| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1021553554 |
| P356 | DOI | 10.1038/GENE.2012.12 |
| P698 | PubMed publication ID | 22551722 |
| P5875 | ResearchGate publication ID | 224887542 |
| P2093 | author name string | C T Watson | |
| F Breden | |||
| P2860 | cites work | The diploid genome sequence of an individual human | Q21090194 |
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| Structural basis of tyrosine sulfation and VH-gene usage in antibodies that recognize the HIV type 1 coreceptor-binding site on gp120 | Q27643185 | ||
| Haploview: analysis and visualization of LD and haplotype maps | Q27860955 | ||
| Recent advances in the genetics of autoimmune disease | Q28238782 | ||
| Efficiency and power in genetic association studies | Q28278645 | ||
| A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 | Q28283861 | ||
| Origins and functional impact of copy number variation in the human genome | Q28730507 | ||
| Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study | Q28943550 | ||
| Missing heritability and strategies for finding the underlying causes of complex disease | Q29614586 | ||
| Somatic generation of antibody diversity | Q29616439 | ||
| Broadly cross-reactive antibodies dominate the human B cell response against 2009 pandemic H1N1 influenza virus infection | Q30398435 | ||
| B cells in autoimmune diseases: insights from analyses of immunoglobulin variable (Ig V) gene usage | Q33286220 | ||
| Combinatorial antibody libraries from survivors of the Turkish H5N1 avian influenza outbreak reveal virus neutralization strategies | Q33328393 | ||
| Physical map of the 3' region of the human immunoglobulin heavy chain locus: clustering of autoantibody-related variable segments in one haplotype | Q33428825 | ||
| The frequency of homozygous deletion of a developmentally regulated Vh gene (Humhv3005) is increased in patients with chronic idiopathic thrombocytopenic purpura | Q33499241 | ||
| The human immunoglobulin heavy variable genes | Q33543808 | ||
| Determination of gene organization in individual haplotypes by analyzing single DNA fragments from single spermatozoa | Q33554290 | ||
| Population-genetic nature of copy number variations in the human genome | Q33630664 | ||
| Evidence for a locus (IDDM16) in the immunoglobulin heavy chain region on chromosome 14q32.3 producing susceptibility to type 1 diabetes | Q58201241 | ||
| Ethnic differences in VH gene polymorphism | Q71556276 | ||
| Simultaneous absence of the human IgG1, IgG2, IgG4 and IgA1 subclasses: immunological and immunogenetical considerations | Q71684366 | ||
| IGH V3-23*01 and its allele V3-23*03 differ in their capacity to form the canonical human antibody combining site specific for the capsular polysaccharide of Haemophilus influenzae type b | Q73622166 | ||
| Susceptibility to multiple sclerosis and the immunoglobulin heavy chain gene cluster | Q77675657 | ||
| Determination of gene organization in the human IGHV region on single chromosomes | Q81471186 | ||
| Structural analysis of substitution patterns in alleles of human immunoglobulin VH genes | Q81647979 | ||
| Segmental duplication as one of the driving forces underlying the diversity of the human immunoglobulin heavy chain variable gene region | Q33805553 | ||
| Rare antibodies from combinatorial libraries suggests an S.O.S. component of the human immunological repertoire | Q33813643 | ||
| Comparison of antibody repertoires produced by HIV-1 infection, other chronic and acute infections, and systemic autoimmune disease | Q33867353 | ||
| Characterization of missing human genome sequences and copy-number polymorphic insertions | Q33875113 | ||
| Susceptibility to multiple sclerosis is associated with the proximal immunoglobulin heavy chain variable region | Q34183158 | ||
| Population and family studies of three disease-related polymorphic genes in systemic lupus erythematosus | Q34210066 | ||
| Molecular basis of an autoantibody-associated restriction fragment length polymorphism that confers susceptibility to autoimmune diseases | Q34225507 | ||
| The human immunoglobulin VH repertoire | Q34312904 | ||
| Population-genetic properties of differentiated human copy-number polymorphisms | Q34687598 | ||
| Wide prevalence of heterosubtypic broadly neutralizing human anti-influenza A antibodies | Q34756837 | ||
| Broad diversity of neutralizing antibodies isolated from memory B cells in HIV-infected individuals | Q34962766 | ||
| HAPPY mapping of a YAC reveals alternative haplotypes in the human immunoglobulin VH locus | Q35036716 | ||
| Limitations of next-generation genome sequence assembly | Q35047159 | ||
| A fetally expressed immunoglobulin VH1 gene belongs to a complex set of alleles | Q35609941 | ||
| Naive antibody gene-segment frequencies are heritable and unaltered by chronic lymphocyte ablation | Q35647840 | ||
| Direct detection of insertion/deletion polymorphisms in an autosomal region by analyzing high-density markers in individual spermatozoa | Q37203928 | ||
| Expression of the immunoglobulin VH gene 51p1 is proportional to its germline gene copy number | Q37354531 | ||
| A defective Vkappa A2 allele in Navajos which may play a role in increased susceptibility to haemophilus influenzae type b disease | Q37354966 | ||
| Novel substitution polymorphisms of human immunoglobulin VH genes in Mexicans | Q38520087 | ||
| Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements. | Q39141906 | ||
| Inherited deletion of immunoglobulin heavy chain constant region genes in normal human individuals | Q39168085 | ||
| Molecular analysis of the T17 immunoglobulin CH multigene deletion (del A1-GP-G2-G4-E). | Q39591553 | ||
| Polymorphism and utilization of human VH Genes. | Q40374426 | ||
| Preferential use of the VH5-51 gene segment by the human immune response to code for antibodies against the V3 domain of HIV-1 | Q41816066 | ||
| The inference of phased haplotypes for the immunoglobulin H chain V region gene loci by analysis of VDJ gene rearrangements. | Q41860468 | ||
| Individual variation in the germline Ig gene repertoire inferred from variable region gene rearrangements. | Q41911217 | ||
| Immunoglobulin heavy chain variable region polymorphisms and multiple sclerosis susceptibility. | Q42622566 | ||
| A segment of human Vh gene locus is duplicated | Q42625986 | ||
| Polymorphism in the immunoglobulin VH gene V1-69 affects susceptibility to rheumatoid arthritis in subjects lacking the HLA-DRB1 shared epitope | Q42674576 | ||
| No evidence for the involvement of interleukin 2 or the immunoglobulin heavy chain gene cluster in determining genetic susceptibility to multiple sclerosis | Q43071810 | ||
| The HuRef Browser: a web resource for individual human genomics | Q43122555 | ||
| Genomic screening by 454 pyrosequencing identifies a new human IGHV gene and sixteen other new IGHV allelic variants. | Q44418690 | ||
| Association of homozygous deletion of the Humhv3005 and the VH3-30.3 genes with renal involvement in systemic lupus erythematosus. | Q44452632 | ||
| Effect of 51p1-related gene copy number (V1-69 locus) on production of hepatitis C-associated cryoglobulins | Q44990800 | ||
| A map of the human immunoglobulin VH locus completed by analysis of the telomeric region of chromosome 14q. | Q48082296 | ||
| IGHV4-39 deletion polymorphism does not associate with risk or outcome of multiple sclerosis | Q48197651 | ||
| A multigene deletion in the human IGH constant region locus involves highly homologous hot spots of recombination | Q48285688 | ||
| Nomenclature of the human immunoglobulin heavy (IGH) genes | Q48739605 | ||
| An utter refutation of the "fundamental theorem of the HapMap". | Q51950798 | ||
| The human immunoglobulin heavy diversity (IGHD) and joining (IGHJ) segments. | Q53344826 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetic variation | Q349856 |
| missing data | Q6878417 | ||
| P304 | page(s) | 363-373 | |
| P577 | publication date | 2012-05-03 | |
| P1433 | published in | Genes and Immunity | Q15745246 |
| P1476 | title | The immunoglobulin heavy chain locus: genetic variation, missing data, and implications for human disease | |
| P478 | volume | 13 |
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| Q41196820 | A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol |
| Q47833098 | A murine Ig light chain transgene reveals IGKV3 gene contributions to anti-collagen types IV and II specificities |
| Q35883727 | Ability to develop broadly neutralizing HIV-1 antibodies is not restricted by the germline Ig gene repertoire |
| Q46655076 | An automated algorithm for extracting functional immunologic V-genes from genomes in jawed vertebrates |
| Q41981966 | Annotation of pseudogenic gene segments by massively parallel sequencing of rearranged lymphocyte receptor loci |
| Q60938455 | Antibody Repertoire Analysis of Hepatitis C Virus Infections Identifies Immune Signatures Associated With Spontaneous Clearance |
| Q42557137 | Antibody engineering and therapeutics, The Annual Meeting of the Antibody Society: December 8-12, 2013, Huntington Beach, CA |
| Q88161098 | Antibody repertoire analysis in polygenic autoimmune diseases |
| Q33705559 | Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania |
| Q30891515 | Automated analysis of high-throughput B-cell sequencing data reveals a high frequency of novel immunoglobulin V gene segment alleles |
| Q89449966 | Blood signatures for second stage human African trypanosomiasis: a transcriptomic approach |
| Q36835759 | Characterization of pathogenic human monoclonal autoantibodies against GM-CSF. |
| Q36742607 | Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation |
| Q36214720 | Cross-reactive and pre-existing antibodies to therapeutic antibodies--Effects on treatment and immunogenicity |
| Q36494999 | DJ Pairing during VDJ Recombination Shows Positional Biases That Vary among Individuals with Differing IGHD Locus Immunogenotypes |
| Q36134501 | Estimating Copy Number and Allelic Variation at the Immunoglobulin Heavy Chain Locus Using Short Reads |
| Q38992740 | Evolution of B cell analysis and Env trimer redesign |
| Q34956008 | Fine mapping of V(D)J recombinase mediated rearrangements in human lymphoid malignancies |
| Q33747916 | Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease |
| Q90101179 | Genetics of rheumatic fever and rheumatic heart disease |
| Q89937719 | Genotyping and Copy Number Analysis of Immunoglobin Heavy Chain Variable Genes Using Long Reads |
| Q90685616 | Germ-line genetic variation in the immunoglobulin heavy chain creates stroke susceptibility in the spontaneously hypertensive rat |
| Q47892454 | Heritability of vaccine-induced measles neutralizing antibody titers |
| Q43071752 | Hypertensive renal injury is associated with gene variation affecting immune signaling |
| Q36583070 | IGHV1-69 polymorphism modulates anti-influenza antibody repertoires, correlates with IGHV utilization shifts and varies by ethnicity |
| Q33627189 | Identification of human neutralizing antibodies against MERS-CoV and their role in virus adaptive evolution |
| Q99240741 | Immune literacy: reading, writing and editing adaptive immunity |
| Q57817492 | Immunoglobulin Light Chain Gene Rearrangements, Receptor Editing and the Development of a Self-Tolerant Antibody Repertoire |
| Q55426539 | In Vitro Evolution of Antibodies Inspired by In Vivo Evolution. |
| Q64255685 | Inference of Diversity Genes and Analysis of Non-canonical V(DD)J Recombination in Immunoglobulins |
| Q91762627 | Influence of Liver Fibrosis on Lobular Zonation |
| Q43795085 | Integrated transcriptome analysis reveals miRNA-mRNA crosstalk in laryngeal squamous cell carcinoma. |
| Q92716462 | Massively parallel single-cell B-cell receptor sequencing enables rapid discovery of diverse antigen-reactive antibodies |
| Q92563047 | Molecular characterization of Bu-1 and TLR2 gene in Haringhata Black chicken |
| Q61797981 | Mosaic deletion patterns of the human antibody heavy chain gene locus shown by Bayesian haplotyping |
| Q47173421 | On being the right size: antibody repertoire formation in the mouse and human |
| Q28607156 | Practical guidelines for B-cell receptor repertoire sequencing analysis |
| Q28818629 | Production of individualized V gene databases reveals high levels of immunoglobulin genetic diversity |
| Q61814105 | Reprogramming the antigen specificity of B cells using genome-editing technologies |
| Q35007784 | Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity |
| Q36501620 | Short-term assessment of BCR repertoires of SLE patients after high dose glucocorticoid therapy with high-throughput sequencing |
| Q34468679 | Soma-to-germline feedback is implied by the extreme polymorphism at IGHV relative to MHC: The manifest polymorphism of the MHC appears greatly exceeded at Immunoglobulin loci, suggesting antigen-selected somatic V mutants penetrate Weismann's Barrie |
| Q47565582 | Structural Determination of the Broadly Reactive Anti-IGHV1-69 Anti-idiotypic Antibody G6 and Its Idiotope |
| Q42069312 | Structures of Preferred Human IgV Genes-Based Protective Antibodies Identify How Conserved Residues Contact Diverse Antigens and Assign Source of Specificity to CDR3 Loop Variation |
| Q57178227 | The Bayesian optimist's guide to adaptive immune receptor repertoire analysis |
| Q38766578 | The Individual and Population Genetics of Antibody Immunity. |
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| Q37137346 | The shape of the lymphocyte receptor repertoire: lessons from the B cell receptor |
| Q22065285 | The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage. |
| Q45324518 | Universal influenza virus vaccines: what can we learn from the human immune response following exposure to H7 subtype viruses? |
| Q33641952 | Visualization and probability-based scoring of structural variants within repetitive sequences |
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