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R. Lorier · SciRah

Researcher profile · Semantic Scholar

R. Lorier

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R. Lorier — researcher profile on SciRah

h-index: 11
Works: 16
Citations: 973

Most-cited papers

An Autoinflammatory Disease Due to Homozygous Deletion of the IL1RN Locus
Sreelatha T. Reddy, S. Jia, R. Geoffrey, R. Lorier +4 more
2009New England Journal of Medicine396 citations Open access
Semantic Scholar
Characterization of 137 genomic DNA reference materials for 28 pharmacogenetic genes: A GeT-RM collaborative project
V. Pratt, R. Everts, P. Aggarwal, B. N. Beyer +11 more
2015Journal of Molecular Diagnostics138 citations Open access
Semantic Scholar
A Clinician-Driven Automated System for Integration of Pharmacogenetic Consults into an Electronic Medical Record
J. Hicks, K. Crews, James M. Hoffman, Nancy M. Kornegay +13 more
2012Clinical pharmacology and therapy94 citations Open access
Semantic Scholar
IL-10 produced by iTreg cells controls colitis and pathogenic ex-iTreg cells during immunotherapy
Erica G. Schmitt, Dipica Haribhai, Jason B. Williams, P. Aggarwal +13 more
2012Journal of Immunology81 citations Open access
Semantic Scholar
Signal transducer of inflammation gp130 modulates atherosclerosis in mice and man
M. Luchtefeld, H. Schunkert, M. Stoll, Tina Selle +20 more
2007Journal of Experimental Medicine69 citations Open access
Semantic Scholar
RNA Expression Profiling of Human iPSC-Derived Cardiomyocytes in a Cardiac Hypertrophy Model
P. Aggarwal, A. Turner, A. Matter, Steven J. Kattman +5 more
2014PLoS ONE53 citations Open access
Semantic Scholar
Concordance of DMET Plus genotypes with orthogonal genotyping methods
C. A. Fernandez, Colton A. Smith, Wenjian Yang, R. Lorier +10 more
2012Clinical pharmacology and therapy43 citations Open access
Semantic Scholar
Copy Number Variation analysis in 98 individuals with PHACE syndrome
D. Siegel, Joseph T. Shieh, Eun-Kyung Kwon, E. Baselga +24 more
2012Journal of Investigative Dermatology30 citations Open access
Semantic Scholar
Pharmacokinetics and pharmacogenomics of daunorubicin in children: a report from the Children’s Oncology Group
P. Thompson, Heather E. Wheeler, Shannon M. Delaney, R. Lorier +7 more
2014Cancer Chemotherapy and Pharmacology26 citations Open access
Semantic Scholar
Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel–Feil and Treacher Collins syndromes
P. Giampietro, L. Armstrong, A. Stoddard, R. Blank +12 more
2015American Journal of Medical Genetics. Part A15 citations
Semantic Scholar
Donor specific phenotypic variation in hiPSC cardiomyocyte-derived exosomes impacts endothelial cell function.
A. Turner, P. Aggarwal, A. Matter, Benjamin Olson +6 more
2021American Journal of Physiology. Heart and Circulatory Physiology14 citations Open access
Semantic Scholar
Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study
Nathan E. Wineinger, N. Pajewski, Richard E. Kennedy, M. Wojczynski +8 more
2011European Journal of Human Genetics10 citations Open access
Semantic Scholar
A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the XIST Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33)
Jess F. Peterson, Donald G Basel, D. Bick, Brett Chirempes +5 more
2017Journal of Pediatric Genetics4 citations Open access
Semantic Scholar
Abstract 16833: Aberrant Intracellular and Exosomal miRNA Expression in a Human iPSC Derived Cardiomyocyte Model of Left Ventricular Hypertrophy
A. Turner, P. Aggarwal, A. Matter, R. Lorier +5 more
20170 citations
Semantic Scholar
Abstracts
P. Aggarwal, B. N. Beyer, U. Broeckel, R. Epstein-Baak +16 more
2014Journal of Molecular Diagnostics0 citations Open access
Semantic Scholar
Abstract 16717: Human Gene Copy Number Spectra Analysis in Congenital Heart Malformations
A. Tomita-Mitchell, Donna K. Mahnke, C. Struble, Maureen E. Tuffnell +11 more
2011Circulation0 citations
Semantic Scholar

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