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 *

308 related articles for article (PubMed ID: 31665216)

  • 1. 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]  

  • 2. No signs of neurodegenerative effects in 15q11.2 BP1-BP2 copy number variant carriers in the UK Biobank.
    Boen R; Kaufmann T; Frei O; van der Meer D; Djurovic S; Andreassen OA; Selmer KK; Alnæs D; Sønderby IE
    Transl Psychiatry; 2023 Feb; 13(1):61. PubMed ID: 36807331
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical features and magnesium levels: Novel insights in 15q11.2 BP1-BP2 copy number variants.
    Meossi C; Carrer A; Ciaccio C; Estienne M; Silipigni R; Sciacca FL; Pantaleoni C; D'Arrigo S; Milani D
    J Intellect Disabil Res; 2023 Jul; 67(7):679-689. PubMed ID: 37129092
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.
    Boen R; Kaufmann T; van der Meer D; Frei O; Agartz I; Ames D; Andersson M; Armstrong NJ; Artiges E; Atkins JR; Bauer J; Benedetti F; Boomsma DI; Brodaty H; Brosch K; Buckner RL; Cairns MJ; Calhoun V; Caspers S; Cichon S; Corvin AP; Crespo-Facorro B; Dannlowski U; David FS; de Geus EJC; de Zubicaray GI; Desrivières S; Doherty JL; Donohoe G; Ehrlich S; Eising E; Espeseth T; Fisher SE; Forstner AJ; Fortaner-Uyà L; Frouin V; Fukunaga M; Ge T; Glahn DC; Goltermann J; Grabe HJ; Green MJ; Groenewold NA; Grotegerd D; Grøntvedt GR; Hahn T; Hashimoto R; Hehir-Kwa JY; Henskens FA; Holmes AJ; Håberg AK; Haavik J; Jacquemont S; Jansen A; Jockwitz C; Jönsson EG; Kikuchi M; Kircher T; Kumar K; Le Hellard S; Leu C; Linden DE; Liu J; Loughnan R; Mather KA; McMahon KL; McRae AF; Medland SE; Meinert S; Moreau CA; Morris DW; Mowry BJ; Mühleisen TW; Nenadić I; Nöthen MM; Nyberg L; Ophoff RA; Owen MJ; Pantelis C; Paolini M; Paus T; Pausova Z; Persson K; Quidé Y; Marques TR; Sachdev PS; Sando SB; Schall U; Scott RJ; Selbæk G; Shumskaya E; Silva AI; Sisodiya SM; Stein F; Stein DJ; Straube B; Streit F; Strike LT; Teumer A; Teutenberg L; Thalamuthu A; Tooney PA; Tordesillas-Gutierrez D; Trollor JN; van 't Ent D; van den Bree MBM; van Haren NEM; Vázquez-Bourgon J; Völzke H; Wen W; Wittfeld K; Ching CRK; Westlye LT; Thompson PM; Bearden CE; Selmer KK; Alnæs D; Andreassen OA; Sønderby IE;
    Biol Psychiatry; 2024 Jan; 95(2):147-160. PubMed ID: 37661008
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition.
    Silva AI; Kirov G; Kendall KM; Bracher-Smith M; Wilkinson LS; Hall J; Ulfarsson MO; Walters GB; Stefansson H; Stefansson K; Linden DEJ; Caseras X
    Biol Psychiatry; 2021 Sep; 90(5):307-316. PubMed ID: 33931204
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.
    Ulfarsson MO; Walters GB; Gustafsson O; Steinberg S; Silva A; Doyle OM; Brammer M; Gudbjartsson DF; Arnarsdottir S; Jonsdottir GA; Gisladottir RS; Bjornsdottir G; Helgason H; Ellingsen LM; Halldorsson JG; Saemundsen E; Stefansdottir B; Jonsson L; Eiriksdottir VK; Eiriksdottir GR; Johannesdottir GH; Unnsteinsdottir U; Jonsdottir B; Magnusdottir BB; Sulem P; Thorsteinsdottir U; Sigurdsson E; Brandeis D; Meyer-Lindenberg A; Stefansson H; Stefansson K
    Transl Psychiatry; 2017 Apr; 7(4):e1109. PubMed ID: 28440815
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
    Chaste P; Sanders SJ; Mohan KN; Klei L; Song Y; Murtha MT; Hus V; Lowe JK; Willsey AJ; Moreno-De-Luca D; Yu TW; Fombonne E; Geschwind D; Grice DE; Ledbetter DH; Lord C; Mane SM; Martin DM; Morrow EM; Walsh CA; Sutcliffe JS; State MW; Martin CL; Devlin B; Beaudet AL; Cook EH; Kim SJ
    Autism Res; 2014 Jun; 7(3):355-62. PubMed ID: 24821083
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
    Silva AI; Ulfarsson MO; Stefansson H; Gustafsson O; Walters GB; Linden DEJ; Wilkinson LS; Drakesmith M; Owen MJ; Hall J; Stefansson K
    Biol Psychiatry; 2019 Apr; 85(7):563-572. PubMed ID: 30583851
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CNVs conferring risk of autism or schizophrenia affect cognition in controls.
    Stefansson H; Meyer-Lindenberg A; Steinberg S; Magnusdottir B; Morgen K; Arnarsdottir S; Bjornsdottir G; Walters GB; Jonsdottir GA; Doyle OM; Tost H; Grimm O; Kristjansdottir S; Snorrason H; Davidsdottir SR; Gudmundsson LJ; Jonsson GF; Stefansdottir B; Helgadottir I; Haraldsson M; Jonsdottir B; Thygesen JH; Schwarz AJ; Didriksen M; Stensbøl TB; Brammer M; Kapur S; Halldorsson JG; Hreidarsson S; Saemundsen E; Sigurdsson E; Stefansson K
    Nature; 2014 Jan; 505(7483):361-6. PubMed ID: 24352232
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families.
    Baldwin I; Shafer RL; Hossain WA; Gunewardena S; Veatch OJ; Mosconi MW; Butler MG
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33562221
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The 15q11.2 BP1-BP2 Microdeletion (
    Rafi SK; Butler MG
    Int J Mol Sci; 2020 May; 21(9):. PubMed ID: 32384786
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Examining neurodevelopmental problems in 15q11.2 (BP1-BP2) copy number variation carriers at ages 9/12 and 18 in a Swedish twin sample.
    Jonsson L; Martin J; Lichtenstein P; Magnusson PKE; Lundström S; Westberg L; Tammimies K
    Mol Genet Genomic Med; 2023 Aug; 11(8):e2191. PubMed ID: 37156729
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank.
    Williams SG; Nakev A; Guo H; Frain S; Tenin G; Liakhovitskaia A; Saha P; Priest JR; Hentges KE; Keavney BD
    Eur J Hum Genet; 2020 Sep; 28(9):1265-1273. PubMed ID: 32327713
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders.
    Picinelli C; Lintas C; Piras IS; Gabriele S; Sacco R; Brogna C; Persico AM
    Am J Med Genet B Neuropsychiatr Genet; 2016 Dec; 171(8):1088-1098. PubMed ID: 27566550
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
    Burnside RD; Pasion R; Mikhail FM; Carroll AJ; Robin NH; Youngs EL; Gadi IK; Keitges E; Jaswaney VL; Papenhausen PR; Potluri VR; Risheg H; Rush B; Smith JL; Schwartz S; Tepperberg JH; Butler MG
    Hum Genet; 2011 Oct; 130(4):517-28. PubMed ID: 21359847
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
    Vanlerberghe C; Petit F; Malan V; Vincent-Delorme C; Bouquillon S; Boute O; Holder-Espinasse M; Delobel B; Duban B; Vallee L; Cuisset JM; Lemaitre MP; Vantyghem MC; Pigeyre M; Lanco-Dosen S; Plessis G; Gerard M; Decamp M; Mathieu M; Morin G; Jedraszak G; Bilan F; Gilbert-Dussardier B; Fauvert D; Roume J; Cormier-Daire V; Caumes R; Puechberty J; Genevieve D; Sarda P; Pinson L; Blanchet P; Lemeur N; Sheth F; Manouvrier-Hanu S; Andrieux J
    Eur J Med Genet; 2015 Mar; 58(3):140-7. PubMed ID: 25596525
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.
    Sønderby IE; van der Meer D; Moreau C; Kaufmann T; Walters GB; Ellegaard M; Abdellaoui A; Ames D; Amunts K; Andersson M; Armstrong NJ; Bernard M; Blackburn NB; Blangero J; Boomsma DI; Brodaty H; Brouwer RM; Bülow R; Bøen R; Cahn W; Calhoun VD; Caspers S; Ching CRK; Cichon S; Ciufolini S; Crespo-Facorro B; Curran JE; Dale AM; Dalvie S; Dazzan P; de Geus EJC; de Zubicaray GI; de Zwarte SMC; Desrivieres S; Doherty JL; Donohoe G; Draganski B; Ehrlich S; Eising E; Espeseth T; Fejgin K; Fisher SE; Fladby T; Frei O; Frouin V; Fukunaga M; Gareau T; Ge T; Glahn DC; Grabe HJ; Groenewold NA; Gústafsson Ó; Haavik J; Haberg AK; Hall J; Hashimoto R; Hehir-Kwa JY; Hibar DP; Hillegers MHJ; Hoffmann P; Holleran L; Holmes AJ; Homuth G; Hottenga JJ; Hulshoff Pol HE; Ikeda M; Jahanshad N; Jockwitz C; Johansson S; Jönsson EG; Jørgensen NR; Kikuchi M; Knowles EEM; Kumar K; Le Hellard S; Leu C; Linden DEJ; Liu J; Lundervold A; Lundervold AJ; Maillard AM; Martin NG; Martin-Brevet S; Mather KA; Mathias SR; McMahon KL; McRae AF; Medland SE; Meyer-Lindenberg A; Moberget T; Modenato C; Sánchez JM; Morris DW; Mühleisen TW; Murray RM; Nielsen J; Nordvik JE; Nyberg L; Loohuis LMO; Ophoff RA; Owen MJ; Paus T; Pausova Z; Peralta JM; Pike GB; Prieto C; Quinlan EB; Reinbold CS; Marques TR; 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; Suzuki IK; Tamnes CK; Teumer A; Thalamuthu A; Tordesillas-Gutiérrez D; Uhlmann A; Ulfarsson MO; van 't Ent D; van den Bree MBM; Vanderhaeghen P; Vassos E; Wen W; Wittfeld K; Wright MJ; Agartz I; Djurovic S; Westlye LT; Stefansson H; Stefansson K; Jacquemont S; Thompson PM; Andreassen OA;
    Transl Psychiatry; 2021 Mar; 11(1):182. PubMed ID: 33753722
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis.
    Mohan KN; Cao Y; Pham J; Cheung SW; Hoffner L; Ou ZZ; Surti U; Cook EH; Beaudet AL
    J Hum Genet; 2019 Mar; 64(3):253-255. PubMed ID: 30542208
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic Diversity of 15q11.2 BP1-BP2 Deletion in Three Korean Families with Development Delay and/or Intellectual Disability: A Case Series and Literature Review.
    Han JY; Park J
    Diagnostics (Basel); 2021 Apr; 11(4):. PubMed ID: 33921555
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: further delineation of an emerging syndrome.
    Cafferkey M; Ahn JW; Flinter F; Ogilvie C
    Am J Med Genet A; 2014 Aug; 164A(8):1916-22. PubMed ID: 24715682
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.