المؤلفون: Levi A. Garraway, Gad Getz, Meenhard Herlyn, Reinhard Dummer, Todd R. Golub, Matthew Meyerson, Roman K. Thomas, William R. Sellers, Glenn Dranoff, F. Stephen Hodi, Casey Gates, Hsiuyi Tseng, Heidi Greulich, Elisabeth Laine, Jennifer M. Marmion, Whei Feng, Wendy Winckler, Rameen Beroukhim, Alissa C. Baker, William M. Lin

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116fa90cddfa9dcfe67f41cce7326a9aTest
https://doi.org/10.1158/0008-5472.c.6497147.v1Test

المؤلفون: Levi A. Garraway, Gad Getz, Meenhard Herlyn, Reinhard Dummer, Todd R. Golub, Matthew Meyerson, Roman K. Thomas, William R. Sellers, Glenn Dranoff, F. Stephen Hodi, Casey Gates, Hsiuyi Tseng, Heidi Greulich, Elisabeth Laine, Jennifer M. Marmion, Whei Feng, Wendy Winckler, Rameen Beroukhim, Alissa C. Baker, William M. Lin

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f7aa981e17f5ada0bcdb0a25354968Test
https://doi.org/10.1158/0008-5472.22373603Test

المؤلفون: David Galimberti, Nikki Bonevich, Aisha Hunt, Jane Faershtein, Brooke McKnight, Jody McIntyre, Michael Hogan, Dinesh Cyanam, Nick Khazanov, Seth Sadis, Casey Gates, Sarah Anstead, Santhoshi Bandla, Joshua Holcomb, Jon Sherlock, Corina Nikoloff, Ken Kopp

المصدر: Cancer Genetics. :S14-S15

مصطلحات موضوعية: Cancer Research, medicine.medical_specialty, Genetics, Cytogenetics, medicine, Computational biology, Biology, Molecular Biology, Clinical decision support system, DNA sequencing

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::7b1e24f5ce4472b18350b0fc8789177fTest
https://doi.org/10.1016/j.cancergen.2019.04.041Test

المؤلفون: Walter J. Muir, Stacey Gabriel, Kimberly Chambert, Carrie Sougnez, Vishwajit L. Nimgaonkar, Michael E. Thase, Matthew Defelice, David Curtis, Jinbo Fan, Jennifer Franklin, Roy H. Perlis, MP D VanBeck, Andrew McQuillin, Mark J. Daly, Nick Bass, P. I. W. de Bakker, Casey Gates, Shaun Purcell, Matthew B. McQueen, Katherine Todd-Brown, Matthew Robinson, Hugh Gurling, Adebayo Anjorin, Pamela Sklar, Douglas Blackwood, Donald J. MacIntyre, Kevin A. McGhee, Gary S. Sachs, M N Ogdie, Stephen V. Faraone, Jordan W. Smoller, Manuel A. R. Ferreira, Andrew Kirby, Brendan Blumenstiel, Kristin G. Ardlie, Jacob Lawrence, Edward M. Scolnick, Alan W. McLean

المصدر: Molecular Psychiatry. 13:558-569

مصطلحات موضوعية: Genetic Markers, Candidate gene, Bipolar Disorder, Genotype, Tetraspanins, Myosin Type V, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Article, Cellular and Molecular Neuroscience, Gene Frequency, Antigens, Neoplasm, Reference Values, medicine, Humans, SNP, ANK3, Bipolar disorder, Medical History Taking, Molecular Biology, Genotyping, Genetics, Membrane Glycoproteins, Myosin Heavy Chains, Genome, Human, Patient Selection, Haplotype, Chromosome Mapping, DNA, medicine.disease, ErbB Receptors, Psychiatry and Mental health

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b854c6215f8e08aed2fe8a3d137244aaTest
https://doi.org/10.1038/sj.mp.4002151Test

المؤلفون: Casey Gates, William M. Lin, Whei Feng, Levi A. Garraway, Matthew Meyerson, Todd R. Golub, Jennifer M. Marmion, F. Stephen Hodi, Meenhard Herlyn, William R. Sellers, Rameen Beroukhim, Gad Getz, Roman K. Thomas, Heidi Greulich, Wendy Winckler, Glenn Dranoff, Alissa C. Baker, Reinhard Dummer, Elisabeth Laine, Hsiuyi Tseng

المساهمون: University of Zurich, Garraway, L A

المصدر: Cancer research

مصطلحات موضوعية: Cancer Research, Loss of Heterozygosity, 610 Medicine & health, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Cell Line, Tumor, medicine, Tensin, PTEN, Cluster Analysis, Humans, 1306 Cancer Research, Receptor, Fibroblast Growth Factor, Type 1, Protein kinase A, Extracellular Signal-Regulated MAP Kinases, Melanoma, 030304 developmental biology, Chromosome Aberrations, 0303 health sciences, Chromosomes, Human, Pair 10, Gene Expression Profiling, PTEN Phosphohydrolase, 10177 Dermatology Clinic, Cancer, DNA, Neoplasm, medicine.disease, Gene expression profiling, Imatinib mesylate, Oncology, 030220 oncology & carcinogenesis, Cutaneous melanoma, Cancer research, biology.protein, 2730 Oncology, raf Kinases, Chromosome Deletion, Mitogen-Activated Protein Kinases, Algorithms

وصف الملف: Lin_Paper_20070616.pdf - application/pdf; Lin_CancRes_2008V.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb528b9445923c15abd8b1842c81a8f1Test

المؤلفون: Zak Kohane, Jeremy Goldberg, Carine Mantoulan, Shaun Purcell, Jessica Brian, Magdalena Laskawiec, Christopher A. Walsh, Irma Moilanen, Ridha Joober, Peter Szatmari, Olena Korvatska, Kerim Munir, James F. Gusella, Rudolph E. Tanzi, David L. Pauls, Generoso G. Gascon, Christine Stevens, Linda Lotspeich, John I. Nurnberger, Ramzi Nazir, Jonathan Green, Brian L. Yaspan, Marion Leboyer, Ann P. Thompson, Shun-Chiao Chang, Carolyn Bridgemohan, Louise Gallagher, Jeff Munson, Michael Gill, Guiqing Cai, Fritz Poustka, Regina Regan, Aislyn Cangialose, Gerard D. Schellenberg, Christopher J. McDougle, Christina Corsello, Wendy Roberts, Thomas H. Wassink, Majid Ghadami, Ellen M. Hanson, Benjamin M. Neale, Stacey Gabriel, Lonnie Zwaigenbaum, John Tsiantis, Hanna Ebeling, Sabine M. Klauck, Elaine LeClair, Bernie Devlin, Steven A. McCarroll, Ashley O'Connor, Andrew Pickles, Emily L. Crawford, Katja Jussila, Helen McConachie, Christopher Gillberg, Brenda E. Barry, Lou Kunkel, Seung Yun Yoo, Jennifer N. Partlow, Stephanie Brewster O'Neil, Ingrid A. Holm, Judith Miller, Guy A. Rouleau, Val C. Sheffield, Catherine Lord, Judith S. Palfrey, Ellen M. Wijsman, Astrid M. Vicente, Azam Hosseinipour, Ronald E. Becker, James S. Sutcliffe, Fred R. Volkmar, Marja Leena Mattila, Katerina Papanikolaou, Jennifer Reichert, Edwin H. Cook, Pamela Sklar, Elena Maestrini, Hilary Coon, Sek Won Kong, Stephen A. Haddad, Todd Green, Gillian Baird, Andrew Kirby, Patrick Bolton, Robert Sean Hill, Eric M. Morrow, Tom Berney, Jonathan L. Haines, Maryam Valujerdi, Casey Gates, David J. Posey, Karola Rehnström, Alistair T. Pagnamenta, Christine M. Freitag, Eric Fombonne, Janice Ware, Christian R. Marshall, Janine A. Lamb, Lauren A. Weiss, Agatino Battaglia, Nancy J. Minshew, Roksana Sasanfar, Elizabeth Baroni, Maretha de Jonge, Lennart von Wendt, Gina Hilton, Dalila Pinto, Nahit Motavalli Mukaddes, Ala Tolouei, Catalina Betancur, Michael Rutter, Tram Tran, Eftichia Duketis, Laurent Mottron, Margaret A. Pericak-Vance, Kristen West, Joachim Hallmayer, Kirsty Wing, Kerstin Wittemeyer, Rachel J. Hundley, Herman van Engeland, Judith Conroy, Mark J. Daly, Asif Hashmi, Michael L. Cuccaro, Geraldine Dawson, Sanna Kuusikko, Richard Anney, Anthony P. Monaco, Brian Winkloski, Samira Al-Saad, Dan E. Arking, Veronica J. Vieland, Stephen W. Scherer, Soher Balkhy, Kara Andresen, Rebecca L. Tomlinson, Joseph D. Buxbaum, Aravinda Chakravarti, Xiao-Qing Liu, Lindsay Jackson, Jaakko Ignatius, Catarina Correia, Leonard Rappaport, Heather Peters, Julie Gauthier, John R. Gilbert, Jeremy R. Parr, Carrie Sougnez, Katherine E. Tansey, Bennett L. Leventha, Annemarie Poustka, Daniel H. Geschwind, Annette Estes, Leena Peltonen, Maryam Rostami, Jeff Salt, David Altshuler, Simon Wallace, Susan E. Bryson, William M. Mahoney, Katy Renshaw, Robert M. Joseph, Lisa H. Albers, Inês Cabrito, Sean Ennis, Vanessa Hus, Guiomar Oliveira, Ann Le Couteur, Joseph Piven, Sandra L. Friedman, Penny Farrar, Joshua M. Korn, Sven Bölte, Camille W. Brune, Esau Simmons, Susan L. Santangelo, Andrew D. Paterson, Rita M. Cantor, Andrew B. West, Finny G Kuruvilla, Tiago R. Magalhaes, Andrew Green, Alison Schonwald, Stephen J. Guter, Anthony J. Bailey, Bernadette Rogé, William M. McMahon

المساهمون: Massachusetts General Hospital [Boston], Harvard Medical School [Boston] (HMS), Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Johns Hopkins University (JHU), Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Génétique de l'autisme = Genetics of Autism (NPS-01), Neuroscience Paris Seine (NPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Betancur, Catalina, University of Helsinki, Neurosciences Paris Seine (NPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), WEISS LA, ARKING DE, GENE DISCOVERY PROJECT OF JOHNS HOPKINS & THE AUTISM CONSORTIUM, DALY MJ, CHAKRAVARTI A, BRUNE CW, WEST K, O'CONNOR A, HILTON G, TOMLINSON RL, WEST AB, COOK EH JR, CHAKRAVARTI A, WEISS LA, GREEN T, CHANG SC, GABRIEL S, GATES C, HANSON EM, KIRBY A, KORN J, KURUVILLA F, MCCARROLL S, MORROW EM, NEALE B, PURCELL S, SASANFAR R, SOUGNEZ C, STEVENS C, ALTSHULER D, GUSELLA J, SANTANGELO SL, SKLAR P, TANZI R, DALY MJ, ANNEY R, BAILEY AJ, BAIRD G, BATTAGLIA A, BERNEY T, BETANCUR C, BÖLTE S, BOLTON PF, BRIAN J, BRYSON SE, BUXBAUM JD, CABRITO I, CAI G, CANTOR RM, COOK EH JR, COON H, CONROY J, CORREIA C, CORSELLO C, CRAWFORD EL, CUCCARO ML, DAWSON G, DE JONGE M, DEVLIN B, DUKETIS E, ENNIS S, ESTES A, FARRAR P, FOMBONNE E, FREITAG CM, GALLAGHER L, GESCHWIND DH, GILBERT J, GILL M, GILLBERG C, GOLDBERG J, GREEN A, GREEN J, GUTER SJ, HAINES JL, HALLMAYER JF, HUS V, KLAUCK SM, KORVATSKA O, LAMB JA, LASKAWIEC M, LEBOYER M, COUTEUR AL, LEVENTHAL BL, LIU XQ, LORD C, LOTSPEICH LJ, MAESTRINI E, MAGALHAES T, MAHONEY W, MANTOULAN C, MCCONACHIE H, MCDOUGLE CJ, MCMAHON WM, MARSHALL CR, MILLER J, MINSHEW NJ, MONACO AP, MUNSON J, NURNBERGER JI JR, OLIVEIRA G, PAGNAMENTA A, PAPANIKOLAOU K, PARR JR, PATERSON AD, PERICAK-VANCE MA, PICKLES A, PINTO D, PIVEN J, POSEY DJ, POUSTKA A, POUSTKA F, REGAN R, REICHERT J, RENSHAW K, ROBERTS W, ROGE B, RUTTER ML, SALT J, SCHELLENBERG GD, SCHERER SW, SHEFFIELD V, SUTCLIFFE JS, SZATMARI P, TANSEY K, THOMPSON AP, TSIANTIS J, VAN ENGELAND H, VICENTE AM, VIELAND VJ, VOLKMAR F, WALLACE S, WASSINK TH, WIJSMAN EM, WING K, WITTEMEYER K, YASPAN BL, ZWAIGENBAUM L, MORROW EM, YOO SY, HILL RS, MUKADDES NM, BALKHY S, GASCON G, AL-SAAD S, HASHMI A, WARE J, JOSEPH RM, LECLAIR E, PARTLOW JN, BARRY B, WALSH CA, PAULS D, MOILANEN I, EBELING H, MATTILA ML, KUUSIKKO S, JUSSILA K, IGNATIUS J, SASANFAR R, TOLOUEI A, GHADAMI M, ROSTAMI M, HOSSEINIPOUR A, VALUJERDI M, SANTANGELO SL, ANDRESEN K, WINKLOSKI B, HADDAD S, KUNKEL L, KOHANE Z, TRAN T, KONG SW, O'NEIL SB, HANSON EM, HUNDLEY R, HOLM I, PETERS H, BARONI E, CANGIALOSE A, JACKSON L, ALBERS L, BECKER R, BRIDGEMOHAN C, FRIEDMAN S, MUNIR K, NAZIR R, PALFREY J, SCHONWALD A, SIMMONS E, RAPPAPORT LA, GAUTHIER J, MOTTRON L, JOOBER R, FOMBONNE E, ROULEAU G, REHNSTROM K, VON WENDT L, PELTONEN L.

المصدر: Nature
Nature, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩
Nature, Nature Publishing Group, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩

مصطلحات موضوعية: Perturbação Autística, Internationality, Genetic Linkage, Genome-wide association study, MESH: Semaphorins, Semaphorins, [SDV.GEN] Life Sciences [q-bio]/Genetics, 0302 clinical medicine, Neurodevelopmental disorder, Heritability of autism, MESH: Nerve Tissue Proteins, Association mapping, Genetics, 0303 health sciences, Multidisciplinary, MESH: Polymorphism, Single Nucleotide, MESH: Genetic Predisposition to Disease, Brain, Chromosome Mapping, Chromosomes, Human, Pair 5, MESH: Membrane Proteins, MESH: Chromosomes, Human, Pair 5, MESH: Autistic Disorder, MESH: Genetic Linkage, Single-nucleotide polymorphism, Nerve Tissue Proteins, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, MESH: Brain, Genetic linkage, medicine, Humans, Genetic Predisposition to Disease, Autistic Disorder, MESH: Sample Size, 030304 developmental biology, Genetic association, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, Membrane Proteins, medicine.disease, Sample Size, Perturbações do Desenvolvimento Infantil e Saúde Mental, MESH: Genome-Wide Association Study, MESH: Internationality, Autism, MESH: Chromosome Mapping, Predisposição Genética para Doença, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::399dbcded0de45863411f1e50a5de20fTest
https://www.hal.inserm.fr/inserm-03135302Test

المؤلفون: Noël P. Burtt, Timothy W. Behrens, Patrick M. Gaffney, Rachel Hackett, Leela Davies, David Altshuler, Melissa Parkin, Deborah S. Cunninghame Graham, Andrew Wong, Robert M. Plenge, Chris Cotsapas, Joan E. Wither, Paul R. Fortin, Casey Gates, Timothy J. Vyse, Candace Guiducci, Mark J. Daly, John D. Rioux, Kathy L. Moser, Robert R. Graham, Christopher J. Lessard, Joanlise M. Leon

المصدر: Nature genetics. 40(9)

مصطلحات موضوعية: Systemic disease, Arthritis, Genome-wide association study, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Article, Arthritis, Rheumatoid, immune system diseases, Immunopathology, Genetics, medicine, Humans, Lupus Erythematosus, Systemic, Genetic Predisposition to Disease, skin and connective tissue diseases, Tumor Necrosis Factor alpha-Induced Protein 3, Autoimmune disease, Lupus erythematosus, Intracellular Signaling Peptides and Proteins, Nuclear Proteins, medicine.disease, Connective tissue disease, DNA-Binding Proteins, Rheumatoid arthritis, Immunology, Chromosomes, Human, Pair 6, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9f47e9ab27a47d3106ed8956c3008d3Test
https://pubmed.ncbi.nlm.nih.gov/19165918Test

المؤلفون: David St Clair, Frank A. Middleton, Peter M. Visscher, Kevin A. McGhee, John L. Waddington, Helena Medeiros, Joshua M. Korn, Vihra Milanova, Gillian Fraser, Stuart MacGregor, David Curtis, Nadine Norton, Nicholas Bass, Ivan Nikolov, Scott Mahon, Jennifer Stone, Kimberly Chambert, Casey Gates, Alan W Maclean, Christopher P. Morley, Margaret Van Beck, Ayman H. Fanous, James A. Knowles, Draga Toncheva, P. Malloy, Jacob Lawrence, Célia Barreto Carvalho, Shaun Purcell, Christina M. Hultman, George Kirov, Digby Quested, Soh Leh Kwan, Carlos N. Pato, Elaine Kenny, Hywel Williams, Vinay Puri, Aiden Corvin, Nicholas John Craddock, Michael Conlon O'Donovan, Nicholas Walker, Nigel Williams, Peter Holmans, Hugh Gurling, Colm O'Dushlaine, Mark J. Daly, Emma Flordal Thelander, Jonathan Pimm, David V. Conti, Michael Gill, Susmita Datta, Derek W. Morris, Douglas M. Ruderfer, Khalid Choudhury, Walter J. Muir, Stacey Gabriel, Ben S. Pickard, Kristen Ardlie, Srinivasa Thirumalai, Michael John Owen, Edward M. Scolnick, Caroline Crombie, Robert Krasucki, M. Helena Azevedo, Michele T. Pato, Steve McCarroll, António Macedo, Lucy Georgieva, Douglas Blackwood, Patrick F. Sullivan, Pamela Sklar, Paul Lichtenstein, Andrew McQuillin, Patrick Sullivan, Carlos Ferreira

المصدر: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

مصطلحات موضوعية: Genetics, Multidisciplinary, biology, CHRNA7, Chromosome, Locus (genetics), Low copy repeats, Genome, Article, Psychiatric Disorder, Genetic, mental disorders, biology.protein, medicine, Schizophrenia, Apathy, Copy-number variation, medicine.symptom, Comparative genomic hybridization

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d81ac4724713772ad334389c90dafed1Test
https://europepmc.org/articles/PMC3912847Test/

المؤلفون: Dyann F. Wirth, Omar Ndir, S. Mboup, Daniel J. Park, David I. Rosen, Casey Gates, Daniel E. Neafsey, Marcelo U. Ferreira, Nathan Houde, Joseph F. Cortese, Daniel L. Hartl, Aditya P Dash, Erin Tyndall, Danny A. Milner, Daouda Ndiaye, Bruce W. Birren, Rachel F. Daniels, Pardis C. Sabeti, Stephen F. Schaffner, Ousmane Sarr, Eric S. Lander, Sandra do Lago Moraes, Nicole Stange-Thomann, Roger C. Wiegand, Chetan E. Chitnis, Amanda K. Lukens, Philip Montgomery, Sarak K. Volkman

المساهمون: Broad Institute of MIT and Harvard, Massachusetts Institute of Technology. Department of Biology, Neafsey, Daniel E., Schaffner, Stephen F., Park, Daniel, Montgomery, Philip, Daniels, Rachel F., Houde, Nathan, Cortese, Joseph F., Tyndall, Erin, Gates, Casey, Stange-Thomann, Nicole, Wiegand, Roger C., Lander, Eric S., Birren, Bruce W., Sabeti, Pardis C.

المصدر: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
BioMed Central Ltd
Genome Biology

مصطلحات موضوعية: Linkage disequilibrium, VARIAÇÃO GENÉTICA, Plasmodium falciparum, 030231 tropical medicine, Population, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, parasitic diseases, Animals, Selection, Genetic, education, Genotyping, Phylogeny, 030304 developmental biology, 2. Zero hunger, Genetics, 0303 health sciences, education.field_of_study, Genetic diversity, Research, respiratory system, Tag SNP, 3. Good health, SNP genotyping, Evolutionary biology, human activities, Genome-Wide Association Study, SNP array

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::891c16333ac5343d0296011c5a4c948dTest

المؤلفون: Matthew DeFelice, Brendan Blumenstiel, Esa Laurila, Marju Orho-Melander, Lauren Gianniny, Mary Fava, John G. Gibbons, Qicheng Ma, Liselotte Hall, Bob Handsaker, Christopher Newton-Cheh, Joel N. Hirschhorn, Stacey Gabriel, Guillaume Lettre, Wendy Brodeur, Carrie Sougnez, Olle Melander, Maria Sterner, Melissa Parkin, Bo Isomaa, Peter Almgren, Lennart Råstam, Marja-Riitta Taskinen, Claire M. Healy, Marketa Sjögren, Jose C. Florez, Richa Saxena, Johan Holmkvist, Ryan Tewhey, Leif Groop, Margareta Svensson, Kieu Nguyen, Jody Camarata, David Altshuler, Kristin Ardlie, Nancy Chia, Noël P. Burtt, Helen N. Lyon, Delwood Richardson, Joanne M. Meyer, Elizabeth K. Speliotes, Peter Nilsson, Aarti Surti, Mark J. Daly, Ulf Lindblad, Rachel Hackett, Paul I.W. de Bakker, Gung-Wei Chirn, Hemang Parikh, Diane Gage, Rachel Barry, Anna Berglund, Thomas E. Hughes, Marcia M. Nizzari, Sekar Kathiresan, Darrell O. Ricke, Malin Svensson, Jeffrey J. Roix, Benjamin F. Voight, Hong Chen, Casey Gates, Candace Guiducci, Valeriya Lyssenko, Tiinamaija Tuomi, Kristina Bengtsson Boström, Shaun Purcell, Joyce Carlson

المصدر: Science (New York, N.Y.). 316(5829)

مصطلحات موضوعية: Blood Glucose, Genetic Markers, Male, Genotype, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Quantitative Trait, Heritable, Meta-Analysis as Topic, SNP, Humans, Genetic Predisposition to Disease, CDKAL1, Alleles, Triglycerides, Genetic association, Adaptor Proteins, Signal Transducing, Aged, Genetics, Multidisciplinary, Glucokinase regulatory protein, Genome, Human, Haplotype, Chromosome Mapping, Middle Aged, Introns, Insulin-Like Growth Factor Binding Proteins, Diabetes Mellitus, Type 2, Haplotypes, Case-Control Studies, biology.protein, Female, Insulin Resistance, Chromosomes, Human, Pair 9, TCF7L2, Epigenetics of diabetes Type 2

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1473b80ffdfa7faf52f3f3b608ab4016Test
https://pubmed.ncbi.nlm.nih.gov/17463246Test