Publications by authors named "Jamie Fisher"

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Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.
Fabiola P Monteiro, Cynthia J Curry, Robert Hevner, Stephen Elliott, Jamie H Fisher

Eur J Med Genet· January 2020

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Discovering Molecules That Regulate Efferocytosis Using Primary Human Macrophages and High Content Imaging.
Sandra Santulli-Marotto, Alexis Gervais, Jamie Fisher, Brandy Strake, Carol Anne Ogden

PLoS One· June 2016

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A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.
Julien L Marcadier, Alan J Mears, Elizabeth A Woods, Jamie Fisher, Cory Airheart

Am J Med Genet A· January 2016

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Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome.
Angela Myers, Jonathan A Bernstein, Marie-Luise Brennan, Cynthia Curry, Edward D Esplin, Jamie Fisher

Am J Med Genet A· November 2014

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Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28.
Karen W Gripp, Cynthia Curry, Ann Haskins Olney, Claudio Sandoval, Jamie Fisher

Am J Med Genet A· September 2014

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IgG variable region and VH CDR3 diversity in unimmunized mice analyzed by massively parallel sequencing.
Jin Lu, Tadas Panavas, Kim Thys, Jeroen Aerssens, Michael Naso, Jamie Fisher

Mol Immunol· February 2014

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Surrogate antibodies that specifically bind and neutralize CCL17 but not CCL22.
Sandra Santulli-Marotto, Jamie Fisher, Theodore Petley, Ken Boakye, Tadas Panavas

Monoclon Antib Immunodiagn Immunother· June 2013

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Investigation of NRXN1 deletions: clinical and molecular characterization.
Mindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, Luis F Escobar, Dima El-Khechen, Jamie Fisher

Am J Med Genet A· April 2013

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Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.
Jill A Rosenfeld, Dina Amrom, Eva Andermann, Frederick Andermann, Martin Veilleux, Jamie Fisher

Neurogenetics· February 2012

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Sherlock Holmes and the strange case of the missing attribution: a historical note on "The Grandfather Passage".
Jamie Reilly, Jamie L Fisher

J Speech Lang Hear Res· February 2012

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Generation and characterization of rat anti-mouse ST2L monoclonal antibodies.
Natalie Fursov, Erin Johnston, Karen Duffy, Adam Cotty, Theodore Petley, Jamie Fisher

Hybridoma (Larchmt)· April 2011

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Novel antagonist antibody to TLR3 blocks poly(I:C)-induced inflammation in vivo and in vitro.
Rachel A Bunting, Karen E Duffy, Roberta J Lamb, Lani R San Mateo, Karen Smalley, Jamie Fisher

Cell Immunol· February 2011

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The use of an anti-CD40 agonist monoclonal antibody during immunizations enhances hybridoma generation.
Michael A Rycyzyn, Kimberly Staquet, Jamie Fisher, Gregory Bannish, Ashlyn Bassiri

Hybridoma (Larchmt)· February 2008

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Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.
Annika M Svensson, Cynthia J Curry, Sarah T South, Heidi Whitby, Teresa M Maxwell, Jamie Fisher

Am J Med Genet A· June 2007

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A rapid and efficient method for generating anti-variable region monoclonal antibodies using type-1 interferons as immune modulators.
Kimberly Staquet, Jamie Fisher, Roberta Lamb, Gregory Bannish, Cynthia Duchala

Hum Antibodies· January 2007

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