Michael F. Seldin

Michael F. Seldin's AcademicInfluence.com Rankings

Michael F. Seldin

Philosophy

#7930

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#11214

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#6310

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philosophy Degrees

Michael F. Seldin

Biology

#10685

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#14037

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Biochemistry

#1713

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#1848

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Philosophy
Biology

Michael F. Seldin's Degrees

PhD Biochemistry University of California, Berkeley
Doctorate Medicine University of California, San Francisco

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Michael F. Seldin's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Uncoupling protein-2: a novel gene linked to obesity and hyperinsulinemia (1997) (1682)
A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. (2004) (1570)
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci (2010) (1285)
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus. (2007) (1041)
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. (2008) (926)
FADD/MORT1 Is a Common Mediator of CD95 (Fas/APO-1) and Tumor Necrosis Factor Receptor-induced Apoptosis (*) (1996) (804)
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus (2009) (782)
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. (2007) (711)
Intestinal Tumorigenesis in Compound Mutant Mice of both Dpc4(Smad4) and Apc Genes (1998) (631)
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis (2007) (592)
Common variants at CD40 and other loci confer risk of rheumatoid arthritis (2008) (550)
Herpesvirus saimiri encodes a new cytokine, IL-17, which binds to a novel cytokine receptor. (1995) (545)
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America (2009) (494)
Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus (2008) (447)
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 orally administered NG-monomethyl-L- arginine (1994) (441)
A genomewide screen in multiplex rheumatoid arthritis families suggests genetic overlap with other autoimmune diseases. (2001) (386)
Human/mouse homology relationships. (1996) (375)
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis (2010) (372)
Accounting for ancestry: population substructure and genome-wide association studies. (2008) (362)
Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci (1992) (356)
Genetic variants at CD28, PRDM1, and CD2/CD58 are associated with rheumatoid arthritis risk (2009) (343)
Products, genetic linkage and limb patterning activity of a murine hedgehog gene. (1994) (330)
A Gene for a Novel Zinc-finger Protein Expressed in Differentiated Epithelial Cells and Transiently in Certain Mesenchymal Cells* (1996) (326)
Mouse Wnt receptor gene Fzd5 is essential for yolk sac and placental angiogenesis. (2001) (324)
Role for ceramide as an endogenous mediator of Fas-induced cytotoxicity. (1995) (319)
BMCP1, a Novel Mitochondrial Carrier with High Expression in the Central Nervous System of Humans and Rodents, and Respiration Uncoupling Activity in Recombinant Yeast* (1998) (315)
REL, a member of the NF-κB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis (2009) (310)
The genetics revolution and the assault on rheumatoid arthritis. (1999) (308)
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers (2016) (267)
Analysis and Application of European Genetic Substructure Using 300 K SNP Information (2008) (261)
Transancestral mapping and genetic load in systemic lupus erythematosus (2017) (253)
Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families. (2003) (247)
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis. (2005) (246)
European Population Substructure: Clustering of Northern and Southern Populations (2006) (245)
MesP1: a novel basic helix-loop-helix protein expressed in the nascent mesodermal cells during mouse gastrulation. (1996) (241)
Herpesvirus Saimiri encodes a new cytokine, IL-17, which binds to a novel cytokine receptor. (1995) (241)
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways (2015) (233)
Regulation of anti-cyclic citrullinated peptide antibodies in rheumatoid arthritis: contrasting effects of HLA-DR3 and the shared epitope alleles. (2005) (217)
Glycine receptor β–subunit gene mutation in spastic mouse associated with LINE–1 element insertion (1994) (211)
Specificity of the STAT4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus (2008) (207)
ADAM-TS5, ADAM-TS6, and ADAM-TS7, Novel Members of a New Family of Zinc Metalloproteases (1999) (206)
Genomic organization, promoter region analysis, and chromosome localization of the mouse bcl-x gene. (1997) (201)
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. (2011) (196)
Dissecting the genetic complexity of the association between human leukocyte antigens and rheumatoid arthritis. (2002) (195)
Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells. (2002) (184)
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. (2004) (176)
Different isozymes of mouse 11 beta-hydroxylase produce mineralocorticoids and glucocorticoids. (1991) (176)
A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping. (2006) (175)
An actively retrotransposing, novel subfamily of mouse L1 elements (1998) (174)
Genotype–phenotype correlations in Peutz-Jeghers syndrome (2004) (174)
An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels (2009) (168)
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. (1994) (167)
New approaches to disease mapping in admixed populations (2011) (157)
Mouse extracellular superoxide dismutase: primary structure, tissue-specific gene expression, chromosomal localization, and lung in situ hybridization. (1997) (156)
Gastrointestinal hamartomatous polyposis in Lkb1 heterozygous knockout mice. (2002) (151)
Modulation of caspase-8 and FLICE-inhibitory protein expression as a potential mechanism of Epstein-Barr virus tumorigenesis in Burkitt's lymphoma. (1999) (150)
Cloning, pharmacological characterization, and genomic localization of the human creatine transporter. (1994) (150)
Genetic analysis of autoimmune gld mice. I. Identification of a restriction fragment length polymorphism closely linked to the gld mutation within a conserved linkage group (1988) (150)
Risk for myasthenia gravis maps to a 151Pro→Ala change in TNIP1 and to human leukocyte antigen‐B*08 (2012) (149)
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 (2005) (146)
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans. (2012) (143)
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. (2012) (143)
Molecular Cloning and Characterization of the Human and Mouse UDP-Glucose Dehydrogenase Genes* (1998) (139)
Molecular cloning and chromosomal localization of the mouse decay-accelerating factor genes. Duplicated genes encode glycosylphosphatidylinositol-anchored and transmembrane forms. (1995) (139)
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 (1994) (137)
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) (2015) (135)
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. (1994) (135)
A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping. (2007) (134)
Colonic hamartoma development by anomalous duplication in Cdx2 knockout mice. (1999) (133)
Ethnic-difference markers for use in mapping by admixture linkage disequilibrium. (2002) (132)
Control of Expression of Insulin Resistance and Hyperglycemia by Different Genetic Factors in Diabetic C57BL/6J Mice (1991) (131)
High-Density SNP Screening of the Major Histocompatibility Complex in Systemic Lupus Erythematosus Demonstrates Strong Evidence for Independent Susceptibility Regions (2009) (127)
Human leukocyte antigen polymorphisms in italian primary biliary cirrhosis: A multicenter study of 664 patients and 1992 healthy controls (2008) (120)
Clinical and Serologic Manifestations of Autoimmune Disease in MRL-lpr/lpr Mice Lacking Nitric Oxide Synthase Type 2 (1997) (117)
Rheumatoid arthritis risk allele PTPRC is also associated with response to anti-tumor necrosis factor alpha therapy. (2010) (117)
Cloning and characterization of the gene for mouse macrophage migration inhibitory factor (MIF). (1995) (112)
Mexican American ancestry-informative markers: examination of population structure and marker characteristics in European Americans, Mexican Americans, Amerindians and Asians (2004) (110)
Primary structure and chromosomal localization of human and mouse rod photoreceptor cGMP-gated cation channel. (1992) (109)
Protocadherin Pcdh2 shows properties similar to, but distinct from, those of classical cadherins. (1995) (108)
Analysis of East Asia Genetic Substructure Using Genome-Wide SNP Arrays (2008) (108)
Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p. (1997) (107)
Chromosomal localization of the human and mouse hyaluronan synthase genes. (1997) (107)
Lymphoid expression and regulation of A20, an inhibitor of programmed cell death. (1995) (105)
TYK2 Protein-Coding Variants Protect against Rheumatoid Arthritis and Autoimmunity, with No Evidence of Major Pleiotropic Effects on Non-Autoimmune Complex Traits (2015) (105)
Hepatocellular carcinoma caused by loss of heterozygosity in Lkb1 gene knockout mice. (2002) (103)
Characterization of mouse thrombospondin 2 sequence and expression during cell growth and development. (1992) (102)
Several Regions in the Major Histocompatibility Complex Confer Risk for Anti-CCP-Antibody Positive Rheumatoid Arthritis, Independent of the DRB1 Locus (2008) (101)
Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort (2007) (100)
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 (2005) (100)
The systemic lupus erythematosus-associated PDCD1 polymorphism PD1.3A in lupus nephritis. (2004) (99)
The human TTP protein: sequence, alignment with related proteins, and chromosomal localization of the mouse and human genes. (1991) (99)
The Family Investigation of Nephropathy and Diabetes (FIND): design and methods. (2005) (96)
Punctin, a Novel ADAMTS-like Molecule, ADAMTSL-1, in Extracellular Matrix* (2002) (95)
Myocyte nuclear factor, a novel winged-helix transcription factor under both developmental and neural regulation in striated myocytes (1994) (94)
Smoking interacts with genetic risk factors in the development of rheumatoid arthritis among older Caucasian women (2006) (93)
European Population Genetic Substructure: Further Definition of Ancestry Informative Markers for Distinguishing among Diverse European Ethnic Groups (2009) (91)
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 (1990) (90)
A Large-Scale Rheumatoid Arthritis Genetic Study Identifies Association at Chromosome 9q33.2 (2008) (90)
The Fcgamma receptor IIIA-158F allele is a major risk factor for the development of lupus nephritis among Caucasians but not non-Caucasians. (2001) (88)
The gene for the homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development (1994) (87)
Argentine population genetic structure: large variance in Amerindian contribution. (2007) (84)
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis (2017) (84)
Report of the second international workshop on human chromosome 1 mapping 1995. (1996) (78)
Genetic Ancestry Is Associated With Subclinical Cardiovascular Disease in African-Americans and Hispanics From the Multi-Ethnic Study of Atherosclerosis (2009) (78)
Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5. (1991) (74)
Nucleotide excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African Americans (2008) (73)
Cloning of a Novel C-type Lectin Expressed by Murine Macrophages* (1998) (73)
Human brain-specific L-proline transporter: molecular cloning, functional expression, and chromosomal localization of the gene in human and mouse genomes. (1995) (72)
Characterization of B61, the Ligand for the Eck Receptor Protein-Tyrosine Kinase (*) (1995) (70)
Classical HLA-DRB1 and DPB1 Alleles Account for HLA Associations with Primary Biliary Cirrhosis (2012) (69)
B94, a primary response gene inducible by tumor necrosis factor-alpha, is expressed in developing hematopoietic tissues and the sperm acrosome. (1994) (67)
Base excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African-Americans. (2009) (66)
Application of Ancestry Informative Markers to Association Studies in European Americans (2008) (64)
Genetic organization of complement receptor-related genes in the mouse (1989) (63)
Fas-mediated apoptosis of proliferating, transiently growth-arrested, and senescent normal human fibroblasts. (2000) (62)
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. (1994) (61)
Genome-Wide Analysis of DNA Methylation, Copy Number Variation, and Gene Expression in Monozygotic Twins Discordant for Primary Biliary Cirrhosis (2014) (60)
Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency (2016) (60)
Establishment of a molecular genetic map of distal mouse chromosome 1: further definition of a conserved linkage group syntenic with human chromosome 1q. (1988) (59)
Interferons as gene activators: a cluster of six interferon-activatable genes is linked to the erythroid alpha-spectrin locus on murine chromosome 1. (1989) (59)
The genetics of human autoimmune disease: A perspective on progress in the field and future directions. (2015) (58)
Encyclopedia of the mouse genome IV. (1994) (58)
Data for Genetic Analysis Workshop 16 Problem 1, association analysis of rheumatoid arthritis data (2009) (58)
Comparison of linkage maps of mouse chromosome 12 derived from laboratory strain intraspecific and Mus spretus interspecific backcrosses. (1989) (57)
Cloning, expression, and chromosomal localization of a novel cadherin-related protein, protocadherin-3. (1995) (57)
Familial leukoencephalopathy in bipolar disorder. (1998) (57)
European genetic ancestry is associated with a decreased risk of lupus nephritis. (2012) (57)
Markers that discriminate between European and African ancestry show limited variation within Africa (2002) (56)
Common variants at CD 40 and other loci confer risk of rheumatoid arthritis (2008) (56)
25‐Hydroxyvitamin D 1α‐Hydroxylase: Structure of the Mouse Gene, Chromosomal Assignment, and Developmental Expression (2001) (55)
The isolation and characterization of the murine T cell antigen receptor zeta chain gene. (1989) (54)
NIH conference. Angioimmunoblastic lymphadenopathy with dysproteinemia. (1988) (54)
The murine fem1 gene family: homologs of the Caenorhabditis elegans sex-determination protein FEM-1. (1998) (53)
A 6000 kb segment of chromosome 1 is conserved in human and mouse. (1989) (52)
A simple and accurate method for determination of microsatellite total allele content differences between DNA pools (2000) (50)
Rat pineal gland phosducin: cDNA isolation, nucleotide sequence, and chromosomal assignment in the mouse. (1991) (49)
Pathway-based analysis of primary biliary cirrhosis genome-wide association studies (2013) (49)
Genome-wide meta-analysis for rheumatoid arthritis (2006) (48)
Functional comparison of the murine macrosialin and human CD68 promoters in macrophage and nonmacrophage cell lines. (1998) (47)
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations (2015) (47)
Chromosomal mapping, isolation, and characterization of the mouse xanthine dehydrogenase gene. (1994) (47)
Admixture mapping as a tool in gene discovery. (2007) (47)
The heat stable antigen (mouse CD24) gene is differentially regulated but has a housekeeping promoter. (1993) (46)
Fine mapping of chromosome 15q25.1 lung cancer susceptibility in African-Americans. (2010) (46)
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 (1994) (45)
The inflammatory disease-associated variants in IL12B and IL23R are not associated with rheumatoid arthritis. (2008) (45)
Genetic Variants of TSLP and Asthma in an Admixed Urban Population (2011) (45)
Cloning and chromosomal mapping of the mouse Mgat3 gene encoding N-acetylglucosaminyltransferase III. (1995) (44)
The functional -169T-->C single-nucleotide polymorphism in FCRL3 is not associated with rheumatoid arthritis in white North Americans. (2006) (44)
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. (1994) (43)
Putative ancestral origins of chromosomal segments in individual african americans: implications for admixture mapping. (2004) (42)
Chromosomal localization of opioid peptide and receptor genes in the mouse. (1995) (42)
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 (1995) (42)
Mouse Sin3A interacts with and can functionally substitute for the amino-terminal repression of the Myc antagonist Mxi1. (1996) (42)
Genetic risk factors for infection in patients with early rheumatoid arthritis (2004) (42)
Multiple Genetic Variants Associated with Primary Biliary Cirrhosis in a Han Chinese Population (2015) (41)
Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients (2018) (41)
Mouse IL-1 receptor antagonist protein. Molecular characterization, gene mapping, and expression of mRNA in vitro and in vivo. (1991) (41)
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data (2016) (40)
Physical and linkage mapping of the human and murine genes for the alpha 1 chain of type IX collagen (COL9A1). (1993) (40)
Gene structure, chromosomal localization, and protein sequence of mouse CD53 (Cd53): evidence that the transmembrane 4 superfamily arose by gene duplication. (1993) (39)
Studies of the lethargic (lh/lh) mouse model of absence seizures: regulatory mechanisms and identification of the lh gene. (1999) (39)
Nucleotide sequence, expression, and chromosomal mapping of Mrp and mapping of five related sequences. (1993) (39)
Construction of a physical map on mouse and human chromosome 1: comparison of 13 Mb of mouse and 11 Mb of human DNA. (1992) (38)
Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits (2007) (38)
Genomic organization, expression, and chromosomal mapping of the mouse adrenomedullin gene. (1996) (38)
Supervised machine learning and logistic regression identifies novel epistatic risk factors with PTPN22 for rheumatoid arthritis (2010) (37)
Genes and (auto)immunity in primary biliary cirrhosis (2005) (37)
Murine common acute lymphoblastic leukemia antigen (CD10 neutral endopeptidase 24.11). Molecular characterization, chromosomal localization, and modeling of the active site. (1992) (37)
Differences in Albuminuria Between Hispanics and Whites: An Evaluation by Genetic Ancestry and Country of Origin: The Multi-Ethnic Study of Atherosclerosis (2010) (37)
Markers informative for ancestry demonstrate consistent megabase-length linkage disequilibrium in the African American population (2003) (36)
Relationship between Adiposity and Admixture in African American and Hispanic American Women (2011) (36)
Immune‐Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA–DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum (2017) (35)
Glycogen synthase: a putative locus for diet-induced hyperglycemia. (1994) (35)
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 (2012) (34)
Clonal expansion of abnormal B cells in old NZB mice (1987) (34)
Amerindian ancestry in Argentina is associated with increased risk for systemic lupus erythematosus (2008) (34)
Cloning, gene structure and genomic localization of an orphan transporter from mouse kidney with six alternatively-spliced isoforms. (1998) (33)
Stronger bone correlates with African admixture in African‐American women (2011) (33)
Replicated association of 17q12-21 with susceptibility of primary biliary cirrhosis in a Japanese cohort. (2011) (33)
T cell receptor gene expression in autoimmune mice. (1986) (32)
Relationship between diabetes risk and admixture in postmenopausal African-American and Hispanic-American women (2012) (32)
A linkage map of mouse chromosome 19: definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus. (1992) (31)
Human immune responses to hapten-conjugated cells. I. Primary and secondary proliferative responses in vitro (1978) (31)
ALOX5 gene variants affect eicosanoid production and response to fish oil supplementation[S] (2011) (31)
Cloning and mapping of the mouse a7-neuronal nicotinic acetylcholine receptor (1995) (30)
A simple and accurate method for determination of microsatellite total allele content differences between DNA pools. (2000) (30)
European population substructure is associated with mucocutaneous manifestations and autoantibody production in systemic lupus erythematosus. (2009) (30)
A hidden Markov modeling approach for admixture mapping based on case‐control data (2004) (29)
A linkage map of mouse Chromosome 1 using an interspecific cross segregating for the gld autoimmunity mutation (2004) (29)
The mouse α1(XII) and human α1(XII)-like collagen genes are localized on mouse chromosome 9 and human chromosome 6 (1992) (29)
CYP1A1/2 haplotypes and lung cancer and assessment of confounding by population stratification. (2009) (29)
Induction of expression of growth-related genes by FGF-4 in mouse fibroblasts. (1996) (28)
Mapping of the genes encoding mouse thromboxane A2 receptor and prostaglandin E receptor subtypes EP2 and EP3. (1994) (28)
Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure (2017) (28)
Mapping of the bcl-2 oncogene on mouse chromosome 1. (1988) (27)
The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus (2011) (27)
Association of SLC11A1 (NRAMP1) with persistent oligoarticular and polyarticular rheumatoid factor-negative juvenile idiopathic arthritis in Finnish patients: haplotype analysis in Finnish families. (2005) (26)
Chromosomal assignment of genes involved in glycosylphosphatidylinositol anchor biosynthesis: implications for the pathogenesis of paroxysmal nocturnal hemoglobinuria (1994) (26)
Cd28 and Ctla-4, two related members of the Ig supergene family, are tightly linked on proximal mouse chromosome 1 (2004) (26)
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs (2021) (26)
Partial structure, chromosome localization, and expression of the mouse Girk4 gene. (1997) (25)
Mapping of eight testis-specific genes to mouse chromosomes. (1997) (24)
Genome‐wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis (2019) (24)
Comparison of interspecific to intersubspecific backcrosses demonstrates species and sex differences in recombination frequency on mouse Chromosome 16 (2004) (23)
Chromosomal assignment of genes involved in glycosylphosphatidylinositol anchor biosynthesis: implications for the pathogenesis of paroxysmal nocturnal hemoglobinuria. (1994) (23)
Renin–angiotensin system gene polymorphisms predict the progression to renal insufficiency among Asians with lupus nephritis (2005) (23)
A single B1 subunit mapped to mouse chromosome 7 may be a common component of Na channel isoforms from brain, skeletal muscle and heart. (1993) (23)
CD1 defines conserved linkage group border between human chromosomes 1 and mouse chromosomes 1 and 3 (2006) (23)
Physical and genetic linkage of the genes encoding Ly-9 and CD48 on mouse and human chromosomes 1 (2004) (23)
Chromosomal localization of the gene encoding the human DNA helicase RECQL and its mouse homologue. (1995) (22)
European population substructure correlates with systemic lupus erythematosus endophenotypes in North Americans of European descent (2010) (20)
Socioeconomic status and lung cancer: unraveling the contribution of genetic admixture. (2013) (20)
Effect of xid on autoimmune C3H-gld/gld mice. (1987) (20)
Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS protein. (1992) (19)
Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994. (1994) (19)
A proximal mouse chromosome 9 linkage map that further defines linkage groups homologous with segments of human chromosomes 11, 15, and 19. (1991) (19)
The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk (2015) (19)
Linkage analysis of rheumatoid arthritis in US and UK families reveals interactions between HLA-DRB1 and loci on chromosomes 6q and 16p. (2006) (19)
Mapping of Abll within a conserved linkage group on distal mouse chromosome 1 syntenic with human chromosome 1 using an interspecific cross. (1989) (18)
Molecular properties and chromosomal location of cadherin-8. (1998) (18)
Characterisation of the mouse homologue of CD151 (PETA-3/SFA-1); genomic structure, chromosomal localisation and identification of 2 novel splice forms. (1998) (18)
Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptor. (1995) (18)
A linkage map of mouse chromosome 8: further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19. (1991) (18)
A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density (2016) (18)
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 (2003) (18)
Specificity of the STAT 4 Genetic Association for Severe Disease Manifestations of Systemic Lupus Erythematosus (2008) (17)
Localization of growth arrest-specific genes on mouse Chromosomes 1, 7, 8, 11, 13, and 16 (2004) (17)
Evidence for malaria selection of a CR1 haplotype in Sardinia (2011) (17)
Physical mapping of a family of interferon-activated genes, serum amyloid P-component, and α-spectrin on mouse chromosome 1 (2006) (17)
Mapping of the genes encoding mouse prostaglandin D, E, and F and prostacyclin receptors. (1996) (17)
Shared susceptibility variations in autoimmune diseases: a brief perspective on common issues (2009) (17)
REL, encoding a member of the NF-kB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis (2020) (16)
Comparison of statistical methods for estimating genetic admixture in a lung cancer study of African Americans and Latinos. (2008) (16)
Mouse thioredoxin gene maps on chromosome 4, whereas its pseudogene maps on chromosome 1. (1994) (16)
Relationship between hypertension and admixture in post-menopausal African American and Hispanic American women (2012) (16)
X chromosome contribution to the genetic architecture of primary biliary cholangitis. (2021) (16)
Chromosomal mapping of the tankyrase gene in human and mouse. (1999) (15)
Localization of mouse melanoma growth stimulatory activity gene (Mgsa) between Afp and Gus on chromosome 5 using interspecific backcross mice. (1990) (15)
Mouse Chromosome 3 (2004) (15)
Mapping of alpha-spectrin on distal mouse chromosome 1. (1987) (15)
Fine mapping of the MHC region identifies major independent variants associated with Han Chinese primary biliary cholangitis. (2019) (14)
Mapping of five subtype genes for muscarinic acetylcholine receptor to mouse chromosomes. (1999) (14)
A glial-specific voltage-sensitive Na channel gene maps close to clustered genes for neuronal isoforms on mouse chromosome 2. (1993) (14)
Genetic Risk and Longitudinal Disease Activity in Systemic Lupus Erythematosus Using Targeted Maximum Likelihood Estimation (2016) (13)
Murine serotonin transporter: sequence and localization to Chromosome 11 (2004) (13)
Chromosomal mapping of the high affinity Fcλ receptor gene (2004) (13)
Genetic mapping and assignment of a long-range repeat cluster to band D of chromosome 1 in Mus musculus and M. spretus. (1992) (13)
Examination of sequence homology between human chromosome 20 and the mouse genome: intense conservation of many genomic elements (2003) (13)
Genetic and molecular genetic studies of murine and human lupus. (1987) (12)
Positional cloning of the Chediak-Higashi syndrome gene: genetic mapping of the beige locus on mouse chromosome 13. (1996) (12)
Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans (2012) (12)
CIITA is not associated with risk of developing rheumatoid arthritis (2011) (11)
Mouse Chromosome 1 (2004) (11)
Human immune responses to hapten-conjugated cells. II. The roles of autologous and allogeneic histocompatibility determinants in proliferative responses in vitro. (1979) (11)
Genetic Analysis of MRL.Ipr Mice: Relationship of the Fas Apoptosis Gene to Disease Manifestations and Renal Disease-modifying Loci By Mark L. Watson,*~ Jaya K. gao,* Gary S. Gilkeson,*$ (1992) (11)
Genetic mapping of the β-arrestin 1 and 2 genes on mouse Chromosomes 7 and 11 respectively (1995) (11)
Genomic structure and chromosomal location of the mouse macrophage C-type lectin gene (1999) (10)
Role of Ia-positive cells in induction of secondary human immune responses to haptens in vitro. (1980) (10)
Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): Generation of a 5-cM, >5 megabase contig on mouse Chromosome 1 (1994) (10)
Relationship between hysterectomy and admixture in African American women. (2013) (10)
Diffuse Pulmonary Gallium Accumulation With a Normal Chest Radiogram in a Homosexual Man With Pneumocystis carinii Pneumonia: A Case Report (1983) (9)
Physical mapping of the retinoid X receptorB gene in mouse and human (2004) (9)
Analysis of maternal-offspring HLA compatibility, parent-of-origin effects, and noninherited maternal antigen effects for HLA-DRB1 in systemic lupus erythematosus. (2010) (9)
Relationship Between Gallbladder Surgery and Ethnic Admixture in African American and Hispanic American Women (2012) (9)
Genetic Variation : Evidence for Multiple Variants Associated with Rheumatoid Arthritis (2005) (8)
Allelic variants of Ly-5 in inbred and natural populations of mice (2004) (8)
Welcome to ‘Genes and Immunity’ (1999) (8)
Advances in Brief Gastrointestinal Hamartomatous Polyposis in Lkb 1 Heterozygous Knockout Mice 1 (2002) (8)
Gene structure and chromosome mapping of mouse transcription elongation factor S-II (Tcea1). (2000) (8)
Molecular Characterization of a Mouse Genomic Element Mobilized by Advanced Glycation Endproduct Modified-DNA (AGE-DNA) (1997) (7)
Partial structure, chromosome localization, and expression of the mouse Icln gene. (1997) (7)
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data (2016) (7)
Pillars Article: Herpesvirus Saimiri Encodes a New Cytokine, IL-17, which Binds to a Novel Cytokine Receptor. Immunity. 1995. 3: 811–821 (2011) (7)
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. (1995) (7)
Advances in Brief Hepatocellular Carcinoma Caused by Loss of Heterozygosity in Lkb 1 Gene Knockout Mice 1 (2002) (7)
Erratum: An actively retrotransposing, novel subfamily of mouse L1 elements (The EMBO Journal (1998) 17 (590-597)) (2001) (7)
PTPN 22 genetic variation : evidence for multiple variants associated with rheumatoid arthritis (2016) (7)
Association of DXA-derived bone mineral density and fat mass with African ancestry. (2013) (7)
Cloning, structural analysis and mapping of the mouse selenocysteine tRNA[Ser]Sec gene (Trsp) (1995) (7)
HLA-DRB1, TAP2/TAP1, and HLA-DPB1 haplotypes in Finnish juvenile idiopathic arthritis: more complexity within the MHC (2004) (7)
Mexican-American admixture mapping analyses for diabetic nephropathy in type 2 diabetes mellitus. (2010) (7)
IL-2 Modulation of Murine T-Cell Oncogene Expression (1987) (6)
Mapping of recombinant retrovirus integration sites that cause expression of the viral genome in murine embryonal carcinoma cells (2004) (6)
Molecular analysis of the murine C4b-binding protein gene. Chromosome assignment and partial gene organization. (1989) (6)
The chromosome 7q region association with rheumatoid arthritis in females in a British population is not replicated in a North American case-control series. (2009) (6)
Independent Origin of c.57 C > T Mutation in MIR184 Associated with Inherited Corneal and Lens Abnormalities (2015) (6)
Genetic mapping of the glycine receptor alpha 3 subunit on mouse chromosome 8. (1994) (6)
The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk (2015) (6)
Physical linkage of genes encoding the lymphocyte adhesion molecules CD2 and its ligand LFA-3 (2006) (5)
Mapping the peroxisome proliferator-activated receptor to Chromosome 15 in the mouse (1994) (5)
Linkage of the mouse Hsp84 heat shock protein structural gene to the H-2 complex (2004) (5)
The mouse alpha 1(XII) and human alpha 1(XII)-like collagen genes are localized on mouse chromosome 9 and human chromosome 6. (1992) (5)
Organization and chromosomal locations of Rap1a/Krev sequences in the mouse (2004) (5)
Mapping of the Ly-4 (L3T4) T-cell differentiation antigen on mouse chromosome 6 by the use of RFLPs in an interspecific cross (2004) (5)
Genome‐wide meta‐analysis identifies susceptibility loci for autoimmune hepatitis type 1 (2022) (5)
Mouse skeletal alpha actin has limited restriction fragment length polymorphism and is not a member of the human 1q-mouse distal chromosome 1 syntatic group. (1987) (5)
Localization of the osteocalcin gene cluster on mouse Chromosome 3 (1994) (5)
The mouse CD7 gene: identification of a new element common to the human CD7 and mouse Thy-1 promoters (1996) (5)
Primary biliary cirrhosis and autoimmunity: evaluating the genetic risk. (2000) (5)
Mouse chromosome 1 (2004) (4)
Genetic mapping of the glycine receptor α3 subunit on mouse Chromosome 8 (1994) (4)
Genetic mapping of the T lymphocyte-specific transcription factor 7 gene on mouse Chromosome 11 (1995) (4)
Encyclopedia of the mouse genome VII. Mouse chromosome 1. (1998) (4)
A comparison of genetic linkage maps surrounding the Lsh/Ity/Bcg disease resistance locus. (1989) (4)
A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis (2010) (4)
Mapping of six germ cell-specific genes to mouse chromosomes (2009) (4)
Genetic variation at the CD28 locus and its impact on expansion of pro-inflammatory CD28 negative T cells in healthy individuals (2017) (4)
Recognition of hapten-modified cells in vitro by human T-lymphocytes. (1979) (4)
Mouse Chromosome 1 (1999) (3)
Relationship between glaucoma and admixture in postmenopausal African American women. (2014) (3)
Admixed populations and autoimmunity. (2008) (3)
Genetic Aspects of Murine Lupus (1987) (3)
Genetic mapping of the integrin alpha 1 gene (Vla1) to mouse chromosome 13. (1992) (3)
Chromosome mapping of the Emr1 gene (1997) (3)
Corrected centromere orientation for mouse Chromosome 19 MIT markers (2004) (3)
Approach to the use of antigen non-specific immunosuppression in systemic lupus erythematosus and other rheumatic autoimmune diseases (1988) (3)
Chromosomal mapping of the high affinity Fc gamma receptor gene. (1992) (3)
Mouse chromosome 3 (2004) (3)
Genetic mapping of the tumor-associated mucin 1 gene on mouse Chromosome 3 (1995) (3)
Mouse chromosome 1 (2009) (2)
Chromosomal mapping of the potassium channel genes Kcnq2 and Kcnq3 in mouse. (1999) (2)
The gene encoding the mouse serum amyloid A protein, apo-SAA5, maps to proximal chromosome 7 (2004) (2)
Localization of mouse parathyroid hormone-like peptide gene (Pthlh) to distal chromosome 6 using interspecific backcross mice and in situ hybridization. (1992) (2)
Gene organization and chromosome mapping of the testis-specific S-II (1998) (2)
Fine-mapping of the 5 p 15 . 33 , 6 p 22 . 1p 21 . 31 , and 15 q 25 . 1 Regions Identi fi es Functional and Histology-Speci fi c Lung Cancer Susceptibility Loci in African-Americans (2013) (2)
Mouse chromosome 1 (2004) (2)
Calendar of Events 1992 (1992) (2)
Genetic mapping of the high-affinity nerve growth factor receptor gene, Ntrk1, to mouse chromosome 3. (1993) (2)
Mouse Cd7 maps to chromosome 11 (2004) (2)
Mapping of the mouse Rar loci encoding retinoic acid receptors RARα, RARβ and RARγ (1993) (2)
New approaches to the genetics of autoimmune disease. (1992) (2)
The mouseCD7 gene: Identification of a new element common to the humanCD7 and mouseThy-1 promoters (2007) (2)
Corrigendum: Genome-Wide Analysis of DNA Methylation, Copy Number Variation, and Gene Expression in Monozygotic Twins Discordant for Primary Biliary Cirrhosis (2014) (2)
Gender and racial differences in rates of total hip replacement. (2003) (2)
Welcome to Volume Two of Genes and Immunity! (2001) (2)
Conservation of the linkage of the murine Itga2b and Itgb3 loci in mouse Chromosome 11 (1999) (1)
No association of ADPRT alleles with SLE susceptibility, severe nephritis or the APLA syndrome (1999) (1)
A Hidden Markov Modeling Approach for Admixture Mapping Based on Case-Control Haplotype Data (2003) (1)
The functional genes for protein synthesis initiation factor 4AI and 4AII map to mouse Chromosomes 11 and 16 (2004) (1)
Mapping of the mouse Rar loci encoding retinoic acid receptors RAR alpha, RAR beta and RAR gamma. (1993) (1)
Assignment1 of Microrchidia (Morc) to mouse chromosome 16 by interspecific backcross linkage analysis and human chromosome 3q13 using somatic cell hybrids and in situ hybridization (2000) (1)
Replication Study of Association of IL13 Pathway Polymorphisms and Asthma Using an Admixed Urban Population. (2009) (1)
Erratum: Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in Europeans (The American Journal of Human Genetics (2012) 91 (778-793)) (2015) (1)
Human histone 3 F2 detects RFLPs in inbred mice, cosegregates with H4F2 and does not map to possible syntenic groups on mouse distal chromosomes 1 and distal chromosomes 3. (1987) (1)
A Large-Scale Rheumatoid Arthritis Genetic Study Identifies TRAF1 Variants on Chr 9q33.2 (2007) (1)
Encyclopedia of the mouse genome V. Mouse chromosome 1. (1996) (1)
Genetic mapping of the mouse topoisomerase II alpha gene to chromosome 11. (1993) (1)
Mouse chromosome 18 (2004) (1)
The 2000 Chromosome Committee Reports for the Mouse Genome (2000) (1)
O28 Largest Genetic Study to Date in Sporadic Inclusion Body Myositis Confirms the Human Leukocyte Antigen as the Most Associated Region and Suggests a Role for C-C Chemokine Receptor Type 5 (2016) (1)
Encyclopedia of the mouse genome V. Mouse chromosome 3. (1996) (1)
Mapping of the genes for four members of the transmembrane 4 superfamily: mouse Cd9, Cd63, Cd81, and Cd82 (2004) (1)
Genetic mapping of the mouse topoisomerase IIα gene to Chromosome 11 (2004) (1)
Mouse Chromosome 19 (2004) (0)
Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581]. (2023) (0)
A Novel Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis (2016) (0)
Subject Index Vol. 60, 1992 (1992) (0)
A molecular genetic approach to gld "autoimmune" disease. (1988) (0)
Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (2021) (0)
1400 DISCOVERY OF A DIRECT ASSOCIATION BETWEEN PRIMARY BILIARY CIRRHOSIS AND LOW BONE MASS: IDENTIFICATION OF TNFSF11/RANKL AS A RISK LOCUS FOR PATIENTS WITH PBC (2012) (0)
Polymorphisms in Thymic Stromal Lymphopoietin (TSLP) Pathways and Asthma in an Urban Admixed Population. (2009) (0)
GENETIC ANCESTRY AND COUNTRY OF ORIGIN (2010) (0)
A regulatory variant at 19p13.3 is associated with primary biliary cholangitis risk and ARID3A expression (2023) (0)
An actively retrotransposing, novel subfamily of mouse L1 elements (2013) (0)
Quantification of pepsin in rennet using a monoclonal antibody-based inhibition ELISA (2020) (0)
Potential Of Integrating Human Genetics and Electronic Medical Records For Drug Discovery : The Example Of TYK2 and Rheumatoid Arthritis (2013) (0)
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 1. (1993) (0)
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 3. (1993) (0)
Positional cloning of the lh absence disease gene (1999) (0)
SocioeconomicStatusandLungCancer:Unravelingthe ContributionofGeneticAdmixture (2013) (0)
Eleventh International Chromosome Conference (2004) (0)
The Isolation and Characterization of Receptor { Chain Gene * the Murine T Cell Antigen (2001) (0)
A highly conserved family of chromosomal proteins are caspase substrates during apoptosis (1999) (0)
Mouse chromosome 1 (2009) (0)
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 Orally Administered NG-Monomethyl-L-Arglnlne (1994) (0)
Genetic mapping of DNA topoisomerase I-related sequences to mouse Chromosomes 2 and 14 (1994) (0)
Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure (2017) (0)
NpgRJ_Ng_2007-27 1..6 (2007) (0)
Replication study and meta-analysis indicate a suggestive association of RUNX3 locus with primary biliary cholangitis (2020) (0)
Replication Of An Association Of The Interleukin-1 Receptor Antagonist Gene With Asthma In An Adult Urban Admixed Population (2010) (0)
Genetic mapping of Pp11r, a thymocyte gene expressed during apoptosis, to mouse Chromosome 15 (2004) (0)
Gender and racial differences in rates of total hip replacement [3] (multiple letters) (2003) (0)
Association of SLC11A1 (NRAMP1) with persistent oligoarticular and polyarticular rheumatoid factor - negative juvenile idiopathic arthritis in Finnis patients (2005) (0)
HLA antigens in angioimmunoblastic lymphadenopathy. (1985) (0)
Genetic admixture and cardiovascular disease risk in postmenopausal Hispanic women. (2022) (0)
Increased sensitivity of gp210 autoantibody detection using a newly designed gp210 antigen. (2021) (0)
ThehumanTTPprotein: sequence, alignment withrelated proteins, andchromosomal localization ofthemouseand humangenes (1991) (0)
Human Immune Responses to Hapten-Conjugated Cells (1979) (0)
1315 REPLICATED ASSOCIATION OF 170.12-21 WITH SUSCEPTIBILITY OF PRIMARY BILIARY CIRRHOSIS IN A JAPANESE COHORT (2011) (0)
Mouse chromosome 3 (2004) (0)
Looking back and looking forward (2003) (0)
Genetic variation at the CD28 locus and its impact on expansion of pro-inflammatory CD28 negative T cells in healthy individuals (2017) (0)
The 36th American Cytogenetics Conference (2000) (0)

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