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2003, Methods in molecular biology, ISBN 9780896039681, Volume 212., xi, 269
Single nucleotide polymorphisms (SNPs) have become the markers of choice in elucidating the relationship between DNA sequence variation and susceptibility to... 
Chromosome polymorphism | Genetic markers | Variation | Human genetics | Laboratory manuals | Human Genetics | Biomedicine
Book
Environmental Health Perspectives, ISSN 0091-6765, 2/2011, Volume 119, Issue 2, pp. 182 - 188
Journal Article
Occupational and Environmental Medicine, ISSN 1351-0711, 01/2017, Volume 74, Issue 1, pp. 30 - 38
Journal Article
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, ISSN 1383-5718, 03/2019, Volume 839, pp. 13 - 20
Journal Article
by Ménard, Sandie and Ménard, Didier and Khim, Nimol and Beghain, Johann and Adegnika, Ayola A and Shafiul-Alam, Mohammad and Amodu, Olukemi and Rahim-Awab, Ghulam and Barnadas, Céline and Berry, Antoine and Boum, Yap and Bustos, Maria D and Cao, Jun and Chen, Jun-Hu and Collet, Louis and Cui, Liwang and Thakur, Garib-Das and Dieye, Alioune and Djallé, Djibrine and Dorkenoo, Monique A and Eboumbou-Moukoko, Carole E and Espino, Fe-Esperanza-Caridad J and Fandeur, Thierry and Ferreira-da-Cruz, Maria-Fatima and Fola, Abebe A and Fuehrer, Hans-Peter and Hassan, Abdillahi M and Herrera, Socrates and Hongvanthong, Bouasy and Houzé, Sandrine and Ibrahim, Maman L and Jahirul-Karim, Mohammad and Jiang, Lubin and Kano, Shigeyuki and Ali-Khan, Wasif and Khanthavong, Maniphone and Kremsner, Peter G and Lacerda, Marcus and Leang, Rithea and Leelawong, Mindy and Li, Mei and Lin, Khin and Mazarati, Jean-Baptiste and Morlais, Isabelle and Muhindo-Mavoko, Hypolite and Musset, Lise and Na-Bangchang, Kesara and Nambozi, Michael and Niaré, Karamoko and Noedl, Harald and Ouédraogo, Jean-Bosco and Pillai, Dylan R and Pradines, Bruno and Quang-Phuc, Bui and Ramharter, Michael and Randrianarivelojosia, Milijaona and Sattabongkot, Jetsumon and Sheikh-Omar, Abdiqani and Silué, Kigbafori D and Sirima, Sodiomon B and Sutherland, Colin and Syafruddin, Din and Tahar, Rachida and Tang, Lin-Hua and Touré, Offianan A and Tshibangu-wa-Tshibangu, Patrick and Vigan-Womas, Inès and Warsame, Marian and Wini, Lyndes and Zakeri, Sedigheh and Kim, Saorin and Eam, Rotha and Berne, Laura and Khean, Chanra and Chy, Sophy and Ken, Malen and Loch, Kaknika and Canier, Lydie and Duru, Valentine and Legrand, Eric and Barale, Jean-Christophe and Stokes, Barbara and Straimer, Judith and Witkowski, Benoit and Fidock, David A and Rogier, Christophe and Ringwald, Pascal and Ariey, Frederic and Mercereau-Puijalon, Odile and KARMA Consortium
The New England Journal of Medicine, ISSN 0028-4793, 06/2016, Volume 374, Issue 25, pp. 2453 - 2464
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, pp. e64683 - e64683
DNA sequence variation within human leukocyte antigen (HLA) genes mediate susceptibility to a wide range of human diseases. The complex genetic structure of... 
CLASSICAL HLA ALLELES | EXTENDED HUMAN MHC | DISEASE ASSOCIATION | GENOTYPE IMPUTATION | MULTIDISCIPLINARY SCIENCES | COMMON DISEASES | SUSCEPTIBILITY | MAJOR HISTOCOMPATIBILITY COMPLEX | HAPLOTYPE | INFERENCE | GENOME-WIDE ASSOCIATION | Haplotypes | Genetic Predisposition to Disease | Genome-Wide Association Study | HapMap Project | Humans | Amino Acids - immunology | Histocompatibility Antigens Class I - immunology | Diabetes Mellitus, Type 1 - genetics | HLA Antigens - immunology | European Continental Ancestry Group | Chromosome Mapping | Histocompatibility Antigens Class I - genetics | HLA Antigens - genetics | Amino Acids - genetics | Linkage Disequilibrium | Histocompatibility Antigens Class II - immunology | Alleles | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 1 - immunology | Histocompatibility Antigens Class II - genetics | Diabetes Mellitus, Type 1 - ethnology | Histocompatibility antigens | Type 1 diabetes | HLA histocompatibility antigens | Amino acids | Disease susceptibility | Genetic aspects | Nucleotide sequencing | Genetic polymorphisms | DNA sequencing | DQA1 protein | Genes | Linkage disequilibrium | Genomes | Single-nucleotide polymorphism | Density | Population genetics | Medical schools | Consortia | Proteins | Drb1 protein | Genetics | Chromosomes | Deoxyribonucleic acid--DNA | Antigens | Nucleotide sequence | Genetic structure | Diabetes mellitus | Rheumatology | Amino acid sequence | Loci | Medicine | Studies | White blood cells | Hospitals | DNA microarrays | Major histocompatibility complex | Acids | Genotyping | Womens health | Computer applications | Histocompatibility antigen HLA | Diabetes | Gene mapping | Histocompatibility | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
Journal of Atherosclerosis and Thrombosis, ISSN 1340-3478, 2011, Volume 18, Issue 1, pp. 56 - 64
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2016, Volume 48, Issue 4, pp. 367 - 373
Journal Article