24/7 Neurocritical Care Nurse Practitioner Coverage Reduced Door-to-Needle Time in Stroke Patients Treated with Tissue Plasminogen Activator

Por Moran, Jennifer L., Nakagawa, Kazuma, Asai, Susan M., Koenig, Matthew A.
Publicado no J Stroke Cerebrovasc Dis (2016)

An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15

Por Fernandez, Liliana, Marchuk, Douglas A., Moran, Jennifer L., Beier, David R., Rockman, Howard A.
Publicado em 2009

De Novo Exon Duplication in a New Allele of Mouse Glra1 (Spasmodic)

Por Holland, Katherine D., Fleming, Michelle T., Cheek, Susannah, Moran, Jennifer L., Beier, David R., Meisler, Miriam H.
Publicado em 2006

A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis

Por Tao, Jianning, Koster, Maranke I., Harrison, Wilbur, Moran, Jennifer L., Beier, David R., Roop, Dennis R., Overbeek, Paul A.
Publicado em 2012

Cholesterol Metabolism Is Required for Intracellular Hedgehog Signal Transduction In Vivo

Por Stottmann, Rolf W., Turbe-Doan, Annick, Tran, Pamela, Kratz, Lisa E., Moran, Jennifer L., Kelley, Richard I., Beier, David R.
Publicado em 2011

Concurrent Lpin1 and Nrcam Mouse Mutations Result in Severe Peripheral Neuropathy with Transitory Hindlimb Paralysis

Por Douglas, Darlene S., Moran, Jennifer L., Bermingham, John R., Chen, Xiang-Jun, Brindley, David N., Soliven, Betty, Beier, David R., Popko, Brian
Publicado em 2009

A family-based study of common polygenic variation and risk of schizophrenia

Por Ruderfer, Douglas M, Kirov, George, Chambert, Kimberly, Moran, Jennifer L, Owen, Michael J, O’Donovan, Michael C, Sklar, Pamela, Purcell, Shaun M
Publicado em 2011

Manic fringe is not required for embryonic development, and fringe family members do not exhibit redundant functions in the axial skeleton, limb, or hindbrain

Por Moran, Jennifer L., Shifley, Emily T., Levorse, John M., Mani, Shyamala, Ostmann, Kristin, Perez-Balaguer, Ariadna, Walker, Dawn M., Vogt, Thomas F., Cole, Susan E.
Publicado em 2009

Latent TGF-β–binding protein 4 modifies muscular dystrophy in mice

Por Heydemann, Ahlke, Ceco, Ermelinda, Lim, Jackie E., Hadhazy, Michele, Ryder, Pearl, Moran, Jennifer L., Beier, David R., Palmer, Abraham A., McNally, Elizabeth M.
Publicado em 2009

Latent TGF-β–binding protein 4 modifies muscular dystrophy in mice

Por Heydemann, Ahlke, Ceco, Ermelinda, Lim, Jackie E., Hadhazy, Michele, Ryder, Pearl, Moran, Jennifer L., Beier, David R., Palmer, Abraham A., McNally, Elizabeth M.
Publicado em 2010

Agouti C57BL/6N embryonic stem cells for mouse genetic resources

Por Pettitt, Stephen J., Liang, Qi, Rairdan, Xin Y., Moran, Jennifer L., Prosser, Haydn M., Beier, David R., Lloyd, Kent, Bradley, Allan, Skarnes, William C.
Publicado em 2009

ENU Mutagenesis in Mice Identifies Candidate Genes For Hypogonadism

Por Weiss, Jeffrey, Hurley, Lisa A., Harris, Rebecca M., Finlayson, Courtney, Tong, Minghan, Fisher, Lisa A., Moran, Jennifer L., Beier, David R., Mason, Christopher, Jameson, J. Larry
Publicado em 2012

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

Por Ruderfer, Douglas M, Lim, Elaine T, Genovese, Giulio, Moran, Jennifer L, Hultman, Christina M, Sullivan, Patrick F, McCarroll, Steven A, Holmans, Peter, Sklar, Pamela, Purcell, Shaun M
Publicado no Eur J Hum Genet (2015)

A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype

Por Dwyer, Noelle D, Manning, Danielle K, Moran, Jennifer L, Mudbhary, Raksha, Fleming, Michael S, Favero, Carlita B, Vock, Vita M, O'Leary, Dennis DM, Walsh, Christopher A, Beier, David R
Publicado em 2011

De novo CNVs in bipolar affective disorder and schizophrenia

Por Georgieva, Lyudmila, Rees, Elliott, Moran, Jennifer L., Chambert, Kimberly D., Milanova, Vihra, Craddock, Nicholas, Purcell, Shaun, Sklar, Pamela, McCarroll, Steven, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Kirov, George
Publicado no Hum Mol Genet (2014)

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia

Por Genovese, Giulio, Fromer, Menachem, Stahl, Eli A., Ruderfer, Douglas M., Chambert, Kimberly, Landén, Mikael, Moran, Jennifer L., Purcell, Shaun M., Sklar, Pamela, Sullivan, Patrick F., Hultman, Christina M., McCarroll, Steven A.
Publicado no Nat Neurosci (2016)

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Por Pocklington, Andrew J., Rees, Elliott, Walters, James T.R., Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter, Moran, Jennifer L., McCarroll, Steven A., Kirov, George, O’Donovan, Michael C., Owen, Michael J.
Publicado no Neuron (2015)

Structural basis of clade-specific HIV-1 neutralization by humanized anti-V3 monoclonal antibody KD-247

Por Kirby, Karen A., Ong, Yee Tsuey, Hachiya, Atsuko, Laughlin, Thomas G., Chiang, Leslie A., Pan, Yun, Moran, Jennifer L., Marchand, Bruno, Singh, Kamalendra, Gallazzi, Fabio, Quinn, Thomas P., Yoshimura, Kazuhisa, Murakami, Toshio, Matsushita, Shuzo, Sarafianos, Stefan G.
Publicado no FASEB J (2015)

Evidence of Common Genetic Overlap Between Schizophrenia and Cognition

Por Hubbard, Leon, Tansey, Katherine E., Rai, Dheeraj, Jones, Peter, Ripke, Stephan, Chambert, Kimberly D., Moran, Jennifer L., McCarroll, Steven A., Linden, David E. J., Owen, Michael J., O’Donovan, Michael C., Walters, James T. R., Zammit, Stanley
Publicado no Schizophr Bull (2016)

Analysis of copy number variations at 15 schizophrenia-associated loci

Por Rees, Elliott, Walters, James T. R., Georgieva, Lyudmila, Isles, Anthony R., Chambert, Kimberly D., Richards, Alexander L., Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O’Donovan, Michael C., Owen, Michael J., Kirov, George
Publicado em 2014