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1Academic Journal
المؤلفون: María de la Puente, Jorge Ruiz-Ramírez, Adrián Ambroa-Conde, Catarina Xavier, Jacobo Pardo-Seco, Jose Álvarez-Dios, Ana Freire-Aradas, Ana Mosquera-Miguel, Theresa E. Gross, Elaine Y. Y. Cheung, Wojciech Branicki, Michael Nothnagel, Walther Parson, Peter M. Schneider, Manfred Kayser, Ángel Carracedo, Maria Victoria Lareu, Christopher Phillips, on behalf of the VISAGE Consortium on behalf of the VISAGE Consortium
المصدر: Genes; Volume 12; Issue 8; Pages: 1284
مصطلحات موضوعية: bio-geographical ancestry, massively parallel sequencing, ancestry informative markers, SNPs, 1000 Genomes, Human Origins SNP array
جغرافية الموضوع: agris
وصف الملف: application/pdf
Relation: Molecular Genetics and Genomics; https://dx.doi.org/10.3390/genes12081284
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المؤلفون: Stefanie Scheiper-Welling, Monika Tabunscik, Theresa E. Gross, Tina Jenewein, Britt M. Beckmann, Constanze Niess, Elise Gradhand, Cora Wunder, Peter M. Schneider, Markus A. Rothschild, Marcel A. Verhoff, Silke Kauferstein
المصدر: International Journal of Legal Medicine. 136:475-482
مصطلحات موضوعية: Pathology and Forensic Medicine
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المؤلفون: Stefanie, Scheiper-Welling, Monika, Tabunscik, Theresa E, Gross, Tina, Jenewein, Britt M, Beckmann, Constanze, Niess, Elise, Gradhand, Cora, Wunder, Peter M, Schneider, Markus A, Rothschild, Marcel A, Verhoff, Silke, Kauferstein
المصدر: International journal of legal medicine. 136(2)
مصطلحات موضوعية: Cohort Studies, Young Adult, Death, Sudden, Cardiac, Adolescent, High-Throughput Nucleotide Sequencing, Humans, Autopsy, Genetic Testing
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المؤلفون: D. Power, S. Olson, Mayra Eduardoff, Masaki Hashiyada, Dennis McNevin, Ana Freire-Aradas, Walther Parson, Ana Mosquera-Miguel, Maria Victoria Lareu, Christopher Phillips, M. de la Puente, Runa Daniel, Robert Lagacé, Sharon Wootton, Kenneth K. Kidd, Peter M. Schneider, C. Oz, L. Dagostino, Theresa E. Gross
المصدر: Forensic Science International: Genetics. 42:213-226
مصطلحات موضوعية: Genetic Markers, 0301 basic medicine, Asia, Oceania, Population, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Pathology and Forensic Medicine, Middle East, 03 medical and health sciences, 0302 clinical medicine, Asia pacific, Gene Frequency, Genotype, Genetics, Humans, Multiplex, East Asia, 030216 legal & forensic medicine, education, education.field_of_study, Massive parallel sequencing, Continental Population Groups, Racial Groups, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, DNA Fingerprinting, Genetics, Population, 030104 developmental biology, Geography, Haplotypes, Evolutionary biology, Legal & Forensic Medicine, Near Oceania
وصف الملف: application/pdf
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5Electronic Resource
المؤلفون: on behalf of the VISAGE Consortium, María de la Puente, Jorge Ruiz-Ramírez, Adrián Ambroa-Conde, Catarina Xavier, Jacobo Pardo-Seco, Jose Álvarez-Dios, Ana Freire-Aradas, Ana Mosquera-Miguel, Theresa E. Gross, Elaine Y.Y. Cheung, Wojciech Branicki, Michael Nothnagel, Walther Parson, Peter M. Schneider, M.H. (Manfred) Kayser, Ángel Carracedo, Maria Victoria Lareu, Christopher Phillips
مصطلحات الفهرس: info:eu-repo/semantics/article
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المؤلفون: Sarah E. Medland, Christopher Phillips, Sijie J. Wu, Ewelina Pośpiech, Lorena Girón-Santamaría, Theresa E. Gross, Ana Freire-Aradas, Ghu Zhu, Shuhua Xu, David Ballard, Manfred Kayser, Yan Chen, Fan Liu, Ana Mosquera-Miguel, Sijia Wang, Marielle Vennemann, Anastasia Aliferi, Peter M. Schneider, Niels Morling, Krystal Breslin, Nicholas G. Martin, Cordula Haas, Li Jin, Susan Walsh, Angel Carracedo, Gabriela Huber, Mario Gysi, Titia Sijen, Denise Syndercombe-Court, Lakshmi Chaitanya, Wojciech Branicki, Jeppe Dyrberg Andersen, Magdalena Kukla-Bartoszek, Małgorzata Skowron, Charanya Muralidharan, Walther Parson, Kristiaan J. van der Gaag
المساهمون: Genetic Identification
المصدر: Pośpiech, E, Chen, Y, Kukla-Bartoszek, M, Breslin, K, Aliferi, A, Andersen, J D, Ballard, D, Chaitanya, L, Freire-Aradas, A, van der Gaag, K J, Girón-Santamaría, L, Gross, T E, Gysi, M, Huber, G, Mosquera-Miguel, A, Muralidharan, C, Skowron, M, Carracedo, Á, Haas, C, Morling, N, Parson, W, Phillips, C, Schneider, P M, Sijen, T, Syndercombe-Court, D, Vennemann, M, Wu, S, Xu, S, Jin, L, Wang, S, Zhu, G, Martin, N G, Medland, S E, Branicki, W, Walsh, S, Liu, F & Kayser, M 2018, ' Towards broadening Forensic DNA Phenotyping beyond pigmentation : Improving the prediction of head hair shape from DNA ', Forensic Science International: Genetics, vol. 37, pp. 241-251 . https://doi.org/10.1016/j.fsigen.2018.08.017
Forensic Science International: Genetics, 37, 241-251. Elsevier Ireland Ltdمصطلحات موضوعية: Adult, 0301 basic medicine, Genotyping Techniques, Single-nucleotide polymorphism, Computational biology, Biology, Polymorphism, Single Nucleotide, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Genotype-phenotype distinction, head hair, Genetics, Humans, SNP, 030216 legal & forensic medicine, Massive parallel sequencing, Models, Genetic, targeted massively parallel sequencing, High-Throughput Nucleotide Sequencing, Paleogenetics, DNA, Sequence Analysis, DNA, Ion semiconductor sequencing, hair shape, DNA prediction, Logistic Models, Phenotype, 030104 developmental biology, Genetic marker, Sample size determination, Forensic DNA Phenotyping, externally visible characteristics, Genome-Wide Association Study, Hair
وصف الملف: application/pdf
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المؤلفون: F.-X. Laurent, M. van den Berge, Guro Dørum, A.D. Roeder, Cordula Haas, Andrea Berti, M. Trautmann, Theresa E. Gross, Denise Syndercombe-Court, Ana Mosquera-Miguel, P. Brito, Athina Vidaki, E. N. Hanssen, Erin K. Hanson, Ewelina Pośpiech, Marie-Louise Kampmann, Niels Morling, Katherine Butler Gettings, K.J. van der Gaag, Maria João Porto, Jack Ballantyne, Manfred Kayser, K. Schulze Johann, J. Vannier, Carolyn R. Steffen, Federica Giangasparo, P. Elsmore, Sabrina Ingold, V. Verdoliva, Walther Parson, Christopher Phillips, S. Hansen, Catarina Xavier, Wojciech Branicki, Peter M. Schneider
المساهمون: Genetic Identification
المصدر: Ingold, S, Dørum, G, Hanson, E, Berti, A, Branicki, W, Brito, P, Elsmore, P, Gettings, K B, Giangasparo, F, Gross, T E, Hansen, S, Hanssen, E N, Kampmann, M-L, Kayser, M, Laurent, F-X, Morling, N, Mosquera-Miguel, A, Parson, W, Phillips, C, Porto, M J, Pośpiech, E, Roeder, A D, Schneider, P M, Johann, K S, Steffen, C R, Syndercombe-Court, D, Trautmann, M, van den Berge, M, van den Gaag, K J, Vannier, J, Verdoliva, V, Vidaki, A, Xavier, C & Ballantyne, J 2018, ' Body fluid identification using a targeted mRNA massively parallel sequencing approach – results of a EUROFORGEN/EDNAP collaborative exercise ', Forensic Science International-Genetics . https://doi.org/10.1016/j.fsigen.2018.01.002
Forensic Science International: Genetics, 34, 105-115. Elsevier Ireland Ltdمصطلحات موضوعية: 0301 basic medicine, Genetic Markers, Male, Saliva, Semen, Computational biology, Biology, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Genetics, Humans, 030216 legal & forensic medicine, RNA, Messenger, Least-Squares Analysis, Menstrual blood, Skin, Body fluid, Messenger RNA, Massive parallel sequencing, body fluid identification, massively parallel sequencing, High-Throughput Nucleotide Sequencing, Ion semiconductor sequencing, mRNA profiling, Menstruation, 030104 developmental biology, MRNA Sequencing, Cervix Mucus, Female, Forensic science, Laboratories, Blood Chemical Analysis
وصف الملف: application/pdf
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المؤلفون: Walther Parson, Wojciech Branicki, Ana Mosquera-Miguel, Carole Ames, Theresa E. Gross, Carsten Hohoff, Ewa Kartasinska, Maria de la Puente, Catarina Xavier, Andrew P. Revoir, Vivian Kalamara, Peter M. Schneider, Ewelina Pośpiech, Christopher Phillips, Athina Vidaki, Magdalena Spólnicka, Manfred Kayser, Ana Freire-Aradas
المساهمون: Universidade de Santiago de Compostela. Departamento de Ciencias Forenses, Anatomía Patolóxica, Xinecoloxía e Obstetricia, e Pediatría, Genetic Identification
المصدر: Forensic Science International: Genetics
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
Forensic Science International: Genetics, 48:102336. Elsevier Ireland Ltd
Minerva: Repositorio Institucional de la Universidad de Santiago de Compostela
Universidad de Santiago de Compostela (USC)مصطلحات موضوعية: 0301 basic medicine, Genetic Markers, Computer science, Appearance and bio-geographical ancestry prediction, Concordance, Genomics, Computational biology, MPS Ion S5, Criminal investigation, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Genetics, Crime scene, Humans, Multiplex, 030216 legal & forensic medicine, AmpliSeq, Massive parallel sequencing, Racial Groups, SNP multiplex, High-Throughput Nucleotide Sequencing, Reproducibility of Results, DNA, Sequence Analysis, DNA, Forensic DNA phenotyping, 16. Peace & justice, DNA Fingerprinting, Identification (information), 030104 developmental biology, Phenotype, DNA profiling, Software
وصف الملف: application/pdf
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المؤلفون: D. Syndercombe Court, R. Banemann, P. Hoff-Olsen, Katherine Butler Gettings, Peter M. Schneider, Adrian Linacre, Priscila Kohler, A. Roseth, Ryan England, M. Mayr-Eduardoff, R.A.H. van Oorschot, Claus Børsting, Francesca Brisighelli, A. Hoffmann, Maria João Porto, Theresa E. Gross, M. Burrington, A.M. Bento, Marcos F. Fondevila, Jennifer E. L. Templeton, Wojciech Branicki, Angel Carracedo, Vlastimil Stenzl, M. Turanská, V. L. Pascali, Cordula Haas, V. Decroyer, Lakshmi Chaitanya, Geraldine O’Donnell, Carla Santos, Catherine McGovern, Niels Morling, Joyce Harteveld, Peter M. Vallone, Runa Daniel, Walther Parson, Tomas Capal, David Ballard, L. Zatkalíková, Christopher Phillips, Titia Sijen, Manfred Kayser
المساهمون: Genetic Identification
المصدر: Forensic Science International: Genetics, 19, 56-67. Elsevier Ireland Ltd
Santos, C, Fondevila, M, Ballard, D, Banemann, R, Bento, A M, Børsting, C, Branicki, W, Brisighelli, F, Burrington, M, Capal, T, Chaitanya, L, Daniel, R, Decroyer, V, England, R, Gettings, K B, Gross, T E, Haas, C, Harteveld, J, Hoff-Olsen, P, Hoffmann, A, Kayser, M, Kohler, P, Linacre, A, Mayr-Eduardoff, M, McGovern, C, Morling, N, O'Donnell, G, Parson, W, Pascali, V L, Porto, M J, Roseth, A, Schneider, P M, Sijen, T, Stenzl, V, Court, D S, Templeton, J E, Turanska, M, Vallone, P M, Oorschot, R A H V, Zatkalikova, L, Carracedo & Phillips, C 2015, ' Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels : Results of a collaborative EDNAP exercise ', Forensic Science International-Genetics, vol. 19, pp. 56-67 . https://doi.org/10.1016/j.fsigen.2015.06.004مصطلحات موضوعية: Forensic Genetics, Genetic Markers, Genotype, Concordance, Aims, Settore BIO/08 - ANTROPOLOGIA, Ancestry-informative marker, Biology, Polymorphism, Single Nucleotide, Bayes analysis, Pathology and Forensic Medicine, Genetics, Humans, principal component analysis (PCA), Indel, Genotyping, Ancestry, ancestry, aims, Electrophoresis, Capillary, DNA, Single-base extension, SNP genotyping, Indels, bayes analysis, Principal component analysis (PCA), DNA profiling, indels, SNPs, SNP array
وصف الملف: application/pdf
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المؤلفون: Iva Gomes, Gustavo Penacino, G. Burgos, E. González, Sean Davison, António Amorim, Teresa Ribeiro, L.F. Jobim, Juan José Builes, Sandra Furfuro, A. Gonzalez-Liñan, A. Sala, L. Rubio, Carlos Martín Restrepo, M. Aler, C. Vilela-Lamego, Maria João Porto, David Parra, P. Brito, E. Betancor, Adriana Castillo, P. Coufalova, Maria Eugenia D’Amato, Q. Huang, M.L.J. Bravo, M.F. Pinheiro, Ana María López-Parra, Oscar Garcia, Gabriela Martínez-Cortés, A. Torres, Rui Pedro Gomes Pereira, Theresa E. Gross, V. Masciovecchio, S. Jiménez, Danilo Faustino Braganholi, J.F. Ferragut, Leonor Gusmão, L. Souto, A. Gaviria, Marcos F. Fondevila, L.S. Solís, Miguel Marino, Juan J. Yunis, Ana Santurtún, Regina Maria Barretto Cicarelli, Paulo Dario, Cecilia Inés Catanesi, Y. Posada, A. Hernández, Iñaki Yurrebaso, Elizeu Fagundes de Carvalho, Sofia L. Marques, Célia Alves, C. Arévalo, E. Streitemberger
المساهمون: Universidad de Cantabria, IPATIMUP (Institute of Molecular Pathology and Immunology of the University of Porto), Universidade do Porto), Instituto de Medicina Legal y Ciencias Forenses de Valencia, FCUP – Faculty of Sciences of the University of Porto, Comisaría General Policía Científica, Laboratorio de Genética Forense del Instituto de Medicina Legal de Las Palmas, Universidade Estadual Paulista (Unesp), GENES SAS, Delegação do Centro, Universidad de Antioquia, Ecuadorian Red Cross, Universidad de Las Américas, Universidade do Estado do Rio de Janeiro (UERJ), Universidad Industrial de Santander (UIS), Instituto Multidisciplinario de Biologia Celular (CONICET-UNLP-CIC), Universidad Nacional de La Plata (UNLP), Institute Criminalistics in Prague, Instituto Nacional de Medicina Legal e Ciências Forenses, University of the Western Cape, Universitat de les Illes Balears, Universidade de Santiago de Compostela, Facultad de Ciencias Médicas – UNCuyo, Basque Country Police, University of Cologne, Forensic Genetics Laboratory, Delegación de Canarias, UCM, Universidad Miguel Hernández, Hospital de Clínicas de, Universidad de Guadalajara (CUCI-UdeG), IACA Laboratorios, Unidad de Analisis de ADN (COFyBCF), University of Antioquia, Genética Molecular de Colombia Ldta, Laboratorio de periciales Médico Legales de la Universidad de Málaga, Universidad de Buenos Aires, University of Cantabria, Laboratorio Clínico Genetix, Universidade de Aveiro, Laboratorio Genia Geo, INTS, Servicios Médicos Yunis Turbay y Cia
المصدر: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
FORENSIC SCIENCE INTERNATIONAL-GENETICS
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
instname
Forensic Science International: Genetics Volume 32, January 2018, Pages 18-25
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESPمصطلحات موضوعية: 0301 basic medicine, Population genetics, Forensic genetics, purl.org/becyt/ford/1 [https], 0302 clinical medicine, Gene Frequency, INDEL Mutation, Ethnicity, Genetics, education.field_of_study, FORENSIC GENETICS, language, Human identification, Databases, Nucleic Acid, Insertion deletion (indel), HUMAN IDENTIFICATION, INSERTION DELETION (INDEL), Population data, Genotype, Medicina, Population, ALLELE FREQUENCY DATABASES, Biology, Polymorphism, Single Nucleotide, Allele frequency databases, Pathology and Forensic Medicine, Cape verde, 03 medical and health sciences, Genetic variation, Humans, 030216 legal & forensic medicine, education, Indel, purl.org/becyt/ford/1.6 [https], Allele frequency, Ciencias Exactas, Racial Groups, POPULATION DATA, DNA Fingerprinting, language.human_language, Genetics, Population, 030104 developmental biology, Genetic distance, Portuguese, Laboratories, Microsatellite Repeats, Demography
وصف الملف: application/pdf
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المؤلفون: M. de la Puente, Carla Santos, Theresa E. Gross, Christina Strobl, D. Syndercombe Court, J. Uacyisrael, M. V. Lareu, Balázs Egyed, Niels Morling, Walther Parson, Claus Børsting, Christian Hussing, L. Fusco, L. Souto, David Ballard, Christopher Phillips, Angel Carracedo, Peter M. Schneider, Mayra Eduardoff
المصدر: Eduardoff, M, Gross, T E, Santos, C, de la puente, M, Ballard, D, Strobl, C, Børsting, C, Morling, N, Fusco, L, Hussing, C, Egyed, B, Souto, L, Uacyisrael, J, Syndercombe Court, D, Carracedo, Á, Lareu, M V, Schneider, P M, Parson, W & Phillips, C 2016, ' Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™ ', Forensic Science International-Genetics, vol. 23, pp. 178-189 . https://doi.org/10.1016/j.fsigen.2016.04.008
مصطلحات موضوعية: Genetic Markers, 0301 basic medicine, Genotype, Population, Single-nucleotide polymorphism, Computational biology, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Forensic ancestry analysis, Databases, Genetic, Genetics, Humans, SNP, Multiplex, Ancestry-informative SNPs, 030216 legal & forensic medicine, Inter-laboratory, education, Genotyping, DNA Primers, education.field_of_study, Massive parallel sequencing, Racial Groups, DNA Degradation, Necrotic, High-Throughput Nucleotide Sequencing, DNA Fingerprinting, SNP genotyping, Genetics, Population, 030104 developmental biology, Ion PGM™, Massively parallel sequencing (MPS)
وصف الملف: application/pdf
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المؤلفون: Theresa E. Gross, Carla Santos, Christina Strobl, Walther Parson, Beatriz Sobrino, Angel Carracedo, Maria Victoria Lareu, Peter M. Schneider, David Ballard, Marcos F. Fondevila, Christopher Phillips, Mayra Eduardoff, M. de la Puente
المصدر: Eduardoff, M, Santos, C, De La Puente, M, Gross, T E, Fondevila, M, Strobl, C, Sobrino, B, Ballard, D, Schneider, P M, Carracedo, Lareu, M V, Parson, W & Phillips, C 2015, ' Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™ ', Forensic Science International-Genetics, vol. 17, 1342, pp. 110-121 . https://doi.org/10.1016/j.fsigen.2015.04.007
مصطلحات موضوعية: Forensic Genetics, Male, Massively parallel sequencing, Genotyping Techniques, Identification SNPs, Computational biology, Biology, Ion Torrent, Polymorphism, Single Nucleotide, DNA sequencing, Pathology and Forensic Medicine, Next generation sequencing, Genetics, Humans, Genotyping, Massive parallel sequencing, High-Throughput Nucleotide Sequencing, Reproducibility of Results, DNA Patterns, Ion semiconductor sequencing, DNA, Sequence Analysis, DNA, SNP genotyping, Forensic identification, Ion PGM™, Female
وصف الملف: application/pdf
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المؤلفون: Christine Keyser, A.M. Bento, Ricky Ansell, Adrian Linacre, Lívia Zatkalíková, David Ballard, Helena Nilsson, Susan Walsh, Titia Sijen, Jens Söchtig, Tomasz Kupiec, Regine Banemann, Wojciech Branicki, Peter M. Vallone, Walther Parson, Vincenzo Lorenzo Pascali, L. Norén, Andreas O. Tillmar, Martina Turanska, Priscila Kohler, Peter M. Schneider, Clémence Hollard, Theresa E. Gross, Jukka U. Palo, Antti Sajantila, Kevin M. Kiesler, Anastassiya Zidkova, Tomas Capal, Lindy Clarisse, Kaye N. Ballantyne, Francesca Brisighelli, Denise Syndercombe-Court, Niels Morling, Manfred Kayser, Cordula Haas, Christiane Maria Bauer, Jeppe Dyrberg Andersen, Lakshmi Chaitanya, Renée Ottens, P. Hoff-Olsen, Maria João Porto, Christopher Phillips, Anglika Minawi
المساهمون: Kayser, Manfred, Genetic Identification
المصدر: Chaitanya, L, Andersen, J D, Morling, N & Kayser, M (ed.) 2014, ' Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour ', Forensic Science International: Genetics, vol. 11, pp. 241-251 . https://doi.org/10.1016/j.fsigen.2014.04.006
Forensic Science International: Genetics, 11, 241-251. Elsevier Ireland Ltdمصطلحات موضوعية: ISFG, genetic structures, Population, Settore BIO/08 - ANTROPOLOGIA, Context (language use), Biology, FDP, Pathology and Forensic Medicine, EDNAP, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, 030216 legal & forensic medicine, education, Multiplex genotyping, Genotyping, 030304 developmental biology, IrisPlex, International level, 0303 health sciences, education.field_of_study, Eye colour prediction, Eye Color, eye colour prediction, DNA, Forensic DNA phenotyping, medicine.anatomical_structure, DNA profiling, Human eye, forensic DNA phenotyping, Forensic genetics
وصف الملف: application/pdf
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المصدر: Forensic Science International: Genetics Supplement Series. 4:e25-e26
مصطلحات موضوعية: Genetics, DNA database, food and beverages, SNP, Single-nucleotide polymorphism, Multiplex, Ancestry-informative marker, Computational biology, Biology, Indel, Pathology and Forensic Medicine