Publications by authors named "Jamie Fisher"

15Publications

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

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.

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

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

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