X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (5885) 5885
Publication (1126) 1126
Book Review (234) 234
Conference Proceeding (32) 32
Newspaper Article (32) 32
Book Chapter (26) 26
Newsletter (20) 20
Dissertation (7) 7
Book / eBook (2) 2
Data Set (1) 1
Magazine Article (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (5034) 5034
humans (3831) 3831
genotype (3790) 3790
female (2383) 2383
polymorphism, single nucleotide (2361) 2361
male (2209) 2209
genetics & heredity (2092) 2092
genomes (2085) 2085
genetics (2011) 2011
genetic aspects (1948) 1948
genomics (1853) 1853
genome-wide association study (1623) 1623
research (1616) 1616
genome-wide association (1592) 1592
genotype & phenotype (1285) 1285
middle aged (1250) 1250
analysis (1220) 1220
studies (1192) 1192
adult (1144) 1144
genes (1121) 1121
article (1105) 1105
phenotype (1102) 1102
genetic predisposition to disease (1063) 1063
risk factors (1037) 1037
single nucleotide polymorphisms (1030) 1030
alleles (1023) 1023
population (1009) 1009
genotypes (998) 998
single-nucleotide polymorphism (995) 995
research article (991) 991
haplotypes (950) 950
aged (910) 910
quantitative trait loci (854) 854
linkage disequilibrium (852) 852
animals (845) 845
risk (831) 831
polymorphism, single nucleotide - genetics (810) 810
genetic variation (794) 794
multidisciplinary sciences (775) 775
disease (731) 731
medicine (711) 711
association (709) 709
gene frequency (700) 700
loci (693) 693
models, genetic (692) 692
case-control studies (688) 688
genetic research (684) 684
gene expression (671) 671
polymorphism (631) 631
science (588) 588
algorithms (579) 579
genotype imputation (577) 577
population genetics (572) 572
variants (557) 557
health aspects (546) 546
genome-wide association studies (534) 534
epidemiology (510) 510
physiological aspects (472) 472
imputation (467) 467
breeding (460) 460
chromosomes (460) 460
metaanalysis (456) 456
biology (454) 454
methods (441) 441
genome-wide association study - methods (439) 439
usage (439) 439
young adult (438) 438
mutation (427) 427
life sciences (426) 426
adolescent (425) 425
agriculture, dairy & animal science (423) 423
genetic association studies (423) 423
cohort studies (419) 419
medical research (415) 415
expression (412) 412
accuracy (410) 410
human genetics (397) 397
genetic predisposition to disease - genetics (388) 388
chromosome mapping (383) 383
psychiatry (379) 379
software (377) 377
cancer (375) 375
genotyping (372) 372
biotechnology & applied microbiology (366) 366
genetic diversity (364) 364
gene (362) 362
biochemistry & molecular biology (361) 361
genetic markers (360) 360
computer simulation (359) 359
computational biology (357) 357
susceptibility (353) 353
bioinformatics (350) 350
selection (349) 349
cattle (347) 347
neurosciences (344) 344
heritability (339) 339
aged, 80 and over (336) 336
european continental ancestry group - genetics (335) 335
pedigree (334) 334
biology and life sciences (330) 330
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


Bioinformatics, ISSN 1367-4803, 03/2015, Volume 31, Issue 5, pp. 782 - 784
Journal Article
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
The American Journal of Human Genetics, ISSN 0002-9297, 01/2016, Volume 98, Issue 1, pp. 116 - 126
We present a genotype imputation method that scales to millions of reference samples. The imputation method, based on the Li and Stephens model and implemented... 
INDIVIDUALS | IDENTITY | GENETIC-VARIATION | HAPLOTYPE MAP | SEQUENCE DATA | GENETICS & HEREDITY | DESCENT | GENOME-WIDE ASSOCIATION | Databases, Genetic | Genotype | Reference Standards | Observations | Genotype & phenotype | Genomes | Simulation | Memory | Index Medicus
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
Journal Article
Journal Article