“Publish or perish”

-Frederick Bieber, Harvard Medical School

(requoted by Charles Lee)


Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, Scherer SW, Lee C. Detection of large-scale variation in the human genome. Nat Genet. 2004 Sep;36(9):949-51.

Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, González JR, Gratacòs M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Zhang J, Armengol L, Conrad DF, Estivill X, *Tyler-Smith C, *Carter NP, Aburatani H, *Lee C, *Jones KW, *Scherer SW, *Hurles ME. Global variation in copy number in the human genome. Nature. 2006 Nov 23;444(7118):444-54. PMCID: PMC2669898 *co-senior author

Lee C, Iafrate AJ, Brothman AR. Copy number variations and clinical cytogenetic diagnosis of constitutional disorders. Nat Genet. 2007 Jul;39(7 Suppl):S48-54.

Perry GH, Dominy NJ, Claw KG, Lee AS, Fiegler H, Redon R, Werner J, Villanea FA, Mountain JL, Misra R, Carter NP, *Lee C, *Stone AC. Diet and the evolution of human amylase gene copy number variation. Nat Genet. 2007 Oct;39(10):1256-60. PMCID: PMC2377015 *co-senior author

Perry GH, Ben-Dor A, Tsalenko A, Sampas N, Rodriguez-Revenga L, Tran CW, Scheffer A, Steinfeld I, Tsang P, Yamada NA, Park HS, Kim JI, Seo JS, Yakhini Z, Laderman S, Bruhn L, Lee C. The fine-scale and complex architecture of human copy-number variation. Am J Hum Genet. 2008 Mar;82(3):685-95. PMCID: PMC2661628

Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, Macarthur DG, Macdonald JR, Onyiah I, Pang AW, Robson S, Stirrups K, Valsesia A, Walter K, Wei J; Wellcome Trust Case Control Consortium, *Tyler-Smith C, *Carter NP, *Lee C, *Scherer SW, *Hurles ME. Origins and functional impact of copy number variation in the human genome. Nature. 2010 Apr 1;464(7289):704-12. PMCID: PMC3330748 *co-senior author

Mills RE, Walter K, Stewart C, Handsaker RE, Chen K, Alkan C, Abyzov A, Yoon SC, Ye K, Cheetham RK, Chinwalla A, Conrad DF, Fu Y, Grubert F, Hajirasouliha I, Hormozdiari F, Iakoucheva LM, Iqbal Z, Kang S, Kidd JM, Konkel MK, Korn J, Khurana E, Kural D, Lam HY, Leng J, Li R, Li Y, Lin CY, Luo R, Mu XJ, Nemesh J, Peckham HE, Rausch T, Scally A, Shi X, Stromberg MP, Stütz AM, Urban AE, Walker JA, Wu J, Zhang Y, Zhang ZD, Batzer MA, Ding L, Marth GT, McVean G, Sebat J, Snyder M, Wang J, Ye K, *Eichler EE, *Gerstein MB, *Hurles ME, *Lee C, *McCarroll SA, *Korbel JO; 1000 Genomes Project. Mapping copy number variation by population-scale genome sequencing. Nature. 2011 Feb 3;470(7332):59-65. PMCID: PMC3077050 *co-senior author

Iskow RC, Gokcumen O, Abyzov A, Malukiewicz J, Zhu Q, Sukumar AT, Pai AA, Mills RE, Habegger L, Cusanovich DA, Rubel MA, Perry GH, Gerstein M, Stone AC, Gilad Y, Lee C. Regulatory element copy number differences shape primate expression profiles. Proc Natl Acad Sci. U S A. 2012 Jul 31;109(31):12656-61. PMCID: PMC3411951

Yang L, Luquette LJ, Gehlenborg N, Xi R, Haseley PS, Hsieh CH, Zhang C, Ren X, Protopopov A, Chin L, Kucherlapati R, Lee C, Park PJ. Diverse mechanisms of somatic structural variations in human cancer genomes. Cell. 2013 May 9;153(4):919-29. PMCID: PMC3704973

Park H, Cho S, Kim H, Na D, Han J, Chae J, Park C, Park O, Min S, Kang J, Choi B, Min J, Kwon J, Suh Y, Kong S, Lee H, Liu E, Kim J, Kim S, *Yang H, *Lee C. Genomic alteration in BCL2L1 and DLC1 contribute to drug sensitivity in gastric cancer. Proc Natl Acad Sci. 2015 Sept.; 112 (40) 12492-12497. PMCID: PMC4603466 *co-senior author

Sudmant PH, Rausch T, Gardner EJ, Handsaker RE, Abyzov A, … , *Mills RE, *Gerstein M, *Bashir A, *Stegle O, *Devine SE, *Lee C, *Eichler EE, *Korbel JO. An integrated map of structural variation in 2,504 human genomes. Nature. 2015 Oct. 1;526 (7571) 75-81. PMCID: PMC4617611 *co-senior author

Zhu Q, High FA, Zhang C, Cereira E, Russell M, Longoni M, Ryan M, Mil-homens A, Bellfy L, Coletti C, Bhayani P, Hila R, Donahoe PK, Lee C. Systematic analysis of copy number variation associated with congenital diaphragmatic hernia. Proc Natl Acad Sci. 2018 May 15;115(20):5247-5252. PMID: 29712845

Chaisson MJP, Sanders AD, Zhao X, Malhotra A, Porubsky D, … , Ye K, Devine SE, Talkowski ME, Mills RE, Marschall T, *Korbel JO, *Eichler EE, *Lee C. Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nat Commun. 2019 Apr 16;10(1):1784 PMID: 30992455 *co-senior author

A complete list of my published work can be found in My Bibliography: