المؤلفون: Manuel Mayhaus, Sandro Sorbi, Peter R. Schofield, A. Rollin, A. Karydas, Alessandro Padovani, Gilles Gasparoni, Peter St George-Hyslop, Carol Dobson-Stone, Stefano F. Cappa, D. S. Knopman, John Hardy, John R. Hodges, Graziella Milan, Florence Pasquier, Christopher Morris, Edward D. Huey, Marc Cruts, Y.A.L. Pijnenburg, R. C. Petersen, Elisa Rubino, P. Scheltens, Vincent Deramecourt, Neil Graff-Radford, Elio Scarpini, Ting Wang, Panagiotis Alexopoulos, Peter Heutink, Lena E. Hjermind, AB Singleton, Jordan Grafman, Elizabeth Thompson, Adrian Danek, Pietro Pietrini, Raffaele Ferrari, Innocenzo Rainero, C. Van Broeckhoven, Rosa Capozzo, Adaikalavan Ramasamy, J. van der Zee, Eric M. Wassermann, Karin Nilsson, Ging-Yuek Robin Hsiung, J. C. van Swieten, Ping Zeng, Rosa Rademakers, Siro Bagnoli, Amalia C. Bruni, Anna Richardson, Dimitrios Kapogiannis, Ian R. A. Mackenzie, Martin N. Rossor, Bruce L. Miller, Roberta Ghidoni, Raffaele Maletta, Massimo Franceschi, Rafael Blesa, Vivianna M. Van Deerlin, Christer Nilsson, Glenda M. Halliday, Jordi Clarimón, John Q. Trojanowski, Michael Tierney, Valeria Novelli, Agustín Ruiz, Didier Hannequin, Giorgio Giaccone, Elise G.P. Dopper, Nicoletta Smirne, F Tagliavini, I. Leber, Julie S. Snowden, Sara Rollinson, Alexis Brice, Ian G. McKeith, John E. Nielsen, Paolo Sorrentino, Véronique Golfier, Maura Gallo, Lauren Bartley, B. F. Boeve, Giancarlo Logroscino, Elena Alonso, Lorenzo Pinessi, Matt Baker, Nigel J. Cairns, Matthias Riemenschneider, William S. Brooks, Alexander Gerhard, Mark Kristiansen, Eric Haan, Israel Hernandez, Ekaterina Rogaeva, Jason D. Warren, Thibaud Lebouvier, Nick C. Fox, Stuart Pickering-Brown, Giacomina Rossi, Carlos Cruchaga, G. Binetti, Maria Landqvist Waldö, William W. Seeley, Jonathan D. Rohrer, Keith A. Josephs, Diego Albani, Wei Gu, Huei-Hsin Chiang, Luigi Ferrucci, H. Zhao, Howie Rosen, Pau Pastor, Alfredo Postiglione, Evelyn Jaros, Livia Bernardi, Dena G. Hernandez, Alberto Lleó, James B. Rowe, Parastoo Momeni, Maria Serpente, Huw R. Morris, Timothy D. Griffiths, Maria Grazia Spillantini, Alan J. Thomas, Maria Elena Conidi, M. Anfossi, Sabrina Pichler, Martine Vercelletto, Murray Grossman, Johannes C. M. Schlachetzki, Gianluigi Forloni, Dennis W. Dickson, Chiara Fenoglio, Olivier Piguet, John B.J. Kwok, Benedetta Nacmias, Harro Seelaar, Robert Perneczky, A. Baborie, Patrizia Rizzu, Y. Gao, Simon Mead, Janine Diehl-Schmid, Sara Ortega-Cubero, Mike A. Nalls, Daniela Galimberti, Annibale Alessandro Puca, Cristina Razquin, Mercè Boada, Johannes Attems, Luisa Benussi, Chiara Cupidi, Irene Piaceri, Xinghao Yu, Joseph E. Parisi, Alexander Kurz, John Collinge, James Uphill, Barbara Borroni, Francesca Frangipane, Caroline Graff, Bernd Ibach, D. M. A. Mann

المساهمون: Amsterdam Neuroscience - Neurodegeneration, Human genetics, Neurology, Apollo - University of Cambridge Repository, Int FTD-Genomics Consortium IFGC

المصدر: Scientific reports, vol 10, iss 1
Scientific Reports, 10(1):12184. Nature Publishing Group
Scientific reports 10(1), 12184 (2020). doi:10.1038/s41598-020-68848-9
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, McKeith, I G, Thomas, A J, Pietrini, P, Huey, E D, Wassermann, E M, Baborie, A, Jaros, E, Tierney, M C, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, George-Hyslop, P S, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, J B, Schlachetzki, J C M, Uphill, J, Collinge, J, Mead, S, Danek, A, Van Deerlin, V M, Grossman, M, Trojanowski, J Q, van der Zee, J, Cruts, M, Van Broeckhoven, C, Cappa, S F, Leber, I, Hannequin, D, Golfier, V, Vercelletto, M, Brice, A, Nacmias, B, Sorbi, S, Bagnoli, S, Piaceri, I, Nielsen, J E, Hjermind, L E, Riemenschneider, M, Mayhaus, M, Ibach, B, Gasparoni, G, Pichler, S, Gu, W, Rossor, M N, Fox, N C, Warren, J D, Spillantini, M G, Morris, H R, Rizzu, P, Heutink, P, Snowden, J S, Rollinson, S, Richardson, A, Gerhard, A, Bruni, A C, Maletta, R, Frangipane, F, Cupidi, C, Bernardi, L, Anfossi, M, Gallo, M, Conidi, M E, Smirne, N, Rademakers, R, Baker, M, Dickson, D W, Graff-Radford, N R, Petersen, R C, Knopman, D, Josephs, K A, Boeve, B F, Parisi, J E, Seeley, W W, Miller, B L, Karydas, A M, Rosen, H, van Swieten, J C, Dopper, E G P, Seelaar, H, Pijnenburg, Y A L, Scheltens, P, Logroscino, G, Capozzo, R, Novelli, V, Puca, A A, Franceschi, M, Postiglione, A, Milan, G, Sorrentino, P, Kristiansen, M, Chiang, H H, Graff, C, Pasquier, F, Rollin, A, Deramecourt, V, Lebouvier, T, Kapogiannis, D, Ferrucci, L, Pickering-Brown, S, Singleton, A B, Hardy, J, Momeni, P, Zhao, H, Zeng, P & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9Test
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, Rowe, J B, Nielsen, J E, Hjermind, L E & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9Test
Scientific reports

مصطلحات موضوعية: 0301 basic medicine, Oncology, lcsh:Medicine, Genome-wide association study, Neurodegenerative, 631/208, 0302 clinical medicine, Leukocytes, Odds Ratio, 2.1 Biological and endogenous factors, Aetiology, Amyotrophic lateral sclerosis, lcsh:Science, Telomerase, Telomere Shortening, education.field_of_study, Multidisciplinary, 692/617, article, Mendelian Randomization Analysis, Amyotrophic Lateral Sclerosis, Asian Continental Ancestry Group, Cholesterol, European Continental Ancestry Group, Genome-Wide Association Study, Humans, Lipoproteins, LDL, Polymorphism, Single Nucleotide, Proportional Hazards Models, Telomere, Frontotemporal Dementia, Single Nucleotide, Neurology, Engineering sciences. Technology, 692/499, medicine.medical_specialty, Lipoproteins, 692/308, Population, White People, LDL, Mendelian randomization (MR) , leukocyte telomere length (LTL) , amyotrophic lateral sclerosis (ALS), 03 medical and health sciences, Medical research, Rare Diseases, Asian People, Internal medicine, Mendelian randomization, Genetics, medicine, Polymorphism, education, Genetic association, business.industry, Proportional hazards model, International FTD-Genomics Consortium, lcsh:R, Neurosciences, Odds ratio, medicine.disease, Computational biology and bioinformatics, Brain Disorders, 030104 developmental biology, Risk factors, lcsh:Q, 631/114, ALS, business, ddc:600, 030217 neurology & neurosurgery

وصف الملف: application/pdf; application/zip; text/xml

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::311860380fb1414204d0afc5fcb0b1d3Test
https://doi.org/10.1038/s41598-020-68848-9Test

المؤلفون: Guey, Stéphanie, Kraemer, Markus, Hervé, Dominique, Ludwig, Thomas, Kossorotoff, Manoëlle, Bergametti, Françoise, Schwitalla, Jan Claudius, Choi, Simone, Broseus, Lucile, Callebaut, Isabelle, Genin, Emmanuelle, Tournier-Lasserve, Elisabeth, Consortium, FREX

المساهمون: unité de recherche de l'institut du thorax UMR1087 UMR6291 (ITX), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)

المصدر: European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2017, Equipe I, 25 (8), pp.995--1003. ⟨10.1038/ejhg.2017.92⟩

مصطلحات موضوعية: Male, 0301 basic medicine, Proband, Heterozygote, medicine.medical_specialty, Adolescent, Ubiquitin-Protein Ligases, [SDV]Life Sciences [q-bio], European Continental Ancestry Group, Mutation, Missense, Gastroenterology, White People, Article, Angiopathy, 03 medical and health sciences, 0302 clinical medicine, Mutation Carrier, Internal medicine, Genetics, Humans, Medicine, Missense mutation, Exome, Moyamoya disease, Child, Preschool, Genetics (clinical), Adenosine Triphosphatases, business.industry, adult, Case-control study, Odds ratio, Middle Aged, medicine.disease, 030104 developmental biology, Child, Preschool, Case-Control Studies, Mutation, Female, Missense, Moyamoya Disease, RING Finger Domains, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e49309f18a38c28af6fb5cea046b94f8Test
https://doi.org/10.1038/ejhg.2017.92Test

المؤلفون: Javier Benitez, Alicia Beeghly-Fadiel, Roger L. Milne, Graham G. Giles, Florentia Fostira, Senno Verhoef, Qin Wang, Simon S. Cross, Jenny Chang-Claude, Jacques Simard, Vessela N. Kristensen, Hoda Anton-Culver, Kathleen E. Malone, Veli-Matti Kosma, Pascal Guénel, Esther M. John, Stig E. Bojesen, Jan Lubinski, Patricia Harrington, Giske Ursin, Muhammad G. Kibriya, Artitaya Lophatananon, Mieke Kriege, Fergus J. Couch, Maria Kabisch, Judith S. Brand, Ute Hamann, Henrik Flyger, Susan L. Neuhausen, Elinor J. Sawyer, Mikael Hartman, Robert Luben, Thilo Dörk, Wanqing Wen, Hiltrud Brauch, Marilie D. Gammon, Xiao-Ou Shu, Ben Shan Zhang, Minouk J. Schoemaker, M. Pilar Zamora, Jirong Long, Rita K. Schmutzler, Natalia Bogdanova, Sofia Khan, Siranoush Manoukian, Anne Lise Børresen-Dale, Barbara Burwinkel, Regina M. Santella, Ian Tomlinson, Manjeet K. Bolla, Shan Wang-Gohrke, Nichola Johnson, Thérèse Truong, Rob B. van der Luijt, Amanda E. Toland, Carl Blomqvist, Catriona McLean, Georgia Chenevix-Trench, Anthony J. Swerdlow, Jingmei Li, Habibul Ahsan, David J. Hunter, Kristiina Aittomäki, Hui Zhao, Hui Miao, Wei Zheng, Olivia Fletcher, Alison M. Dunning, Marjanka K. Schmidt, Kenneth Muir, Per Hall, Farzana Jasmine, Eunjung Lee, Melissa C. Southey, Robert Winqvist, Janet E. Olson, Anna Jakubowska, Paul D.P. Pharoah, Martine Dumont, Dieter Flesch-Janys, Barbara Perkins, Douglas F. Easton, Christopher A. Haiman, Jonine D. Figueroa, Julia A. Knight, Kamila Czene, Loic Le Marchand, Katri Pylkäs, Angela Cox, Maartje J. Hooning, Kyriaki Michailidou, John L. Hopper, Qiuyin Cai, Volker Arndt, Heli Nevanlinna, Sara Lindström, Hanne Meijers-Heijboer, Sara Margolin, Zhiguo Zhao, Mitul Shah, Matthias W. Beckmann, Alfons Meindl, Martha J. Shrubsole, Paolo Peterlongo, Frederik Marmé, Peter Kraft, Irene L. Andrulis, Annika Lindblom, Diana Torres, Anja Rudolph, Arto Mannermaa, Graham Casey, Alice S. Whittemore, Hermann Brenner, Patrick Neven, Kelly-Anne Phillips, Peter A. Fasching, Montserrat Garcia-Closas

المساهمون: Human genetics, CCA - Cancer biology, Wang, Jean [0000-0002-9139-0627], Luben, Robert [0000-0002-5088-6343], Dunning, Alison [0000-0001-6651-7166], Pharoah, Paul [0000-0001-8494-732X], Easton, Douglas [0000-0003-2444-3247], Apollo - University of Cambridge Repository, Medical Oncology

المصدر: Zhao, Z, Wen, W, Michailidou, K, Bolla, M K, Wang, Q, Zhang, B, Long, J, Shu, X-O, Schmidt, M K, Milne, R L, Garcia-Closas, M, Chang-Claude, J, Lindstrom, S, Bojesen, S E, Ahsan, H, Aittomaki, K, Andrulis, I L, Anton-Culver, H, Arndt, V, Beckmann, M W, Beeghly-Fadiel, A, Benitez, J, Blomqvist, C, Bogdanova, N V, Borresen-Dale, A-L, Brand, J, Brauch, H, Brenner, H, Burwinkel, B, Cai, Q, Casey, G, Chenevix-Trench, G, Couch, F J, Cox, A, Cross, S S, Czene, K, Doerk, T, Dumont, M, Fasching, P A, Figueroa, J, Flesch-Janys, D, Fletcher, O, Flyger, H, Fostira, F, Gammon, M, Giles, G G, Guenel, P, Haiman, C A, Hamann, U, Harrington, P, Hartman, M, Hooning, M J, Hopper, J L, Jakubowska, A, Jasmine, F, John, E M, Johnson, N, Kabisch, M, Khan, S, Kibriya, M, Knight, J A, Kosma, V-M, Kriege, M, Kristensen, V, Le Marchand, L, Lee, E, Li, J, Lindblom, A, Lophatananon, A, Luben, R, Lubinski, J, Malone, K E, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, McLean, C, Meijers-Heijboer, H, Meindl, A, Miao, H, Muir, K, Neuhausen, S L, Nevanlinna, H, Neven, P, Olson, J E, Perkins, B, Peterlongo, P, Phillips, K-A, Pylkas, K, Rudolph, A, Santella, R, Sawyer, E J, Schmutzler, R K, Schoemaker, M, Shah, M, Shrubsole, M, Southey, M C, Swerdlow, A J, Toland, A E, Tomlinson, I, Torres, D, Therese Truong, Ursin, G, Van Der Luijt, R B, Verhoef, S, Wang-Gohrke, S, Whittemore, A S, Winqvist, R, Zamora, M P, Zhao, H, Dunning, A M, Simard, J, Hall, P, Kraft, P, Pharoah, P, Hunter, D, Easton, D F & Zheng, W 2016, ' Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry ', CCC. Cancer Causes and Control, vol. 27, no. 5, pp. 679-693 . https://doi.org/10.1007/s10552-016-0741-6Test
CCC. Cancer Causes and Control, 27(5), 679-693. Springer Netherlands
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Zhao, Zhiguo; Wen, Wanqing; Michailidou, Kyriaki; Bolla, Manjeet K; Wang, Qin; Zhang, Ben; et al.(2016). Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.. Cancer causes & control : CCC, 27(5), 679-693. doi: 10.1007/s10552-016-0741-6. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/9dr7h6bxTest
Cancer Causes & Control, 27(5), 679-693. Springer Netherlands
Cancer Causes & Control, 27(5), 679. Springer Netherlands

مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, endocrine system diseases, Epidemiology, Genome-wide association study, Type 2 diabetes, Breast cancer, 0302 clinical medicine, Risk Factors, Ethnicity, Odds Ratio, GWAS, Non-U.S. Gov't, Research Support, Non-U.S. Gov't, Middle Aged, 3. Good health, 030220 oncology & carcinogenesis, Public Health and Health Services, Female, medicine.medical_specialty, Oncology and Carcinogenesis, European Continental Ancestry Group, Non-P.H.S, Ethnic Groups, Breast Neoplasms, Research Support, Polymorphism, Single Nucleotide, Article, White People, N.I.H, 03 medical and health sciences, Research Support, N.I.H., Extramural, SDG 3 - Good Health and Well-being, Internal medicine, Genetic susceptibility, Journal Article, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, business.industry, Case-control study, Genetic Variation, Extramural, nutritional and metabolic diseases, Cancer, Odds ratio, medicine.disease, Obesity, 030104 developmental biology, Diabetes Mellitus, Type 2, Case-Control Studies, U.S. Gov't, business, Research Support, U.S. Gov't, Non-P.H.S, Demography

وصف الملف: application/pdf; image/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e548fd0236c68d3466b287e02b88a9b5Test
https://doi.org/10.1007/s10552-016-0741-6Test

المؤلفون: Torben Hansen, Lise Pedersen, Ulrik Lausten-Thomsen, Palle Skov Bratholm, Cilius Esmann Fonvig, Christine Bøjsøe, Jens-Christian Holm, Tenna Ruest Haarmark Nielsen, Oluf Pedersen

المصدر: Nielsen, T R H, Lausten-Thomsen, U, Fonvig, C E, Bøjsøe, C, Pedersen, L, Bratholm, P S, Hansen, T, Pedersen, O & Holm, J-C 2017, ' Dyslipidemia and reference values for fasting plasma lipid concentrations in Danish/North-European White children and adolescents ', B M C Pediatrics, vol. 17, 116 . https://doi.org/10.1186/s12887-017-0868-yTest
BMC Pediatrics, Vol 17, Iss 1, Pp 1-11 (2017)
Nielsen, T R H, Lausten-Thomsen, U, Esmann Fonvig, C, Bøjsøe, C, Pedersen, L, Bratholm, P S, Hansen, T, Pedersen, O & Holm, J-C 2017, ' Dyslipidemia and reference values for fasting plasma lipid concentrations in Danish/North-European White children and adolescents ', BMC Pediatrics, vol. 17, 116 . https://doi.org/10.1186/s12887-017-0868-yTest
BMC Pediatrics

مصطلحات موضوعية: Male, Pediatric Obesity, Pediatrics, Denmark, 030204 cardiovascular system & hematology, Overweight, 0302 clinical medicine, Prevalence, Dyslipidemias/blood, Medicine, Child, education.field_of_study, lcsh:RJ1-570, Fasting, Lipids, Europe, Triglycerides/blood, Cholesterol, Cohort, language, Female, medicine.symptom, Research Article, medicine.medical_specialty, Adolescent, European Continental Ancestry Group, Population, 030209 endocrinology & metabolism, Cholesterol/blood, White People, Childhood obesity, Europe/epidemiology, Reference values, Danish, Young Adult, 03 medical and health sciences, Journal Article, Humans, Obesity, education, Triglycerides, Dyslipidemias, business.industry, lcsh:Pediatrics, Odds ratio, medicine.disease, Denmark/epidemiology, language.human_language, Pediatric Obesity/blood, Cross-Sectional Studies, Logistic Models, Case-Control Studies, Pediatrics, Perinatology and Child Health, business, Biomarkers, Biomarkers/blood, Dyslipidemia

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::118729a7b4886b272823386d99e756baTest
https://doi.org/10.1186/s12887-017-0868-yTest

المؤلفون: Vladimir Vukovic, Rosarita Amore, Emanuele Leoncini, Carolina Ianuale, Stefania Boccia, Roberta Pastorino, Maria Rosaria Gualano

المصدر: BMC Cancer

مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, medicine.medical_specialty, European Continental Ancestry Group, CYP1A2, Population, Single-nucleotide polymorphism, Genome-wide association study, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, Cancer, Meta-analysis, Polymorphism, Susceptibility, Cytochrome P-450 CYP1A2, Genome-Wide Association Study, Humans, Neoplasms, Risk Factors, Genetic Predisposition to Disease, Genetics, 0302 clinical medicine, Internal medicine, Genetic model, medicine, education, Settore MED/42 - IGIENE GENERALE E APPLICATA, Genetic association, education.field_of_study, Bladder cancer, business.industry, Single Nucleotide, Odds ratio, medicine.disease, 030104 developmental biology, 030220 oncology & carcinogenesis, business, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80297c720c92bec500047b47d338fd7eTest
https://doi.org/10.1186/s12885-016-2096-5Test

المؤلفون: John I. Nurnberger, Arpana Agrawal, Nancy L. Saccone, Samuel Kuperman, Jen C. Wang, Louis Fox, John Kramer, Kathleen K. Bucholz, John P. Rice, Eric O. Johnson, Howard J. Edenberg, Jay A. Tischfield, Alison Goate, Tatiana Foroud, Sarah Bertelsen, Laura J. Bierut, Victor Hesselbrock, Marc A. Schuckit, Naomi Breslau, Richard A. Grucza, Bernice Porjesz

المصدر: Molecular psychiatry
Molecular psychiatry, vol 17, iss 4

مصطلحات موضوعية: Male, alcohol dependence, Alcohol, Medical and Health Sciences, Substance Misuse, Alcohol Use and Health, chemistry.chemical_compound, 0302 clinical medicine, genetics, protective allele, African Continental Ancestry Group, Psychiatry, Genetics, 0303 health sciences, alcohol dehydrogenase, ADH1B, Single Nucleotide, Biological Sciences, Middle Aged, 3. Good health, Alcoholism, Psychiatry and Mental health, Mental health, Female, Adult, Adolescent, Alcohol Drinking, Genotype, European Continental Ancestry Group, Black People, Biology, association study, Polymorphism, Single Nucleotide, White People, Article, 03 medical and health sciences, Cellular and Molecular Neuroscience, Humans, Polymorphism, Allele, Molecular Biology, Allele frequency, Alleles, Aged, 030304 developmental biology, Psychology and Cognitive Sciences, Alcohol dependence, Case-control study, Odds ratio, Confidence interval, Brain Disorders, Good Health and Well Being, chemistry, Case-Control Studies, 030217 neurology & neurosurgery, Demography

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d02d05e4bb4f9183f1fd95d42987160Test
https://doi.org/10.1038/mp.2011.124Test

المؤلفون: Lorena Garcia, Rami Nassir, Matthew A. Allison, John A Robbins, JoAnn E. Manson, Heather M. Ochs-Balcom, Russell Shigeta, Lihong Qi, Michael F. Seldin, Fran Tylavsky, Roman Kosoy

المصدر: International journal of obesity (2005)
International journal of obesity (2005), vol 36, iss 2

مصطلحات موضوعية: Gerontology, Endocrinology, Diabetes and Metabolism, Medicine (miscellaneous), waist to hip ratio, Medical and Health Sciences, Cohort Studies, Waist–hip ratio, Indians, Odds Ratio, Medicine, Amerindian admixture, Adiposity, African Americans, education.field_of_study, Nutrition and Dietetics, Hispanic or Latino, Middle Aged, African admixture, Phenotype, Adipose Tissue, Quartile, Body Composition, Female, Hispanic Americans, North American, Genotype, European Continental Ancestry Group, Population, waist-to-hip ratio, European admixture, body mass index, Ancestry-informative marker, White People, Article, Education, post-menopausal women, Endocrinology & Metabolism, Clinical Research, Humans, Obesity, education, Africa South of the Sahara, Waist-Hip Ratio, business.industry, nutritional and metabolic diseases, Odds ratio, medicine.disease, United States, Confidence interval, Black or African American, Indians, North American, Women's Health, post–menopausal women, business, Body mass index, Demography

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a04e8c53754e7030d7d0d9e53a3b846Test
https://doi.org/10.1038/ijo.2011.84Test

المؤلفون: Søren Rasmussen, Janne Schurmann Tolstrup, Børge G. Nordestgaard, Morten Grønbæk, Anne Tybjærg-Hansen

المصدر: Tolstrup, J S, Nordestgaard, B G, Rasmussen, S, Tybjaerg-Hansen, A & Grønbaek, M 2008, ' Alcoholism and alcohol drinking habits predicted from alcohol dehydrogenase genes ', Pharmacogenomics Journal, vol. 8, no. 3, pp. 220-7 . https://doi.org/10.1038/sj.tpj.6500471Test

مصطلحات موضوعية: Asian Continental Ancestry Group, Male, Alcohol Drinking, Genotype, Epidemiology, European Continental Ancestry Group, Population, Alcohol, White People, chemistry.chemical_compound, Asian People, Genetics, Humans, Medicine, Alcohol tolerance, education, Alcohol dehydrogenase, Pharmacology, education.field_of_study, Ethanol, biology, business.industry, Alcohol Dehydrogenase, ADH1B, Odds ratio, Confidence interval, Alcoholism, chemistry, Attributable risk, biology.protein, Molecular Medicine, Female, business, Demography

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39c5d463e83527bb5404ca21ccf694b7Test
https://doi.org/10.1038/sj.tpj.6500471Test

المؤلفون: Bobby P. C. Koeleman, Juan-Manuel Anaya, Elena Sánchez, Miguel A. López-Nevot, María Francisca González-Escribano, Javier Martin, E de Ramón, Miguel A. González-Gay, José Mario Sabio, Norberto Ortego-Centeno, Luis Miguel Gómez

المصدر: Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario

مصطلحات موضوعية: Male, single nucleotide, Chromosomes, Human, Pair 22, Pathogenesis, Promoter regions (genetics), Gene Frequency, pair 22, Polymorphism (computer science), Genotype, Odds Ratio, Haplotype, Lupus Erythematosus, Systemic, Macrophage migration-inhibitory factors, Promoter Regions, Genetic, Middle aged, skin and connective tissue diseases, Genetics (clinical), Priority journal, Allele, education.field_of_study, Chromosome Mapping, Odds ratio, Middle Aged, Statistical significance, Polymerase chain reaction, Female, Macrophage migration inhibition factor, Adult, Chromosome mapping, Confidence intervals, Immunology, Population, Major clinical study, Case-control studies, Biology, Polymorphism, Single Nucleotide, White People, Article, Chromosomes, Systemic lupus erythematosus, Microsatellite repeats, Confidence Intervals, Genetic susceptibility, Genetics, medicine, Humans, human, Polymorphism, education, Macrophage Migration-Inhibitory Factors, Allele frequency, Alleles, Polymorphism, Genetic, Genetic polymorphism, Lupus erythematosus, systemic, medicine.disease, Gene frequency, Clinical feature, Haplotypes, Case-Control Studies, Genetic association, Macrophage migration inhibitory factor, genetic, Controlled study, Microsatellite Repeats, European continental ancestry group

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::698ec41a327a871a45f790a9d3affe66Test
https://doi.org/10.1038/sj.gene.6364310Test

المؤلفون: Gavin R. Norton, Angela J. Woodiwiss, Patrick H Dessein, Ahmed Solomon

المساهمون: Clinical sciences

المصدر: Arthritis Research & Therapy

مصطلحات موضوعية: Carotid Artery Diseases, medicine.medical_specialty, Waist, Cross-sectional study, European Continental Ancestry Group, Immunology, Population, White People, Body Mass Index, Arthritis, Rheumatoid, Waist–hip ratio, Rheumatology, Risk Factors, Internal medicine, medicine, Humans, Immunology and Allergy, Obesity, education, Abdominal obesity, Aged, African Americans, Medicine(all), education.field_of_study, Waist-Hip Ratio, business.industry, Odds ratio, Middle Aged, medicine.disease, Black or African American, Cross-Sectional Studies, Physical therapy, Female, medicine.symptom, business, Body mass index, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c933954252e8b927192c5eac77148b35Test
https://doi.org/10.1186/ar3784Test