BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 38172840)

  • 21. Prenatal diagnosis of 15q11.2 microdeletion fetuses in Eastern China: 21 case series and literature review.
    Jiang XL; Liang B; Zhao WT; Lin N; Huang HL; Cai MY; Xu LP
    J Matern Fetal Neonatal Med; 2023 Dec; 36(2):2262700. PubMed ID: 37770195
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review.
    Butler MG
    Int J Mol Sci; 2023 Feb; 24(5):. PubMed ID: 36901699
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. Further phenotypic expansion of 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome.
    Jerkovich AM; Butler MG
    J Pediatr Genet; 2014; 3(1):41-44. PubMed ID: 25309804
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature.
    Farrell M; Lichtenstein M; Harner MK; Crowley JJ; Filmyer DM; Lázaro-Muñoz G; Dietterich TE; Bruno LM; Shaughnessy RA; Biondi TF; Burkholder S; Donmoyer J; Berg JS; Szatkiewicz J; Sullivan PF; Josiassen RC
    Transl Psychiatry; 2020 Jan; 10(1):42. PubMed ID: 32066678
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?
    Maya I; Perlman S; Shohat M; Kahana S; Yacobson S; Tenne T; Agmon-Fishman I; Tomashov Matar R; Basel-Salmon L; Sukenik-Halevy R
    J Clin Med; 2020 Aug; 9(8):. PubMed ID: 32796639
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Expanding the BP1-BP2 15q11.2 Microdeletion Phenotype: Tracheoesophageal Fistula and Congenital Cataracts.
    Wong D; Johnson SM; Young D; Iwamoto L; Sood S; Slavin TP
    Case Rep Genet; 2013; 2013():801094. PubMed ID: 23864968
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies.
    Jähn JA; von Spiczak S; Muhle H; Obermeier T; Franke A; Mefford HC; Stephani U; Helbig I
    Epilepsy Res; 2014 Jan; 108(1):109-16. PubMed ID: 24246141
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal ultrasound features and genetic analysis for 17q12 microdeletion syndrome.
    Zhang Z; Pan L; Chen K; Tan R
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2021 Dec; 46(12):1370-1374. PubMed ID: 35232906
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion.
    Kuroda Y; Ohashi I; Naruto T; Ida K; Enomoto Y; Saito T; Nagai JI; Yanagi S; Ueda H; Kurosawa K
    J Hum Genet; 2018 Nov; 63(11):1185-1188. PubMed ID: 30108319
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features.
    Abdelmoity AT; LePichon JB; Nyp SS; Soden SE; Daniel CA; Yu S
    J Dev Behav Pediatr; 2012 Sep; 33(7):570-6. PubMed ID: 22922608
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome.
    Davis KW; Serrano M; Loddo S; Robinson C; Alesi V; Dallapiccola B; Novelli A; Butler MG
    Int J Mol Sci; 2019 Mar; 20(6):. PubMed ID: 30909440
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [15Q11.2 (BP1-BP2) microdeletion, a new syndrome with variable expressivity].
    Sempere Pérez A; Manchón Trives I; Palazón Azorín I; Alcaraz Más L; Pérez Lledó E; Galán Sánchez F
    An Pediatr (Barc); 2011 Jul; 75(1):58-62. PubMed ID: 21419731
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rare missense TUBGCP5 gene variant in a patient with primary microcephaly.
    Maver A; Čuturilo G; Kovanda A; Miletić A; Peterlin B
    Eur J Med Genet; 2019 Dec; 62(12):103598. PubMed ID: 30543990
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 15q11.2 microdeletion and FMR1 premutation in a family with intellectual disabilities and autism.
    Madrigal I; Rodríguez-Revenga L; Xunclà M; Milà M
    Gene; 2012 Oct; 508(1):92-5. PubMed ID: 22842191
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.