X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (198) 198
Publication (42) 42
Conference Proceeding (3) 3
Book Review (2) 2
Book / eBook (1) 1
Book Chapter (1) 1
Dissertation (1) 1
Patent (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (100) 100
index medicus (86) 86
medical and health sciences (84) 84
medicin och hälsovetenskap (84) 84
female (54) 54
male (54) 54
genome-wide association study (44) 44
clinical medicine (42) 42
klinisk medicin (42) 42
polymorphism, single nucleotide (40) 40
genetics (37) 37
genetics & heredity (37) 37
risk factors (37) 37
research (36) 36
diabetes (35) 35
genetic predisposition to disease (35) 35
middle aged (35) 35
diabetes mellitus, type 2 - genetics (33) 33
endokrinologi och diabetes (33) 33
endocrinology and diabetes (32) 32
genetic aspects (31) 31
genomes (30) 30
studies (29) 29
article (28) 28
medical genetics (28) 28
aged (27) 27
genome-wide association (27) 27
genotype (27) 27
type 2 diabetes (27) 27
adult (26) 26
medicinsk genetik (26) 26
basic medicine (23) 23
medicinska och farmaceutiska grundvetenskaper (23) 23
meta-analysis (22) 22
case-control studies (21) 21
polymorphism, single nucleotide - genetics (20) 20
abridged index medicus (19) 19
cohort studies (19) 19
risk (19) 19
genetic variation (18) 18
loci (17) 17
alleles (16) 16
body mass index (15) 15
disease (15) 15
genomics (15) 15
metaanalysis (15) 15
multidisciplinary sciences (15) 15
cardiovascular disease (14) 14
diabetes mellitus, type 2 (14) 14
expression (14) 14
genes (14) 14
genetic loci (13) 13
genetic research (13) 13
health aspects (13) 13
hypertension (13) 13
medical research (13) 13
medicine (13) 13
obesity (13) 13
variants (13) 13
cardiac and cardiovascular systems (12) 12
diabetes mellitus (12) 12
european continental ancestry group - genetics (12) 12
genealogy (12) 12
internal medicine (12) 12
kardiologi (12) 12
pharmacogenetics (12) 12
physiological aspects (12) 12
association (11) 11
cardiac & cardiovascular systems (11) 11
common variants (11) 11
dk/atira/pure/subjectarea/asjc/1300/1311 (11) 11
endocrinology & metabolism (11) 11
gene expression (11) 11
gene frequency (11) 11
mortality (11) 11
population (11) 11
blood pressure (10) 10
genetic predisposition to disease - genetics (10) 10
meta-analysis as topic (10) 10
quantitative trait loci (10) 10
susceptibility loci (10) 10
atherosclerosis (9) 9
biomedical research (9) 9
cardiovascular diseases (9) 9
cholesterol (9) 9
drug therapy (9) 9
genome, human (9) 9
glucose (9) 9
insulin (9) 9
metabolic disorders (9) 9
aged, 80 and over (8) 8
analysis (8) 8
coronary artery disease - genetics (8) 8
diabetes mellitus, type 2 - blood (8) 8
epidemiology (8) 8
european continental ancestry group (8) 8
genome-wide association study - methods (8) 8
insulin-resistance (8) 8
lipoproteins (8) 8
metabolism (8) 8
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Shungin, Dmitry and Winkler, Thomas W and Croteau-Chonka, Damien C and Ferreira, Teresa and Locke, Adam E and Mägi, Reedik and Strawbridge, Rona J and Pers, Tune H and Fischer, Krista and Justice, Anne E and Workalemahu, Tsegaselassie and Wu, Joseph M. W and Buchkovich, Martin L and Heard-Costa, Nancy L and Roman, Tamara S and ng, Alexander W and Song, Ci and Gustafsson, Stefan and Day, Felix R and Esko, Tonu and Fall, Tove and Kutalik, Zoltán and Luan, Jian'an and Randall, Joshua C and Scherag, Ané and Vedantam, Sailaja and Wood, Anew R and Chen, Jin and Fehrmann, Rudolf and Karjalainen, Juha and Kahali, Bratati and Liu, Ching-Ti and Schmidt, Ellen M and Absher, Devin and Amin, Najaf and Anderson, Denise and Beekman, Marian and Bragg-Gresham, Jennifer L and Buyske, Steven and Demirkan, Ayse and Ehret, Georg B and Feitosa, Mary F and Goel, Anuj and Jackson, Anne U and Johnson, Toby and Kleber, Marcus E and Kristiansson, Kati and Mangino, Massimo and Mateo Leach, Irene and Medina-Gomez, Carolina and Palmer, Cameron D and Pasko, Dorota and Pechlivanis, Sonali and Peters, Marjolein J and Prokopenko, Inga and Stančáková, Alena and Ju Sung, Yun and Tanaka, Toshiko and Teumer, Alexander and van Vliet-Ostaptchouk, Jana V and Yengo, Loïc and Zhang, Weihua and Albrecht, Eva and Ärnlöv, Johan and Arscott, Gillian M and Bandinelli, Stefania and Barrett, Amy and Bellis, Claire and Bennett, Amanda J and Berne, Christian and Blüher, Matthias and Böhringer, Stefan and Bonnet, Fabrice and Böttcher, Yvonne and Bruinenberg, Marcel and Carba, Delia B and Caspersen, Ida H and Clarke, Robert and Daw, E. Warwick and Deelen, Joris and Deelman, Ewa and Delgado, Graciela and Doney, Alex S. F and Eklund, Niina and Erdos, Michael R and Estrada, Karol and Eury, Elodie and Frieich, Nele and Garcia, Melissa E and Gieaitis, Vilmantas and Gigante, Bruna and Go, Alan S and Golay, Alain and Grallert, Harald and Grammer, Tanja B and Gräßler, Jürgen and Grewal, Jagvir and Groves, Christopher J and Haller, Toomas and Hallmans, Goran and ... and PAGE Consortium and LifeLines Cohort Study and CARDIOGRAMplusC4D Consortium and MuTHER Consortium and ICBP and ADIPOGEN Consortium and CKDGen Consortium and GEFOS Consortium and Int Endogene Consortium and GENIE Consortium and MAGIC Investigators and ReproGen Consortium and GLGC and ADIPOGen Consortium and International Endogene Consortium and The PAGE Consortium and The International Endogene Consortium and The MAGIC Investigators and The ReproGen Consortium and The CKDGen Consortium and The ADIPOGen Consortium and The ICBP and The CARDIOGRAMplusC4D Consortium and The GENIE Consortium and The GLGC and The GEFOS Consortium and The MuTHER Consortium and The LifeLines Cohort Study and Högskolan Dalarna and Akademin Utbildning, hälsa och samhälle and Medicinsk vetenskap
Nature, ISSN 0028-0836, 2015, Volume 518, Issue 7538, pp. 187 - U378
Body fat distribution is a heritable trait and a well-established predictor of adverse metabolic outcomes, independent of overall adiposity. To increase our... 
HUMAN HEIGHT | ABDOMINAL ADIPOSITY | MULTIDISCIPLINARY SCIENCES | COMMON SNPS | SUSCEPTIBILITY LOCI | GLYCEMIC TRAITS | FALSE DISCOVERY | MESENCHYMAL STEM-CELLS | GENOME-WIDE ASSOCIATION | ADIPOGENIC DIFFERENTIATION | SEXUAL-DIMORPHISM | Body Mass Index | Genome-Wide Association Study | Age Factors | Neovascularization, Physiologic - genetics | Epigenesis, Genetic | Humans | Male | Continental Population Groups - genetics | Sex Characteristics | Obesity - genetics | Europe - ethnology | Genome, Human - genetics | Adipose Tissue - metabolism | Insulin - metabolism | Models, Biological | Adipocytes - metabolism | Insulin Resistance - genetics | Polymorphism, Single Nucleotide - genetics | Female | Body Fat Distribution | Transcription, Genetic - genetics | Adipogenesis - genetics | Waist-Hip Ratio | Quantitative Trait Loci - genetics | Adipose tissues | Quantitative trait loci | Genetic research | Genetic aspects | Research | Metabolism | Health aspects | Studies | Body mass index | Genealogy | Body fat | Insulin resistance | Genetics | Genomes | Abdomen | Meta-analysis | Index Medicus | Life Sciences | Adipocytes/metabolism Adipogenesis/genetics Adipose Tissue/metabolism Age Factors Body Fat Distribution Body Mass Index Continental Population Groups/genetics Epigenesis, Genetic Europe/ethnology Female Genome, Human/genetics Genome-Wide Association Study Humans Insulin/metabolism Insulin Resistance/genetics Male Models, Biological Neovascularization, Physiologic/genetics Obesity/genetics Polymorphism, Single Nucleotide/genetics Quantitative Trait Loci/genetics Sex Characteristics Transcription, Genetic/genetics Waist-Hip Ratio | Clinical Medicine | Hälsa och välfärd | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Health and Welfare
Journal Article
by Dastani, Zari and Hivert, Marie-France and Timpson, Nicholas and Perry, John R. B and Yuan, Xin and Scott, Robert A and Henneman, Peter and Heid, Iris M and Kizer, Jorge R and Lyytikäinen, Leo-Pekka and Fuchsberger, Christian and Tanaka, Toshiko and Morris, Anew P and Small, Kerrin and Isaacs, Aaron and Beekman, Marian and Coassin, Stefan and Lohman, Kurt and Qi, Lu and Kanoni, Stavroula and Pankow, James S and Uh, Hae-Won and Wu, Ying and Bidulescu, Aurelian and Rasmussen-Torvik, Laura J and Greenwood, Celia M. T and Ladouceur, Martin and Grimsby, Jonna and Manning, Alisa K and Liu, Ching-Ti and Kooner, Jaspal and Mooser, Vincent E and Vollenweider, Peter and Kapur, Karen A and Chambers, John and Wareham, Nicholas J and Langenberg, Claudia and Frants, Rune and Willems-Vandijk, Ko and Oostra, Ben A and Willems, Sara M and Lamina, Claudia and Winkler, Thomas W and Psaty, Bruce M and Tracy, Russell P and Brody, Jennifer and Chen, Ida and Viikari, Jorma and Kähönen, Mika and Pramstaller, Peter P and Evans, David M and St Pourcain, Beate and Sattar, Naveed and Wood, Anew R and Bandinelli, Stefania and Carlson, Olga D and Egan, Josephine M and Böhringer, Stefan and van Heemst, Diana and Kedenko, Lyudmyla and Kristiansson, Kati and Nuotio, Marja-Liisa and Loo, Britt-Marie and Harris, Tamara and Garcia, Melissa and Kanaya, Alka and Haun, Margot and Klopp, Norman and Wichmann, H.-Erich and Deloukas, Panos and Katsareli, Efi and Couper, David J and Duncan, Bruce B and Kloppenburg, Margreet and Adair, Linda S and Borja, Judith B and Wilson, James G and Musani, Solomon and Guo, Xiuqing and Johnson, Toby and Semple, Robert and Teslovich, Tanya M and Allison, Matthew A and Redline, Susan and Buxbaum, Sarah G and Mohlke, Karen L and Meulenbelt, Ingrid and Ballantyne, Christie M and Dedoussis, George V and Hu, Frank B and Liu, Yongmei and Paulweber, Bernhard and Spector, Timothy D and Slagboom, P. Eline and Ferrucci, Luigi and Jula, Antti and Perola, Markus and Raitakari, Olli and Florez, Jose C and Salomaa, Veikko and ... and GLGC Investigators and DIAGRAM Consortium and MAGIC Consortium and MuTHER Consortium and Global B Pgen Consortium and MAGIC investigators and Procardis Consortium and DIAGRAM+ Consortium and GLGC Consortium and GIANT Consortium
PLoS genetics, ISSN 1553-7390, 2012, Volume 8, Issue 3, pp. e1002607 - e1002607
Journal Article
by Webb, Thomas R., PhD|Erdmann, Jeanette, PhD|Stirrups, Kathleen E., PhD|Stitziel, Nathan O., MD, PhD|Masca, Nicholas G.D., PhD|Jansen, Henning, MD|Kanoni, Stavroula, PhD|Nelson, Christopher P., PhD|Ferrario, Paola G., PhD|König, Inke R., PhD|Eicher, John D., PhD|Johnson, Andrew D., PhD|Hamby, Stephen E., PhD|Betsholtz, Christer, PhD|Ruusalepp, Arno, MD, PhD|Franzén, Oscar, PhD|Schadt, Eric E., MD, PhD|Björkegren, Johan L.M., MD, PhD|Weeke, Peter E., MD, PhD|Auer, Paul L., PhD|Schick, Ursula M., PhD|Lu, Yingchang, MD, PhD|Zhang, He, PhD|Dube, Marie-Pierre, PhD|Goel, Anuj, MSc|Farrall, Martin, MD|Peloso, Gina M., PhD|Won, Hong-Hee, PhD|Do, Ron, PhD|van Iperen, Erik, MSc|Kruppa, Jochen, PhD|Mahajan, Anubha, PhD|Scott, Robert A., PhD|Willenborg, Christina, PhD|Braund, Peter S., PhD|van Capelleveen, Julian C., MD|Doney, Alex S.F., MD, PhD|Donnelly, Louise A., PhD|Asselta, Rosanna, PhD|Merlini, Pier A., MD|Duga, Stefano, PhD|Marziliano, Nicola, PhD|Denny, Josh C., MD, MS|Shaffer, Christian, BS|El-Mokhtari, Nour Eddine, MD|Franke, Andre, PhD|Heilmann, Stefanie, PhD|Hengstenberg, Christian, MD|Hoffmann, Per, PhD|Holmen, Oddgeir L., MD|Hveem, Kristian, MD, PhD|Jansson, Jan-Håkan, MD, PhD|Jöckel, Karl-Heinz, PhD|Kessler, Thorsten, MD|Kriebel, Jennifer, PhD|Laugwitz, Karl L., MD|Marouli, Eirini, MSc|Martinelli, Nicola, MD, PhD|McCarthy, Mark I., MD|Van Zuydam, Natalie R., PhD|Meisinger, Christa, MD, MPH|Esko, Tõnu, PhD|Mihailov, Evelin, MSc|Escher, Stefan A., PhD|Alver, Maris, MSc|Moebus, Susanne, PhD|Morris, Andrew D., MD|Virtamo, Jarma, MD, PhD|Nikpay, Majid, PhD|Olivieri, Oliviero, MD|Provost, Sylvie, MSc|AlQarawi, Alaa, BSc|Robertson, Neil R., MSc|Akinsansya, Karen O., PhD|Reilly, Dermot F., PhD|Vogt, Thomas F., PhD|Yin, Wu, PhD|Asselbergs, Folkert W., MD, PhD|Kooperberg, Charles, PhD|Jackson, Rebecca D., MD|Stahl, Eli, PhD|Müller-Nurasyid, Martina, PhD|Strauch, Konstantin, PhD|Varga, Tibor V., PhD|Waldenberger, Melanie, PhD|Zeng, Lingyao, MSc|Chowdhury, Rajiv, MD, PhD|Salomaa, Veikko, MD, PhD|Ford, Ian, PhD|Jukema, J. Wouter, MD, PhD|Amouyel, Philippe, MD, PhD|Kontto, Jukka, MSSc|Nordestgaard, Børge G., MD, DMSc|Ferrières, Jean, MD|Saleheen, Danish, MBBS, PhD|Sattar, Naveed, PhD|Surendran, Praveen, PhD|Wagner, Aline, MD, PhD|Young, Robin, PhD|Howson, Joanna M.M., PhD|Butterworth, Adam S., PhD|Danesh, John, DPhil|Ardissino, Diego, MD|Bottinger, Erwin P., MD|Erbel, Raimund, MD|Franks, Paul W., PhD|Girelli, Domenico, MD, PhD|Hall, Alistair S., MD, PhD|Hovingh, G. Kees, MD, PhD|Kastrati, Adnan, MD|Lieb, Wolfgang, MD, MSc|Meitinger, Thomas, MD|Kraus, William E., MD|Shah, Svati H., MD, MPH|McPherson, Ruth, MD, PhD|Orho-Melander, Marju, PhD|Melander, Olle, MD, PhD|Metspalu, Andres, MD, PhD|Palmer, Colin N.A., PhD|Peters, Annette, PhD|Rader, Daniel J., MD|Reilly, Muredach P., MB, BCh, MSCE|Loos, Ruth J.F., PhD|Reiner, Alex P., MD, MSc|Roden, Dan M., MD|Tardif, Jean-Claude, MD|Thompson, John R., PhD|Wareham, Nicholas J., MB, BS, PhD|Watkins, Hugh, MD, PhD|Willer, Cristen J., PhD|Samani, Nilesh J., MD|Schunkert, Heribert, MD|Deloukas, Panos, PhD|Kathiresan, Sekar, MD and Wellcome Trust Case Control and MORGAM Investigators and Myocardial Infarction Genetics and Wellcome Trust Case Control Consortium and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
Journal of the American College of Cardiology, ISSN 0735-1097, 2017, Volume 69, Issue 7, pp. 823 - 836
Abstract Background Genome-wide association studies have so far identified 56 loci associated with risk of coronary artery disease (CAD). Many CAD loci show... 
Cardiovascular | Internal Medicine | expression quantitative trait loci | genetics | genome-wide association | single nucleotide polymorphism | cholesteryl ester transfer protein | COMMON VARIANTS | SR-BI | CARDIAC & CARDIOVASCULAR SYSTEMS | CETP MASS | RISK | PHOSPHOLIPASE A | HEART-DISEASE | SCAVENGER RECEPTOR | ABDOMINAL AORTIC-ANEURYSM | DENSITY-LIPOPROTEIN RECEPTOR | Genome-Wide Association Study | Gene Frequency | Humans | Coronary Artery Disease - genetics | Female | Male | Coronary Artery Disease - epidemiology | Genetic Pleiotropy | Polymorphism, Single Nucleotide | Genetic Loci | Odds Ratio | Case-Control Studies | Coronary heart disease | Analysis | Genealogy | Cardiovascular disease | Genomes | Metabolism | Gene expression | Blood | Risk factors | Studies | Celiac disease | Lipoproteins | Coronary vessels | Rheumatoid arthritis | Quality control | Calcification | Diabetes | Bioinformatics | Index Medicus | Abridged Index Medicus | LD, linkage disequilibrium | CETP, cholesteryl ester transfer protein | eQTL, expression quantitative trait locus | CAD, coronary artery disease | GWAS, genome-wide association study | BMI, body mass index | SNP, single nucleotide polymorphism | HDL, high-density lipoprotein | LDL, low-density lipoprotein | Original Investigation | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Kardiologi | Medical Genetics | Medicinsk genetik | Clinical Medicine | Cardiac and Cardiovascular Systems | Medicinska och farmaceutiska grundvetenskaper
Journal Article
by Mahajan, Anubha and Go, Min Jin and Zhang, Weihua and Below, Jennifer E and Gaulton, Kyle J and Ferreira, Teresa and Horikoshi, Momoko and Johnson, Anew D and Ng, Maggie C. Y and Prokopenko, Inga and Saleheen, Danish and Wang, Xu and Zeggini, Eleftheria and Abecasis, Goncalo R and Adair, Linda S and Almgren, Peter and Atalay, Mustafa and Aung, Tin and Baldassarre, Damiano and Balkau, Beverley and Bao, Yuqian and Barnett, Anthony H and Barroso, Ines and Basit, Abdul and Been, Latonya F and Beilby, John and Bell, Graeme I and Benediktsson, Rafn and Bergman, Richard N and Boehm, Bernhard O and Boerwinkle, Eric and Bonnycastle, Lori L and Burtt, Noël and Cai, Qiuyin and Campbell, Harry and Carey, Jason and Cauchi, Stephane and Caulfield, Mark and Chan, Juliana C. N and Chang, Li-Ching and Chang, Tien-Jyun and Chang, Yi-Cheng and Charpentier, Guillaume and Chen, Chien-Hsiun and Chen, Han and Chen, Yuan-Tsong and Chia, Kee-Seng and Chidambaram, Manickam and Chines, Peter S and Cho, Nam H and Cho, Young Min and Chuang, Lee-Ming and Collins, Francis S and Cornelis, Marilyn C and Couper, David J and Crenshaw, Anew T and van Dam, Rob M and Danesh, John and Das, Debashish and de Faire, Ulf and Dedoussis, George and Deloukas, Panos and Dimas, Antigone S and Dina, Christian and Doney, Alex S. F and Donnelly, Peter J and Dorkhan, Mozhgan and van Duijn, Cornelia and Dupuis, Josée and Edkins, Sarah and Elliott, Paul and Emilsson, Valur and Erbel, Raimund and Eriksson, Johan G and Escobedo, Jorge and Esko, Tonu and Eury, Elodie and Florez, Jose C and Fontanillas, Pierre and Forouhi, Nita G and Forsen, Tom and Fox, Caroline and Fraser, Ross M and Frayling, Timothy M and Froguel, Philippe and Frossard, Philippe and Gao, Yutang and Gertow, Karl and Gieger, Christian and Gigante, Bruna and Grallert, Harald and Grant, George B and Groop, Leif C and Groves, Christopher J and Grundberg, Elin and Guiducci, Candace and Hamsten, Anders and Han, Bok-Ghee and Hara, Kazuo and Hassanali, Neelam and ... and South Asian Type Diabet SAT2D Cons and DIAbet Genetics Replication & Meta and Mexican Amer Type 2 Diabet MAT2D C and Asian Genetic Epidemiology Network and Type 2 Diabet Genetic Exploration and South Asian Type 2 Diabetes (SAT2D) Consortium and Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and Type 2 Diabetes Genetic Exploration by Nex-generation sequencing in muylti-Ethnic Samples (T2D-GENES) Consortium and DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Mexican American Type 2 Diabetes (MAT2D) Consortium and Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples (T2D-GENES) Consortium and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 3, pp. 234 - 244
Journal Article