| 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 |
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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 |
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| 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 receivedat lea |
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| This Month in the Journal |
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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 |
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| Letter from the Editor |
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| Announcements11Announcements 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 lea |
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| This Month in the Journal |
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| This Month in the Journal |
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| This Month in the Journal |
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| This Month in the Journal |
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| Announcements |
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| This Month in the Journal |
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| Editorial Reviewers for 2005 |
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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 l |
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| Employment Opportunities; Conference |
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| Contents of Volume 77 |
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| 2004 Cotterman Award Winners |
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| 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 |
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| Embracing Our Duty |
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| This Month in the Journal |
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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 |
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| 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 |
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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 |
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| Employment Opportunities; Conferences; Symposium |
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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 |
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| This Month in the Journal |
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| This Month in the Journal |
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| Contents of Volume 76 |
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| Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios |
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✓ |
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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 |
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| Erratum |
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| 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 |
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| The Role of Mannosylated Enzyme and the Mannose Receptor in Enzyme Replacement Therapy |
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| Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts Syndrome: No Phenotype-Genotype Correlation |
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| A Homozygous Missense Mutation in TGM5 Abolishes Epidermal Transglutaminase 5 Activity and Causes Acral Peeling Skin Syndrome |
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| Genetic Testing for Cancer: Psychological Approaches for Helping Patients and Families. |
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| GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study |
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| 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 |
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| Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination |
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| Preferential Transmission of Paternal Alleles at Risk Genes in Attention-Deficit/Hyperactivity Disorder |
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| The Effect of Single-Nucleotide Polymorphism Marker Selection on Patterns of Haplotype Blocks and Haplotype Frequency Estimates |
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| Identification of an X-Chromosomal Locus and Haplotype Modulating the Phenotype of a Mitochondrial DNA Disorder |
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| Comparative Genomics and Gene Expression Analysis Identifies BBS9, a New Bardet-Biedl Syndrome Gene |
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| Discriminating Power of Localized Three-Dimensional Facial Morphology |
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| NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome |
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| The Y Deletion gr/gr and Susceptibility to Testicular Germ Cell Tumor |
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| Velo-cardio-facial Syndrome: A Model for Understanding Microdeletion Disorders. |
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| Recent Spread of a Y-Chromosomal Lineage in Northern China and Mongolia |
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| 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 |
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✓ |
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European Samples |
| A Genomewide Linkage Study of 1,933 Families Affected by Premature Coronary Artery Disease: The British Heart Foundation (BHF) Family Heart Study |
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| Erratum |
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| Mutations in TCF8 Cause Posterior Polymorphous Corneal Dystrophy and Ectopic Expression of COL4A3 by Corneal Endothelial Cells |
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| A Constrained-Likelihood Approach to Marker-Trait Association Studies |
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| Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus |
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| Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment. |
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| High-Resolution Whole-Genome Association Study of Parkinson Disease |
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| High-Resolution Identification of Chromosomal Abnormalities Using Oligonucleotide Arrays Containing 116,204 SNPs |
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| Multiple Correcting COL17A1 Mutations in Patients with Revertant Mosaicism of Epidermolysis Bullosa |
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| Handling Marker-Marker Linkage Disequilibrium: Pedigree Analysis with Clustered Markers |
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| Reply to Castiglia et al. |
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| Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor |
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| Curcumin Treatment Abrogates Endoplasmic Reticulum Retention and Aggregation-Induced Apoptosis Associated with Neuropathy-Causing Myelin Protein Zero–Truncating Mutants |
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| The Heritage of Pathogen Pressures and Ancient Demography in the Human Innate-Immunity CD209/CD209L Region |
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| Evidence for Widespread Reticulate Evolution within Human Duplicons |
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| Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome |
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| Narrowing the Candidate Region for Congenital Diaphragmatic Hernia in Chromosome 15q26: Contradictory Results |
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| Promoter and 3′-Untranslated-Region Haplotypes in the Vitamin D Receptor Gene Predispose to Osteoporotic Fracture: The Rotterdam Study |
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| A Novel Method with Improved Power To Detect Recombination Hotspots from Polymorphism Data Reveals Multiple Hotspots in Human Genes |
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| Severely Incapacitating Mutations in Patients with Extreme Short Stature Identify RNA-Processing Endoribonuclease RMRP as an Essential Cell Growth Regulator |
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| Genetics of Developmental Disabilities. |
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| A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis |
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| Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q |
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| Loss of Desmoplakin Tail Causes Lethal Acantholytic Epidermolysis Bullosa* |
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| Neurofibromatosis: A Handbook for Patients, Families, and Healthcare Professionals, |
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| PTPN22 Genetic Variation: Evidence for Multiple Variants Associated with Rheumatoid Arthritis |
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| Assessment of the Effect of Age at Onset on Linkage to Bipolar Disorder: Evidence on Chromosomes 18p and 21q |
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| Linkage Disequilibrium Mapping of Quantitative-Trait Loci by Selective Genotyping |
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| Identification of Four Gene Variants Associated with Myocardial Infarction |
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| Charting the Ancestry of African Americans |
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| Sex, Not Genotype, Determines Recombination Levels in Mice |
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| Diagnostic Genome Profiling in Mental Retardation |
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| The β-Globin Recombinational Hotspot Reduces the Effects of Strong Selection around HbC, a Recently Arisen Mutation Providing Resistance to Malaria |
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| Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample |
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| A Hybrid Design for Studying Genetic Influences on Risk of Diseases with Onset Early in Life |
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| Meiotic Synapsis Proceeds from a Limited Number of Subtelomeric Sites in the Human Male |
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| The Use of Racial, Ethnic, and Ancestral Categories in Human Genetics Research |
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| A Variant in XPNPEP2 Is Associated with Angioedema Induced by Angiotensin I–Converting Enzyme Inhibitors |
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| Genetic Evidence for a Distinct Subtype of Schizophrenia Characterized by Pervasive Cognitive Deficit |
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| The BTNL2 Gene and Sarcoidosis Susceptibility in African Americans and Whites |
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| On Rapid Simulation of P Values in Association Studies |
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| Y-Chromosome Evidence of Southern Origin of the East Asian–Specific Haplogroup O3-M122 |
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| Genomewide Significant Linkage to Migrainous Headache on Chromosome 5q21 |
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| Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin |
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✓ |
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Ancient European Origin |
| Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males |
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| Genomewide Linkage Study in 1,176 Affected Sister Pair Families Identifies a Significant Susceptibility Locus for Endometriosis on Chromosome 10q26 |
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| An Algorithm to Construct Genetically Similar Subsets of Families with the Use of Self-Reported Ethnicity Information |
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| Recent Developments in Genomewide Association Scans: A Workshop Summary and Review |
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| Differential X Reactivation in Human Placental Cells: Implications for Reversal of X Inactivation |
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| Reply to Lin |
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| Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism |
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| Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification |
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| A Mutation in the Variable Repeat Region of the Aggrecan Gene (AGC1) Causes a Form of Spondyloepiphyseal Dysplasia Associated with Severe, Premature Osteoarthritis |
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| Susceptibility Genes for Age-Related Maculopathy on Chromosome 10q26 |
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| A High-Density SNP Genomewide Linkage Scan for Chronic Lymphocytic Leukemia–Susceptibility Loci |
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| A High-Density Screen for Linkage in Multiple Sclerosis |
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| Erratum |
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| Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations |
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| Weighting Affected Sib Pairs by Marker Informativity |
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| 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 |
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| A Genomewide Scan for Intelligence Identifies Quantitative Trait Loci on 2q and 6p |
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| A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy |
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| Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome |
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| Use of the Term “Antley-Bixler Syndrome”: Minimizing Confusion |
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| Dysregulation of Chondrogenesis in Human Cleidocranial Dysplasia |
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| LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century |
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✓ |
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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 |
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| Identification of Risk and Age-at-Onset Genes on Chromosome 1p in Parkinson Disease |
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| Allelic Heterogeneity at the Serotonin Transporter Locus (SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors |
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| “Antley-Bixler Syndrome”—A Reply to Cragun and Hopkin |
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| A Combined Genomewide Linkage Scan of 1,233 Families for Prostate Cancer–Susceptibility Genes Conducted by the International Consortium for Prostate Cancer Genetics |
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| A “Fille du Roy” Introduced the T14484C Leber Hereditary Optic Neuropathy Mutation in French Canadians |
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✓ |
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French Canadians |
| How Malaria Has Affected the Human Genome and What Human Genetics Can Teach Us about Malaria |
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| Guide to Mutation Detection |
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| Germline Susceptibility to Colorectal Cancer Due to Base-Excision Repair Gene Defects |
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| An Entropy-Based Statistic for Genomewide Association Studies |
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| Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy |
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| Polymorphisms within the C-Reactive Protein (CRP) Promoter Region Are Associated with Plasma CRP Levels |
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| Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS |
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| Identifying Novel Genes for Atherosclerosis through Mouse-Human Comparative Genetics |
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| Biotin-Responsive Basal Ganglia Disease Maps to 2q36.3 and Is Due to Mutations in SLC19A3 |
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| Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems |
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| Disentangling Fetal and Maternal Susceptibility for Pre-Eclampsia: A British Multicenter Candidate-Gene Study |
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| Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene |
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| Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells |
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| Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia |
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| Strong Association of the Y402H Variant in Complement Factor H at 1q32 with Susceptibility to Age-Related Macular Degeneration |
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| Segmental Duplications and Copy-Number Variation in the Human Genome |
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| 3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome |
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| Identification of a Major Recombination Hotspot in Patients with Short Stature and SHOX Deficiency |
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| A Powerful and Robust Method for Mapping Quantitative Trait Loci in General Pedigrees |
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| Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations |
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| Single-Gene Disorders: What Role Could Moonlighting Enzymes Play? |
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| 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 |
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| Rational Inferences about Departures from Hardy-Weinberg Equilibrium |
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| Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion |
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| Joint Modeling of Linkage and Association: Identifying SNPs Responsible for a Linkage Signal |
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| Replication of Autism Linkage: Fine-Mapping Peak at 17q21 |
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| A Genomewide Exploration Suggests a New Candidate Gene at Chromosome 11q23 as the Major Determinant of Plasma Homocysteine Levels: Results from the GAIT Project |
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| Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT |
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| In Silico Analysis of Disease-Association Mapping Strategies Using the Coalescent Process and Incorporating Ascertainment and Selection |
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| Alternative Splicing Suggests Extended Function of PEX26 in Peroxisome Biogenesis |
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| Facioscapulohumeral Muscular Dystrophy: Clinical Medicine and Molecular Cell Biology. |
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| Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits |
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| ERRATUM |
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| A Novel Linkage to Generalized Vitiligo on 4q13-q21 Identified in a Genomewide Linkage Analysis of Chinese Families |
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| Human Evolutionary Genetics: Origins, Peoples and Disease. |
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| Germline BHD-Mutation Spectrum and Phenotype Analysis of a Large Cohort of Families with Birt-Hogg-Dubé Syndrome |
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| Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human Genome |
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| A Note on Exact Tests of Hardy-Weinberg Equilibrium |
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| The Dual Origin of the Malagasy in Island Southeast Asia and East Africa: Evidence from Maternal and Paternal Lineages |
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| Identifying Candidate Hirschsprung Disease–Associated RET Variants |
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| Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design |
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| Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization |
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| Autosomal Recessive Primary Microcephaly (MCPH): A Review of Clinical, Molecular, and Evolutionary Findings |
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| A Novel STX16 Deletion in Autosomal Dominant Pseudohypoparathyroidism Type Ib Redefines the Boundaries of a cis-Acting Imprinting Control Element of GNAS |
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| The Epsin 4 Gene on Chromosome 5q, Which Encodes the Clathrin-Associated Protein Enthoprotin, Is Involved in the Genetic Susceptibility to Schizophrenia |
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| Quantitative Founder-Effect Analysis of French Canadian Families Identifies Specific Loci Contributing to Metabolic Phenotypes of Hypertension |
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✓ |
|
French Canadian Families |
| Diversity and Function of Mutations in P450 Oxidoreductase in Patients with Antley-Bixler Syndrome and Disordered Steroidogenesis |
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| Nonparametric Tests of Association of Multiple Genes with Human Disease |
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| Single- and Multilocus Allelic Variants within the GABAB Receptor Subunit 2 (GABAB2) Gene Are Significantly Associated with Nicotine Dependence |
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| Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome |
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| Localization of a Type 1 Diabetes Locus in the IL2RA/CD25 Region by Use of Tag Single-Nucleotide Polymorphisms |
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| Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis |
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| Saami and Berbers—An Unexpected Mitochondrial DNA Link |
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| Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism |
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| Population Genetics of CAPN10 and GPR35: Implications for the Evolution of Type 2 Diabetes Variants |
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| The X in Sex: How the X Chromosome Controls our Lives. |
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| Position Effects Due to Chromosome Breakpoints that Map ∼900 Kb Upstream and ∼1.3 Mb Downstream of SOX9 in Two Patients with Campomelic Dysplasia |
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| Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations |
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✓ |
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|
European Populations |
| Erratum |
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| Erratum |
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| No Convincing Evidence of Linkage for Restless Legs Syndrome on Chromosome 9p |
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| Analysis of Families in the Multiple Autoimmune Disease Genetics Consortium (MADGC) Collection: the PTPN22 620W Allele Associates with Multiple Autoimmune Phenotypes |
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| Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease |
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| Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia |
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| Erratum |
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| Genetic Association Analysis Using Data from Triads and Unrelated Subjects |
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| Genomewide Significant Linkage to Stuttering on Chromosome 12 |
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| Fine Mapping of Chromosome 17 Translocation Breakpoints ⩾900 Kb Upstream of SOX9 in Acampomelic Campomelic Dysplasia and a Mild, Familial Skeletal Dysplasia |
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| A Comparison of Linkage Disequilibrium Patterns and Estimated Population Recombination Rates across Multiple Populations |
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| Effects of Updating Linkage Evidence across Subsets of Data: Reanalysis of the Autism Genetic Resource Exchange Data Set |
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| Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations |
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| 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 |
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| A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms |
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| Reply to Ray and Weeks: Linkage for Restless Legs Syndrome on Chromosome 9p Is Significant |
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| Gene-Environment Interaction Effects on the Development of Immune Responses in the 1st Year of Life |
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| PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome |
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|
| Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations |
|
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|
✓ |
|
|
|
European Populations |
| The Principles of Clinical Cytogenetics, second edition. |
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| The D4Z4 Repeat–Mediated Pathogenesis of Facioscapulohumeral Muscular Dystrophy |
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|
| Accuracy of Haplotype Reconstruction from Haplotype-Tagging Single-Nucleotide Polymorphisms |
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| Accounting for Decay of Linkage Disequilibrium in Haplotype Inference and Missing-Data Imputation |
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|
| Association between the Gene Encoding 5-Lipoxygenase–Activating Protein and Stroke Replicated in a Scottish Population |
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| Rapid Simulation of P Values for Product Methods and Multiple-Testing Adjustment in Association Studies |
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|
| Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy |
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|
| No Evidence of Association or Interaction between the IL4RA, IL4, and IL13 Genes in Type 1 Diabetes |
|
|
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|
|
| Possible Genomic Imprinting of Three Human Obesity–Related Genetic Loci |
|
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|
| A 4-bp Deletion in the Birt-Hogg-Dubé Gene (FLCN) Causes Dominantly Inherited Spontaneous Pneumothorax |
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|
| Polymorphisms in the Tyrosine Kinase 2 and Interferon Regulatory Factor 5 Genes Are Associated with Systemic Lupus Erythematosus |
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|
| Association Testing in a Linked Region Using Large Pedigrees |
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|
| Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome |
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|
| Functional Consequences of PRODH Missense Mutations |
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|
| Population Structure, Admixture, and Aging-Related Phenotypes in African American Adults: The Cardiovascular Health Study |
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|
| 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 |
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| Constitutional Rearrangement of the Architectural Factor HMGA2: A Novel Human Phenotype Including Overgrowth and Lipomas |
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|
| Dent Disease with Mutations in OCRL1 |
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|
| Contrasting Effects of Natural Selection on Human and Chimpanzee CC Chemokine Receptor 5 |
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|
| Introductory Speech for Neil Risch* |
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|
| Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation |
|
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|
|
| High-Resolution Mapping of Genotype-Phenotype Relationships in Cri du Chat Syndrome Using Array Comparative Genomic Hybridization |
|
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|
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|
|
| 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 |
|
|
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|
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|
|
| Genetic Structure, Self-Identified Race/Ethnicity, and Confounding in Case-Control Association Studies |
|
|
|
|
|
|
✓ |
|
Self-Identified Race/Ethnicity |
| ERRATUM |
|
|
|
|
|
|
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|
|
| What Is Special about the “Human” in “Human Genetics”?* |
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|
|
| Ethnicity and Human Genetic Linkage Maps |
|
|
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|
|
| Introductory Speech for Louis Kunkel* |
|
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|
| Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy |
|
|
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|
|
| Fine Mapping and Positional Candidate Studies Identify HLA-G as an Asthma Susceptibility Gene on Chromosome 6p21 |
|
|
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|
|
| Introductory Speech for Robert J. Gorlin* |
|
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|
|
| And the Band Played On…* |
|
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|
| Mutations in the d-2-Hydroxyglutarate Dehydrogenase Gene Cause d-2-Hydroxyglutaric Aciduria |
|
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|
| The Genetics of Renal Disease. |
|
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| Inborn Errors of Development: The Molecular Basis of Clinical Disorders of Morphogenesis. |
|
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|
| Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation |
|
|
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|
|
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|
|
|
| ERRATUM |
|
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|
| The SNP Endgame: A Multidisciplinary Approach* |
|
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|
|
| A New Susceptibility Locus for Migraine with Aura in the 15q11-q13 Genomic Region Containing Three GABA-A Receptor Genes |
|
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|
|
| Role of Replication and CpG Methylation in Fragile X Syndrome CGG Deletions in Primate Cells |
|
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|
|
| Cloning of the DMD Gene* |
|
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|
| Regression Mapping of Association between the Human Leukocyte Antigen Region and Graves Disease |
|
|
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|
|
| A Whole-Genome Scan for 24-Hour Respiration Rate: A Major Locus at 10q26 Influences Respiration During Sleep |
|
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|
|
| Extreme Heterogeneity in the Molecular Events Leading to the Establishment of Chiasmata during Meiosis I in Human Oocytes |
|
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|
|
| Sex-Specific Genetic Architecture of Whole Blood Serotonin Levels |
|
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|
|
| Long-Range Control of Gene Expression: Emerging Mechanisms and Disruption in Disease |
|
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|
|
| Prospects for Admixture Mapping of Complex Traits |
|
|
|
|
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|
|
| 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 |
|
|
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|
|
| Mutations within the Programmed Cell Death 10 Gene Cause Cerebral Cavernous Malformations |
|
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|
| Examining the Farming/Language Dispersal Hypothesis. |
|
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| Erratum |
|
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|
| Systematic Evaluation of Genetic Variation at the Androgen Receptor Locus and Risk of Prostate Cancer in a Multiethnic Cohort Study |
|
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|
|
| 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 |
|
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|
|
| The R620W Polymorphism of the Protein Tyrosine Phosphatase PTPN22 Is Not Associated with Multiple Sclerosis |
|
|
|
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|
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|
|
| Erratum |
|
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|
|
| Robust Multipoint Identical-by-Descent Mapping for Affected Relative Pairs |
|
|
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|
|
| Mapping of a Major Locus that Determines Telomere Length in Humans |
|
|
|
|
|
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|
|
| Malic Enzyme 2 May Underlie Susceptibility to Adolescent-Onset Idiopathic Generalized Epilepsy |
|
|
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|
|
| Mathematical Assumptions versus Biological Reality: Myths in Affected Sib Pair Linkage Analysis |
|
|
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|
|
| Mapping a Mendelian Form of Intracranial Aneurysm to 1p34.3-p36.13 |
|
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|
| Statistical Methods in Genetic Epidemiology. |
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|
| Association between Maternal Age and Meiotic Recombination for Trisomy 21 |
|
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| Erratum |
|
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|
| Strong Evidence of Linkage Disequilibrium between Polymorphisms at the IRF6 Locus and Nonsyndromic Cleft Lip With or Without Cleft Palate, in an Italian Population |
|
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|
|
| Mapping of the Major Psoriasis-Susceptibility Locus (PSORS1) in a 70-Kb Interval around the Corneodesmosin Gene (CDSN) |
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