The Genetics of Adult-Onset Neuropsychiatric Disease: Complexities and Conundra?
暂无分享,去创建一个
Richard Mayeux | Nancy C Andreasen | N. Andreasen | P. S. St George-Hyslop | R. Mayeux | L. Farrer | J. Kennedy | Lindsay A Farrer | James L Kennedy | Peter St George-Hyslop | J. Kennedy
[1] H. Stefánsson,et al. Neuregulin 1 and susceptibility to schizophrenia. , 2002, American journal of human genetics.
[2] Leena Peltonen,et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. , 2003, American journal of human genetics.
[3] A. Paterson,et al. Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity. , 1998, JAMA.
[4] A. Paterson,et al. Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance? , 2003, Schizophrenia bulletin.
[5] G. Schellenberg,et al. Tau is a candidate gene for chromosome 17 frontotemporal dementia , 1998, Annals of neurology.
[6] M. Owen,et al. Susceptibility locus for Alzheimer's disease on chromosome 10. , 2000, Science.
[7] N. Risch. Searching for genetic determinants in the new millennium , 2000, Nature.
[8] M A Pericak-Vance,et al. Fine mapping of autistic disorder to chromosome 15q11‐q13 by use of phenotypic subtypes. , 2003, American journal of human genetics.
[9] Ricardo Segurado,et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis. , 2003, American journal of human genetics.
[10] W. Rocca,et al. Epidemiology of clinically diagnosed Alzheimer's disease , 1986, Annals of neurology.
[11] A. Petronis,et al. Human morbid genetics revisited: relevance of epigenetics. , 2001, Trends in genetics : TIG.
[12] D. Botstein,et al. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease , 2003, Nature Genetics.
[13] Nancy J. Cox,et al. Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans , 1999, Nature Genetics.
[14] M. Pericak-Vance,et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease , 1991, Nature.
[15] M. Egan,et al. The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal Function , 2003, Cell.
[16] J. Rommens,et al. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene , 1995, Nature.
[17] P. Sham,et al. Genetic and physiological data implicating the new human gene G72 and the gene for d-amino acid oxidase in schizophrenia , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[18] M. Tohen,et al. Textbook in psychiatric epidemiology , 2002 .
[19] R. Rosenberg. Molecular neurogenetics: the genome is settling the issue. , 1997, JAMA.
[20] A. Petronis. The Genes for Major Psychosis: Aberrant Sequence or Regulation? , 2000, Neuropsychopharmacology.
[21] Michael C O'Donovan,et al. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. , 2003, American journal of human genetics.
[22] P. Visscher,et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. , 2003, American journal of human genetics.
[23] A. Caspi,et al. Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene , 2003, Science.
[24] M G McInnis,et al. Evidence for genetic linkage of Alzheimer's disease to chromosome 10q. , 2000, Science.
[25] A. D. Roses,et al. Association of apolipoprotein E allele €4 with late-onset familial and sporadic Alzheimer’s disease , 2006 .
[26] P. M. Conneally,et al. Identification of Novel Genes in Late-Onset Alzheimer's Disease , 2000, Experimental Gerontology.
[27] J. H. Lee,et al. Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean Hispanics. , 2002, American journal of human genetics.
[28] D. Selkoe,et al. Additive Effects of PS1 and APP Mutations on Secretion of the 42-Residue Amyloid β-Protein , 1998, Neurobiology of Disease.
[29] J. Blangero,et al. Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. , 2000, Science.
[30] Weiming Xia,et al. Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid β-protein in both transfected cells and transgenic mice , 1997, Nature Medicine.
[31] Michael J Owen,et al. Recent advances in the genetics of schizophrenia. , 2003, Human molecular genetics.
[32] M. Albert,et al. Results of a high-resolution genome screen of 437 Alzheimer's disease families. , 2003, Human molecular genetics.
[33] J. Beckmann,et al. A highly significant association between a COMT haplotype and schizophrenia. , 2002, American journal of human genetics.
[34] S. Christian,et al. Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. , 2003, American journal of human genetics.
[35] F. McMahon,et al. Linkage of bipolar affective disorder to chromosome 18 markers in a new pedigree series. , 1997, American journal of human genetics.
[36] S. Gabriel,et al. Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus , 2002, Molecular Psychiatry.
[37] R. Straub,et al. Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia. , 2002, American journal of human genetics.
[38] David A Lewis,et al. Schizophrenia as a disorder of neurodevelopment. , 2002, Annual review of neuroscience.
[39] Steven A. Crone,et al. Gene Targeting Reveals Multiple Essential Functions of the Neuregulin Signaling System during Development of the Neuroendocrine and Nervous Systems , 2002, Annals of the New York Academy of Sciences.
[40] J. Growdon,et al. Risk of dementia among relatives of Alzheimer's disease patients in the MIRAGE study , 1996, Neurology.
[41] I. Gottesman,et al. The endophenotype concept in psychiatry: etymology and strategic intentions. , 2003, The American journal of psychiatry.
[42] D. Botstein,et al. Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect. , 1995, American journal of human genetics.
[43] D. Blake,et al. Dysbindin, a Novel Coiled-coil-containing Protein That Interacts with the Dystrobrevins in Muscle and Brain* , 2001, The Journal of Biological Chemistry.
[44] L R Goldin,et al. A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[45] D. Pollen,et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease , 1995, Nature.
[46] D. Pfaff,et al. Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[47] A. Gronenborn,et al. Experimental support for the "hydrophobic zipper" hypothesis. , 1994, Science.
[48] P. Muglia,et al. The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: evidence from a family-based association study. , 2002, American journal of human genetics.
[49] J. Karlawish,et al. Alzheimer Disease: Current Concepts and Emerging Diagnostic and Therapeutic Strategies , 2003, Annals of Internal Medicine.
[50] U. Finckh,et al. The future of genetic association studies in Alzheimer disease , 2003, Journal of Neural Transmission.
[51] R. Coppola,et al. Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia. , 2003, Archives of general psychiatry.
[52] E. Lander,et al. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease , 2003, Nature Genetics.
[53] Peter McGuffin,et al. Psychiatric Genetics and Genomics , 2002 .