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Hoevels, Fritz Erik [Author]; Priskil, Peter [Author]; MacRae, Ralph [Author] ; Ahriman-Verlag Freiburg im BreisgauDie Oper auf dem ProkrustesbettClose
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You can manage bookmarks using lists, please log in to your user account for this.Freiburg: Ahriman-Verlag, [2016]
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Lynch, Derek; MacRae, Rod; Martin, RalphThe Carbon and Global Warming Potential Impacts of Organic Farming: Does It Have a Significant Role in an Energy Constrained World?View onlineSchließen
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Published in: Sustainability
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MacRae, Duncan; Ross, Ralph; van den Haag, ErnestThe Fabric of Society: An Introduction to the Social SciencesView onlineSchließen
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Published in: The American Journal of Psychology
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Holt, Charles C.; MacRae, C. Duncan; Schweitzer, Stuart O.; Smith, Ralph E.Manpower Proposals for Phase IIIView onlineSchließen
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Published in: Brookings Papers on Economic Activity
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Holt, Charles C.; MacRae, C. Duncan; Schweitzer, Stuart O.; Smith, Ralph E.Manpower Proposals for Phase IIIView onlineSchließen
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Published in: Brookings Papers on Economic Activity
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Hambrick, Ralph; Bardach, Eugene; Chelimsky, Eleanor; Shadish, William R.; deLeon, Peter; Fischer, Frank; MacRae, Duncan; Whittington, DaleBuilding the Policy Studies Enterprise: A Work in ProgressView onlineSchließen
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Published in: Public Administration Review
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Creek, Darren J.; Chua, Hwa H.; Cobbold, Simon A.; Nijagal, Brunda; MacRae, James I.; Dickerman, Benjamin K.; Gilson, Paul R.; Ralph, Stuart A.; McConville, Malcolm J.Metabolomics-Based Screening of the Malaria Box Reveals both Novel and Established Mechanisms of ActionView onlineSchließen
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Published in: Antimicrobial Agents and Chemotherapy
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Allen, Stacey M.; Lim, Erin E.; Jortzik, Esther; Preuss, Janina; Chua, Hwa Huat; MacRae, James I.; Rahlfs, Stefan; Haeussler, Kristina; Downton, Matthew T.; McConville, Malcolm J.; Becker, Katja; Ralph, Stuart A.Plasmodium falciparum glucose‐6‐phosphate dehydrogenase 6‐phosphogluconolactonase is a potential drug targetView onlineSchließen
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Published in: The FEBS Journal
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Wang, Thomas J.; Nam, Byung-Ho; D’Agostino, Ralph B.; Wolf, Philip A.; Lloyd-Jones, Donald M.; MacRae, Calum A.; Wilson, Peter W.; Polak, Joseph F.; O’Donnell, Christopher J.Carotid Intima-Media Thickness Is Associated With Premature Parental Coronary Heart Disease : The Framingham Heart Study : The Framingham Heart StudyView onlineSchließen
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Published in: Circulation
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Moss, Alastair J.; Sim, Alisia M.; Adamson, Philip D.; Seidman, Michael A.; Andrews, Jack P. M.; Doris, Mhairi K.; Shah, Anoop S. V.; BouHaidar, Ralph; Alcaide-Corral, Carlos J.; Williams, Michelle C.; Leipsic, Jonathon A.; Dweck, Marc R.; MacRae, Vicky E.; Newby, David E.; Tavares, Adriana A. S.; Sellers, Stephanie L.Ex vivo 18F-fluoride uptake and hydroxyapatite deposition in human coronary atherosclerosisView onlineSchließen
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Published in: Scientific Reports
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Wild, Philipp S.; Felix, Janine F.; Schillert, Arne; Teumer, Alexander; Chen, Ming-Huei; Leening, Maarten J.G.; Völker, Uwe; Großmann, Vera; Brody, Jennifer A.; Irvin, Marguerite R.; Shah, Sanjiv J.; Pramana, Setia; Lieb, Wolfgang; Schmidt, Reinhold; Stanton, Alice V.; Malzahn, Dörthe; Smith, Albert Vernon; Sundström, Johan; Minelli, Cosetta; Ruggiero, Daniela; Lyytikäinen, Leo-Pekka; Tiller, Daniel; Smith, J. Gustav; Monnereau, Claire; [...]Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and functionView onlineSchließen
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Published in: Journal of Clinical Investigation
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Geng, Linda N; Kohler, Jennefer N; Levonian, Peter; Bernstein, Jonathan A; Ford, James M; Ahuja, Neera; Witteles, Ronald; Hom, Jason; Wheeler, Matthew; Acosta, Maria T; Adams, David R; Aday, Aaron; Alejandro, Mercedes E; Allard, Patrick; Ashley, Euan A; Azamian, Mahshid S; Bacino, Carlos A; Bademci, Guney; Baker, Eva; Balasubramanyam, Ashok; Baldridge, Dustin; Barbouth, Deborah; Batzli, Gabriel F; Beggs, Alan H; [...]Genomics in medicine: a novel elective rotation for internal medicine residentsView onlineSchließen
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Published in: Postgraduate Medical Journal
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Lu, Jinfeng; Toro, Camilo; Adams, David R.; Acosta, Maria T.; Adam, Margaret; Alvarez, Raquel L.; Alvey, Justin; Amendola, Laura; Andrews, Ashley; Ashley, Euan A.; Bacino, Carlos A.; Bademci, Guney; Balasubramanyam, Ashok; Baldridge, Dustin; Bale, Jim; Bamshad, Michael; Barbouth, Deborah; Bayrak-Toydemir, Pinar; Beck, Anita; Beggs, Alan H.; Behrens, Edward; Bejerano, Gill; Bellen, Hugo J.; Bennett, Jimmy; [...]LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variantsView onlineSchließen
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Published in: BMC Genomics
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Srivastava, Siddharth; Shaked, Hagar Mor; Gable, Kenneth; Gupta, Sita D; Pan, Xueyang; Somashekarappa, Niranjanakumari; Han, Gongshe; Mohassel, Payam; Gotkine, Marc; Doney, Elizabeth; Goldenberg, Paula; Tan, Queenie K G; Gong, Yi; Kleinstiver, Benjamin; Wishart, Brian; Cope, Heidi; Pires, Claudia Brito; Stutzman, Hannah; Spillmann, Rebecca C; Alejandro, Mercedes E; Azamian, Mahshid S; Bacino, Carlos A; Balasubramanyam, Ashok; Burrage, Lindsay C; [...]SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegiaView onlineSchließen
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Published in: Brain
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Morimoto, Marie; Bhambhani, Vikas; Gazzaz, Nour; Davids, Mariska; Sathiyaseelan, Paalini; Macnamara, Ellen F.; Lange, Jennifer; Lehman, Anna; Zerfas, Patricia M.; Murphy, Jennifer L.; Acosta, Maria T.; Wang, Camille; Alderman, Emily; Adam, Margaret; Alvarez, Raquel L.; Alvey, Justin; Amendola, Laura; Andrews, Ashley; Ashley, Euan A.; Azamian, Mahshid S.; Bacino, Carlos A.; Bademci, Guney; Balasubramanyam, Ashok; Baldridge, Dustin; [...]Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairmentView onlineSchließen
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Published in: npj Genomic Medicine
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Tepe, Burak; Macke, Erica L.; Niceta, Marcello; Weisz Hubshman, Monika; Kanca, Oguz; Schultz-Rogers, Laura; Zarate, Yuri A.; Schaefer, G. Bradley; Granadillo De Luque, Jorge Luis; Wegner, Daniel J.; Cogne, Benjamin; Gilbert-Dussardier, Brigitte; Le Guillou, Xavier; Wagner, Eric J.; Pais, Lynn S.; Neil, Jennifer E.; Mochida, Ganeshwaran H.; Walsh, Christopher A.; Magal, Nurit; Drasinover, Valerie; Shohat, Mordechai; Schwab, Tanya; Schmitz, Chris; Clark, Karl; [...]Bi-allelic variants in INTS11 are associated with a complex neurological disorderView onlineSchließen
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Published in: The American Journal of Human Genetics
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Miller, Ilana M.; Yashar, Beverly M.; Acosta, Maria T.; Adam, Margaret; Adams, David R.; Agrawal, Pankaj B.; Alvey, Justin; Amendola, Laura; Andrews, Ashley; Ashley, Euan A.; Azamian, Mahshid S.; Bacino, Carlos A.; Bademci, Guney; Baker, Eva; Balasubramanyam, Ashok; Baldridge, Dustin; Bale, Jim; Bamshad, Michael; Barbouth, Deborah; Bayrak-Toydemir, Pinar; Beck, Anita; Beggs, Alan H.; Behrens, Edward; Bejerano, Gill; [...]Continuing a search for a diagnosis: the impact of adolescence and family dynamicsView onlineSchließen
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Published in: Orphanet Journal of Rare Diseases
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Niggl, Eva; Bouman, Arjan; Briere, Lauren C.; Hoogenboezem, Remco M.; Wallaard, Ilse; Park, Joohyun; Admard, Jakob; Wilke, Martina; Harris-Mostert, Emilio D.R.O.; Elgersma, Minetta; Bain, Jennifer; Balasubramanian, Meena; Banka, Siddharth; Benke, Paul J.; Bertrand, Miriam; Blesson, Alyssa E.; Clayton-Smith, Jill; Ellingford, Jamie M.; Gillentine, Madelyn A.; Goodloe, Dana H.; Haack, Tobias B.; Jain, Mahim; Krantz, Ian; Luu, Sharon M.; [...]HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorderView onlineSchließen
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Published in: The American Journal of Human Genetics
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Koop, Klaas; Yuan, Weimin; Tessadori, Federico; Rodriguez-Polanco, Wilmer R; Grubbs, Jeremy; Zhang, Bo; Osmond, Matt; Graham, Gail; Sawyer, Sarah; Conboy, Erin; Vetrini, Francesco; Treat, Kayla; Płoski, Rafal; Pienkowski, Victor Murcia; Kłosowska, Anna; Fieg, Elizabeth; Krier, Joel; Mallebranche, Coralie; Alban, Ziegler; Aldinger, Kimberly A; Ritter, Deborah; Macnamara, Ellen; Sullivan, Bonnie; Herriges, John; [...]Macrocephaly and developmental delay caused by missense variants in RAB5CView onlineSchließen
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Published in: Human Molecular Genetics
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Morleo, Manuela; Venditti, Rossella; Theodorou, Evangelos; Briere, Lauren C.; Rosello, Marion; Tirozzi, Alfonsina; Tammaro, Roberta; Al-Badri, Nour; High, Frances A.; Shi, Jiahai; Putti, Elena; Ferrante, Luigi; Cetrangolo, Viviana; Torella, Annalaura; Walker, Melissa A.; Tenconi, Romano; Iascone, Maria; Mei, Davide; Guerrini, Renzo; van der Smagt, Jasper; Kroes, Hester Y.; van Gassen, Koen L.I.; Bilal, Muhammad; Umair, Muhammad; [...]De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signalingView onlineSchließen
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Published in: The American Journal of Human Genetics