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MOLLY MCLELLAN, DO
DO
Family Medicine Physician
NPI: 1952930216IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
DR.0067195(CO)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 2020
Research & Publications (20)
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation.
PMID 19668202·Nat Methods·2009
8-other
Recurring mutations found by sequencing an acute myeloid leukemia genome.
PMID 19657110·N Engl J Med·2009
5-case
Acquired copy number alterations in adult acute myeloid leukemia genomes.
PMID 19651600·Proc Natl Acad Sci U S A·2009
8-other
VarScan: variant detection in massively parallel sequencing of individual and pooled samples.
PMID 19542151·Bioinformatics·2009
8-other
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome.
PMID 18987736·Nature·2008
8-other
Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma.
PMID 18632602·Cancer Res·2008
7-preclinical
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.
PMID 18628315·J Med Genet·2008
8-other
Somatic mutations and germline sequence variants in the expressed tyrosine kinase genes of patients with de novo acute myeloid leukemia.
PMID 18270328·Blood·2008
8-other
Bacterial community structure of acid-impacted lakes: what controls diversity?
PMID 18245245·Appl Environ Microbiol·2008
8-other
Identification of somatic JAK1 mutations in patients with acute myeloid leukemia.
PMID 18160671·Blood·2008
7-preclinical
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.
PMID 17660820·Nat Genet·2007
8-other
Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia.
PMID 17494858·Blood·2007
3-trial
Mutational analysis of EGFR and related signaling pathway genes in lung adenocarcinomas identifies a novel somatic kinase domain mutation in FGFR4.
PMID 17487277·PLoS One·2007
8-other
PolyScan: an automatic indel and SNP detection approach to the analysis of human resequencing data.
PMID 17416743·Genome Res·2007
8-other
Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome.
PMID 16825992·J Pediatr Hematol Oncol·2006
8-other
Reduced PU.1 expression causes myeloid progenitor expansion and increased leukemia penetrance in mice expressing PML-RARalpha.
PMID 16113082·Proc Natl Acad Sci U S A·2005
7-preclinical
Integration of complementary and alternative medicine in a major pediatric teaching hospital: an initial overview.
PMID 15865507·J Altern Complement Med·2005
8-other
Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
PMID 15815621·Nature·2005
7-preclinical
Comparison of genome degradation in Paratyphi A and Typhi, human-restricted serovars of Salmonella enterica that cause typhoid.
PMID 15531882·Nat Genet·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1025 PENNOCK PL
FORT COLLINS, CO 80524 - Phone
- (970) 495-8800
Quick Facts
- NPI
- 1952930216
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 6
- Publications
- 20
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