Literature DB >> 1570835

Sensitivity of lod scores to changes in diagnostic status.

S E Hodge1, D A Greenberg.   

Abstract

This paper investigates effects on lod scores when one individual in a data set changes diagnostic or recombinant status. First we examine the situation in which a single offspring in a nuclear family changes status. The nuclear-family situation, in addition to being of interest in its own right, also has general theoretical importance, since nuclear families are "transparent"; that is, one can track genetic events more precisely in nuclear families than in complex pedigrees. We demonstrate that in nuclear families log10 [(1-theta)/theta] gives an upper limit on the impact that a single offspring's change in status can have on the lod score at that recombination fraction (theta). These limits hold for a fully penetrant dominant condition and fully informative marker, in either phase-known or phase-unknown matings. Moreover, log10 [(1-theta)/theta] (where theta denotes the value of theta at which Zmax occurs) gives an upper limit on the impact of a single offspring's status change on the maximum lod score (Zmax). In extended pedigrees, in contrast to nuclear families, no comparable limit can be set on the impact of a single individual on the lod score. Complex pedigrees are subject to both stabilizing and destabilizing influences, and these are described. Finally, we describe a "sensitivity analysis," in which, after all linkage analysis is completed, every informative individual in the data set is changed, one at a time, to see the effect which each separate change has on the lod scores. The procedure includes identifying "critical individuals," i.e., those who would have the greatest impact on the lod scores, should their diagnostic status in fact change. To illustrate use of the sensitivity analysis, we apply it to the large bipolar pedigree reported by Egeland et al. and Kelsoe et al. We show that the changes in lod scores observed there, on the order of 1.1-1.2 per person, are not unusual. We recommend that investigators include a sensitivity analysis as a standard part of reporting the results of a linkage analysis.

Entities:  

Mesh:

Year:  1992        PMID: 1570835      PMCID: PMC1682606     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  9 in total

1.  Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis.

Authors:  D E Weeks; T Lehner; E Squires-Wheeler; C Kaufmann; J Ott
Journal:  Genet Epidemiol       Date:  1990       Impact factor: 2.135

2.  Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish.

Authors:  J R Kelsoe; E I Ginns; J A Egeland; D S Gerhard; A M Goldstein; S J Bale; D L Pauls; R T Long; K K Kidd; G Conte
Journal:  Nature       Date:  1989-11-16       Impact factor: 49.962

3.  Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree.

Authors:  J L Kennedy; L A Giuffra; H W Moises; L L Cavalli-Sforza; A J Pakstis; J R Kidd; C M Castiglione; B Sjogren; L Wetterberg; K K Kidd
Journal:  Nature       Date:  1988-11-10       Impact factor: 49.962

4.  Localization of a susceptibility locus for schizophrenia on chromosome 5.

Authors:  R Sherrington; J Brynjolfsson; H Petursson; M Potter; K Dudleston; B Barraclough; J Wasmuth; M Dobbs; H Gurling
Journal:  Nature       Date:  1988-11-10       Impact factor: 49.962

Review 5.  Genetic linkage and complex diseases, with special reference to psychiatric disorders.

Authors:  N Risch
Journal:  Genet Epidemiol       Date:  1990       Impact factor: 2.135

6.  Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p.

Authors:  S J Bale; N C Dracopoli; M A Tucker; W H Clark; M C Fraser; B Z Stanger; P Green; H Donis-Keller; D E Housman; M H Greene
Journal:  N Engl J Med       Date:  1989-05-25       Impact factor: 91.245

Review 7.  Bipolar affective disorders linked to DNA markers on chromosome 11.

Authors:  J A Egeland; D S Gerhard; D L Pauls; J N Sussex; K K Kidd; C R Allen; A M Hostetter; D E Housman
Journal:  Nature       Date:  1987 Feb 26-Mar 4       Impact factor: 49.962

8.  Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36.

Authors:  L A Cannon-Albright; D E Goldgar; E C Wright; A Turco; M Jost; L J Meyer; M Piepkorn; J J Zone; M H Skolnick
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

9.  Possible linkage of a breast cancer-susceptibility locus to the ABO locus: sensitivity of LOD scores to a single new recombinant observation.

Authors:  M H Skolnick; E A Thompson; D T Bishop; L A Cannon
Journal:  Genet Epidemiol       Date:  1984       Impact factor: 2.135

  9 in total
  10 in total

1.  Eye tracking dysfunction in families with multiple cases of schizophrenia.

Authors:  V Arolt; R Lencer; A Nolte; M Pinnow; E Schwinger
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1996       Impact factor: 5.270

2.  A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3.

Authors:  Pedro Fernandez; Johanna Moolman-Smook; Paul Brink; Valerie Corfield
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

3.  Chromosome 20 shows linkage with DSM-IV nicotine dependence in Finnish adult smokers.

Authors:  Kaisu Keskitalo-Vuokko; Jenni Hällfors; Ulla Broms; Michele L Pergadia; Scott F Saccone; Anu Loukola; Pamela A F Madden; Jaakko Kaprio
Journal:  Nicotine Tob Res       Date:  2011-10-29       Impact factor: 4.244

4.  Replication of genetic linkage by follow-up of previously studied pedigrees.

Authors:  E S Gershon; L R Goldin
Journal:  Am J Hum Genet       Date:  1994-04       Impact factor: 11.025

5.  Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds.

Authors:  S M Gorski; K J Adams; P H Birch; B N Chodirker; C R Greenberg; P J Goodfellow
Journal:  Hum Genet       Date:  1994-08       Impact factor: 4.132

6.  An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family.

Authors:  T P Atkinson; A A Schäffer; B Grimbacher; H W Schroeder; C Woellner; C S Zerbe; J M Puck
Journal:  Am J Hum Genet       Date:  2001-08-21       Impact factor: 11.025

7.  Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group.

Authors:  M Krajinovic; B Pinamonti; G Sinagra; M Vatta; G M Severini; J Milasin; A Falaschi; F Camerini; M Giacca; L Mestroni
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

8.  Phenotypic variation of tuberous sclerosis in a single extended kindred.

Authors:  S L Smalley; F Burger; M Smith
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

9.  Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice?

Authors:  P Heutink; B J van de Wetering; A J Pakstis; R Kurlan; P Sandor; B A Oostra; L A Sandkuijl
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

10.  Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5-6.0 Hz polyspike waves.

Authors:  Jenny E Wight; Viet-Huong Nguyen; Marco T Medina; Christopher Patterson; Reyna M Durón; Yolly Molina; Yu-Chen Lin; Iris E Martínez-Juárez; Adriana Ochoa; Aurelio Jara-Prado; Miyabi Tanaka; Dongsheng Bai; Sumaya Aftab; Julia N Bailey; Antonio V Delgado-Escueta
Journal:  Mol Genet Genomic Med       Date:  2016-01-23       Impact factor: 2.183

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.