المؤلفون: Wim Teughels, Nadine Schlueter, Maria Clotilde Carra, Iain L. C. Chapple, Nigel Pitts, David J. Manton, Marja L. Laine, Peter Lingström, Maria Grazia Cagetti, Fabio Cocco, Eduardo Montero, Philippe P. Hujoel, Andreas G. Schulte, Cor van Loveren, Fridus van der Weijden, Philippe Bouchard, Svante Twetman, Guglielmo Campus, Luigi Nibali, Alexandre R. Vieira, Hélène Rangé

المساهمون: Periodontology, Preventive Dentistry, Parodontologie (OII, ACTA), Preventieve tandheelkunde (OII, ACTA)

المصدر: Journal of Clinical Periodontology, 44(S18), S39-S51. Blackwell Munksgaard
Chapple, I L C, Bouchard, P, Cagetti, M G, Campus, G, Carra, M-C, Cocco, F, Nibali, L, Hujoel, P, Laine, M L, Lingstrom, P, Manton, D J, Montero, E, Pitts, N, Rangé, H, Schlueter, N, Teughels, W, Twetman, S, van Loveren, C, van der Weijden, F, Vieira, A R & Schulte, A G 2017, ' Interaction of lifestyle, behaviour or systemic diseases with dental caries and periodontal diseases: consensus report of group 2 of the joint EFP/ORCA workshop on the boundaries between caries and periodontal diseases ', Journal of Clinical Periodontology, vol. 44, no. S18, pp. S39-S51 . https://doi.org/10.1111/jcpe.12685

مصطلحات موضوعية: Health Behavior, Dentistry, Fc gamma receptor IIA (Fc gamma RIIA) gene, vitamin C, vitamin D, PROGRESSION, Disease, Bioinformatics, SUPPLEMENTATION, gingival bleeding, Gingivitis, 0302 clinical medicine, Risk Factors, OBSTRUCTIVE SLEEP-APNEA, Tooth loss, genetics, 030212 general & internal medicine, prognostic factor, VITAMIN-D, periodontitis, RISK, diabetes, starch, oral hygiene frequency, vitamin B12, ASSOCIATION, nutrition, risk factor, prediction factor, Periodontics, genome wide association study (GWAS), medicine.symptom, Life Sciences & Biomedicine, periodontal diseases, gingivitis, acquired risk factors, macronutrient, malnutrition, Biology, Dental Caries, smoking, DIET, 03 medical and health sciences, single nucleotide polymorphism (SNP), SDG 3 - Good Health and Well-being, Dentistry, Oral Surgery & Medicine, Vitamin D and neurology, medicine, micronutrient, Humans, Risk factor, ORAL-HEALTH, hyposalivation, Life Style, Periodontal Diseases, caries, Periodontitis, vitamin D receptor (VDR) gene, saliva, Science & Technology, candidate gene study (CGS), fluoride, ASCORBIC-ACID DEPLETION, business.industry, polyunsaturated fatty acid (PUFA), 030206 dentistry, GLOBAL BURDEN, medicine.disease, Chronic periodontitis, amelogenin (AMELX) gene, sugars, carbohydrate, aquaporin (AQP5) gene, Attributable risk, Interleukin 10 (IL10) gene, business, protein

وصف الملف: Print

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53d5f87461b9abcbb299613cd716fe39
https://doi.org/10.1111/jcpe.12685

المؤلفون: Luis R. Lopes, Perry M. Elliott

المصدر: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1832:2451-2461

مصطلحات موضوعية: Candidate gene, Cardiomyopathy, Population, Heart failure, Genome-wide association study, Biology, Bioinformatics, symbols.namesake, Candidate gene study, Risk Factors, Genetics, medicine, Genetic predisposition, Animals, Humans, GWAS, Genetic Predisposition to Disease, education, Molecular Biology, education.field_of_study, High-throughput sequencing, medicine.disease, Muscle disease, Mendelian inheritance, symbols, Molecular Medicine, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a409fe106f8c932792fba303993fbebf
https://doi.org/10.1016/j.bbadis.2012.12.012

المؤلفون: Samuel Kuperman, Frank Visscher, Kirsten R. Müller-Vahl, Eun-Young Shin, Jennifer Tübing, Els van den Ban, Sina Wanderer, Hyun Ju Hong, Yun-Joo Koh, Jungeun Song, Gary A. Heiman, Lonneke Elzerman, Donald L. Gilbert, Derek Gordon, Laura Ibanez-Gomez, Keun-Ah Cheon, Douglas Londono, Young Key Kim, Bennett L. Leventhal, Alexander Münchau, Odette Fründt, Andrea G. Ludolph, Astrid Morer, Sodahm Kook, Thomas V. Fernandez, Lawrence W. Brown, Marcos Madruga-Garrido, Ewgeni Jakubovski, Jay A. Tischfield, Mohamed Abdulkadir, Blanca Garcia-Delgar, Carolin Fremer, Samuel H. Zinner, Pablo Mir, Robert A. King, Martin Woods, Veit Roessner, Young Shin Kim, Isobel Heyman, Tara Murphy, Athanasios Maras, Dong-Ho Song, Pieter J. Hoekstra, Tammy Hedderly, Barbara J. Coffey, Andrea Dietrich, Chaim Huyser, Dorothy E. Grice, Kerstin J. Plessen

المساهمون: Clinical Cognitive Neuropsychiatry Research Program (CCNP), Child Psychiatry, Child and Adolescent Psychiatry / Psychology

المصدر: European Archives of Psychiatry and Clinical Neuroscience, 268(3), 301-316. SPRINGER HEIDELBERG
European archives of psychiatry and clinical neuroscience, 268(3), 301-316. Springer Verlag
European Archives of Psychiatry and Clinical Neuroscience
European Archives of Psychiatry and Clinical Neuroscience, 268(3), 301-316. D. Steinkopff-Verlag
European archives of psychiatry and clinical neuroscience, vol 268, iss 3

مصطلحات موضوعية: 0301 basic medicine, Male, Candidate gene, Genome-wide association study, Tryptophan Hydroxylase, Obsessive–compulsive disorder, Severity of Illness Index, Linkage Disequilibrium, PICALM, 0302 clinical medicine, Candidate gene study, Obsessive-compulsive disorder, Pharmacology (medical), Child, POPULATION, Psychiatry, Genetics, LA-TOURETTE-SYNDROME, education.field_of_study, SLITRK1 GENE, Single Nucleotide, General Medicine, Transmission disequilibrium test, Middle Aged, 3. Good health, Psychiatry and Mental health, COMPREHENSIVE METAANALYSIS, Child, Preschool, HISTIDINE-DECARBOXYLASE, Cognitive Sciences, Female, Microtubule-Associated Proteins, Adult, Adolescent, Genotype, Clinical Sciences, Population, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Young Adult, SNP, Humans, Polymorphism, GENOME-WIDE ASSOCIATION, AUTISM, Preschool, education, Biological Psychiatry, FAMILY-BASED ASSOCIATION, Genetic association, Family Health, Original Paper, Tourette syndrome, Neurosciences, OBSESSIVE-COMPULSIVE DISORDER, Transmission Disequilibrium Test, CROSS-DISORDER, 030104 developmental biology, Attention-deficit/hyperactivity disorder, Tic Disorders, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c080118db5a7932f73b32854e2647093
https://doi.org/10.1007/s00406-017-0808-8

المؤلفون: Mahlman, M. (Mari)

المساهمون: Hallman, M. (Mikko), Rämet, M. (Mika), Karjalainen, M. (Minna)

مصطلحات موضوعية: bronkopulmonaalinen dysplasia, ehdokasgeenitutkimus, pulmonary inflammation, Kit ligandi, behavioral disciplines and activities, ennenaikainen syntymä, C-reactive protein, vascular endothelial growth factor receptor 2, mental disorders, bronchopulmonary dysplasia, genetic polymorphism, verisuonten endoteelikasvutekijä, genome-wide association study, C-reaktiivinen proteiini, vascular endothelial growth factor, Kit ligand, geneettinen assosiaatiotutkimus, koko genomin assosiaatiotutkimus, twins, premature birth, keskosuus, premature infant, kaksoset, geenipolymorfismi, keuhkojen tulehdusreaktio, genetic association study, candidate gene study, keskosen krooninen keuhkosairaus

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2423::cc12aa7d424d372abb93956a233ba232
http://urn.fi/urn:isbn:9789526219530

المؤلفون: Biju Viswanath, Abhishek Purty, Jack Samuels, Gerald Nestadt

المصدر: Indian Journal of Psychiatry

مصطلحات موضوعية: Candidate gene, Genome-wide association study, Review Article, Biology, Serotonergic, 03 medical and health sciences, 0302 clinical medicine, Candidate gene study, mental disorders, medicine, family study, genetics, 030212 general & internal medicine, Epigenetics, twin study, Gene, linkage study, Genetics, genome-wide association study, Heritability, Twin study, 030227 psychiatry, obsessive-compulsive disorder, Psychiatry and Mental health, medicine.anatomical_structure, Dopaminergic pathways

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7444d7286b9106ffab34fcc82ebfce2
https://doi.org/10.4103/psychiatry.indianjpsychiatry_518_18

المؤلفون: Barić, Ana, Brčić, Luka, Gračan, Sanda, Torlak Lovrić, Vesela, Gunjača, Ivana, Šimunac, Marta, Boban, Mladen, Zemunik, Tatijana, Polašek, Ozren, Barbalić, Maja, Punda, Ante, Boraska Perica, Vesna

مصطلحات موضوعية: endocrine system, endocrine system diseases, Hashimoto's thyroiditis, hypothyroidism, candidate gene study, genetic epidemiology, single nucleotide polymorphism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::865510729ecf7787d03a8a87a31c009a
https://www.bib.irb.hr/974888

المؤلفون: Karppanen, Tiina, Kaartokallio, Tea, Klemetti, Miira M, Heinonen, Seppo, Kajantie, Eero, Kere, Juha, Kivinen, Katja, Pouta, Anneli, Staff, Anne Cathrine, Laivuori, Hannele

مصطلحات موضوعية: Adult, Genotype, Models, Biological, Polymorphism, Single Nucleotide, Body Mass Index, Candidate gene study, Pre-Eclampsia, Pregnancy, Risk Factors, Odds Ratio, Humans, Genetic Predisposition to Disease, 3' Untranslated Regions, reproductive and urinary physiology, Alleles, Genetic Association Studies, 2. Zero hunger, Overweight, Preeclampsia, female genital diseases and pregnancy complications, 3. Good health, Gene Expression Regulation, Case-Control Studies, embryonic structures, Regulator of G-protein signaling 2, Female, Biomarkers, RGS Proteins

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fc06ef7763702136db20006d587727ec

المؤلفون: Amin, Hasnat A

المساهمون: Blakemore-Walters, A I F, Drenos, F

مصطلحات موضوعية: UK Biobank, Ageing, Candidate gene study, Newcastle 85 Plus study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_______900::67dbd1d3c6a441f7e9c8d0d9a2a81d05
https://bura.brunel.ac.uk/handle/2438/25514

المؤلفون: Eero Kajantie, Miira M. Klemetti, Katja Kivinen, Juha Kere, Seppo Heinonen, Tea Kaartokallio, Hannele Laivuori, Tiina Karppanen, Anne Cathrine Staff, Anneli Pouta

المساهمون: Karppanen, Tiina [0000-0002-0954-478X], Apollo - University of Cambridge Repository, Medicum, Pregnancy and Genes, Department of Medical and Clinical Genetics, Clinicum, Department of Obstetrics and Gynecology, Children's Hospital, Lastentautien yksikkö, University of Helsinki, Juha Kere / Principal Investigator, Institute for Molecular Medicine Finland, HUS Gynecology and Obstetrics

المصدر: BMC Genetics

مصطلحات موضوعية: 0301 basic medicine, BLOOD-PRESSURE, 030204 cardiovascular system & hematology, Overweight, Body Mass Index, 0302 clinical medicine, Candidate gene study, Pre-Eclampsia, 3123 Gynaecology and paediatrics, Pregnancy, Risk Factors, Polymorphism (computer science), Odds Ratio, ANXIETY, Genetics(clinical), 3' Untranslated Regions, reproductive and urinary physiology, Genetics (clinical), METABOLIC SYNDROME, 2. Zero hunger, Genetics, C1114G POLYMORPHISM, female genital diseases and pregnancy complications, 3. Good health, ANGIOTENSIN-II, CARDIOVASCULAR-DISEASE, embryonic structures, Regulator of G-protein signaling 2, Female, medicine.symptom, Research Article, Adult, Genotype, Biology, Models, Biological, Polymorphism, Single Nucleotide, Preeclampsia, 03 medical and health sciences, medicine, Humans, Genetic Predisposition to Disease, METAANALYSIS, Alleles, Genetic Association Studies, OBESITY-RELATED HYPERTENSION, Case-control study, Odds ratio, medicine.disease, Angiotensin II, 030104 developmental biology, Gene Expression Regulation, 3121 General medicine, internal medicine and other clinical medicine, Case-Control Studies, RISK-FACTORS, 3111 Biomedicine, Metabolic syndrome, Body mass index, Biomarkers, RGS Proteins

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c48b0cb04d97f3e16d91afd4d00dcccd
https://doi.org/10.1186/s12863-016-0428-8

المؤلفون: Tatijana Zemunik, Vesna Boraska Perica, Nikolina Vidan, Maja Barbalić, Luka Brčić, Vesela Torlak Lovrić, Sanda Gračan, Dubravka Brdar, Ozren Polasek, Ana Barić, Ante Punda

المصدر: Autoimmunity. 49:480-485

مصطلحات موضوعية: Male, 0301 basic medicine, endocrine system diseases, Autoantigens, Thyroiditis, 0302 clinical medicine, Iron-Binding Proteins, Immunology and Allergy, Aged, 80 and over, biology, Thyroid, Middle Aged, Hashimoto's thyroiditis, thyroid peroxidase autoantibody, candidate gene study, genetic epidemiology, single-nucleotide polymorphism, Anti-thyroid autoantibodies, Phenotype, medicine.anatomical_structure, Female, Adult, endocrine system, medicine.medical_specialty, Genotype, Immunology, 030209 endocrinology & metabolism, Single-nucleotide polymorphism, Hashimoto Disease, Iodide Peroxidase, Polymorphism, Single Nucleotide, Young Adult, 03 medical and health sciences, Thyroid peroxidase, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Alleles, Aged, Autoantibodies, business.industry, Autoantibody, Case-control study, Genetic Variation, medicine.disease, 030104 developmental biology, Endocrinology, Genetic epidemiology, Case-Control Studies, biology.protein, business, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::425327eef2c3fde7a93c0726467ff459
https://doi.org/10.1080/08916934.2016.1191475