Lab Publications


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* indicates co-authorship
Pre-print

Wojcik GL, Fuchsberger C, Taliun D, Welch R, Martin AR, Shringarpure S, Carlson CS, Abecasis G, Kang HM, Boehnke M, Bustamante CD, Gignoux CR, and Kenny EE. Imputation aware tag SNP selection to improve power for large and multi-ethnic association studies BioRxiv (2017) [BioRxiv]

Daya M, Rafaels N, Chavan S, Johnston HR, Shetty A, Gignoux CR, Boorgula MP, Campbell M, Maul P, Maul T, Vergara C, Levin AM, Wojcik G, Torgerson DG, Ortega VE, Doumatey A, Araujo MI, Avila PC, Bleecker E, Bustamante CD, Caraballo L, Dunston GM, Faruque MU, Ferguson T, Figueiredo C, Ford JG, Gourraud PA, Hansel NN, Hernanadez RD, Herrera-Paz EF, Kenny EE, Knight-Madden J, Kumar R, Lange LA, Lange EM, Lizee A, Mayorga A, Meyeers D, Nicolae DL, O’Connor TD, Oliveria RR, Olopade CO, Olopade O, Qin ZS, Rotimi C, Watson H, Wilks RJ, Williams KL, Wilson JG, Ober C, Burchard EG, Beaty TH, Taub MA, Ruczinski I, Mathias RA and Barnes KC. Genome-wide association study of asthma in individuals of African ancestry reveals novel asthma susceptibility loci. BioRxiv (2017) [BioRxiv]

2017

Belbin GM, Odgis J, Sorokin EP, Yee MC, Kohli S, Glicksberg BS, Gignoux CR, Wojcik GL, Van Vleck T, Jeff JM, Linderman M, Schurmann C, Ruderfer D, Cai X, Merkelson A, Justice AE, Young KL, Graff M, North KE, Peter U, James R, Hindorff L, Kornreich R, Edelmann L, Gottesman O, Stahl EEA, Cho JH, Loos RJF, Bottinger EP, Nadkarni GN, Abul-husn NS, Kenny EE. Genetic Identification of a common collagen disease in Puerto Ricans via identity-by-descent mapping in a health system. eLife 6:e25060 (2017) [BioRxiv][Open access]

Hellwege JN, Jeff JM, Wise LA, Gallagher CS, Wellons M, Hartmann KE, Jones SF, Torstenson ES, Dickinson S, Ruiz-Narváez EA, Rohland N, Allen A, Reich D, Tandon A, Pasaniuc B, Mancuso N, Im HK, Hinds DA, Palmer JR, Rosenberg L, Denny JC, Roden DM, Stewart EA, Morton CC, Kenny EE, Edwards TL, Velez Edwards DR. A multi-stage genome-wide association study of uterine fibroids in African Americans.Hum Genet (2017) Aug 23. doi: 10.1007/s00439-017-1836-1 [Journal]

Johnston HR, Hu Y, Gao J, O’Connor T, Abecasis G, Wojcik G, Gignoux CR, Gourraud PA, Lizee A, Hansen M, Genuario R, Bullis D, Lawley C, Kenny EE, Bustamante CD, Beaty T, Mathias R, Barnes K, Qin Z and CAAPA Consortium. Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome. Sci Reports 7:46398 (2017) [Open access]

Martin AR, Gignoux CR, Walters RK, Wojcik GL, Neale BM, Gravel S, Daly MJ, Bustamante CD, Kenny EE. Human demographic history impacts genetic risk prediction across diverse populations Am J Hum Genet 100(4):635-649 (2017) [Journal]

Nadkarni GN, Galarneau G, Ellis SB, Nadukur R, Zhang J, Scott SA, Schurmann C, Li R, Rasmussen-Torvik LJ, Kho AN, Hayes MG, Pacheco JA, Manolio TA, Chisholm RL, Roden DM, Denny JC, Kenny EE, Bottinger EP. Apolipoprotein L1 variants and blood pressure traits in African Americans. J Am College Cardiol 69(12):1564-1574 (2017) [Journal]

Levin M, Joseph TT, Jeff JM, Nadukuru R, Ellis SB, Bottinger EP, Kenny EE. iGAS: A framework for using electronic intraoperative medical records for genomic discovery. J Biomed Infor 67:80-89 (2017) [Journal]

2016

Bien S, Wojcik GL, Zubair N, Gignoux CR, Martin AR, Kocarnik JM, Martin LW, Buyske S, Haessler J, Walker RW, Cheng I, Graff M, Xia L, Franceschini N, Matise T, James R, Hindorff L, Le Marchand L, North KE, Haiman CA, Peters U, Loos RJ, Kooperberg CL, Bustamante CD, Kenny EE, Carlson CS; PAGE Study. Strategies for enriching variant coverage in candidate disease loci on a multiethnic genotyping array. PLoS One 11(12):e0167758 (2016) [Open Access]

Kessler MD, Yerges-Armstrong L, Taub MA, Shetty AC, Maloney K, Jeng LJ, Ruczinski I, Levin AM, Williams LK, Beaty TH, Mathias RA, Barnes KC; Consortium on Asthma among African-ancestry Populations in the Americas (CAAPA), O’Connor TD. Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry. Nat Commun 11;7:12521 (2016) [Open Access]

Mathias RA, Taub M, O'Connor TD, Fu W, Gignoux C, Vergara C, Torgerson D, Pino-Yanes M, Shringarpure S, Huang L, Rafaels N, Ortega V, Levin AL, Padhukasahasram B, Eng C, Delmy-Aracely Mejia-Mejia, Trevor Ferguson Johnston HR, Qin ZS, Wilson AF, Marrugo J, Lange LA, Kumar R, Avila P, Maria Yazdanbakhsh, Williams LK, Watson H, Ware LB, Olopade S, Oliveira R, Ober C, Nicholae D, Meyers D, Mayorga A, Knight-Madden J, Hartart T, Hansel N, Foreman M, Ford J, Figueiredo C, Faruque M, Georgia M. Dunston, Philip J. Cooper, Luis Caraballo, Esteban G. Burchard, Eugene Bleecker, Barreto M, Araujo M, Herrera-Paz EF, Gietzen K, Grus WE, Bustamante CD, Kenny EE, Bamshad M, Hernandez R, Akey J, Beaty TH, Ruckzinski I, CAAPA, and Kathleen C. Barnes A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome. Nat Commun 11;7:12522 (2016) [Open Access]

Baharian S, Barakatt M, Gignoux CR, Maples BK, Kenny EE, Aldrich M, Bustamante CD and Gravel S. Population structure in African-Americans. PLoS Genet 12(5):e1006059 (2016) [Open Access]

Cooke TF, Yee MC, Muzzio M, Adams A, Bell R, Cornejo OE, Bustamante CD and Kenny EE Genotyping-by-sequencing in human population genetics and methods for correcting genotyping errors PLoS Genet 12(2):e1005631 (2016) [Open Access]

2015

The 1000 Genomes Project. A Global Reference for the Human Genome. (2015) Nature 526:68-74 [Open Access]

Goes FS, McGrath J, Avramopoulos D, Wolyniec P, Pirooznia M, Ruczinski I, Nestadt G, Kenny EE, Vacic V, Peters I, Lencz T, Darvasi A, Mulle JG, Warren ST and Pulver AE. Genome-wide association of schizophrenia in the Ashkenazi Jews. Am J Med Genet B Neuropsychiatr Genet. 168(8):649-59 (2015) [Journal]

Vilhjálmsson BJ, Yang J, Finucane H, Gusev A, Lindström S, Ripke S, Genovese G, Loh PR, Bhatia G, Do R, Hayeck T, Won HH, Schizophrenia Working Group of the Psychiatric Genomics Consortium, the Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) study, Kathiresan S, Pato M, Pato C, Tamimi R, Stahl E, Zaitlen N, Pasaniuc B, Belbin GM, Kenny EE, Schierup MK, De Jager P, Patsopoulos NA, McCarroll S, Daly M, Purcell S, Chasman D, Neale B, Goddard M, Visscher P, Kraft P, Patterson N, Price AL. Modeling linkage disequilibrium increases accuracy of polygenic risk scores. Am J Hum Genet 97(4):576-92 (2015) [ Open Access]

Auer PL, Nalls M, Meschia JF, Worrall BB, Longstreth WT Jr, et al. Rare and Coding Region Genetic Variants Associated with Risk of Ischemic Stroke: The NHLBI Exome Sequence Project. JAMA neurology 72(7):781-8 (2015) [Open Access]

2014

Udler MS, Nadkarni GN, Belbin G, Lotay V, Wyatt C, Gottesman O, Bottinger EP, Kenny EE, Peter I. Effect of Genetic African Ancestry on eGFR and Kidney Disease. (2014) J Am Soc Nephrol ePub ahead of print [Pubmed] [Journal]

Moreno-Estrada A, Gignoux CR, Fernandez-Lopez JC, Zakharia F, Sikora M, Contreras AV, Acuna-Alonzo V, Sandoval K, Eng C, Romero-Hidalgo S, Ortiz-Tello P, Robles V, Kenny EE, Nuno I, Huntsman S, Galanter JM, Via M, Ford JG, Chapela R, Rodriguez-Cintron W, Rodriguez-Santana JR, Romieu I, Sienra JJ, del Rio Navarro B, London S, Garcia-Herrera R, Estrada K, Hidalgo-Miranda A, Jimenez-Sanchez G, Carnevale A, Soberon X, Canizales-Quinteros S, Rangel-Villalobos H, Silva-Zolezzi I, Gonzlez Burchard E and Bustamante CD. The Genetic History and Structure of Mexican Populations. (2014) Science 344(6189):1280-5. [Pubmed] [Journal]

Vacic V, Ozelius LJ, Clarke LJ, Bar-Shira A, Gana-Weisz M, Gurevich T, Gusev A, Kedmi M, Kenny EE, Liu X, Mejia-Santana H, Mirelman A, Raymond D, Saunders-Pullman R, Desnick RJ, Atzmon G, Burns ER, Ostrer H, Hakonarson H, Bergman A, Barzilai N, Darvasi A, Peter I, Guha S, Lencz T, Giladi N, Marder K, Pe’er I, Bressman SB, and Orr-Urtreger A. Genome-wide mapping of identical-by-descent segments in an Ashkenazi Parkinson disease cohort identifies associated haplotypes. (2014) Hum Mol Genet [Pubmed] [Journal-Free]

Martin A, Tse G, Bustamante CD and Kenny EE. Imputation-based assessment of next generation rare exome variant arrays. (2014) Pacific Symp Biocomput 19;241-52 [Pubmed] [Journal-Free]

2013

Gravel S, Zakharia F, Byrnes JK, Muzzio M, Moreno-Estrada A, Rodriguez-Flores JL, Kenny EE, Gignoux CR, Maples BK, Guiblet W, Dutil J, Sandoval K, Bedoya G, The 1000 Genomes Project, Oleksyk TK, Ruiz-Linares A, Burchard EG, Martinez-Cruzado JC, Bustamante CD. Reconstructing Native American Migrations from Whole-genome and Whole-exome Data (2013) PLoS Genet 9(12):1004703 [Pubmed] [Journal-Free]

Khurana E, Fu Y, Colonna V, Mu XJ, Kang HM, Lappalainen T, Sboner A, Lochovsky L, Chen J, Harmanci A, Das J, Abyzov A, Balasubramanian S, Beal K, Chakravarty D, Challis D, Chen Y, Clarke D, Clarke L, Cunningham F, Evani US, Flicek P, Fragoza R, Garrison E, Gibbs R, Gümüş ZH, Herrero J, Kitabayashi N, Kong Y, Lage K, Liluashvili V, Lipkin SM, MacArthur DG, Marth G, Muzny D, Pers TM, Ritchie GRS, Rosenfeld JA, Sisu C, Wei X, Wilson M, Xue Y, Yu F, 1000 Genomes Project Consortium, Dermitzakis ET, Yu H, Rubin M, Tyler-Smith C, Gerstein M, Integrative annotation of variants from 1092 humans: application to cancer genomics. Science 342:6154 [PubMed] [Journal]

Maples B, Gravel S, Kenny EE* and Bustamante CD*. RFMix: A Discriminative Modeling Approach for Rapid and Robust Local-Ancestry Inference. (2013) Am J Hum Genet. (13)00289-9 [PubMed] [Journal] [NRG-highlight] [Software]

Genovese G, Handsaker RE, Li H, Kenny EE and McCarroll SA. Mapping the Human Reference Genome’s Missing Sequence by Three-Way Admixture in Latino Genomes (2013) Am J Hum Genet. 93(3):411-21 [Pubmed] [Journal] [NRG-hightlight] [Science Daily]

Guo DC, Regalado E, Casteel DE, Santos-Cortez RL, Gong L, Kim JJ, Dyack S, Horne SG, Chang G, Jondeau G, Boileau C, Coselli JS, Li Z, Leal SM, Shendure J, Rieder MJ, Bamshad MJ, Nickerson DA; GenTAC Registry Consortium; National Heart, Lung, and Blood Institute Grand Opportunity Exome Sequencing Project, Kim C, Milewicz DM. Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections. (2013) Am J Hum Genet. 93(2):398-404 [PubMed] [Journal]

O'Connor TD, Kiezun A, Bamshad M, Rich SS, Smith JD, Turner E; NHLBIGO Exome Sequencing Project; ESP Population Genetics, Statistical Analysis Working Group, Leal SM, Akey JM. Fine-scale patterns of population stratification confound rare variant association tests. PLoS One. (2013) 8(7):e65834 [PubMed] [Journal-Free]

Johnsen JM, Auer PL, Morrison AC, Jiao S, Wei P, Haessler J, Fox K, McGee SR, Smith JD, Carlson CS, Smith N, Boerwinkle E, Kooperberg C, Nickerson DA, Rich SS, Green D, Peters U, Cushman M, Reiner AP; NHLBI Exome Sequencing Project. Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood. (2013) 122(4):590-7. [PubMed] [Journal-Free]

Faraco J*, Lin L*, Kornum B, Kenny EE, Trynka G, Einen M,Rico T, Lichtner P, Arnulf I, Dauvilliers Y, Lecendreux M, Javidi S, Geisler P, Mayer G, Pizza F, Poli F, Plazzi G, Overeem S, Gert S, Lammers J, Kemlink D, Sonka K, Nevsimalova S, Rouleau G, Desautels A, Montplaisir J, Hor H, Frauscher B, Ehrmann L, Högl B, Jennum P, Bourgin P, Chen W, Concannon P,Thompson S, Damotte V, Fontaine B, Breban M, Gieger C, Klopp N, Deloukas P, Wijmenga C, Hallmayer J, Onengut-Gumuscu S, Rich SS, Winkelmann J and Mignot E. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. (2013) PLoS Genet 9(2):e1003270 [PubMed] [Journal - Free]

Norton N, Li D, Rampersaud E, Morales A, Martin ER, Zuchner S, Guo S, Gonzalez M, Hedges DJ, Robertson PD, Krumm N, Nickerson DA, Hershberger RE; National Heart, Lung, and Blood Institute GO Exome Sequencing Project and the Exome Sequencing Project Family Studies Project Team. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy.Circ Cardiovasc Genet. 2013 Apr;6(2):144-53 [PubMed] [Journal]

Fu W, O'Connor TD, Jun G, Kang HM, Abecasis G, Leal SM, Gabriel S, Altshuler D, Shendure J, Nickerson DA, Bamshad MJ; NHLBI Exome Sequencing Project, Akey JM. Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. (2013) Nature 493(7431):216-20 [Pubmed] [Journal]

2012

McVean and the 1000 Genomes Project Consortium An integrated map of genetic variation from 1,092 human genomes. (2012) Nature 491(7422):56-65 [PubMed] [Journal - Free] [GB-editorial] More...

Boileau C, Guo DC, Hanna N, Regalado ES, Detaint D, Gong L, Varret M, Prakash SK, Li AH, d‘Indy H, Braverman AC, Grandchamp B, Kwartler CS, Gouya L, Santos-Cortez RL, Abifadel M, Leal SM, Muti C, Shendure J, Gross MS, Rieder MJ, Vahanian A, Nickerson DA, Michel JB; National Heart, Lung, and Blood Institute (NHLBI) Go Exome Sequencing Project, Jondeau G, Milewicz DM. TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome. (2012) Nat Genet. 44(8):916-21 [Pubmed] [Journal]

Emond MJ, Louie T, Emerson J, Zhao W, Mathias RA, Knowles MR, Wright FA, Rieder MJ, Tabor HK, Nickerson DA, Barnes KC; National Heart, Lung, and Blood Institute (NHLBI) GO Exome Sequencing Project; Lung GO, Gibson RL, Bamshad MJ.Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis. (2012) Nat Genet. 44(8):886-9 [Pubmed] [Journal]

Tennessen JA*, Bigham AW*, O’Connor TD*, Fu W, Kenny EE, Gravel S, McGee S, Do R, Liu X, Jun G, Kang HM, Jordan D, Leal SM, Gabriel S, Rieder MJ, Abecasis G, Altshuler D, Nickerson DA, Boerwinkle E, Sunyaev S, Bustamante CD, Bamshad MJ, Akey JM, BroadGO, SeattleGO, on behalf of the NHLBI Exome Sequencing Project (2012) Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science 337 6090;64-9 [PubMed] [Journal]

Kenny EE*, Timpson N*, Sikora M, Yee MC, Moreno AE, Stoneking M, Bustamante CD and Myles S (2012) Melanesian blond hair caused by a radical amino acid change in TYRP1 Science 336(6081):554 [Pubmed][Journal - Free]

Kenny EE, Atzmon G, Bergman A, Chowders J, Darvasi A, Desnick JR, Eliakim R, Erazo M, Gregersen P, Hakonarson H, Karban A, Mayer L, McGovern D, Mitchell A, Mulle J, Ostrer H, Ozelius L, Pulver A, Ullman T, Waterman M, Pe’er I, Peters I and Cho J (2012) Genome-wide scan of Ashkenazi Jewish Crohn’s Disease suggest novel susceptibility loci unique to this population PLoS Genet, 8(3);e1002559 [PubMed] [Journal - Free]

2011

Gusev A, Shah MJ, Kenny EE, Ramachandran A, Lowe JK, Salit J, Lee C, Hansen S, Joseph E, Levandowsky E, Pearlstein K, Weaver T, Quynh D, Peckham H, McLaughlin S, Lyons M, Sheth V, Stoffel M, Friedman JM, Breslow JL and Pe’er I (2011) Low-pass genomewide sequencing and variant imputation using identity-by-descent in an isolated human population Genetics, 190(2):679-89 [PubMed] [Journal - Free]

Kenny EE and Bustamante CD (2011) SnapShot: human biomedical genomics Cell 147(1): 248 [PubMed] [Journal]

Gusev A, Kenny EE, Lowe JK, Salit J, Saxena R, Kathiresan S, Altshuler DM, Friedman JM, Breslow JL, Pe’er I.  (2011) DASH: A method for IBD-based haplotype discovery uncovers association to recent variation.  Amer J of Hum Genet 88(6):706-17 [PubMed] [Journal - Free]

Kenny EE, Kim M, Gusev A, Lowe JK, Salit J, Smith JG, Kovvali S, Min Kang H, Newton-Cheh C, Daly M, Stoffel M, Altshuler DM, Friedman JM, Eskin E, Breslow JL and Pe’er I (2011) Increased power of mixed-models facilitates association mapping of 10 loci for metabolic traits in an isolated population Hum Mol Genet 20(4):827-39 [PubMed] [Journal - Free]

2010

Kenny EE Genome-scale genetics: lessons from founder populations. (2010) Ph.D. Thesis, The Rockefeller University [Free Text]

2009

Kenny EE, Gusev A, Riegel K, Lütjohann D, Lowe JK, Salit J, Maller JB, Stoffel M, Daly MJ, Altshuler DM, Friedman JM, Breslow JL, Pe’er I and Sehayek E (2009) Systematic haplotype analysis resolves a complex locus affecting plasma plant sterol levels in a Micronesian Island population Proc Natl Acad Sci 106(33):13886-91 [PubMed] [Journal - Free]

Lowe JK, Maller JB, Pe’er I, Neale BM, Salit J, Kenny EE, Shea JL, Burkhardt R, Ji W, Noel M, Nee Foo J,  Blundell ML, Garcia L, Sullivan ML, Lee HE, Utterman A, Ferdowsian H, Lifton RP, Breslow JL, Stoffel M,  Daly MJ, Altshuler DM, Friedman JM (2009) Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae PLoS Genet 5(2):31000365 [PubMed] [Journal - Free]

Burkhardt R, Kenny EE and Breslow JL (2009) Genome-wide associations and lipid risk factors Current Cardiovascular Lipid Reports 3(1):12-17 [Available on request]

2008 and earlier

Burkhardt R, Kenny EE, Lowe JK, Birkeland A, Josowitz R, Noel M, Salit J, Maller JB, Pe’er I, Daly MJ, Altshuler D, Stoffel M, Friedman JM and Breslow JL (2008) Common SNPs in HMGCR in Micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon 13 ATVB28:11 2078-84 [PubMed] [Journal - Free]

Schwarz EM, Antoshechkin I, Bastiani C, Bieri T, Blasiar D, Canaran P, Chan J, Chen CK, Chen N, Chen WJ, Davis P, Fiedler TJ, Girard L, Harris TW,Kenny EE, Kishore R, Lawson D, Lee R, Müller HM, Nakamura C, Ozersky P, Petcherski A, Rogers A, Spooner W, Tuli MA, Van Auken K, Wang Q, Durbin R, Spieth J, Stein LD, Sternberg PW (2006) Wormbase: better software, richer content. Nucleic Acids Res 1:34 Database issue; D475-8
[PubMed] [Journal]

Chen N, Harris TW, Antoshechkin I, Bastiani C, Bieri T, Blasiar D, Bradnam K, Canaran P, Chan J, Chen CK, Chen WJ, Davis P, Kenny EE, Kishore R, Lawson D, Lee R, Müller HM, Nakamura C, Ozersky P, Petcherski A, Rogers A, Sabo A, Schwarz EM, Van Auken K, Wang Q, Durbin R, Spieth J, Sternberg PW, Stein LD (2005) Wormbase: a comprehensive data resource for Caenorhabditis biology and genomics. Nucleic Acids Res. 1:33 Database issue; D383-9
[PubMed] [Journal - Free]

Müller HM, Kenny EE, Sternberg PW (2004) Textpresso: an ontology-based information retrieval and extraction system for biological literature PLoS Biol 2(11); e309
[PubMed] [Journal - Free]

Harris TW, Chen N, Cunningham F, Tello-Ruiz M, Antoshechkin I, Bastiani C, Bieri T, Blasiar D, Bradnam K, Chan J, Chen CK, Chen WJ, Davis P, Kenny EE, Kishore R, Lawson D, Lee R, Müller HM, Nakamura C, Ozersky P, Petcherski A, Rogers A, Sabo A, Schwarz EM, Van Auken K, Wang Q, Durbin R, Spieth J, Sternberg PW, Stein LD (2004) Wormbase: a multi-species resource for nematode biology and genomics. Nucleic Acids Res. 1:32 Database issue; D411-7
[PubMed] [Journal - Free]

Harris TW, Lee R, Schwarz EM, Bradnam K, Lawson D, Chen W, Chen N, Blasiar D, Kenny EE, Cunningham F,  Kishore R, Chan J, Muller HM,  Petcherski A, Thorisson G, Day A, Bieri T, Rogers A, Chen CK,  Durbin R, Spieth J, Sternberg PW, Stein LD (2003) Wormbase: a cross-species database for comparative genomics. Nucleic Acids Res 1:31(1):133-7
[PubMed] [Journal - Free]

Mayer C, Köher C, Kenny EE, Prusko C, RajBhandary UL (2003) Initiator tRNA: effects of overproduction of aminoacyl-tRNA synthetases, methionyl-tRNA formyltransferase and initiation factor 2 on activity in initiation. Biochemistry 42(17):4787-99 [PubMed] [Journal]