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1. Full Text Disproportionate Sterilization of Latinos Under California's Eugenic Sterilization Program, 1920-1945
by Novak, NL and Lira, N and O'Connor, KE and Harlow, SD and Kardia, SLR and Stern, AM
AMERICAN JOURNAL OF PUBLIC HEALTH, ISSN 0090-0036, 05/2018, Volume 108, Issue 5, pp. 611 - 613
Objectives. To compare population-based sterilization rates between Latinas/os and non-Latinas/os sterilized under California's eugenics law. Methods. We used... 
PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | HEALTH | CARE | RACE | Eugenics - legislation & jurisprudence | Hispanic Americans - history | History, 20th Century | Humans | Sterilization - legislation & jurisprudence | Eugenics - statistics & numerical data | Hispanic Americans - statistics & numerical data | Male | California | Sterilization - statistics & numerical data | Sterilization - history | Eugenics - history | Female | Reproductive health | Hispanic Americans | Gender | Datasets | Confidence intervals | Censuses | Sterilization | Race | Population | Poisson density functions | Public health | Age | Statistical analysis | Eugenics | Residence | Minority & ethnic groups | Patients | Health care services policy | Trust | Girls | Census | Ethnicity | Womens health | Genetic engineering | Age differences
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2. Full Text Synergistic polymorphisms of β 1- and α 2C-adrenergic receptors and the risk of congestive heart failure
by Small, Kersten M and Wagoner, Lynne E and Levin, Albert M and Kardia, Sharon L. R and Liggett, Stephen B
New England Journal of Medicine, ISSN 0028-4793, 10/2002, Volume 347, Issue 15, pp. 1135 - 1142
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3. Full Text Genome-wide association study identifies 74 loci associated with educational attainment
by Okbay, Aysu and Beauchamp, Jonathan and Fontana, M.A and Lee, James J and Pers, Tune and Rietveld, C.A and Turley, Patrick and Chen, G.-B and Emilsson, Valur and Meddens, S.F.W and Oskarsson, S and Pickrell, J.K and Thom, K and Timshel, P and Vlaming, Ronald and Abdellaoui, Abdel and Ahluwalia, Tarunveer Singh and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, G and Brandsma, Johan and Pina Concas, M and Derringer, J and Furlotte, N.A and Galesloot, Tessel and Girotto, S and Gupta, R and Hall, Leanne M and Harris, Sarah and Hofer, E and Horikoshi, M and Huffman, Jennifer E and Kaasik, K and Kalafati, Ioanna-Panagiota and Karlsson, Robert and Kong, Augustine and Lahti, Jari and Lee, Sven and Deleeuw, C and Lind, Penelope and Lindgren, K.-O and Liu, T and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Mike and Most, Peter and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter and Qian, Y and Raitakari, Olli and Rueedi, R and Salvi, E and Schmidt, B and Schraut, K.E and Shi, J and Smith, Albert Vernon and Poot, Raymond and St Pourcain, Beate and Teumer, Alexander and Thorleifsson, Gudmar and Verweij, Niek and Vuckovic, gana and Wellmann, J and Westra, Harm-Jan and Yang, J and Zhao, W and Zhu, Z and Alizadeh, Behrooz and Amin, Najaf and Bakshi, A and Baumeister, Sebastian and Biino, G and Bønnelykke, Klaus and Boyle, Patricia and Campbell, Harry and Cappuccio, F.P and Davies, Gail and Neve, Jan-Emmanuel and Deloukas, Panagiotis and Demuth, Ilja and Ding, J and Eibich, P and Eisele, L and Eklund, Niina and Evans, David and Faul, Jessica D and Feitosa, Mary Furlan and Forstner, Aneas and Gandin, Ilaria and Gunnarsson, B and Halldorsson, Bjarni and Harris, Tamara and Holliday, Elizabeth and Heath, Anew C and Hocking, L.J and Homuth, Georg and Horan, Mike and ... and LifeLines Cohort Study and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 05/2016, Volume 533, Issue 7604, pp. 539 - 542
textabstractEducational attainment is strongly influenced by social and other environmental factors, but genetic factors are estimated to account for at least... 
IQ | ACHIEVEMENT | TRAITS | MULTIDISCIPLINARY SCIENCES | HERITABILITY | Genome-Wide Association Study | Gene Expression Regulation - genetics | Humans | Molecular Sequence Annotation | Computational Biology | Fetus - metabolism | United Kingdom | Cognition | Educational Status | Bipolar Disorder - genetics | Gene-Environment Interaction | Brain - metabolism | Schizophrenia - genetics | Polymorphism, Single Nucleotide - genetics | Alzheimer Disease - genetics | Quantitative trait loci | Academic achievement | Genome-wide association studies | Genetic aspects | Observations | Studies | Genomes | Gene expression | Genes | Educational attainment | Meta-analysis | Quantitative Finance | Samhällsvetenskap | Biological Sciences | Social Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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4. Full Text Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
by Okbay, Aysu and Baselmans, B.M.L and Neve, Jan-Emmanuel and Turley, Patrick and Nivard, Michel and Fontana, M.A and Meddens, S.F.W and Linnér, R.K and Rietveld, C.A and Derringer, J and Gratten, Jacob and Lee, James J and Liu, J.Z and Vlaming, Ronald and SAhluwalia, T and Buchwald, J and Cavadino, Alana and Frazier-Wood, Alexis C and Furlotte, N.A and Garfield, V and Geisel, M.H and Gonzalez, Juan R and Haitjema, S and Karlsson, Robert and Der Laan, S.W and Ladwig, Karl-Heinz and Lahti, Jari and Lee, Sven and Lind, Penelope and Liu, T and Matteson, L and Mihailov, Evelin and Miller, Mike and CMinica, C and MNolte, I and Mook-Kanamori, Dennis and Most, Peter and Oldmeadow, Christopher and Qian, Yong and Raitakari, Olli and Rawal, R and Realo, A and Rueedi, R and Schmidt, B and Smith, Albert Vernon and Stergiakouli, Evangelia and Tanaka, Toshiko and Taylor, Kent and Wedenoja, J and Wellmann, J and Westra, Harm-Jan and MWillems, S and Zhao, W and Study, LifeLines Cohort and Amin, Najaf and Bakshi, A and Boyle, Patricia and Cherney, S and Cox, S.R and Davies, Gail and Davis, Oliver S and Ding, Jun and Direk, Nese and Eibich, P and Emeny, Rebecca and Fatemifar, G and Faul, J.D and Ferrucci, Luigi and Forstner, Aneas and Gieger, Christian and Gupta, R and Harris, Tamara B and Harris, Juliette and Holliday, Elizabeth and Hottenga, Jouke Jan and Jager, Philip and Kaakinen, Marika and Kajantie, Eero and Karhunen, V and Kolcic, Ivana and Kumari, Meena and Launer, Lenore and Franke, Lude and Li-Gao, R and Koini, M and Loukola, Anu and Marques-Vidal, P and Montgomery, Grant and Mosing, Miriam and Paternoster, Lavinia and Pattie, Alison and Petrovic, Katja and Pulkki-R'back, L and Quaye, Lydia and R'ikkönen, K and Rudan, Igor and Scott, Rodney and Smith, Jennifer A and Sutin, A.R and Trzaskowski, M and ... and LifeLines Cohort Study
Nature Genetics, ISSN 1061-4036, 06/2016, Volume 48, Issue 6, pp. 624 - 633
textabstractVery few genetic variants have been associated with depression and neuroticism, likely because of limitations on sample size in previous studies.... 
PERSONALITY | COMMON VARIANTS | HUMAN HEIGHT | METAANALYSIS | DISEASE | GENETICS & HEREDITY | RISK | MAJOR DEPRESSION | HAPPINESS | HERITABILITY | RESOURCE | Neuroticism | Genome-Wide Association Study | Phenotype | Humans | Bayes Theorem | Anxiety Disorders - genetics | Polymorphism, Single Nucleotide | Depression - genetics | Genome-wide association studies | Genetic variation | Depression, Mental | Genetic aspects | Identification and classification | Methods | Risk factors | Studies | Psychological aspects | Consortia | Social sciences | Quality control | Personality | Genomes | Behavior | Mental depression | Statistics | Epidemiology | Meta-analysis | Quantitative Finance
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5. Full Text Genetic modification of triggers of acute myocardial infarction: results from a case-crossover study in Costa Rica
by Mittleman, Murray and Mostofsky, Elizabeth and Wang, Dongqing and Baylin, Ana and Campos, Hannia and Kardia, Sharon L
Circulation, ISSN 0009-7322, 03/2017, Volume 135, Issue 10
Diet | Genetic variation | Analysis | Genetic aspects | Coffee | Health aspects | Heart attack | Risk factors
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6. Full Text GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment
by Cornelius A. Rietveld and Sarah E. Medland and Jaime Derringer and Jian Yang and Tõnu Esko and Nicolas W. Martin and Harm-Jan Westra and Konstantin Shakhbazov and Abdel Abdellaoui and Arpana Agrawal and Eva Albrecht and Behrooz Z. Alizadeh and Najaf Amin and John Barnard and Sebastian E. Baumeister and Kelly S. Benke and Lawrence F. Bielak and Jeffrey A. Boatman and Patricia A. Boyle and Gail Davies and Christiaan de Leeuw and Niina Eklund and Daniel S. Evans and Rudolf Ferhmann and Krista Fischer and Christian Gieger and Håkon K. Gjessing and Sara Hägg and Jennifer R. Harris and Caroline Hayward and Christina Holzapfel and Carla A. Ibrahim-Verbaas and Erik Ingelsson and Bo Jacobsson and Peter K. Joshi and Astanand Jugessur and Marika Kaakinen and Stavroula Kanoni and Juha Karjalainen and Ivana Kolcic and Kati Kristiansson and Zoltán Kutalik and Jari Lahti and Sang H. Lee and Peng Lin and Penelope A. Lind and Yongmei Liu and Kurt Lohman and Marisa Loitfelder and George McMahon and Pedro Marques Vidal and Osorio Meirelles and Lili Milani and Ronny Myhre and Marja-Liisa Nuotio and Christopher J. Oldmeadow and Katja E. Petrovic and Wouter J. Peyrot and Ozren Polašek and Lydia Quaye and Eva Reinmaa and John P. Rice and Thais S. Rizzi and Helena Schmidt and Reinhold Schmidt and Albert V. Smith and Jennifer A. Smith and Toshiko Tanaka and Antonio Terracciano and Matthijs J. H. M. van der Loos and Veronique Vitart and Henry Völzke and Jürgen Wellmann and Lei Yu and Wei Zhao and Jüri Allik and John R. Attia and Stefania Bandinelli and François Bastardot and Jonathan Beauchamp and David A. Bennett and Klaus Berger and Laura J. Bierut and Dorret I. Boomsma and Ute Bültmann and Harry Campbell and Christopher F. Chabris and Lynn Cherkas and Mina K. Chung and Francesco Cueca and Mariza de Andrade and Philip L. De Jager and Jan-Emmanuel De Neve and Ian J. Deary and George V. Dedoussis and Panos Deloukas and Maria Dimitriou and Guðný Eiríksdóttir and Martin F. Elderson and Johan G. Eriksson and ... and LifeLines Cohort Study and The LifeLines Cohort Study and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper
Science, ISSN 0036-8075, 6/2013, Volume 340, Issue 6139, pp. 1467 - 1471
A genome-wide association study (GWAS) of educational attainment was conducted in a discovery sample of 101,069 individuals and a replication sample of 25,490.... 
Medical research | Phenotypes | Psychology | REPORTS | Personality traits | Genetic research | Research facilities | Genetics | Epidemiology | Research universities | Educational attainment | MULTIDISCIPLINARY SCIENCES | LOCI | ENVIRONMENT | Genome-Wide Association Study | Endophenotypes | Humans | Female | Male | Cognition | Educational Status | Polymorphism, Single Nucleotide | Genetic Loci | Multifactorial Inheritance | Academic achievement | Genetic aspects | Research | Single nucleotide polymorphisms | Genetic variation | Genomics | Science education | Medical and Health Sciences | Medicin och hälsovetenskap
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7. Full Text Laying Anchor: Inserting Precision Health into a Public Health Genetics Policy Course
by Modell, Stephen M and Citrin, Toby and Kardia, Sharon L R
Healthcare (Basel, Switzerland), ISSN 2227-9032, 08/2018, Volume 6, Issue 3, p. 93
The United States Precision Medicine Initiative (PMI) was announced by then President Barack Obama in January 2015. It is a national effort designed to take... 
Professionals | Genomics | Genomes | Family medical history | Presentations | Literacy | Medicine | Ethics | Genetic counseling | Students | Genetics | Drug therapy | Public health | Cancer | cardiovascular disease | precision public health | education | genetics | population health | health disparities | health policy | race | precision medicine | cancer
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8. Full Text The transcriptional landscape of age in human peripheral blood
by Peters, Marjolein and Joehanes, Roby and Pilling, Luke and Schurmann, Claudia and Conneely, Karen N and Powell, Joseph and Reinmaa, Eva and Sutphin, George L and Zhernakova, Alexana and Schramm, Katharina and Wilson, Yana A and Kobes, Sayuko and Tukiainen, Taru and Ramos, Yolande and Göring, Harald H and Fornage, Myriam and Liu, Yongmei and Gharib, Sina and Stranger, Barbara and Jager, Philip and Aviv, Abraham and Levy, Daniel and Murabito, Joanne and Munson, Peter J and Huan, Tianxiao and Hofman, Albert and Uitterlinden, Ané and Rivadeneira Ramirez, Fernando and van Rooij, Jeroen and Stolk, Lisette and Broer, Linda and Verbiest, Michael and Jhamai, Mila and Arp, Pascal and Metspalu, Anes and Tserel, Liina and Milani, Lili and Samani, Nilesh and Peterson, Pärt and Kasela, Silva and Codd, Veryan and Peters, Annette and Ward-Caviness, Cavin K and Herder, Christian and Waldenberger, Melanie and Roden, Michael and Singmann, Paula and Zeilinger, Sonja and Illig, Thomas and Homuth, Georg and Grabe, Hans Jörgen and Völzke, Henry and Steil, Leif and Kocher, Thomas and Murray, Anna and Melzer, David and Yaghootkar, Hanieh and Bandinelli, S and Moses, Eric and Kent, Jack and Curran, Joanne and Johnson, Matthew and Williams-Blangero, Sarah and Westra, Harm-Jan and McRae, Allan F and Smith, Jennifer A and Kardia, Sharon and Hovatta, Iiris and Perola, Markus and Ripatti, Samuli and Salomaa, Veikko and Henders, Anjali and Martin, Nicholas and Smith, Alicia K and Mehta, Divya and Binder, Elisabeth B and Nylocks, K. Maria and Kennedy, Elizabeth M and Klengel, Torsten and Ding, Jingzhong and Suchy-Dicey, Astrid and Enquobahrie, D and Brody, Jennifer and Rotter, Jerome I and Chen, Yii-Der I and Houwing-Duistermaat, Jeanine and Kloppenburg, Margreet and Slagboom, Eline and Helmer, Quinta and Hollander, Wouter and Bean, Shannon and Raj, Towfique and Bakhshi, Noman and Wang, Qiao Ping and Oyston, Lisa J and Psaty, Bruce and Tracy, Russell and Montgomery, Grant and Turner, Stephen and Blangero, John and ... and NABEC UKBEC Consortium and NABEC/UKBEC Consortium
Nature Communications, ISSN 2041-1723, 10/2015, Volume 6, Issue 1, p. 8570
textabstractDisease incidences increase with age, but the molecular characteristics of ageing that lead to increased disease susceptibility remain inadequately... 
LIFE-SPAN | OXIDATIVE STRESS | METHYLATION | PROFILES | GLYCOSAMINOGLYCANS | HUMAN LONGEVITY | DROSOPHILA-MELANOGASTER | MULTIDISCIPLINARY SCIENCES | PATTERNS | GENE-EXPRESSION CHANGES | GENOME-WIDE ASSOCIATION | Aging - blood | DNA Methylation | Humans | Transcriptome | European Continental Ancestry Group | Gene Expression Profiling | Biomarkers - blood
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9. Full Text Rare and low-frequency coding variants alter human adult height
by Marouli, Eirini and Graff, Mariaelisa and Medina-Gomez, Carolina and Lo, Ken Sin and Wood, Anew R and Kjaer, Troels R and Fine, Rebecca S and Lu, Yingchang and Schurmann, Claudia and Highland, Heather M and Rüeger, Sina and Thorleifsson, Gudmar and Justice, Anne E and Lamparter, David and Stirrups, Kathleen E and Turcot, Valérie and Young, Kristin L and Winkler, Thomas W and Esko, Tõnu and Karaderi, Tugce and Locke, Adam E and Masca, Nicholas G. D and Ng, Maggie C. Y and Mudgal, Poorva and Rivas, Manuel A and Vedantam, Sailaja and Mahajan, Anubha and Guo, Xiuqing and Abecasis, Goncalo and Aben, Katja K and Adair, Linda S and Alam, Dewan S and Albrecht, Eva and Allin, Kristine H and Allison, Matthew and Amouyel, Philippe and Appel, Emil V and Arveiler, Dominique and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Banas, Bernhard and Bang, Lia E and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bonnycastle, Lori L and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Burt, Amber A and Butterworth, Adam S and Carey, David J and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Auey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Galbany, Jordi Corominas and Cox, Amanda J and Cuellar-Partida, Gabriel and Danesh, John and Davies, Gail and de Bakker, Paul I. W and de Borst, Gert J and de Denus, Simon and de Groot, Mark C. H and de Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and den Hollander, Anneke I and Dennis, Joe G and Di Angelantonio, Emanuele and nos, Fotios and Du, Mengmeng and Dunning, Alison M and Easton, Douglas F and Ebeling, Tapani and Edwards, Todd L and Ellinor, Patrick T and Elliott, Paul and Evangelou, Evangelos and Farmaki, Aliki-Eleni and Faul, Jessica D and ... and EPIC-CVD Consortium and GoT2D Genes Consortium and MAGIC Investigators and Global Lipids Genetics Consortium and EPIC-InterAct Consortium and ReproGen Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and The EPIC-InterAct Consortium and CHD Exome+ Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Nature, ISSN 0028-0836, 2017, Volume 542, Issue 7640, pp. 186 - 190
Height is a highly heritable, classic polygenic trait with approximately 700 common associated variants identified through genome-wide association studies so... 
MISSING HERITABILITY | GENETIC ARCHITECTURE | INTERLEUKIN-11 | MUTATIONS | MULTIDISCIPLINARY SCIENCES | GENOME-WIDE ASSOCIATION | Stature | Genetic aspects | Observations | Genetic variation | Studies | Datasets | Disease | Genes | Deoxyribonucleic acid--DNA | Hälsovetenskaper | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Medical and Health Sciences | Medicin och hälsovetenskap | Public Health, Global Health, Social Medicine and Epidemiology | Health Sciences
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10. Full Text A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
by Manning, Alisa K and Hivert, Marie-France and Scott, Robert A and Grimsby, Jonna L and Bouatia-Naji, Nabila and Chen, Han and Rybin, Denis and Liu, Ching-Ti and Bielak, Lawrence F and Prokopenko, Inga and Amin, Najaf and Barnes, Daniel and Cadby, Gemma and Hottenga, Jouke-Jan and Ingelsson, Erik and Jackson, Anne U and Johnson, Toby and Kanoni, Stavroula and Ladenvall, Claes and Lagou, Vasiliki and Lahti, Jari and Lecoeur, Cecile and Liu, Yongmei and Martinez-Larrad, Maria Teresa and Montasser, May E and Navarro, Pau and Perry, John R. B and Rasmussen-Torvik, Laura J and Salo, Perttu and Sattar, Naveed and Shungin, Dmitry and Strawbridge, Rona J and Tanaka, Toshiko and van Duijn, Cornelia M and An, Ping and de Anade, Mariza and Anews, Jeanette S and Aspelund, Thor and Atalay, Mustafa and Aulchenko, Yurii and Balkau, Beverley and Bandinelli, Stefania and Beckmann, Jacques S and Beilby, John P and Bellis, Claire and Bergman, Richard N and Blangero, John and Boban, Mladen and Boehnke, Michael and Boerwinkle, Eric and Bonnycastle, Lori L and Boomsma, Dorret I and Borecki, Ingrid B and Boettcher, Yvonne and Bouchard, Claude and Brunner, Eric and Budimir, Danijela and Campbell, Harry and Carlson, Olga and Chines, Peter S and Clarke, Robert and Collins, Francis S and Corbaton-Anchuelo, Arturo and Couper, David and de Faire, Ulf and Dedoussis, George V and Deloukas, Panos and Dimitriou, Maria and Egan, Josephine M and Eiriksdottir, Gudny and Erdos, Michael R and Eriksson, Johan G and Eury, Elodie and Ferrucci, Luigi and Ford, Ian and Forouhi, Nita G and Fox, Caroline S and Franzosi, Maria Grazia and Franks, Paul W and Frayling, Timothy M and Froguel, Philippe and Galan, Pilar and de Geus, Eco and Gigante, Bruna and Glazer, Nicole L and Goel, Anuj and Groop, Leif and Gudnason, Vilmundur and Hallmans, Goeran and Hamsten, Anders and Hansson, Ola and Harris, Tamara B and Hayward, Caroline and Heath, Simon and Hercberg, Serge and Hicks, Anew A and Hingorani, Aroon and Hofman, Albert and Hui, Jennie and Hung, Joseph and ... and DIAGRAM Consortium and MUTHER Consortium and DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Multiple Tissue Human Expression Resource (MUTHER) Consortium and The Multiple Tissue Human Expression Resource (MUTHER) Consortium and Medicinska fakulteten and Institutionen för odontologi and Institutionen för folkhälsa och klinisk medicin and Näringsforskning and Umeå universitet and Medicin
Nature Genetics, ISSN 1061-4036, 06/2012, Volume 44, Issue 6, pp. 659 - 669
Recent genome-wide association studies have described many loci implicated in type 2 diabetes (T2D) pathophysiology and beta-cell dysfunction but have... 
COMMON VARIANTS | ASSOCIATION ANALYSIS | ENVIRONMENT INTERACTION | OBESITY | GLUCOSE | SUSCEPTIBILITY | GENETICS & HEREDITY | TYPE-2 DIABETES RISK | LOCI | POLYMORPHISM | CORONARY-ARTERY-DISEASE | Body Mass Index | Genome-Wide Association Study | Insulin - metabolism | Cholesterol, HDL - metabolism | Diabetes Mellitus, Type 2 - genetics | Humans | Insulin Resistance - genetics | Polymorphism, Single Nucleotide | Blood Glucose - metabolism | Type 2 diabetes | Insulin resistance | Genetic aspects | Research | Genetic variation | Risk factors | Body mass index | Hyperglycemia | Genomics | Diabetes | Glucose | Insulin | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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