Lehoczky JA and Tabin CJ. (2018) Rethinking WNT signaling.  Nature, 557(7706):495-496. [News & Views] Pubmed

Lehoczky JA (2017) Are fingernails a key to unlocking the puzzle of mammalian limb regeneration?  Experimental Dermatology, 19(4):417-418. [Viewpoint] Pubmed

Lehoczky JA (2016) Digit tip regeneration and beyond: Schwann cell progenitors to the rescue. Cell Stem Cell, 19(4):417-418.  [Preview]  Elsevier

Lehoczky JA and Tabin CJ. (2015) Lgr6 marks nail stem cells and is required for digit tip regeneration. PNAS, 112(43):13249-54.  PubMed

Lehoczky JA and Tabin CJ. (2013) Advances in understanding limb regeneration in a developmental and evolutionary context. in “Advances in Evolutionary Developmental Biology.” J.T. Streelman, ed. John Wiley and Sons. Hoboken, NJ.  [Book Chapter]  Wiley

Lehoczky JA, Thomas PE, Patrie KM, Owens KM, et al. (2013) A novel intergenic ETnII-B insertion mutation causes multiple malformations in Polypodia mice. PLoS Genetics, 9(12):e1003967.  PubMed

Whited JL*, Lehoczky JA*, and Tabin CJ. (2012) Inducible genetic system for the axolotl. PNAS, 109(34):13662-7. (* equal contribution)  PubMed

Lehoczky JA, Robert B, and Tabin CJ. (2011) Mouse digit tip regeneration is mediated by fate-restricted progenitor cells. PNAS, 108(51):20609-14.  PubMed

Whited JL, Lehoczky JA, Austin CA, and Tabin CJ. (2011) Dynamic expression of two thrombospondins during axolotl limb regeneration. Developmental Dynamics, 240(5):1249-58.  PubMed

Persampieri J, Ritter D, Lees D, Lehoczky J, Li Q, Guo S, and Chuang JH. (2008) cneViewer: a database of conserved noncoding elements for studies of tissue-specific gene regulation. Bioinformatics, 24(20):2418-9.  PubMed

Lehoczky JA and Innis JW. (2008) Homopolymeric amino acid tracts emerged early in the mammalian lineage: analysis of monotreme N-terminal HOXA13. Evolution & Development, 10(4):433-8.  PubMed

Lehoczky JA and Innis JW. (2008) BAC transgenic analysis reveals enhancers sufficient for Hoxa13 and neighborhood gene expression in mouse embryonic distal limbs and genital bud. Evolution & Development, 10(4):421-32.  PubMed

Lehoczky JA and Innis JW. (2007) A mouse transgene drives embryonic dorsal posterior commissure expression. Transgenic Research, 16(6):823-8.  PubMed

Lehoczky JA, Cai WW, Douglas JA, Moran JL, Beier DR, and Innis JW. (2006) Description and genetic mapping of Polypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations. Mammalian Genome, 17(9):903-13.  PubMed

Williams ME, Lehoczky JA, and Innis JW. (2006) A group 13 homeodomain is neither necessary nor sufficient for posterior prevalence in the mouse limb. Developmental Biology, 297(2):493-507.  PubMed

Zody MC, et al. (2006) DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. Nature, 440 (7087):1045-9.  PubMed

Nusbaum C, et al. (2005) DNA sequence and analysis of human chromosome 18. Nature. 437(7058):551-5.  PubMed

Lehoczky JA, Williams ME, and Innis JW. (2004) Conserved expression domains among genes upstream of HoxA and HoxD clusters suggests global gene enhancers existed prior to cluster duplication. Evolution & Development, 6(6):423-30.  PubMed

Askew DJ, Askew YS, Kato Y, Turner RF, Dewar K, Lehoczky J, Silverman GA. (2004) Comparative genomic analysis of the clade B serpin cluster at human chromosome 18q21: amplification within the mouse squamous cell carcinoma antigen gene locus. Genomics, 84(1):176-84.  PubMed

Wechsler SB, Lehoczky JA, Hall JG, and Innis JW. (2004) Tibial aplasia, lower extremity mirror image polydactyly, brachyphalangy, craniofacial dysmorphism and genital hypoplasia: further delineation and mutational analysis. Clinical Dysmorphology, 13(2):63-9.  PubMed

Keegan CE, Vilain E, Mohammed M, Lehoczky J, Dobyns WB, Archer SM, and Innis JW. (2004) Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal. American Journal of Medical Genetics, 125A(3):293-8.  PubMed

Liu S, Lu W, Obara T, Kuida S, Lehoczky J, Dewar K, Drummond IA, and Beier DR. (2002) A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish. Development, 129(24):5839-46.  PubMed

Stojanovic N, Chang JL, Lehoczky J, Zody MC, and Dewar K. (2002) Identification of mixups among DNA sequencing plates. Bioinformatics, 18(11):1418-26.  PubMed

Park SS, Stankiewicz P, Bi W, Shaw C, Lehoczky J, Dewar K, Birren B, and Lupski JR. (2002) Structure and evolution of the Smith-Magenis Syndrome repeat gene clusters, SMS-REPs. Genome Research, 12(5):729-38.  PubMed

Askew YS, Pak SC, Luke CJ, Askew DJ, Cataltepe S, Mills DR, Kato H, Lehoczky J, Dewar K, Birren B, and Silverman GA. (2001) SERPINB12 is a novel member of the human ov-serpin family that is widely expressed and inhibits trypsin-like serine proteinases. J. Biol. Chem., 276(52):49320-30.  PubMed

Watters J, Dewar K, Lehoczky J, Boyartchuk V, and Dietrich W. (2001) Kif1C, a kinesin-like motor protein, mediates mouse macrophage resistance to anthrax lethal factor. Current Biology, 11(19):1503-11.  PubMed

Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, Kann L, Lehoczky J, et al. (2001) Initial sequencing and analysis of the human genome. Nature, 409(6822):860-921.  PubMed

Miyoshi K, Cui Y, Riedlinger G, Robinson P, Lehoczky J, Zon L, Oka T, Dewar K, and Hennighausen L. (2000) Structure of the mouse Stat 3/5 locus, evolution from Drosophila to zebrafish to mouse. Genomics, 71(2):150-55.  PubMed

Onyango P, Miller W, Lehoczky J, Leung C, Birren B, Wheelan S, Dewar K, and Feinberg A. (2000) Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain. Genome Research, 10(11):1697-1710.  PubMed

Wiltshire T, Pletcher M, Cole S, Villanueva M, Birren B, Lehoczky J, Dewar K, and Reeves R. (1999) Perfect conserved linkage across the entire mouse chromosome 10 region homologous to human chromosome 21. Genome Research, 9(12):1214-22.  PubMed