List of works - Michael E. March

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

scientific article

A signaling network stimulated by β2 integrin promotes the polarization of lytic granules in cytotoxic cells

scientific article

ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor

scientific article published on 01 July 2019

Activation, coactivation, and costimulation of resting human natural killer cells

scientific article published on December 2006

Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned.

scientific article published on 21 July 2015

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study

scientific article

Association of novel rare coding variants with juvenile idiopathic arthritis

scientific article published on 06 January 2021

Common variants at 5q33.1 predispose to migraine in African-American children.

scientific article

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

scientific article

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

scientific article published on 30 November 2017

Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells.

scientific article

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

scientific article published on 18 January 2016

Essential role for the C-terminal noncatalytic region of SHIP in FcgammaRIIB1-mediated inhibitory signaling

scientific article

Genetic Underpinnings of Asthma and Related Traits

Genome-wide association study (GWAS) approaches to sleep phenotypes

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

scientific article published on 28 September 2016

Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations

scientific article published on 17 August 2017

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

scientific article

Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients

scientific article published on 02 December 2020

Identification of Target Genes at Juvenile Idiopathic Arthritis GWAS Loci in Human Neutrophils

article

Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy

scientific article

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

scientific article

Novel locus for atopic dermatitis in African Americans and replication in European Americans

scientific article published on 09 November 2018

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

scholarly article by Dong Li published in June 2018

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

scientific article published on 14 January 2020

Recruitment of activation receptors at inhibitory NK cell immune synapses

scientific article

Regulation of the immune response by SHIP.

scientific article

Stress and Bronchodilator Response in Children with Asthma

scientific article published in July 2015

Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion

scientific article published on 8 September 2005

Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant

scientific article

The genetic basis of eosinophilic esophagitis

scientific article published on 11 September 2015

β2 integrin induces TCRζ-Syk-phospholipase C-γ phosphorylation and paxillin-dependent granule polarization in human NK cells

scientific article published on 26 January 2011

List of works by Michael E. March

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

A signaling network stimulated by β2 integrin promotes the polarization of lytic granules in cytotoxic cells

ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor

Activation, coactivation, and costimulation of resting human natural killer cells

Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned.

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study

Association of novel rare coding variants with juvenile idiopathic arthritis

Common variants at 5q33.1 predispose to migraine in African-American children.

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells.

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

Essential role for the C-terminal noncatalytic region of SHIP in FcgammaRIIB1-mediated inhibitory signaling

Genetic Underpinnings of Asthma and Related Traits

Genome-wide association study (GWAS) approaches to sleep phenotypes

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients

Identification of Target Genes at Juvenile Idiopathic Arthritis GWAS Loci in Human Neutrophils

Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

Novel locus for atopic dermatitis in African Americans and replication in European Americans

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Recruitment of activation receptors at inhibitory NK cell immune synapses

Regulation of the immune response by SHIP.

Stress and Bronchodilator Response in Children with Asthma

Synergy among receptors on resting NK cells for the activation of natural cytotoxicity and cytokine secretion

Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant

The genetic basis of eosinophilic esophagitis

β2 integrin induces TCRζ-Syk-phospholipase C-γ phosphorylation and paxillin-dependent granule polarization in human NK cells