| scholarly article | Q13442814 |
| P50 | author | Rachel L Kember | Q56678788 |
| P2093 | author name string | David Craig | |
| Wencheng Liu | |||
| Steven M Paul | |||
| Ingrid Lindquist | |||
| Christopher Brown | |||
| Sara Nasser | |||
| Janice A Egeland | |||
| Benjamin Georgi | |||
| Maja Bućan | |||
| P2860 | cites work | A flexible and accurate genotype imputation method for the next generation of genome-wide association studies | Q21129496 |
| A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline | Q22251083 | ||
| The genetics of bipolar disorder: genome ‘hot regions,’ genes, new potential candidates and future directions | Q22251105 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| In search of low-frequency and rare variants affecting complex traits | Q24618492 | ||
| Identifying autism loci and genes by tracing recent shared ancestry | Q24655308 | ||
| Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder | Q24655630 | ||
| Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM) | Q24671756 | ||
| Merlin--rapid analysis of dense genetic maps using sparse gene flow trees | Q27860829 | ||
| A method and server for predicting damaging missense mutations | Q27860835 | ||
| Mutations in BRIP1 confer high risk of ovarian cancer | Q28249514 | ||
| Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays | Q28263829 | ||
| Whole-genome association study of bipolar disorder | Q28271419 | ||
| Genome-wide association analysis identifies 13 new risk loci for schizophrenia | Q28297287 | ||
| A rare variant in MYH6 is associated with high risk of sick sinus syndrome | Q28306661 | ||
| Essential regulation of CNS angiogenesis by the orphan G protein-coupled receptor GPR124. | Q28507603 | ||
| GPR124, an orphan G protein-coupled receptor, is required for CNS-specific vascularization and establishment of the blood–brain barrier | Q28509184 | ||
| Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene | Q28775974 | ||
| Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes | Q28943290 | ||
| Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry | Q28943449 | ||
| CNVs conferring risk of autism or schizophrenia affect cognition in controls | Q29308426 | ||
| Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder | Q29417107 | ||
| Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 | Q29417143 | ||
| Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. | Q29417150 | ||
| Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 | ||
| Distribution and intensity of constraint in mammalian genomic sequence | Q29614574 | ||
| PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data | Q29614933 | ||
| Multipoint Quantitative-Trait Linkage Analysis in General Pedigrees | Q29614967 | ||
| Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children | Q29615807 | ||
| Robust relationship inference in genome-wide association studies | Q30429726 | ||
| Catecholamine receptor polymorphisms affect decision-making in C. elegans | Q30503390 | ||
| A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. | Q33595430 | ||
| Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information | Q33910988 | ||
| dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations | Q33945578 | ||
| Neurocognitive phenotypes and genetic dissection of disorders of brain and behavior | Q34009035 | ||
| Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21q | Q34114496 | ||
| Use of population isolates for mapping complex traits | Q34185425 | ||
| A diagnostic interview: the schedule for affective disorders and schizophrenia | Q34269355 | ||
| A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish | Q34379627 | ||
| Changing the landscape of autism research: the autism genetic resource exchange | Q34417603 | ||
| Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish | Q34511287 | ||
| Rare Variant Analysis for Family-Based Design | Q34558081 | ||
| Research diagnostic criteria: rationale and reliability | Q34711463 | ||
| Integrative modeling of eQTLs and cis-regulatory elements suggests mechanisms underlying cell type specificity of eQTLs | Q34917186 | ||
| Variance component model to account for sample structure in genome-wide association studies | Q34971144 | ||
| Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. | Q35476021 | ||
| Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect | Q35644150 | ||
| Genetic dissection of a behavioral quantitative trait locus shows that Rgs2 modulates anxiety in mice. | Q50989320 | ||
| Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population | Q51574823 | ||
| Robust estimation of critical values for genome scans to detect linkage | Q51989476 | ||
| Implementing a unified approach to family-based tests of association | Q52072093 | ||
| Amish Study, II: Consensus diagnoses and reliability results | Q52096580 | ||
| Determining trait locus position from multipoint analysis: Accuracy and power of three different statistics | Q52936287 | ||
| A direct approach to false discovery rates | Q56622258 | ||
| A survey of genetic human cortical gene expression | Q57272923 | ||
| Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder | Q57410923 | ||
| A locus for bipolar affective disorder on chromosome 4p | Q57416170 | ||
| Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families | Q59698063 | ||
| Risks of affective illness among first-degree relatives of bipolar I old-order Amish probands | Q68030975 | ||
| Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia | Q78035307 | ||
| Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission | Q80051194 | ||
| A germline variant in the TP53 polyadenylation signal confers cancer susceptibility | Q35687702 | ||
| The epidemiology of mood disorders | Q35946041 | ||
| A second-generation combined linkage physical map of the human genome | Q36177402 | ||
| A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2. | Q36360605 | ||
| GIGI: an approach to effective imputation of dense genotypes on large pedigrees | Q36742599 | ||
| Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms | Q36959677 | ||
| Quantitative trait loci for aggressive behavior in Drosophila melanogaster | Q37260638 | ||
| Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways | Q37347882 | ||
| Genetics of bipolar disorder: successful start to a long journey | Q37368587 | ||
| Voltage-gated potassium channels as therapeutic targets | Q37464784 | ||
| Genetics, medicine, and the Plain people | Q37561095 | ||
| Evaluating empirical bounds on complex disease genetic architecture | Q39329664 | ||
| Bipolar affective disorders linked to DNA markers on chromosome 11 | Q39461777 | ||
| Analysis of a t(18;21)(p11.1;p11.1) translocation in a family with schizophrenia | Q39848269 | ||
| Neuronal cell adhesion genes: Key players in risk for schizophrenia, bipolar disorder and other neurodevelopmental brain disorders? | Q41505838 | ||
| Genetic overlap between autism, schizophrenia and bipolar disorder | Q42179071 | ||
| Next-generation association studies for complex traits | Q42323465 | ||
| Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands | Q42616389 | ||
| Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility | Q42649179 | ||
| Identification of low-frequency variants associated with gout and serum uric acid levels | Q42726171 | ||
| HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity | Q43180179 | ||
| Identification of novel loci for bipolar I disorder in a multi-stage genome-wide association study. | Q43498601 | ||
| Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits | Q44274525 | ||
| Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder | Q44841212 | ||
| Computational Techniques for Human Genome Resequencing Using Mated Gapped Reads | Q44976858 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bipolar disorder | Q131755 |
| whole genome sequencing | Q2068526 | ||
| P304 | page(s) | e1004229 | |
| P577 | publication date | 2014-03-13 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate | |
| P478 | volume | 10 |
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| Q34463175 | A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder |
| Q33921014 | A population-specific reference panel empowers genetic studies of Anabaptist populations |
| Q52358336 | An examination of multiple classes of rare variants in extended families with bipolar disorder |
| Q90133772 | Clinical and genetic validity of quantitative bipolarity |
| Q34537225 | Commonalities in Development of Pure Breeds and Population Isolates Revealed in the Genome of the Sardinian Fonni's Dog |
| Q89865831 | Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates |
| Q35246537 | Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder |
| Q91497049 | De novo variation in bipolar disorder |
| Q44104317 | Disruption of sonic hedgehog signaling in Ellis-van Creveld dwarfism confers protection against bipolar affective disorder |
| Q40779420 | Exome Sequencing of Familial Bipolar Disorder |
| Q58090958 | Exome sequencing in large, multiplex bipolar disorder families from Cuba |
| Q36598985 | Expanding the phenotype half of the genotype-phenotype space |
| Q36296198 | Family studies to find rare high risk variants in migraine |
| Q54966377 | From the Psychiatrist's Couch to Induced Pluripotent Stem Cells: Bipolar Disease in a Dish. |
| Q33905738 | Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder. |
| Q57473369 | Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree |
| Q38733245 | Genetics of Bipolar Disorder: Recent Update and Future Directions. |
| Q50343363 | Genetics of bipolar disorder |
| Q91657755 | Health Needs Assessment of Five Pennsylvania Plain Populations |
| Q47978042 | Health Needs Assessment of Plain Populations in Lancaster County, Pennsylvania. |
| Q41985304 | High-throughput sequencing of the synaptome in major depressive disorder |
| Q34080310 | Integrated neurobiology of bipolar disorder |
| Q26827615 | Molecular and genetic basis of depression |
| Q37193071 | Molecular circadian rhythm shift due to bright light exposure before bedtime is related to subthreshold bipolarity |
| Q38246508 | New developments in the genetics of bipolar disorder. |
| Q27028029 | On the Teneurin track: a new synaptic organization molecule emerges |
| Q48092656 | Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder. |
| Q35212607 | Rare variants in neuronal excitability genes influence risk for bipolar disorder |
| Q57316758 | Rediscovering the value of families for psychiatric genetics research |
| Q47212535 | The Sardinian Puzzle: Concentration of Major Psychoses and Suicide in the Same Sub-Regions Across One Century. |
| Q92453423 | The genetics of bipolar disorder |
| Q26797377 | Toward a Deeper Understanding of the Genetics of Bipolar Disorder |
| Q35837073 | Transcriptomic Analysis of Induced Pluripotent Stem Cells Derived from Patients with Bipolar Disorder from an Old Order Amish Pedigree |
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| Q37200175 | Variants in Ion Channel Genes Link Phenotypic Features of Bipolar Illness to Specific Neurobiological Process Domains |
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