The American Journal of Human Genetics - 2005

269 articles | Last updated: 2025-12-03 14:12:57
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T A T A T A T A
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This Month in the Journal
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Announcements11. Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to [email protected]. Submission must be received at
Letter from the Editor
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This Month in the Journal
This Month in the Journal
This Month in the Journal
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Announcements
This Month in the Journal
Editorial Reviewers for 2005
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Employment Opportunities; Conference
Contents of Volume 77
2004 Cotterman Award Winners
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Embracing Our Duty
This Month in the Journal
This Month in the Journal
This Month in the Journal
Announcements11. Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to [email protected]. Submission must be received at
Announcements**Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to [email protected]. Submission must be received at le
Announcements11. Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to [email protected]. Submission must be received at
Employment Opportunities; Conferences; Symposium
Announcements11. Announcements are published free of charge for members of The American Society of Human Genetics (ASHG). Please e-mail announcements to [email protected]. Submission must be received at
This Month in the Journal
This Month in the Journal
Contents of Volume 76
Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios Ashkenazi Jewish
Genomewide High-Density SNP Linkage Analysis of 236 Japanese Families Supports the Existence of Schizophrenia Susceptibility Loci on Chromosomes 1p, 14q, and 20p
Erratum
Replication of Putative Candidate-Gene Associations with Rheumatoid Arthritis in >4,000 Samples from North America and Sweden: Association of Susceptibility with PTPN22, CTLA4, and PADI4
The Role of Mannosylated Enzyme and the Mannose Receptor in Enzyme Replacement Therapy
Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts Syndrome: No Phenotype-Genotype Correlation
A Homozygous Missense Mutation in TGM5 Abolishes Epidermal Transglutaminase 5 Activity and Causes Acral Peeling Skin Syndrome
Genetic Testing for Cancer: Psychological Approaches for Helping Patients and Families.
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Robust Estimation of Experimentwise P Values Applied to a Genome Scan of Multiple Asthma Traits Identifies a New Region of Significant Linkage on Chromosome 20q13
Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination
Preferential Transmission of Paternal Alleles at Risk Genes in Attention-Deficit/Hyperactivity Disorder
The Effect of Single-Nucleotide Polymorphism Marker Selection on Patterns of Haplotype Blocks and Haplotype Frequency Estimates
Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder
Comparative Genomics and Gene Expression Analysis Identifies BBS9, a New Bardet-Biedl Syndrome Gene
Discriminating Power of Localized Three-Dimensional Facial Morphology
NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome
The Y Deletion gr/gr and Susceptibility to Testicular Germ Cell Tumor
Velo-cardio-facial Syndrome: A Model for Understanding Microdeletion Disorders.
Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia
Genomewide Scan and Fine-Mapping Linkage Studies in Four European Samples with Bipolar Affective Disorder Suggest a New Susceptibility Locus on Chromosome 1p35-p36 and Provides Further Evidence of Loc European Samples
A Genomewide Linkage Study of 1,933 Families Affected by Premature Coronary Artery Disease: The British Heart Foundation (BHF) Family Heart Study
Erratum
Mutations in TCF8 Cause Posterior Polymorphous Corneal Dystrophy and Ectopic Expression of COL4A3 by Corneal Endothelial Cells
A Constrained-Likelihood Approach to Marker-Trait Association Studies
Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus
Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment.
High-Resolution Whole-Genome Association Study of Parkinson Disease
High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs
Multiple Correcting COL17A1 Mutations in Patients with Revertant Mosaicism of Epidermolysis Bullosa
Handling Marker-Marker Linkage Disequilibrium: Pedigree Analysis with Clustered Markers
Reply to Castiglia et al.
Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor
Curcumin Treatment Abrogates Endoplasmic Reticulum Retention and Aggregation-Induced Apoptosis Associated with Neuropathy-Causing Myelin Protein Zero–Truncating Mutants
The Heritage of Pathogen Pressures and Ancient Demography in the Human Innate-Immunity CD209/CD209L Region
Evidence for Widespread Reticulate Evolution within Human Duplicons
Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome
Narrowing the Candidate Region for Congenital Diaphragmatic Hernia in Chromosome 15q26: Contradictory Results
Promoter and 3′-Untranslated-Region Haplotypes in the Vitamin D Receptor Gene Predispose to Osteoporotic Fracture: The Rotterdam Study
A Novel Method with Improved Power To Detect Recombination Hotspots from Polymorphism Data Reveals Multiple Hotspots in Human Genes
Severely Incapacitating Mutations in Patients with Extreme Short Stature Identify RNA-Processing Endoribonuclease RMRP as an Essential Cell Growth Regulator
Genetics of Developmental Disabilities.
A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis
Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q
Loss of Desmoplakin Tail Causes Lethal Acantholytic Epidermolysis Bullosa*
Neurofibromatosis: A Handbook for Patients, Families, and Healthcare Professionals,
PTPN22 Genetic Variation: Evidence for Multiple Variants Associated with Rheumatoid Arthritis
Assessment of the Effect of Age at Onset on Linkage to Bipolar Disorder: Evidence on Chromosomes 18p and 21q
Linkage Disequilibrium Mapping of Quantitative-Trait Loci by Selective Genotyping
Identification of Four Gene Variants Associated with Myocardial Infarction
Charting the Ancestry of African Americans
Sex, Not Genotype, Determines Recombination Levels in Mice
Diagnostic Genome Profiling in Mental Retardation
The β-Globin Recombinational Hotspot Reduces the Effects of Strong Selection around HbC, a Recently Arisen Mutation Providing Resistance to Malaria
Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample
A Hybrid Design for Studying Genetic Influences on Risk of Diseases with Onset Early in Life
Meiotic Synapsis Proceeds from a Limited Number of Subtelomeric Sites in the Human Male
The Use of Racial, Ethnic, and Ancestral Categories in Human Genetics Research
A Variant in XPNPEP2 Is Associated with Angioedema Induced by Angiotensin I–Converting Enzyme Inhibitors
Genetic Evidence for a Distinct Subtype of Schizophrenia Characterized by Pervasive Cognitive Deficit
The BTNL2 Gene and Sarcoidosis Susceptibility in African Americans and Whites
On Rapid Simulation of P Values in Association Studies
Y-Chromosome Evidence of Southern Origin of the East Asian–Specific Haplogroup O3-M122
Genomewide Significant Linkage to Migrainous Headache on Chromosome 5q21
Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin Ancient European Origin
Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males
Genomewide Linkage Study in 1,176 Affected Sister Pair Families Identifies a Significant Susceptibility Locus for Endometriosis on Chromosome 10q26
An Algorithm to Construct Genetically Similar Subsets of Families with the Use of Self-Reported Ethnicity Information
Recent Developments in Genomewide Association Scans: A Workshop Summary and Review
Differential X Reactivation in Human Placental Cells: Implications for Reversal of X Inactivation
Reply to Lin
Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism
Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification
A Mutation in the Variable Repeat Region of the Aggrecan Gene (AGC1) Causes a Form of Spondyloepiphyseal Dysplasia Associated with Severe, Premature Osteoarthritis
Susceptibility Genes for Age-Related Maculopathy on Chromosome 10q26
A High-Density SNP Genomewide Linkage Scan for Chronic Lymphocytic Leukemia–Susceptibility Loci
A High-Density Screen for Linkage in Multiple Sclerosis
Erratum
Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations
Weighting Affected Sib Pairs by Marker Informativity
A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmopl
A Genomewide Scan for Intelligence Identifies Quantitative Trait Loci on 2q and 6p
A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome
Use of the Term “Antley-Bixler Syndrome”: Minimizing Confusion
Dysregulation of Chondrogenesis in Human Cleidocranial Dysplasia
LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century European and North African Families
An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repe
Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson Disease
Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors
“Antley-Bixler Syndrome”—A Reply to Cragun and Hopkin
A Combined Genomewide Linkage Scan of 1,233 Families for Prostate Cancer–Susceptibility Genes Conducted by the International Consortium for Prostate Cancer Genetics
A “Fille du Roy” Introduced the T14484C Leber Hereditary Optic Neuropathy Mutation in French Canadians French Canadians
How Malaria Has Affected the Human Genome and What Human Genetics Can Teach Us about Malaria
Guide to Mutation Detection
Germline Susceptibility to Colorectal Cancer Due to Base-Excision Repair Gene Defects
An Entropy-Based Statistic for Genomewide Association Studies
Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy
Polymorphisms within the C-Reactive Protein (CRP) Promoter Region Are Associated with Plasma CRP Levels
Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS
Identifying Novel Genes for Atherosclerosis through Mouse-Human Comparative Genetics
Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3
Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems
Disentangling Fetal and Maternal Susceptibility for Pre-Eclampsia: A British Multicenter Candidate-Gene Study
Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene
Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells
Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
Strong Association of the Y402H Variant in Complement Factor H at 1q32 with Susceptibility to Age-Related Macular Degeneration
Segmental Duplications and Copy-Number Variation in the Human Genome
3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome
Identification of a Major Recombination Hotspot in Patients with Short Stature and SHOX Deficiency
A Powerful and Robust Method for Mapping Quantitative Trait Loci in General Pedigrees
Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations
Single-Gene Disorders: What Role Could Moonlighting Enzymes Play?
Fatal Congenital Heart Glycogenosis Caused by a Recurrent Activating R531Q Mutation in the γ2-Subunit of AMP-Activated Protein Kinase (PRKAG2), Not by Phosphorylase Kinase Deficiency
Rational Inferences about Departures from Hardy-Weinberg Equilibrium
Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion
Joint Modeling of Linkage and Association: Identifying SNPs Responsible for a Linkage Signal
Replication of Autism Linkage: Fine-Mapping Peak at 17q21
A Genomewide Exploration Suggests a New Candidate Gene at Chromosome 11q23 as the Major Determinant of Plasma Homocysteine Levels: Results from the GAIT Project
Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT
In Silico Analysis of Disease-Association Mapping Strategies Using the Coalescent Process and Incorporating Ascertainment and Selection
Alternative Splicing Suggests Extended Function of PEX26 in Peroxisome Biogenesis
Facioscapulohumeral Muscular Dystrophy: Clinical Medicine and Molecular Cell Biology.
Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits
ERRATUM
A Novel Linkage to Generalized Vitiligo on 4q13-q21 Identified in a Genomewide Linkage Analysis of Chinese Families
Human Evolutionary Genetics: Origins, Peoples and Disease.
Germline BHD-Mutation Spectrum and Phenotype Analysis of a Large Cohort of Families with Birt-Hogg-Dubé Syndrome
Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human Genome
A Note on Exact Tests of Hardy-Weinberg Equilibrium
The Dual Origin of the Malagasy in Island Southeast Asia and East Africa: Evidence from Maternal and Paternal Lineages
Identifying Candidate Hirschsprung Disease–Associated RET Variants
Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design
Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization
Autosomal Recessive Primary Microcephaly (MCPH): A Review of Clinical, Molecular, and Evolutionary Findings
A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS
The Epsin 4 Gene on Chromosome 5q, Which Encodes the Clathrin-Associated Protein Enthoprotin, Is Involved in the Genetic Susceptibility to Schizophrenia
Quantitative Founder-Effect Analysis of French Canadian Families Identifies Specific Loci Contributing to Metabolic Phenotypes of Hypertension French Canadian Families
Diversity and Function of Mutations in P450 Oxidoreductase in Patients with Antley-Bixler Syndrome and Disordered Steroidogenesis
Nonparametric Tests of Association of Multiple Genes with Human Disease
Single- and Multilocus Allelic Variants within the GABAB Receptor Subunit 2 (GABAB2) Gene Are Significantly Associated with Nicotine Dependence
Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome
Localization of a Type 1 Diabetes Locus in the IL2RA/CD25 Region by Use of Tag Single-Nucleotide Polymorphisms
Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis
Saami and Berbers—An Unexpected Mitochondrial DNA Link
Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism
Population Genetics of CAPN10 and GPR35: Implications for the Evolution of Type 2 Diabetes Variants
The X in Sex: How the X Chromosome Controls our Lives.
Position Effects Due to Chromosome Breakpoints that Map ∼900 Kb Upstream and ∼1.3 Mb Downstream of SOX9 in Two Patients with Campomelic Dysplasia
Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations European Populations
Erratum
Erratum
No Convincing Evidence of Linkage for Restless Legs Syndrome on Chromosome 9p
Analysis of Families in the Multiple Autoimmune Disease Genetics Consortium (MADGC) Collection: the PTPN22 620W Allele Associates with Multiple Autoimmune Phenotypes
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease
Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia
Erratum
Genetic Association Analysis Using Data from Triads and Unrelated Subjects
Genomewide Significant Linkage to Stuttering on Chromosome 12
Fine Mapping of Chromosome 17 Translocation Breakpoints ⩾900 Kb Upstream of SOX9 in Acampomelic Campomelic Dysplasia and a Mild, Familial Skeletal Dysplasia
A Comparison of Linkage Disequilibrium Patterns and Estimated Population Recombination Rates across Multiple Populations
Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set
Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations
Variation in Antiviral 2′,5′-Oligoadenylate Synthetase (2′5′AS) Enzyme Activity Is Controlled by a Single-Nucleotide Polymorphism at a Splice-Acceptor Site in the OAS1 Gene
A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms
Reply to Ray and Weeks: Linkage for Restless Legs Syndrome on Chromosome 9p Is Significant
Gene-Environment Interaction Effects on the Development of Immune Responses in the 1st Year of Life
PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome
Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations European Populations
The Principles of Clinical Cytogenetics, second edition.
The D4Z4 Repeat–Mediated Pathogenesis of Facioscapulohumeral Muscular Dystrophy
Accuracy of Haplotype Reconstruction from Haplotype-Tagging Single-Nucleotide Polymorphisms
Accounting for Decay of Linkage Disequilibrium in Haplotype Inference and Missing-Data Imputation
Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population
Rapid Simulation of P Values for Product Methods and Multiple-Testing Adjustment in Association Studies
Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy
No Evidence of Association or Interaction between the IL4RA, IL4, and IL13 Genes in Type 1 Diabetes
Possible Genomic Imprinting of Three Human Obesity–Related Genetic Loci
A 4-bp Deletion in the Birt-Hogg-Dubé Gene (FLCN) Causes Dominantly Inherited Spontaneous Pneumothorax
Polymorphisms in the Tyrosine Kinase 2 and Interferon Regulatory Factor 5 Genes Are Associated with Systemic Lupus Erythematosus
Association Testing in a Linked Region Using Large Pedigrees
Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome
Functional Consequences of PRODH Missense Mutations
Population Structure, Admixture, and Aging-Related Phenotypes in African American Adults: The Cardiovascular Health Study
Regulation of α-Synuclein Expression by Poly (ADP Ribose) Polymerase-1 (PARP-1) Binding to the NACP-Rep1 Polymorphic Site Upstream of the SNCA Gene
Constitutional Rearrangement of the Architectural Factor HMGA2: A Novel Human Phenotype Including Overgrowth and Lipomas
Dent Disease with Mutations in OCRL1
Contrasting Effects of Natural Selection on Human and Chimpanzee CC Chemokine Receptor 5
Introductory Speech for Neil Risch*
Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
High-Resolution Mapping of Genotype-Phenotype Relationships in Cri du Chat Syndrome Using Array Comparative Genomic Hybridization
Genomewide Scan for Affective Disorder Susceptibility Loci in Families of a Northern Swedish Isolated Population Northern Swedish Isolated Population
Parental Phenotypes in Family-Based Association Analysis
Genetic Structure, Self-Identified Race/Ethnicity, and Confounding in Case-Control Association Studies Self-Identified Race/Ethnicity
ERRATUM
What Is Special about the “Human” in “Human Genetics”?*
Ethnicity and Human Genetic Linkage Maps
Introductory Speech for Louis Kunkel*
Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy
Fine Mapping and Positional Candidate Studies Identify HLA-G as an Asthma Susceptibility Gene on Chromosome 6p21
Introductory Speech for Robert J. Gorlin*
And the Band Played On…*
Mutations in the d-2-Hydroxyglutarate Dehydrogenase Gene Cause d-2-Hydroxyglutaric Aciduria
The Genetics of Renal Disease.
Inborn Errors of Development: The Molecular Basis of Clinical Disorders of Morphogenesis.
Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation
ERRATUM
The SNP Endgame: A Multidisciplinary Approach*
A New Susceptibility Locus for Migraine with Aura in the 15q11-q13 Genomic Region Containing Three GABA-A Receptor Genes
Role of Replication and CpG Methylation in Fragile X Syndrome CGG Deletions in Primate Cells
Cloning of the DMD Gene*
Regression Mapping of Association between the Human Leukocyte Antigen Region and Graves Disease
A Whole-Genome Scan for 24-Hour Respiration Rate: A Major Locus at 10q26 Influences Respiration During Sleep
Extreme Heterogeneity in the Molecular Events Leading to the Establishment of Chiasmata during Meiosis I in Human Oocytes
Sex-Specific Genetic Architecture of Whole Blood Serotonin Levels
Long-Range Control of Gene Expression: Emerging Mechanisms and Disruption in Disease
Prospects for Admixture Mapping of Complex Traits
Identification of a 3.0-kb Major Recombination Hotspot in Patients with Sotos Syndrome Who Carry a Common 1.9-Mb Microdeletion
Genetic Investigation of Quantitative Traits Related to Autism: Use of Multivariate Polygenic Models with Ascertainment Adjustment
Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations
Examining the Farming/Language Dispersal Hypothesis.
Erratum
Systematic Evaluation of Genetic Variation at the Androgen Receptor Locus and Risk of Prostate Cancer in a Multiethnic Cohort Study
Corrections to the Parameterization of Constraints on Allele Sharing in Sibling Pairs Alter Covariate-Parameter Estimates but Not Sharing-Probability Estimates or Power of Tests for Linkage
The R620W Polymorphism of the Protein Tyrosine Phosphatase PTPN22 Is Not Associated with Multiple Sclerosis
Erratum
Robust Multipoint Identical-by-Descent Mapping for Affected Relative Pairs
Mapping of a Major Locus that Determines Telomere Length in Humans
Malic Enzyme 2 May Underlie Susceptibility to Adolescent-Onset Idiopathic Generalized Epilepsy
Mathematical Assumptions versus Biological Reality: Myths in Affected Sib Pair Linkage Analysis
Mapping a Mendelian Form of Intracranial Aneurysm to 1p34.3-p36.13
Statistical Methods in Genetic Epidemiology.
Association between Maternal Age and Meiotic Recombination for Trisomy 21
Erratum
Strong Evidence of Linkage Disequilibrium between Polymorphisms at the IRF6 Locus and Nonsyndromic Cleft Lip With or Without Cleft Palate, in an Italian Population
Mapping of the Major Psoriasis-Susceptibility Locus (PSORS1) in a 70-Kb Interval around the Corneodesmosin Gene (CDSN)