المؤلفون: Diana I. Cruz-Dávalos, María A. Nieves-Colón, Alexandra Sockell, G. David Poznik, Hannes Schroeder, Anne C. Stone, Carlos D. Bustamante, Anna-Sapfo Malaspinas, María C. Ávila-Arcos

المصدر: BMC Genomics, Vol 19, Iss 1, Pp 1-16 (2018)

مصطلحات موضوعية: Ancient DNA, Capture-enrichment, Y chromosome, Biotechnology, TP248.13-248.65, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12864-018-4945-x; https://doaj.org/toc/1471-2164

URL الوصول: https://doaj.org/article/816d1d78e11d419083ab8853a8bf6c49

المؤلفون: Lynne Krohn, Karl Heilbron, Cornelis Blauwendraat, Regina H. Reynolds, Eric Yu, Konstantin Senkevich, Uladzislau Rudakou, Mehrdad A. Estiar, Emil K. Gustavsson, Kajsa Brolin, Jennifer A. Ruskey, Kathryn Freeman, Farnaz Asayesh, Ruth Chia, Isabelle Arnulf, Michele T. M. Hu, Jacques Y. Montplaisir, Jean-Fran(c(c))ois Gagnon, Alex Desautels, Yves Dauvilliers, Gian Luigi Gigli, Mariarosaria Valente, Francesco Janes, Andrea Bernardini, Birgit Högl, Ambra Stefani, Abubaker Ibrahim, Karel ( (S))onka, David Kemlink, Wolfgang Oertel, Annette Janzen, Giuseppe Plazzi, Francesco Biscarini, Elena Antelmi, Michela Figorilli, Monica Puligheddu, Brit Mollenhauer, Claudia Trenkwalder, Friederike Sixel-Döring, Val('(e))rie Cochen De Cock, Christelle Charley Monaca, Anna Heidbreder, Luigi Ferini-Strambi, Femke Dijkstra, Mineke Viaene, Beatriz Abril, Bradley F. Boeve, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Daniella Coker, Gabriel Cuellar Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez-Brant, Pierre Fontanillas, Will Freyman, Pooja M. Gandhi, Barry Hicks, David A. Hinds, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Keng-Han Lin, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Joanna L. Mountain, Priyanka Nandakumar, Elizabeth S. Noblin, Jared O'Connell, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Alejandro Hernandez, Corinna Wong, Christophe Toukam Tchakout('(e)), Sonja W. Scholz, Mina Ryten, Sara Bandres-Ciga, Alastair Noyce, Paul Cannon, Lasse Pihlstr(o)m, Mike A. Nalls, Andrew B. Singleton, Guy A. Rouleau, Ronald B. Postuma, Ziv Gan-Or and

المساهمون: Lynne Krohn, Karl Heilbron, Cornelis Blauwendraat, Regina H. Reynold, Eric Yu, Konstantin Senkevich, Uladzislau Rudakou, Mehrdad A. Estiar, Emil K. Gustavsson, Kajsa Brolin, Jennifer A. Ruskey, Kathryn Freeman, Farnaz Asayesh, Ruth Chia, Isabelle Arnulf, Michele T. M. Hu, Jacques Y. Montplaisir, Jean-Fran{\c{c}}ois Gagnon, Alex Desautel, Yves Dauvillier, Gian Luigi Gigli, Mariarosaria Valente, Francesco Jane, Andrea Bernardini, Birgit Högl, Ambra Stefani, Abubaker Ibrahim, Karel {\v{S}}onka, David Kemlink, Wolfgang Oertel, Annette Janzen, Giuseppe Plazzi, Francesco Biscarini, Elena Antelmi, Michela Figorilli, Monica Puligheddu, Brit Mollenhauer, Claudia Trenkwalder, Friederike Sixel-Döring, Val{\'{e}}rie Cochen De Cock, Christelle Charley Monaca, Anna Heidbreder, Luigi Ferini-Strambi, Femke Dijkstra, Mineke Viaene, Beatriz Abril, Bradley F. Boeve, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bulli, Daniella Coker, Gabriel Cuellar Partida, Devika Dhamija, Sayantan Da, Sarah L. Elson, Teresa Filshtein, Kipper Fletez-Brant, Pierre Fontanilla, Will Freyman, Pooja M. Gandhi, Barry Hick, David A. Hind, Ethan M. Jewett, Yunxuan Jiang, Katelyn Kukar, Keng-Han Lin, Maya Lowe, Jey C. McCreight, Matthew H. McIntyre, Steven J. Micheletti, Meghan E. Moreno, Joanna L. Mountain, Priyanka Nandakumar, Elizabeth S. Noblin, Jared O'Connell, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Alejandro Hernandez, Corinna Wong, Christophe Toukam Tchakout{\'{e}}, Sonja W. Scholz, Mina Ryten, Sara Bandres-Ciga, Alastair Noyce, Paul Cannon

مصطلحات موضوعية: Brain Genome-Wide Association Study Humans Parkinson Disease / genetics REM Sleep Behavior Disorder / genetics Synucleinopathies

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/36470867; info:eu-repo/semantics/altIdentifier/wos/WOS:000952021200016; volume:13; issue:1; firstpage:1; lastpage:16; numberofpages:16; journal:NATURE COMMUNICATIONS; https://hdl.handle.net/11585/918305; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85143480320; https://www.nature.com/articles/s41467-022-34732-5

الاتاحة: https://hdl.handle.net/11585/918305
https://doi.org/10.1038/s41467-022-34732-5
https://www.nature.com/articles/s41467-022-34732-5

المؤلفون: Steven J Micheletti, Kasia Bryc, Samantha G Ancona Esselmann, William A Freyman, Meghan E Moreno, G David Poznik, Anjali J Shastri, Sandra Beleza, Joanna L Mountain, M Agee, S Aslibekyan, A Auton, R Bell, S Clark, S Das, S Elson, K Fletez-Brant, P Fontanillas, P Gandhi, K Heilbron, B Hicks, D Hinds, K Huber, E Jewett, Y Jiang, A Kleinman, K Lin, N Litterman, J McCreight, M McIntyre, K McManus, S Mozaffari, P Nandakumar, L Noblin, C Northover, J O’Connell, A Petrakovitz, S Pitts, J Shelton, S Shringarpure, C Tian, J Tung, R Tunney, V Vacic, X Wang, A Zare

مصطلحات موضوعية: Uncategorized, genetics, population genetics, slave trade, Africa, Americas, identity by descent, ancestry, admixture, migration, history

Relation: 2381/12770804.v1; https://figshare.com/articles/journal_contribution/Genetic_Consequences_of_the_Transatlantic_Slave_Trade_in_the_Americas/12770804

الاتاحة: https://figshare.com/articles/journal_contribution/Genetic_Consequences_of_the_Transatlantic_Slave_Trade_in_the_Americas/12770804

المؤلفون: James R. Ashenhurst, Hoang Nhan, Janie F. Shelton, Shirley Wu, Joyce Y. Tung, Sarah L. Elson, James K. Stoller, Michelle Agee, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Briana Cameron, Daniella Coker, Gabriel Cuellar Partida, Devika Dhamija, Sayantan Das, Teresa Filshtein, Kipper Fletez-Brant, Pierre Fontanillas, Will Freyman, Pooja M. Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Katelyn Kukar, Vanessa A. Lane, Keng-Han Lin, Maya Lowe, Marie K. Luff, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Steven J. Micheletti, Meghan E. Moreno, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Anjali J. Shastri, Jingchunzi Shi, Suyash Shringarpure, Chao Tian, Vinh Tran, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton

المصدر: Chest. 161:373-381

مصطلحات موضوعية: Male, Pulmonary and Respiratory Medicine, Pediatrics, medicine.medical_specialty, Genotype, Critical Care and Intensive Care Medicine, Direct-To-Consumer Screening and Testing, alpha 1-Antitrypsin Deficiency, Health care, Prevalence, medicine, Humans, Genetic Testing, Allele frequency, Genetic testing, COPD, Alpha 1-antitrypsin deficiency, medicine.diagnostic_test, business.industry, Behavior change, Primary care physician, Odds ratio, Middle Aged, medicine.disease, Female, Self Report, Cardiology and Cardiovascular Medicine, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b448c00c09f424d8a138e26d18ba6147
https://doi.org/10.1016/j.chest.2021.09.041

المؤلفون: Kristi Krebs, Jonas Bovijn, Neil Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson, Dage Särg, Erik Abner, Triin Laisk, Yang Luo, Line Skotte, Frank Geller, Bjarke Feenstra, Wei Wang, Adam Auton, Soumya Raychaudhuri, Tõnu Esko, Andres Metspalu, Sven Laur, Dan M. Roden, Wei-Qi Wei, Michael V. Holmes, Cecilia M. Lindgren, Elizabeth J. Phillips, Reedik Mägi, Lili Milani, João Fadista, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah K. Clark, Sarah L. Elson, Kipper Fletez-Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja M. Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng-Han Lin, Nadia K. Litterman, Marie K. Luff, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A.M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare

المساهمون: Institute for Molecular Medicine Finland, University of Helsinki

المصدر: The American Journal of Human Genetics. 107:612-621

مصطلحات موضوعية: 0301 basic medicine, Genome-wide association study, Human leukocyte antigen, HYPERSENSITIVITY REACTIONS, FREQUENCY, BIOBANK, MECHANISMS, PTPN22, 03 medical and health sciences, 0302 clinical medicine, MANAGEMENT, Genetics, medicine, SNP, Allele, METAANALYSIS, Genetics (clinical), business.industry, 1184 Genetics, developmental biology, physiology, ADVERSE DRUG-REACTIONS, POLYMORPHISM, HLA-B, 3. Good health, HLA, Penicillin, 030104 developmental biology, 030220 oncology & carcinogenesis, Pharmacogenomics, Immunology, T-CELLS, business, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b449294124373a0265767122010de84
https://doi.org/10.1016/j.ajhg.2020.08.008

المؤلفون: Nadia Litterman, Steven J. Micheletti, Janie F. Shelton, Joanna L. Mountain, Michelle Agee, Samantha G. Ancona Esselmann, Sayantan Das, Ethan M. Jewett, S. Clark, A. Petrakovitz, Karl Heilbron, Suyash Shringarpure, Jeffery R. O'Connell, G. David Poznik, Pierre Fontanillas, Kipper Fletez-Brant, Keng-Han Lin, Sahar V. Mozaffari, William A. Freyman, Joyce Y. Tung, Carrie Northover, Anjali J. Shastri, Kimberly F. McManus, Adam Auton, Aaron Kleinman, L. Noblin, P. Gandhi, Xin Wang, Vladimir Vacic, Chao Tian, Karen E. Huber, Jennifer C. McCreight, Yunxuan Jiang, R. Tunney, Robert K. Bell, Sarah L. Elson, Barry W. Hicks, A. Zare, Sandra Beleza, Stella Aslibekyan, David A. Hinds, Meghan E. Moreno, Steven J. Pitts, Kasia Bryc, Matthew H. McIntyre, P. Nandakumar

المصدر: American Journal of Human Genetics

مصطلحات موضوعية: Disembarkation, Variable survival, Present day, migration, identity by descent, Article, 03 medical and health sciences, 0302 clinical medicine, genetics, slave trade, Genetics (clinical), Historical record, 030304 developmental biology, 0303 health sciences, ancestry, Genetic data, population genetics, Forced migration, Geography, Africa, Ethnology, admixture, history, Americas, 030217 neurology & neurosurgery, Regional differences

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08defb0a0eff823c05e153d1f0c5274
http://europepmc.org/articles/PMC7413858

المؤلفون: Upekha E. Liyanage, Stuart MacGregor, D. Timothy Bishop, Jianxin Shi, Jiyuan An, Jue Sheng Ong, Xikun Han, Richard A. Scolyer, Nicholas G. Martin, Sarah E. Medland, Enda M. Byrne, Adèle C. Green, Robyn P.M. Saw, John F. Thompson, Jonathan Stretch, Andrew Spillane, Yunxuan Jiang, Chao Tian, Scott G. Gordon, David L. Duffy, Catherine M. Olsen, David C. Whiteman, Georgina V. Long, Mark M. Iles, Maria Teresa Landi, Matthew H. Law, Michelle Agee, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Briana Cameron, Daniella Coker, Gabriel Cuellar Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez-Brant, Pierre Fontanillas, Will Freyman, Pooja M. Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Aaron Kleinman, Katelyn Kukar, Keng-Han Lin, Maya Lowe, Marie K. Luff, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Steven J. Micheletti, Meghan E. Moreno, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Jared O'Connell, Aaron A. Petrakovitz, G. David Poznik, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton

المصدر: The Journal of investigative dermatology. 142(6)

مصطلحات موضوعية: Genetics, Linkage disequilibrium, Skin Neoplasms, Genome-wide association study, Cell Biology, Dermatology, Biology, Biochemistry, Identity by descent, Genetic analysis, Genetic correlation, Polymorphism, Single Nucleotide, Minor allele frequency, Phenotype, Genetic Loci, Cutaneous melanoma, Humans, Genetic Predisposition to Disease, Molecular Biology, Melanoma, Genetic association, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::581d67a66b4cc294aa0af7b7ad820155
https://pubmed.ncbi.nlm.nih.gov/34813871

المؤلفون: Peter R. Wilton, Chuong B. Do, Adam Auton, J. Michael Macpherson, Joanna L. Mountain, Eric Durand, G. David Poznik

مصطلحات موضوعية: Projection (relational algebra), business.industry, Computer science, Haplotype, Inference, Pattern recognition, Artificial intelligence, business, Pipeline (software), Classifier (UML)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e6266f004458b1d690fd73d0a76da89f
https://doi.org/10.1101/2021.01.19.427308

المؤلفون: Sarah L. Elson, Joyce Y. Tung, Yunxuan Jiang, Kimberly F. McManus, Joanna L. Mountain, Nadia K. Litterman, Chao Tian, Karen E. Huber, Michelle Agee, G. David Poznik, Sohini Ramachandran, Keng-Han Lin, Pierre Fontanillas, J. Fah Sathirapongsasuti, Adam Auton, Elizabeth S. Noblin, Jennifer C. McCreight, Robert K. Bell, Matthew H. McIntyre, Xin Wang, Barry W. Hicks, Aaron Kleinman, Vladimir Vacic, Samuel Pattillo Smith, Suyash Shringarpure, Nicholas A. Furlotte, Ethan M. Jewett, Katarzyna Bryc, Carrie A.M. Northover, David A. Hinds, Priyanka Nakka, Janie F. Shelton, Steven J. Pitts, Anne H. O’Donnell-Luria

المصدر: American Journal of Human Genetics

مصطلحات موضوعية: 0301 basic medicine, Male, congenital, hereditary, and neonatal diseases and abnormalities, uniparental disomy, Population, Aneuploidy, 030105 genetics & heredity, Runs of Homozygosity, Biology, Identity by descent, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Genomic Imprinting, Genetics, medicine, Prevalence, Humans, education, Genetics (clinical), education.field_of_study, runs of homozygosity, Homozygote, medicine.disease, Uniparental disomy, 3. Good health, 030104 developmental biology, Phenotype, Nondisjunction, Autism, Female, identity-by-descent, Chromosome 22

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84b3745c1654fb180bf762c63aaf72d9
https://pubmed.ncbi.nlm.nih.gov/31607426

المؤلفون: María C. Ávila-Arcos, M. Thomas P. Gilbert, Morten E. Allentoft, Anna-Sapfo Malaspinas, Eske Willerslev, Michael W. Dee, José Alfredo Samaniego, Martin Sikora, Hannes Schroeder, Meredith L. Carpenter, Thomas W. Stafford, Antonio Salas, G. David Poznik, Marcela Sandoval-Velasco, Philip L. F. Johnson, Carlos Bustamante, Ludovic Orlando, José Víctor Moreno-Mayar, Jay B. Haviser

المصدر: Proceedings of the National Academy of Sciences
Schroeder, H, Avila-Arcos, M C, Malaspinas, A-S, Poznik, G D, Sandoval-Velasco, M, Carpenter, M L, Moreno-Mayar, J V, Sikora, M, Johnson, P L F, Allentoft, M E, Samaniego, J A, Haviser, J B, Dee, M W, Stafford, T W, Salas, A, Orlando, L, Willerslev, E, Bustamante, C D & Gilbert, M T P 2015, ' Genome-wide ancestry of 17th-century enslaved Africans from the Caribbean ', Proceedings of the National Academy of Sciences of the United States of America, vol. 112, no. 12, pp. 3669-3673 . https://doi.org/10.1073/pnas.1421784112

مصطلحات موضوعية: Genetic Markers, EUROPE, MITOCHONDRIAL-DNA, Genomic data, Population, Ethnic group, Black People, Enslaved Persons, Biology, SEQUENCE, DNA, Mitochondrial, Caribbean region, Ethnicity, genomics, ANCIENT DNA, Cluster Analysis, Humans, POPULATION-STRUCTURE, education, ancient DNA, slave trade, Historical record, Probability, Likelihood Functions, Principal Component Analysis, education.field_of_study, Caribbean island, Chromosomes, Human, Y, Multidisciplinary, Enslavement, Genome, Human, AMERICANS, Bayes Theorem, SAINT, Sequence Analysis, DNA, Biological Sciences, Genealogy, Genetics, Population, Ancient DNA, Archaeology, Caribbean Region, Haplotypes, ORIGINS, Africa, Algorithms, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::937a51a154b03b95f6e04d19c8aae555
https://doi.org/10.1073/pnas.1421784112

المؤلفون: Hannes Schroeder, Carlos Bustamante, Alexandra Sockell, Maria A. Nieves-Colón, Anna-Sapfo Malaspinas, María C. Ávila-Arcos, Anne C. Stone, Diana I. Cruz Dávalos, G. David Poznik

المصدر: Cruz-Davalos, D I, Nieves-Colon, M A, Sockell, A, Poznik, G D, Schroeder, H, Stone, A C, Bustamante, C D, Malaspinas, A-S & Ávila-Arcos, M C 2018, ' In-solution Y-chromosome capture-enrichment on ancient DNA libraries ', BMC Genomics, vol. 19 . https://doi.org/10.1186/s12864-018-4945-x
BMC Genomics
BMC Genomics, Vol 19, Iss 1, Pp 1-16 (2018)

مصطلحات موضوعية: 0106 biological sciences, 0303 health sciences, Endogenous content, lcsh:QH426-470, Ancient DNA, Y chromosome, lcsh:Biotechnology, Capture-enrichment, Genomics, Biology, 010603 evolutionary biology, 01 natural sciences, Haplogroup, lcsh:Genetics, 03 medical and health sciences, chemistry.chemical_compound, chemistry, Recovery rate, Evolutionary biology, lcsh:TP248.13-248.65, DNA, 030304 developmental biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c73612970e883d4ac6510b74c02bfde

المؤلفون: Diana I, Cruz-Dávalos, María A, Nieves-Colón, Alexandra, Sockell, G David, Poznik, Hannes, Schroeder, Anne C, Stone, Carlos D, Bustamante, Anna-Sapfo, Malaspinas, María C, Ávila-Arcos

المصدر: BMC Genomics
BMC genomics, vol. 19, no. 1, pp. 608

مصطلحات موضوعية: Chromosomes, Human, Y, Whole Genome Sequencing, Ancient DNA, Y chromosome, Methodology Article, DNA, Ancient/analysis, DNA, Ancient/isolation & purification, Gene Library, Genomics, History, Ancient, Humans, Sequence Analysis, DNA/methods, Whole Genome Sequencing/methods, Capture-enrichment, Sequence Analysis, DNA, DNA, Ancient

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::84734006a321d8747114ea297606b90b
https://pubmed.ncbi.nlm.nih.gov/30107783

المؤلفون: Simon Rasmussen, Søren Brunak, Vera Warmuth, Michael DeGiorgio, Thorfinn Sand Korneliussen, David J. Meltzer, Shane M. Doyle, Ramneek Gupta, Morten Rasmussen, Francois Balloux, Michael R. Waters, Lauri Saag, Peter D. Heintzman, Mattias Jakobsson, Ida Moltke, Thomas W. Stafford, Sarah L. Anzick, Carlos Bustamante, Anders Albrechtsen, Omar E. Cornejo, Rasmus Nielsen, Mait Metspalu, Ripan S. Malhi, Valborg Gudmundsdottir, Morten E. Allentoft, Anna-Sapfo Malaspinas, Anders Eriksson, Matthew J. Collins, Tracey Pierre, G. David Poznik, Rachita Yadav, Margarida C. Lopes, Thomas Sicheritz-Pontén, Jesper Stenderup, Andrea Manica, Monika Karmin, Ludovic Orlando, Pontus Skoglund, Kristiina Tambets, V. Samuel Stockton White, Ian Barnes, Eske Willerslev

المصدر: Nature
Rasmussen, M, Anzick, S L, Waters, M R, Skoglund, P, Degiorgio, M, Stafford, T W, Rasmussen, S, Moltke, I, Albrechtsen, A, Doyle, S M, Poznik, G D, Gudmundsdottir, V, Yadav, R, Malaspinas, A S, Samuel Stockton White, V, Allentoft, M E, Cornejo, O E, Tambets, K, Eriksson, A, Heintzman, P D, Karmin, M, Korneliussen, T S, Meltzer, D J, Pierre, T L, Stenderup, J, Saag, L, Warmuth, V M, Lopes, M C, Malhi, R S, Brunak, S, Sicheritz-Ponten, T, Barnes, I, Collins, M, Orlando, L, Balloux, F, Manica, A, Gupta, R, Metspalu, M, Bustamante, C D, Jakobsson, M, Nielsen, R & Willerslev, E 2014, ' The genome of a Late Pleistocene human from a Clovis burial site in western Montana ', Nature, vol. 506, no. 7487, pp. 225-229 . https://doi.org/10.1038/nature13025

مصطلحات موضوعية: Gene Flow, Male, Asia, Burial, Pleistocene, Molecular Sequence Data, Population Dynamics, Population, Biology, Solutrean, DNA, Mitochondrial, Bone and Bones, Article, Indigenous, Gene flow, 03 medical and health sciences, Humans, 0601 history and archaeology, education, History, Ancient, Phylogeny, 030304 developmental biology, 0303 health sciences, geography, education.field_of_study, Chromosomes, Human, Y, Multidisciplinary, geography.geographical_feature_category, Models, Genetic, Montana, 060102 archaeology, Genome, Human, Radiometric Dating, Infant, Last Glacial Maximum, 06 humanities and the arts, Emigration and Immigration, Before Present, Archaeology, Europe, Haplotypes, Indians, North American, Ice sheet

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25c269ae00b6e39cbd2a75473dc726ed
https://doi.org/10.1038/nature13025

المؤلفون: Stephen S. Rich, Adam M. Smiles, Jan Skupien, G. David Poznik, Andrzej S. Krolewski, James H. Warram, Josyf C. Mychaleckyj, Marcus G. Pezzolesi

المصدر: Kidney International. 80:105-111

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, genetic association, type 1 diabetes, Locus (genetics), Single-nucleotide polymorphism, Type 2 diabetes, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, Article, White People, Nephropathy, Diabetic nephropathy, 03 medical and health sciences, 0302 clinical medicine, Intergenic region, Asian People, Diabetes mellitus, Internal medicine, medicine, Humans, Diabetic Nephropathies, Genetic Predisposition to Disease, 030304 developmental biology, Genetics, 0303 health sciences, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 11, diabetic nephropathy, Middle Aged, medicine.disease, Diabetes Mellitus, Type 1, Endocrinology, Diabetes Mellitus, Type 2, Nephrology, Case-Control Studies, DNA, Intergenic, Female, type 2 diabetes, Genome-Wide Association Study, Kidney disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811631c499db469dfa2a31a002367ee9
https://doi.org/10.1038/ki.2011.64

المؤلفون: Masahiko Kure, Jonathon Dunn, G. David Poznik, James H. Warram, Jan Skupien, Marcus G. Pezzolesi, Andrzej S. Krolewski, Josyf C. Mychaleckyj, Pisut Katavetin

المصدر: Molecular Genetics and Metabolism. 103:60-65

مصطلحات موضوعية: Adult, Adolescent, Genotype, Endocrinology, Diabetes and Metabolism, Population, Single-nucleotide polymorphism, Genome-wide association study, Locus (genetics), Biology, Biochemistry, Article, End stage renal disease, Young Adult, Endocrinology, Genetic variation, Genetics, Humans, Diabetic Nephropathies, Genetic Predisposition to Disease, Allele, Child, education, Molecular Biology, Alleles, Genetic association, education.field_of_study, Infant, Newborn, Genetic Variation, Infant, Matrix Metalloproteinases, Diabetes Mellitus, Type 1, Child, Preschool, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d7d81c451e89c9f59dd59d67a46cfe9
https://doi.org/10.1016/j.ymgme.2011.01.001

المؤلفون: James H. Warram, Marcus G. Pezzolesi, Josyf C. Mychaleckyj, Andrzej S. Krolewski, Stephen S. Rich, Jan Skupien, Pisut Katavetin, Masahiko Kure, G. David Poznik

المصدر: Diabetes

مصطلحات موضوعية: Adult, Male, Adolescent, Endocrinology, Diabetes and Metabolism, 030232 urology & nephrology, Blood Pressure, Genome-wide association study, Locus (genetics), Single-nucleotide polymorphism, Kidney, Polymorphism, Single Nucleotide, White People, Nephropathy, Diabetic nephropathy, 03 medical and health sciences, 0302 clinical medicine, Cell Movement, Reference Values, Diabetes mellitus, Genetics, Ethnicity, Internal Medicine, medicine, Humans, Diabetic Nephropathies, Genetic Predisposition to Disease, Age of Onset, Child, Adaptor Proteins, Signal Transducing, 030304 developmental biology, Glycated Hemoglobin, 0303 health sciences, Type 1 diabetes, business.industry, Middle Aged, medicine.disease, Diabetes Mellitus, Type 2, Child, Preschool, Original Article, Female, Allelic heterogeneity, business, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41c702ecbc1243e19232f638d7e5cf69
https://doi.org/10.2337/db09-0641

المؤلفون: Daryl Waggott, Masahiko Kure, Pisut Katavetin, Michael L. Merchant, James H. Warram, Jonathon Dunn, Andrew D. Paterson, Alessandro Doria, Krzysztof Wanic, Jacek Bochenski, Shelley B. Bull, John J. Rogus, G. David Poznik, William H. Walker, Paweł Wołkow, Daniel P.K. Ng, Jon B. Klein, Adam M. Smiles, Stephen S. Rich, Marcus G. Pezzolesi, Michelle T. Barati, Luis Henrique Santos Canani, Andrew P. Boright, Lucia Mirea, Grzegorz Placha, Bozena Krolewski, Josyf C. Mychaleckyj, Andrzej S. Krolewski

المصدر: Diabetes

مصطلحات موضوعية: Oncology, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Genome-wide association study, Single-nucleotide polymorphism, 030204 cardiovascular system & hematology, Kidney, Polymorphism, Single Nucleotide, Diabetic nephropathy, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Diabetes mellitus, Internal Medicine, Genetic predisposition, Genetics, Medicine, Humans, Diabetic Nephropathies, Genetic Predisposition to Disease, 030304 developmental biology, 0303 health sciences, Type 1 diabetes, Proteinuria, business.industry, Genome, Human, Microfilament Proteins, Chromosome Mapping, Membrane Proteins, medicine.disease, 3. Good health, Cytoskeletal Proteins, Endocrinology, Diabetes Mellitus, Type 1, Kidney Failure, Chronic, Original Article, medicine.symptom, business, Kidney disease, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b7476248c834b649ec45b679b6350e3
http://europepmc.org/articles/PMC2682673

المؤلفون: James H. Warram, Shin-ichi Araki, Luis Henrique Santos Canani, Andrzej S. Krolewski, Krzysztof Wanic, Jonathon Dunn, John J. Rogus, William F. Walker, G. David Poznik, Adam M. Smiles, Yuichiro Makita, Marcus G. Pezzolesi, Dariusz Moczulski

المصدر: Diabetes

مصطلحات موضوعية: Adult, Male, Genetic Linkage, Endocrinology, Diabetes and Metabolism, 030232 urology & nephrology, Chromosomes, Human, Pair 20, Genomics, Single-nucleotide polymorphism, Disease, Polymorphism, Single Nucleotide, Diabetic nephropathy, 03 medical and health sciences, 0302 clinical medicine, Genetic linkage, Internal Medicine, medicine, Genetics, Humans, Diabetic Nephropathies, Genetic Predisposition to Disease, Allele, 030304 developmental biology, Family Health, 0303 health sciences, Type 1 diabetes, business.industry, Siblings, Middle Aged, medicine.disease, 3. Good health, Diabetes Mellitus, Type 1, Kidney Failure, Chronic, Chromosomes, Human, Pair 6, Female, Chromosomes, Human, Pair 3, business, Kidney disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09a7fb921a424a886cc138cfc8a33427
http://europepmc.org/articles/PMC2518505

المؤلفون: Thomas Willems, Chris Tyler-Smith, Yaniv Erlich, G. David Poznik, Melissa Gymrek

المصدر: American journal of human genetics. 98(5)

مصطلحات موضوعية: 0301 basic medicine, Male, Mutation rate, Genotype, Population, Locus (genetics), Biology, Genome, Article, 03 medical and health sciences, 0302 clinical medicine, Mutation Rate, Genetics, Humans, Genetics(clinical), Y-STR, 1000 Genomes Project, education, Genetics (clinical), education.field_of_study, Chromosomes, Human, Y, Genome, Human, humanities, 030104 developmental biology, Haplotypes, Mutation, Microsatellite, Human genome, 030217 neurology & neurosurgery, Microsatellite Repeats

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c878e88e558cc2a3d5f092e30cb45e58
https://pubmed.ncbi.nlm.nih.gov/27126583

المؤلفون: G. David Poznik, Chris Tyler-Smith, Yaniv Erlich, Thomas Willems, Melissa Gymrek

مصطلحات موضوعية: 0303 health sciences, Mutation rate, 030305 genetics & heredity, Genomics, Computational biology, Biology, Dinucleotide Repeat, Genome, humanities, 03 medical and health sciences, Chromosome (genetic algorithm), Microsatellite, Y-STR, 1000 Genomes Project, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4635de01e64fb63508d38e20e7a6c02
https://doi.org/10.1101/036590