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1. Full Text Low Temperature Fluidity of Lubricating Oils Under Slow Cool Conditions
by Schmidt, G. M., author
SAE technical paper series, Volume 831718.
A Slow Cool Fluidity Test (SCFT) was developed to detect gelation of oils. In this test, SAE 10W multigrade oils of known poor field experience solidified at... 
Engine lubricants | Tests and Testing
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2. Full Text Synthetics as Future Diesel Engine Lubricants
by Schmidt, G. M., author
SAE technical paper series, Volume 841366.
Synthetic oils of polyol ester, polyalphaolefin, and diester type were tested in heavy-duty diesel engines used in agricultural applications. Evaluation... 
Synthetic lubricants | Diesel / Compression Ignition engines | Gas turbines | Lubricants | Engine lubricants | Wear | Agricultural vehicles and equipment
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3. Full Text Performance of Multigrade Oils in Off-Highway Diesel Engines
by Schmidt, G. M., author
SAE technical paper series, Volume 801348.
A number of multigrade diesel engine oils meeting API Service Classification CD, including those of Super Tractor Oil Universal (STUO) type, were tested in a... 
Diesel / Compression Ignition engines | Performance tests | Lubricants | Engine lubricants
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4. Full Text Illuminating gravitational waves: A concordant picture of photons from a neutron star merger
by Kasliwal, M.M and Nakar, E and Singer, L.P and Kaplan, D.L and Cook, D.O and Sistine, A. Van and Ghosh, S and Hinderer, T and Kupfer, T and Nichols, D and Nissanke, S and Schmidt, P and Williamson, A.R and Zhang, C and Zhao, W and Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States) and Fysikum and Naturvetenskapliga fakulteten and Institutionen för astronomi and Stockholms universitet and Oskar Klein-centrum för kosmopartikelfysik (OKC)
Science, ISSN 0036-8075, 2017, Volume 358, Issue 6370, pp. 1559 - 1565
Merging neutron stars offer an excellent laboratory for simultaneously studying strong-field gravity and matter in extreme environments. We establish the... 
MULTIDISCIPLINARY SCIENCES | Neutron stars | Photons | Observations | Natural history | Radio waves | Heavy elements | Galaxies | Merging | Gravitational waves | Stars | Luminosity | Neutrons | Emission | Waves | Flux (rate) | Extreme environments | Forging | Gravity | Light speed | Space telescopes | Gamma ray bursts | Emissions | Gamma rays | Observatories | Wavelengths | Telescopes | Acquisitions & mergers | ASTRONOMY AND ASTROPHYSICS | Fysik | Physical Sciences | Astronomi, astrofysik och kosmologi | Naturvetenskap | Natural Sciences | Astronomy, Astrophysics and Cosmology
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5. Full Text Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
by Davies, Gail and Lam, Max and Harris, Sarah E and Trampush, Joey W and Luciano, Michelle and Hill, W David and Hagenaars, Saskia P and Ritchie, Stuart J and Marioni, Riccardo E and Fawns-Ritchie, Chloe and Liewald, David C M and Okely, Judith A and Ahola-Olli, Ari V and Barnes, Catriona L K and Bertram, Lars and Bis, Joshua C and Burdick, Katherine E and Christoforou, Andrea and DeRosse, Pamela and Djurovic, Srdjan and Espeseth, Thomas and Giakoumaki, Stella and Giddaluru, Sudheer and Gustavson, Daniel E and Hayward, Caroline and Hofer, Edith and Ikram, M Arfan and Karlsson, Robert and Knowles, Emma and Lahti, Jari and Leber, Markus and Li, Shuo and Mather, Karen A and Melle, Ingrid and Morris, Derek and Oldmeadow, Christopher and Palviainen, Teemu and Payton, Antony and Pazoki, Raha and Petrovic, Katja and Reynolds, Chandra A and Sargurupremraj, Muralidharan and Scholz, Markus and Smith, Jennifer A and Smith, Albert V and Terzikhan, Natalie and Thalamuthu, Anbupalam and Trompet, Stella and van der Lee, Sven J and Ware, Erin B and Windham, B Gwen and Wright, Margaret J and Yang, Jingyun and Yu, Jin and Ames, David and Amin, Najaf and Amouyel, Philippe and Andreassen, Ole A and Armstrong, Nicola J and Assareh, Amelia A and Attia, John R and Attix, Deborah and Avramopoulos, Dimitrios and Bennett, David A and Böhmer, Anne C and Boyle, Patricia A and Brodaty, Henry and Campbell, Harry and Cannon, Tyrone D and Cirulli, Elizabeth T and Congdon, Eliza and Conley, Emily Drabant and Corley, Janie and Cox, Simon R and Dale, Anders M and Dehghan, Abbas and Dick, Danielle and Dickinson, Dwight and Eriksson, Johan G and Evangelou, Evangelos and Faul, Jessica D and Ford, Ian and Freimer, Nelson A and Gao, He and Giegling, Ina and Gillespie, Nathan A and Gordon, Scott D and Gottesman, Rebecca F and Griswold, Michael E and Gudnason, Vilmundur and Harris, Tamara B and Hartmann, Annette M and Hatzimanolis, Alex and Heiss, Gerardo and Holliday, Elizabeth G and Joshi, Peter K and Kähönen, Mika and Kardia, Sharon L R and Karlsson, Ida and Kleineidam, Luca and ...
Nature communications, ISSN 2041-1723, 05/2019, Volume 10, Issue 1, pp. 2068 - 5
Christina M. Lill, who contributed to analysis of data, was inadvertently omitted from the author list in the originally published version of this article.... 
Cognitive ability
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6. Full Text Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
by Lange, Leslie A and Lange, Ethan M and Lange, Christoph and Hu, Youna and Zhang, Qunyuan and Zhang, Ji and Zhang, He and Xue, Chenyi and Schmidt, Ellen M and Tang, Hua and Tang, Zheng-Zheng and Bizon, Chris and Smith, Nicholas L and Smith, Joshua D and Smith, Albert V and Turner, Emily H and Jun, Goo and Kang, Hyun Min and Peloso, Gina and Auer, Paul L and Auer, Paul and Li, Kuo-ping and Li, Mingyao and Li, Yun and Li, Bingshan and Li, Dalin and Flannick, Jason and Fuchsberger, Christian and Gaulton, Kyle and Lindgren, Cecilia and Locke, Adam and Manning, Alisa and Sim, Xueling and Rivas, Manuel A and Holmen, Oddgeir L and Gottesman, Omri and Lu, Yingchang and Ruderfer, Douglas and Stahl, Eli A and Duan, Qing and Durda, Peter and Durda, J. Peter and Jiao, Shuo and Isaacs, Aaron and Hofman, Albert and Bis, Joshua C and Bis, Joshua and Correa, Adolfo and Griswold, Michael E and Jakobsdottir, Johanna and Schreiner, Pamela and Schreiner, Pamela J and Feitosa, Mary F and Huffman, Jennifer E and Crosby, Jacy and Wassel, Chrstina L and Wassel, Christina L and Do, Ron and Franceschini, Nora and Martin, Lisa and Martin, Lisa W and Martin, Thomas R and Robinson, Jennifer G and Assimes, Themistocles L and Crosslin, David R and Rosenthal, Elisabeth A and Tsai, Michael Y and Tsai, Michael and Rieder, Mark J and Farlow, Deborah N and Folsom, Aaron R and Lumley, Thomas and Fox, Ervin R and Fox, Caroline S and Fox, P. Keolu and Fox, Ervin and Carlson, Christopher S and Peters, Ulrike and Jackson, Rebecca D and Jackson, Rebecca and van Duijn, Cornelia M and Uitterlinden, André G and Levy, Daniel and Rotter, Jerome I and Taylor, Herman A and Taylor, Kira C and Taylor, Kent and Gudnason, Vilmundur and Siscovick, David S and Fornage, Myriam and Borecki, Ingrid B and Hayward, Caroline and Rudan, Igor and Chen, Wei-Min and Chen, Y. Eugene and Chen, Donna T and Chen, Ida Y and Bottinger, Erwin P and Loos, Ruth J.F and Sætrom, Pål and ... and NHLBI Grand Opportunity Exome Sequ and NHLBI Grand Opportunity Exome Sequencing Project and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
The American Journal of Human Genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 233 - 245
Elevated low-density lipoprotein cholesterol (LDL-C) is a treatable, heritable risk factor for cardiovascular disease. Genome-wide association studies (GWASs)... 
OBJECTIVES | HEART-DISEASE | PLASMA | GENE | SUSCEPTIBILITY | GENETICS & HEREDITY | DENSITY-LIPOPROTEIN-CHOLESTEROL | Dyslipidemias - genetics | Genetic Code | Follow-Up Studies | Humans | Middle Aged | Male | Proprotein Convertases - genetics | Exome | Dyslipidemias - blood | Serine Endopeptidases - genetics | Adult | Female | Receptors, LDL - genetics | Genome-Wide Association Study | Gene Frequency | Genotype | Sequence Analysis, DNA | Cholesterol, LDL - genetics | Phenotype | Apolipoproteins E - blood | Apolipoproteins E - genetics | Aged | Polymorphism, Single Nucleotide | Cohort Studies | Lipase - genetics | Proprotein Convertase 9 | Genetic code | Genetic variation | Physiological aspects | Genetic research | Cholesterol, LDL | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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7. Operative treatment of deep vein thrombosis (author's transl)
by Nedjabat, T and Birtel, F J and Neuhaus, G and Thelen, M and Schmidt, I
Zentralblatt fur Chirurgie, ISSN 0044-409X, 1979, Volume 104, Issue 8, p. 529
From 1973 to 1977 a total of 63 patients with thrombosis of the deep veins in leg and pelvis and in the V. cava inferior was treated by operative thrombectomy.... 
Femoral Vein | Vena Cava, Inferior | Humans | Middle Aged | Male | Iliac Vein | Postoperative Care | Adolescent | Thrombophlebitis - diagnosis | Adult | Female | Aged | Thrombophlebitis - surgery | Postoperative Complications | Methods
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8. Full Text Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa
by Duncan, Laramie and Yilmaz, Zeynep and Gaspar, Helena and Walters, Raymond and Goldstein, Jackie and Anttila, Verneri and Bulik-Sullivan, Brendan and Ripke, Stephan and Thornton, Laura and Hinney, Anke and Daly, Mark and Sullivan, Patrick F and Zeggini, Eleftheria and Breen, Gerome and Bulik, Cynthia M and Gaspar, Héléna and Adan, Roger and Alfredsson, Lars and Ando, Tetsuya and Andreassen, Ole and Aschauer, Harald and Baker, Jessica and Barrett, Jeffrey and Bencko, Vladimir and Bergen, Andrew and Berrettini, Wade and Birgegård, Andreas and Boni, Claudette and Perica, Vesna Boraska and Brandt, Harry and Burghardt, Roland and Carlberg, Laura and Cassina, Matteo and Cesta, Carolyn and Cichon, Sven and Clementi, Maurizio and Cohen-Woods, Sarah and Coleman, Joni and Cone, Roger and Courtet, Philippe and Crawford, Steven and Crow, Scott and Crowley, Jim and Danner, Unna and Davis, Oliver and de Zwaan, Martina and Dedoussis, George and Degortes, Daniela and DeSocio, Janiece and Dick, Danielle and Dikeos, Dimitris and Dina, Christian and Ding, Bo and Dmitrzak-Weglarz, Monika and Docampo, Elisa and Egberts, Karin and Ehrlich, Stefan and Escaramís, Geòrgia and Esko, Tõnu and Espeseth, Thomas and Estivill, Xavier and Favaro, Angela and Fernández-Aranda, Fernando and Fichter, Manfred and Finan, Chris and Fischer, Krista and Floyd, James and Föcker, Manuel and Foretova, Lenka and Forzan, Monica and Fox, Caroline and Franklin, Christopher and Gaborieau, Valerie and Gallinger, Steven and Gambaro, Giovanni and Giegling, Ina and Gonidakis, Fragiskos and Gorwood, Philip and Gratacos, Monica and Guillaume, Sébastien and Guo, Yiran and Hakonarson, Hakon and Halmi, Katherine and Harrison, Rebecca and Hatzikotoulas, Konstantinos and Hauser, Joanna and Hebebrand, Johannes and Helder, Sietske and Hendriks, Judith and Herms, Stefan and Herpertz-Dahlmann, Beate and Herzog, Wolfgang and Hilliard, Christopher and Huckins, Laura and Hudson, James and Huemer, Julia and Imgart, Hartmut and Inoko, Hidetoshi and Jall, Sigrid and Jamain, Stephane and ... and Eatint Disorders Working Grp and Eating Disorders Working Group of the Psychiatric Genomics Consortium and Institute of Neuroscience and Physiology and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institutionen för neurovetenskap och fysiologi
American Journal of Psychiatry, ISSN 0002-953X, 09/2017, Volume 174, Issue 9, pp. 850 - 858
Objective:The authors conducted a genome-wide association study of anorexia nervosa and calculated genetic correlations with a series of psychiatric,... 
GWAS | METAANALYSIS | PSYCHIATRIC-DISORDERS | RISK | SCHIZOPHRENIA | UPDATE | EATING-DISORDERS | TRAITS | Journal Article | PSYCHIATRY | Anorexia Nervosa - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Phenotype | Humans | Linkage Disequilibrium - genetics | Polymorphism, Single Nucleotide - genetics | Case-Control Studies | Genotype | Development and progression | Genetic aspects | Anorexia nervosa | Metabolism | Health aspects | Anorèxia nerviosa | Genetics | Genètica | Metabolisme | Life Sciences | Clinical Medicine | Psykiatri | Klinisk medicin | Psychiatry
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9. A highly sensitive determination of immunoglobulin G and M with sensibilized latex particles (author's transl)
by Schmidt, W A and Klein, M and Brade, H
Immunitat und Infektion, 02/1977, Volume 5, Issue 1, p. 30
Latexparticles, sensitized with heavy chain specific anti-human IgG and IgM, were used for the detection of IgG and IgM in sera of adults and newborn infants.... 
Microspheres | Animals | Immune Sera | Rabbits - immunology | Humans | Immunoglobulin M - analysis | Adult | Immunoglobulin G - analysis | Fetal Blood | Infant, Newborn | Latex
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10. Full Text Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations
by Ganesh, Santhi K and Chasman, Daniel I and Larson, Martin G and Guo, Xiuqing and Verwoert, Germain and Bis, Joshua C and Gu, Xiangjun and Smith, Albert V and Yang, Min-Lee and Zhang, He and Zhang, Feng and Zhang, Yan and Ehret, Georg and Rose, Lynda M and Hwang, Shih-Jen and Papanicolau, George J and Sijbrands, Eric J and Rice, Kenneth and Eiriksdottir, Gudny and Pihur, Vasyl and Ridker, Paul M and Vasan, Ramachandran S and Newton-Cheh, Christopher and Johnson, Andrew D and Johnson, Toby and Gateva, Vesela and Tobin, Martin D and Bochud, Murielle and Coin, Lachlan and Najjar, Samer S and Zhao, Jing Hua and Heath, Simon C and Eyheramendy, Susana and Papadakis, Konstantinos and Voight, Benjamin F and Scott, Laura J and Farrall, Martin and Tanaka, Toshiko and Wallace, Chris and Chambers, John C and Khaw, Kay-Tee and Nilsson, Peter and van der Harst, Pim and Polidoro, Silvia and Grobbee, Diederick E and Onland-Moret, N. Charlotte and Bots, Michiel L and Wain, Louise V and Elliott, Katherine S and Elliott, Paul and Teumer, Alexander and Luan, Jian’an and Lucas, Gavin and Kuusisto, Johanna and Burton, Paul R and Hadley, David and McArdle, Wendy L and Brown, Morris and Dominiczak, Anna and Newhouse, Stephen J and Samani, Nilesh J and Webster, John and Zeggini, Eleftheria and Beckmann, Jacques S and Bergmann, Sven and Lim, Noha and Song, Kijoung and Vollenweider, Peter and Waeber, Gerard and Waterworth, Dawn M and Yuan, Xin and Groop, Leif and Orho-Melander, Marju and Allione, Alessandra and Di Gregorio, Alessandra and Guarrera, Simonetta and Panico, Salvatore and Ricceri, Fulvio and Romanazzi, Valeria and Sacerdote, Carlotta and Vineis, Paolo and Barroso, Inês and Sandhu, Manjinder S and Luben, Robert N and Crawford, Gabriel J and Jousilahti, Pekka and Perola, Markus and Boehnke, Michael and Bonnycastle, Lori L and Collins, Francis S and Jackson, Anne U and Mohlke, Karen L and Stringham, Heather M and Valle, Timo T and Willer, Cristen J and Willer, Cristen J and Bergman, Richard N and Morken, Mario A and Döring, Angela and Gieger, Christian and ... and Global Blood Pressure Genetics Con and Global Blood Pressure Genetics Consortium
The American Journal of Human Genetics, ISSN 0002-9297, 07/2014, Volume 95, Issue 1, pp. 49 - 65
Blood pressure (BP) is a heritable, quantitative trait with intraindividual variability and susceptibility to measurement error. Genetic studies of BP... 
HEART | VARIABILITY | TRACKING | GENETICS & HEREDITY | CARDIOVASCULAR-DISEASE |