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 *

237 related articles for article (PubMed ID: 29562078)

  • 1. Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
    Huguet G; Schramm C; Douard E; Jiang L; Labbe A; Tihy F; Mathonnet G; Nizard S; Lemyre E; Mathieu A; Poline JB; Loth E; Toro R; Schumann G; Conrod P; Pausova Z; Greenwood C; Paus T; Bourgeron T; Jacquemont S;
    JAMA Psychiatry; 2018 May; 75(5):447-457. PubMed ID: 29562078
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome.
    Douard E; Zeribi A; Schramm C; Tamer P; Loum MA; Nowak S; Saci Z; Lord MP; Rodríguez-Herreros B; Jean-Louis M; Moreau C; Loth E; Schumann G; Pausova Z; Elsabbagh M; Almasy L; Glahn DC; Bourgeron T; Labbe A; Paus T; Mottron L; Greenwood CMT; Huguet G; Jacquemont S
    Am J Psychiatry; 2021 Jan; 178(1):87-98. PubMed ID: 32911998
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.
    Huguet G; Schramm C; Douard E; Tamer P; Main A; Monin P; England J; Jizi K; Renne T; Poirier M; Nowak S; Martin CO; Younis N; Knoth IS; Jean-Louis M; Saci Z; Auger M; Tihy F; Mathonnet G; Maftei C; Léveillé F; Porteous D; Davies G; Redmond P; Harris SE; Hill WD; Lemyre E; Schumann G; Bourgeron T; Pausova Z; Paus T; Karama S; Lippe S; Deary IJ; Almasy L; Labbe A; Glahn D; Greenwood CMT; Jacquemont S
    Mol Psychiatry; 2021 Jun; 26(6):2663-2676. PubMed ID: 33414497
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of copy number variation across the genome with neuropsychiatric traits in the general population.
    Guyatt AL; Stergiakouli E; Martin J; Walters J; O'Donovan M; Owen M; Thapar A; Kirov G; Rodriguez S; Rai D; Zammit S; Gaunt TR
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jul; 177(5):489-502. PubMed ID: 29687944
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank.
    Birnbaum R; Mahjani B; Loos RJF; Sharp AJ
    JAMA Psychiatry; 2022 Mar; 79(3):250-259. PubMed ID: 35080590
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Copy number variations and cognitive phenotypes in unselected populations.
    Männik K; Mägi R; Macé A; Cole B; Guyatt AL; Shihab HA; Maillard AM; Alavere H; Kolk A; Reigo A; Mihailov E; Leitsalu L; Ferreira AM; Nõukas M; Teumer A; Salvi E; Cusi D; McGue M; Iacono WG; Gaunt TR; Beckmann JS; Jacquemont S; Kutalik Z; Pankratz N; Timpson N; Metspalu A; Reymond A
    JAMA; 2015 May; 313(20):2044-54. PubMed ID: 26010633
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Copy number variation and neuropsychiatric problems in females and males in the general population.
    Martin J; Tammimies K; Karlsson R; Lu Y; Larsson H; Lichtenstein P; Magnusson PKE
    Am J Med Genet B Neuropsychiatr Genet; 2019 Sep; 180(6):341-350. PubMed ID: 30307693
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort.
    Alexander-Bloch A; Huguet G; Schultz LM; Huffnagle N; Jacquemont S; Seidlitz J; Saci Z; Moore TM; Bethlehem RAI; Mollon J; Knowles EK; Raznahan A; Merikangas A; Chaiyachati BH; Raman H; Schmitt JE; Barzilay R; Calkins ME; Shinohara RT; Satterthwaite TD; Gur RC; Glahn DC; Almasy L; Gur RE; Hakonarson H; Glessner J
    JAMA Psychiatry; 2022 Jul; 79(7):699-709. PubMed ID: 35544191
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs).
    Hall JH; Chawner SJRA; ; Wolstencroft J; Skuse D; Hall J; Holmans P; Owen MJ; van den Bree MBM
    Transl Psychiatry; 2024 Jun; 14(1):259. PubMed ID: 38890284
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Schizophrenia genetic variants are not associated with intelligence.
    van Scheltinga AF; Bakker SC; van Haren NE; Derks EM; Buizer-Voskamp JE; Cahn W; Ripke S; ; Ophoff RA; Kahn RS
    Psychol Med; 2013 Dec; 43(12):2563-70. PubMed ID: 23410598
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The copy number variant architecture of psychopathology and cognitive development in the ABCD
    Sha Z; Sun KY; Jung B; Barzilay R; Moore TM; Almasy L; Forsyth JK; Prem S; Gandal MJ; Seidlitz J; Glessner JT; Alexander-Bloch AF
    medRxiv; 2024 May; ():. PubMed ID: 38798629
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.
    Safizadeh Shabestari SA; Nassir N; Sopariwala S; Karimov I; Tambi R; Zehra B; Kosaji N; Akter H; Berdiev BK; Uddin M
    Hum Genet; 2023 Aug; 142(8):1201-1213. PubMed ID: 36383254
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.
    Szatkiewicz JP; Neale BM; O'Dushlaine C; Fromer M; Goldstein JI; Moran JL; Chambert K; Kähler A; Magnusson PK; Hultman CM; Sklar P; Purcell S; McCarroll SA; Sullivan PF
    Mol Psychiatry; 2013 Nov; 18(11):1178-84. PubMed ID: 23938935
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Impact of Copy Number Variants and Polygenic Risk Scores on Psychopathology in the UK Biobank.
    Mollon J; Schultz LM; Huguet G; Knowles EEM; Mathias SR; Rodrigue A; Alexander-Bloch A; Saci Z; Jean-Louis M; Kumar K; Douard E; Almasy L; Jacquemont S; Glahn DC
    Biol Psychiatry; 2023 Oct; 94(7):591-600. PubMed ID: 36764568
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease.
    Lemire G; Sanchis-Juan A; Russell K; Baxter S; Chao KR; Singer-Berk M; Groopman E; Wong I; England E; Goodrich J; Pais L; Austin-Tse C; DiTroia S; O'Heir E; Ganesh VS; Wojcik MH; Evangelista E; Snow H; Osei-Owusu I; Fu J; Singh M; Mostovoy Y; Huang S; Garimella K; Kirkham SL; Neil JE; Shao DD; Walsh CA; Argilli E; Le C; Sherr EH; Gleeson JG; Shril S; Schneider R; Hildebrandt F; Sankaran VG; Madden JA; Genetti CA; Beggs AH; Agrawal PB; Bujakowska KM; Place E; Pierce EA; Donkervoort S; Bönnemann CG; Gallacher L; Stark Z; Tan TY; White SM; Töpf A; Straub V; Fleming MD; Pollak MR; Õunap K; Pajusalu S; Donald KA; Bruwer Z; Ravenscroft G; Laing NG; MacArthur DG; Rehm HL; Talkowski ME; Brand H; O'Donnell-Luria A
    Am J Hum Genet; 2024 May; 111(5):863-876. PubMed ID: 38565148
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Similar Rates of Deleterious Copy Number Variants in Early-Onset Psychosis and Autism Spectrum Disorder.
    Brownstein CA; Douard E; Mollon J; Smith R; Hojlo MA; Das A; Goldman M; Garvey E; Cabral K; Li J; Bowen J; Rao AS; Genetti C; Carroll D; Knowles EEM; Deaso E; Agrawal PB; Beggs AH; D'Angelo E; Almasy L; Alexander-Bloch A; Saci Z; Moreau CA; Huguet G; Deo AJ; Jacquemont S; Glahn DC; Gonzalez-Heydrich J
    Am J Psychiatry; 2022 Nov; 179(11):853-861. PubMed ID: 36000218
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.
    Luo R; Sanders SJ; Tian Y; Voineagu I; Huang N; Chu SH; Klei L; Cai C; Ou J; Lowe JK; Hurles ME; Devlin B; State MW; Geschwind DH
    Am J Hum Genet; 2012 Jul; 91(1):38-55. PubMed ID: 22726847
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
    ; van der Meer D; Sønderby IE; Kaufmann T; Walters GB; Abdellaoui A; Ames D; Amunts K; Andersson M; Armstrong NJ; Bernard M; Blackburn NB; Blangero J; Boomsma DI; Brodaty H; Brouwer RM; Bülow R; Cahn W; Calhoun VD; Caspers S; Cavalleri GL; Ching CRK; Cichon S; Ciufolini S; Corvin A; Crespo-Facorro B; Curran JE; Dalvie S; Dazzan P; de Geus EJC; de Zubicaray GI; de Zwarte SMC; Delanty N; den Braber A; Desrivieres S; Di Forti M; Doherty JL; Donohoe G; Ehrlich S; Eising E; Espeseth T; Fisher SE; Fladby T; Frei O; Frouin V; Fukunaga M; Gareau T; Glahn DC; Grabe HJ; Groenewold NA; Gústafsson Ó; Haavik J; Haberg AK; Hashimoto R; Hehir-Kwa JY; Hibar DP; Hillegers MHJ; Hoffmann P; Holleran L; Hottenga JJ; Hulshoff Pol HE; Ikeda M; Jacquemont S; Jahanshad N; Jockwitz C; Johansson S; Jönsson EG; Kikuchi M; Knowles EEM; Kwok JB; Le Hellard S; Linden DEJ; Liu J; Lundervold A; Lundervold AJ; Martin NG; Mather KA; Mathias SR; McMahon KL; McRae AF; Medland SE; Moberget T; Moreau C; Morris DW; Mühleisen TW; Murray RM; Nordvik JE; Nyberg L; Olde Loohuis LM; Ophoff RA; Owen MJ; Paus T; Pausova Z; Peralta JM; Pike B; Prieto C; Quinlan EB; Reinbold CS; Reis Marques T; Rucker JJH; Sachdev PS; Sando SB; Schofield PR; Schork AJ; Schumann G; Shin J; Shumskaya E; Silva AI; Sisodiya SM; Steen VM; Stein DJ; Strike LT; Tamnes CK; Teumer A; Thalamuthu A; Tordesillas-Gutiérrez D; Uhlmann A; Úlfarsson MÖ; van 't Ent D; van den Bree MBM; Vassos E; Wen W; Wittfeld K; Wright MJ; Zayats T; Dale AM; Djurovic S; Agartz I; Westlye LT; Stefánsson H; Stefánsson K; Thompson PM; Andreassen OA
    JAMA Psychiatry; 2020 Apr; 77(4):420-430. PubMed ID: 31665216
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of copy number variants in the genetic architecture of common familial epilepsies.
    Epi4K Consortium
    Epilepsia; 2024 Mar; 65(3):792-804. PubMed ID: 38101940
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.