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Sherlock Holmes and the Strange Case of the Missing Attribution: A Historical Note on "The Grandfather Passage"

Journal of speech, language, and hearing research, 2012-02, Vol.55 (1), p.84-88

2012

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

European journal of medical genetics, 2020-01, Vol.63 (1), p.103624-103624, Article 103624

2020

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Perinatal features of the RASopathies: Noonan syndrome, Cardiofaciocutaneous syndrome and Costello syndrome

American journal of medical genetics. Part A, 2014-11, Vol.164A (11), p.2814-2821

2014

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Ecstasy Inside the Lines

Harvard review (Cambridge, Mass. 1992), 2024-01 (61), p.36-191

Fisher, Jamie

2024

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

PloS one, 2015-12, Vol.10 (12), p.e0145078-e0145078

2015

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Ecstasy Inside the Lines

Harvard review (Cambridge, Mass. 1992), 2022-06 (61), p.36

Fisher, Jamie

2022

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An item response theory and factor analytic examination of two prominent maximizing tendency scales

Judgment and Decision Making, 2012-09, Vol.7 (5), p.644-658

2012

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Woman in a Picture Hat, Looking out into the Water.(Short story)

The Literary review (Teaneck), 2016-09, Vol.59 (4), p.96

Fisher, Jamie

2016

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

American journal of medical genetics. Part A, 2014-09, Vol.164A (9), p.2240-2249

2014

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Generation and characterization of rat anti-mouse ST2L monoclonal antibodies

Hybridoma (2005), 2011-04, Vol.30 (2), p.153-162

2011

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

Molecular immunology, 2014-02, Vol.57 (2), p.274-283

2014

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Investigation of NRXN1 deletions: Clinical and molecular characterization

American journal of medical genetics. Part A, 2013-04, Vol.161A (4), p.717-731

2013

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

American journal of medical genetics. Part A, 2016-01, Vol.170A (1), p.11-18

2016

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An Analysis of Paper-Based Assessment vs. Computer-Based Assessment: A Quantitative Inferential Research Study

Fisher, Jamie M

2018

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Threshold Effects of Landscape Structure on Biological Control in Agroecosystems

Ecological applications, 2002-02, Vol.12 (1), p.52-65

2002

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Effects of interferon-a and interferon-b on development of antigen-specific B cells and hybridoma generation (38.28)

The Journal of immunology (1950), 2009-04, Vol.182 (1_Supplement), p.38-38.28

2009

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Discovering Molecules That Regulate Efferocytosis Using Primary Human Macrophages and High Content Imaging: e0145078

PloS one, 2015-12, Vol.10 (12)

2015

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

Cellular immunology, 2011, Vol.267 (1), p.9-16

2011

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Tri-occurrence of attenuated familial adenomatous polyposis, Lynch syndrome, and hereditary breast and ovarian cancer: A case report with implications for treatment and surveillance

Meta Gene, 2022-02, Vol.31, p.101001, Article 101001

2022

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Surrogate antibodies that specifically bind and neutralize CCL17 but not CCL22

Monoclonal antibodies in immunodiagnosis and immunotherapy, 2013-06, Vol.32 (3), p.162-171

2013

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Complex Syntax Production in Preschool Teacher Talk

Fisher, Jamie D

2013

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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

American journal of medical genetics. Part A, 2007-06, Vol.143A (12), p.1348-1353

2007

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A Tale of Young Flames, and Their Dark Futures, After a Coup: Fiction

New York Times (Online), 2024-04-27

Fisher, Jamie

2024

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The High-Risk Feat of Bringing ‘American Born Chinese’ to TV

New York Times (Online), 2023-05-24

Fisher, Jamie

2023

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Sherlock Holmes and the Strange Case of the Missing Attribution: A Historical Note on "The Grandfather Passage"

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

Perinatal features of the RASopathies: Noonan syndrome, Cardiofaciocutaneous syndrome and Costello syndrome

Ecstasy Inside the Lines

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

Ecstasy Inside the Lines

An item response theory and factor analytic examination of two prominent maximizing tendency scales

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

Woman in a Picture Hat, Looking out into the Water.(Short story)

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

Generation and characterization of rat anti-mouse ST2L monoclonal antibodies

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

Investigation of NRXN1 deletions: Clinical and molecular characterization

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

An Analysis of Paper-Based Assessment vs. Computer-Based Assessment: A Quantitative Inferential Research Study

Threshold Effects of Landscape Structure on Biological Control in Agroecosystems

Effects of interferon-a and interferon-b on development of antigen-specific B cells and hybridoma generation (38.28)

Discovering Molecules That Regulate Efferocytosis Using Primary Human Macrophages and High Content Imaging: e0145078

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

Tri-occurrence of attenuated familial adenomatous polyposis, Lynch syndrome, and hereditary breast and ovarian cancer: A case report with implications for treatment and surveillance

Surrogate antibodies that specifically bind and neutralize CCL17 but not CCL22

Complex Syntax Production in Preschool Teacher Talk

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

A Tale of Young Flames, and Their Dark Futures, After a Coup: Fiction

The High-Risk Feat of Bringing ‘American Born Chinese’ to TV

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