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1. 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 (London), ISSN 0028-0836, 2015, Volume 526, Issue 7571, pp. 68 - 74
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | 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 | Index Medicus
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2. Full Text The genetic architecture of type 2 diabetes
by Fuchsberger, Christian and Flannick, Jason and Teslovich, Tanya M and Mahajan, Anubha and Agarwala, Vineeta and Gaulton, Kyle J and Ma, Clement and Fontanillas, Pierre and Moutsianas, Loukas and McCarthy, Davis J and Rivas, Manuel A and Perry, John R. B and Sim, Xueling and Blackwell, Thomas W and Robertson, Neil R and Rayner, N. William and Cingolani, Pablo and Locke, Adam E and Fernandez Tajes, Juan and Highland, Heather M and Dupuis, Josee and Chines, Peter S and Lindgren, Cecilia M and Hartl, Christopher and Jackson, Anne U and Chen, Han and Huyghe, Jeroen R and van de Bunt, Martijn and Pearson, Richard D and Kumar, Ashish and Müller-Nurasyid, Martina and Grarup, Niels and Stringham, Heather M and Gamazon, Eric R and Lee, Jaehoon and Chen, Yuhui and Scott, Robert A and Below, Jennifer E and Chen, Peng and Huang, Jinyan and Go, Min Jin and Stitzel, Michael L and Pasko, Dorota and Parker, Stephen C. J and Varga, Tibor V and Green, Todd and Beer, Nicola L and Day-Williams, Aaron G and Ferreira, Teresa and Fingerlin, Tasha and Horikoshi, Momoko and Hu, Cheng and Huh, Iksoo and Ikram, Mohammad Kamran and Kim, Bong-Jo and Kim, Yongkang and Kim, Young Jin and Kwon, Min-Seok and Lee, Juyoung and Lee, Selyeong and Lin, Keng-Han and Maxwell, Taylor J and Nagai, Yoshihiko and Wang, Xu and Welch, Ryan P and Yoon, Joon and Zhang, Weihua and Barzilai, Nir and Voight, Benjamin F and Han, Bok-Ghee and Jenkinson, Christopher P and Kuulasmaa, Teemu and Kuusisto, Johanna and Manning, Alisa and Ng, Maggie C. Y and Palmer, Nicholette D and Balkau, Beverley and Stancáková, Alena and Abboud, Hanna E and Boeing, Heiner and Gieaitis, Vilmantas and Prabhakaran, Dorairaj and Gottesman, Omri and Scott, James and Carey, Jason and Kwan, Phoenix and Grant, George and Smith, Joshua D and Neale, Benjamin M and Purcell, Shaun and Butterworth, Adam S and Howson, Joanna M. M and Lee, Heung Man and Lu, Yingchang and Kwak, Soo-Heon and Zhao, Wei and Danesh, John and Lam, Vincent K. L and Park, Kyong Soo and Saleheen, Danish and ... and GoT2D Consortium and T2D-Genes Consortium
Nature (London), ISSN 0028-0836, 2016, Volume 536, Issue 7614, pp. 41 - +
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Exome | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Sample Size | DNA Mutational Analysis | Diabetes Mellitus, Type 2 - genetics | Humans | Alleles | Genetic Variation - genetics | Genotyping Techniques | Europe - ethnology | Type 2 diabetes | Genomic structural variations | Nucleotide sequencing | Research | Analysis | DNA sequencing | Studies | Genetics | Genomes | Diabetes | Health risk assessment | Genes | Index Medicus | health risk | ancestry | pathology | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | Article | genetic structure | Klinisk medicin | genetic code | genetics | Endokrinologi och diabetes | genetic predisposition | Diabetes Mellitus, Type 2 | priority journal | ethnology | human | sample size | Endocrinology and Diabetes | Genetic Predisposition to Disease | gene sequence | Europe | genotyping technique | physiology | genetic variation | European | genotype | non insulin dependent diabetes mellitus | genome | Clinical Medicine | genetic analysis | exome | controlled study | allele | genome-wide association study | dna mutational analysis | diabetes
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3. Full Text A Bibliometric Analysis on Top‐Cited Articles in Pain Research
by Chuang, Kun‐Yang and Ho, Yuh‐Shan
Pain medicine (Malden, Mass.), ISSN 1526-2375, 05/2014, Volume 15, Issue 5, pp. 732 - 744
Scientometrics | Web of Science | Major Contribution Index | Pain Research | Article Life | Highly Cited | Article life | Web of science | Highly cited | Pain research | Major contribution index | Medicine, General & Internal | Anesthesiology | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Publishing - trends | Pain Management - trends | Chronic Pain - therapy | Biomedical Research - trends | Bibliometrics | Humans | Analysis | Chronic pain | Bibliographic data bases | Pain | Index Medicus
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4. Full Text Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
by Mahajan, Anubha and Wessel, Jennifer and Willems, Sara M and Zhao, Wei and Robertson, Neil R and Chu, Audrey Y and Gan, Wei and Kitajima, Hidetoshi and Taliun, Daniel and Rayner, N. William and Guo, Xiuqing and Lu, Yingchang and Li, Man and Jensen, Richard A and Hu, Yao and Huo, Shaofeng and Lohman, Kurt K and Zhang, Weihua and Cook, James P and Prins, Bram Peter and Flannick, Jason and Grarup, Niels and Trubetskoy, Vassily Vladimirovich and Kravic, Jasmina and Kim, Young Jin and Rybin, Denis V and Yaghootkar, Hanieh and Müller-Nurasyid, Martina and Meidtner, Karina and Li-Gao, Ruifang and Varga, Tibor V and Marten, Jonathan and Li, Jin and Smith, Albert Vernon and An, Ping and Ligthart, Symen and Gustafsson, Stefan and Malerba, Giovanni and Demirkan, Ayse and Tajes, Juan Fernandez and Steinthorsdottir, Valgerdur and Wuttke, Matthias and Lecoeur, Cécile and Preuss, Michael and Bielak, Lawrence F and Graff, Marielisa and Highland, Heather M and Justice, Anne E and Liu, Dajiang J and Marouli, Eirini and Peloso, Gina Marie and Warren, Helen R and Afaq, Saima and Afzal, Shoaib and Ahlqvist, Emma and Bang, Lia B and Bertoni, Alain G and Bombieri, Cristina and Bork-Jensen, Jette and Brandslund, Ivan and Brody, Jennifer A and Burtt, Noël P and Canouil, Mickaël and Chen, Yii-Der Ida and Cho, Yoon Shin and Christensen, Cramer and Eastwood, Sophie V and Eckardt, Kai-Uwe and Fischer, Krista and Gambaro, Giovanni and Giedraitis, Vilmantas and Grove, Megan L and De Haan, Hugoline G and Hackinger, Sophie and Hai, Yang and Han, Sohee and Tybjærg-Hansen, Anne and Hivert, Marie-France and Isomaa, Bo and Jäger, Susanne and Jørgensen, Marit E and Jørgensen, Torben and Käräjämäki, Annemari and Kim, Bong-Jo and Kim, Sung Soo and Koistinen, Heikki A and Kovacs, Peter and Kriebel, Jennifer and Kronenberg, Florian and Läll, Kristi and Lange, Leslie A and Lee, Jung-Jin and Lehne, Benjamin and Li, Huaixing and Lin, Keng-Hung and Linneberg, Allan and Liu, Ching-Ti and Liu, Jun and Loh, Marie and Mägi, Reedik and ...
Nature genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 559 - 571
ancestry group | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | Article | genetic association | odds ratio | Klinisk medicin | genetic code | Medicinsk genetik | Medical Genetics | Endokrinologi och diabetes | gene mapping | priority journal | human | Endocrinology and Diabetes | Basic Medicine | gene sequence | disease predisposition | genetic variability | non insulin dependent diabetes mellitus | gene locus | genome | Clinical Medicine | Medicinska och farmaceutiska grundvetenskaper
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5. Full Text Review article: next‐generation transformative advances in the pathogenesis and management of autoimmune hepatitis
by Czaja, A. J
Alimentary pharmacology & therapeutics, ISSN 0269-2813, 11/2017, Volume 46, Issue 10, pp. 920 - 937
Gastroenterology & Hepatology | Pharmacology & Pharmacy | Life Sciences & Biomedicine | Science & Technology | Hepatitis, Autoimmune - physiopathology | Genome-Wide Association Study | Hepatitis, Autoimmune - therapy | Humans | Gastrointestinal Microbiome | Cues | Biotechnology | Chromatin | Transcription | Pathogenesis | Liver | Environmental changes | Antagonists | Genomes | Epidemiology | Hepatitis | Immunosuppression | Microorganisms | Major histocompatibility complex | Reviews | Bibliographies | Bibliographic literature | Intestine | Epigenetics | Genetics | Immune system | Index Medicus
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