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Variants at chromosome 20 (ASIP locus) and melanoma risk.
Maccioni L, Rachakonda PS, Scherer D, Bermejo JL, Planelles D, Requena C, Hemminki K, Nagore E, Kumar R.
Int J Cancer. 2013 Jan 1;132(1):42-54. doi: 10.1002/ijc.27648. Epub 2012 Jun 13.
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Gelastic seizures in ring chromosome 20 syndrome: a case report with video illustration.
Dimova P, Boneva I, Todorova A, Minotti L, Kahane P.
Epileptic Disord. 2012 Jun;14(2):181-6. doi: 10.1684/epd.2012.0508.
Sequence and expression analysis of gaps in human chromosome 20.
Minocherhomji S, Seemann S, Mang Y, El-Schich Z, Bak M, Hansen C, Papadopoulos N, Josefsen K, Nielsen H, Gorodkin J, Tommerup N, Silahtaroglu A.
Nucleic Acids Res. 2012 Aug;40(14):6660-72. Epub 2012 Apr 17.
Ring chromosome 20 syndrome: electroclinical description of six patients and review of the literature.
Elens I, Vanrykel K, De Waele L, Jansen K, Segeren M, Van Paesschen W, Ceulemans B, Boel M, Frijns JP, Buyse G, Lagae L.
Epilepsy Behav. 2012 Apr;23(4):409-14. doi: 10.1016/j.yebeh.2012.02.008. Epub 2012 Mar 15. Review.
Ring chromosome 20.
Daber RD, Conlin LK, Leonard LD, Canevini MP, Vignoli A, Hosain S, Brown LW, Spinner NB.
Eur J Med Genet. 2012 May;55(5):381-7. doi: 10.1016/j.ejmg.2012.02.004. Epub 2012 Feb 22. Review.
Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis.
Pressato B, Valli R, Marletta C, Mare L, Montalbano G, Lo Curto F, Pasquali F, Maserati E.
Br J Haematol. 2012 May;157(4):503-5. doi: 10.1111/j.1365-2141.2012.09033.x. Epub 2012 Feb 1. No abstract available.
Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness.
Bigdeli TB, Maher BS, Zhao Z, Oord EJ, Thiselton DL, Sun J, Webb BT, Amdur RL, Wormley B, O'Neill FA, Walsh D, Riley BP, Kendler KS, Fanous AH.
PLoS One. 2011;6(12):e21440. doi: 10.1371/journal.pone.0021440. Epub 2011 Dec 29.
Chromosome 20 shows linkage with DSM-IV nicotine dependence in Finnish adult smokers.
Keskitalo-Vuokko K, Hällfors J, Broms U, Pergadia ML, Saccone SF, Loukola A, Madden PA, Kaprio J.
Nicotine Tob Res. 2012 Feb;14(2):153-60. doi: 10.1093/ntr/ntr153. Epub 2011 Oct 29.
New association between ring chromosome 20 syndrome and hypomelanosis of Ito.
Cappanera S, Passamonti C, Zamponi N.
Pediatr Neurol. 2011 Nov;45(5):341-3. doi: 10.1016/j.pediatrneurol.2011.08.006.
Characterization of a complex rearrangement of a chromosome 20 by FISH and array CGH.
Bertini V, Valetto A, Baroncelli GI, Simi P.
Eur J Med Genet. 2011 Jul-Aug;54(4):e419-24. doi: 10.1016/j.ejmg.2011.03.004. Epub 2011 Mar 24.
Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients.
Conlin LK, Kramer W, Hutchinson AL, Li X, Riethman H, Hakonarson H, Mulley JC, Scheffer IE, Berkovic SF, Hosain SA, Spinner NB.
J Med Genet. 2011 Jan;48(1):1-9. doi: 10.1136/jmg.2010.080382. Epub 2010 Oct 23.
Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib).
Bastepe M, Altug-Teber O, Agarwal C, Oberfield SE, Bonin M, Jüppner H.
Bone. 2011 Mar 1;48(3):659-62. doi: 10.1016/j.bone.2010.10.168. Epub 2010 Oct 19.
Paternal mosaic inv(20) resulting in a recombinant chromosome 20 in two siblings.
Wang BT, Hemmat M, Jayakar P, Boyar F, Chan P, El Naggar M, Anguiano A.
Pediatr Int. 2010 Jun;52(3):492-5. doi: 10.1111/j.1442-200X.2010.03041.x. No abstract available.
The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion.
Mackinnon RN, Selan C, Wall M, Baker E, Nandurkar H, Campbell LJ.
Genes Chromosomes Cancer. 2010 Nov;49(11):998-1013. doi: 10.1002/gcc.20806.
Update on "two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20".
Descipio C, Morrissette JD, Conlin LK, Clark D, Kaur M, Coplan J, Riethman H, Spinner NB, Krantz ID.
Am J Med Genet A. 2010 Jun;152A(6):1599. doi: 10.1002/ajmg.a.33390. No abstract available.
Modest association of malignant melanoma with the rs910873 and rs1885120 markers on chromosome 20: a population-based study.
Debniak T, Gapska P, Serrano-Fernandez P, Rassoud I, Cybulski C, Maleszka R, Sulikowski M, Narod S, Lubiński J.
Melanoma Res. 2010 Apr;20(2):159-60. doi: 10.1097/CMR.0b013e32833716e6. No abstract available.
Two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20.
Am J Med Genet A. 2010 Feb;152A(2):373-82. doi: 10.1002/ajmg.a.33219.
BAK1 gene variation and abdominal aortic aneurysms-variants are likely due to sequencing of a processed gene on chromosome 20.
Hatchwell E.
Hum Mutat. 2010 Jan;31(1):108-9; author reply 110-1. doi: 10.1002/humu.21147. No abstract available.
Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20.
Callier P, Faivre L, Pigeonnat S, Quilichini B, Marle N, Thauvin-Robinet C, Mosca AL, Masurel-Paulet A, Rousseau T, Sagot P, Laurent N, Mugneret F.
Prenat Diagn. 2009 Oct;29(10):1002-5. doi: 10.1002/pd.2333. No abstract available.
Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children.
Vignoli A, Canevini MP, Darra F, La Selva L, Fiorini E, Piazzini A, Lazzarotto F, Zucca C, Dalla Bernardina B.
Epilepsia. 2009 Nov;50(11):2420-7. doi: 10.1111/j.1528-1167.2009.02176.x. Epub 2009 Jul 2.
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