Volume 41, Issue 1

Search all Behavior Genetics articles

January 2011

Learning Disabilities

Issue Editors:

Brett Miller,
Elena L. Grigorenko

17 articles in this issue

Moving Closer to a Public Health Model of Language and Learning Disabilities: The Role of Genetics and the Search for Etiologies
Brett Miller
Peggy McCardle
Original Research 13 January 2011 Pages: 1 - 5
In Search of the Perfect Phenotype: An Analysis of Linkage and Association Studies of Reading and Reading-Related Processes
Thomas Skiba
Nicole Landi
Elena L. Grigorenko
Original Research 19 January 2011 Pages: 6 - 30
Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization
Kevin Rubenstein
Mark Matsushita
Ellen M. Wijsman
ORIGINAL RESEARCH 18 September 2010 Pages: 31 - 42
Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan
Idor Svensson
Staffan Nilsson
Erland Hjelmquist
ORIGINAL RESEARCH 23 September 2010 Pages: 43 - 49
Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits
Timothy C. Bates
Michelle Luciano
Nicholas G. Martin
ORIGINAL RESEARCH 15 October 2010 Pages: 50 - 57
A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression
Haiying Meng
Natalie R. Powers
Jeffrey R. Gruen
ORIGINAL RESEARCH 02 November 2010 Pages: 58 - 66
Pleiotropic Effects of DCDC2 and DYX1C1 Genes on Language and Mathematics Traits in Nuclear Families of Developmental Dyslexia
Cecilia Marino
Sara Mascheretti
Massimo Molteni
ORIGINAL RESEARCH 03 November 2010 Pages: 67 - 76
Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia
Adrienne Elbert
Maureen W. Lovett
Cathy L. Barr
Original Research 05 January 2011 Pages: 77 - 89
Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects
D. F. Newbury
S. Paracchini
A. P. Monaco
Original Research Open access 17 December 2010 Pages: 90 - 104
An Examination of Candidate Gene SNPs for Dyslexia in an Indian Sample
Shyamala K. Venkatesh
Anand Siddaiah
Nallur B. Ramachandra
Original Research 04 January 2011 Pages: 105 - 109
Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia
Darina Czamara
Jennifer Bruder
Gerd Schulte-Körne
ORIGINAL RESEARCH 21 November 2010 Pages: 110 - 119
An Application of the Elastic Net for an Endophenotype Analysis
Dean Palejev
Wookyeon Hwang
Elena L. Grigorenko
Original Research 13 January 2011 Pages: 120 - 124
A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1
Roberta Buonincontri
Iben Bache
Niels Tommerup
ORIGINAL RESEARCH 27 August 2010 Pages: 125 - 133
SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations
Hans Matsson
Kristiina Tammimies
Myriam Peyrard-Janvid
Original Research 04 January 2011 Pages: 134 - 140
Gene-Environment Interaction in the Etiology of Mathematical Ability Using SNP Sets
Sophia J. Docherty
Yulia Kovas
Robert Plomin
ORIGINAL RESEARCH Open access 27 October 2010 Pages: 141 - 154
Influence of Candidate Genes on Attention Problems in Children: A Longitudinal Study
Catherina E. M. van Beijsterveldt
Christel M. Middeldorp
Dorret I. Boomsma
ORIGINAL RESEARCH Open access 30 October 2010 Pages: 155 - 164
A Family Based Association Study of DRD4, DAT1, and 5HTT and Continuous Traits of Attention-Deficit Hyperactivity Disorder
L. Cinnamon Bidwell
Erik G. Willcutt
Bruce F. Pennington
Original Research 05 January 2011 Pages: 165 - 174

Volume 41, Issue 1

Moving Closer to a Public Health Model of Language and Learning Disabilities: The Role of Genetics and the Search for Etiologies

In Search of the Perfect Phenotype: An Analysis of Linkage and Association Studies of Reading and Reading-Related Processes

Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization

Familial Dyslexia in a Large Swedish Family: A Whole Genome Linkage Scan

Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits

A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

Pleiotropic Effects of DCDC2 and DYX1C1 Genes on Language and Mathematics Traits in Nuclear Families of Developmental Dyslexia

Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

An Examination of Candidate Gene SNPs for Dyslexia in an Indian Sample

Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia

An Application of the Elastic Net for an Endophenotype Analysis

A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1

SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations

Gene-Environment Interaction in the Etiology of Mathematical Ability Using SNP Sets

Influence of Candidate Genes on Attention Problems in Children: A Longitudinal Study

A Family Based Association Study of DRD4, DAT1, and 5HTT and Continuous Traits of Attention-Deficit Hyperactivity Disorder

Navigation