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Genetic Testing Utilization in the U.S. Registry for Childhood Interstitial and Diffuse Lung Diseases
Voss, Laura A., Nevel, Rebekah J., Wambach, Jennifer A., Nogee, Lawrence M., Deterding, Robin R., Casey, Alicia M., O'Connor, Michael G., Craven, Daniel I., Taylor, Jane B., Deutsch, Gail H., Tam‐Williams, Jade B., Steffes, Lea C., Brennan, Steven K., Santiago, Maria T., Sadreameli, Sara C., Heras, Andrea F., Powers, Michael R., Popova, Antonia P., Bansal, Manvi, Hamvas, Aaron, Gower, William A., Urrego, Fernando, Young, Lisa R.
Published in Pediatric pulmonology (01.04.2025)
Published in Pediatric pulmonology (01.04.2025)
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Effect of Direct-to-Consumer Genomewide Profiling to Assess Disease Risk
Bloss, Cinnamon S, Schork, Nicholas J, Topol, Eric J
Published in The New England journal of medicine (10.02.2011)
Published in The New England journal of medicine (10.02.2011)
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Celebrity Influence and Identification: A Test of the Angelina Effect
Kosenko, Kami A., Binder, Andrew R., Hurley, Ryan
Published in Journal of health communication (03.03.2016)
Published in Journal of health communication (03.03.2016)
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Evaluation of the prevalence and prospective clinical impact of the JAK2 V617F mutation in coronary patients
Muendlein, Axel, Gasser, Klaus, Kinz, Elena, Stark, Nicole, Leiherer, Andreas, Rein, Philipp, Saely, Christoph H., Grallert, Harald, Peters, Annette, Drexel, Heinz, Lang, Alois H.
Published in American journal of hematology (01.03.2014)
Published in American journal of hematology (01.03.2014)
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Presymptomatic genetic testing in CADASIL
Reyes, S., Kurtz, A., Hervé, D., Tournier-Lasserve, E., Chabriat, H.
Published in Journal of neurology (01.10.2012)
Published in Journal of neurology (01.10.2012)
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Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines
Marcus, Rebecca K., Geurts, Jennifer L., Grzybowski, Jessica A., Turaga, Kiran K., Clark Gamblin, T., Strong, Kimberly A., Johnston, Fabian M.
Published in Familial cancer (01.12.2015)
Published in Familial cancer (01.12.2015)
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Whole-genome sequencing in German clinical practice : Economic impacts of its use in selected areas of application
Plöthner, Marika, Frank, Martin, Graf von der Schulenburg, J-Matthias
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01.02.2017)
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01.02.2017)
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Genetic testing behavior and reporting patterns in electronic medical records for physicians trained in a primary care specialty or subspecialty
Ronquillo, J. G., Li, C., Lester, W. T.
Published in Journal of the American Medical Informatics Association : JAMIA (01.07.2012)
Published in Journal of the American Medical Informatics Association : JAMIA (01.07.2012)
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The use of genetic programming in the analysis of quantitative gene expression profiles for identification of nodal status in bladder cancer
Mitra, Anirban P, Almal, Arpit A, George, Ben, Fry, David W, Lenehan, Peter F, Pagliarulo, Vincenzo, Cote, Richard J, Datar, Ram H, Worzel, William P
Published in BMC cancer (16.06.2006)
Published in BMC cancer (16.06.2006)
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Decreasing uptake of predictive testing for Huntington's disease in a German centre: 12 years' experience (1993–2004)
Bernhardt, Christiane, Schwan, Anne-Marie, Kraus, Peter, Epplen, Joerg Thomas, Kunstmann, Erdmute
Published in European journal of human genetics : EJHG (01.03.2009)
Published in European journal of human genetics : EJHG (01.03.2009)
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Predictive genetic testing for hereditary non‐polyposis colorectal cancer: Uptake and long‐term satisfaction
Aktan‐Collan, Katja, Mecklin, Jukka‐Pekka, Järvinen, Heikki, Nyström‐Lahti, Minna, Peltomäki, Päivi, Söderling, Ismo, Uutela, Antti, de la Chapelle, Albert, Kääriäinen, Helena
Published in International journal of cancer (20.01.2000)
Published in International journal of cancer (20.01.2000)
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