Kalen Mc Gowan | Researcher Profile | Sotabase

Career

· Human Resources Generalist, Watchfire2025–

· Office Support Specialist, University of Illinois Urbana-Champaign2021–2025

· Senior Claims Technician, Blue Cross and Blue Shield of Illinois, Montana, New Mexico, Oklahoma & Texas2019–2021

Publications (52)

NALP1 in vitiligo-associated multiple autoimmune disease.

New England Journal of Medicine · 2007

635

cited

Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.

New England Journal of Medicine · 2010

391

cited

Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo

Nature Genetics · 2012

338

cited

Crossinhibitory Activities of Ngn1 and Math1 Allow Specification of Distinct Dorsal Interneurons

Neuron · 2001

324

cited

Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia

Nature Genetics · 2015

287

cited

Resistance Mechanisms to Targeted Therapies in ROS1+ and ALK+ Non–small Cell Lung Cancer

Clinical Cancer Research · 2018

212

cited

NLRP1 haplotypes associated with vitiligo and autoimmunity increase interleukin-1β processing via the NLRP1 inflammasome

Proceedings of the National Academy of Sciences of the United States of America · 2013

207

cited

Early disease onset and increased risk of other autoimmune diseases in familial generalized vitiligo.

Pigment Cell Research · 2005

197

cited

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell–Cell Adhesion Structures

JACC Clinical Electrophysiology · 2018

165

cited

Comparison of Molecular Testing Modalities for Detection of ROS1 Rearrangements in a Cohort of Positive Patient Samples

Journal of Thoracic Oncology · 2017

145

cited

Novel vitiligo susceptibility loci on chromosomes 7 (AIS2) and 8 (AIS3), confirmation of SLEV1 on chromosome 17, and their roles in an autoimmune diathesis.

American Journal of Human Genetics · 2004

123

cited

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy

JACC: Basic to Translational Science · 2016

106

cited

A genomewide screen for generalized vitiligo: confirmation of AIS1 on chromosome 1p31 and evidence for additional susceptibility loci.

American Journal of Human Genetics · 2003

104

cited

Common variants in FOXP1 are associated with generalized vitiligo

Nature Genetics · 2010

104

cited

Stimulation of NeuroD activity by huntingtin and huntingtin-associated proteins HAP1 and MLK2

Proceedings of the National Academy of Sciences of the United States of America · 2003

cited

Role of Titin Missense Variants in Dilated Cardiomyopathy

Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease · 2015

cited

Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.

Journal of Investigative Dermatology · 2010

cited

Clinical and biochemical characterization of four patients with mutations in ECHS1

Orphanet Journal of Rare Diseases · 2015

cited

Mutations in the accessory subunit NDUFB10 result in isolated complex I deficiency and illustrate the critical role of intermembrane space import for complex I holoenzyme assembly

Human Molecular Genetics · 2016

cited

Decreased Levels of BAG3 in a Family With a Rare Variant and in Idiopathic Dilated Cardiomyopathy

Journal of Cellular Physiology · 2014

cited

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