Skip to Main Content
CKG
Home
Home
Home
TKG
Author details
Breadcrumb
Author Details
Full Name
Patrice M Milos
Affiliation
ORCID
Career Start Year
1982
Papers
64
H Index
39
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
27090146
Orthogonal NGS for High Throughput Clinical Diagnostics.
Sci Rep
2016
25100654
Deadenylase depletion protects inherited mRNAs in primordial germ cells.
Development
2014
24658703
Brown fat determination and development from muscle precursor cells by novel action of bone morphogenetic protein 6.
PLoS ONE
2014
23563143
On the importance of small changes in RNA expression.
Methods
2013
23636849
Somatic alterations contributing to metastasis of a castration-resistant prostate cancer.
Hum Mutat
2013
22144202
Profiling of short RNAs using Helicos single-molecule sequencing.
Methods in Molecular Biology
2012
22753024
An in-depth map of polyadenylation sites in cancer.
Nucleic Acids Res
2012
22531001
Genome-wide identification and characterization of replication origins by deep sequencing.
Genome Biol
2012
22820990
Direct sequencing of Arabidopsis thaliana RNA reveals patterns of cleavage and polyadenylation.
Nature Structural and Molecular Biology
2012
22763454
RNA sequencing of pancreatic circulating tumour cells implicates WNT signalling in metastasis.
Nature
2012
21765009
Single-step capture and sequencing of natural DNA for detection of BRCA1 mutations.
Genome Research
2012
21875357
Native molecular state of adeno-associated viral vectors revealed by single-molecule sequencing.
Human Gene Therapy
2012
21552279
Genome-wide mapping of 5-hydroxymethylcytosine in embryonic stem cells.
Nature
2011
21349208
The properties and applications of single-molecule DNA sequencing.
2011
21390249
A comparison of single molecule and amplification based sequencing of cancer transcriptomes.
PLoS One
2011
21431761
RNA sequencing and quantitation using the Helicos Genetic Analysis System.
Methods in Molecular Biology
2011
21431762
Transcriptome profiling using single-molecule direct RNA sequencing.
Methods in Molecular Biology
2011
21431759
Helicos single-molecule sequencing of bacterial genomes.
Methods in Molecular Biology
2011
21191423
RNA sequencing: advances, challenges and opportunities.
Nature Reviews Genetics
2011
21573114
Protocol dependence of sequencing-based gene expression measurements.
PLoS ONE
2011
21957044
Single-molecule direct RNA sequencing without cDNA synthesis.
Wiley interdisciplinary reviews. RNA
2011
20580974
Single-molecule sequencing: sequence methods to enable accurate quantitation.
Methods in Enzymology
2010
21176148
The majority of total nuclear-encoded non-ribosomal RNA in a human cell is 'dark matter' un-annotated RNA.
BMC Biol
2010
21124451
The Lkb1 metabolic sensor maintains haematopoietic stem cell survival.
Nature
2010
21145465
Comprehensive polyadenylation site maps in yeast and human reveal pervasive alternative polyadenylation.
Cell
2010
19946276
Chromatin profiling by directly sequencing small quantities of immunoprecipitated DNA.
Nat Methods
2010
20133332
Digital transcriptome profiling from attomole-level RNA samples.
Genome Res
2010
20639869
Amplification-free digital gene expression profiling from minute cell quantities.
Nat Methods
2010
20671709
New class of gene-termini-associated human RNAs suggests a novel RNA copying mechanism.
Nature
2010
19817551
Emergence of single-molecule sequencing and potential for molecular diagnostic applications.
Expert Review of Molecular Diagnostics
2009
19581875
Quantification of the yeast transcriptome by single-molecule sequencing.
Nature Biotechnology
2009
19776739
Direct RNA sequencing.
Nature
2009
18193046
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.
Nat Genet
2008
18384261
Helicos BioSciences.
Pharmacogenomics
2008
17728769
New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
Nat Genet
2007
17096118
Paraoxonase 2 (PON2) polymorphisms and development of renal dysfunction in type 2 diabetes: UKPDS 76.
Diabetologia
2006
17161064
Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes.
American Heart Journal
2006
16338273
Drug-metabolizing enzymes: evidence for clinical utility of pharmacogenomic tests.
Clin Pharmacol Ther
2005
15939053
CETP polymorphisms associated with HDL cholesterol may differ from those associated with cardiovascular disease.
Atherosclerosis
2005
16103896
An association study of 43 SNPs in 16 candidate genes with atorvastatin response.
Pharmacogenomics Journal
2005
15681846
Cholesteryl ester transfer protein variants have differential stability but uniform inhibition by torcetrapib.
Journal of Biological Chemistry
2005
14984737
Association between single-nucleotide polymorphisms in the endothelial lipase (LIPG) gene and high-density lipoprotein cholesterol levels.
2004
15450208
Highly polymorphic repeat region in the CETP promoter induces unusual DNA structure.
2004
15606999
Emerging strategies and applications of pharmacogenomics.
Human Genomics
2004
15606997
Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels.
Hum Genomics
2004
15324321
Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol.
Clinical Genetics
2004
15522280
Role of a KCNH2 polymorphism (R1047 L) in dofetilide-induced Torsades de Pointes.
Journal of Molecular and Cellular Cardiology
2004
12955294
The serotonin transporter polymorphism, 5HTTLPR, is associated with a faster response time to sertraline in an elderly population with major depressive disorder.
Psychopharmacology
2004
12818401
Polymorphisms in the CETP gene and association with CETP mass and HDL levels.
Atherosclerosis
2003
11741249
CYP2D6 genotyping as an alternative to phenotyping for determination of metabolic status in a clinical trial setting.
2000
1 - 50 of 64
Column Actions
Search
Recommended Authors
Collaborators
Philipp Kapranov
Co-authored papers
9
Christopher Hart
Co-authored papers
5
Kathleen E Steinmann
Co-authored papers
5
Albert B Seymour
Co-authored papers
4
Bino John
University of Pittsburgh School of Medicine
Co-authored papers
3
Stanley Letovsky
Co-authored papers
3
Aviv Regev
Broad Institute of MIT and Harvard
Co-authored papers
3
A P Monaghan
University of Missouri Kansas City School of Medicine
Co-authored papers
3
Kelly A Frazer
University of California, USA Institute for Genomic Medicine
Co-authored papers
3
Nabeel Bardeesy
Massachusetts General Hospital
Co-authored papers
3
David A Hinds
23andMe Inc.
Co-authored papers
2
Sylvain Foissac
Co-authored papers
2
David R Cox
Rinat (Pfizer Inc.)
Co-authored papers
2
Bradley E Bernstein
Broad Institute of MIT and Harvard
Co-authored papers
2
Dennis G Ballinger
Memorial Sloan-Kettering Cancer Center
Co-authored papers
2
Alon Goren
Co-authored papers
2
George Steven Bova
Prostate Cancer Research Center, Tampere University and Tays Cancer Center
Co-authored papers
1
Nicholas Rhind
Co-authored papers
1
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers
1
Francesco Ferrari
Co-authored papers
1
Marcia M Nizzari
Co-authored papers
1
Chad Nusbaum
Co-authored papers
1
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers
1
Francis S Collins
University of Michigan ann arbor
Co-authored papers
1
Chandan Kumar-Sinha
Co-authored papers
1
Stephen T Sherry
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers
1
James Scott
Co-authored papers
1
Timothy J Triche
Center for Epigenetics, Van Andel Research Institute
Co-authored papers
1
Peter Donnelly
University of Oxford
Co-authored papers
1
Xuhong Cao
Michigan Center for Translational Pathology.
Co-authored papers
1
1 - 30