Christophe G. Lambert

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Douglas J. PerkinsProfessor of Medicine, University of New MexicoVerifierad e-postadress på salud.unm.edu
Samuel B. AnyonaMaseno UniversityVerifierad e-postadress på maseno.ac.ke
Evans RaballahSenior Lecturer, Masinde Muliro University of Science and TechnologyVerifierad e-postadress på mmust.ac.ke
Anastasiya NestsiarovichWestchester Medical CenterVerifierad e-postadress på wcmc.com
Professor Collins OumaMaseno UniversityVerifierad e-postadress på maseno.ac.ke
Dr. Elly Ochieng MundeKirinyaga University School of Health Sciences Department of Clinical MedicineVerifierad e-postadress på kyu.ac.ke
Tudor OpreaCEO, Expert Systems IncVerifierad e-postadress på expertsystems.inc
Cristian BologaResearch Professor, University of New MexicoVerifierad e-postadress på salud.unm.edu
Benjamin H McMahonLos Alamos National LaboratoryVerifierad e-postadress på lanl.gov
edward dratzMontana State UniversityVerifierad e-postadress på montana.edu
Annette S. CrisantiAssociate Professor, University of New MexicoVerifierad e-postadress på salud.unm.edu
Stuart J. NelsonClinical Professor, George Washington UniversityVerifierad e-postadress på gwu.edu
Kristan Alexander SchneiderProfessor for Modeling and Simulation, Hochschule MittweidaVerifierad e-postadress på hs-mittweida.de
Nicolas W HengartnerLos Alamos National LaboratoryVerifierad e-postadress på lanl.gov
heidi hammProfessor of PharmacologyVerifierad e-postadress på vanderbilt.edu
Alexandra YinglingResearch Scientist; Center for Global Health, University of New Mexico Health Sciences CenterVerifierad e-postadress på salud.unm.edu
Orrin B. MyersProfessor, University of New MexicoVerifierad e-postadress på salud.unm.edu
Praveen KumarResearch Assistant Professor, University of New MexicoVerifierad e-postadress på unm.edu
Karen HoClene Nanomedicine, IncVerifierad e-postadress på clene.com
Patrick RyanJanssen Research and DevelopmentVerifierad e-postadress på cornell.edu

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Christophe G. Lambert

Professor of Medicine, University of New Mexico; Chairman, Golden Helix

Verifierad e-postadress på unm.edu - Startsida

clinical research informatics bioinformatics machine learning systems thinking human longevity


Titel Sortera efter citat Sortera efter år Sortera efter titel	Citeras av Citeras av	År
The MicroArray Quality Control (MAQC)-II study of common practices for the development and validation of microarray-based predictive models L Shi, G Campbell, WD Jones, F Campagne, Z Wen, SJ Walker, Z Su, ... Nature biotechnology 28 (8), 827-838, 2010	878	2010
Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia T Lencz, C Lambert, P DeRosse, KE Burdick, TV Morgan, JM Kane, ... Proceedings of the National Academy of Sciences 104 (50), 19942-19947, 2007	468	2007
Risk of hydroxychloroquine alone and in combination with azithromycin in the treatment of rheumatoid arthritis: a multinational, retrospective study JCE Lane, J Weaver, K Kostka, T Duarte-Salles, MTF Abrahao, H Alghoul, ... The Lancet Rheumatology 2 (11), e698-e711, 2020	304*	2020
Analysis of a Large Structure/Biological Activity Data Set Using Recursive Partitioning A Rusinko III, MW Farmen, CG Lambert, PL Brown, SS Young J. Chem. Inf. Comput. Sci 39, 1017-1026, 1999	258	1999
NMR structure of a receptor-bound G-protein peptide EA Dratz, JE Furstenau, CG Lambert, DL Thireault, H Rarick, T Schepers, ... Nature 363 (6426), 276-281, 1993	221	1993
Renin–angiotensin system blockers and susceptibility to COVID-19: an international, open science, cohort analysis DR Morales, MM Conover, SC You, N Pratt, K Kostka, T Duarte-Salles, ... The Lancet Digital Health 3 (2), e98-e114, 2021	149	2021
Multipole-based algorithms for efficient calculation of forces and potentials in macroscopic periodic assemblies of particles CG Lambert Duke University, 1994	129	1994
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population N Matsunami, D Hadley, CH Hensel, GB Christensen, C Kim, E Frackelton, ... PloS one 8 (1), e52239, 2013	89	2013
Bipolar disorder and diabetes mellitus: evidence for disease-modifying effects and treatment implications EF Charles, CG Lambert, B Kerner International Journal of Bipolar Disorders 4 (13), 2016	73	2016
Technical reproducibility of genotyping SNP arrays used in genome-wide association studies H Hong, L Xu, J Liu, WD Jones, Z Su, B Ning, R Perkins, W Ge, K Miclaus, ... Public Library of Science 7 (9), e44483, 2012	73	2012
Learning from our GWAS mistakes: from experimental design to scientific method CG Lambert, LJ Black Biostatistics 13 (2), 195-203, 2012	69	2012
Genome-wide association study in bipolar patients stratified by co-morbidity B Kerner, CG Lambert, BO Muthen PLoS One 6 (12), e28477, 2011	66	2011
Bridging islands of information to establish an integrated knowledge base of drugs and health outcomes of interest RD Boyce, PB Ryan, GN Norén, MJ Schuemie, C Reich, J Duke, ... Drug Safety 37 (8), 557-567, 2014	63	2014
Efficient on-line nonparametric kernel density estimation CG Lambert, SE Harrington, CR Harvey, A Glodjo Algorithmica 25, 37-57, 1999	63	1999
Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome KS Ho, ST South, A Lortz, CH Hensel, MR Sdano, RJ Vanzo, MM Martin, ... Journal of Medical Genetics, 2016	56	2016
Mixture deconvolution and analysis of Ames mutagenicity data SS Young, VK Gombar, MR Emptage, NF Cariello, C Lambert Chemometrics and Intelligent Laboratory Systems 60 (1-2), 5-11, 2002	55	2002
Statistical deconvoluting of mixtures MW Farmen, CG Lambert, AR Rusinko III, SS Young US Patent 6,434,542, 2002	51	2002
The MAQC-II Project: A comprehensive study of common practices for the development and validation of microarray-based predictive models. L Shi, G Campbell, W Jones, F Campagne, Z Wen, S Walker, Z Su, T Chu, ... Nature biotechnology 28 (8), 827-838, 2010	50	2010
Hypothyroidism risk compared among nine common bipolar disorder therapies in a large US cohort CG Lambert, AJ Mazurie, NR Lauve, NG Hurwitz, SS Young, ... Bipolar disorders 18 (3), 247-260, 2016	47	2016
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population N Matsunami, CH Hensel, L Baird, J Stevens, B Otterud, T Leppert, ... Molecular Autism 5 (5), 2014	45	2014

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