Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (523) 523
Publication (97) 97
Book Review (14) 14
Conference Proceeding (11) 11
Book Chapter (5) 5
Book / eBook (2) 2
Data Set (1) 1
Magazine Article (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (294) 294
index medicus (275) 275
female (168) 168
male (159) 159
medical and health sciences (145) 145
medicin och hälsovetenskap (145) 145
genetics (137) 137
genetic aspects (131) 131
polymorphism, single nucleotide (128) 128
research (125) 125
diabetes mellitus, type 2 - genetics (124) 124
genetics & heredity (123) 123
genome-wide association study (109) 109
adult (107) 107
genome-wide association (103) 103
type 2 diabetes (99) 99
genotype (97) 97
genetic predisposition to disease (91) 91
genomes (91) 91
diabetes (87) 87
genetic variation (86) 86
risk factors (85) 85
middle aged (78) 78
body mass index (76) 76
article (71) 71
endocrinology & metabolism (70) 70
abridged index medicus (69) 69
studies (69) 69
aged (67) 67
clinical medicine (67) 67
endokrinologi och diabetes (67) 67
klinisk medicin (67) 67
endocrinology and diabetes (66) 66
risk (64) 64
alleles (61) 61
genomics (61) 61
obesity (61) 61
phenotype (52) 52
loci (51) 51
population (51) 51
polymorphism, single nucleotide - genetics (49) 49
case-control studies (48) 48
disease (48) 48
physiological aspects (48) 48
medical genetics (45) 45
meta-analysis (45) 45
obesity - genetics (44) 44
medicinsk genetik (42) 42
multidisciplinary sciences (42) 42
variants (41) 41
european continental ancestry group - genetics (40) 40
genetic predisposition to disease - genetics (40) 40
basic medicine (39) 39
association (38) 38
health aspects (38) 38
medicinska och farmaceutiska grundvetenskaper (38) 38
gene expression (37) 37
metaanalysis (37) 37
gene frequency (36) 36
genes (36) 36
medicine (34) 34
polymorphism (34) 34
single nucleotide polymorphisms (34) 34
epidemiology (33) 33
insulin-resistance (33) 33
analysis (31) 31
susceptibility loci (31) 31
united kingdom (31) 31
cohort studies (30) 30
gene loci (30) 30
medical research (30) 30
quantitative trait loci (30) 30
common variants (29) 29
genetic research (29) 29
biochemistry & molecular biology (28) 28
genome, human (28) 28
research article (28) 28
body-mass index (27) 27
expression (27) 27
body height - genetics (26) 26
genome-wide association studies (26) 26
linkage disequilibrium (26) 26
mellitus (26) 26
diabetes mellitus (25) 25
mutation (25) 25
diabetes mellitus, type 2 (24) 24
insulin resistance (24) 24
cardiovascular disease (23) 23
chromosome mapping (23) 23
insulin (22) 22
susceptibility (22) 22
biology (21) 21
genetic loci (21) 21
glucose (21) 21
haplotypes (21) 21
odds ratio (21) 21
proteins (21) 21
european continental ancestry group (20) 20
transcription factors - genetics (20) 20
aged, 80 and over (19) 19
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


1. Full Text Hundreds of variants clustered in genomic loci and biological pathways affect human height
by Allen, H.L and Estrada Gil, Karol and Lettre, Guillaume and Berndt, Sonja and Rivadeneira Ramirez, Fernando and Willer, Cristen and Jackson, Anne and Vedantam, Sailaja and Raychaudhuri, Soumya and Ferreira, Teresa and Wood, Anew and Weyant, Robert and Segrè, Ayellet and Speliotes, Elizabeth and Wheeler, Eleanor and Soranzo, Nicole and Park, J.H and Yang, Joanna and Gudbjartsson, Daniel and Heard-Costa, Nancy and Randall, Joshua and Qi, Lu and Smith, Albert Vernon and Mägi, Reedik and Pastinen, Tomi and Liang, Liming and Heid, Iris and Luan, J and Thorleifsson, Gudmar and Winkler, Thomas and Goddard, Michael and Lo, K.S and Palmer, Cameron and Workalemahu, Tsegaselassie and Aulchenko, Yurii and Johansson, Åsa and Zillikens, Carola and Feitosa, Mary Furlan and Esko, Tõnu and Johnson, Toby and Ketkar, Shamika and Kraft, Peter and Mangino, Massimo and Prokopenko, Inga and Absher, Devin and Albrecht, Eva and Ernst, Florian and Glazer, Nicole and Hayward, Caroline and Hottenga, Jouke Jan and Jacobs, Kevin and Knowles, Joshua and Kutalik, Zoltán and Monda, Keri and Polasek, Ozren and Preuss, Michael and Rayner, Nigel William and Robertson, Neil and Steinthorsdottir, Valgerdur and Tyrer, Jonathan and Voight, Benjamin and Wiklund, Freik and Xu, Jianfeng and Zhao, Jing Hua and Nyholt, Dale and Pellikka, Niina and Perola, Markus and Perry, John and Surakka, Ida and Tammesoo, M.L and Altmaier, Elizabeth and Amin, Najaf and Aspelund, Thor and Bhangale, Tushar and Boucher, Gabrielle and Chasman, Daniel and Chen, Constance and Coin, Lachlan and Cooper, Matthew and Dixon, Anna and Gibson, Quince and Grundberg, Elin and Hao, Ke and Junttila, Juhani and Kaplan, Robert and Kettunen, Johannes and König, Inke and Kwan, Tony and Lawrence, Robert and Levinson, Douglas and Lorentzon, Mattias and McKnight, Barbara and Morris, Anew and Müller, Martina and Ngwa, J.S and Purcell, Shaun and Rafelt, Suzanne and Salem, Rany and Salvi, Erika and Sanna, Serena and ... and Procardis Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature: international weekly journal of science, ISSN 0028-0836, 10/2010, Volume 467, Issue 7317, pp. 832 - 838
textabstractMost common human traits and diseases have a polygenic pattern of inheritance: DNA sequence variants at many genetic loci influence the phenotype.... 
COMMON VARIANTS | POPULATION | DISEASES | WIDE ASSOCIATION ANALYSIS | MULTIDISCIPLINARY SCIENCES | GROWTH | SNPS | TRAITS | HERITABILITY | ADULT | STRATIFICATION | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Metabolic Networks and Pathways - genetics | Phenotype | Humans | Genetic Loci - genetics | Polymorphism, Single Nucleotide - genetics | Body Height - genetics | Chromosomes, Human, Pair 3 - genetics | Genome, Human - genetics | Confidence intervals | Genetics | Independent sample | Meta-analysis | Index Medicus | Life Sciences | Naturvetenskap | Natural Sciences | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts
by Vimaleswaran, K.S and Berry, D.J and Lu, C and Tikkanen, E and Pilz, S and Hiraki, L.T and Cooper, J.D and Dastani, Z and Li, R and Houston, D.K and Wood, A.R and Michaelsson, K and Vandenput, L and Zgaga, L and Yerges-Armstrong, L.M and McCarthy, M.I and Dupuis, J and Kaakinen, M and Kleber, M.E and Jameson, K and Arden, N and Raitakari, O and Viikari, J and Lohman, K.K and Ferrucci, L and Melhus, H and Ingelsson, E and Byberg, L and Lind, L and Lorentzon, M and Salomaa, V and Campbell, H and Dunlop, M and Mitchell, B.D and Herzig, K.H and Pouta, A and Hartikainen, A.L and Streeten, E.A and Theodoratou, E and Jula, A and Wareham, N.J and Ohlsson, C and Frayling, T.M and Kritchevsky, S.B and Spector, T.D and Richards, J.B and Lehtimaki, T and Ouwehand, W.H and Kraft, P and Cooper, C and Marz, W and Power, C and Loos, R.J and Wang, T.J and Jarvelin, M.R and Whittaker, J.C and Hingorani, A.D and Hypponen, E and Kiemeney, L.A.L.M and Genetic Invest Anthropometric Trai and Genetic Investigation of Anthropometric Traits-GIANT Consortium and the Genetic Investigation of Anthropometric Traits (GIANT) consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Institutionen för kirurgiska vetenskaper and Klinisk farmakogenomik och osteoporos
PLoS Medicine, ISSN 1549-1277, 2013, Volume 10, Issue 2, pp. e1001383 - e1001383
BACKGROUND: Obesity is associated with vitamin D deficiency, and both are areas of active public health concern. We explored the causality and direction of the... 
CARDIOVASCULAR-DISEASE RISK | MEDICINE, GENERAL & INTERNAL | COMMON OBESITY | INSTRUMENTAL VARIABLES | D DEFICIENCY | 25-HYDROXYVITAMIN D | BODY-MASS INDEX | GENETIC-VARIANTS | D INSUFFICIENCY | PREVALENCE | GENOME-WIDE ASSOCIATION | Multivariate Analysis | Humans | Middle Aged | Male | North America | Obesity - genetics | Mendelian Randomization Analysis | Aged, 80 and over | Adult | Female | Obesity - diagnosis | Body Mass Index | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Vitamin D Deficiency - genetics | Risk Assessment | Europe | Risk Factors | Obesity - ethnology | Linear Models | Biomarkers - blood | Evidence-Based Medicine | Vitamin D - blood | Vitamin D Deficiency - ethnology | Vitamin D Deficiency - prevention & control | Phenotype | Vitamin D Deficiency - diagnosis | Obesity - therapy | Vitamin D - analogs & derivatives | Aged | Polymorphism, Single Nucleotide | Obesity | Vitamin D | Physiological aspects | Calcifediol | Social medicine | Alfacalcidol | Research | Health aspects | Studies | Body mass index | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text The genetic architecture of type 2 diabetes
by Fuchsberger, Christian and Flannick, Jason and Teslovich, Tanya M and Mahajan, Anubha and Agarwala, Vineeta and Gaulton, Kyle J and Ma, Clement and Fontanillas, Pierre and Moutsianas, Loukas and McCarthy, Davis J and Rivas, Manuel A and Perry, John R. B and Sim, Xueling and Blackwell, Thomas W and Robertson, Neil R and Rayner, N. William and Cingolani, Pablo and Locke, Adam E and Fernandez Tajes, Juan and Highland, Heather M and Dupuis, Josee and Chines, Peter S and Lindgren, Cecilia M and Hartl, Christopher and Jackson, Anne U and Chen, Han and Huyghe, Jeroen R and van de Bunt, Martijn and Pearson, Richard D and Kumar, Ashish and Müller-Nurasyid, Martina and Grarup, Niels and Stringham, Heather M and Gamazon, Eric R and Lee, Jaehoon and Chen, Yuhui and Scott, Robert A and Below, Jennifer E and Chen, Peng and Huang, Jinyan and Go, Min Jin and Stitzel, Michael L and Pasko, Dorota and Parker, Stephen C. J and Varga, Tibor V and Green, Todd and Beer, Nicola L and Day-Williams, Aaron G and Ferreira, Teresa and Fingerlin, Tasha and Horikoshi, Momoko and Hu, Cheng and Huh, Iksoo and Ikram, Mohammad Kamran and Kim, Bong-Jo and Kim, Yongkang and Kim, Young Jin and Kwon, Min-Seok and Lee, Juyoung and Lee, Selyeong and Lin, Keng-Han and Maxwell, Taylor J and Nagai, Yoshihiko and Wang, Xu and Welch, Ryan P and Yoon, Joon and Zhang, Weihua and Barzilai, Nir and Voight, Benjamin F and Han, Bok-Ghee and Jenkinson, Christopher P and Kuulasmaa, Teemu and Kuusisto, Johanna and Manning, Alisa and Ng, Maggie C. Y and Palmer, Nicholette D and Balkau, Beverley and Stancáková, Alena and Abboud, Hanna E and Boeing, Heiner and Gieaitis, Vilmantas and Prabhakaran, Dorairaj and Gottesman, Omri and Scott, James and Carey, Jason and Kwan, Phoenix and Grant, George and Smith, Joshua D and Neale, Benjamin M and Purcell, Shaun and Butterworth, Adam S and Howson, Joanna M. M and Lee, Heung Man and Lu, Yingchang and Kwak, Soo-Heon and Zhao, Wei and Danesh, John and Lam, Vincent K. L and Park, Kyong Soo and Saleheen, Danish and ... and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Allmänmedicin and Umeå universitet and Medicin
Nature, ISSN 0028-0836, 2016, Volume 536, Issue 7614, pp. 41 - +
The genetic architecture of common traits, including the number, frequency, and effect sizes of inherited variants that contribute to individual risk, has been... 
Exome | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Sample Size | DNA Mutational Analysis | Diabetes Mellitus, Type 2 - genetics | Humans | Alleles | Genetic Variation - genetics | Genotyping Techniques | Europe - ethnology | Type 2 diabetes | Genomic structural variations | Nucleotide sequencing | Research | Analysis | DNA sequencing | Studies | Genetics | Genomes | Diabetes | Health risk assessment | Genes | Index Medicus | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
by Speliotes, Elizabeth and Willer, Cristen and Berndt, Sonja and Monda, Keri and Thorleifsson, Gudmar and Jackson, Anne and Allen, H.L and Lindgren, Cecilia and Luan, J and Mägi, Reedik and Randall, Joshua and Vedantam, Sailaja and Winkler, Thomas and Qi, Lu and Workalemahu, Tsegaselassie and Heid, Iris and Steinthorsdottir, Valgerdur and Stringham, Heather and Wheeler, Eleanor and Wood, Anew and Ferreira, Teresa and Weyant, Robert and Segrè, Ayellet and Eestrada, Karol and Liang, Liming and Nemesh, James and Park, J.H and Gustafsson, Stefan and Kilpeläinen, Tuomas and Yang, Joanna and Bouatia-Naji, Nabila and Eesko, Tõnu and Feitosa, Mary Furlan and Kutalik, Zoltán and Mangino, Massimo and Raychaudhuri, Soumya and Scherag, Ane and Smith, Albert Vernon and Welch, Ryan and Zhao, Jing Hua and Aben, Katja and Absher, Devin and Amin, Najaf and Dixon, Anna and Fisher, Eeva and Glazer, Nicole and Goddard, Michael and Heard-Costa, Nancy and Hoesel, Volker and Hottenga, Jouke Jan and Johansson, Åsa and Johnson, Toby and Ketkar, Shamika and Lamina, Claudia and Li, Shengxu and Moffatt, Miriam and Myers, Richard and Narisu, Narisu and Perry, John and Peters, Marjolein and Preuss, Michael and Ripatti, Samuli and Rivadeneira Ramirez, Fernando and Sandholt, Camilla and Scott, Laura and Timpson, Nicholas and Tyrer, Jonathan and Wingerden, Sophie and White, Charles and Wiklund, Freik and Barlassina, Christina and Chasman, Daniel and Cooper, Matthew and Jansson, J.O and Lawrence, Robert and Pellikka, Niina and Prokopenko, Inga and Shi, Jianxin and Thiering, Eelisabeth and Alavere, Helene and Alibrandi, Maria and Almgren, Peter and Arnold, Alice and Aspelund, Thor and Atwood, Larry and Balkau, Beverley and Balmforth, Anthony and Bennett, Amanda and Ben-Shlomo, Y and Bergman, Richard and Bergmann, Sven and Biebermann, Heike and Blakemore, Alexana and Boes, Tanja and Bonnycastle, Lori and Bornstein, Stefan and Brown, Morris and Buchanan, Thomas and Busonero, F and Campbell, Harry and ... and MAGIC and Procardis Consortium and on behalf of Procardis Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 11/2010, Volume 42, Issue 11, pp. 937 - 948
textabstractObesity is globaLy prevalent and highly heritable, but its underlying genetic factors remain largely elusive. To identify genetic loci for obesity... 
COMMON VARIANTS | GLUCOSE-HOMEOSTASIS | FTO GENE | GENETICS & HEREDITY | EARLY-ONSET | MELANOCORTIN-4 RECEPTOR GENE | RISK | GASTRIC-INHIBITORY POLYPEPTIDE | ADULT OBESITY | FAT MASS | GENOME-WIDE ASSOCIATION | Body Mass Index | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Humans | Body Size - genetics | Chromosome Mapping | Polymorphism, Single Nucleotide | Body Weight - genetics | Obesity - genetics | Body Height - genetics | Measurement | Body mass index | Obesity | Genetic aspects | Research | Risk factors | Studies | Medical research | Hospitals | Biomedical research | Councils | Risk assessment | Genetics | Society | Charitable foundations | Public health | Index Medicus | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
by Dupuis, Josée and Langenberg, Claudia and Prokopenko, Inga and Saxena, Richa and Soranzo, Nicole and Jackson, Anne and Wheeler, Eleanor and Glazer, Nicole and Bouatia-Naji, Nabila and Gloyn, Anna and Lindgren, Cecilia and Mägi, Reedik and Morris, Anew and Randall, Joshua and Johnson, Toby and Elliott, Paul and Rybin, Denis and Thorleifsson, Gudmar and Steinthorsdottir, Valgerdur and Henneman, Peter and Grallert, Harald and Dehghan, Abbas and JanHottenga, Jouke and Franklin, Christopher and Navarro, Pau and Song, Kijoung and Goel, Anuj and Perry, John and Egan, Josephine and Lajunen, Taina and Grarup, Niels and Sparsø, Thomas and Doney, Alex and Voight, Benjamin and Stringham, Heather and Li, Man and Kanoni, Stavroula and Shrader, Peter and Cavalcanti-Proença, Christine and Kumari, Meena and Qi, Lu and Timpson, Nicholas and Gieger, Christian and Zabena, Carina and Rocheleau, Ghislain and Ingelsson, Erik and An, Ping and O´Connell, J.R and Luan, J and McCarroll, Steven and Payne, Felicity and Roccasecca, R.M and Pattou, François and Sethupathy, Praveen and Ardlie, Kristin and Ariyurek, Yavuz and Balkau, Beverley and Barter, Phil and Beilby, John and Ben-Shlomo, Y and Benediktsson, Rafn and Bennett, Amanda and Bergmann, Sven and Bochud, Murielle and Boerwinkle, Eric and Bonnefond, Amélie and Bonnycastle, Lori and Borch-Johnsen, K and Böttcher, Yvonne and Brunner, Eric and Bumpstead, Suzannah and Charpentier, Guillaume and IdaChen, Yii and Chines, Peter and Clarke, R and McOin, Lachlan and Cooper, Matthew and Cornelis, Marilyn and Crawford, Gabe and Crisponi, Laura and Day, Ian and Geus, Eco and Delplanque, Jerome and Dina, Christian and Erdos, Michael and Fedson, Annette and Fischer-Rosinsky, Antje and Forouhi, Nita and Fox, Caroline and Frants, Rune and GraziaFranzosi, Maria and Galan, Pilar and Goodarzi, Mark and Graessler, Jürgen and Groves, Christopher and Grundy, Scott and Gwilliam, Rhian and Gyllensten, Ulf and Hadjadj, Samy and Hallmans, Göran and ... and DIAGRAM Consortium and Global BPgen Consortium and Anders Hamsten Procardis Consortiu and GIANT Consortium and MAGIC Investigators and Anders Hamsten on behalf of Procardis Consortium and MAGIC investigators and the MAGIC investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Allmänmedicin and Näringsforskning and Umeå universitet and Medicin
Nature Genetics, ISSN 1061-4036, 02/2010, Volume 42, Issue 2, pp. 105 - 116
textabstractLevels of circulating glucose are tightly regulated. To identify new loci influencing glycemic traits, we performed meta-analyses of 21 genome-wide... 
CIRCADIAN CLOCK | DISEASE RISK | TRIGLYCERIDE LEVELS | INSULIN-RESISTANCE | GENETICS & HEREDITY | BETA-CELL DYSFUNCTION | PLASMA-GLUCOSE | MODEL ASSESSMENT | FOLLOW-UP | GENOME-WIDE ASSOCIATION | ESSENTIAL COMPONENTS | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Reproducibility of Results | Quantitative Trait, Heritable | Diabetes Mellitus, Type 2 - genetics | Humans | Gene Expression Regulation | Genetic Loci - genetics | Databases, Genetic | DNA Copy Number Variations - genetics | Fasting - blood | Adolescent | Alleles | Polymorphism, Single Nucleotide - genetics | Adult | Blood Glucose - genetics | Blood Glucose - metabolism | Child | Homeostasis - genetics | Quantitative Trait Loci - genetics | Type 2 diabetes | Homeostasis | Physiological aspects | Genetic aspects | Research | Insulin | Health aspects | Risk factors | Studies | Hyperglycemia | Diabetes | Sample size | Meta-analysis | Index Medicus | Clinical Medicine | Medical and Health Sciences | Endokrinologi och diabetes | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights