17
results
for author:"Clark L.N."
in Literature Citations
| Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. Sidransky E., Nalls M.A., Aasly J.O., Aharon-Peretz J., Annesi G., Barbosa E.R., Bar-Shira A., Berg D., Bras J., Brice A. et al. N. Engl. J. Med. 361:1651-1661(2009) · Mapped (11) |
| Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor. Clark L.N., Kisselev S., Park N., Ross B., Verbitsky M., Rios E., Alcalay R.N., Lee J.H., Louis E.D. Parkinsonism Relat. Disord. 0:0-0(2009) · Mapped (15) |
| Association of glucocerebrosidase mutations with dementia with lewy bodies. Clark L.N., Kartsaklis L.A., Wolf Gilbert R., Dorado B., Ross B.M., Kisselev S., Verbitsky M., Mejia-Santana H., Cote L.J., Andrews H. et al. Arch. Neurol. 66:578-583(2009) · Mapped (17) |
| Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method. Wang Y., Clark L.N., Louis E.D., Mejia-Santana H., Harris J., Cote L.J., Waters C., Andrews H., Ford B., Frucht S. et al. Arch. Neurol. 65:467-474(2008) · Mapped (14) |
| Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Clark L.N., Ross B.M., Wang Y., Mejia-Santana H., Harris J., Louis E.D., Cote L.J., Andrews H., Fahn S., Waters C. et al. Neurology 69:1270-1277(2007) · Mapped (11) |
| Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene. Clark L.N., Haamer E., Mejia-Santana H., Harris J., Lesage S., Durr A., Bs S.J., Hedrich K., Louis E.D., Cote L.J. et al. Mov. Disord. 22:932-937(2007) · Mapped (14) |
| Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Clark L.N., Wang Y., Karlins E., Saito L., Mejia-Santana H., Harris J., Louis E.D., Cote L.J., Andrews H., Fahn S. et al. Neurology 67:1786-1791(2006) · Mapped (4) |
| Case-control study of the parkin gene in early-onset Parkinson disease. Clark L.N., Afridi S., Karlins E., Wang Y., Mejia-Santana H., Harris J., Louis E.D., Cote L.J., Andrews H., Fahn S. et al. Arch. Neurol. 63:548-552(2006) · Mapped (14) |
| The genome of the African trypanosome Trypanosoma brucei. Berriman M., Ghedin E., Hertz-Fowler C., Blandin G., Renauld H., Bartholomeu D.C., Lennard N.J., Caler E., Hamlin N.E., Haas B. et al. Science 309:416-422(2005) · UniProtKB (4,402) |
| Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity. Clark L.N., Nicolai A., Afridi S., Harris J., Mejia-Santana H., Strug L., Cote L.J., Louis E.D., Andrews H., Waters C. et al. Mov. Disord. 20:100-103(2005) · Mapped (11) |
| Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations. Clark L.N., Afridi S., Mejia-Santana H., Harris J., Louis E.D., Cote L.J., Andrews H., Singleton A., Wavrant De-Vrieze F., Hardy J. et al. Mov. Disord. 19:796-800(2004) · UniProtKB (1) |
| The DNA sequence of chromosome I of an African trypanosome: gene content, chromosome organisation, recombination and polymorphism. Hall N., Berriman M., Lennard N.J., Harris B.R., Hertz-Fowler C., Bart-Delabesse E.N., Gerrard C.S., Atkin R.J., Barron A.J., Bowman S. et al. Nucleic Acids Res. 31:4864-4873(2003) · UniProtKB (474) |
| The DNA sequence and comparative analysis of human chromosome 20. Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L. et al. Nature 414:865-871(2001) · UniProtKB (802) |
| Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Clark L.N., Poorkaj P., Wszolek Z., Geschwind D.H., Nasreddine Z.S., Miller B., Li D., Payami H., Awert F., Markopoulou K. et al. Proc. Natl. Acad. Sci. U.S.A. 95:13103-13107(1998) · UniProtKB (1) |
| Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hewitt J.E., Lyle R., Clark L.N., Valleley E.M., Wright T.J., Wijmenga C., van Deutekom J.C., Francis F., Sharpe P.T., Hofker M. Hum. Mol. Genet. 3:1287-1295(1994) · UniProtKB (2) |
| Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11. Wright T.J., Wijmenga C., Clark L.N., Frants R.R., Williamson R., Hewitt J.E. Hum. Mol. Genet. 2:1673-1678(1993) · UniProtKB (1) |
| The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes. Lyle R., Wright T.J., Clark L.N., Hewitt J.E. Genomics 28:389-397(1995) · UniProtKB (1) |
