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Infrared observations of the black-hole candidate V861 Sco.
Published in:
Nature, 1979, v. 278, n. 5701, p. 233, doi. 10.1038/278233a0
By:
- JAMESON, R. F.;
- SHERRINGTON, M. R.;
- KING, A. R.;
- GILES, A. B.
Publication type:
Article
Genetic linkage analysis of manic depression in Iceland.
Published in:
1993
By:
- Curtis, D;
- Sherrington, R;
- Brett, P;
- Holmes, D S;
- Kalsi, G;
- Brynjolfsson, J;
- Petursson, H;
- Rifkin, L;
- Murphy, P;
- Moloney, E
Publication type:
journal article
A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12.
Published in:
Molecular Psychiatry, 2005, v. 10, n. 6, p. 545, doi. 10.1038/sj.mp.4001601
By:
- Shink, E.;
- Morissette, J.;
- Sherrington, R.;
- Barden, N.
Publication type:
Article
Molecular genetics and heterogeneity in manic depression.
Published in:
Molecular Neurobiology, 1988, v. 2, n. 2, p. 125, doi. 10.1007/BF02935342
By:
- Gurling, H.;
- Sherrington, R.;
- Brynjolfsson, J.;
- Potter, M.;
- McInnis, M.;
- Petursson, H.;
- Hodgkinson, S.
Publication type:
Article
Business Management of the Public Services.
Published in:
Public Administration, 1930, v. 8, n. 1, p. 31, doi. 10.1111/j.1467-9299.1930.tb02884.x
By:
- Sherrington, C. E. R.
Publication type:
Article
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1...
Published in:
Nature, 1995, v. 376, n. 6543, p. 775, doi. 10.1038/376775a0
By:
- Rogaev, E.I.;
- Sherrington, R.
Publication type:
Article
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.
Published in:
Nature, 1995, v. 375, n. 6534, p. 754, doi. 10.1038/375754a0
By:
- Sherrington, R.;
- Rogaev, E.I.
Publication type:
Article
C.1 The molecular diagnostic landscape of children with seizure onset in the first three years of life.
Published in:
2023
By:
- McKnight, D;
- McLaughlin, H;
- Grayson, C;
- Sherrington, R;
- Butterfield, N;
- Aradhya, S;
- DeRienzo, L;
- Morales, A;
- Willcock, A;
- Johnson, B
Publication type:
Abstract
Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant.
Published in:
Human Molecular Genetics, 1996, v. 5, n. 7, p. 985, doi. 10.1093/hmg/5.7.985
By:
- Sherrington, R.;
- Froelich, S.;
- Sorbi, S.;
- Campion, D.;
- Chi, H.;
- Rogaeva, E. A.;
- Levesque, G.;
- Rogaev, E. I.;
- Lin, C.;
- Liang, Y.;
- Ikeda, M.;
- Mar, L.;
- Brice, A.;
- Agid, Y.;
- Percy, M.E.;
- Clerget-Darpoux, F.;
- Piacentini, S.;
- Marcon, G.;
- Nacmias, B.;
- Amaducci, L.
Publication type:
Article
Intergenerational Instability of the CAG Repeat of the Gene for Machado-Joseph Disease (MJD1) is Affected by the Genotype of the Normal Chromosome: Implications for the Molecular Mechanisms of the Instability of the CAG Repeat.
Published in:
Human Molecular Genetics, 1996, v. 5, n. 7, p. 923, doi. 10.1093/hmg/5.7.923
By:
- Igarashi, S.;
- Takiyama, Y.;
- Cancel, G.;
- Rogaeva, E. A.;
- Sasaki, H.;
- Wakisaka, A.;
- Zhou, Y.-X.;
- Takano, H.;
- Endo, K.;
- Sanpei, K.;
- Oyake, M.;
- Tanaka, H.;
- Stevanin, G.;
- Abbas, N.;
- Dürr, A.;
- Rogaev, E. I.;
- Sherrington, R.;
- Tsuda, T.;
- Ikeda, M.;
- Cassa, E.
Publication type:
Article
Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.
Published in:
Human Molecular Genetics, 1995, v. 4, n. 7, p. 1137
By:
- Takiyama, Y.;
- Igasrashi, S.;
- Rogaeva, E.A.;
- Endo, K.;
- Rogaev, E.I.;
- Tanaka, H.;
- Sherrington, R.;
- Sanpei, K.;
- Liang, Y.;
- Saito, M.;
- Tsuda, T.;
- Takano, H.;
- Ikeda, M.;
- Lin, C.;
- Chi, H.;
- Kennedy, J. L.;
- Lang, A. E.;
- Wherrett, J.R.;
- Segawa, M.;
- Nomura, Y.
Publication type:
Article

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