Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: a preliminary report.
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Laura J. Bierut | Alan R. Sanders | O. Colin Stine | Pablo V. Gejman | Tatiana Foroud | Howard J. Edenberg | Elliot S. Gershon | Francis J. McMahon | Marvin J. Miller | John I. Nurnberger | F. McMahon | L. Bierut | J. Nurnberger | M. Blehar | T. Reich | A. Goate | E. Gershon | T. Foroud | J. Badner | S. Detera-Wadleigh | O. C. Stine | D. Meyers | H. Edenberg | A. Sanders | P. Gejman | J. Rice | S. Simpson | P. Conneally | L. Goldin | J. Depaulo | Alison Goate | Theodore Reich | Diane Kazuba | Lynn R. Goldin | J. Guroff | D. Kazuba | Judith A. Badner | Deborah A. Meyers | Mary C. Blehar | J. Raymond DePaulo | Sevilla D. Detera-Wadleigh | Elizabeth S. Bowman | Aimee R. Mayeda | Leela Rau | Carrie Smiley | P. Michael Conneally | Sylvia G. Simpson | M. G. Mclnnis | Juliet J. Guroff | Elizabeth S. Maxwell | John R. Rice | M. Mclnnis | E. Bowman | A. Mayeda | L. Rau | C. Smiley | O. Stine | J. DePaulo | Carrie Smiley
[1] R. Elston,et al. A comparison of sib‐pair linkage tests for disease susceptibility loci , 1985, Genetic epidemiology.
[2] O. Mors,et al. A possible locus for manic depressive illness on chromosome 16p13 , 1995, Psychiatric genetics.
[3] J. Nurnberger,et al. Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q. , 1996, American journal of human genetics.
[4] T. Hudson,et al. Direct detection of novel expanded trinucleotide repeats in the human genome , 1993, Nature Genetics.
[5] A Chromosome‐based method to infer IBD scores for missing and ambiguous markers , 1995, Genetic epidemiology.
[6] J. Nurnberger,et al. A linkage study of bipolar illness. , 1997, Archives of general psychiatry.
[7] D J Schaid,et al. Genotype relative risks: methods for design and analysis of candidate-gene association studies. , 1993, American journal of human genetics.
[8] J. Todd,et al. A genome-wide search for human type 1 diabetes susceptibility genes , 1994, Nature.
[9] D E Weeks,et al. A multilocus extension of the affected-pedigree-member method of linkage analysis. , 1992, American journal of human genetics.
[10] J. Nurnberger,et al. A family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands. , 1982, Archives of general psychiatry.
[11] S. Hodge,et al. Do bilineal pedigrees represent a problem for linkage analysis? basic principles and simulation results for single‐gene diseases with no heterogeneity , 1992, Genetic epidemiology.
[12] L. DeLisi,et al. A controlled family study of chronic psychoses. Schizophrenia and schizoaffective disorder. , 1988, Archives of general psychiatry.
[13] F. Goodwin. Manic-Depressive Illness , 1990 .
[14] H. Pétursson,et al. Linkage findings in bipolar disorder , 1995, Nature Genetics.
[15] J. Nurnberger,et al. Genomic Screening for Genes Predisposing to Bipolar Disease , 1992 .
[16] John P. Rice,et al. The familial transmission of bipolar illness. , 1987, Archives of general psychiatry.
[17] 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.
[18] John P. Rice,et al. A meta‐analysis of chromosome 18 linkage data for bipolar illness , 1997, Genetic epidemiology.
[19] L Kruglyak,et al. Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.
[20] M. McInnis,et al. Genes with triplet repeats: candidate mediators of neuropsychiatric disorders , 1993, Trends in Neurosciences.
[21] R. Straub,et al. A potential vulnerability locus for schizophrenia on chromosome 6p24–22: evidence for genetic heterogeneity , 1995, Nature Genetics.
[22] T. Reich,et al. Family history studies: V. The genetics of mania. , 1969, The American journal of psychiatry.
[23] M. Pericak-Vance,et al. Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[24] M. Leboyer,et al. Tyrosine hydroxylase polymorphisms associated with manic-depressive illness , 1990, The Lancet.
[25] H. Pétursson,et al. Molecular genetic evidence for heterogeneity in manic depression , 1987, Nature.
[26] N. Craddock,et al. Expanded CAG repeats in schizophrenia and bipolar disorder , 1995, Nature Genetics.
[27] J. Weissenbach,et al. A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish , 1996, Nature Genetics.
[28] K. Kidd,et al. Bipolar affective disorders linked to DNA markers on chromosome 11 , 1987, Nature.
[29] K. Kidd,et al. Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish , 1989, Nature.
[30] J. Rommens,et al. Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families , 1994, Nature Genetics.
[31] W. Ewens,et al. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). , 1993, American journal of human genetics.
[32] Patrick Dowd,et al. Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families , 1994, Nature Genetics.
[33] A. Bertelsen,et al. A Danish Twin Study of Manic-Depressive Disorders , 1977, British Journal of Psychiatry.
[34] J. R. Alexander,et al. Diminished support for linkage between manic depressive illness and X–chromosome markers in three Israeli pedigrees , 1993, Nature Genetics.
[35] L. Peltonen,et al. Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree. , 1995, Genome research.
[36] D. Gerhard,et al. A follow-up report of a genome search for affective disorder predisposition loci in the Old Order Amish. , 1996, American journal of human genetics.
[37] John P. Rice,et al. Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. , 1997, American journal of medical genetics.
[38] F. McMahon,et al. Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q. , 1997, American journal of medical genetics.
[39] K. Lange,et al. The affected-pedigree-member method of linkage analysis. , 1988, American journal of human genetics.
[40] R. Murray,et al. Linkage studies of bipolar disorder with chromosome 18 markers. , 1999, American journal of medical genetics.
[41] A. Frances. The Diagnostic Interview for Genetic Studies , 1994 .
[42] S. Barondes,et al. Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23 , 1996, Nature Genetics.
[43] J. Nurnberger,et al. Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[44] D. Clair,et al. A locus for bipolar affective disorder on chromosome 4p , 1996, Nature Genetics.
[45] S. Detera-Wadleigh,et al. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter. , 1994, American journal of medical genetics.
[46] F. McMahon,et al. Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12. , 1997, American journal of medical genetics.
[47] E. Gershon,et al. Close linkage of c-Harvey-ras-1 and the insulin gene to affective disorder is ruled out in three North American pedigrees , 1987, Nature.
[48] J. Mendlewicz,et al. POLYMORPHIC DNA MARKER ON X CHROMOSOME AND MANIC DEPRESSION , 1987, The Lancet.
[49] F. McMahon,et al. Anticipation in bipolar affective disorder. , 1993, American journal of human genetics.
[50] N. Risch. Linkage strategies for genetically complex traits. I. Multilocus models. , 1990, American journal of human genetics.
[51] E. Lander,et al. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results , 1995, Nature Genetics.
[52] Francis S. Collins,et al. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer , 1994, Nature Genetics.
[53] C. Falk,et al. Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations , 1987, Annals of human genetics.
[54] M. Zompo,et al. Is bipolar disorder linked to Xq28? , 1994, Nature Genetics.
[55] J. Mendlewicz,et al. Adoption study supporting genetic transmission in manic–depressive illness , 1977, Nature.
[56] D J Schaid,et al. Comparison of statistics for candidate-gene association studies using cases and parents. , 1994, American journal of human genetics.
[57] R. Todd,et al. Population frequencies of tyrosine hydroxylase restriction fragment length polymorphisms in bipolar affective disorder , 1989, Biological Psychiatry.
[58] N. Risch. Linkage strategies for genetically complex traits. II. The power of affected relative pairs. , 1990, American journal of human genetics.
[59] D. Housman,et al. Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1. , 1994, American journal of medical genetics.
[60] N. Risch,et al. Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. , 1990, American journal of human genetics.
[61] E. Gershon,et al. Manic depressive illness not linked to factor IX region in an independent series of pedigrees. , 1990, Genomics.
[62] N. Craddock,et al. Familial Cosegregation of Major Affective Disorder and Darier's Disease (Keratosis Follicularis) , 1994, British Journal of Psychiatry.
[63] D. Botstein,et al. A manic depressive history , 1996, Nature Genetics.
[64] G. Schellenberg,et al. Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease , 1996, Nature Medicine.
[65] J. Fleiss,et al. Linkage studies with X-chromosome markers in bipolar (manic-depressive) and unipolar (depressive) illnesses. , 1974, Biological psychiatry.
[66] J. Badner,et al. Bipolar disorder and chromosome 18: An analysis of multiple data sets , 1997, Genetic epidemiology.
[67] N. Freimer,et al. Use of linkage disequilibrium approaches to map genes for bipolar disorder in the Costa Rican population. , 1996, American journal of medical genetics.
[68] H. Coon,et al. A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance. , 1993, American journal of human genetics.
[69] M. Boehnke,et al. Allele frequency estimation from data on relatives. , 1991, American journal of human genetics.
[70] N. Freimer,et al. Incorrect specification of marker allele frequencies: effects on linkage analysis. , 1993, American journal of human genetics.
[71] A. Young,et al. A polymorphic DNA marker genetically linked to Huntington's disease , 1983, Nature.
[72] N. Risch,et al. Genetic linkage between X-chromosome markers and bipolar affective illness , 1987, Nature.
[73] John P. Rice,et al. Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X. , 1997, American journal of medical genetics.
[74] E. Gershon,et al. X-chromosome markers and manic-depressive illness. Rejection of linkage to Xq28 in nine bipolar pedigrees. , 1990, Archives of general psychiatry.