Rong Chen

Получаване на мой собствен потребителски профил

Позовавания

	Всички	От 2018
Позовавания	15871	6874
h-индекс	58	43
i10-индекс	102	86

1500

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1125

20032004200520062007200820092010201120122013201420152016201720182019202020212022202348 81 162 160 238 304 298 450 656 883 1145 1099 1028 1193 1077 1191 1140 1207 1467 1369 487

Публичен достъп

Преглед на всички

74 статии

1 статия

налични

неналични

Въз основа на изисквания при финансирането

Съавтори

Atul J. ButteDirector, Bakar Computational Health Sciences Institute, University of California, San FranciscoПотвърден имейл адрес: ucsf.edu
Li LiSVP Clinical Informatics, Sema4; Assistant Professor, Mount Sinai School of MedicineПотвърден имейл адрес: sema4.com
Eric SchadtProfessor of Genetics and Genomic Sciences, Mount Sinai School of MedicineПотвърден имейл адрес: mssm.edu
Joel DudleyInstitute Director and Associate Professor, Icahn School of Medicine at Mount SinaiПотвърден имейл адрес: mssm.edu
Alexander A MorganKhosla VenturesПотвърден имейл адрес: stanford.edu
Zhiping WengDirector, Professor of Program in Bioinformatics and Integrative Biology, University ofПотвърден имейл адрес: umassmed.edu
Benjamin GlicksbergVP Data Science & Machine Learning, Character Biosciences | Adjunct Professor, Icahn School ofПотвърден имейл адрес: mssm.edu
William OhChief Medical Officer, Prostate Cancer Foundation; Clinical Professor of Medicine, Mount SinaiПотвърден имейл адрес: pcf.org
Minnie SarwalProfessor, UCSF, Stanford UniversityПотвърден имейл адрес: ucsf.edu
Chirag J PatelAssociate Professor of Biomedical Informatics, Harvard UniversityПотвърден имейл адрес: hms.harvard.edu
Julian MintserisHarvard Medical SchoolПотвърден имейл адрес: hms.harvard.edu
Tara SigdelAssoc. Professor, UCSF Medical SchoolПотвърден имейл адрес: ucsf.edu
Keiichi KodamaAssistant Professor of Pediatrics at UCSFПотвърден имейл адрес: ucsf.edu
Michael SnyderStanford UniversityПотвърден имейл адрес: stanford.edu
Jörg HakenbergIllumina, Inc.Потвърден имейл адрес: illumina.com
Scott NewmanGeneDxПотвърден имейл адрес: sema4.com
David RuauCSO @ Sensyne HealthПотвърден имейл адрес: cam.ac.uk
Robert P. SebraProfessor, Genetics & Genomic Sciences, Icahn School of Medicine at Mount SinaiПотвърден имейл адрес: mssm.edu
Brian G. PierceAssistant Professor, Department of Cell Biology and Molecular Genetics, IBBR, University of MarylandПотвърден имейл адрес: umd.edu
Euan A. AshleyAssociate Dean, Professor of Medicine, Genetics & Biomedical Data Science, Stanford UniversityПотвърден имейл адрес: stanford.edu

Следене

Rong Chen

Director of Clinical Genome Informatics & Assistant Professor, Mount Sinai School of Medicine

Потвърден имейл адрес: mssm.edu - Начална страница

Precision Medicine Translational Bioinformatics Genomics Big Data NGS


Заглавие Сортиране по цитати Сортиране по година Сортиране по заглавие	Позовавания Позовавания	Година
ZDOCK: an initial‐stage protein‐docking algorithm R Chen, L Li, Z Weng Proteins: Structure, Function, and Bioinformatics 52 (1), 80-87, 2003	1545	2003
Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes R Chen, GI Mias, J Li-Pook-Than, L Jiang, HYK Lam, R Chen, E Miriami, ... Cell 148 (6), 1293-1307, 2012	1300	2012
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, 2010	802	2010
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. SMIII Consortium. Nature Biotechnology 32 (9), 903-914, 2014	773	2014
Clinical assessment incorporating a personal genome EA Ashley, AJ Butte, MT Wheeler, R Chen, TE Klein, FE Dewey, ... The Lancet 375 (9725), 1525-1535, 2010	767	2010
AKI in hospitalized patients with COVID-19 L Chan, K Chaudhary, A Saha, K Chauhan, A Vaid, S Zhao, I Paranjpe, ... Journal of the American Society of Nephrology 32 (1), 151-160, 2021	583	2021
Performance comparison of exome DNA sequencing technologies MJ Clark, R Chen, HYK Lam, KJ Karczewski, R Chen, G Euskirchen, ... Nature Biotechnology, 2011	573	2011
Identification of type 2 diabetes subgroups through topological analysis of patient similarity L Li, WY Cheng, BS Glicksberg, O Gottesman, R Tamler, R Chen, ... Science translational medicine 7 (311), 311ra174-311ra174, 2015	529	2015
Docking unbound proteins using shape complementarity, desolvation, and electrostatics R Chen, Z Weng Proteins: Structure, Function, and Bioinformatics 47 (3), 281-294, 2002	461	2002
RDOCK: refinement of rigid‐body protein docking predictions L Li, R Chen, Z Weng Proteins: Structure, Function, and Bioinformatics 53 (3), 693-707, 2003	370	2003
Network-based elucidation of human disease similarities reveals common functional modules enriched for pluripotent drug targets S Suthram, JT Dudley, AP Chiang, R Chen, TJ Hastie, AJ Butte PLoS computational biology 6 (2), e1000662, 2010	364	2010
Protein–protein docking benchmark 2.0: an update J Mintseris, K Wiehe, B Pierce, R Anderson, R Chen, J Janin, Z Weng Proteins: Structure, Function, and Bioinformatics 60 (2), 214-216, 2005	360	2005
Integrating statistical pair potentials into protein complex prediction J Mintseris, B Pierce, K Wiehe, R Anderson, R Chen, Z Weng Proteins: Structure, Function, and Bioinformatics 69 (3), 511-520, 2007	356	2007
A novel shape complementarity scoring function for protein‐protein docking R Chen, Z Weng Proteins: Structure, Function, and Bioinformatics 51 (3), 397-408, 2003	350	2003
A protein–protein docking benchmark R Chen, J Mintseris, J Janin, Z Weng Proteins: Structure, Function, and Bioinformatics 52 (1), 88-91, 2003	349	2003
Performance comparison of whole-genome sequencing platforms HYK Lam, MJ Clark, R Chen, R Chen, G Natsoulis, M O'Huallachain, ... Nature Biotechnology, 2011	342	2011
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases R Chen, L Shi, J Hakenberg, B Naughton, P Sklar, J Zhang, H Zhou, ... Nature biotechnology 34 (5), 531-538, 2016	322	2016
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway GM Enns, V Shashi, M Bainbridge, MJ Gambello, FR Zahir, T Bast, ... Genetics in Medicine 16 (10), 751-758, 2014	200	2014
Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease association R Chen, EV Davydov, M Sirota, AJ Butte PloS one 5 (10), e13574, 2010	193	2010
Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence FE Dewey, R Chen, SP Cordero, KE Ormond, C Caleshu, KJ Karczewski, ... PLoS Genet 7 (9), e1002280, 2011	155	2011

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