X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (99) 99
humans (87) 87
female (50) 50
male (47) 47
genetics & heredity (43) 43
ophthalmology (36) 36
beer (29) 29
biochemistry (29) 29
chemistry (29) 29
enzymology (29) 29
genetic predisposition to disease (29) 29
metallurgy (29) 29
microbiology (29) 29
mutation or genetic engineering (29) 29
spirits (29) 29
vinegar (29) 29
wine (29) 29
genetics (27) 27
compositions thereof (26) 26
culture media (26) 26
microorganisms or enzymes (26) 26
propagating, preserving or maintaining microorganisms (26) 26
compositions or test papers therefor (25) 25
condition-responsive control in microbiological orenzymological processes (25) 25
measuring or testing processes involving enzymes, nucleicacids or microorganisms (25) 25
processes of preparing such compositions (25) 25
adult (24) 24
article (24) 24
macular degeneration (24) 24
middle aged (24) 24
genome-wide association study (23) 23
aged (22) 22
biochemistry & molecular biology (21) 21
eye diseases (21) 21
genomics (21) 21
myopia - genetics (21) 21
genotype (20) 20
macular degeneration - genetics (20) 20
myopia (20) 20
genetic linkage (19) 19
genome-wide association (19) 19
polymorphism, single nucleotide (19) 19
animals (18) 18
genomes (16) 16
agriculture (15) 15
animal husbandry (15) 15
care of birds, fishes, insects (15) 15
fishing (15) 15
forestry (15) 15
genetic aspects (15) 15
human necessities (15) 15
hunting (15) 15
new breeds of animals (15) 15
population (15) 15
rearing or breeding animals, not otherwise provided for (15) 15
trapping (15) 15
aged, 80 and over (14) 14
cataract - genetics (14) 14
chromosome mapping (14) 14
hygiene (14) 14
medical or veterinary science (14) 14
mutation (14) 14
preparations for medical, dental, or toilet purposes (14) 14
prevalence (14) 14
testing (14) 14
gene expression (13) 13
mice (13) 13
retina (13) 13
disease (12) 12
european continental ancestry group - genetics (12) 12
fermentation or enzyme-using processes to synthesise a desiredchemical compound or composition or to separate optical isomersfrom a racemic mixture (12) 12
genetic structures (12) 12
investigating or analysing materials by determining theirchemical or physical properties (12) 12
measuring (12) 12
physics (12) 12
refractive error (12) 12
risk factors (12) 12
analysis (11) 11
base sequence (11) 11
complement factor-h (11) 11
gene (11) 11
general tagging of cross-sectional technologies spanning over several sections of the ipc (11) 11
general tagging of new technological developments (11) 11
molecular sequence data (11) 11
refractive errors - genetics (11) 11
research (11) 11
specific therapeutic activity of chemical compounds ormedicinal preparations (11) 11
technical subjects covered by former us classification (11) 11
technical subjects covered by former uspc (11) 11
technical subjects covered by former uspc cross-reference art collections [xracs] and digests (11) 11
variants (11) 11
adolescent (10) 10
alleles (10) 10
genetic markers (10) 10
ocular refraction (10) 10
phenotype (10) 10
polymorphism, single nucleotide - genetics (10) 10
research article (10) 10
studies (10) 10
susceptibility (10) 10
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1284 - 1287
Genotype imputation is a key component of genetic association studies, where it increases power, facilitates meta-analysis, and aids interpretation of signals.... 
Haplotypes | Genome-Wide Association Study | Algorithms | Computer Simulation | Humans | Genotype | Internet | Studies | Genotype & phenotype | Accuracy | Researchers | Computer simulation | Software | Genomes | Methods | Index Medicus
Journal Article
by Verhoeven, Virginie J. M and Hysi, Pirro G and Wojciechowski, Robert and Fan, Qiao and Guggenheim, Jeremy A and Höhn, René and Macgregor, Stuart and Hewitt, Alex W and Nag, Abhishek and Cheng, Ching-Yu and Yonova-Doing, Ekaterina and Zhou, Xin and Ikram, M. Kamran and Buitendijk, Gabriëlle H. S and McMahon, George and Kemp, John P and Pourcain, Beate St and Simpson, Claire L and Mäkelä, Kari-Matti and Lehtimäki, Terho and Kähönen, Mika and Paterson, Anew D and Hosseini, S. Mohsen and Wong, Hoi Suen and Xu, Liang and Jonas, Jost B and Pärssinen, Olavi and Wedenoja, Juho and Yip, Shea Ping and Ho, Daniel W. H and Pang, Chi Pui and Chen, Li Jia and Burdon, Kathryn P and Craig, Jamie E and Klein, Barbara E. K and Klein, Ronald and Haller, Toomas and Metspalu, Anes and Khor, Chiea-Chuen and Tai, E.-Shyong and Aung, Tin and Vithana, Eranga and Tay, Wan-Ting and Barathi, Veluchamy A and Chen, Peng and Li, Ruoying and Liao, Jiemin and Zheng, Yingfeng and Ong, Rick T and Döring, Angela and Evans, David M and Timpson, Nicholas J and Verkerk, Annemieke J. M. H and Meitinger, Thomas and Raitakari, Olli and Hawthorne, Felicia and Spector, Tim D and Karssen, Lennart C and Pirastu, Mario and Murgia, Federico and Ang, Wei and Mishra, Aniket and Montgomery, Grant W and Pennell, Craig E and Cumberland, Phillippa M and Cotlarciuc, Ioana and Mitchell, Paul and Wang, Jie Jin and Schache, Maria and Janmahasathian, Sarayut and Igo, Robert P and Lass, Jonathan H and Chew, Emily and Iyengar, Sudha K and Gorgels, Theo G. M. F and Rudan, Igor and Hayward, Caroline and Wright, Alan F and Polasek, Ozren and Vatavuk, Zoran and Wilson, James F and Fleck, Brian and Zeller, Tanja and Mirshahi, Alireza and Müller, Christian and Uitterlinden, Ané G and Rivadeneira, Fernando and Vingerling, Johannes R and Hofman, Albert and Oostra, Ben A and Amin, Najaf and Bergen, Arthur A. B and teo, Yik-Ying and Rahi, Jugnoo S and Vitart, Veronique and Williams, Cathy and Baird, Paul N and Wong, Tien-Yin and Oexle, Konrad and Pfeiffer, Norbert and ... and Fuchs' Genetics Multi-Ctr Study Gr and Diabet Control Complications Trial and WTCCC2 and CREAM and Consortium for Refractive Error and Myopia (CREAM) and Fuchs' Genetics Multi-Center Study Group and Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and Wellcome Trust Case Control Consortium 2 (WTCCC2) and The Fuchs' Genetics Multi-Center Study Group and The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 3, pp. 314 - 318
Journal Article
by McCarthy, Shane and Das, Sayantan and Kretzschmar, Warren and Delaneau, Olivier and Wood, Anew R and Teumer, Alexander and Kang, Hyun Min and Fuchsberger, Christian and Danecek, Petr and Sharp, Kevin and Luo, Yang and Sidorel, Carlo and Kwong, Alan and Timpson, Nicholas and Koskinen, Seppo and Vrieze, Scott and Scott, Laura J and Zhang, He and Mahajan, Anubha and Veldink, Jan and Peters, Ulrike and Pato, Carlos and van Duijn, Cornelia M and Gillies, Christopher E and Gandin, Ilaria and Mezzavilla, Massimo and Gilly, Arthur and Cocca, Massimiliano and Traglia, Michela and Angius, Anea and Barrett, Jeffrey C and Boomsma, Dorrett and Branham, Kari and Breen, Gerome and Brummett, Chad M and Busonero, Fabio and Campbell, Harry and Chan, Anew and Che, Sai and Chew, Emily and Collins, Francis S and Corbin, Laura J and Smith, George Davey and Dedoussis, George and Dorr, Marcus and Farmaki, Aliki-Eleni and Ferrucci, Luigi and Forer, Lukas and Fraser, Ross M and Gabriel, Stacey and Levy, Shawn and Groop, Leif and Harrison, Tabitha and Hattersley, Anew and Holmen, Oddgeir L and Hveem, Kristian and Kretzler, Matthias and Lee, James C and McGue, Matt and Meitinger, Thomas and Melzer, David and Min, Josine L and Mohlke, Karen L and Vincent, John B and Nauck, Matthias and Nickerson, Deborah and Palotie, Aarno and Pato, Michele and Pirastu, Nicola and McInnis, Melvin and Richards, J. Brent and Sala, Cinzia and Salomaa, Veikko and Schlessinger, David and Schoenherr, Sebastian and Slagboom, P. Eline and Small, Kerrin and Spector, Timothy and Stambolian, Dwight and Tuke, Marcus and Tuomilehto, Jaakko and van den Berg, Leonard H and Van Rheenen, Wouter and Volker, Uwe and Wijmenga, Cisca and Toniolo, Daniela and Zeggini, Eleftheria and Gasparini, Paolo and Sampson, Matthew G and Wilson, James F and Frayling, Timothy and de Bakker, Paul I. W and Swertz, Morris A and McCarroll, Steven and Kooperberg, Charles and Dekker, Annelot and Altshuler, David and Willer, Cristen and Iacono, William and Ripatti, Samuli and ... and Haplotype Reference Consortium and the Haplotype Reference Consortium and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1279 - 1283
Journal Article
by Fritsche, Lars G and Igl, Wilmar and Bailey, Jessica N. Cooke and Grassmann, Felix and Sengupta, Sebanti and Bragg-Gresham, Jennifer L and Burdon, Kathryn and Hebbring, Scott J and Wen, Cindy and Gorski, Mathias and Kim, Ivana K and Cho, David and Zack, Donald and Souied, Eric and Scholl, Henik and Bala, Elisa and ELee, Kristine and Hunter, David J and Sardell, Rebecca J and Mitchell, Paul and Merriam, Joanna E and Cipriani, Francesco and Hoffman, Joshua D and Schick, Tina and Lechanteur, Yara T.E and Guymer, Robyn and Johnson, Matthew and Jiang, Yingda and Stanton, Chloe M and Buitendijk, Gabrielle and Zhan, Xiaowei and Kwong, Alan M and Boleda, Alexis and Brooks, Matthew and Gieser, Linn and Ratna Priya, Rinki and Branham, Kari E and Foerster, Johanna R and Heckenlively, John R and Othman, Mohammad I and Vote, Brendan J and Liang, Helena Hai and Souzeau, Emmanuelle and McAllister, Ian L and Isaacs, Timothy and Hall, Janette and Lake, Stewart and Mackey, David A and Constable, Ian J and Craig, Jamie E and Kitchner, Terrie E and Yang, Zhenglin and Su, Zhiguang and Luo, Hongrong and Chen, Daniel and Ouyang, Hong and Flagg, Ken and Lin, Danni and Mao, Guanping and Ferreyra, Henry and Stark, Klaus and Strachwitz, Claudia and Wolf, Armin and Brandl, Caroline and Rudolph, Guenther and Olden, Matthias and Morrison, Margaux A and Morgan, Denise and Schu, Matthew and Ahn, Jeeyun and Silvestri, Giuliana and ETsironi, Evangelia and Park, Kyu Hyung and Farrer, Lindsay and Orlin, Anton and Brucker, Alexander and Li, Mingyao and Curcio, Christine A and Mohand-Sa'd, Saddek and Sahel, José-Alain and Audo, Isabelle and Benchaboune, Mustapha and Cree, Angela and Rennie, Christina A and Goverdhan, Srinivas V and Grunin, Michelle and Hagbi-Levi, Shira and Campochiaro, Peter and Katsanis, Nicholas and Holz, Frank G and Blond, Frédéric and Blanché, Hél'ne and Deleuze, Jean-Fran'ois and Igo Jr., Robert and Truitt, Barbara and Peachey, Neal S and Meuer, Stacy M and Myers, Chelsea E and Moore, Emily L and Klein, Ronald and ...
Nature Genetics, ISSN 1061-4036, 02/2016, Volume 48, Issue 2, pp. 134 - 143
Journal Article
by Fritsche, Lars G and Chen, Wei and Schu, Matthew and Yaspan, Brian L and Yu, Yi and Thorleifsson, Gudmar and Zack, Donald J and Arakawa, Satoshi and Cipriani, Valentina and Ripke, Stephan and Igo, Robert P and Buitendijk, Gabriëlle H. S and Sim, Xueling and Weeks, Daniel E and Guymer, Robyn H and Merriam, Joanna E and Francis, Peter J and Hannum, Gregory and Agarwal, Anita and Armbrecht, Ana Maria and Audo, Isabelle and Aung, Tin and Barile, Gaetano R and Benchaboune, Mustapha and Bird, Alan C and Bishop, Paul N and Branham, Kari E and Brooks, Matthew and Brucker, Alexander J and Cade, William H and Cain, Melinda S and Campochiaro, Peter A and Chan, Chi-Chao and Cheng, Ching-Yu and Chew, Emily Y and Chin, Kimberly A and Chowers, Itay and Clayton, David G and Cojocaru, Radu and Conley, Yvette P and Cornes, Belinda K and Daly, Mark J and Dhillon, Baljean and Edwards, Albert O and Evangelou, Evangelos and Fagerness, Jesen and Ferreyra, Henry A and Friedman, James S and Geirsdottir, Asbjorg and George, Ronnie J and Gieger, Christian and Gupta, Neel and Hagstrom, Stephanie A and Harding, Simon P and Haritoglou, Christos and Heckenlively, John R and Holz, Frank G and Hughes, Guy and Ioannidis, John P. A and Ishibashi, Tatsuro and Joseph, Peronne and Jun, Gyungah and Kamatani, Yoichiro and Katsanis, Nicholas and N Keilhauer, Claudia and Khan, Jane C and Kim, Ivana K and Kiyohara, Yutaka and Klein, Barbara E. K and Klein, Ronald and Kovach, Jaclyn L and Kozak, Igor and Lee, Clara J and Lee, Kristine E and Lichtner, Peter and Lotery, Andrew J and Meitinger, Thomas and Mitchell, Paul and Mohand-Saïd, Saddek and Moore, Anthony T and Morgan, Denise J and Morrison, Margaux A and Myers, Chelsea E and Naj, Adam C and Nakamura, Yusuke and Okada, Yukinori and Orlin, Anton and Ortube, M Carolina and Othman, Mohammad I and Pappas, Chris and Park, Kyu Hyung and Pauer, Gayle J. T and Peachey, Neal S and Poch, Olivier and Priya, Rinki Ratna and Reynolds, Robyn and Richardson, Andrea J and Ripp, Raymond and Rudolph, Guenther and Ryu, Euijung and ... and AMD Gene Consortium and The AMD Gene Consortium
Nature Genetics, ISSN 1061-4036, 04/2013, Volume 45, Issue 4, pp. 433 - 439
Journal Article
by Cheng, Ching-Yu and Schache, Maria and Ikram, M. Kamran and Ikram, M. Kamran and Young, Terri L and Young, Terri L and Guggenheim, Jeremy A and Guggenheim, Jeremy A and Vitart, Veronique and MacGregor, Stuart and Verhoeven, Virginie J.M and Verhoeven, Virginie J.M and Barathi, Veluchamy A and Liao, Jiemin and Hysi, Pirro G and Hysi, Pirro G and Bailey-Wilson, Joan E and St. Pourcain, Beate and Kemp, John P and McMahon, George and Timpson, Nicholas J and Evans, David M and Montgomery, Grant W and Mishra, Aniket and Wang, Jie Jin and Wang, Jie Jin and Wang, Ya Xing and Rochtchina, Elena and Polasek, Ozren and Wright, Alan F and Wright, Alan F and Amin, Najaf and van Leeuwen, Elisabeth M and Wilson, James F and Wilson, James F and Wilson, Joan E. Bailey and Pennell, Craig E and van Duijn, Cornelia M and de Jong, Paulus T.V.M and Vingerling, Johannes R and Zhou, Xin and Zhou, Xiangtian and Chen, Peng and Chen, Li Jia and Chen, Wei and Li, Ruoying and Tay, Wan-Ting and Zheng, Yingfeng and Zheng, D and Chew, Merwyn and Chew, Emily Y and Chew, Emily and Rahi, Jugnoo S and Yoshimura, Nagahisa and Yamashiro, Kenji and Miyake, Masahiro and Delcourt, Cécile and Maubaret, Cecilia and Williams, T and Williams, Katie M and Williams, Cathy and Northstone, Kate and Ring, Susan M and Davey-Smith, George and Craig, Jamie E and Burdon, Kathryn P and Fogarty, Rhys D and Iyengar, Sudha K and Igo, Robert P and Janmahasathian, Sarayut and Stambolian, Dwight and Lu, Yi and Jonas, Jost B and Xu, Liang and Saw, Seang-Mei and Baird, Paul N and Mitchell, Paul and Nangia, Vinay and Hayward, Caroline and Campbell, C and Campbell, Harry and Rudan, Igor and Vatavuk, Zoran and Paterson, Andrew D and Hosseini, S. Mohsen and Fondran, Jeremy R and Feng, Sheng and Klaver, Caroline C and Klaver, Caroline C.W and van Duijn, Cornelia M and Metspalu, Andres and Haller, Toomas and Mihailov, Evelin and Pärssinen, Olavi and Wedenoja, Juho and Wojciechowski, Robert and Pfeiffer, Norbert and Höhn, René and Pang, Chi Pui and Meitinger, Thomas and ... and Consortium Refractive Error Myopia and Fuchs Genetics Multictr Study Grp and Diabet Control Complications Trial and Wellcome Trust Case Control Consor and Fuchs' Genetics Multi-Center Study Group and Consortium for Refractive Error and Myopia and Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group and Wellcome Trust Case Control Consortium 2
The American Journal of Human Genetics, ISSN 0002-9297, 08/2013, Volume 93, Issue 2, pp. 264 - 277
Journal Article