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The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Huntington’s disease genetics

Myers, Richard H.·2004·NeuroRX
DOI 10.1602/neurorx.1.2.255
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Research works printed but not linked: 27

  1. Myers RH, Marans K, MacDonald ME. Huntington’s disease. In: Genetic instabilities and hereditary neurological diseases (Warren ST, Wells RT, eds), pp 301–323. New York: Academic Press, 1998.
  2. Gusella JF, Wexler NS, Conneally PM, Naylor SL, Anderson MA, Tanzi RE et al. A polymorphic DNA marker genetically linked to Huntington’s disease.Nature 306: 234–238, 1983. · DOI
  3. Chong SS, Almqvist E, Telenius H, LaTray L, Nichol K, Bourdelat-Parks B et al. Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses.Hum Mol Genet 6: 301–309, 1997. · DOI
  4. Maat-Kievit A, Losekoot M, Van Den Boer-Van Den Berg H, Van Ommen GJ, Niermeijer M, Breuning M et al. New problems in testing for Huntington’s disease: the issue of intermediate and reduced penetrance alleles.J Med Genet 38: E12, 2001. · DOI
  5. Merritt AD, Conneally PM, Rahman NF, Drew AL. Juvenile Huntington’s chorea. In: Progress in neurogenetics. (Barbeau A, Brunette TR, eds), pp 645–650. Amsterdam: Excerpta Medica Foundation, 1969.
  6. Zühlke C, Olaf R, Bockel B, Lange H, Thies U. Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene.Hum Mol Genet 2: 2063–2067, 1993. · DOI
  7. Ranen NG, Stine CO, Abbott MH, Sherr M, Codori AM, Franz ML et al. Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington’s disease.Am J Hum Genet 57: 593–602, 1995.
  8. Djoussé L, Knowlton B, Hayden M, Almqvist EW, Brinkman R, Ross C et al. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease.Am J Med Genet 119a: 279–282, 2003. · DOI · Paper page
  9. Rosenblatt A, Brinkman RR, Liang KY, Almqvist EW, Margolis RL, Huang CY et al. Familial influence on age of onset among siblings with Huntington disease.Am J Med Genet 105: 399–403, 2001. · DOI
  10. Li J-L, Hayden M, Almqvist EW, Brinkman R, Durr A, Dode C et al. A genome scan for modifiers of age at onset in Huntington’s disease: the HD MAPS Study.Am J Hum Genet 73: 682–687, 2003. · DOI · Paper page
  11. Bates G. Huntingtin aggregation and toxicity in Huntington’s disease.Lancet 361: 1642–1644, 2003. · DOI
  12. Beal MF. Coenzyme Q10 as a possible treatment for neurodegenerative diseases.Free Radic Res 36: 455–460, 2002. · DOI
  13. Ross CA. Polyglutamine pathogenesis: emergence of unifying mechanisms for Huntington’s disease and related disorders.Neuron 35: 819–822, 2002. · DOI
  14. Almqvist EW, Bloch M, Brinkman R, Craufurd D, Hayden MR. A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease.Am J Hum Genet 64: 1293–1304, 1999. · DOI
  15. Taylor CA, Myers RH. Long-term psychological impact of Huntington’s disease linkage testing.Am J Med Genet 70: 365–370, 1997. · DOI
  16. Nance MA, Myers RH, and US Huntington Disease Genetic Testing Group. Trends in predictive and prenatal testing for Huntington disease, 1993–1999.Am J Hum Genet 65: A406, 1999.
  17. Farrer LA. Suicide and attempted suicide in Huntington disease: implications for preclinical testing of persons at risk.Am J Med Genet 24: 305–311, 1986. · DOI
  18. Schoenfeld M, Myers RH, Cupples LA, Berkman B, Sax DS, Clark E. Increased rate of suicide among patients with Huntington’s disease.J Neurol Neurosurg Psychiatry 47: 1283–1287, 1984. · DOI
  19. Almqvist EW, Elterman DS, MacLeod PM, Hayden MR. High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia.Clin Genet 60: 198–205, 2001. · DOI
  20. Hayden MR. Huntington’s chorea. New York: Springer, 1981. · DOI
  21. Visintainer CL, Matthias-Hagen V, Nance MA. U.S. Huntington Disease Genetic Testing Group. Anonymous predictive testing for Huntington’s disease in the United States.Genet Testing 5: 213–218, 2001. · DOI
  22. Tyler A, Morris M, Lazarou L, Meredith L, Myring J, Harper P. Presymptomatic testing for Huntington’s disease in Wales 1987–1990.Br J Psychiatry 161: 481–488, 1992. · DOI
  23. Hersch SM, Jones R, Koroshetz WJ, Quaid K. The neurogenetics genie: testing for the Huntington’s disease mutation.Neurology 44: 1369–1373, 1990. · DOI
  24. Guidelines for the molecular genetics predictive testing Huntington’s disease.Neurology 44:1533–1536, 1994. · DOI
  25. Bui TH, Harper JC. Preimplantation genetic diagnosis.Clin Obstet Gynecol 45: 640–648, 2002. · DOI
  26. Pickering S, Polidoropoulos N, Caller J, Scriven P, Ogilvie CM, Braude P. Preimplantation Genetic Diagnosis Study Group. Strategies and outcomes of the first 100 cycles of preimplantation genetic diagnosis at the Guy’s and St. Thomas’ Center.Fertil Steril 79: 81–90, 2003. · DOI
  27. Stern HJ, Harton GL, Sisson ME, Jones SL, Fallon LA, Thorsell LP et al. Non-disclosing preimplantation genetic diagnosis for Huntington disease.Prenat Diagn 22: 503–507, 2002. · DOI

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Metadata

Authors
Myers, R. H.
Venue
NeuroRX
Publisher
Springer Science and Business Media LLC
Published
2004-04
Volume
1
Issue
2
Pages
255-262
ISSN
1545-5343
DOI
10.1602/neurorx.1.2.255
Cited by
301
References
2
Language
en

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