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by Zanoni, Paolo and Khetarpal, Sumeet A and Larach, Daniel B and Hancock-Cerutti, William F and Millar, John S and Cuchel, Marina and DerOhannessian, Stephanie and Kontush, Anatol and Surenan, Praveen and Saleheen, Danish and Trompet, Stella and Jukema, J. Wouter and de Craen, Anton and Deloukas, Panos and Sattar, Naveed and Ford, Ian and Packard, Chris and Majumder, Abdullah al Shafi and Alam, Dewan S and Di Angelantonio, Emanuele and Abecasis, Goncalo and Chowdhury, Rajiv and Erdmann, Jeanette and Nordestgaard, Børge G and Nielsen, Sune F and Tybjærg-Hansen, Anne and Schmidt, Ruth Frikke and Kuulasmaa, Kari and Liu, Dajiang J and Perola, Markus and Blankenberg, Stefan and Salomaa, Veikko and Männistö, Satu and Amouyel, Philippe and Arveiler, Dominique and Ferrieres, Jean and Müller-Nurasyid, Martina and Ferrario, Marco and Kee, Frank and Willer, Cristen J and Samani, Nilesh and Schunkert, Heribert and Butterworth, Adam S and Howson, Joanna M. M and Peloso, Gina M and Stitziel, Nathan O and Danesh, John and Kathiresan, Sekar and Rader, Daniel J and Watson, Sarah and Schmidt, Ellen M and Sengupta, Sebanti and Gustafsson, Stefan and Kanoni, Stavroula and Ganna, Anea and Chen, Jin and Buchkovich, Martin L and Mora, Samia and Beckmann, Jacques S and Bragg-Gresham, Jennifer L and Chang, Hsing-Yi and Demirkan, Ayşe and den Hertog, Heleen M and Do, Ron and Donnelly, Louise A and Ehret, Georg B and Esko, Tõnu and Feitosa, Mary F and Ferreira, Teresa and Fischer, Krista and Fontanillas, Pierre and Fraser, Ross M and Freitag, Daniel F and Gurdasani, Deepti and Heikkilä, Kauko and Hyppönen, Elina and Isaacs, Aaron and Jackson, Anne U and Johansson, Åsa and Johnson, Toby and Kaakinen, Marika and Kettunen, Johannes and Kleber, Marcus E and Li, Xiaohui and Luan, Jian'an and Lyytikäinen, Leo-Pekka and Magnusson, Patrik K. E and Mangino, Massimo and Mihailov, Evelin and Montasser, May E and Nolte, Ilja M and O'Connell, Jeffrey R and Palmer, Cameron D and Petersen, Ann-Kristin and Sanna, Serena and Saxena, Richa and Service, Susan K and Shah, Sonia and Shungin, Dmitry and Sidore, Carlo and ... and Consortium, CE and Global Lipids Genetics Consortium and CARDIoGRAM Exome Consortium and CHD Exome+ Consortium
Science, ISSN 0036-8075, 2016, Volume 351, Issue 6278, pp. 1166 - 1171
Journal Article
12/2010
Dietary fat intake is extremely low in most communities with vitamin A deficiency. However, its role in vitamin A status of pregnant and lactating women is... 
Pregnancy | Vitamin A | Bangladesh | Fat supplementation | Community-based studies | Infant | Vitamin A deficiency | Postpartum
Web Resource
by Marouli, Eirini and Graff, Mariaelisa and Medina-Gomez, Carolina and Lo, Ken Sin and Wood, Anew R and Kjaer, Troels R and Fine, Rebecca S and Lu, Yingchang and Schurmann, Claudia and Highland, Heather M and Rüeger, Sina and Thorleifsson, Gudmar and Justice, Anne E and Lamparter, David and Stirrups, Kathleen E and Turcot, Valérie and Young, Kristin L and Winkler, Thomas W and Esko, Tõnu and Karaderi, Tugce and Locke, Adam E and Masca, Nicholas G. D and Ng, Maggie C. Y and Mudgal, Poorva and Rivas, Manuel A and Vedantam, Sailaja and Mahajan, Anubha and Guo, Xiuqing and Abecasis, Goncalo and Aben, Katja K and Adair, Linda S and Alam, Dewan S and Albrecht, Eva and Allin, Kristine H and Allison, Matthew and Amouyel, Philippe and Appel, Emil V and Arveiler, Dominique and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Banas, Bernhard and Bang, Lia E and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bonnycastle, Lori L and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Burt, Amber A and Butterworth, Adam S and Carey, David J and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Auey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Galbany, Jordi Corominas and Cox, Amanda J and Cuellar-Partida, Gabriel and Danesh, John and Davies, Gail and de Bakker, Paul I. W and de Borst, Gert J and de Denus, Simon and de Groot, Mark C. H and de Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and den Hollander, Anneke I and Dennis, Joe G and Di Angelantonio, Emanuele and nos, Fotios and Du, Mengmeng and Dunning, Alison M and Easton, Douglas F and Ebeling, Tapani and Edwards, Todd L and Ellinor, Patrick T and Elliott, Paul and Evangelou, Evangelos and Farmaki, Aliki-Eleni and Faul, Jessica D and ... and EPIC-CVD Consortium and GoT2D Genes Consortium and MAGIC Investigators and Global Lipids Genetics Consortium and EPIC-InterAct Consortium and ReproGen Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and CHD Exome+ Consortium and The EPIC-InterAct Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature, ISSN 0028-0836, 2017, Volume 542, Issue 7640, pp. 186 - 190
Height is a highly heritable, classic polygenic trait with approximately 700 common associated variants identified through genome-wide association studies so... 
MULTIDISCIPLINARY SCIENCES | MISSING HERITABILITY | GENETIC ARCHITECTURE | INTERLEUKIN-11 | MICE | MUTATIONS | GENOME-WIDE ASSOCIATION | Cell Adhesion Molecules - genetics | Gene Frequency - genetics | Humans | Glycoproteins - metabolism | Male | Intercellular Signaling Peptides and Proteins - metabolism | Hedgehog Proteins - genetics | Proteolysis | NADPH Oxidases - genetics | Adult | Female | Interleukin-11 Receptor alpha Subunit - genetics | Somatomedins - metabolism | Glycosaminoglycans - biosynthesis | Glycoproteins - genetics | Multifactorial Inheritance - genetics | Procollagen N-Endopeptidase - genetics | Intercellular Signaling Peptides and Proteins - genetics | Interferon Regulatory Factors - genetics | Proteoglycans - biosynthesis | NADPH Oxidase 4 | Body Height - genetics | Genome, Human - genetics | Phenotype | Receptors, Androgen - genetics | Alleles | Genetic Variation - genetics | Pregnancy-Associated Plasma Protein-A - metabolism | ADAMTS Proteins - genetics | Stature | Genetic aspects | Observations | Genetic variation | Studies | Datasets | Disease | Genes | Deoxyribonucleic acid--DNA | Index Medicus | Hälsovetenskaper | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Medical and Health Sciences | Medicin och hälsovetenskap | Public Health, Global Health, Social Medicine and Epidemiology | Health Sciences
Journal Article
Journal Article
by Howson, Joanna M M and Zhao, Wei and Barnes, Daniel R and Ho, Weang-Kee and Young, Robin and Paul, Dirk S and Waite, Lindsay L and Freitag, Daniel F and Fauman, Eric B and Salfati, Elias L and Sun, Benjamin B and Eicher, John D and Johnson, Andrew D and Sheu, Wayne H H and Nielsen, Sune F and Lin, Wei-Yu and Surendran, Praveen and Malarstig, Anders and Wilk, Jemma B and Tybjærg-Hansen, Anne and Rasmussen, Katrine L and Kamstrup, Pia R and Deloukas, Panos and Erdmann, Jeanette and Kathiresan, Sekar and Samani, Nilesh J and Schunkert, Heribert and Watkins, Hugh and Do, Ron and Rader, Daniel J and Johnson, Julie A and Hazen, Stanley L and Quyyumi, Arshed A and Spertus, John A and Pepine, Carl J and Franceschini, Nora and Justice, Anne and Reiner, Alex P and Buyske, Steven and Hindorff, Lucia A and Carty, Cara L and North, Kari E and Kooperberg, Charles and Boerwinkle, Eric and Young, Kristin and Graff, Mariaelisa and Peters, Ulrike and Absher, Devin and Hsiung, Chao A and Lee, Wen-Jane and Taylor, Kent D and Chen, Ying-Hsiang and Lee, I-Te and Guo, Xiuqing and Chung, Ren-Hua and Hung, Yi-Jen and Rotter, Jerome I and Juang, Jyh-Ming J and Quertermous, Thomas and Wang, Tzung-Dau and Rasheed, Asif and Frossard, Philippe and Alam, Dewan S and Majumder, Abdulla Al Shafi and Di Angelantonio, Emanuele and Chowdhury, Rajiv and Chen, Yii-Der Ida and Nordestgaard, Børge G and Assimes, Themistocles L and Danesh, John and Butterworth, Adam S and Saleheen, Danish and EPIC-CVD and CARDIoGRAMplusC4D
Nature Genetics, ISSN 1061-4036, 07/2017, Volume 49, Issue 7, pp. 1113 - 1119
Journal Article
Bulletin of the World Health Organization, ISSN 0042-9686, 10/2013, Volume 91, Issue 10, pp. 757 - 764
Journal Article
Journal Article
by Turcot, Valérie and Lu, Yingchang and Highland, Heather M and Schurmann, Claudia and Justice, Anne E and Fine, Rebecca S and Bradfield, Jonathan P and Esko, Tõnu and Giri, Ayush and Graff, Mariaelisa and Guo, Xiuqing and Hendricks, Audrey E and Karaderi, Tugce and Lempradl, Adelheid and Locke, Adam E and Mahajan, Anubha and Marouli, Eirini and Sivapalaratnam, Suthesh and Young, Kristin L and Alfred, Tamuno and Feitosa, Mary F and Masca, Nicholas G. D and Manning, Alisa K and Medina-Gomez, Carolina and Mudgal, Poorva and Ng, Maggie C. Y and Reiner, Alex P and Vedantam, Sailaja and Willems, Sara M and Winkler, Thomas W and Abecasis, Gonçalo and Aben, Katja K and Alam, Dewan S and Alharthi, Sameer E and Allison, Matthew and Amouyel, Philippe and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Bang, Lia E and Barroso, Inês and Bastarache, Lisa and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boehnke, Michael and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Brumat, Marco and Burt, Amber A and Butterworth, Adam S and Campbell, Peter T and Cappellani, Stefania and Carey, David J and Catamo, Eulalia and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der I and Chowdhury, Rajiv and Christensen, Cramer and Chu, Audrey Y and Cocca, Massimiliano and Cook, James P and Corley, Janie and Corominas Galbany, Jordi and Cox, Amanda J and Crosslin, David S and Cuellar-Partida, Gabriel and D'Eustacchio, Angela and Danesh, John and Davies, Gail and Bakker, Paul I. W and Groot, Mark C. H and Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and Heijer, Martin and Hollander, Anneke I and Ruijter, Hester M and Dennis, Joe G and Denny, Josh C and Angelantonio, Emanuele and Drenos, Fotios and Du, Mengmeng and Dubé, Marie-Pierre and Dunning, Alison M and Easton, Douglas F and Edwards, Todd L and ... and Chd Exome Consortium and EPIC InterAct Consortium and Global Lipids Genetic Consortium and GoT2D Genes Consortium and MAGIC Investigators and Understanding Soc Sci Grp and ReproGen Consortium and Interval Study and Epic-Cvd Consortium and ExomeBP Consortium and T2D-Genes Consortium and INTERVAL Study and EPIC-CVD Consortium and EPIC InterAct Consortium and CHD Exome+ Consortium and Understanding Society Scientific Group and The MAGIC Investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature Genetics, ISSN 1061-4036, 01/2018, Volume 50, Issue 1, pp. 26 - 35
Journal Article
by Zhao, Wei and Rasheed, Asif and Tikkanen, Emmi and Lee, Jung-Jin and Butterworth, Adam S and Howson, Joanna M. M and Assimes, Themistocles L and Chowdhury, Rajiv and Orho-Melander, Marju and Damrauer, Scott and Small, Aeron and Asma, Senay and Imamura, Minako and Yamauch, Toshimasa and Chambers, John C and Chen, Peng and Sapkota, Bishwa R and Shah, Nabi and Jabeen, Sehrish and Surendran, Praveen and Lu, Yingchang and Zhang, Weihua and Imran, Atif and Abbas, Shahid and Majeed, Faisal and Trindade, Kevin and Qamar, Nadeem and Mallick, Nadeem Hayyat and Yaqoob, Zia and Saghir, Tahir and Hasan Rizvi, Syed Nadeem and Memon, Anis and Rasheed, Syed Zahed and Memon, Fazal-Ur-Rehman and Mehmood, Khalid and Ahmed, Naveeduddin and Hussain Qureshi, Irshad and Tanveer-Us-Salam, Tanveer-Us-Salam and Iqbal, Wasim and Malik, Uzma and Mehra, Narinder and Kuo, Jane Z and Sheu, Wayne H.-H and Guo, Xiuqing and Hsiung, Chao A and Juang, Jyh-Ming J and Taylor, Kent D and Hung, Yi-Jen and Lee, Wen-Jane and Quertermous, Thomas and Lee, I-Te and Hsu, Chih-Cheng and Bottinger, Erwin P and Ralhan, Sarju and Teo, Yik Ying and Wang, Tzung-Dau and Alam, Dewan S and Di Angelantonio, Emanuele and Epstein, Steve and Nielsen, Sune F and Nordestgaard, Borge G and Tybjaerg-Hansen, Anne and Young, Robin and Benn, Marianne and Frikke-Schmidt, Ruth and Kamstrup, Pia R and Jukema, J. Wouter and Sattar, Naveed and Smit, Roelof and Chung, Ren-Hua and Liang, Kae-Woei and Anand, Sonia and Sanghera, Dharambir K and Ripatti, Samuli and Loos, Ruth J. F and Kooner, Jaspal S and Tai, E. Shyong and Rotter, Jerome I and Ida Chen, Yii-Der and Frossard, Philippe and Maeda, Shiro and Kadowaki, Takashi and Reilly, Muredach and Pare, Guillaume and Melander, Olle and Salomaa, Veikko and Rader, Daniel J and Danesh, John and Voight, Benjamin F and Saleheen, Danish and EPIC-CVD Consortium and CHD Exome Consortium and EPIC-Interact Consortium and Michigan Biobank and CHD Exome+ Consortium and Diabetes - Cardiovascular Disease and Diabetes - kardiovaskulär sjukdom and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Lund University and EpiHealth: Epidemiology for Health and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 10/2017, Volume 49, Issue 10, pp. 1450 - 1457
To evaluate the shared genetic etiology of type 2 diabetes (T2D) and coronary heart disease (CHD), we conducted a genome-wide, multi-ancestry study of genetic... 
METAANALYSIS | AP2 | VARIANTS | ACID-BINDING PROTEIN | GENETICS & HEREDITY | ATHEROSCLEROSIS | RISK | GENETIC ARCHITECTURE | MENDELIAN RANDOMIZATION | GENOME-WIDE ASSOCIATION | ARTERY-DISEASE | Diabetes Mellitus, Type 2 - genetics | Humans | Asian Continental Ancestry Group - genetics | Genetic Loci - genetics | Coronary Disease - epidemiology | Mutation, Missense | Molecular Targeted Therapy | Diabetes Mellitus, Type 2 - epidemiology | Diabetes Mellitus, Type 2 - etiology | HLA-DRB5 Chains - genetics | Metabolic Syndrome - epidemiology | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Comorbidity | Risk Factors | Coronary Disease - etiology | Europe - epidemiology | Asia - epidemiology | Metabolic Networks and Pathways - genetics | Coronary Disease - genetics | Metabolic Syndrome - genetics | Biomarkers | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 2 - drug therapy | Quantitative trait loci | Type 2 diabetes | Genetic variation | Genetic aspects | Health aspects | Coronary heart disease | Risk factors | Drugs | Diabetes mellitus | Cardiovascular disease | Triglycerides | Genomes | Genetic diversity | Adipocytes | Risk analysis | Fatty acids | Loci | Coronary artery disease | Meta-analysis | Proteins | Pathways | Etiology | Atherosclerosis | Gene loci | Histocompatibility antigen HLA | Diabetes | Cardiovascular diseases | Bioinformatics | Heart diseases | Index Medicus | Medical and Health Sciences | single nucleotide polymorphism | major clinical study | ischemic heart disease | Genetic Loci | HLA DRB5 gene | genetic risk | genetic predisposition | East Asian | Diabetes Mellitus, Type 2 | genetic susceptibility | metabolic syndrome X | Basic Medicine | gene | Europe | Caucasian | genetic variation | European Continental Ancestry Group | South Asian | European | non insulin dependent diabetes mellitus | Metabolic Networks and Pathways | HLA-DRB5 Chains | metabolism | molecularly targeted therapy | comparative study | HLA DRB5 antigen | CCDC92 gene | Medicin och hälsovetenskap | Article | fatty acid binding protein 4 | missense mutation | Medicinsk genetik | Medical Genetics | genetics | Coronary Disease | icosapentaenoic acid ethyl ester | priority journal | human | risk factor | genetic variability | gene locus | comorbidity | biological marker | controlled study | Asian continental ancestry group | Asia | genome-wide association study | Medicinska och farmaceutiska grundvetenskaper
Journal Article