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938 results

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A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.
Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR, et al. Haines JL, et al. Among authors: reyes c. Nat Genet. 1996 Aug;13(4):469-71. doi: 10.1038/ng0896-469. Nat Genet. 1996. PMID: 8696344
Linkage analysis of candidate myelin genes in familial multiple sclerosis.
Seboun E, Oksenberg JR, Rombos A, Usuku K, Goodkin DE, Lincoln RR, Wong M, Pham-Dinh D, Boesplug-Tanguy O, Carsique R, Fitoussi R, Gartioux C, Reyes C, Ribierre F, Faure S, Fizames C, Gyapay G, Weissenbach J, Dautigny A, Rimmler JB, Garcia ME, Pericak-Vance MA, Haines JL, Hauser SL. Seboun E, et al. Among authors: reyes c. Neurogenetics. 1999 Sep;2(3):155-62. doi: 10.1007/s100480050076. Neurogenetics. 1999. PMID: 10541588
A first high-density map of 981 biallelic markers on human chromosome 14.
Escary JL, Bottius E, Prince N, Reyes C, Fiawoumo Y, Caloustian C, Bruls T, Fujiyama A, Cooper RS, Adeyemo AA, Lathrop GM, Weissenbach J, Gyapay G, Foglio M, Beckmann JS. Escary JL, et al. Among authors: reyes c. Genomics. 2000 Dec 1;70(2):153-64. doi: 10.1006/geno.2000.6369. Genomics. 2000. PMID: 11112343
Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore Sequencing.
Reyes CJ, Laabs BH, Schaake S, Lüth T, Ardicoglu R, Rakovic A, Grütz K, Alvarez-Fischer D, Jamora RD, Rosales RL, Weyers I, König IR, Brüggemann N, Klein C, Dobricic V, Westenberger A, Trinh J. Reyes CJ, et al. Neurol Genet. 2021 Jul 6;7(4):e608. doi: 10.1212/NXG.0000000000000608. eCollection 2021 Aug. Neurol Genet. 2021. PMID: 34250228 Free PMC article.
A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.
Westenberger A, Reyes CJ, Saranza G, Dobricic V, Hanssen H, Domingo A, Laabs BH, Schaake S, Pozojevic J, Rakovic A, Grütz K, Begemann K, Walter U, Dressler D, Bauer P, Rolfs A, Münchau A, Kaiser FJ, Ozelius LJ, Jamora RD, Rosales RL, Diesta CCE, Lohmann K, König IR, Brüggemann N, Klein C. Westenberger A, et al. Among authors: reyes cj. Ann Neurol. 2019 Jun;85(6):812-822. doi: 10.1002/ana.25488. Epub 2019 May 3. Ann Neurol. 2019. PMID: 30973967
Prodromal X-Linked Dystonia-Parkinsonism is Characterized by a Subclinical Motor Phenotype.
Steinhardt J, Hanssen H, Heldmann M, Sprenger A, Laabs BH, Domingo A, Reyes CJ, Prasuhn J, Brand M, Rosales R, Münte TF, Klein C, Westenberger A, Oropilla JQ, Diesta C, Brüggemann N. Steinhardt J, et al. Among authors: reyes cj. Mov Disord. 2022 Jul;37(7):1474-1482. doi: 10.1002/mds.29033. Epub 2022 May 2. Mov Disord. 2022. PMID: 35491955
DNA Methylation as a Potential Molecular Mechanism in X-linked Dystonia-Parkinsonism.
Krause C, Schaake S, Grütz K, Sievert H, Reyes CJ, König IR, Laabs BH, Jamora RD, Rosales RL, Diesta CCE, Pozojevic J, Gemoll T, Westenberger A, Kaiser FJ, Klein C, Kirchner H. Krause C, et al. Among authors: reyes cj. Mov Disord. 2020 Dec;35(12):2220-2229. doi: 10.1002/mds.28239. Epub 2020 Sep 10. Mov Disord. 2020. PMID: 32914507
Elucidating Hexanucleotide Repeat Number and Methylation within the X-Linked Dystonia-Parkinsonism (XDP)-Related SVA Retrotransposon in TAF1 with Nanopore Sequencing.
Lüth T, Laβ J, Schaake S, Wohlers I, Pozojevic J, Jamora RDG, Rosales RL, Brüggemann N, Saranza G, Diesta CCE, Schlüter K, Tse R, Reyes CJ, Brand M, Busch H, Klein C, Westenberger A, Trinh J. Lüth T, et al. Among authors: reyes cj. Genes (Basel). 2022 Jan 11;13(1):126. doi: 10.3390/genes13010126. Genes (Basel). 2022. PMID: 35052466 Free PMC article.
938 results