1q21.1 Duplication syndrome and epilepsy: Case report and review

Tekijä Gourari, Ioulia, Schubert, Romaine, Prasad, Aparna
Julkaisussa Neurol Genet (2018)

Anergy in CD4 Memory T Lymphocytes: II. Abrogation of TCR-induced Formation of Membrane Signaling Complexes

Tekijä Lee, William T., Prasad, Aparna, Watson, Andrew R. O.
Julkaistu 2012

The terminal nerve plays a prominent role in GnRH-1 neuronal migration independent from proper olfactory and vomeronasal connections to the olfactory bulbs

Tekijä Taroc, Ed Zandro M., Prasad, Aparna, Lin, Jennifer M., Forni, Paolo E.
Julkaisussa Biol Open (2017)

The First Type III Domain of Fibronectin is Associated with the Expression of Cytokines within the Lung Tumor Microenvironment

Tekijä Zheng, Mingzhe, Jones, David M., Horzempa, Carol, Prasad, Aparna, McKeown-Longo, Paula J.
Julkaistu 2011

Comparative gene expression profiling between optic nerve and spinal cord injury in Xenopus laevis reveals a core set of genes inherent in successful regeneration of vertebrate cen...

Tekijä Belrose, Jamie L., Prasad, Aparna, Sammons, Morgan A., Gibbs, Kurt M., Szaro, Ben G.
Julkaisussa BMC Genomics (2020)

Induction of Purkinje fiber differentiation by coronary arterialization

Tekijä Hyer, Jeanette, Johansen, Mikkel, Prasad, Aparna, Wessels, Andy, Kirby, Margaret L., Gourdie, Robert G., Mikawa, Takashi
Julkaistu 1999

Interpretation errors in focused cardiac ultrasound by novice pediatric emergency medicine fellow sonologists

Tekijä Thomas-Mohtat, Rosemary, Sable, Craig, Breslin, Kristen, Weinberg, Jacqueline G., Prasad, Aparna, Zinns, Lauren, Cohen, Joanna S.
Julkaisussa Crit Ultrasound J (2018)

Markers of Cardiovascular Dysfunction in Adolescents With Anorexia Nervosa

Tekijä Morris, Reshmi, Prasad, Aparna, Asaro, Joseph, Guzman, Marla, Sanders, Leslie, Hauck, Amanda, Singh, Gautam K., Levy, Philip T.
Julkaisussa Glob Pediatr Health (2017)

High resolution radiation hybrid maps of bovine chromosomes 19 and 29: comparison with the bovine genome sequence assembly

Tekijä Prasad, Aparna, Schiex, Thomas, McKay, Stephanie, Murdoch, Brenda, Wang, Zhiquan, Womack, James E, Stothard, Paul, Moore, Stephen S
Julkaistu 2007

Variant detection and the Autism sequencing project

Tekijä Buske, Orion, Dzamba, Misko, Foong, Justin, Lau, Lynette, Fiume, Marc, Marshall, Christian, Walker, Susan, Prasad, Aparna, Brudno, Michael
Julkaistu 2011

Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis

Tekijä Prasad, Aparna, Sdano, Matthew A., Vanzo, Rena J., Mowery-Rushton, Patricia A., Serrano, Moises A., Hensel, Charles H., Wassman, E. Robert
Julkaisussa BMC Med Genet (2018)

The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism

Tekijä Vanzo, Rena J., Prasad, Aparna, Staunch, Lauren, Hensel, Charles H., Serrano, Moises A., Wassman, E. Robert, Kaplun, Alexander, Grandin, Temple, Boles, Richard G.
Julkaisussa J Pers Med (2020)

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Dis...

Tekijä Ho, Karen S., Wassman, E. Robert, Baxter, Adrianne L., Hensel, Charles H., Martin, Megan M., Prasad, Aparna, Twede, Hope, Vanzo, Rena J., Butler, Merlin G.
Julkaisussa Int J Mol Sci (2016)

A 2cM genome-wide scan of European Holstein cattle affected by classical BSE

Tekijä Prasad Aparna, McKay Stephanie, Settles Matthew, Stothard Paul, Laegreid William W, Clawson Michael L, Murdoch Brenda M, Wang Zhiquan, Moore Stephen S, Williams John L
Julkaistu 2010-03-01

A 2cM genome-wide scan of European Holstein cattle affected by classical BSE

Tekijä Murdoch, Brenda M, Clawson, Michael L, Laegreid, William W, Stothard, Paul, Settles, Matthew, McKay, Stephanie, Prasad, Aparna, Wang, Zhiquan, Moore, Stephen S, Williams, John L
Julkaistu 2010

A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder

Tekijä Prasad, Aparna, Merico, Daniele, Thiruvahindrapuram, Bhooma, Wei, John, Lionel, Anath C., Sato, Daisuke, Rickaby, Jessica, Lu, Chao, Szatmari, Peter, Roberts, Wendy, Fernandez, Bridget A., Marshall, Christian R., Hatchwell, Eli, Eis, Peggy S., Scherer, Stephen W.
Julkaistu 2012

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders

Tekijä Wassman, E. Robert, Ho, Karen S., Bertrand, Diana, Davis, Kyle W., Martin, Megan M., Page, Stephanie, Peiffer, Andreas, Prasad, Aparna, Serrano, Moises A., Twede, Hope, Vanzo, Rena, Scherer, Stephen W., Uddin, Mohammed, Hensel, Charles H.
Julkaisussa Neurol Genet (2019)

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

Tekijä Costain, Gregory, Walker, Susan, Argiropoulos, Bob, Baribeau, Danielle A., Bassett, Anne S., Boot, Erik, Devriendt, Koen, Kellam, Barbara, Marshall, Christian R., Prasad, Aparna, Serrano, Moises A., Stavropoulos, D. James, Twede, Hope, Vermeesch, Joris R., Vorstman, Jacob A. S., Scherer, Stephen W.
Julkaisussa J Neurodev Disord (2019)

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

Tekijä Pinto, Dalila, Darvishi, Katayoon, Shi, Xinghua, Rajan, Diana, Rigler, Diane, Fitzgerald, Tom, Lionel, Anath C, Thiruvahindrapuram, Bhooma, MacDonald, Jeffrey R, Mills, Ryan, Prasad, Aparna, Noonan, Kristin, Gribble, Susan, Prigmore, Elena, Donahoe, Patricia K, Smith, Richard S, Park, Ji Hyeon, Hurles, Matthew E, Carter, Nigel P, Lee, Charles, Scherer, Stephen W, Feuk, Lars
Julkaistu 2011

A second generation radiation hybrid map to aid the assembly of the bovine genome sequence

Tekijä Jann, Oliver C, Aerts, Jan, Jones, Michelle, Hastings, Nicola, Law, Andy, McKay, Stephanie, Marques, Elisa, Prasad, Aparna, Yu, Jody, Moore, Stephen S, Floriot, Sandrine, Mahé, Marie-Françoise, Eggen, André, Silveri, Licia, Negrini, Riccardo, Milanesi, Elisabetta, Ajmone-Marsan, Paolo, Valentini, Alessio, Marchitelli, Cinzia, Savarese, Maria C, Janitz, Michal, Herwig, Ralf, Hennig, Steffen, Gorni, Chiara, Connor, Erin E, Sonstegard, Tad S, Smith, Timothy, Drögemüller, Cord, Williams, John L
Julkaistu 2006