Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
editorial
. 1996 Nov;59(5):973–979.

Anticipation: an old idea in new genes.

M G McInnis
PMCID: PMC1914846  PMID: 8900222

Full text

PDF
973

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Asherson P., Walsh C., Williams J., Sargeant M., Taylor C., Clements A., Gill M., Owen M., McGuffin P. Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia? Br J Psychiatry. 1994 May;164(5):619–624. doi: 10.1192/bjp.164.5.619. [DOI] [PubMed] [Google Scholar]
  2. Bassett A. S., Honer W. G. Evidence for anticipation in schizophrenia. Am J Hum Genet. 1994 May;54(5):864–870. [PMC free article] [PubMed] [Google Scholar]
  3. Bleyl S., Nelson L., Odelberg S. J., Ruttenberg H. D., Otterud B., Leppert M., Ward K. A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12. Am J Hum Genet. 1995 Feb;56(2):408–415. [PMC free article] [PubMed] [Google Scholar]
  4. Bonifati V., Fabrizio E., Vanacore N., De Mari M., Meco G. Familial Parkinson's disease: a clinical genetic analysis. Can J Neurol Sci. 1995 Nov;22(4):272–279. doi: 10.1017/s0317167100039469. [DOI] [PubMed] [Google Scholar]
  5. Borgaonkar D. S., Shah S. A. The xyy chromosome male--or syndrome? Prog Med Genet. 1974;10:135–222. [PubMed] [Google Scholar]
  6. Campuzano V., Montermini L., Moltò M. D., Pianese L., Cossée M., Cavalcanti F., Monros E., Rodius F., Duclos F., Monticelli A. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science. 1996 Mar 8;271(5254):1423–1427. doi: 10.1126/science.271.5254.1423. [DOI] [PubMed] [Google Scholar]
  7. Cheng J. T., Liu A., Wasmuth J., Liu B. P., Truong D. Clinical evidence of genetic anticipation in adult-onset idiopathic dystonia. Neurology. 1996 Jul;47(1):215–219. doi: 10.1212/wnl.47.1.215. [DOI] [PubMed] [Google Scholar]
  8. Engström C., Thornlund A. S., Johansson E. L., Långström M., Chotai J., Adolfsson R., Nylander P. O. Anticipation in unipolar affective disorder. J Affect Disord. 1995 Oct 9;35(1-2):31–40. doi: 10.1016/0165-0327(95)00035-l. [DOI] [PubMed] [Google Scholar]
  9. Filla A., De Michele G., Cavalcanti F., Pianese L., Monticelli A., Campanella G., Cocozza S. The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia. Am J Hum Genet. 1996 Sep;59(3):554–560. [PMC free article] [PubMed] [Google Scholar]
  10. Gispert S., Santos N., Damen R., Voit T., Schulz J., Klockgether T., Orozco G., Kreuz F., Weissenbach J., Auburger G. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity. Am J Hum Genet. 1995 Jan;56(1):183–187. [PMC free article] [PubMed] [Google Scholar]
  11. Goldberg Y. P., Nicholson D. W., Rasper D. M., Kalchman M. A., Koide H. B., Graham R. K., Bromm M., Kazemi-Esfarjani P., Thornberry N. A., Vaillancourt J. P. Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract. Nat Genet. 1996 Aug;13(4):442–449. doi: 10.1038/ng0896-442. [DOI] [PubMed] [Google Scholar]
  12. Hodge S. E., Wickramaratne P. Statistical pitfalls in detecting age-of-onset anticipation: the role of correlation in studying anticipation and detecting ascertainment bias. Psychiatr Genet. 1995 Spring;5(1):43–47. doi: 10.1097/00041444-199521000-00007. [DOI] [PubMed] [Google Scholar]
  13. Holmberg M., Johansson J., Forsgren L., Heijbel J., Sandgren O., Holmgren G. Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1. Hum Mol Genet. 1995 Aug;4(8):1441–1445. doi: 10.1093/hmg/4.8.1441. [DOI] [PubMed] [Google Scholar]
  14. Höweler C. J., Busch H. F., Geraedts J. P., Niermeijer M. F., Staal A. Anticipation in myotonic dystrophy: fact or fiction? Brain. 1989 Jun;112(Pt 3):779–797. doi: 10.1093/brain/112.3.779. [DOI] [PubMed] [Google Scholar]
  15. Kawaguchi Y., Okamoto T., Taniwaki M., Aizawa M., Inoue M., Katayama S., Kawakami H., Nakamura S., Nishimura M., Akiguchi I. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet. 1994 Nov;8(3):221–228. doi: 10.1038/ng1194-221. [DOI] [PubMed] [Google Scholar]
  16. Knight S. J., Flannery A. V., Hirst M. C., Campbell L., Christodoulou Z., Phelps S. R., Pointon J., Middleton-Price H. R., Barnicoat A., Pembrey M. E. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell. 1993 Jul 16;74(1):127–134. doi: 10.1016/0092-8674(93)90300-f. [DOI] [PubMed] [Google Scholar]
  17. Koide R., Ikeuchi T., Onodera O., Tanaka H., Igarashi S., Endo K., Takahashi H., Kondo R., Ishikawa A., Hayashi T. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nat Genet. 1994 Jan;6(1):9–13. doi: 10.1038/ng0194-9. [DOI] [PubMed] [Google Scholar]
  18. La Spada A. R., Wilson E. M., Lubahn D. B., Harding A. E., Fischbeck K. H. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature. 1991 Jul 4;352(6330):77–79. doi: 10.1038/352077a0. [DOI] [PubMed] [Google Scholar]
  19. Lezin A., Cancel G., Stevanin G., Smadja D., Vernant J. C., Dürr A., Martial J., Buisson G. G., Bellance R., Chneiweiss H. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families. Hum Genet. 1996 May;97(5):671–676. doi: 10.1007/BF02281881. [DOI] [PubMed] [Google Scholar]
  20. Lindblad K., Nylander P. O., De bruyn A., Sourey D., Zander C., Engström C., Holmgren G., Hudson T., Chotai J., Mendlewicz J. Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method. Neurobiol Dis. 1995 Feb;2(1):55–62. doi: 10.1006/nbdi.1995.0006. [DOI] [PubMed] [Google Scholar]
  21. Lindblad K., Schalling M. Clinical implications of unstable DNA repeat sequences. Acta Paediatr. 1996 Mar;85(3):265–271. doi: 10.1111/j.1651-2227.1996.tb14011.x. [DOI] [PubMed] [Google Scholar]
  22. Mahadevan M., Tsilfidis C., Sabourin L., Shutler G., Amemiya C., Jansen G., Neville C., Narang M., Barceló J., O'Hoy K. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. Science. 1992 Mar 6;255(5049):1253–1255. doi: 10.1126/science.1546325. [DOI] [PubMed] [Google Scholar]
  23. McInnis M. G., McMahon F. J., Chase G. A., Simpson S. G., Ross C. A., DePaulo J. R., Jr Anticipation in bipolar affective disorder. Am J Hum Genet. 1993 Aug;53(2):385–390. [PMC free article] [PubMed] [Google Scholar]
  24. Morrison A. W. Anticipation in Menière's disease. J Laryngol Otol. 1995 Jun;109(6):499–502. doi: 10.1017/s0022215100130567. [DOI] [PubMed] [Google Scholar]
  25. Newbury-Ecob R. A., Leanage R., Raeburn J. A., Young I. D. Holt-Oram syndrome: a clinical genetic study. J Med Genet. 1996 Apr;33(4):300–307. doi: 10.1136/jmg.33.4.300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Nylander P. O., Engström C., Chotai J., Wahlström J., Adolfsson R. Anticipation in Swedish families with bipolar affective disorder. J Med Genet. 1994 Sep;31(9):686–689. doi: 10.1136/jmg.31.9.686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. O'Donovan M. C., Guy C., Craddock N., Murphy K. C., Cardno A. G., Jones L. A., Owen M. J., McGuffin P. Expanded CAG repeats in schizophrenia and bipolar disorder. Nat Genet. 1995 Aug;10(4):380–381. doi: 10.1038/ng0895-380. [DOI] [PubMed] [Google Scholar]
  28. Orr H. T., Chung M. Y., Banfi S., Kwiatkowski T. J., Jr, Servadio A., Beaudet A. L., McCall A. E., Duvick L. A., Ranum L. P., Zoghbi H. Y. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet. 1993 Jul;4(3):221–226. doi: 10.1038/ng0793-221. [DOI] [PubMed] [Google Scholar]
  29. Peral B., Ong A. C., San Millán J. L., Gamble V., Rees L., Harris P. C. A stable, nonsense mutation associated with a case of infantile onset polycystic kidney disease 1 (PKD1). Hum Mol Genet. 1996 Apr;5(4):539–542. doi: 10.1093/hmg/5.4.539. [DOI] [PubMed] [Google Scholar]
  30. Pierpont J. W., St Jacques D., Seaver L. H., Erickson R. P. A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3. Clin Genet. 1995 Mar;47(3):139–143. doi: 10.1111/j.1399-0004.1995.tb03946.x. [DOI] [PubMed] [Google Scholar]
  31. Planté-Bordeneuve V., Taussig D., Thomas F., Ziégler M., Said G. A clinical and genetic study of familial cases of Parkinson's disease. J Neurol Sci. 1995 Nov;133(1-2):164–172. doi: 10.1016/0022-510x(95)00190-d. [DOI] [PubMed] [Google Scholar]
  32. Polito J. M., 2nd, Rees R. C., Childs B., Mendeloff A. I., Harris M. L., Bayless T. M. Preliminary evidence for genetic anticipation in Crohn's disease. Lancet. 1996 Mar 23;347(9004):798–800. doi: 10.1016/s0140-6736(96)90870-3. [DOI] [PubMed] [Google Scholar]
  33. Presciuttini S., Varesco L., Sala P., Gismondi V., Rossetti C., Bafico A., Ferrara G. B., Bertario L. Age of onset in familial adenomatous polyposis: heterogeneity within families and among APC mutations. Ann Hum Genet. 1994 Oct;58(Pt 4):331–342. doi: 10.1111/j.1469-1809.1994.tb00730.x. [DOI] [PubMed] [Google Scholar]
  34. Ranen N. G., Stine O. C., Abbott M. H., Sherr M., Codori A. M., Franz M. L., Chao N. I., Chung A. S., Pleasant N., Callahan C. Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease. Am J Hum Genet. 1995 Sep;57(3):593–602. [PMC free article] [PubMed] [Google Scholar]
  35. Ross C. A., McInnis M. G., Margolis R. L., Li S. H. Genes with triplet repeats: candidate mediators of neuropsychiatric disorders. Trends Neurosci. 1993 Jul;16(7):254–260. doi: 10.1016/0166-2236(93)90175-l. [DOI] [PubMed] [Google Scholar]
  36. Scheffer I. E., Jones L., Pozzebon M., Howell R. A., Saling M. M., Berkovic S. F. Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation. Ann Neurol. 1995 Oct;38(4):633–642. doi: 10.1002/ana.410380412. [DOI] [PubMed] [Google Scholar]
  37. Taneja K. L., McCurrach M., Schalling M., Housman D., Singer R. H. Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues. J Cell Biol. 1995 Mar;128(6):995–1002. doi: 10.1083/jcb.128.6.995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Thibaut F., Martinez M., Petit M., Jay M., Campion D. Further evidence for anticipation in schizophrenia. Psychiatry Res. 1995 Nov 29;59(1-2):25–33. doi: 10.1016/0165-1781(95)02778-5. [DOI] [PubMed] [Google Scholar]
  39. Trenkwalder C., Seidel V. C., Gasser T., Oertel W. H. Clinical symptoms and possible anticipation in a large kindred of familial restless legs syndrome. Mov Disord. 1996 Jul;11(4):389–394. doi: 10.1002/mds.870110407. [DOI] [PubMed] [Google Scholar]
  40. Verkerk A. J., Pieretti M., Sutcliffe J. S., Fu Y. H., Kuhl D. P., Pizzuti A., Reiner O., Richards S., Victoria M. F., Zhang F. P. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell. 1991 May 31;65(5):905–914. doi: 10.1016/0092-8674(91)90397-h. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES