| Q33589660 | A 6000 kb segment of chromosome 1 is conserved in human and mouse. |
| Q36542251 | A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density |
| Q62734302 | A Genomewide Screen in Multiplex Rheumatoid Arthritis Families Suggests Genetic Overlap with Other Autoimmune Diseases |
| Q49133415 | A Single B1 Subunit Mapped to Mouse Chromosome 7 May Be a Common Component of Na Channel Isoforms from Brain, Skeletal Muscle and Heart |
| Q24634112 | A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis |
| Q33675881 | A genome-wide association study identifies six novel risk loci for primary biliary cholangitis |
| Q35788496 | A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping |
| Q35070442 | A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping |
| Q72632850 | A glial-specific voltage-sensitive Na channel gene maps close to clustered genes for neuronal isoforms on mouse chromosome 2 |
| Q48290845 | A glutaminase (gis) gene maps to mouse chromosome 1, rat chromosome 9, and human chromosome 2. |
| Q30962764 | A hidden Markov modeling approach for admixture mapping based on case-control data. |
| Q24629130 | A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus |
| Q33354118 | A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2. |
| Q45341202 | A linkage map of mouse chromosome 1 using an interspecific cross segregating for the gld autoimmunity mutation |
| Q28183783 | A linkage map of mouse chromosome 19: definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus |
| Q68302487 | A linkage map of mouse chromosome 8: Further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19 |
| Q28267921 | A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis |
| Q68166997 | A molecular genetic linkage map of mouse chromosome 7 |
| Q44586822 | A proximal mouse chromosome 9 linkage map that further defines linkage groups homologous with segments of human chromosomes 11, 15, and 19 |
| Q41727943 | A simple and accurate method for determination of microsatellite total allele content differences between DNA pools |
| Q22010980 | ADAM-TS8, a novel metalloprotease of the ADAM-TS family located on mouse chromosome 9 and human chromosome 11 |
| Q34776325 | ALOX5 gene variants affect eicosanoid production and response to fish oil supplementation |
| Q34598361 | Accounting for ancestry: population substructure and genome-wide association studies |
| Q43799396 | Admixed populations and autoimmunity |
| Q35135891 | Admixture mapping as a tool in gene discovery |
| Q69902903 | Allelic variants of Ly-5 in inbred and natural populations of mice |
| Q40104504 | Amerindian ancestry in Argentina is associated with increased risk for systemic lupus erythematosus |
| Q68760258 | Ampd-2 maps to distal mouse chromosome 3 in linkage with Ampd-1 |
| Q42637048 | An actively retrotransposing, novel subfamily of mouse L1 elements |
| Q33486736 | An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels |
| Q33315564 | Analysis and application of European genetic substructure using 300 K SNP information |
| Q21562489 | Analysis of East Asia genetic substructure using genome-wide SNP arrays |
| Q46014753 | Analysis of MHC region genetics in Finnish patients with juvenile idiopathic arthritis: evidence for different locus-specific effects in polyarticular vs pauciarticular subsets and a shared DRB1 epitope. |
| Q34167918 | Analysis of maternal-offspring HLA compatibility, parent-of-origin effects, and noninherited maternal antigen effects for HLA-DRB1 in systemic lupus erythematosus |
| Q42690314 | Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure |
| Q34804773 | Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America |
| Q33315565 | Application of ancestry informative markers to association studies in European Americans |
| Q35125497 | Argentine population genetic structure: large variance in Amerindian contribution |
| Q73145884 | Assignment of microrchidia (Morc) to mouse chromosome 16 by interspecific backcross linkage analysis and human chromosome 3q13 using somatic cell hybrids and in situ hybridization |
| Q36736449 | Association of DXA-derived bone mineral density and fat mass with African ancestry |
| Q34079062 | Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort |
| Q42644623 | Association of SLC11A1 (NRAMP1) with persistent oligoarticular and polyarticular rheumatoid factor-negative juvenile idiopathic arthritis in Finnish patients: haplotype analysis in Finnish families |
| Q46041669 | Association of angiotensin-converting enzyme polymorphisms with systemic lupus erythematosus and nephritis: analysis of 644 SLE families |
| Q28265206 | Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX |
| Q37030914 | Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans. |
| Q37292697 | Base excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African-Americans |
| Q34418188 | CD1 defines conserved linkage group border between human chromosomes 1 and mouse chromosomes 1 and 3. |
| Q36253879 | CIITA is not associated with risk of developing rheumatoid arthritis |
| Q34477176 | CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification |
| Q44635940 | Cd28 and Ctla-4, two related members of the Ig supergene family, are tightly linked on proximal mouse chromosome 1 |
| Q36761303 | Characterization of an atypical member of the Na+/Cl(-)-dependent transporter family: chromosomal localization and distribution in GABAergic and glutamatergic neurons in the rat brain. |
| Q28288104 | Chromosomal assignment of two ADAM genes, TACE (ADAM17) and MLTNB (ADAM19), to human chromosomes 2 and 5, respectively, and of Mltnb to mouse chromosome 11 |
| Q62394150 | Chromosomal mapping of the high affinity Fc gamma receptor gene |
| Q42155343 | Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis |
| Q36380452 | Clinical and serologic manifestations of autoimmune disease in MRL-lpr/lpr mice lacking nitric oxide synthase type 2. |
| Q34341595 | Cloning of cDNA and genomic DNA encoding human type XVIII collagen and localization of the alpha 1(XVIII) collagen gene to mouse chromosome 10 and human chromosome 21. |
| Q24313513 | Cloning of the human glycine transporter type 1: molecular and pharmacological characterization of novel isoform variants and chromosomal localization of the gene in the human and mouse genomes |
| Q28278564 | Cloning of the human tissue inhibitor of metalloproteinase-4 gene (TIMP4) and localization of the TIMP4 and Timp4 genes to human chromosome 3p25 and mouse chromosome 6, respectively |
| Q28511186 | Cloning, gene structure and genomic localization of an orphan transporter from mouse kidney with six alternatively-spliced isoforms |
| Q24336176 | Cloning, pharmacological characterization, and genomic localization of the human creatine transporter |
| Q77926135 | Colonic hamartoma development by anomalous duplication in Cdx2 knockout mice |
| Q37376871 | Common variants at CD40 and other loci confer risk of rheumatoid arthritis |
| Q37378028 | Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency |
| Q67868000 | Comparison of interspecific to intersubspecific backcrosses demonstrates species and sex differences in recombination frequency on mouse Chromosome 16 |
| Q57000963 | Comparison of linkage maps of mouse chromosome 12 derived from laboratory strain intraspecific and Mus spretus interspecific backcrosses |
| Q37289097 | Comparison of statistical methods for estimating genetic admixture in a lung cancer study of African Americans and Latinos |
| Q77778144 | Conservation of the linkage of the murine Itga2b and Itgb3 loci in mouse chromosome 11 |
| Q28207585 | Construction of a physical map on mouse and human chromosome 1: comparison of 13 Mb of mouse and 11 Mb of human DNA |
| Q70731837 | Corrected centromere orientation for mouse chromosome 19 MIT markers |
| Q46101994 | Corrigendum: Genome-Wide Analysis of DNA Methylation, Copy Number Variation, and Gene Expression in Monozygotic Twins Discordant for Primary Biliary Cirrhosis |
| Q31154891 | Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits |
| Q33519271 | Data for Genetic Analysis Workshop 16 Problem 1, association analysis of rheumatoid arthritis data |
| Q43422939 | Definition of mouse chromosome 1 and 3 gene linkage groups that are conserved on human chromosome 1: evidence that a conserved linkage group spans the centromere of human chromosome 1. |
| Q34169210 | Differences in albuminuria between Hispanics and whites: an evaluation by genetic ancestry and country of origin: the multi-ethnic study of atherosclerosis |
| Q40749783 | Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells |
| Q35834701 | Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis |
| Q68956744 | Effect of xid on autoimmune C3H-gld/gld mice |
| Q72676004 | Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 1 |
| Q72676064 | Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 3 |
| Q71519522 | Encyclopedia of the mouse genome V. Mouse chromosome 1 |
| Q71519545 | Encyclopedia of the mouse genome V. Mouse chromosome 3 |
| Q46333644 | Encyclopedia of the mouse genome VII. Mouse chromosome 1. |
| Q68413535 | Establishment of a molecular genetic map of distal mouse chromosome 1: further definition of a conserved linkage group syntenic with human chromosome 1q |
| Q37361406 | Ethnic-difference markers for use in mapping by admixture linkage disequilibrium |
| Q37398821 | European genetic ancestry is associated with a decreased risk of lupus nephritis |
| Q24648104 | European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups |
| Q37634162 | European population substructure correlates with systemic lupus erythematosus endophenotypes in North Americans of European descent |
| Q37335908 | European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus |
| Q21092502 | European population substructure: clustering of northern and southern populations |
| Q46541550 | Evidence for malaria selection of a CR1 haplotype in Sardinia |
| Q38412152 | Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicine |
| Q45995448 | Examination of sequence homology between human chromosome 20 and the mouse genome: intense conservation of many genomic elements. |
| Q57186231 | Familial antiphospholipid antibody syndrome: Criteria for disease and evidence for autosomal dominant inheritance |
| Q31056324 | FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data |
| Q73677692 | Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p |
| Q34083676 | Fine mapping of chromosome 15q25.1 lung cancer susceptibility in African-Americans |
| Q91765524 | Fine mapping of the MHC region identifies major independent variants associated with Han Chinese primary biliary cholangitis |
| Q36589343 | Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans |
| Q44449408 | Finnish case-control and family studies support PTPN22 R620W polymorphism as a risk factor in rheumatoid arthritis, but suggest only minimal or no effect in juvenile idiopathic arthritis |
| Q34522435 | Gastrointestinal hamartomatous polyposis in Lkb1 heterozygous knockout mice |
| Q46791617 | Gender and racial differences in rates of total hip replacement |
| Q48081432 | Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP-3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10. |
| Q28117598 | Gene structure, chromosomal localization, and protein sequence of mouse CD53 (Cd53): evidence that the transmembrane 4 superfamily arose by gene duplication |
| Q36202209 | Genes and (auto)immunity in primary biliary cirrhosis |
| Q57186365 | Genetic Mapping of the High-Affinity Nerve Growth Factor Receptor Gene, Ntrk1, to Mouse Chromosome 3 |
| Q36232118 | Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci |
| Q73485705 | Genetic analysis of multiplex rheumatoid arthritis families |
| Q37482665 | Genetic ancestry is associated with subclinical cardiovascular disease in African-Americans and Hispanics from the multi-ethnic study of atherosclerosis |
| Q55514451 | Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients. |
| Q36732133 | Genetic mapping of DNA topoisomerase I-related sequences to mouse chromosomes 2 and 14. |
| Q40712860 | Genetic mapping of Pp11r, a thymocyte gene expressed during apoptosis, to mouse chromosome 15. |
| Q57186323 | Genetic mapping of the ?-arrestin 1 and 2 genes on mouse Chromosomes 7 and 11 respectively |
| Q57186310 | Genetic mapping of the T lymphocyte-specific transcription factor 7 gene on mouse chromosome 11 |
| Q57186335 | Genetic mapping of the glycine receptor ?3 subunit on mouse Chromosome 8 |
| Q67577186 | Genetic mapping of the integrin alpha 1 gene (Vla1) to mouse chromosome 13 |
| Q57186389 | Genetic mapping of the mouse topoisomerase II? gene to Chromosome 11 |
| Q48074165 | Genetic mapping of the tumor-associated mucin 1 gene on mouse chromosome 3. |
| Q42939540 | Genetic organization of complement receptor-related genes in the mouse. |
| Q67244136 | Genetic relationships of Mlsa among polymorphic loci on distal mouse chromosome 1 |
| Q37227144 | Genetic risk and longitudinal disease activity in systemic lupus erythematosus using targeted maximum likelihood estimation. |
| Q57332116 | Genetic risk factors for infection in patients with early rheumatoid arthritis |
| Q35125868 | Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk |
| Q34037986 | Genetic variants of TSLP and asthma in an admixed urban population |
| Q41331832 | Genetic variation at the CD28 locus and its impact on expansion of pro-inflammatory CD28 negative T cells in healthy individuals |
| Q35754934 | Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) |
| Q92259854 | Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis |
| Q36568293 | Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations |
| Q37683538 | Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis |
| Q24306903 | Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci |
| Q29417131 | Genome-wide association study identifies novel loci predisposing to cutaneous melanoma |
| Q28281906 | Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci |
| Q28943317 | Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis |
| Q83151084 | Genome-wide meta-analysis for rheumatoid arthritis |
| Q62394171 | Genomic organization of adrenergic and serotonin receptors in the mouse: Linkage mapping of sequence-related genes provides a method for examining mammalian chromosome evolution |
| Q31422581 | Genomic structure and chromosomal location of the mouse macrophage C-type lectin gene. |
| Q48082303 | Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion. |
| Q34235447 | Glycogen synthase: a putative locus for diet-induced hyperglycemia. |
| Q46972523 | HLA-DRB1, TAP2/TAP1, and HLA-DPB1 haplotypes in Finnish juvenile idiopathic arthritis: more complexity within the MHC. |
| Q34526330 | Hepatocellular carcinoma caused by loss of heterozygosity in Lkb1 gene knockout mice |
| Q38436416 | Herpesvirus saimiri encodes a new cytokine, IL-17, which binds to a novel cytokine receptor |
| Q44922542 | High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33. |
| Q21092448 | High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions |
| Q34317235 | Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL1 maps to human chromosome 1q21, a region that is frequently altered in preneoplastic and neoplastic disease. |
| Q36992568 | Human leukocyte antigen polymorphisms in Italian primary biliary cirrhosis: a multicenter study of 664 patients and 1992 healthy controls |
| Q48079752 | Identification of OX40 ligand and preliminary characterization of its activities on OX40 receptor. |
| Q24336310 | Identification of a putative gamma-aminobutyric acid (GABA) receptor subunit rho2 cDNA and colocalization of the genes encoding rho2 (GABRR2) and rho1 (GABRR1) to human chromosome 6q14-q21 and mouse chromosome 4 |
| Q39021882 | Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum |
| Q24617796 | Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants |
| Q35789165 | Independent origin of c.57 C > T mutation in MIR184 associated with inherited corneal and lens abnormalities |
| Q36087896 | International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways |
| Q67577242 | Linkage analysis demonstrates that the Timp-2 locus is on mouse chromosome 11 |
| Q57306858 | Linkage analysis of rheumatoid arthritis in US and UK families reveals interactions between HLA–DRB1 and loci on chromosomes 6q and 16p |
| Q42824684 | Localization of growth arrest-specific genes on mouse chromosomes 1, 7, 8, 11, 13, and 16. |
| Q34244874 | Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7. |
| Q72690204 | Localization of the osteocalcin gene cluster on mouse chromosome 3 |
| Q44435255 | Long-range restriction site mapping of a syntenic segment conserved between human chromosome 1 and mouse chromosome 3. |
| Q33917780 | MHC associations with clinical and autoantibody manifestations in European SLE. |
| Q69371102 | Mapping of Abll within a conserved linkage group on distal mouse chromosome 1 syntenic with human chromosome 1 using an interspecific cross |
| Q69900963 | Mapping of alpha-spectrin on distal mouse chromosome 1 |
| Q34449720 | Mapping of eight testis-specific genes to mouse chromosomes |
| Q73150853 | Mapping of five subtype genes for muscarinic acetylcholine receptor to mouse chromosomes |
| Q54279099 | Mapping of recombinant retrovirus integration sites that cause expression of the viral genome in murine embryonal carcinoma cells |
| Q48055366 | Mapping of six germ-cell-specific genes to mouse chromosomes |
| Q34368125 | Mapping of the 75-kDa inositol polyphosphate-5-phosphatase (Inpp5b) to distal mouse chromosome 4 and its exclusion as a candidate gene for dysgenetic lens |
| Q69916163 | Mapping of the Ly-4 (L3T4) T-cell differentiation antigen on mouse chromosome 6 by the use of RFLPs in an interspecific cross |
| Q69916103 | Mapping of the bcl-2 oncogene on mouse chromosome 1 |
| Q34374794 | Mapping of the calcium-sensing receptor gene (CASR) to human chromosome 3q13.3-21 by fluorescence in situ hybridization, and localization to rat chromosome 11 and mouse chromosome 16. |
| Q28291650 | Mapping of the genes encoding mouse prostaglandin D, E, and F and prostacyclin receptors |
| Q71819466 | Mapping of the genes for four members of the transmembrane 4 superfamily: mouse Cd9, Cd63, Cd81, and Cd82 |
| Q67522993 | Mapping of the mouse Rxr loci encoding nuclear retinoid X receptors RXR alpha, RXR beta, and RXR gamma |
| Q72297603 | Mapping of the taurine transporter gene to mouse chromosome 6 and to the short arm of human chromosome 3 |
| Q46776110 | Mapping of two mouse membrane-type matrix metalloproteinase (MT-MMP) genes, Mmp15 and Mmp16, to mouse chromosomes 8 and 4, respectively |
| Q46170684 | Markers informative for ancestry demonstrate consistent megabase-length linkage disequilibrium in the African American population |
| Q34159421 | Markers that discriminate between European and African ancestry show limited variation within Africa |
| Q46243435 | Mexican American ancestry-informative markers: examination of population structure and marker characteristics in European Americans, Mexican Americans, Amerindians and Asians |
| Q34258558 | Mexican-American admixture mapping analyses for diabetic nephropathy in type 2 diabetes mellitus |
| Q32169917 | Molecular characterization of a mouse genomic element mobilized by advanced glycation endproduct modified-DNA (AGE-DNA). |
| Q24568305 | Molecular characterization of murine and human OX40/OX40 ligand systems: identification of a human OX40 ligand as the HTLV-1-regulated protein gp34 |
| Q28266045 | Molecular properties and chromosomal location of cadherin-8 |
| Q48086970 | Mouse Cd7 maps to chromosome 11. |
| Q71846580 | Mouse Elk oncogene maps to chromosome X and a novel Elk oncogene (Elk3) maps to chromosome 10 |
| Q72160459 | Mouse chromosome 1 |
| Q73535247 | Mouse chromosome 1 |
| Q35675696 | Mouse chromosome 1. |
| Q41692772 | Mouse chromosome 1. |
| Q44036292 | Mouse chromosome 1. |
| Q67871546 | Mouse chromosome 18 |
| Q35675802 | Mouse chromosome 19. |
| Q67871556 | Mouse chromosome 3 |
| Q72160509 | Mouse chromosome 3 |
| Q35675814 | Mouse chromosome 3. |
| Q37523829 | Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5 |
| Q41615335 | Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population |
| Q37498799 | Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus |
| Q48137908 | Murine serotonin transporter: sequence and localization to chromosome 11. |
| Q28742230 | New approaches to disease mapping in admixed populations |
| Q37325986 | Nucleotide excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African Americans |
| Q41543179 | Nucleotide sequence, expression, and chromosomal mapping of Mrp and mapping of five related sequences |
| Q73860274 | PARP alleles and SLE: failure to confirm association with disease susceptibility |
| Q34114509 | PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis |
| Q48052603 | Partial structure, chromosome localization, and expression of the mouse Girk4 gene. |
| Q48052602 | Partial structure, chromosome localization, and expression of the mouse Icln gene |
| Q37191674 | Pathway-based analysis of primary biliary cirrhosis genome-wide association studies |
| Q24324590 | Physical and genetic linkage of the genes encoding Ly-9 and CD48 on mouse and human chromosomes 1 |
| Q28256553 | Physical and linkage mapping of the human and murine genes for the alpha 1 chain of type IX collagen (COL9A1) |
| Q57186434 | Physical linkage of genes encoding the lymphocyte adhesion molecules CD2 and its ligand LFA-3 |
| Q43762143 | Physical mapping of a family of interferon-activated genes, serum amyloid P-component, and alpha-spectrin on mouse chromosome 1. |
| Q57186279 | Positional cloning of the Chediak-Higashi syndrome gene: genetic mapping of the beige locus on mouse chromosome 13 |
| Q43611215 | Primary biliary cirrhosis and autoimmunity: evaluating the genetic risk. |
| Q28216248 | Punctin, a novel ADAMTS-like molecule, ADAMTSL-1, in extracellular matrix |
| Q34342474 | Putative ancestral origins of chromosomal segments in individual african americans: implications for admixture mapping |
| Q37248628 | REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis |
| Q42674479 | Regulation of anti-cyclic citrullinated peptide antibodies in rheumatoid arthritis: contrasting effects of HLA-DR3 and the shared epitope alleles |
| Q35601633 | Relationship between diabetes risk and admixture in postmenopausal African-American and Hispanic-American women |
| Q39295211 | Relationship between gallbladder surgery and ethnic admixture in African American and Hispanic American women |
| Q35845618 | Relationship between glaucoma and admixture in postmenopausal African American women |
| Q36731618 | Relationship between hysterectomy and admixture in African American women |
| Q35607376 | Relationship of pain and ancestry in African American women |
| Q46100560 | Renin-angiotensin system gene polymorphisms predict the progression to renal insufficiency among Asians with lupus nephritis |
| Q83911029 | Replicated association of 17q12-21 with susceptibility of primary biliary cirrhosis in a Japanese cohort |
| Q104104590 | Replication study and meta-analysis indicate a suggestive association of RUNX3 locus with primary biliary cholangitis |
| Q36839197 | Rheumatoid arthritis risk allele PTPRC is also associated with response to anti-tumor necrosis factor alpha therapy |
| Q28943379 | Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08 |
| Q37070948 | STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus |
| Q47985297 | Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families |
| Q34756777 | Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus |
| Q83208728 | Shared susceptibility variations in autoimmune diseases: a brief perspective on common issues |
| Q72771913 | Single-strand conformational polymorphism (SSCP) mapping of the mouse genome: integration of the SSCP, microsatellite, and gene maps of mouse chromosome 1 |
| Q35637941 | Smoking interacts with genetic risk factors in the development of rheumatoid arthritis among older Caucasian women. |
| Q87259111 | Socioeconomic status and lung cancer: unraveling the contribution of genetic admixture |
| Q33339386 | Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus |
| Q46225372 | Stronger bone correlates with African admixture in African-American women |
| Q24300819 | Structure, expression, and genetic linkage of the mouse BCM1 (OX45 or Blast-1) antigen. Evidence for genetic duplication giving rise to the BCM1 region on mouse chromosome 1 and the CD2/LFA3 region on mouse chromosome 3 |
| Q35053753 | Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis |
| Q24657292 | TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study |
| Q28545832 | TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits |
| Q36005358 | The Family Investigation of Nephropathy and Diabetes (FIND): design and methods |
| Q46334533 | The Fcgamma receptor IIIA-158F allele is a major risk factor for the development of lupus nephritis among Caucasians but not non-Caucasians |
| Q37578078 | The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers |
| Q34912912 | The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series |
| Q41365044 | The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk |
| Q87174182 | The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk |
| Q70576513 | The functional genes for protein synthesis initiation factor 4AI and 4AII map to mouse chromosomes 11 and 16 |
| Q57533002 | The functional −169T→C single-nucleotide polymorphism inFCRL3 is not associated with rheumatoid arthritis in white North Americans |
| Q71867342 | The gene encoding the mouse serum amyloid A protein, apo-SAA5, maps to proximal chromosome 7 |
| Q36236745 | The genetics of human autoimmune disease: A perspective on progress in the field and future directions |
| Q33656090 | The genetics revolution and the assault on rheumatoid arthritis |
| Q34309796 | The highly conserved defender against the death 1 (DAD1) gene maps to human chromosome 14q11-q12 and mouse chromosome 14 and has plant and nematode homologs |
| Q34291573 | The human myeloid cell nuclear differentiation antigen gene is one of at least two related interferon-inducible genes located on chromosome 1q that are expressed specifically in hematopoietic cells. |
| Q34781620 | The inflammatory disease-associated variants in IL12B and IL23R are not associated with rheumatoid arthritis |
| Q46114766 | The influence of genetic variation in the HLA-DRB1 and LTA-TNF regions on the response to treatment of early rheumatoid arthritis with methotrexate or etanercept |
| Q24294442 | The mouse alpha 1(XII) and human alpha 1(XII)-like collagen genes are localized on mouse chromosome 9 and human chromosome 6 |
| Q36362801 | The role of nitric oxide in the pathogenesis of spontaneous murine autoimmune disease: increased nitric oxide production and nitric oxide synthase expression in MRL-lpr/lpr mice, and reduction of spontaneous glomerulonephritis and arthritis by orall |
| Q36070941 | The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus. |
| Q68716759 | The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q |
| Q28239517 | The systemic lupus erythematosus-associated PDCD1 polymorphism PD1.3A in lupus nephritis |
| Q38676110 | Transancestral mapping and genetic load in systemic lupus erythematosus |
| Q37120830 | Two independent alleles at 6q23 associated with risk of rheumatoid arthritis |
| Q36365695 | Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans |