Lon Phan

Laboratory of Molecular Growth Regulation, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA

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Papers24 papers

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Database resources of the National Center for Biotechnology Information

Eric W Sayers, Jeffrey Beck,Evan E Bolton, Devon Bourexis, James R Brister,Kathi Canese,Donald C Comeau, Kathryn Funk,Sunghwan Kim, William Klimke,Aron Marchler-Bauer,Melissa Landrum

Nucleic acids research, (2020)

WOSBibtex

iCn3D, a Web-based 3D Viewer for Sharing 1D/2D/3D Representations of Biomolecular Structures

Jiyao Wang,Philippe Youkharibache,Dachuan Zhang,Christopher J Lanczycki,Renata C Geer,Thomas Madej,Lon Phan,Minghong Ward,Shennan Lu,Gabriele H Marchler,Yanli Wang,Stephen H Bryant

BIOINFORMATICS, no. 1 (2019): 131-135

Cited by5WOSEIBibtex

SPDI: Data Model for Variants and Applications at NCBI

J. Bradley Holmes, Eric Moyer,Lon Phan,Donna Maglott,Brandi L. Kattman

bioRxiv, pp.537449-33, (2019)

Cited by4WOSBibtex

iCn3D, a Web-based 3D Viewer for the Visualization of Biomolecular Structure and Sequence Annotation

Jiyao Wang,Philippe Youkharibache,Dachuan Zhang,Christopher J Lanczycki,Renata C Geer, Tom Madej,Lon Phan,Minghong Ward, Shennan Lu,Gabriele H Marchler,Yanli Wang,Stephen H Bryant

bioRxiv, pp.501692-13, (2018)

Bibtex

tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine

Chih-Hsuan Wei,Lon Phan, Juliana Feltz, Rama Maiti,Tim Hefferon,Zhiyong Lu

BIOINFORMATICS, no. 1 (2018): 80-87

Cited by38EIWOSBibtex

The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool

Steven Flygare, Edgar Javier Hernandez,Lon Phan,Barry Moore,Man Li,Anthony Fejes,Hao Hu,Karen Eilbeck,Chad D. Huff,Lynn Jorde,Martin G. Reese,Mark Yandell

BMC Bioinformatics, no. 1 (2018): 57:1-57:13

Cited by10EIWOSBibtex

LitVar: a semantic search engine for linking genomic variant data in PubMed and PMC

Alexis Allot,Yifan Peng,Chih-Hsuan Wei,Kyubum Lee,Lon Phan,Zhiyong Lu

Nucleic acids research, (2018)

Cited by3WOSEIBibtex

Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites

Amrita Roy Choudhury,Tiejun Cheng,Lon Phan,Stephen H. Bryant,Yanli Wang

BIOINFORMATICS, no. 11 (2017): 1621-1629

EIWOSBibtex

dbVar structural variant cluster set for data analysis and variant comparison

Lon Phan, Jeffrey Hsu, Le Quang Minh Tri,Michaela Willi, Tamer Mansour, Yan Kai,John Garner, John Lopez,Ben Busby

F1000Research, (2016): 673

WOSBibtex

A global reference for human genetic variation

Altshuler David M.,Durbin Richard M.,Abecasis Goncalo R.,Bentley David R., Chakravarti Aravinda,Clark Andrew G.,Donnelly Peter,Eichler Evan E.,Flicek Paul,Gabriel Stacey B.,Gibbs Richard A.,Green Eric D.

NATURE, no. 7571 (2015): 68-+

Cited by2788Bibtex

Database resources of the National Center for Biotechnology Information

Zhiyong Lu,Thomas L Madden,Kevin D Clark,Michael Dicuccio, Ilya Dondoshansky,Paul Kitts,S F Krasnov,David Landsman,David J Lipman, Vyacheslav Gorelenkov, M Hoeppner, Melissa K Johnson

Nucleic Acids Research, (2014)

EIBibtex

An integrated map of genetic variation from 1,092 human genomes

NATURE, no. 7422 (2012): 56-65

Cited by5419Bibtex

An integrated map of genetic variation from 1,092 human genomes

Abigail W Bigham,Andrea Angius, Paul Anderson,Hyun Min Kang,Goncalo R Abecasis,Leslie P Michelson, Jeffrey A Rosenfeld,Luke J Tallon, Ankit Maroo, Scott E Devine,Tuuli Lappalainen,Emmanouil T Dermitzakis

Nature, (2012)

Cited by2427Bibtex

The completion of the Mammalian Gene Collection

Gary F. Temple,Daniela S. Gerhard,Rebekah S. Rasooly,Elise A. Feingold,Peter J. Good,Cristen P. Robinson,Allison Mandich,Jeffery G. Derge,Jeanne R. Lewis,Debonny Shoaf,Francis S. Collins,Wonhee Jang

Genome Research, no. 12 (2009): 2324-2333

Cited by93WOSSCOPUSBibtex

The NCBI dbGaP database of genotypes and phenotypes

Matthew D Mailman,Michael Feolo,Yumi Jin,Masato Kimura,Kimberly Tryka,Rinat Bagoutdinov,Luning Hao,Anne Kiang,Justin Paschall,Lon Phan,Natalia Popova,Stephanie Pretel

Nature Genetics, no. 10 (2007): 1181-1186

Cited by776WOSNATUREBibtex

Domains of eIF1A that mediate binding to eIF2, eIF3 and eIF5B and promote ternary complex recruitment in vivo

DeAnne S Olsen,Erin M Savner,Amy Mathew,Fan Zhang,Thanuja Krishnamoorthy,Lon Phan,Alan G Hinnebusch

EMBO JOURNAL, no. 2 (2003): 193.0-204.0

Cited by79WOSBibtex

Sequence variations in the public human genome data reflect a bottlenecked population history

Gabor Marth,Greg Schuler,Raymond Yeh,Ruth Davenport,Richa Agarwala,Deanna Church,Sarah Wheelan,Jonathan Baker,Ming Ward,Michael Kholodov,Lon Phan,Eva Czabarka

Proceedings of the National Academy of Sciences of the United States of America, no. 1 (2003): 376-381

Cited by105WOSBibtex

The structure of single-nucleotide variation in overlapping regions of human genome sequence

G Marth,G Schuler,R Yeh, R Davenport,R Agarwala,D Church, S Wheelan,J Baker,M Ward, M Kholdov,L Phan,H Harpending

ANTHROPOLOGICAL SCIENCE, no. 1.0 (2003): 63-63

Bibtex

Analysis and reconstitution of translation initiation in vitro

Katsura Asano,Lon Phan,Thanuja Krishnamoorthy,Graham D Pavitt,Edith Gomez,Ernest M Hannig,Joseph Nika,Thomas F Donahue,Han-kuei Huang,Alan G Hinnebusch

Methods in Enzymology, (2002): 221-247

Cited by21WOSEIBibtex

Development and characterization of a reconstituted yeast translation initiation system

MIKKEL A. ALGIRE,DAVID MAAG,PETER SAVIO,MICHAEL G. ACKER,SALVADOR Z. TARUN,ALAN B. SACHS,KATSURA ASANO,KLAUS H. NIELSEN,DEANNE S. OLSEN,LON PHAN,ALAN G. HINNEBUSCH,JON R. LORSCH

Rna-a Publication of The Rna Society, no. 3 (2002): 382-397

Cited by9WOSBibtex

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