X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (27) 27
index medicus (21) 21
female (13) 13
gene expression (13) 13
genetics & heredity (13) 13
male (13) 13
genomes (12) 12
middle aged (11) 11
dna methylation (9) 9
genomics (9) 9
genotype (9) 9
cohort studies (8) 8
article (7) 7
association (7) 7
expression (7) 7
genome-wide association study (7) 7
aged (6) 6
genetic aspects (6) 6
genetic variation (6) 6
multidisciplinary sciences (6) 6
osteoporosis (6) 6
population (6) 6
quantitative trait loci (6) 6
risk factors (6) 6
studies (6) 6
alleles (5) 5
biochemistry & molecular biology (5) 5
disease (5) 5
dna methylation - genetics (5) 5
fractures (5) 5
genetic predisposition to disease (5) 5
genome-wide association (5) 5
meta-analysis (5) 5
metaanalysis (5) 5
polymorphism, single nucleotide - genetics (5) 5
research (5) 5
risk (5) 5
variants (5) 5
analysis (4) 4
animals (4) 4
apoptosis (4) 4
blood (4) 4
body-mass index (4) 4
bone-mineral density (4) 4
deoxyribonucleic acid--dna (4) 4
endocrinology & metabolism (4) 4
european continental ancestry group - genetics (4) 4
fractures, bone - genetics (4) 4
gene expression profiling (4) 4
gene expression regulation (4) 4
gene-expression (4) 4
genes (4) 4
genetics (4) 4
linkage disequilibrium (4) 4
medical research (4) 4
methylation (4) 4
obesity (4) 4
phenotype (4) 4
polymorphism, single nucleotide (4) 4
transcription factors (4) 4
transcription factors - metabolism (4) 4
adult (3) 3
body mass index (3) 3
bone density (3) 3
bone density - genetics (3) 3
cell line, tumor (3) 3
dna (3) 3
dna-binding proteins - genetics (3) 3
gene (3) 3
genetic research (3) 3
genome, human (3) 3
genome-wide association study - methods (3) 3
loci (3) 3
medical and health sciences (3) 3
medicin och hälsovetenskap (3) 3
mendelian randomization (3) 3
methods (3) 3
mice (3) 3
mutation (3) 3
netherlands (3) 3
osteoporosis - genetics (3) 3
polymorphism (3) 3
prostatic neoplasms - metabolism (3) 3
proteins (3) 3
quantitative trait loci - genetics (3) 3
receptor (3) 3
science (3) 3
smoking (3) 3
transcriptome (3) 3
zinc-finger protein (3) 3
abridged index medicus (2) 2
activation (2) 2
adolescent (2) 2
age (2) 2
aged, 80 and over (2) 2
architecture (2) 2
arthritis (2) 2
binding sites (2) 2
biomedical research (2) 2
biophysics (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


P L o S Genetics (Print), ISSN 1553-7390, 04/2009, Volume 5, Issue 4, pp. e1000445 - e1000445
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 131 - 138
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 139 - 145
Journal Article
by Zheng, Hou-Feng and Forgetta, Vincenzo and Hsu, Yi-Hsiang and Estrada, Karol and Rosello-Diez, Alberto and Leo, Paul J and Dahia, Chitra L and Park-Min, Kyung Hyun and Tobias, Jonathan H and Kooperberg, Charles and Kleinman, Aaron and Styrkarsdottir, Unnur and Liu, Ching-Ti and Uggla, Charlotta and Evans, Daniel S and Nielson, Carrie M and Walter, Klaudia and Pettersson-Kymmer, Ulrika and Mccarthy, Shane and Eriksson, Joel and Kwan, Tony and Jhamai, Mila and Trajanoska, Katerina and Memari, Yasin and Min, Josine and Huang, Jie and Danecek, Petr and Wilmot, Beth and Li, Rui and Chou, Wen-Chi and Mokry, Lauren E and Moayyeri, Alireza and Claussnitzer, Melina and Cheng, Chia-Ho and Cheung, Warren and Medina-Gómez, Carolina and Ge, Bing and Chen, Shu-Huang and Choi, Kwangbom and Oei, Ling and Fraser, James and Kraaij, Robert and Hibbs, Matthew A and Gregson, Celia L and Paquette, Denis and Hofman, Albert and Wibom, Carl and Tranah, Gregory J and Marshall, Mhairi and Gardiner, Brooke B and Cremin, Katie and Auer, Paul and Hsu, Li and Ring, Sue and Tung, Joyce Y and Thorleifsson, Gudmar and Enneman, Anke W and van Schoor, Natasja M and de Groot, Lisette C. P. G. M and van der Velde, Nathalie and Melin, Beatrice and Kemp, John P and Christiansen, Claus and Sayers, Aian and Zhou, Yanhua and Calderari, Sophie and van Rooij, Jeroen and Carlson, Chris and Peters, Ulrike and Berlivet, Soizik and Dostie, Josée and Uitterlinden, Ane G and Williams, Stephen R and Farber, Charles and Grinberg, Daniel and LaCroix, Anea Z and Haessler, Jeff and Chasman, Daniel I and Giulianini, Franco and Rose, Lynda M and Ridker, Paul M and Eisman, John A and Nguyen, Tuan V and Center, Jacqueline R and Nogues, Xavier and Garcia-Giralt, Natalia and Launer, Lenore L and Gudnason, Vilmunder and Mellström, Dan and Vandenput, Liesbeth and Amin, Najaf and van Duijn, Cornelia M and Karlsson, Magnus K and Ljunggren, Östen and Svensson, Olle and Hallmans, Göran and Rousseau, François and Giroux, Sylvie and Bussière, Johanne and Arp, Pascal P and ... and AOGC Consortium and UK10K Consortium and Medicinska fakulteten and Institutionen för strålningsvetenskaper and Umeå universitet and Institutionen för folkhälsa och klinisk medicin and Institutionen för farmakologi och klinisk neurovetenskap and Farmakologi and Enheten för biobanksforskning and Näringsforskning and Institutionen för kirurgisk och perioperativ vetenskap
Nature, ISSN 0028-0836, 2015, Volume 526, Issue 7571, pp. 112 - +
The extent to which low-frequency (minor allele frequency (MAF) between 1-5%) and rare (MAF <= 1%) variants contribute to complex traits and disease in the... 
WIDE ASSOCIATION LOCI | MINERAL DENSITY | METAANALYSIS | VARIANTS | GENE | ENGRAILED-1 | MULTIDISCIPLINARY SCIENCES | MOUSE | HUMAN-DISEASES | COMPLEX TRAITS | OSTEOPOROSIS | European Continental Ancestry Group - genetics | Gene Frequency - genetics | Genetic Predisposition to Disease - genetics | Genomics | Humans | Genotype | Bone Density - genetics | Sequence Analysis, DNA | Europe - ethnology | Fractures, Bone - genetics | Genome, Human - genetics | Homeodomain Proteins - genetics | Exome - genetics | Animals | Wnt Proteins - genetics | Bone and Bones - metabolism | Female | Genetic Variation - genetics | Mice | Disease Models, Animal | Quantitative trait loci | Fractures | Bones | Genetic aspects | Nucleotide sequencing | Identification and classification | Density | Methods | DNA sequencing | Proteins | Studies | Osteoporosis | Ethnicity | Population | Bone density | Genomes | Neck | Meta-analysis | Malalties | Aspectes genètics | Ossos | Hälsovetenskaper | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Medical and Health Sciences | Medicin och hälsovetenskap | Public Health, Global Health, Social Medicine and Epidemiology | Health Sciences | HNE Voeding en Gezondheid in de Levenscyclus | Wereldvoeding | VLAG | Chair Nutrition and Health over the Lifecourse | Global Nutrition | HNE Nutrition and Health over the Lifecourse
Journal Article
by Peters, Marjolein and Joehanes, Roby and Pilling, Luke and Schurmann, Claudia and Conneely, Karen N and Powell, Joseph and Reinmaa, Eva and Sutphin, George L and Zhernakova, Alexana and Schramm, Katharina and Wilson, Yana A and Kobes, Sayuko and Tukiainen, Taru and Ramos, Yolande and Göring, Harald H and Fornage, Myriam and Liu, Yongmei and Gharib, Sina and Stranger, Barbara and Jager, Philip and Aviv, Abraham and Levy, Daniel and Murabito, Joanne and Munson, Peter J and Huan, Tianxiao and Hofman, Albert and Uitterlinden, Ané and Rivadeneira Ramirez, Fernando and van Rooij, Jeroen and Stolk, Lisette and Broer, Linda and Verbiest, Michael and Jhamai, Mila and Arp, Pascal and Metspalu, Anes and Tserel, Liina and Milani, Lili and Samani, Nilesh and Peterson, Pärt and Kasela, Silva and Codd, Veryan and Peters, Annette and Ward-Caviness, Cavin K and Herder, Christian and Waldenberger, Melanie and Roden, Michael and Singmann, Paula and Zeilinger, Sonja and Illig, Thomas and Homuth, Georg and Grabe, Hans Jörgen and Völzke, Henry and Steil, Leif and Kocher, Thomas and Murray, Anna and Melzer, David and Yaghootkar, Hanieh and Bandinelli, S and Moses, Eric and Kent, Jack and Curran, Joanne and Johnson, Matthew and Williams-Blangero, Sarah and Westra, Harm-Jan and McRae, Allan F and Smith, Jennifer A and Kardia, Sharon and Hovatta, Iiris and Perola, Markus and Ripatti, Samuli and Salomaa, Veikko and Henders, Anjali and Martin, Nicholas and Smith, Alicia K and Mehta, Divya and Binder, Elisabeth B and Nylocks, K. Maria and Kennedy, Elizabeth M and Klengel, Torsten and Ding, Jingzhong and Suchy-Dicey, Astrid and Enquobahrie, D and Brody, Jennifer and Rotter, Jerome I and Chen, Yii-Der I and Houwing-Duistermaat, Jeanine and Kloppenburg, Margreet and Slagboom, Eline and Helmer, Quinta and Hollander, Wouter and Bean, Shannon and Raj, Towfique and Bakhshi, Noman and Wang, Qiao Ping and Oyston, Lisa J and Psaty, Bruce and Tracy, Russell and Montgomery, Grant and Turner, Stephen and Blangero, John and ... and NABEC UKBEC Consortium and NABEC/UKBEC Consortium
Nature Communications, ISSN 2041-1723, 10/2015, Volume 6, Issue 1, p. 8570
textabstractDisease incidences increase with age, but the molecular characteristics of ageing that lead to increased disease susceptibility remain inadequately... 
LIFE-SPAN | OXIDATIVE STRESS | METHYLATION | PROFILES | GLYCOSAMINOGLYCANS | HUMAN LONGEVITY | DROSOPHILA-MELANOGASTER | MULTIDISCIPLINARY SCIENCES | PATTERNS | GENE-EXPRESSION CHANGES | GENOME-WIDE ASSOCIATION | Aging - blood | DNA Methylation | Humans | Transcriptome | European Continental Ancestry Group | Gene Expression Profiling | Biomarkers - blood
Journal Article
by Shvetsova, Ekaterina and Sofronova, Alina and Monajemi, Ramin and Gagalova, Kristina and Draisma, Harmen H. M and White, Stefan J and Santen, Gijs W. E and Chuva de Sousa Lopes, Susana M and Heijmans, Bastiaan T and van Meurs, Joyce and Jansen, Rick and Franke, Lude and Kiełbasa, Szymon M and den Dunnen, Johan T and ‘t Hoen, Peter A. C and Heijmans, Bastiaan T and ‘t Hoen, Peter A. C and van Meurs, Joyce and Boomsma, Dorret I and Pool, René and van Dongen, Jenny and Hottenga, Jouke J and van Greevenbroek, Marleen Mj and Stehouwer, Coen Da and van der Kallen, Carla Jh and Schalkwijk, Casper G and Wijmenga, Cisca and Zhernakova, Sasha and Tigchelaar, Ettje F and Slagboom, P Eline and Beekman, Marian and Deelen, Joris and van Heemst, Diana and Veldink, Jan H and van den Berg, Leonard H and van Duijn, Cornelia M and Hofman, Bert A and Uitterlinden, André G and Jhamai, P Mila and Verbiest, Michael and Suchiman, H Eka D and Verkerk, Marijn and van der Breggen, Ruud and van Rooij, Jeroen and Lakenberg, Nico and Mei, Hailiang and Bot, Jan and Zhernakova, Dasha V and van ’t Hof, Peter and Deelen, Patrick and Nooren, Irene and Moed, Matthijs and Vermaat, Martijn and Luijk, René and Jan Bonder, Marc and van Iterson, Maarten and van Dijk, Freerk and van Galen, Michiel and Arindrarto, Wibowo and Kiełbasa, Szymon M and Swertz, Morris A and van Zwet, Erik W and Isaacs, Aaron and Jansen, Rick and Franke, Lude and Francioli, Lc and Menelaou, A and Pulit, Sl and van Dijk, F and Palamara, Pf and Elbers, Cc and Neerincx, Pb and Ye, K and Guryev, V and Kloosterman, Wp and Deelen, P and Abdellaoui, A and van Leeuwen, Em and van Oven, M and Vermaat, M and Li, M and Laros, Jf and Karssen, Lc and Kanterakis, A and Amin, N and Hottenga, Jj and Lameijer, Ew and Kattenberg, M and Dijkstra, M and Byelas, H and van Setten, J and van Schaik, Bd and Bot, J and Nijman, Ij and Renkens, I and Marschall, T and Schönhuth, A and Hehir-Kwa, Jy and Handsaker, Re and Polak, P and ... and GoNL Consortium and BIOS Consortium and GoNL consortium and BIOS consortium
European Journal of Human Genetics, ISSN 1018-4813, 03/2019, Volume 27, Issue 3, pp. 455 - 465
X-inactivation is a well-established dosage compensation mechanism ensuring that X-chromosomal genes are expressed at comparable levels in males and females.... 
VARIABILITY | TRANSLOCATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | DMD LOCUS | GENETICS & HEREDITY | ADRENOLEUKODYSTROPHY | CONSEQUENCES | PATTERNS | DUCHENNE MUSCULAR-DYSTROPHY | CHROMOSOME-INACTIVATION | EXPRESSION | CARRIERS | Dosage compensation | Alleles | Population | Genomes | Negative selection | Females | Ribonucleic acid--RNA | Chromosomes | Embryos | Blood | Hemopoiesis
Journal Article
Genome Biology, ISSN 1474-7596, 01/2017, Volume 18, Issue 1, p. 19
Journal Article
by Porcu, E and Rueger, S and Lepik, K and Agbessi, M and Ahsan, H and Alves, I and Andiappan, A and Arindrarto, W and Awadalla, P and Battle, A and Beutner, F and Bonder, MJ and Boomsma, D and Christiansen, M and Claringbould, A and Deelen, P and Esko, T and Fave, MJ and Franke, L and Frayling, T and Gharib, SA and Gibson, G and Heijmans, BT and Hemani, G and Jansen, R and Kahonen, M and Kalnapenkis, A and Kasela, S and Kettunen, J and Kim, Y and Kirsten, H and Kovacs, P and Krohn, K and Kronberg-Guzman, J and Kukushkina, V and Lee, B and Lehtimaki, T and Loeffler, M and Marigorta, UM and Mei, HL and Milani, L and Montgomery, GW and Muller-Nurasyid, M and Nauck, M and Nivard, M and Penninx, B and Perola, M and Pervjakova, N and Pierce, BL and Powell, J and Prokisch, H and Psaty, BM and Raitakari, OT and Ripatti, S and Rotzschke, O and Saha, A and Scholz, M and Schramm, K and Seppala, I and Slagboom, EP and Stehouwer, CDA and Stumvoll, M and Sullivan, P and t Hoen, PAC and Teumer, A and Thiery, J and Tong, L and Tonjes, A and van Dongen, J and van Iterson, M and van Meurs, J and Veldink, JH and Verlouw, J and Visscher, PM and Volker, U and Vosa, U and Westra, HJ and Wijmenga, C and Yaghootkar, H and Yang, J and Zeng, B and Zhang, FT and Beekman, M and Boomsma, DI and Bot, J and Deelen, J and Hofman, BA and Hottenga, JJ and Isaacs, A and Jhamai, PM and Kielbasa, SM and Lakenberg, N and Luijk, R and Mei, H and Moed, M and Nooren, I and Pool, R and Schalkwijk, CG and Slagboom, PE and Suchiman, HED and ... and eQTLGen Consortium and BIOS Consortium
NATURE COMMUNICATIONS, ISSN 2041-1723, 07/2019, Volume 10, Issue 1, pp. 3300 - 12
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex traits, but their biological interpretation often remains... 
OBESITY | VARIANTS | STATISTICS | INSTRUMENTAL VARIABLES | MULTIDISCIPLINARY SCIENCES | DISEASE | MUTATION | PLEIOTROPY | ASSOCIATION | EXPRESSION | FAMILY | Quantitative trait loci | Pleiotropy | Randomization | Phenotypes | Encephalopathy | Genomes | Single-nucleotide polymorphism | Mutation | Gene expression | Statistics
Journal Article