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humans (38) 38
index medicus (29) 29
arrangements or adaptations of heating, cooling, ventilating,or other air-treating devices specially for passenger or goodsspaces of vehicles (23) 23
performing operations (23) 23
transporting (23) 23
vehicles in general (23) 23
male (21) 21
research (20) 20
electricity (19) 19
polymorphism, single nucleotide (19) 19
female (18) 18
genetics & heredity (17) 17
basic electric elements (16) 16
genetics (16) 16
processes or means, e.g. batteries, for the direct conversionof chemical into electrical energy (16) 16
article (15) 15
genome, human (15) 15
climate change mitigation technologies related totransportation (14) 14
general tagging of cross-sectional technologies spanning over several sections of the ipc (14) 14
general tagging of new technological developments (14) 14
technical subjects covered by former uspc cross-reference art collections [xracs] and digests (14) 14
technologies or applications for mitigation or adaptation againstclimate change (14) 14
genetic variation (13) 13
genomics (13) 13
genotype (13) 13
genetic aspects (12) 12
human genome (12) 12
electric equipment or propulsion of electrically-propelledvehicles (11) 11
electrodynamic brake systems for vehicles, in general (11) 11
magnetic suspension or levitation for vehicles (11) 11
medical and health sciences (11) 11
medicin och hälsovetenskap (11) 11
genome-wide association (10) 10
genome-wide association study (10) 10
genomes (10) 10
multidisciplinary sciences (10) 10
mutation (10) 10
studies (10) 10
analysis (9) 9
obesity (9) 9
adult (8) 8
aged (8) 8
blasting (8) 8
disease (8) 8
genotype & phenotype (8) 8
heating (8) 8
lighting (8) 8
mechanical engineering (8) 8
population genetics (8) 8
risk (8) 8
risk factors (8) 8
weapons (8) 8
arrangement or mounting of plural diverse prime-movers invehicles (7) 7
arrangement or mounting of propulsion units or oftransmissions in vehicles (7) 7
arrangements in connection with cooling, air intake, gasexhaust or fuel supply of propulsion units, in vehicles (7) 7
auxiliary drives for vehicles (7) 7
genetics, population (7) 7
instrumentation or dashboards for vehicles (7) 7
polymorphism (7) 7
population (7) 7
algorithms (6) 6
alleles (6) 6
body mass index (6) 6
clinical medicine (6) 6
common variants (6) 6
gene expression (6) 6
gene frequency (6) 6
klinisk medicin (6) 6
methods (6) 6
middle aged (6) 6
polymorphism, single nucleotide - genetics (6) 6
variants (6) 6
animals (5) 5
biochemistry & molecular biology (5) 5
cell biology (5) 5
chromosome mapping (5) 5
combined heating and refrigeration systems (5) 5
conjoint control of vehicle sub-units of different type ordifferent function (5) 5
control systems specially adapted for hybrid vehicles (5) 5
endocrinology and diabetes (5) 5
endokrinologi och diabetes (5) 5
haplotypes - genetics (5) 5
heat pump systems (5) 5
liquefaction solidification of gases (5) 5
manufacture or storage of ice (5) 5
mathematics (5) 5
mice (5) 5
refrigeration or cooling (5) 5
road vehicle drive control systems for purposes not related tothe control of a particular sub-unit (5) 5
sequence analysis, dna (5) 5
single nucleotide polymorphisms (5) 5
aged, 80 and over (4) 4
brain (4) 4
continental population groups - genetics (4) 4
evolution (4) 4
evolution, molecular (4) 4
genealogy (4) 4
genetic research (4) 4
genome, human - genetics (4) 4
glucose-homeostasis (4) 4
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1. Full Text Mapping copy number variation by population-scale genome sequencing
by Mills, Ryan E and Walter, Klaudia and Stewart, Chip and Handsaker, Robert E and Chen, Ken and Alkan, Can and Abyzov, Alexej and Yoon, Seungtai Chris and Ye, Kai and Cheetham, R. Keira and Chinwalla, Asif and Conrad, Donald F and Fu, Yutao and Grubert, Fabian and Hajirasouliha, Iman and Hormozdiari, Fereydoun and Iakoucheva, Lilia M and Iqbal, Zamin and Kang, Shuli and Kidd, Jeffrey M and Konkel, Miriam K and Korn, Joshua and Khurana, Ekta and Kural, Deniz and Lam, Hugo Y. K and Leng, Jing and Li, Ruiqiang and Li, Yingrui and Lin, Chang-Yun and Luo, Ruibang and Mu, Xinmeng Jasmine and Nemesh, James and Peckham, Heather E and Rausch, Tobias and Scally, Aylwyn and Shi, Xinghua and Stromberg, Michael P and Sütz, Adrian M and Urban, Alexander Eckehart and Walker, Jerilyn A and Wu, Jiantao and Zhang, Yujun and Zhang, Zhengdong D and Batzer, Mark A and Ding, Li and Marth, Gabor T and McVean, Gil and Sebat, Jonathan and Snyder, Michael and Wang, Jun and Ye, Kenny and Eichler, Evan E and Gerstein, Mark B and Hurles, Matthew E and Lee, Charles and McCarroll, Steven A and Korbel, Jan O and Collins, Francis S and Altshuler, D.L and Durbin, R.M and Abecasis, G.R and Bentley, D.R and Chakravarti, A and Clark, A.G and De La Vega, F.M and Donnelly, P and Egholm, M and Flicek, P and Gabriel, S.B and Gibbs, R.A and Knoppers, B.M and Lander, E.S and Lehrach, H and Mardis, E.R and McVean, G.A and Nickerson, D.A and Peltonen, L and Schafer, A.J and Sherry, S.T and Wilson, R.K and Deiros, D and Metzker, M and Muzny, D and Reid, J and Wheeler, D and Li, J and Jian, M and Li, G and Liang, H and Tian, G and Wang, B and Wang, W and Yang, H and Zhang, X and Zheng, H and Ambrogio, L and Bloom, T and Cibulskis, K and Fennell, T.J and Jaffe, D.B and ... and 1000 Genomes Project
Nature, ISSN 0028-0836, 02/2011, Volume 470, Issue 7332, pp. 59 - 65
Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in extent, origin and functional impact. Despite progress in... 
SHORT-READ | MULTIDISCIPLINARY SCIENCES | SNPS | SEGMENTAL DUPLICATIONS | COMMON | POLYMORPHISM | REARRANGEMENTS | STRUCTURAL VARIATION | DELETIONS | INSERTIONS | Genetics, Population | Genetic Predisposition to Disease - genetics | Reproducibility of Results | Genomics | Humans | Gene Duplication - genetics | Genotype | DNA Copy Number Variations - genetics | Sequence Analysis, DNA | Genome, Human - genetics | Mutagenesis, Insertional - genetics | Sequence Deletion - genetics | Genotype & phenotype | Algorithms | Methods
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2. Full Text A global reference for human genetic variation
by Altshuler, D.M and Albers, C.A and Abecasis, G.R and et al and Genomes Project Consortium and 1000 Genomes Project Consortium and The 1000 Genomes Project Consortium
Nature, ISSN 0028-0836, 2015, Volume 526, Issue 7571, pp. 68 - 74
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set... 
BAYES FACTORS | INDIVIDUALS | COMPLEMENT FACTOR-H | POPULATION HISTORY | MULTIDISCIPLINARY SCIENCES | MUTATION | DISEASE | SUSCEPTIBILITY | MACULAR DEGENERATION | VARIANT | GENOME-WIDE ASSOCIATION | Rare Diseases - genetics | Genome-Wide Association Study | Datasets as Topic | Demography | Disease Susceptibility | Physical Chromosome Mapping | Humans | Genetics, Population - standards | Genomics - standards | Genotype | INDEL Mutation - genetics | Sequence Analysis, DNA | Genome, Human - genetics | Haplotypes - genetics | Exome - genetics | Reference Standards | Genetics, Medical | Internationality | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | High-Throughput Nucleotide Sequencing | Quantitative Trait Loci - genetics | Genetic research | Nucleotide sequencing | Observations | Genetic variation | Methods | DNA sequencing | Studies | Haplotypes | Genotype & phenotype | Accuracy | Genealogy | Population | Genomes | Genetic diversity | Mitochondrial DNA | Binding sites
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3. 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 | OBESITY | METAANALYSIS | FTO GENE | GLUCOSE | GENETICS & HEREDITY | EARLY-ONSET | GASTRIC-INHIBITORY POLYPEPTIDE | WEIGHT | 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 | Charitable foundations | Public health | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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4. Full Text An integrated map of genetic variation from 1,092 human genomes
by Altshuler, David M and Durbin, Richard M and Abecasis, Gonçalo R and Bentley, David R and Chakravarti, Aravinda and Clark, Andrew G and Donnelly, Peter and Eichler, Evan E and Flicek, Paul and Gabriel, Stacey B and Gibbs, Richard A and Green, Eric D and Hurles, Matthew E and Knoppers, Bartha M and Korbel, Jan O and Lander, Eric S and Lee, Charles and Lehrach, Hans and Mardis, Elaine R and Marth, Gabor T and McVean, Gil A and Nickerson, Deborah A and Schmidt, Jeanette P and Sherry, Stephen T and Wang, Jun and Wilson, Richard K and Dinh, Huyen and Kovar, Christie and Lee, Sandra and Lewis, Lora and Muzny, Donna and Reid, Jeff and Wang, Min and Fang, Xiaodong and Guo, Xiaosen and Jian, Min and Jiang, Hui and Jin, Xin and Li, Guoqing and Li, Jingxiang and Li, Yingrui and Li, Zhuo and Liu, Xiao and Lu, Yao and Ma, Xuedi and Su, Zhe and Tai, Shuaishuai and Tang, Meifang and Wang, Bo and Wang, Guangbiao and Wu, Honglong and Wu, Renhua and Yin, Ye and Zhang, Wenwei and Zhao, Jiao and Zhao, Meiru and Zheng, Xiaole and Zhou, Yan and Gupta, Namrata and Clarke, Laura and Leinonen, Rasko and Smith, Richard E and Zheng-Bradley, Xiangqun and Grocock, Russell and Humphray, Sean and James, Terena and Kingsbury, Zoya and Sudbrak, Ralf and Albrecht, Marcus W and Amstislavskiy, Vyacheslav S and Borodina, Tatiana A and Lienhard, Matthias and Mertes, Florian and Sultan, Marc and Timmermann, Bernd and Yaspo, Marie-Laure and Fulton, Lucinda and Fulton, Robert and Weinstock, George M and Balasubramaniam, Senduran and Burton, John and Danecek, Petr and Keane, Thomas M and Kolb-Kokocinski, Anja and McCarthy, Shane and Stalker, James and Quail, Michael and Davies, Christopher J and Gollub, Jeremy and Webster, Teresa and Wong, Brant and Zhan, Yiping and Auton, Adam and Yu, Fuli and Bainbridge, Matthew and Challis, Danny and Evani, Uday S and Lu, James and Nagaswamy, Uma and Sabo, Aniko and ... and 1000 Genomes Project Consortium and The 1000 Genomes Project Consortium
Nature, ISSN 0028-0836, 11/2012, Volume 491, Issue 7422, pp. 56 - 65
By characterizing the geographic and functional spectrum of human genetic variation, the 1000 Genomes Project aims to build a resource to help to understand... 
RARE | VARIANTS | MULTIDISCIPLINARY SCIENCES | MUTATION | POPULATION-STRUCTURE | RISK | LOCI | WIDE ASSOCIATION | COPY NUMBER VARIATION | Genetics, Population | Conserved Sequence - genetics | Genome-Wide Association Study | Genomics | Humans | Binding Sites - genetics | Continental Population Groups - genetics | Genome, Human - genetics | Transcription Factors - metabolism | Haplotypes - genetics | Genetics, Medical | Nucleotide Motifs | Alleles | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Evolution, Molecular | Sequence Deletion - genetics | Chromosome mapping | Human genome | Genetic variation | Identification and classification | Methods | Studies | Haplotypes | Accuracy | Algorithms | Genealogy | Genetics | Data processing | Principal components analysis | Statistical methods | Genomes | Genoma humà
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