Akalal DB, Yu D and Davis RLThe Long-Term Memory Trace Formed in the Drosophila{alpha}/{beta} Mushroom Body Neurons Is Abolished in Long-Term Memory Mutants. J Neurosci .Apr 2011, 31: 5643-7. PMID: 21490205.

Akman HO, Raghavan A and Craigen WJAnimal Models of Glycogen Storage disease. Prog Mol Biol Transl Sci. 2011, 100:369-88. PMID: 21377631.

Akman, HO, Sheiko T, Tay, SK, Finegold, MJ, Dimauro, S, Craigen, WJGeneration of a novel mouse model that recapitulates early and adult onset glycogenosis type IV. Hum Mol Genet Nov 2011, 20(22):4430-9. PMID: 21856731.

Allen EG, Hunter JE, Rusin M, Juncos JL, Novak G, Hamilton D, Shubeck L, Charen K,Sherman SLNeuropsychological findings for 107 older premutation carrier males and their non-carrier siblings from families with fragile X syndrome. Neuropsychology, in press, 2011.

Anderson AE, Karandikar UG, Pepple KL, Chen Z, Bergmann A, and Mardon GThe enhancer of trithorax and polycomb gene Caf1/p55 is essential for cell survival and patterning in Drosophila development. Development Apr 2011 [Epub], 138:1957-66. PMCID: PMC3082301.

Anflous-Pharayra K, Lei N, Armstrong DL and Craigen WJVDAC3 has differing mitochondrial functions in two types of striated muscles. Biochim Biophys Acta Jan 2011, 1807:150-6. PMCID: PMC2998388.

Auffray C, Caulfield T, Khoury MJ, Lupski JR, Schwab M and Veenstra T. Genome medicine: past, present, and future. Genome Med Jan 2011, 3:6. PMID: 21345269.

Bayat V, Jaiswal M and Bellen HJThe BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases. Curr Opn Neurobiol Feb 2011, 21:182-8. PMID 20832291.

Bellen HJ, Levis RW, He Y, Carlson JW, Evans-Holm M, Bae E, Kim J, Metaxakis A, Savakis C, Schulze KL, Hoskins RA, and Spradling AC. The Drosophila gene disruption project: progress using transposons with distinctive site-specificities. Genetics 2011, in press.

Belmont JW, Craigen W, Martinez H and Jefferies JL. Genetic disorders with both hearing loss and cardiovascular abnormalities. Adv Otorhinolaryngol Feb 2011, 70:66-74. PMID: 21358187.

Berens P, Ecker AS, Gerwinn S, Tolias AS, and Bethge M. Reassessing optimal neural population codes with neurometric functions. Proc Natl Acad Sci U S A. 2011 Mar 15;108(11):4423-8. PMID: 21368193.

Boone, PM, Reiter, RJ, Glaze, DG, Tan, DX, Lupski, JR, Potocki, L. Abnormal circadian rhythm of melatonin in Smith-Magenis syndrome patients with RAI1 point mutations. Am J Med Genet Aug 2011;155A(8):2024-7. PMID: 21739587.

Boone PM, Wiszniewski W and Lupski JRGenomic Medicine and Neurologic Disease. Human Genetics 2011, in press.

Brunetti-Pierri N, Pignatelli R, Fouladi N, Towbin JA, Belmont JWCraigen WJ, Wong LJ, Jefferies JL and Scaglia F. Dilation of the root in mitochondrial disease patients. Mol Genet Metab Feb 2011 Epub ahead of print. PMID: 21406331.

Brunetti-Pierri, N*, Lanpher B*, Erez A, Ananieva EA, Islam M, Marini JC, Sun Q, Yu C, Hedge M, Li J, Wynn RM, Chuang CT, Hutson S and Lee BPhenylbutyrate therapy for maple syrup urine disease. Human Molecular Genetics Feb 2011, 20:631-40 (2011). *equal contribution. PMCID: PMC3024040.

Carvalho, CMB, Ramocki, MB, Pehlivan, D, Seaver, L, Friehling, L, Lee, S, del Gaudio, D, Peters, SU, Withers, M, Liu, P, Cheung, SW, Zoghbi, HY, Hastings, P, Lupski, JRInverted genomic segments and complex rearrangements are mediated by inverted repeats in the human genome. Nat Genet Oct 2011, 43:1074-1081. PMID: 21964572.

Carvalho CM, Zhang F and Lupski JRStructural variation of the human genome: mechanisms, assays, and role in male infertility. Syst Biol Reprod Med Feb 2011, 57:3-16. PMID: 21210740.

Chinen J, Martinez-Gallo M M, Gu W, Cols M, Cerutti A, Radigan L, Zhang L, Potocki L, Withers M, Lupski JR and Cunningham-Rundles C. Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndrome. J Allergy Clin Immunol Apr 2011, Epub ahead of print. PMID: 21514638.

Clericuzio C, Harutyunyan K, Jin W, Erickson R, Irvine AD, McLean WH, Wen Y, Bagatelle R, Griffin TA, Shwayder TA, Plon SE and Wang LLIdentification of a Novel C16orf57 Mutation in Athabaskan Patients with Poikiloderma with Neutropenia. Am J Med Genet A Feb 2011,155:337-342. PMCID: PMC3069503.

Cooper ECMade for "anchorin": Kv7.2/7.3 (KCNQ2/KCNQ3) channels and the modulation of neuronal excitability in vertebrate axons. Semin Cell Dev Biol Apr 2011, 22:185-92. PMCID: PMC3070838.

Dettman EJ, Simko SJ, Ayanga B, Carofino BL, Margolin JF, Morse HC 3rd and Justice M. Prdm14 initiates lymphoblastic leukemia after expanding a population of cells resembling common lymphoid progenitors. Oncogene Feb 2011 Epub ahead of print.

Fakhro KA, Choi M, Ware SM, Belmont JW, Towbin JA, Lifton RP, et al. Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning. Proc Natl Acad Sci U S A. Feb 2011, 108:2915-20. PMCID: PMC3041108.

Frost JD. Jr, Lee CL, Hrachovy RA and Swann JWHigh frequency EEG activity associated with Ictal events in an animal model of infantile spasms. Epilepsia Jan 2011 52:53–62. PMID: 21204817

Fruhman G, El-Hattab AW, Belmont JW, Patel A, Cheung SW and Sutton VR. Suspected trisomy 22: Modification, clarification, or confirmation of the diagnosis by aCGH. Am J Med Genet A Feb 2011, 155:434-8. PMID: 21271668.

Fryer, JD, Yu, P, Kang, H, Mandel-Brehm, C, Carter, AN, Crespo-Barreto, J, Gao, Y, Flora, A, Shaw, C, Orr, HT, and Zoghbi, HYExercise and genetic rescue of SCA1 via the transcriptional repressor capicua. Science Nov 2011, 334:690-3. PMID: 22053053.

Gehrking KM, Andresen JM, Duvick L, Lough J, Zoghbi HY and Orr HT. Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model. Hum Mol Genet, Apr 2011 Epub ahead of print. PMID: 21427130.

Grammatikakis I, Goo YH, Echeverria GV and Cooper TAIdentification of MBNL1 and MBNL3 domains required for splicing activation and repression. Nucleic Acids Res Apr 2011 39(7):2769-80. PMCID: PMC3074124.

Gross, C and Bassell, GJExcess protein synthesis in FXS patient lymphoblastoid cells can be rescued with a p110?-selective inhibitor. Molecular Medicine Dec 2011. PMID: 22207187.

Gross, C, Yao, X, Pang, DL and Bassell, GJFragile X Mental Retardation protein regulates protein expression and mRNA translation of the potassium channel, Kv4.2. Journal of Neuroscience Apr 2011, 13;31(15):5693-5698. PMID: 21490210.

Guo, Q, Li, H, Gaddam, SSK, Justice, NJ, Robertson, CS, and Zheng, HAmyloid precursor protein revisited: Neuronal-specific expression and the highly stable nature of soluble derivatives. J Biol Chem 2011, In press. PMID: 22144675.

Guo W, Allan AM, Zong R, Zhang L, Johnson EB, Schaller EG, Murthy AC, Goggin SL, Eisch AJ, Oostra BA, Nelson DL, Jin P and Zhao X. Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning. Nat Med Apr 2011. PMID: 21516088. Epub ahead of print.

Hamilton SM, Spencer CM, Harrison WR, Yuva-Paylor LA, Graham DF, Daza RA, Hevner RF, Overbeek PA, Paylor RMultiple autism-like behaviors in a novel transgenic mouse model. Behav Brain Res. Mar 2011, 218:29-41. PMCID: PMC3022332.

Hawkins SM, Creighton CJ, Han DY, Zariff A, Anderson ML, Gunaratne PH and Matzuk MM. Functional microRNA involved in endometriosis. Mol Endocrinol May 2011, 25:821-32. PMCID: PMC3082329.

Hu C, Cela RG, Suzuki M, Lee B and Lipshutz GS. Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII. Proceedings of the National Academy of Sciences USA 2011, in press.

Iakova P, Timchenko L and Timchenko NA. Intracellular signaling and hepatocellular carcinoma. Semin Cancer Biol Feb 2011, 21:28-34. PMID: 20850540.

Iwamori T, Lin YN, Ma L, Iwamori N and Matzuk MMIdentification and characterization of RBM44 as a novel intercellular bridge protein. PLoS One Feb 2011, 6:e17066. PMCID: PMC3045441.

Iwamori N, Zhao M, Meistrich ML and Matzuk MMThe Testis-Enriched Histone Demethylase, KDM4D, Regulates Methylation of Histone H3 Lysine 9 During Spermatogenesis in the Mouse but Is Dispensable for Fertility. Biol Reprod Feb 2011, Epub ahead of print. PMID: 21293030.

Jafar-Nejad P, Richman R, Orr HT and Zoghbi HYRegional rescue of spinocerebellar ataxia type 1 phenotypes by 14-3-3{varepsilon} haploinsufficiency in mice underscores complex pathogenicity in neurodegeneration. Proc Natl Acad Sci USA Feb 2011, 108:2142-7. PMCID: PMC3033247.

Jiang Y, Scott KL, Kwak SJ, Chen R and Mardon GSds22/PP1 links epithelial integrity and tumor suppression via regulation of myosin II and JNK signaling. Oncogene Mar 2011 Epub ahead of print. PMID: 21399659.

Juncos, JL, Lazarus JT, Allen EG, Shubeck L, Rusin M, Novak G, Hamilton D, Rohr J,Sherman SLNew clinical findings in the Fragile X associated tremor ataxia syndrome. Neurogenetics, in press, 2011.

Kelley BP, F. Malfait, L. Bonafe, D. Baldridge, S. Symoens, N. Elcioglu, C. Verellen-Dumoulin, Y. Gillerot, D. Napierala, D. Krakow, P. Beighton, A. Superti-Furga, Anne De Paepe, Lionel Van Malderghem, and Lee BMutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome. Journal of Bone and Mineral Research 2011, in press.

Klisch, TJ, Xi Y, Flora A, Wang L, Li W and Zoghbi HYThe in vivo Atoh1 targetome reveals how a proneural transcription factor regulates neurogenesis. Proc Natl Acad Sci USA Feb 2011,108: 3288-93: PMCID: PMC3044384.

Ku S, Tolias AS, Logothetis NK and Goense J. fMRI of the face-processing network in the ventral temporal lobe of awake and anesthetized macaques. Neuron 2011, in press.

Lee OH, Kim H, He Q, Baek HJ, Yang D, Chen LY, Liang J, Chae HK, Safari A, Liu D, Songyang Z. Genome-wide YFP fluorescence complementation screen identifies new regulators for telomere signaling in human cells. Mol Cell Proteomics Feb 2011. 10:M110.001628. PMCID: PMC3033672.

Leitão-Gonçalves R, Ermanoska B, Jacobs A, De Vriendt E, Timmerman V, Lupski JR, Callaerts P, Jordanova A. Drosophila as a platform to predict the pathogenicity of novel aminoacyl-tRNA synthetase mutations in CMT. Amino Acids Mar 2011 Epub ahead of print. PMID: 21384131.

Levenga J, Hayashi S, de Vrij FM, Koekkoek SK, van der Linde HC, Nieuwenhuizen I, Song C, Buijsen RA, Pop AS, Gomezmancilla B, Nelson DL, Willemsen R, Gasparini F, Oostra BA. AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome. Neurobiol Dis Jun 2011, 42:311-17. PMID: 21316452.

Liu, P, Erez, A, Nagamani, SCS, Dhar, S, Mitchel, CL, Zhang, F, Withers, M, Brinkman, L, Daniel L, Acevedo, C, Delgado, M, Dolores, A, Freedenberg, D, Garnica, A, Grebe, TA, Immken, L, Lalani, S, McLean, SD, Northrup, H, Scaglia, F, Strathearn, L, Trapane, P, Kang, S-HL, Patel, A, Cheung, SW, Hastings, PJ, Stankiewicz, P, Lupski, JR, Bi, W. Chromosome catastrophes involve replication mechanisms generating complex rearrangements. Cell Sep 2011,146:889-903. PMID: 21925314.

Liu, P, Lacaria, M, Zhang, F, Withers, M, Hastings, P, Lupski, JRFrequency of nonallelic homologous recombination is correlated with length of homology: Evidence that ectopic synapsis preceded ectopic crossing-over. Am J Hum Genet Oct 2011, 89:580-588. PMID: 21981782.

Liu P, Erez A, Sreenath Nagamani SC, Bi W, Carvalho CM, Simmons AD, Wiszniewska J, Fang P, Eng PA, Cooper ML, Sutton VR, Roeder ER, Bodensteiner JB, Delgado MR, Prakash SK, Belmont JW, Stankiewicz P, Berg JS, Shinawi M, Patel A, Cheung SW and Lupski JR.Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications. Hum Mol Genet May 2011, 20:1975-88. PMCID: PMC3080608.

Ma W, Kim H, and Songyang ZStudying of Telomeric Protein–Protein Interactions by Bi-Molecular Fluorescence Complementation (BiFC) and Peptide Array-Based Assays. Methods in Molecular Biology 2011, in press.

Maricich SM, Aqeeb KA, Moayedi Y, Mathes EL, Patel MS, Chitayat D, Lyon G, Leroy JG,Zoghbi HYPontocerebellar hypoplasia: review of classification and genetics, and exclusion of several genes known to be important for cerebellar development. J Child Neurol Mar 2011,26:288-94. PMID: 21383226.

Martinez HR, Belmont JW, Craigen WJ, Taylor MD and Jefferies JL. Left ventricular noncompaction in Sotos syndrome. Am J Med Genet A May 2011 59:1115-8. PMID: 21484993.

McBride KL, Zender GA, Fitzgerald-Butt SM, Seagraves NJ, Fernbach SD, Zapata G, Lewin M, Towbin JA and Belmont JWAssociation of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects. Birth Defects Res A Clin Mol Teratol. March 2011,91:182-82. PMID: 21290564.

McCauley, MD, Wang, T, Mike, E, Herrera, J, Beavers, DL, Huang, TW, Ward, CS, Skinner, S, Percy, AK, Glaze, DG, Wehrens, XH, Neul, JLPathogenesis of lethal cardiac arrhythmias in mecp2 mutant mice: implication for therapy in Rett syndrome. Sci Transl Med Dec 2011;3(113):113ra125. PMID: 22174313.

McGraw, CM, Samaco, RC, Zoghbi, HYAdult neural function requires MeCP2. Science Jul 2011, 8;333(6039):186. PMID: 21636743.

Meerbrey KL, Hu G, Kessler JD, Roarty K, Li MZ, Fang JE, Herschkowitz JI, Burrows AE, Ciccia A, Sun T, Schmitt EM, Bernardi RJ, Fu X, Bland CS, Cooper TA, Schiff R, Rosen JM,Westbrook TF, Elledge SJ. The pINDUCER lentiviral toolkit for inducible RNA interference n vitro and in vivo. Proc Natl Acad Sci USA Mar 2011, 108:3665-70. PMCID: PMC3048138.

Merveille AC, Davis EE, Becker-Heck A, Legendre M, Amirav I, Bataille G, Belmont J, et al. CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Nat Genet Jan 2011, 43:72-8. PMID: 21131972.

Muddashetty RS, Nalavadi V, Gross, C, Yao, X, Warren ST and Bassell GJ. Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation and mGluR signaling. Mol Cell. 2011 Jun 10;42(5):673-88.

Nagamani, SC, Erez, A, Bader, P, Lalani, SR, Scott, DA, Scaglia, F, Plon, SE, Tsai, CH, Reimschisel, T, Roeder, E, Malphrus, AD, Eng, PA, Hixson, PM, Kang, SH, Stankiewicz, P, Patel, A, Cheung, SW. Phenotypic manifestations of copy number variation in chromosome 16p13.11. Eur J Hum Genet Mar 2011, 19(3):280-6, PMID: 21150890.

Nègre N, Brown CD, Ma L, Bristow CA, Miller SW, Wagner U, Kheradpour P, Eaton ML, Loriaux P, Sealfon R, Li Z, Ishii H, Spokony RF, Chen J, Hwang L, Cheng C, Auburn RP, Davis MB, Domanus M, Shah PK, Morrison CA, Zieba J, Suchy S, Senderowicz L, Victorsen A, Bild NA, Grundstad AJ, Hanley D, MacAlpine DM, Mannervik M, Venken K, Bellen H, White R, Gerstein M, Russell S, Grossman RL, Ren B, Posakony JW, Kellis M and White KP. A cis-regulatory map of the Drosophila genome. Nature Mar 2011, 471:527-31. PMID: 21430782. Commentary in Nature March 2011, 471:458-9.

Orengo JP, Ward AJ and Cooper TAAlternative splicing dysregulation secondary to skeletal muscle regeneration. Ann Neurol Apr 2011, 69:681-90. PMCID: PMC3082633.

Ou Z, Stankiewicz P, Xia Z, Breman AM,…….Lupski JR and Cheung SW. Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes. Genome Res Jan 2011, PMCID: PMC3012924.

Palmieri, M, Impey, S, Kang, H, di Ronza, A, Pelz, C, Sardiello, M, Ballabio, A. Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways. Hum Mol Genet Oct 2011; 20(19):3852-66. PMID: 21752829.

Shaw CA, Li Y, Wiszniewska J, Chasse S, Zaidi SN, Jin W, Dawson B, Wilhelmsen K, Lupski JRBelmont JW, Doody RS and Szigeti K. Olfactory copy number association with age at onset of Alzheimer disease. Neurology Apr 2011, 76:1302-9. PMID: 21482944.

Shim, DJ, Yang, L, Reed, JG, Noebels, JL, Chiao, PJ, and Zheng, HDisruption of the NF-?B/I?B? autoinhibitory loop improves cognitive performance and promotes hyperexcitability of hippocampal neurons. Mol Neurodegen Jun 2011; 6:42. PMID: 21663635.

Soler-Alfonso C, Motil KJ, Turk CL, Robbins-Furman P, Friedman EM, Zhang F, Lupski JR, Fraley JK and Potocki L. Potocki-Lupski syndrome: a microduplication syndrome associated with oropharyngeal dysphagia and failure to thrive. J Pediatr Apr 2011, 158:655-659. PMID:21168152.

Spencer CM, Alekseyenko O, Hamilton SM, Thomas AM, Serysheva E, Yuva-Paylor LA and Paylor RModifying behavioral phenotypes in Fmr1 KO mice: Genetic background differences reveal autistic-like responses. Autism Res. Feb 2011, 4:40-56. PMCID: PMC3059810.

Stewart, LR, Hall, AL, Kang, SH, Shaw, CA, Beaudet, ALHigh frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy. BMC Med Genet Nov 2011, 12:154. PMID: 22118685.

Sun, YG, Wu, CS, Lu, HC, Beierlein, M. Target-dependent control of synaptic inhibition by endocannabinoids in the thalamus. J Neurosci Jun 2011, 31(25):9222-30. PMID: 21697372.

Sun T, Aceto N, Meerbrey KL, Kessler JD, Zhou C, Migliaccio I, Nguyen DX, Pavlova NN, Botero M, Huang J, Bernardi RJ, Schmitt E, Hu G, Li MZ, Dephoure N, Gygi SP, Rao M, Creighton CJ, Hilsenbeck SG, Shaw CA, Muzny D, Gibbs RA, Wheeler DA, Osborne CK, Schiff R, Bentires-Alj M, Elledge SJ, Westbrook TFActivation of multiple proto-oncogenic tyrosine kinases in breast cancer via loss of the PTPN12 phosphatase. Cell Mar 2011, 144:703-18. PMD: 21376233.

Sunnen, CN, Brewster, AL, Lugo, JN, Vanegas, F, Turcios, E, Mukhi, S, Parghi, D, D'Arcangelo, G, Anderson, AE. Inhibition of the mammalian target of rapamycin blocks epilepsy progression in NS-Pten conditional knockout mice. Epilepsia Nov 2011, 52:2065-2075. PMID: 21973019.

Susuki K, Raphael AR, Ogawa Y, Stankewich MC, Peles E, Talbot WS and Rasband MN. Schwann Cell spectrins modulate peripheral nerve myelination. Proc Natl Acad Sci U S A. 2011 May 10;108(19):8009-14. PMID: 21518878.

Swanger SA, Yao X, Gross C and Bassell GJAutomated 4D analysis of dendritic spine morphology: applications to stimulus-induced spine remodeling and pharmacological rescue in a disease model. Molecular Brain Oct 2011, 4(1):38-46. PMID: 21982080.

Thomas AM, Bui N, Graham D, Perkins JR, Yuva-Paylor LA and Paylor RGenetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome. Behav Brain Res. 2011 Oct 1;223(2):310-21.

Tolias KF, Duman J G, Um K. Control of synapse development and plasticity by Rho GTPase regulatory proteins. Prog Neurobiol. 2011 Jul;94(2):133-48.

Tomson SN, Avidan N, Lee K, Sarma AK, Tushe R, Milewicz DM, Bray M, Leal SM and Eagleman DM. The genetics of colored sequence synesthesia: Suggestive evidence of linkage to 16q and genetic heterogeneity for the condition. Behav Brain Res. 2011 Sep 30;223(1):48-52.

Tong, C, Ohyama, T, Tien, A, Rajan, A, Haueter, CM, Bellen, HJRich regulates target specificity of photoreceptor cells and N-Cadherin trafficking in the Drosophila visual system via Rab6. Neuron Aug 2011, 71:447-459. PMID: 21835342.

Veeraragavan, S, Bui, N, Perkins, JR, Yuva-Paylor, LA, and Paylor, R. The modulation of fragile X behaviors by the muscarinic M4 antagonist, tropicamide. Behav Neurosci. Oct 2011, 125, 783-790. PMID: 21942438.

Veeraragavan S, Bui N, Perkins JR, Yuva-Paylor LA, Carpenter RL and Paylor R. Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome. Psychopharmacology (Berl). 2011 Sep;217(1):143-51.

van Bon BW, Balciuniene J, Fruhman G, Nagamani SC, Broome DL, Cameron E, Martinet D, Roulet E, Jacquemont S, Beckmann JS, Irons M, Potocki L, Lee B, ...Lupski JR, de Vries BB. The Phenotype of recurrent 10q22q23 deletions and duplications. Eur J Hum Genet. 2011 Apr;19(4):400-8. PMID: 21248748.

Wang, B, Harrison, W, Overbeek, P and Zheng, HTransposon mutagenesis with coat color genotyping identifies an essential role of SKOR2 in Sonic Hedgehog signaling and cerebellum development. 2011, Development; 138(20): 4487-97. PMID: 21937600.

Ward, CS, Arvide, EM, Huang, TW, Yoo, J, Noebels, JL and Neul, JLMeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan. J Neuroscience Jul 2011, 13;31(28):10359-70. PMID: 21753013.

Wat MJ, Veenma D, Hogue J, Holder AM, Yu Z, Wat JJ, ….. and Scott DAGenomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia. J Med Genet May 2011, 48:299-307.

Wiszniewski W, Lewis RA, Stockton DW, Peng J, Mardon G, Chen R, and Lupski J.Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis. Hum Genet Mar 2011, 129:319-27. PMID: 21153841.

Zhu PJ, Huang W, Kalikulov D, Yoo JW, Placzek AN, Stoica L, Zhou H, Bell JC, Friedlander MJ, Krnjevic K, Noebels JL, and Costa-Mattioli M. Suppression of PKR promotes network excitability and enhanced cognition by interferon-γ-mediated disinhibition. Cell. 2011 Dec 9;147(6):1384-96. PMID: 22153080.