Kyle Walsh

Origins and prevalence of the American Founder Mutation of MSH2.

Teaching medical interviewing to patients: the other side of the encounter.

Inflammatory mediators of liver ischemia-reperfusion injury.

Properties of a nonlinear version of the stimulus-frequency otoacoustic emission.

Overshoot measured physiologically and psychophysically in the same human ears.

Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism.

Overshoot using very short signal delays.

A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.

Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: a systematic review and meta-analysis.

The emotional journey of women experiencing a breast abnormality.

Attempted replication of 50 reported asthma risk genes identifies a SNP in RAD50 as associated with childhood atopic asthma.

Decreased use of non-steroidal anti-inflammatory drugs for the treatment of juvenile idiopathic arthritis in the era of modern aggressive treatment.

Genetic signatures of exceptional longevity in humans.

Disease risk prediction with rare and common variants.

Cigarette smoking and risk of meningioma: the effect of gender.

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.

Cigarette smoking associated with lung adenocarcinoma in situ in a large case-control study (SFBALCS).

A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation.

Whole-exome sequencing of a pedigree segregating asthma.

Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach.

Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans.

Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans.

Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies.

Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology.

Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: evidence for distinct pathways of gliomagenesis.

Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype.

Peripheral monocyte count is associated with case fatality after intracerebral hemorrhage.

GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL.

The role of KIR genes and their cognate HLA class I ligands in childhood acute lymphoblastic leukemia.

Selective attention reduces physiological noise in the external ear canals of humans. I: auditory attention.

Selective attention reduces physiological noise in the external ear canals of humans. II: visual attention.

Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia.

The epidemiology of glioma in adults: a "state of the science" review.

Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.

Familial gliomas: cases in two pairs of brothers.

Germline mutations in shelterin complex genes are associated with familial glioma.

Survival and low-grade glioma: the emergence of genetic information.

Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children.

Response to "the epidemiology of glioma in adults: a 'state of the science' review".

CDKN2A loss is associated with shortened overall survival in lower-grade (World Health Organization Grades II-III) astrocytomas.

Cancer. The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer.

Changes in otoacoustic emissions during selective auditory and visual attention.

Telomere maintenance and the etiology of adult glioma.

Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors.

Monocyte Count and 30-Day Case Fatality in Intracerebral Hemorrhage.

Response to Letter Regarding Article, "Monocyte Count and 30-Day Case Fatality in Intracerebral Hemorrhage".

A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution.

Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA.

Longer genotypically-estimated leukocyte telomere length is associated with increased adult glioma risk.