A Multi-Platform Draft de novo Genome Assembly and Comparative Analysis for the Scarlet Macaw (Ara macao)

Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease

(2017) Erin L. Heinzen et al.   JOURNAL OF ALZHEIMERS DISEASE

Multiple loci influencing hippocampal degeneration identified by genome scan

(2012) Scott A. Melville et al.   ANNALS OF NEUROLOGY

Titin mutation segregates with hereditary myopathy with early respiratory failure

(2012) Gerald Pfeffer et al.   BRAIN

Will the real aging Sirtuin please stand up?

(2012) Chen-Yu Liao et al.   CELL RESEARCH

Genome-wide association study of lung function decline in adults with and without asthma

(2012) Medea Imboden et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

(2012) Brian J. O’Roak et al.   NATURE

A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity

(2012) Lorna M. Lopez et al.   NEUROBIOLOGY OF AGING

Gene-Based Analysis of Regionally Enriched Cortical Genes in GWAS Data Sets of Cognitive Traits and Psychiatric Disorders

(2012) Kari M. Ersland et al.   PLoS One

Neuropeptide Y2 Receptor (NPY2R) Expression in Saliva Predicts Feeding Immaturity in the Premature Neonate

(2012) Jill L. Maron et al.   PLoS One

Disruption of ATP-binding cassette B8 in mice leads to cardiomyopathy through a decrease in mitochondrial iron export

(2012) Y. Ichikawa et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders

(2012) Patrícia BS Celestino-Soper et al.   Molecular Cytogenetics

A locally funded Puerto Rican parrot (Amazona vittata) genome sequencing project increases avian data and advances young researcher education

(2012) Taras K Oleksyk et al.   GigaScience

Birds and longevity: Does flight driven aerobicity provide an oxidative sink?

(2011) Anthony J.R. Hickey et al.   AGEING RESEARCH REVIEWS

GWAS Findings for Human Iris Patterns: Associations with Variants in Genes that Influence Normal Neuronal Pattern Development

(2011) Mats Larsson et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-Wide Association Scan for Survival on Dialysis in African-Americans with Type 2 Diabetes

(2011) Mariana Murea et al.   AMERICAN JOURNAL OF NEPHROLOGY

A Comprehensive Genetic Association Study of Alzheimer Disease in African Americans

(2011) Mark W. Logue   ARCHIVES OF NEUROLOGY

TimeTree2: species divergence times on the iPhone

(2011) S. Kumar et al.   BIOINFORMATICS

A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genes

(2011) David Della-Morte et al.   BMC Medical Genetics

Does the oxidative stress theory of aging explain longevity differences in birds? I. Mitochondrial ROS production

(2011) Magdalene K. Montgomery et al.   EXPERIMENTAL GERONTOLOGY

Comparative analysis of microsatellite variability in five macaw species (Psittaciformes, Psittacidae): application for conservation

(2011) Flavia T. Presti et al.   GENETICS AND MOLECULAR BIOLOGY

Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function

(2011) Jiyeon Choi et al.   HUMAN MOLECULAR GENETICS

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration

(2011) Yi Yu et al.   HUMAN MOLECULAR GENETICS

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

(2011) Simon Mead et al.   HUMAN MOLECULAR GENETICS

Genetic mapping of the major histocompatibility complex in the zebra finch (Taeniopygia guttata)

(2011) Robert Ekblom et al.   IMMUNOGENETICS

Predicted metabolizable energy density and amino acid profile of the crop contents of free-living scarlet macaw chicks (Ara macao)

(2011) J. Cornejo et al.   JOURNAL OF ANIMAL PHYSIOLOGY AND ANIMAL NUTRITION

Genome-Wide Association Study Implicates PARD3B-Based AIDS Restriction

(2011) J. L. Troyer et al.   JOURNAL OF INFECTIOUS DISEASES

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

(2011) Hossein Najmabadi et al.   NATURE

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

(2011) Vladimir Vacic et al.   NATURE

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

(2011) Irina Voineagu et al.   NATURE

Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci

(2011) Jaspal S Kooner et al.   NATURE GENETICS

Sex-chromosome evolution: recent progress and the influence of male and female heterogamety

(2011) Hans Ellegren   NATURE REVIEWS GENETICS

Genome-Wide Association Study Identifies Loci for Body Composition and Structural Soundness Traits in Pigs

(2011) Bin Fan et al.   PLoS One

Genome-Wide Polymorphism and Comparative Analyses in the White-Tailed Deer (Odocoileus virginianus): A Model for Conservation Genomics

(2011) Christopher M. Seabury et al.   PLoS One

In Silico Gene Prioritization by Integrating Multiple Data Sources

(2011) Yixuan Chen et al.   PLoS One

Wolf–Hirschhorn syndrome candidate 1 is involved in the cellular response to DNA damage

(2011) Ildiko Hajdu et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Roles of SATB2 in Osteogenic Differentiation and Bone Regeneration

(2011) Jin Zhang et al.   TISSUE ENGINEERING PART A

Cdk5rap2 exposes the centrosomal root of microcephaly syndromes

(2011) Timothy L. Megraw et al.   TRENDS IN CELL BIOLOGY

SNW1 Orchestrates BMP Signaling in Early Embryonic Patterning

(2011) Caitlin Sedwick   PLOS BIOLOGY

Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry

(2011) Amidou N'Diaye et al.   PLoS Genetics

A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci

(2011) Jonathan P. Bradfield et al.   PLoS Genetics

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

(2011) John P Hussman et al.   Molecular Autism

Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association

(2010) Cammon B. Arrington et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

(2010) Thais S. Rizzi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Association of retinoic acid receptor genes with meningomyelocele

(2010) Phong X. Tran et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Gene duplication and fragmentation in the zebra finch major histocompatibility complex

(2010) Christopher N Balakrishnan et al.   BMC BIOLOGY

Genome-wide analysis of tandem repeats in Daphnia pulex - a comparative approach

(2010) Christoph Mayer et al.   BMC GENOMICS

Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry

(2010) Nicholas L. Smith et al.   Circulation-Cardiovascular Genetics

Genomic Variation Associated With Mortality Among Adults of European and African Ancestry With Heart Failure

(2010) Alanna C. Morrison et al.   Circulation-Cardiovascular Genetics

Synteny Conservation of Chicken Macrochromosomes 1–10 in Different Avian Lineages Revealed by Cross-Species Chromosome Painting

(2010) I. Nanda et al.   CYTOGENETIC AND GENOME RESEARCH

Boc modifies the holoprosencephaly spectrum of Cdo mutant mice

(2010) W. Zhang et al.   Disease Models & Mechanisms

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

(2010) Stuart Macgregor et al.   HUMAN MOLECULAR GENETICS

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

(2010) Denise Horn et al.   HUMAN MUTATION

A genome-wide association study for diabetic nephropathy genes in African Americans

(2010) Caitrin W. McDonough et al.   KIDNEY INTERNATIONAL

Adaptive Evolution of Four Microcephaly Genes and the Evolution of Brain Size in Anthropoid Primates

(2010) S. H. Montgomery et al.   MOLECULAR BIOLOGY AND EVOLUTION

The genome of a songbird

(2010) Wesley C. Warren et al.   NATURE

Hundreds of variants clustered in genomic loci and biological pathways affect human height

(2010) Hana Lango Allen et al.   NATURE

Genome-wide association study of hematological and biochemical traits in a Japanese population

(2010) Yoichiro Kamatani et al.   NATURE GENETICS

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

(2010) Nona Sotoodehnia et al.   NATURE GENETICS

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

(2010) Benjamin F Voight et al.   NATURE GENETICS

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

(2010) Li Shen et al.   NEUROIMAGE

Being Attractive Brings Advantages: The Case of Parrot Species in Captivity

(2010) Daniel Frynta et al.   PLoS One

The Mohawk homeobox gene is a critical regulator of tendon differentiation

(2010) Y. Ito et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder

(2010) Ke-Sheng Wang et al.   SCHIZOPHRENIA RESEARCH

Genome-Wide Association Study of Height and Body Mass Index in Australian Twin Families

(2010) Jimmy Z. Liu et al.   Twin Research and Human Genetics

Multi-Platform Next-Generation Sequencing of the Domestic Turkey (Meleagris gallopavo): Genome Assembly and Analysis

(2010) Rami A. Dalloul et al.   PLOS BIOLOGY

Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in Spinocerebellar Ataxia Type 1 Pathogenesis

(2010) Juan Crespo-Barreto et al.   PLoS Genetics

An Integration of Genome-Wide Association Study and Gene Expression Profiling to Prioritize the Discovery of Novel Susceptibility Loci for Osteoporosis-Related Traits

(2010) Yi-Hsiang Hsu et al.   PLoS Genetics

Genome-Wide Identification of Susceptibility Alleles for Viral Infections through a Population Genetics Approach

(2010) Matteo Fumagalli et al.   PLoS Genetics

Impaired sociability and cognitive function in Nrcam-null mice

(2009) Sheryl S. Moy et al.   BEHAVIOURAL BRAIN RESEARCH

Evidence of uneven selective pressure on different subsets of the conserved human genome; implications for the significance of intronic and intergenic DNA

(2009) Scott Davidson et al.   BMC GENOMICS

Single nucleotide polymorphism discovery in rainbow trout by deep sequencing of a reduced representation library

(2009) Cecilia Sánchez et al.   BMC GENOMICS

A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations

(2009) Fabio Marroni et al.   Circulation-Cardiovascular Genetics

Genetic modulation of striatal volume by loci on Chrs 6 and 17 in BXD recombinant inbred mice

(2009) G. D. Rosen et al.   GENES BRAIN AND BEHAVIOR

Identification of 15 loci influencing height in a Korean population

(2009) Jae-Jung Kim et al.   JOURNAL OF HUMAN GENETICS

Hippocampal and Cognitive Aging across the Lifespan: A Bioenergetic Shift Precedes and Increased Cholesterol Trafficking Parallels Memory Impairment

(2009) I. Kadish et al.   JOURNAL OF NEUROSCIENCE

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

(2009) Katharine M. Brauch et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Evolution of the Vertebrate Gene Regulatory Network Controlled by the Transcriptional Repressor REST

(2009) R. Johnson et al.   MOLECULAR BIOLOGY AND EVOLUTION

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

(2009) J Elia et al.   MOLECULAR PSYCHIATRY

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

(2009) Elisabeth Mangold et al.   NATURE GENETICS

INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse

(2009) Monique Jacoby et al.   NATURE GENETICS

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

(2009) Daniel F Gudbjartsson et al.   NATURE GENETICS

Genomewide Association Studies of Stroke

(2009) M. Arfan Ikram et al.   NEW ENGLAND JOURNAL OF MEDICINE

Genome-wide Association Study and Follow-up Analysis of Adiposity Traits in Hispanic Americans: The IRAS Family Study

(2009) Jill M. Norris et al.   Obesity

Gene Expression in Skeletal Muscle Biopsies from People with Type 2 Diabetes and Relatives: Differential Regulation of Insulin Signaling Pathways

(2009) Jane Palsgaard et al.   PLoS One

Mutation Analysis of FOXF2 in Patients with Disorders of Sex Development (DSD) in Combination with Cleft Palate

(2009) U. Jochumsen et al.   Sexual Development

Multi-Organ Expression Profiling Uncovers a Gene Module in Coronary Artery Disease Involving Transendothelial Migration of Leukocytes and LIM Domain Binding 2: The Stockholm Atherosclerosis Gene Expression (STAGE) Study

(2009) Sara Hägg et al.   PLoS Genetics

Expression of avianprickle genes during early development and organogenesis

(2008) Oliver Cooper et al.   DEVELOPMENTAL DYNAMICS

Differential expression of Eya1 and Eya2 during chick early embryonic development

(2008) Tadashi Ishihara et al.   GENE EXPRESSION PATTERNS

Quality scores and SNP detection in sequencing-by-synthesis systems

(2008) W. Brockman et al.   GENOME RESEARCH

Genome-based prediction of common diseases: advances and prospects

(2008) A. C. J.W. Janssens et al.   HUMAN MOLECULAR GENETICS

Support for the minimal essential MHC hypothesis: a parrot with a single, highly polymorphic MHC class II B gene

(2008) Colin R. Hughes et al.   IMMUNOGENETICS

SDF2L1, a Component of the Endoplasmic Reticulum Chaperone Complex, Differentially Interacts with α-, β-, and θ-Defensin Propeptides

(2008) Prasad Tongaonkar et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Cross-species amplification and optimization of microsatellite markers for use in six Neotropical parrots

(2008) KARA J. GEBHARDT et al.   Molecular Ecology Resources

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

(2008) James Bruce Stewart et al.   NATURE REVIEWS GENETICS

Satb2 Is a Postmitotic Determinant for Upper-Layer Neuron Specification in the Neocortex

(2008) Olga Britanova et al.   NEURON

ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations

(2008) F. Gianfrancesco et al.   NEUROSCIENCE

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE

The epsin 4 gene is associated with psychotic disorders in families of Latin American origin

(2008) M ESCAMILLA et al.   SCHIZOPHRENIA RESEARCH

Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry

(2008) E. M. Morrow et al.   SCIENCE

Foraging Ecology Of Parrots In A Modified Landscape: Seasonal Trends And Introduced Species

(2008) Greg D. Matuzak et al.   Wilson Journal of Ornithology