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Author Details
Full Name
Kurt N Hetrick
Affiliation
Center for Inherited Disease Research, Johns Hopkins School of Medicine
ORCID
Career Start Year
2007
Papers
24
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36018819
Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men.
Hum Mol Genet
2023
37733366
Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer.
JAMA Oncol
2023
36921087
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.
Am J Respir Crit Care Med
2023
34782259
Complete CFTR gene sequencing in 5,058 individuals with cystic fibrosis informs variant-specific treatment.
J Cyst Fibros
2022
32853339
Germline Sequencing DNA Repair Genes in 5545 Men With Aggressive and Nonaggressive Prostate Cancer.
J Natl Cancer Inst
2021
29859855
Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma.
EBioMedicine
2018
28075488
Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation Sequencing.
Curr Protoc Hum Genet
2017
26239294
Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans.
Mol Psychiatry
2016
26595808
Whole-Exome Sequencing in Familial Parkinson Disease.
JAMA Neurol
2016
27416908
A germline ERBB3 variant is a candidate for predisposition to erythroid MDS/erythroleukemia.
Leukemia
2016
25569433
Assessment of incidental findings in 232 whole-exome sequences from the Baylor-Hopkins Center for Mendelian Genomics.
Genet Med
2015
26166479
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities.
Am J Hum Genet
2015
25803036
Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.
PLoS One
2015
24387990
Mutations in PCYT1A, encoding a key regulator of phosphatidylcholine metabolism, cause spondylometaphyseal dysplasia with cone-rod dystrophy.
Am J Hum Genet
2014
25565926
Novel Deletion of SERPINF1 Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families.
Mol Syndromol
2014
24595103
Mutations in Alström protein impair terminal differentiation of cardiomyocytes.
Nat Commun
2014
22561516
Detectable clonal mosaicism from birth to old age and its relationship to cancer.
Nat Genet
2012
23103226
Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data.
Am J Hum Genet
2012
21478196
Performance assessment of copy number microarray platforms using a spike-in experiment.
Bioinformatics
2011
21829596
Copy number variation in familial Parkinson disease.
PLoS One
2011
19910028
A genome-wide association study on African-ancestry populations for asthma.
J Allergy Clin Immunol
2010
19661241
R/Bioconductor software for Illumina's Infinium whole-genome genotyping BeadChips.
Bioinformatics
2009
20018050
Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data.
BMC Proc
2009
17463248
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Science
2007
1 - 24 of 24
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The Institute of Cancer Research
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