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1. Full Text COPYRIGHT, PRESERVATION, AND ARCHIVES: An Interview with Eric Schwartz
by DAVID PIERCE and Eric Schwartz
Moving image (Minneapolis, Minn.), ISSN 1532-3978, 10/2009, Volume 9, Issue 2, pp. 105 - 148
Copyright laws | Motion picture industry | Archival preservation | Copyrights | Fair use | Libraries | Movies | Archives | Film preservation | Film archives | Copyright | Motion picture film | Schwartz, Eric | Preservation | Interviews | film preservation | copyright | film | dramatic arts | interview
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2. Full Text Copyright, preservation, and archives: an interview with Eric Schwartz
by Pierce, David
Moving image (Minneapolis, Minn.), ISSN 1532-3978, 09/2009, Volume 9, Issue 2, p. 104
Copyright | Television program reviews | Television programs | Social networks
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3. Full Text Making the White man's West
: Whiteness and the creation of the American West
by Pierce, Jason (Jason Eric)
2016, ISBN 1607323958, xxv, 296
Cultural pluralism | British Americans | Race identity | Frontier and pioneer life | West (U.S.) History | Whites | History | Racism | West (U.S.) Race relationsHistory | Social Science | 20th century | West (U.S.) | 19th century | Race relations | British Americans - West (U.S.) - History
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4. Full Text Genome Editing for Inherited Retinal Degenerations
by Pierce, Eric
Ophthalmology (Rochester, Minn.), ISSN 0161-6420, 09/2018, Volume 125, Issue 9, pp. 1431 - 1432
Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Retina | Retinitis Pigmentosa | Retinal Degeneration - genetics | Humans | Gene Editing | Clustered Regularly Interspaced Short Palindromic Repeats
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5. Full Text Development of Transient Simulation Methodologies for Underhood Hot Spot Analysis of a Truck
by Pryor, Joshua, author and Pierce, Matt, author and Fremond, Eric, author and Michou, Yanick, author
SAE technical paper series, Volume 2011-01-0651.
Trucks | Product development | Simulation and modeling
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6. Full Text Performance Measurement of Vehicle Antilock Braking Systems (Abs)
by Khanse, Karan R., author and Pierce, Eric, author and Ng, Michael, author and Taheri, Saied, author
SAE technical paper series, Volume 2015-01-0591.
Performance tests | Measurements | Anti-lock braking
eJournal
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7. Full Text Analysis of protein-coding genetic variation in 60,706 humans
by Lek, M and Karczewski, K.J and Minikel, E.V and Samocha, K.E and Posthuma, D and Exome Aggregation Consortium, [Unknown] and Exome Aggregation Consortium
Nature (London), ISSN 0028-0836, 2016, Volume 536, Issue 7616, pp. 285 - 291
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic aspects | Research | Man | Human beings | Genetic variation | Analysis | Datasets | Proteins | Databases | Disease | Genes | Principal components analysis | Genetics | Genomes | Index Medicus | Medicin och hälsovetenskap
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8. Improving America's schools
: the role of incentives
by Hanushek, Eric A. 1943- (Eric Alan) and Jorgenson, Dale Weldeau, 1933
1996, ISBN 0309054362, viii, 268
Educational change | School improvement programs | School management and organization
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9. Full Text The mutational constraint spectrum quantified from variation in 141,456 humans
by Karczewski, Konrad J and Francioli, Laurent C and Tiao, Grace and Cummings, Beryl B and Alfoldi, Jessica and Wang, Qingbo and Collins, Ryan L and Laricchia, Kristen M and Ganna, Andrea and Birnbaum, Daniel P and Gauthier, Laura D and Brand, Harrison and Solomonson, Matthew and Watts, Nicholas A and Rhodes, Daniel and Singer-Berk, Moriel and England, Eleina M and Seaby, Eleanor G and Kosmicki, Jack A and Walters, Raymond K and Tashman, Katherine and Farjoun, Yossi and Banks, Eric and Poterba, Timothy and Wang, Arcturus and Seed, Cotton and Whiffin, Nicola and Chong, Jessica X and Samocha, Kaitlin E and Pierce-Hoffman, Emma and Zappala, Zachary and O'Donnell-Luria, Anne H and Minikel, Eric Vallabh and Weisburd, Ben and Lek, Monkol and Ware, James S and Vittal, Christopher and Armean, Irina M and Bergelson, Louis and Cibulskis, Kristian and Connolly, Kristen M and Covarrubias, Miguel and Donnelly, Stacey and Ferriera, Steven and Gabriel, Stacey and Gentry, Jeff and Gupta, Namrata and Jeandet, Thibault and Kaplan, Diane and Llanwarne, Christopher and Munshi, Ruchi and Novod, Sam and Petrillo, Nikelle and Roazen, David and Ruano-Rubio, Valentin and Saltzman, Andrea and Schleicher, Molly and Soto, Jose and Tibbetts, Kathleen and Tolonen, Charlotte and Wade, Gordon and Talkowski, Michael E and Neale, Benjamin M and Daly, Mark J and MacArthur, Daniel G and Genome Aggregation Database Consor and Genome Aggregation Database Consortium
Nature (London), ISSN 0028-0836, 05/2020, Volume 581, Issue 7809, pp. 434 - 443
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Gene silencing | Control | Human genome | Gene mutations | Genetic variation | Analysis | Identification and classification | Genomics | Genes | Genetic aspects | Genomes | Nucleotide sequencing | Cells | DNA sequencing | Deactivation | Natural populations | Cardiovascular disease | Biology | Organisms | Agglomeration | Mutation rates | Inactivation | Gene sequencing | Datasets | Proteins | Genetic variance | Annotations | Gene disruption | Quality | Extremely low frequencies | Population | Physiology | Mutation | Index Medicus | Genetik | Biological Sciences | Medicinsk genetik | Basic Medicine | Medical Genetics | Naturvetenskap | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Genetics | Biologi | Natural Sciences
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10. Full Text SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research
by Feliciano, Pamela and Daniels, Amy M and Green Snyder, LeeAnne and Beaumont, Amy and Camba, Alexies and Esler, Amy and Gulsrud, Amanda G and Mason, Andrew and Gutierrez, Anibal and Nicholson, Amy and Paolicelli, Anna Marie and McKenzie, Alexander P and Rachubinski, Angela L and Stephens, Alexandra N and Simon, Andrea R and Stedman, Amy and Shocklee, Amanda D and Swanson, Amy and Finucane, Brenda and Hilscher, Brittani A and Hauf, Brenda and O’Roak, Brian J and McKenna, Brooke and Robertson, Beverly E and Rodriguez, Barbara and Vernoia, Brianna M and Van Metre, Bonnie and Bradley, Catherine and Cohen, Cheryl and Erickson, Craig A and Harkins, Christina and Hayes, Caitlin and Lord, Catherine and Martin, Christa Lese and Ortiz, Crissy and Ochoa-Lubinoff, Cesar and Peura, Christine and Rice, Catherine E and Rosenberg, Cordelia R and Smith, Christopher J and Thomas, Carrie and Taylor, Cora M and White, Loran Casey and Walston, Corrie H and Amaral, David G and Coury, Daniel Lee and Sarver, Dustin E and Istephanous, Dalia and Li, Deana and Nugyen, Dzung Cong and Fox, Emily A and Butter, Eric M and Berry-Kravis, Elizabeth and Courchesne, Eric and Fombonne, Eric J and Hofammann, Eugenia and Lamarche, Elena and Wodka, Ericka L and Matthews, Emily T and O’Connor, Eirene and Palen, Emily and Miller, Fiona and Dichter, Gabriel S and Marzano, Gabriela and Stein, Gail and Hutter, Hanna and Kaplan, Hannah E and Li, Hai and Lechniak, Holly and Schneider, Hoa Lam and Zaydens, Hana and Arriaga, Ivette and Gerdts, Jennifer A and Cubells, Joseph F and Cordova, Jeanette M and Gunderson, Jaclyn and Lillard, Joseph and Manoharan, Julie and McCracken, James T and Michaelson, Jacob J and Neely, Jason and Orobio, Jessica and Pandey, Juhi and Piven, Joseph and Scherr, Jessica and Sutcliffe, James S and Tjernagel, Jennifer and Wallace, Jermel and Callahan, Kristen and Dent, Katherine and Schweers, Kathryn A and Hamer, Kira E and Law, J. Kiely and Lowe, Kathryn and O’Brien, Kaela and Smith, Kaitlin and Pawlowski, Katherine G and Pierce, Karen L and Roeder, Katherine and Abbeduto, Leonard J and ... and The SPARK Consortium and SPARK Consortium and SPARK Consortium. Electronic address: pfeliciano@simonsfoundation.org
Neuron (Cambridge, Mass.), ISSN 0896-6273, 02/2018, Volume 97, Issue 3, pp. 488 - 493
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Autism Spectrum Disorder - genetics | Genetic Predisposition to Disease | Autism Spectrum Disorder - epidemiology | United States | Humans | Biomedical Research | Gene-Environment Interaction | Cohort Studies | Patient Selection | Autism | Family | Congenital diseases | Working groups | Genomics | Genes | Families & family life | Systematic review | Genomes | Research | Environmental risk | Meta-analysis | Studies | Consortia | Researchers | Mutation | Pollutants | Index Medicus
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11. Full Text C3a triggers formation of sub-retinal pigment epithelium deposits via the ubiquitin proteasome pathway
by Fernandez-Godino, Rosario and Pierce, Eric A
Scientific reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 9679 - 14
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Ubiquitin | Complement receptors | Deposits | Complement component C3a | Fetuses | Retina | Epithelium | Retinal pigment epithelium | Gelatinase A | Macular degeneration | Complement activation | Complement component C3 | Collagen | Extracellular matrix | Age
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12. Full Text Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
by Stessman, H.A and Xiong, B and Coe, B.P and Wang, T and Hoekzema, K and Fenckova, M and Kvarnung, M and Gerdts, J and Trinh, S and Cosemans, N and Vives, L and Lin, J and Turner, T.N and Santen, G and Ruivenkamp, C and Kriek, M and Haeringen, A. van and Aten, E and Friend, K and Liebelt, J and Barnett, C and Haan, E and Shaw, M and Gecz, J and Anderlid, B.M and Nordgren, A and Lindstrand, A and Schwartz, C and Kooy, R.F and Vandeweyer, G and Helsmoortel, C and Romano, C and Alberti, A and Vinci, M and Avola, E and Giusto, S and Courchesne, E and Pramparo, T and Pierce, K and Nalabolu, S and Amaral, D.G and Scheffer, I.E and Delatycki, M.B and Lockhart, P.J and Hormozdiari, F and Harich, B and Castells Nobau, A and Xia, K and Peeters, H and Nordenskjold, M and Schenck, A and Bernier, R.A and Eichler, E.E
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 4, pp. 515 - 526
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Autistic Disorder - genetics | Phenotype | Humans | Female | Male | Developmental Disabilities - genetics | Mutation - genetics | Intellectual Disability - genetics | Consortia | Autism | Councils | Intellectual disabilities | Genes | Mutation | Siblings | Index Medicus | Medicin och hälsovetenskap
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