António Manuel Hespanha (1945–2019)
Cardim, Pedro, Schwartz, Stuart B.
Published in The Hispanic American historical review (01.08.2020)
Published in The Hispanic American historical review (01.08.2020)
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Journal Article
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
Mefford, Heather C, Sharp, Andrew J, Baker, Carl, Itsara, Andy, Jiang, Zhaoshi, Buysse, Karen, Huang, Shuwen, Maloney, Viv K, Crolla, John A, Baralle, Diana, Collins, Amanda, Mercer, Catherine, Norga, Koen, de Ravel, Thomy, Devriendt, Koen, Bongers, Ernie M.H.F, de Leeuw, Nicole, Reardon, William, Gimelli, Giorgio, Gimelli, Stefania, Bena, Frederique, Hennekam, Raoul C, Male, Alison, Gaunt, Lorraine, Clayton-Smith, Jill, Simonic, Ingrid, Park, Soo Mi, Mehta, Sarju G, Nik-Zainal, Serena, Woods, C. Geoffrey, Firth, Helen V, Parkin, Georgina, Fichera, Marco, Reitano, Santina, Giudice, Mariangela Lo, Li, Kelly E, Casuga, Iris, Broomer, Adam, Conrad, Bernard, Schwerzmann, Markus, Räber, Lorenz, Gallati, Sabina, Striano, Pasquale, Coppola, Antonietta, Tolmie, John L, Tobias, Edward S, Lilley, Chris, Armengol, Lluis, Spysschaert, Yves, Verloo, Patrick, De Coene, Anja, Goossens, Linde, Mortier, Geert, Speleman, Frank, van Binsbergen, Ellen, Nelen, Marcel R, Hochstenbach, Ron, Poot, Martin, Gallagher, Louise, Gill, Michael, McClellan, Jon, King, Mary-Claire, Regan, Regina, Skinner, Cindy, Stevenson, Roger E, Antonarakis, Stylianos E, Chen, Caifu, Estivill, Xavier, Menten, Björn, Gribble, Susan, Schwartz, Charles E, Schwartz, Stuart, Sutcliffe, James S, Walsh, Tom, Knight, Samantha J.L, Sebat, Jonathan, Romano, Corrado, Veltman, Joris A, de Vries, Bert B.A, Vermeesch, Joris R, Barber, John C.K, Willatt, Lionel, Tassabehji, May, Eichler, Evan E
Published in The New England journal of medicine (16.10.2008)
Published in The New England journal of medicine (16.10.2008)
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Journal Article
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
Burnside, Rachel D., Pasion, Romela, Mikhail, Fady M., Carroll, Andrew J., Robin, Nathaniel H., Youngs, Erin L., Gadi, Inder K., Keitges, Elizabeth, Jaswaney, Vikram L., Papenhausen, Peter R., Potluri, Venkateswara R., Risheg, Hiba, Rush, Brooke, Smith, Janice L., Schwartz, Stuart, Tepperberg, James H., Butler, Merlin G.
Published in Human genetics (01.10.2011)
Published in Human genetics (01.10.2011)
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Journal Article
Assessment of 2q23.1 Microdeletion Syndrome Implicates MBD5 as a Single Causal Locus of Intellectual Disability, Epilepsy, and Autism Spectrum Disorder
Talkowski, Michael E., Mullegama, Sureni V., Rosenfeld, Jill A., van Bon, Bregje W.M., Shen, Yiping, Repnikova, Elena A., Gastier-Foster, Julie, Thrush, Devon Lamb, Kathiresan, Sekar, Ruderfer, Douglas M., Chiang, Colby, Hanscom, Carrie, Ernst, Carl, Lindgren, Amelia M., Morton, Cynthia C., An, Yu, Astbury, Caroline, Brueton, Louise A., Lichtenbelt, Klaske D., Ades, Lesley C., Fichera, Marco, Romano, Corrado, Innis, Jeffrey W., Williams, Charles A., Bartholomew, Dennis, Van Allen, Margot I., Parikh, Aditi, Zhang, Lilei, Wu, Bai-Lin, Pyatt, Robert E., Schwartz, Stuart, Shaffer, Lisa G., de Vries, Bert B.A., Gusella, James F., Elsea, Sarah H.
Published in American journal of human genetics (07.10.2011)
Published in American journal of human genetics (07.10.2011)
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Journal Article
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
Eichler, Evan E, Sharp, Andrew J, Hansen, Sierra, Selzer, Rebecca R, Cheng, Ze, Regan, Regina, Hurst, Jane A, Stewart, Helen, Price, Sue M, Blair, Edward, Hennekam, Raoul C, Fitzpatrick, Carrie A, Segraves, Rick, Richmond, Todd A, Guiver, Cheryl, Albertson, Donna G, Pinkel, Daniel, Eis, Peggy S, Schwartz, Stuart, Knight, Samantha J L
Published in Nature genetics (01.09.2006)
Published in Nature genetics (01.09.2006)
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Journal Article
Segmental Duplications and Copy-Number Variation in the Human Genome
Sharp, Andrew J., Locke, Devin P., McGrath, Sean D., Cheng, Ze, Bailey, Jeffrey A., Vallente, Rhea U., Pertz, Lisa M., Clark, Royden A., Schwartz, Stuart, Segraves, Rick, Oseroff, Vanessa V., Albertson, Donna G., Pinkel, Daniel, Eichler, Evan E.
Published in American journal of human genetics (01.07.2005)
Published in American journal of human genetics (01.07.2005)
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Journal Article
Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant NIPT results
Caldwell, Samantha, Sagaser, Katelynn, Nelson, Zoe, Frey, Jennifer, Wardrop, Jenna, Boomer, Theresa, McCullough, Ron, Schwartz, Stuart
Published in American journal of medical genetics. Part A (01.11.2020)
Published in American journal of medical genetics. Part A (01.11.2020)
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Journal Article
Hematologists' barriers and enablers to screening and recruiting patients to a chimeric antigen receptor (CAR) T cell therapy trial: a theory-informed interview study
Castillo, Gisell, Lalu, Manoj, Asad, Sarah, Foster, Madison, Kekre, Natasha, Fergusson, Dean, Hawrysh, Terry, Atkins, Harold, Thavorn, Kednapa, Montroy, Joshua, Schwartz, Stuart, Holt, Robert, Broady, Raewyn, Presseau, Justin
Published in Current controlled trials in cardiovascular medicine (25.03.2021)
Published in Current controlled trials in cardiovascular medicine (25.03.2021)
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Journal Article
An energy-efficient approach to power control and receiver design in wireless data networks
Meshkati, F., Poor, H.V., Schwartz, S.C., Mandayam, N.B.
Published in IEEE transactions on communications (01.11.2005)
Published in IEEE transactions on communications (01.11.2005)
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Journal Article
Navigating choice in the face of uncertainty: using a theory informed qualitative approach to identifying potential patient barriers and enablers to participating in an early phase chimeric antigen receptor T (CAR-T) cell therapy trial
Castillo, Gisell, Lalu, Manoj M, Asad, Sarah, Foster, Madison, Kekre, Natasha, Fergusson, Dean A, Hawrysh, Terry, Atkins, Harold, Thavorn, Kednapa, Montroy, Joshua, Schwartz, Stuart, Holt, Robert A, Broady, Raewyn, Presseau, Justin
Published in BMJ open (19.03.2021)
Published in BMJ open (19.03.2021)
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Journal Article
P571: Detection of isodisomy utilizing SNP microarray: Frequency, ascertainment, and implications
Molinari, Sharon, Williams, Niecy, Phillips, Karen, Haskell, Gloria, Penton, Andrea, Gadi, Inder, Arreola, Alexandra, Schwartz, Stuart
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Assessing spatiotemporal variations of greenness in the Baltimore–Washington corridor area
Tang, Junmei, Chen, Fang, Schwartz, Stuart S.
Published in Landscape and urban planning (15.04.2012)
Published in Landscape and urban planning (15.04.2012)
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Journal Article
Recent Segmental Duplications in the Human Genome
Bailey, Jeffrey A., Gu, Zhiping, Clark, Royden A., Reinert, Knut, Samonte, Rhea V., Schwartz, Stuart, Adams, Mark D., Myers, Eugene W., Li, Peter W., Eichler, Evan E.
Published in Science (American Association for the Advancement of Science) (09.08.2002)
Published in Science (American Association for the Advancement of Science) (09.08.2002)
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Journal Article
Clinical significance and mechanisms associated with segmental UPD
Papenhausen, Peter R, Kelly, Carla A, Harris, Samuel, Caldwell, Samantha, Schwartz, Stuart, Penton, Andrea
Published in Molecular cytogenetics (20.07.2021)
Published in Molecular cytogenetics (20.07.2021)
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Journal Article