Barry Moore

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Hao HuAmazonGeverifieerd e-mailadres voor amazon.com
Chad HuffAssistant Professor of Epidemiology, MD Anderson Cancer CenterGeverifieerd e-mailadres voor mdanderson.org
John F. AtkinsResearch Professor, University College Cork (UCC), IrelandGeverifieerd e-mailadres voor genetics.utah.edu
Karen EilbeckProfessor, Biomedical Informatics, University of UtahGeverifieerd e-mailadres voor genetics.utah.edu
Sofia RobbStowers Institute for Medical ResearchGeverifieerd e-mailadres voor stowers.org
Brandi Cantarel, PhDForm BioGeverifieerd e-mailadres voor formbio.com
Kai WangChildren's Hospital of PhiladelphiaGeverifieerd e-mailadres voor email.chop.edu
Gholson LyonInstitute for Basic Research in Developmental DisabilitiesGeverifieerd e-mailadres voor opwdd.ny.gov
Reid Robison, MD MBABoard-certified Psychiatrist. Co-Founded Genomics (acquired 2016), Polizzi Free Clinic. Board ChairGeverifieerd e-mailadres voor utahresearch.org
Hakon HakonarsonDirector, Center for Applied Genomics, CHOP, UPENNGeverifieerd e-mailadres voor email.chop.edu
Lincoln SteinDirector of Informatics and Biocomputing, Ontario Institute for Cancer Research Geverifieerd e-mailadres voor oicr.on.ca
Colin BatchelorRoyal Society of Chemistry, UKGeverifieerd e-mailadres voor rsc.org
Paul FlicekThe Jackson Laboratory, University of CambridgeGeverifieerd e-mailadres voor jax.org
W. Evan JohnsonProfessor of MedicineGeverifieerd e-mailadres voor rutgers.edu
Pavel Baranov, "Pasha"Professor of Biomolecular Informatics, University College Cork, IrelandGeverifieerd e-mailadres voor ucc.ie
Ivaylo P IvanovNational Institutes of Health, Bethesda, MDGeverifieerd e-mailadres voor nih.gov
Olivier FayetCNRSGeverifieerd e-mailadres voor ibcg.biotoul.fr
Zev N KronenbergPacBioGeverifieerd e-mailadres voor pacb.com
Christopher J MungallLawrence Berkeley National LaboratoryGeverifieerd e-mailadres voor lbl.gov

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Barry Moore

Department of Human Genetics, University of Utah

Geverifieerd e-mailadres voor genetics.utah.edu

Human Medical Genetics Genomics Biomedical Ontologies


Titel Sorteren op citaties Sorteren op jaar Sorteren op titel	Geciteerd door Geciteerd door	Jaar
MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomes BL Cantarel, I Korf, SMC Robb, G Parra, E Ross, B Moore, C Holt, ... Genome research 18 (1), 188-196, 2008	1787	2008
Genome annotation and curation using MAKER and MAKER‐P MS Campbell, C Holt, B Moore, M Yandell Current protocols in bioinformatics 48 (1), 4.11. 1-4.11. 39, 2014	618	2014
Genome sequence of the necrotrophic plant pathogen Pythium ultimum reveals original pathogenicity mechanisms and effector repertoire CA Lévesque, H Brouwer, L Cano, JP Hamilton, C Holt, E Huitema, ... Genome biology 11, 1-22, 2010	422	2010
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency AF Rope, K Wang, R Evjenth, J Xing, JJ Johnston, JJ Swensen, ... The American Journal of Human Genetics 89 (1), 28-43, 2011	281	2011
A probabilistic disease-gene finder for personal genomes M Yandell, C Huff, H Hu, M Singleton, B Moore, J Xing, LB Jorde, ... Genome research 21 (9), 1529-1542, 2011	257	2011
Comparison of approaches for rational siRNA design leading to a new efficient and transparent method O Matveeva, Y Nechipurenko, L Rossi, B Moore, P Sætrom, AY Ogurtsov, ... Nucleic acids research 35 (8), e63, 2007	188	2007
VAAST 2.0: Improved variant classification and disease‐gene identification using a conservation‐controlled amino acid substitution matrix H Hu, CD Huff, B Moore, S Flygare, MG Reese, M Yandell Genetic epidemiology 37 (6), 622-634, 2013	171	2013
The maize mitochondrial genome: dynamic, yet functional C Fauron, M Casper, Y Gao, B Moore TRENDS in Genetics 11 (6), 228-235, 1995	169	1995
Quantitative measures for the management and comparison of annotated genomes K Eilbeck, B Moore, C Holt, M Yandell BMC bioinformatics 10, 1-15, 2009	153	2009
Quadruplet codons: implications for code expansion and the specification of translation step size B Moore, BC Persson, CC Nelson, RF Gesteland, JF Atkins Journal of molecular biology 298 (2), 195-209, 2000	144	2000
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ... Genome biology 15, 1-18, 2014	119	2014
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data H Hu, JC Roach, H Coon, SL Guthery, KV Voelkerding, RL Margraf, ... Nature biotechnology 32 (7), 663-669, 2014	113	2014
A standard variation file format for human genome sequences MG Reese, B Moore, C Batchelor, F Salas, F Cunningham, GT Marth, ... Genome biology 11, 1-9, 2010	108	2010
A functional–1 ribosomal frameshift signal in the human paraneoplastic Ma3 gene NM Wills, B Moore, A Hammer, RF Gesteland, JF Atkins Journal of Biological Chemistry 281 (11), 7082-7088, 2006	96	2006
Coordinated control of senescence by lncRNA and a novel T-box3 co-repressor complex P Kumar P, U Emechebe, R Smith, S Franklin, B Moore, M Yandell, ... Elife 3, e02805, 2014	90	2014
Uteroplacental insufficiency increases visceral adiposity and visceral adipose PPARγ2 expression in male rat offspring prior to the onset of obesity LA Joss-Moore, Y Wang, MS Campbell, B Moore, X Yu, CW Callaway, ... Early Human Development 86 (3), 179-185, 2010	81	2010
Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications GJ Lyon, T Jiang, R Van Wijk, W Wang, PM Bodily, J Xing, L Tian, ... Discovery medicine 12 (62), 41, 2011	80	2011
Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications GJ Lyon, T Jiang, R Van Wijk, W Wang, PM Bodily, J Xing, L Tian, ... Discovery medicine 12 (62), 41, 2011	80	2011
Novel venom peptides from the cone snail Conus pulicarius discovered through next-generation sequencing of its venom duct transcriptome AO Lluisma, BA Milash, B Moore, BM Olivera, PK Bandyopadhyay Marine genomics 5, 43-51, 2012	78	2012
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases FM De La Vega, S Chowdhury, B Moore, E Frise, J McCarthy, ... Genome Medicine 13, 1-19, 2021	68	2021

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