Evidence for Linkage and Association with Reading Disability, on 6p21

Slides:



Advertisements
Similar presentations
Previous Estimates of Mitochondrial DNA Mutation Level Variance Did Not Account for Sampling Error: Comparing the mtDNA Genetic Bottleneck in Mice and.
Advertisements

Functional Analysis of the Neurofibromatosis Type 2 Protein by Means of Disease- Causing Point Mutations Renee P. Stokowski, David R. Cox The American.
Gene Preference in Maple Syrup Urine Disease Mary M. Nellis, Dean J. Danner The American Journal of Human Genetics Volume 68, Issue 1, Pages (January.
Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery Herbert A. Lubs, Roger E. Stevenson, Charles E. Schwartz The American Journal.
The Trimmed-Haplotype Test for Linkage Disequilibrium
Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set  Christopher W. Bartlett, Rhinda.
Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1
Transmission/Disequilibrium Tests for Extended Marker Haplotypes
Genetic Linkage of Paget Disease of the Bone to Chromosome 18q
Molecular Genetics of Pediatric Soft Tissue Tumors
Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia  Natalie Cope, Denise Harold, Gary Hill, Valentina.
D. E. Grice, K. A. Halmi, M. M. Fichter, M. Strober, D. B. Woodside, J
Model-Free Linkage Analysis with Covariates Confirms Linkage of Prostate Cancer to Chromosomes 1 and 4  Katrina A.B. Goddard, John S. Witte, Brian K.
Genomewide Linkage Scan Identifies a Novel Susceptibility Locus for Restless Legs Syndrome on Chromosome 9p  Shenghan Chen, William G. Ondo, Shaoqi Rao,
A Major Susceptibility Locus Influencing Plasma Triglyceride Concentrations Is Located on Chromosome 15q in Mexican Americans  Ravindranath Duggirala,
CHEK2*1100delC and Susceptibility to Breast Cancer: A Collaborative Analysis Involving 10,860 Breast Cancer Cases and 9,065 Controls from 10 Studies 
Linkage Disequilibrium Mapping of Schizophrenia Susceptibility to the CAPON Region of Chromosome 1q22  Linda M. Brzustowicz, Jaime Simone, Paria Mohseni,
Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome.
A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q  S.C.
Meta-analysis of Genetic-Linkage Analysis of Quantitative-Trait Loci
Accounting for Linkage in Family-Based Tests of Association with Missing Parental Genotypes  Eden R. Martin, Meredyth P. Bass, Elizabeth R. Hauser, Norman.
Ren-Hua Chung, Richard W. Morris, Li Zhang, Yi-Ju Li, Eden R. Martin 
Anxiety with Panic Disorder Linked to Chromosome 9q in Iceland
Malic Enzyme 2 May Underlie Susceptibility to Adolescent-Onset Idiopathic Generalized Epilepsy  David A. Greenberg, Eftihia Cayanis, Lisa Strug, Sudhir.
Linkage Thresholds for Two-stage Genome Scans
A Combined Linkage-Physical Map of the Human Genome
The Novel Genetic Disorder Microhydranencephaly Maps to Chromosome 16p  
Caroline Durrant, Krina T. Zondervan, Lon R
A 77-Kilobase Region of Chromosome 6p22
The American Journal of Human Genetics 
Elizabeth Theusch, Analabha Basu, Jane Gitschier 
Weight Loss after Gastric Bypass Is Associated with a Variant at 15q26
Highly Significant Linkage to the SLI1 Locus in an Expanded Sample of Individuals Affected by Specific Language Impairment    The American Journal of.
Gene Expression in Skin and Lymphoblastoid Cells: Refined Statistical Method Reveals Extensive Overlap in cis-eQTL Signals  Jun Ding, Johann E. Gudjonsson,
Kristina Allen-Brady, Peggy A. Norton, James M
Use of a Quantitative Trait to Map a Locus Associated with Severity of Positive Symptoms in Familial Schizophrenia to Chromosome 6p  L.M. Brzustowicz,
Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region 
Familial Juvenile Hyperuricemic Nephropathy: Localization of the Gene on Chromosome 16p11.2—and Evidence for Genetic Heterogeneity  Blanka Stibůrková,
Two Families with Familial Amyotrophic Lateral Sclerosis Are Linked to a Novel Locus on Chromosome 16q  Deborah M. Ruddy, Matthew J. Parton, Ammar Al-Chalabi,
Hal M. Hoffman, Fred A. Wright, David H. Broide, Alan A
Stephen C. Pratt, Mark J. Daly, Leonid Kruglyak 
Model-Free Linkage Analysis with Covariates Confirms Linkage of Prostate Cancer to Chromosomes 1 and 4  Katrina A.B. Goddard, John S. Witte, Brian K.
Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design  Veronique Vitart,
A Syndrome of Severe Mental Retardation, Spasticity, and Tapetoretinal Degeneration Linked to Chromosome 15q24  S.J. Mitchell, D.P. McHale, D.A. Campbell,
The SNP Endgame: A Multidisciplinary Approach*
Family-Based Tests of Association in the Presence of Linkage
Erratum The American Journal of Human Genetics
Linkage Analysis Identifies a Novel Locus for Restless Legs Syndrome on Chromosome 2q in a South Tyrolean Population Isolate  Irene Pichler, Fabio Marroni,
William F. Forrest, Eleanor Feingold 
Michael P. Epstein, Xihong Lin, Michael Boehnke 
On a Randomization Procedure in Linkage Analysis
D. E. Grice, K. A. Halmi, M. M. Fichter, M. Strober, D. B. Woodside, J
Homozygosity and Linkage-Disequilibrium Mapping of the Syndrome of Congenital Hypoparathyroidism, Growth and Mental Retardation, and Dysmorphism to a.
James A. Lautenberger, J. Claiborne Stephens, Stephen J
Long Homozygous Chromosomal Segments in Reference Families from the Centre d'Étude du Polymorphisme Humain  Karl W. Broman, James L. Weber  The American.
Genomewide Linkage Analysis of Quantitative Spirometric Phenotypes in Severe Early- Onset Chronic Obstructive Pulmonary Disease  Edwin K. Silverman, Lyle.
Gonçalo R. Abecasis, Emiko Noguchi, Andrea Heinzmann, James A
David B. Allison, Bonnie Thiel, Pamela St. Jean, Robert C
Suzanne M. Leal, Jurg Ott  The American Journal of Human Genetics 
Increasing the Power and Efficiency of Disease-Marker Case-Control Association Studies through Use of Allele-Sharing Information  Tasha E. Fingerlin,
Identifying Novel Genes for Atherosclerosis through Mouse-Human Comparative Genetics  Xiaosong Wang, Naoki Ishimori, Ron Korstanje, Jarod Rollins, Beverly.
Genomewide Search and Genetic Localization of a Second Gene Associated with Autosomal Dominant Branchio-Oto-Renal Syndrome: Clinical and Genetic Implications 
Table of contents The Journal for Nurse Practitioners
Genome Scan of Human Systemic Lupus Erythematosus by Regression Modeling: Evidence of Linkage and Epistasis at 4p   C. Gray-McGuire, K.L. Moser,
Markers for Mapping by Admixture Linkage Disequilibrium in African American and Hispanic Populations  Michael W. Smith, James A. Lautenberger, Hyoung.
Tao Wang, Robert C. Elston  The American Journal of Human Genetics 
A Quantitative-Trait Locus on Chromosome 6p Influences Different Aspects of Developmental Dyslexia  Simon E. Fisher, Angela J. Marlow, Janine Lamb, Elena.
Alice S. Whittemore, Jerry Halpern 
Gonçalo R. Abecasis, Janis E. Wigginton 
The Size Distribution of Homozygous Segments in the Human Genome
Presentation transcript:

Evidence for Linkage and Association with Reading Disability, on 6p21 D.E. Kaplan, J. Gayán, J. Ahn, T.-W. Won, D. Pauls, R.K. Olson, J.C. DeFries, F. Wood, B.F. Pennington, G.P. Page, S.D. Smith, J.R. Gruen  The American Journal of Human Genetics  Volume 70, Issue 5, Pages 1287-1298 (May 2002) DOI: 10.1086/340449 Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 1 Location and distribution of the 29 STR markers used for linkage and association studies as described elsewhere (J. Ahn, T.-W. Won, D. E. Kaplan, E. R. Londin, P. Kuzmic, J. Gelernter, and J. R. Gruen, unpublished data). The American Journal of Human Genetics 2002 70, 1287-1298DOI: (10.1086/340449) Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 2 T scores across the chromosomal region for the most significant test of linkage for each phenotype. Chromosomal location (in cM) is expressed proximally from JA01. The American Journal of Human Genetics 2002 70, 1287-1298DOI: (10.1086/340449) Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 3 Significant results from QTDT output for the orthogonal model of association with environmental, polygenic, and additive major locus variance-components modeling. All results with P <.02 are graphed corresponding to table 3. Significance levels are shown on the basis of the nominal P values from the QTDT output. The American Journal of Human Genetics 2002 70, 1287-1298DOI: (10.1086/340449) Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 4 Graphical output from GOLD (Abecasis and Cookson 2000), showing intermarker linkage disequilibrium (D′) independent of reading phenotype data. The American Journal of Human Genetics 2002 70, 1287-1298DOI: (10.1086/340449) Copyright © 2002 The American Society of Human Genetics Terms and Conditions