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المؤلفون: Frank Rühle, Anika Witten, Andre Franke, Monika Stoll, Verena Limperger, Andrei Barysenka, Andreas Huge, Mona Riemenschneider, Rolf M. Mesters, Ulrike Nowak-Göttl, Astrid Arning, Anne Krümpel, Christine Heller, Wolfgang Lieb, Milan Hiersche
المساهمون: RS: FHML MaCSBio, RS: CARIM - R1.01 - Blood proteins & engineering, Biochemie
المصدر: Blood, 129(6), 783-790. The American Society of Hematology
مصطلحات موضوعية: Male, 0301 basic medicine, FAMILY-BASED TESTS, Genome-wide association study, 030204 cardiovascular system & hematology, Bioinformatics, medicine.disease_cause, Biochemistry, Cohort Studies, 0302 clinical medicine, Polymorphism (computer science), Glucuronosyltransferase, Child, RISK, Genetics, Mutation, GTPase-Activating Proteins, Chromosome Mapping, High-Throughput Nucleotide Sequencing, Venous Thromboembolism, Hematology, Child, Preschool, Chromosomes, Human, Pair 6, Female, Adolescent, Immunology, DNA-SEQUENCING DATA, Nerve Tissue Proteins, Single-nucleotide polymorphism, Biology, Thrombophilia, Polymorphism, Single Nucleotide, 03 medical and health sciences, GTP-Binding Proteins, LINKAGE, medicine, Humans, Genetic Predisposition to Disease, GENOME-WIDE ASSOCIATION, Nuclear family, METAANALYSIS, Genetic association, RELEASE, Siblings, Infant, Membrane Proteins, Cell Biology, medicine.disease, ARTERIAL ISCHEMIC-STROKE, 030104 developmental biology, Genetic Loci, THROMBOPHILIA, DISEQUILIBRIUM, Venous thromboembolism, Genome-Wide Association Study
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5852c888fd76966a7a3fc32126b86c81
https://doi.org/10.1182/blood-2016-07-728840 -
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المؤلفون: Benjamin Brokinkel, Stephan Köhnemann, Astrid Jeibmann, Walter Stummer, Klaus Berger, Christian Ewelt, Markus Holling, Ulrike Nowak-Göttl, Astrid Arning, Jürgen Wellmann, Monika Stoll
المساهمون: Biochemie, RS: FHML MaCSBio, RS: CARIM - R1.06 - Genetic Epidemiology and Genomics of cardiovascular diseases
المصدر: Journal of Neurosurgery, 125(2), 269-274. American Association of Neurological Surgeons
مصطلحات موضوعية: Male, 0301 basic medicine, Population, ADAMTS, Single-nucleotide polymorphism, Bioinformatics, vascular disorders, Pathogenesis, 03 medical and health sciences, ADAMTS Proteins, 0302 clinical medicine, Genetic variation, Familial predisposition, Humans, Medicine, education, genes, education.field_of_study, business.industry, Genetic Variation, Intracranial Aneurysm, General Medicine, Middle Aged, ADAMTS13, ADAMTS2, 030104 developmental biology, cerebral aneurysm, Case-Control Studies, Female, business, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::490037ecccb6a7bdd06a5428442dec59
https://doi.org/10.3171/2015.7.JNS154 -
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المؤلفون: Monika Stoll, Anika Witten, Christina Strauss, Frank Rühle, Ulrike Nowak-Göttl, Astrid Arning, Andrei Barysenka
المصدر: Circulation: Cardiovascular Genetics. 9:357-367
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, DNA Mutational Analysis, ADAMTS13 Protein, Single-nucleotide polymorphism, 030204 cardiovascular system & hematology, Bioinformatics, Polymorphism, Single Nucleotide, Linkage Disequilibrium, 03 medical and health sciences, 0302 clinical medicine, INDEL Mutation, Von Willebrand factor, Predictive Value of Tests, Risk Factors, hemic and lymphatic diseases, von Willebrand Factor, Genetic variation, Genetics, medicine, Humans, Pediatric stroke, Genetic Predisposition to Disease, Protein Interaction Domains and Motifs, Age of Onset, Child, Genotyping, Genetics (clinical), biology, ADAMTS, Haplotype, Infant, Newborn, High-Throughput Nucleotide Sequencing, Infant, Reproducibility of Results, medicine.disease, ADAMTS13, Stroke, Phenotype, 030104 developmental biology, Haplotypes, Case-Control Studies, Child, Preschool, biology.protein, Female, Cardiology and Cardiovascular Medicine, Protein Binding
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1245002f3fea3211e1590702452578a
https://doi.org/10.1161/circgenetics.115.001184 -
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المؤلفون: Anika Witten, Ulrike Nowak-Göttl, Monika Stoll, Gerhard Kurlemann, Milan Hiersche, Karin Kurnik, Astrid Arning, Daniela Manner
المصدر: Blood. 120:5231-5236
مصطلحات موضوعية: Adult, Male, Immunology, Genome-wide association study, Single-nucleotide polymorphism, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Biochemistry, medicine, Humans, Pediatric stroke, Gene Regulatory Networks, Genetic Predisposition to Disease, Age of Onset, Child, Stroke, Genetic association, Genetics, Systems Biology, ADAMTS, Infant, Cell Biology, Hematology, Transmission disequilibrium test, medicine.disease, ADAM Proteins, Child, Preschool, Female, Algorithms, Genome-Wide Association Study, SNP array
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::286b46019b28ca9924ed9bc34dc367f9
https://doi.org/10.1182/blood-2012-07-442038 -
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المؤلفون: Peter J. Francis, Subhabrata Chakrabarti, Mark McEvoy, Usha Chakravarthy, Masakazu Akahori, Astrid Arning, Giuliana Silvestri, Inderjeet Kaur, Ammarin Thakkinstian, Takeshi Iwata, Gareth J. McKay, Euijung Ryu, John Attia, Albert O. Edwards, Johanna M. Seddon
المصدر: Thakkinstian, A, McEvoy, M, Chakravarthy, U, Chakrabarti, S, McKay, G J, Ryu, E, Silvestri, G, Kaur, I, Francis, P, Iwata, T, Akahori, M, Arning, A, Edwards, A O, Seddon, J M & Attia, J 2012, ' The association between complement component 2/complement factor B polymorphisms and age-related macular degeneration: A HuGE review and meta-analysis ' American Journal of Epidemiology, vol. 176, no. 5, pp. 361-72 . DOI: 10.1093/aje/kws031
مصطلحات موضوعية: Oncology, medicine.medical_specialty, Epidemiology, Genome-wide association study, Single-nucleotide polymorphism, Bioinformatics, Polymorphism, Single Nucleotide, Complement factor B, Macular Degeneration, Age related, Internal medicine, medicine, Humans, Allele, Association (psychology), Allele frequency, Complement component 2, business.industry, Odds ratio, Macular degeneration, Complement C2, medicine.disease, Minor allele frequency, Meta-analysis, HUMAN GENOME EPIDEMIOLOGY (HuGE) REVIEW, business, Complement Factor B
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10b0ce40e62d1d1762aab814a6a9b1b
https://doi.org/10.1093/aje/kws031 -
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المؤلفون: Monika Stoll, Astrid Arning, Albrecht Lommatzsch, Daniel Pauleikhoff, Hans-Werner Hense, Martha Dietzel, Britta Heimes
المصدر: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 252(8)
مصطلحات موضوعية: Oncology, Male, medicine.medical_specialty, genetic structures, Genotyping Techniques, Retinal Drusen, Drusen, Polymorphism, Single Nucleotide, White People, Cellular and Molecular Neuroscience, Macular Degeneration, Internal medicine, Age related, Germany, medicine, Humans, Prospective Studies, Prospective cohort study, Aged, Aged, 80 and over, business.industry, Disease progression, Proteins, Macular degeneration, Middle Aged, medicine.disease, Phenotype, eye diseases, Sensory Systems, Ophthalmology, Cross-Sectional Studies, Complement Factor H, Disease Progression, Female, sense organs, business, ATP Binding Cassette Transporter 1
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المصدر: Blood. 118:3336-3336
مصطلحات موضوعية: Genetics, Immunology, Haplotype, Single-nucleotide polymorphism, Genome-wide association study, Cell Biology, Hematology, Transmission disequilibrium test, Biology, Bioinformatics, Biochemistry, Chromosome 15, Genotype, Multiple comparisons problem, SNP array
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::24b333fee34c1ef57a3598239c326b69
https://doi.org/10.1182/blood.v118.21.3336.3336
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