Mathematics for the analysis of algorithms

por Greene, Daniel H, Knuth, Donald Ervin
Publicado 1982

Mathematics for the analysis of algorithms

por Greene, Daniel H, Knuth, Donald Ervin
Publicado 1990

Mathematics for the analysis of algorithms

por Greene, Daniel H, Knuth, Donald Ervin
Publicado 1981

Phenotype Similarity Regression for Identifying the Genetic Determinants of Rare Diseases

por Greene, Daniel, Richardson, Sylvia, Turro, Ernest
Publicado 2016

ontologyX: a suite of R packages for working with ontological data

por Greene, Daniel, Richardson, Sylvia, Turro, Ernest
Publicado 2017

A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases

por Greene, Daniel, Richardson, Sylvia, Turro, Ernest
Publicado 2017

Motivating Proactive Biorisk Management

por Greene, Daniel, Palmer, Megan J., Relman, David A.
Publicado 2023

Comparison of Optical Coherence Tomography Findings in a Patient with Central Retinal Artery Occlusion in One Eye and End-stage Glaucoma in the Fellow Eye

por Greene, Daniel P., Richards, Charles P., Ghazi, Nicola G.
Publicado 2012

Climate effects on nesting phenology in Nebraska turtles

por Hedrick, Ashley R., Greene, Daniel U., Lewis, Erin L., Hood, Andrew S., Iverson, John B.
Publicado 2021

A comparison of animal color measurements using a commercially available digital color sensor and photograph analysis

por Potash, Alex D, Greene, Daniel U, Foursa, Gabrielle A, Mathis, Verity L, Conner, L Mike, McCleery, Robert A
Publicado 2020

Interactive effects of severe drought and grazing on the life history cycle of a bioindicator species

por Fritts, Sarah Rebecah, Grisham, Blake A., Cox, Robert D., Boal, Clint W., Haukos, David A., McDaniel, Patricia, Hagen, Christian A., Greene, Daniel U.
Publicado 2018

A novel missense variant in SLC18A2 causes recessive brain monoamine vesicular transport disease and absent serotonin in platelets

por Padmakumar, Manisha, Jaeken, Jaak, Ramaekers, Vincent, Lagae, Lieven, Greene, Daniel, Thys, Chantal, Van Geet, Chris, BioResource, NIHR, Stirrups, Kathleen, Downes, Kate, Turro, Ernest, Freson, Kathleen
Publicado 2019

MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases

por Ratnaike, Thiloka E, Greene, Daniel, Wei, Wei, Sanchis-Juan, Alba, Schon, Katherine R, van den Ameele, Jelle, Raymond, Lucy, Horvath, Rita, Turro, Ernest, Chinnery, Patrick F
Publicado 2021

Effectiveness of a 16-Week High-Intensity Cardioresistance Training Program in Adults

por Greenlee, Tina A., Greene, Daniel R., Ward, Nathan J., Reeser, Ginger E., Allen, Courtney M., Baumgartner, Nicholas W., Cohen, Neal J., Kramer, Arthur F., Hillman, Charles H., Barbey, Aron K.
Publicado 2017

Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia

por Bariana, Tadbir K., Labarque, Veerle, Heremans, Jessica, Thys, Chantal, De Reys, Mara, Greene, Daniel, Jenkins, Benjamin, Grassi, Luigi, Seyres, Denis, Burden, Frances, Whitehorn, Deborah, Shamardina, Olga, Papadia, Sofia, Gomez, Keith, BioResource, NIHR, Van Geet, Chris, Koulman, Albert, Ouwehand, Willem H., Ghevaert, Cedric, Frontini, Mattia, Turro, Ernest, Freson, Kathleen
Publicado 2019

Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function

por Chan, Melissa V., Hayman, Melissa A., Sivapalaratnam, Suthesh, Crescente, Marilena, Allan, Harriet E., Edin, Matthew L., Zeldin, Darryl C., Milne, Ginger L., Stephens, Jonathan, Greene, Daniel, Hanif, Moghees, O’Donnell, Valerie B., Dong, Liang, Malkowski, Michael G., Lentaigne, Claire, Wedderburn, Katherine, Stubbs, Matthew, Downes, Kate, Ouwehand, Willem H., Turro, Ernest, Hart, Daniel P., Freson, Kathleen, Laffan, Michael A., Warner, Timothy D.
Publicado 2020

Genetic association analysis of 77,539 genomes reveals rare disease etiologies

por Greene, Daniel, Pirri, Daniela, Frudd, Karen, Sackey, Ege, Al-Owain, Mohammed, Giese, Arnaud P. J., Ramzan, Khushnooda, Riaz, Sehar, Yamanaka, Itaru, Boeckx, Nele, Thys, Chantal, Gelb, Bruce D., Brennan, Paul, Hartill, Verity, Harvengt, Julie, Kosho, Tomoki, Mansour, Sahar, Masuno, Mitsuo, Ohata, Takako, Stewart, Helen, Taibah, Khalid, Turner, Claire L. S., Imtiaz, Faiqa, Riazuddin, Saima, Morisaki, Takayuki, Ostergaard, Pia, Loeys, Bart L., Morisaki, Hiroko, Ahmed, Zubair M., Birdsey, Graeme M., Freson, Kathleen, Mumford, Andrew, Turro, Ernest
Publicado 2023

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

por Tuijnenburg, Paul, Lango Allen, Hana, Burns, Siobhan O., Greene, Daniel, Jansen, Machiel H., Staples, Emily, Stephens, Jonathan, Carss, Keren J., Biasci, Daniele, Baxendale, Helen, Thomas, Moira, Chandra, Anita, Kiani-Alikhan, Sorena, Longhurst, Hilary J., Seneviratne, Suranjith L., Oksenhendler, Eric, Simeoni, Ilenia, de Bree, Godelieve J., Tool, Anton T.J., van Leeuwen, Ester M.M., Ebberink, Eduard H.T.M., Meijer, Alexander B., Tuna, Salih, Whitehorn, Deborah, Brown, Matthew, Turro, Ernest, Thrasher, Adrian J., Smith, Kenneth G.C., Thaventhiran, James E., Kuijpers, Taco W.
Publicado 2018

Next‐generation sequencing for the diagnosis of MYH9‐RD: Predicting pathogenic variants

por Bury, Loredana, Megy, Karyn, Stephens, Jonathan C., Grassi, Luigi, Greene, Daniel, Gleadall, Nick, Althaus, Karina, Allsup, David, Bariana, Tadbir K., Bonduel, Mariana, Butta, Nora V., Collins, Peter, Curry, Nicola, Deevi, Sri V. V., Downes, Kate, Duarte, Daniel, Elliott, Kim, Falcinelli, Emanuela, Furie, Bruce, Keeling, David, Lambert, Michele P., Linger, Rachel, Mangles, Sarah, Mapeta, Rutendo, Millar, Carolyn M., Penkett, Christopher, Perry, David J., Stirrups, Kathleen E., Turro, Ernest, Westbury, Sarah K., Wu, John, BioResource, NIHR, Gomez, Keith, Freson, Kathleen, Ouwehand, Willem H., Gresele, Paolo, Simeoni, Ilenia
Publicado 2019