Genet B Neuropsychiatr Genet; 2020 Sep; 183(6):380-391. PubMed ID: 32652891
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.