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Genes and Immunity, ISSN 1466-4879, 06/2011, Volume 12, Issue 4, pp. 270 - 279
Journal Article
BMC MEDICINE, ISSN 1741-7015, 07/2019, Volume 17, Issue 1, pp. 135 - 19
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2013, Volume 8, Issue 8, p. e69404
Protein tyrosine phosphatase non-receptor type 22 (PTPN22) is a negative regulator of T-cell activation associated with several autoimmune diseases, including... 
RHEUMATOID-ARTHRITIS | OF-FUNCTION VARIANT | C1858T POLYMORPHISM | GENETIC ASSOCIATION | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | SINGLE-NUCLEOTIDE POLYMORPHISM | LYMPHOID TYROSINE PHOSPHATASE | AUTOIMMUNE-DISEASE | GENOME-WIDE ASSOCIATION | R620W POLYMORPHISM | Antibodies, Anticardiolipin - immunology | Haplotypes | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Hispanic Americans - genetics | Gene Frequency | Humans | Protein Tyrosine Phosphatase, Non-Receptor Type 22 - genetics | African Americans - genetics | Genotype | Logistic Models | Linkage Disequilibrium | Phenotype | Asian Americans - genetics | Immunoglobulin G - immunology | Lupus Erythematosus, Systemic - ethnology | Lupus Erythematosus, Systemic - genetics | Lupus Erythematosus, Systemic - immunology | Genetic Predisposition to Disease - ethnology | Polymorphism, Single Nucleotide | Lupus | Tyrosine | Autoimmunity | Systemic lupus erythematosus | Phosphatases | Autoantibodies | Immunoglobulin G | Genetic aspects | T cells | Health sciences | Disease | Physicians | Lymphocytes T | Phosphatase | Proteins | Cell activation | Immunology | Medical research | Rheumatic diseases | Rheumatology | Ethnic factors | Children & youth | Medicine | Chronic conditions | Hospitals | Gene frequency | Collaboration | Rheumatoid arthritis | Cardiolipin | Autoimmune diseases | Protein-tyrosine-phosphatase
Journal Article
by Zouk, Hana and Venner, Eric and Lennon, Niall J and Muzny, Donna M and Abrams, Debra and Adunyah, Samuel and Albertson-Junkans, Ladia and Ames, Darren C and Appelbaum, Paul and Aronson, Samuel and Aufox, Sharon and Babb, Lawrence J and Balasubramanian, Adithya and Bangash, Hana and Basford, Melissa and Bastarache, Lisa and Baxter, Samantha and Behr, Meckenzie and Benoit, Barbara and Bhoj, Elizabeth and Bielinski, Suzette J and Bland, Sarah T and Blout, Carrie and Borthwick, Kenneth and Bottinger, Erwin P and Bowser, Mark and Brand, Harrison and Brilliant, Murray and Brodeur, Wendy and Caraballo, Pedro and Carrell, David and Carroll, Andrew and Almoguera, Berta and Castillo, Lisa and Castro, Victor and Chandanavelli, Gauthami and Chiang, Theodore and Chisholm, Rex L and Christensen, Kurt D and Chung, Wendy and Chute, Christopher G and City, Brittany and Cobb, Beth L and Connolly, John J and Crane, Paul and Crew, Katherine and Crosslin, David and De Andrade, Mariza and De la Cruz, Jessica and Denson, Shawn and Denny, Josh and DeSmet, Tim and Dikilitas, Ozan and Friedrich, Christopher and Fullerton, Stephanie M and Funke, Birgit and Gabriel, Stacey and Gainer, Vivian and Gharavi, Ali and Glazer, Andrew M and Glessner, Joseph T and Goehringer, Jessica and Gordon, Adam S and Graham, Chet and Green, Robert C and Gundelach, Justin H and Dayal, Jyoti and Hain, Heather S and Hakonarson, Hakon and Harden, Maegan V and Harley, John and Harr, Margaret and Hartzler, Andrea and Hayes, M. Geoffrey and Hebbring, Scott and Henrikson, Nora and Hershey, Andrew and Hoell, Christin and Holm, Ingrid and Howell, Kayla M and Hripcsak, George and Hu, Jianhong and Jarvik, Gail P and Jayaseelan, Joy C and Jiang, Yunyun and Joo, Yoonjung Yoonie and Jose, Sheethal and Josyula, Navya Shilpa and Justice, Anne E and Kalla, Sara E and Kalra, Divya and Karlson, Elizabeth and Kelly, Melissa A and Keating, Brendan J and Kenny, Eimear E and Key, Dustin and Kiryluk, Krzysztof and Kitchner, Terrie and Klanderman, Barbara and Klee, Eric and ... and eMERGE Consortium and eMERGE Consortium. Electronic address: agibbs@bcm.edu
The American Journal of Human Genetics, ISSN 0002-9297, 09/2019, Volume 105, Issue 3, pp. 588 - 605
The advancement of precision medicine requires new methods to coordinate and deliver genetic data from heterogeneous sources to physicians and patients. The... 
clinical sequencing | eMERGE | electronic health record | next generation sequencing | harmonization | FRAMEWORK | TRISOMY-12 MOSAICISM | VARIANTS | GENETICS & HEREDITY | FEATURES | Usage | Research | Nucleotide sequencing | DNA sequencing
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 02/2017, Volume 195, Issue 4, pp. 456 - 463
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 05/2015, Volume 96, Issue 5, pp. 731 - 739
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 07/2018, Volume 27, Issue 13, pp. 2392 - 2404
Abstract Systemic lupus erythematosus (SLE or lupus) (OMIM: 152700) is a chronic autoimmune disease with debilitating inflammation that affects multiple organ... 
RHEUMATOID-ARTHRITIS | POPULATION | GENETIC SUSCEPTIBILITY LOCI | AUTOIMMUNE-DISEASES | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | STAT4 | FAMILIAL AGGREGATION | ADMIXTURE | ERYTHEMATOSUS | GENOME-WIDE ASSOCIATION | IFN-ALPHA | Association Studies
Journal Article