المؤلفون: Singhal P; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA., Veturi Y; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA., Dudek SM; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA., Lucas A; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA., Frase A; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA., van Steen K; Department of Human Genetics, Katholieke Universiteit Leuven, ON4 Herestraat 49, 3000 Leuven, Belgium., Schrodi SJ; Laboratory of Genetics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53706, USA., Fasel D; Columbia University, New York, NY 10027, USA., Weng C; Columbia University, New York, NY 10027, USA., Pendergrass R; Genentech, San Francisco, CA 94080, USA., Schaid DJ; Mayo Clinic, Rochester, MN 55902, USA., Kullo IJ; Mayo Clinic, Rochester, MN 55902, USA., Dikilitas O; Mayo Clinic, Rochester, MN 55902, USA., Sleiman PMA; Children's Hospital of Pennsylvania, Philadelphia, PA 19104, USA., Hakonarson H; Children's Hospital of Pennsylvania, Philadelphia, PA 19104, USA., Moore JH; Department of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA., Williams SM; Department of Genetics and Genome Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA., Ritchie MD; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: marylyn@pennmedicine.upenn.edu., Verma SS; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: shefali.setiaverma@pennmedicine.upenn.edu.

المصدر: American journal of human genetics [Am J Hum Genet] 2023 Apr 06; Vol. 110 (4), pp. 575-591.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genome-Wide Association Study* , Epistasis, Genetic*, Linkage Disequilibrium/genetics ; Genotype ; Biological Specimen Banks ; United Kingdom ; Polymorphism, Single Nucleotide/genetics

المؤلفون: Schrodi SJ; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, United States of America.; Computation and Informatics in Biology and Medicine, University of Wisconsin-Madison, Madison, WI, United States of America.

المصدر: PloS one [PLoS One] 2016 Apr 29; Vol. 11 (4), pp. e0154472. Date of Electronic Publication: 2016 Apr 29 (Print Publication: 2016).

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

مواضيع طبية MeSH: Genome-Wide Association Study* , Models, Genetic* , Polymorphism, Single Nucleotide*, Female ; Genetic Markers ; Humans ; Male

المؤلفون: Ye Z; Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI, USA., Mayer J; Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI, USA., Ivacic L; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, USA., Zhou Z; Parkland Center for Clinical Innovation, Parkland Health and Hospital System, Dallas, TX, USA., He M; 1] Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI, USA [2] Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, USA., Schrodi SJ; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, USA., Page D; Computation and Informatics in Biology and Medicine, University of Wisconsin Madison, Madison, WI, USA., Brilliant MH; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, USA., Hebbring SJ; 1] Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, USA [2] Computation and Informatics in Biology and Medicine, University of Wisconsin Madison, Madison, WI, USA.

المصدر: European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Apr; Vol. 23 (4), pp. 523-9. Date of Electronic Publication: 2014 Jul 30.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Validation Study

بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Phenotype* , Polymorphism, Single Nucleotide*, Genome-Wide Association Study/*methods, Databases, Genetic ; Electronic Health Records ; Genetic Predisposition to Disease/genetics ; Genotype ; Humans ; Macular Degeneration/genetics ; Proteins/genetics ; Reproducibility of Results

المؤلفون: Nair, Rajan P, Duffin, Kristina Callis, Helms, Cynthia, Ding, Jun, Stuart, Philip E, Goldgar, David, Gudjonsson, Johann E, Li, Yun, Tejasvi, Trilokraj, Feng, Bing-Jian, Ruether, Andreas, Schreiber, Stefan, Weichenthal, Michael, Gladman, Dafna, Rahman, Proton, Schrodi, Steven J, Prahalad, Sampath, Guthery, Stephen L, Fischer, Judith, Liao, Wilson, Kwok, Pui-Yan, Menter, Alan, Lathrop, G Mark, Wise, Carol A, Begovich, Ann B, Voorhees, John J, Elder, James T, Krueger, Gerald G, Bowcock, Anne M, Abecasis, Gonçalo R

المصدر: Nature Genetics. 41(2)

مصطلحات موضوعية: Genetics, Human Genome, Psoriasis, Autoimmune Disease, Aetiology, 2.1 Biological and endogenous factors, Skin, Adult, Case-Control Studies, DNA-Binding Proteins, Female, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study, HLA-C Antigens, Humans, Interleukin-12 Subunit p40, Interleukin-13, Interleukin-23, Interleukin-4, Intracellular Signaling Peptides and Proteins, Male, Middle Aged, NF-kappa B, Nuclear Proteins, Polymorphism, Single Nucleotide, Signal Transduction, Tumor Necrosis Factor alpha-Induced Protein 3, Young Adult, Collaborative Association Study of Psoriasis, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0xc5k746

المؤلفون: Nair, Rajan P, Duffin, Kristina Callis, Helms, Cynthia, Ding, Jun, Stuart, Philip E, Goldgar, David, Gudjonsson, Johann E, Li, Yun, Tejasvi, Trilokraj, Feng, Bing-Jian, Ruether, Andreas, Schreiber, Stefan, Weichenthal, Michael, Gladman, Dafna, Rahman, Proton, Schrodi, Steven J, Prahalad, Sampath, Guthery, Stephen L, Fischer, Judith, Liao, Wilson, Kwok, Pui-Yan, Menter, Alan, Lathrop, G Mark, Wise, Carol A, Begovich, Ann B, Voorhees, John J, Elder, James T, Krueger, Gerald G, Bowcock, Anne M, Abecasis, Gonçalo R, Collaborative Association Study of Psoriasis

المصدر: Nature genetics. 41(2)

مصطلحات موضوعية: Collaborative Association Study of Psoriasis, Humans, Psoriasis, Genetic Predisposition to Disease, Intracellular Signaling Peptides and Proteins, DNA-Binding Proteins, NF-kappa B, Nuclear Proteins, Interleukin-4, Interleukin-13, HLA-C Antigens, Case-Control Studies, Signal Transduction, Gene Frequency, Polymorphism, Single Nucleotide, Adult, Middle Aged, Female, Male, Interleukin-23, Interleukin-12 Subunit p40, Genome-Wide Association Study, Young Adult, Tumor Necrosis Factor alpha-Induced Protein 3, Genetics, Autoimmune Disease, Clinical Research, 2.1 Biological and endogenous factors, Inflammatory and immune system, Skin, Developmental Biology, Biological Sciences, Medical and Health Sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0xc5k746

المؤلفون: Singhal, Pankhuri, Veturi, Yogasudha, Dudek, Scott M, Lucas, Anastasia, Frase, Alex, Van Steen, Kristel, Schrodi, Steven J, Fasel, David, Weng, Chunhua, Pendergrass, Rion, Schaid, Daniel J, Kullo, Iftikhar J, Dikilitas, Ozan, Sleiman, Patrick M A, Hakonarson, Hakon, Moore, Jason H, Williams, Scott M, Ritchie, Marylyn D, Verma, Shefali S

المصدر: American Journal of Human Genetics, 110 (4), 575 - 591 (2023-04-06)

مصطلحات موضوعية: complex human disease, epistasis, essential genes, evolution, interchromosomal, linkage disequilibrium, long-range, pleiotropy, variable expressivity, Linkage Disequilibrium/genetics, Genotype, Biological Specimen Banks, United Kingdom, Polymorphism, Single Nucleotide/genetics, Genome-Wide Association Study, Epistasis, Genetic, Polymorphism, Single Nucleotide, Genetics, Genetics (clinical), Life sciences, Sciences du vivant

Relation: https://api.elsevier.com/content/article/PII:S0002929723000915?httpAccept=text/xml; urn:issn:0002-9297; urn:issn:1537-6605

URL الوصول: https://orbi.uliege.be/handle/2268/304724

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