Publications by authors named "Jamie Fisher"

15Publications

Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.

Authors:
Fabiola P Monteiro Cynthia J Curry Robert Hevner Stephen Elliott Jamie H Fisher John Turocy William B Dobyns Larissa A Costa Erika Freitas João Paulo Kitajima Fernando Kok

Eur J Med Genet 2020 Jan 25;63(1):103624. Epub 2019 Jan 25.

Mendelics Genomic Analysis, CEP 04013-000, São Paulo, SP, Brazil; Neurogenetics, Neurology Department, Hospital das Clínicas da Universidade de São Paulo, São Paulo, SP, Brazil. Electronic address:

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January 2020

Discovering Molecules That Regulate Efferocytosis Using Primary Human Macrophages and High Content Imaging.

Authors:
Sandra Santulli-Marotto Alexis Gervais Jamie Fisher Brandy Strake Carol Anne Ogden Chelsea Riveley Jill Giles-Komar

PLoS One 2015 16;10(12):e0145078. Epub 2015 Dec 16.

Janssen Research & Development, LLC, 1400 Welsh & McKean Rds., Spring House, PA, 19477, United States of America.

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June 2016

A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.

Authors:
Julien L Marcadier Alan J Mears Elizabeth A Woods Jamie Fisher Cory Airheart Wen Qin Chandree L Beaulieu David A Dyment A Micheil Innes Cynthia J Curry

Am J Med Genet A 2016 Jan 16;170A(1):11-8. Epub 2015 Sep 16.

Genetic Medicine Central California, Fresno, California.

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January 2016

Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome.

Authors:
Angela Myers Jonathan A Bernstein Marie-Luise Brennan Cynthia Curry Edward D Esplin Jamie Fisher Margaret Homeyer Melanie A Manning Eric A Muller Anna-Kaisa Niemi Laurie H Seaver Susan R Hintz Louanne Hudgins

Am J Med Genet A 2014 Nov 22;164A(11):2814-21. Epub 2014 Sep 22.

Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, California.

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November 2014

Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28.

Authors:
Karen W Gripp Cynthia Curry Ann Haskins Olney Claudio Sandoval Jamie Fisher Jessica Xiao-Ling Chong Lisa Pilchman Rebecca Sahraoui Deborah L Stabley Katia Sol-Church

Am J Med Genet A 2014 Sep 18;164A(9):2240-9. Epub 2014 Jun 18.

Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, Delaware.

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September 2014

IgG variable region and VH CDR3 diversity in unimmunized mice analyzed by massively parallel sequencing.

Authors:
Jin Lu Tadas Panavas Kim Thys Jeroen Aerssens Michael Naso Jamie Fisher Michael Rycyzyn Raymond W Sweet

Mol Immunol 2014 Feb 8;57(2):274-83. Epub 2013 Nov 8.

Biologics Research, 1400 McKean Road, Spring House, PA 19477, United States.

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February 2014

Surrogate antibodies that specifically bind and neutralize CCL17 but not CCL22.

Authors:
Sandra Santulli-Marotto Jamie Fisher Theodore Petley Ken Boakye Tadas Panavas Jennifer Luongo Karl Kavalkovich Michael Rycyzyn Bingyuan Wu Lester Gutshall Ana Coelho Cory M Hogaboam Mary Ryan

Monoclon Antib Immunodiagn Immunother 2013 Jun;32(3):162-71

Janssen Research & Development, Radnor, Pennsylvania 19087, USA.

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June 2013

Investigation of NRXN1 deletions: clinical and molecular characterization.

Authors:
Mindy Preston Dabell Jill A Rosenfeld Patricia Bader Luis F Escobar Dima El-Khechen Stephanie E Vallee Mary Beth Palko Dinulos Cynthia Curry Jamie Fisher Raymond Tervo Mark C Hannibal Kiana Siefkas Philip R Wyatt Lauren Hughes Rosemarie Smith Sara Ellingwood Yves Lacassie Tracy Stroud Sandra A Farrell Pedro A Sanchez-Lara Linda M Randolph Dmitriy Niyazov Cathy A Stevens Cheri Schoonveld David Skidmore Sara MacKay Judith H Miles Manikum Moodley Adam Huillet Nicholas J Neill Jay W Ellison Blake C Ballif Lisa G Shaffer

Am J Med Genet A 2013 Apr 12;161A(4):717-31. Epub 2013 Mar 12.

Signature Genomic Laboratories, PerkinElmer, Inc., Spokane, WA, USA.

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April 2013

Sherlock Holmes and the strange case of the missing attribution: a historical note on "The Grandfather Passage".

Authors:
Jamie Reilly Jamie L Fisher

J Speech Lang Hear Res 2012 Feb;55(1):84-8

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February 2012

Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.

Authors:
Jill A Rosenfeld Dina Amrom Eva Andermann Frederick Andermann Martin Veilleux Cynthia Curry Jamie Fisher Stephen Deputy Arthur S Aylsworth Cynthia M Powell Kandamurugu Manickam Bryce Heese Melissa Maisenbacher Cathy Stevens Jay W Ellison Sheila Upton John Moeschler Wilfredo Torres-Martinez Abby Stevens Robert Marion Elaine Maria Pereira Melanie Babcock Bernice Morrow Trilochan Sahoo Allen N Lamb Blake C Ballif Alex R Paciorkowski Lisa G Shaffer

Neurogenetics 2012 Feb 5;13(1):31-47. Epub 2012 Jan 5.

Signature Genomic Laboratories, PerkinElmer, Inc., 2820 N. Astor St., Spokane, WA 99207, USA.

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February 2012

Generation and characterization of rat anti-mouse ST2L monoclonal antibodies.

Authors:
Natalie Fursov Erin Johnston Karen Duffy Adam Cotty Theodore Petley Jamie Fisher Haiyan Jiang Michael A Rycyzyn Jill Giles-Komar Gordon Powers

Hybridoma (Larchmt) 2011 Apr;30(2):153-62

Biologics Research, Centocor, Radnor, Pennsylvania, USA.

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April 2011

Novel antagonist antibody to TLR3 blocks poly(I:C)-induced inflammation in vivo and in vitro.

Authors:
Rachel A Bunting Karen E Duffy Roberta J Lamb Lani R San Mateo Karen Smalley Holly Raymond Xuesong Liu Ted Petley Jamie Fisher Heena Beck Richard A Flavell Lena Alexopoulou Christine K Ward

Cell Immunol 2011 2;267(1):9-16. Epub 2010 Nov 2.

Immunology Discovery Department, Centocor Research & Development, Inc., Radnor, PA, USA.

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February 2011

The use of an anti-CD40 agonist monoclonal antibody during immunizations enhances hybridoma generation.

Authors:
Michael A Rycyzyn Kimberly Staquet Jamie Fisher Gregory Bannish Ashlyn Bassiri Cindy Duchala Jill Giles-Komar

Hybridoma (Larchmt) 2008 Feb;27(1):25-30

Department of Cellular Biology, Centocor R&D, Inc., Radnor, Pennsylvania 19087, USA.

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February 2008

Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.

Authors:
Annika M Svensson Cynthia J Curry Sarah T South Heidi Whitby Teresa M Maxwell Emily Aston Jamie Fisher C E Carmack Alicia Scheffer Aimee Abu-Shamsieh Arthur R Brothman

Am J Med Genet A 2007 Jun;143A(12):1348-53

Cytogenetics Laboratory, Department of Pediatrics, University of Utah, Salt Lake City, UT 84132-2117, USA.

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June 2007

A rapid and efficient method for generating anti-variable region monoclonal antibodies using type-1 interferons as immune modulators.

Authors:
Kimberly Staquet Jamie Fisher Roberta Lamb Gregory Bannish Cynthia Duchala M Lamine Mbow Michael A Rycyzyn Jill Giles-Komar

Hum Antibodies 2006 ;15(3):61-9

Centocor Research & Development Inc., 145 King of Prussia Rd., Radnor, PA 19087, USA.

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January 2007