Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study
Lavedan, C, Licamele, L, Volpi, S, Hamilton, J, Heaton, C, Mack, K, Lannan, R, Thompson, A, Wolfgang, C D, Polymeropoulos, M H
Published in Molecular psychiatry (01.08.2009)
Published in Molecular psychiatry (01.08.2009)
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Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia
Volpi, S, Heaton, C, Mack, K, Hamilton, J B, Lannan, R, Wolfgang, C D, Licamele, L, Polymeropoulos, M H, Lavedan, C
Published in Molecular psychiatry (01.11.2009)
Published in Molecular psychiatry (01.11.2009)
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Tasimelteon treatment entrains the circadian clock and demonstrates significant benefit on sleep and wake parameters in totally blind individuals with non-24 hour circadian rhythms
Lockley, S, Dressman, M, Torres, R, Lavedan, C, Licamele, L, Polymeropoulos, M
Published in Sleep medicine (01.12.2013)
Published in Sleep medicine (01.12.2013)
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Myotonic dystrophy : size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism
LAVEDAN, C, HOFMANN-RADVANYI, H, SHELBOURNE, P, RABES, J.-P, DUROS, C, SAVOY, D, DEHAUPAS, I, LUCE, S, JOHNSON, K, JUNIEN, C
Published in American journal of human genetics (01.05.1993)
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Published in American journal of human genetics (01.05.1993)
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Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy
ASHIZAWA, T, ANVRET, M, JUNIEN, C, KOCH, M. C, KORNELUK, R. G, LAVEDAN, C, MIKI, T, MULLEY, J. C, LOPEZ DE MUNAIN, A, NOVELLI, G, ROSES, A. D, SELTZER, W. K, BAIGET, M, SHAW, D. J, SMEETS, H, SUTHERLAND, G. R, YAMAGATA, H, HARPER, P. S, BARCELO, J. M, BRUNNER, H, COBO, A. M, DALLAPICCOLA, B, FENWICK, R. G, GRANDELL, U, HARLEY, H
Published in American journal of human genetics (01.03.1994)
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Published in American journal of human genetics (01.03.1994)
Journal Article
Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophy
Lavedan, C, Hofmann-Radvanyi, H, Rabes, J.P, Roume, J, Junien, C
Published in The Lancet (British edition) (23.01.1993)
Published in The Lancet (British edition) (23.01.1993)
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Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease
Lavedan, C, Buchholtz, S, Auburger, G, Albin, R L, Athanassiadou, A, Blancato, J, Burguera, J A, Ferrell, R E, Kostic, V, Leroy, E, Leube, B, Mota-Vieira, L, Papapetropoulos, T, Pericak-Vance, M A, Pinkus, J, Scott, W K, Ulm, G, Vasconcelos, J, Vilchez, J J, Nussbaum, R L, Polymeropoulos, M H
Published in DNA research (31.12.1998)
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Published in DNA research (31.12.1998)
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Contig map of the Parkinson's disease region on 4q21-q23
Lavedan, C, Dehejia, A, Pike, B, Dutra, A, Leroy, E, Ide, S E, Root, H, Rubenstein, J, Boyer, R L, Chandrasekharappa, S, Makalowska, I, Nussbaum, R L, Polymeropoulos, M H
Published in DNA research (28.02.1998)
Published in DNA research (28.02.1998)
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The ubiquitin pathway in Parkinson's disease
Leroy, Elisabeth, Boyer, Rebecca, Auburger, Georg, Leube, Barbara, Ulm, Gudrun, Mezey, Eva, Harta, Gyongyi, Brownstein, Michael J, Jonnalagada, Sobhanadditya, Chernova, Tanya, Dehejia, Anindya, Lavedan, Christian, Gasser, Thomas, Steinbach, Peter J, Wilkinson, Keith D, Polymeropoulos, Mihael H
Published in Nature (London) (01.10.1998)
Published in Nature (London) (01.10.1998)
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Mutation in the α-synuclein gene identified in families with Parkinson's disease
POLYMEROPOULOS, M. H, LAVEDAN, C, STENROOS, E. S, CHANDRASEKHARAPPA, S, ATHANASSIADOU, A, PAPAPETROPOULOS, T, JOHNSON, W. G, LAZZARINI, A. M, DUVOISIN, R. C, DI LORIO, G, GOLBE, L. I, NUSSBAUM, R. L, LEROY, E, IDE, S. E, DEHEJIA, A, DUTRA, A, PIKE, B, ROOT, H, RUBENSTEIN, J, BOYER, R
Published in Science (American Association for the Advancement of Science) (27.06.1997)
Published in Science (American Association for the Advancement of Science) (27.06.1997)
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French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion
Lavedan, C, Hofmann-Radvanyi, H, Boileau, C, Bonaïti-Pellié, C, Savoy, D, Shelbourne, P, Duros, C, Rabes, J P, Dehaupas, I, Luce, S
Published in Journal of medical genetics (01.01.1994)
Published in Journal of medical genetics (01.01.1994)
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NcoI RFLP at 19q13 identified by the DNA sequence pW119B (D19S169)
Lavedan, C, Savoy, D, Simon, M, Wieringa, B, Junien, C
Published in Nucleic acids research (25.10.1991)
Published in Nucleic acids research (25.10.1991)
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Journal Article
Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers
Lavedan, C, Hofmann, H, Shelbourne, P, Duros, C, Savoy, D, Johnson, K, Junien, C
Published in Journal of medical genetics (01.02.1991)
Published in Journal of medical genetics (01.02.1991)
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