Jay Tischfield - Publications

Affiliations: 
Graduate School - New Brunswick Rutgers University, New Brunswick, New Brunswick, NJ, United States 
Area:
Microbiology Biology

216 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Cao X, Zhang Y, Abdulkadir M, Deng L, Fernandez TV, Garcia-Delgar B, Hagstrøm J, Hoekstra PJ, King RA, Koesterich J, Kuperman S, Morer A, Nasello C, Plessen KJ, Thackray JK, ... ... Tischfield JA, et al. Whole-exome sequencing identifies genes associated with Tourette's disorder in multiplex families. Molecular Psychiatry. PMID 33837273 DOI: 10.1038/s41380-021-01094-1  0.6
2020 Thapa KS, Chen AB, Lai D, Xuei X, Wetherill L, Tischfield JA, Liu Y, Edenberg HJ. Identification of Functional Genetic Variants Associated with Alcohol Dependence and Related Phenotypes Using a High-Throughput Assay. Alcoholism, Clinical and Experimental Research. PMID 33119910 DOI: 10.1111/acer.14492  0.48
2020 Simonet NG, Thackray JK, Vazquez BN, Ianni A, Espinosa-Alcantud M, Morales-Sanfrutos J, Hurtado-Bagès S, Sabidó E, Buschbeck M, Tischfield J, De La Torre C, Esteller M, Braun T, Olivella M, Serrano L, et al. SirT7 auto-ADP-ribosylation regulates glucose starvation response through mH2A1. Science Advances. 6: eaaz2590. PMID 32832656 DOI: 10.1126/Sciadv.Aaz2590  0.44
2020 Lai D, Kapoor M, Wetherill L, Schwandt M, Ramchandani VA, Goldman D, Chao M, Almasy L, Bucholz K, Hart RP, Kamarajan C, Meyers JL, Nurnberger JI, Tischfield J, Edenberg HJ, et al. Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32652861 DOI: 10.1002/Ajmg.B.32805  0.48
2019 Wetherill L, Lai D, Johnson EC, Anokhin A, Bauer L, Bucholz KK, Dick DM, Hariri AR, Hesselbrock V, Kamarajan C, Kramer J, Kuperman S, Meyers JL, Nurnberger JI, Schuckit M, ... ... Tischfield J, et al. ERRATUM: Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans. Genes, Brain, and Behavior. 18: e12608. PMID 31667958 DOI: 10.1111/Gbb.12608  0.48
2019 Salvatore JE, Barr PB, Stephenson M, Aliev F, Kuo SI, Su J, Agrawal A, Almasy L, Bierut L, Bucholz K, Chan G, Edenberg HJ, Johnson EC, McCutcheon VV, Meyers JL, ... ... Tischfield J, et al. Sibling comparisons elucidate the associations between educational attainment polygenic scores and alcohol, nicotine and cannabis. Addiction (Abingdon, England). PMID 31659820 DOI: 10.1111/Add.14815  0.48
2019 Meyers JL, Chorlian DB, Johnson EC, Pandey AK, Kamarajan C, Salvatore JE, Aliev F, Subbie-Saenz de Viteri S, Zhang J, Chao M, Kapoor M, Hesselbrock V, Kramer J, Kuperman S, Nurnberger J, ... Tischfield J, et al. Association of Polygenic Liability for Alcohol Dependence and EEG Connectivity in Adolescence and Young Adulthood. Brain Sciences. 9. PMID 31627376 DOI: 10.3390/Brainsci9100280  0.48
2019 Rao X, Thapa KS, Chen AB, Lin H, Gao H, Reiter JL, Hargreaves KA, Ipe J, Lai D, Xuei X, Wang Y, Gu H, Kapoor M, Farris SP, Tischfield J, et al. Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders. Molecular Psychiatry. PMID 31477794 DOI: 10.1038/S41380-019-0508-Z  0.48
2019 Lai D, Wetherill L, Kapoor M, Johnson EC, Schwandt M, Ramchandani VA, Goldman D, Joslyn G, Rao X, Liu Y, Farris S, Mayfield RD, Dick D, Hesselbrock V, Kramer J, ... ... Tischfield J, et al. Genome-wide association studies of the self-rating of effects of ethanol (SRE). Addiction Biology. e12800. PMID 31270906 DOI: 10.1111/Adb.12800  0.48
2019 Vazquez BN, Thackray JK, Simonet NG, Chahar S, Kane-Goldsmith N, Newkirk SJ, Lee S, Xing J, Verzi MP, An W, Vaquero A, Tischfield JA, Serrano L. SIRT7 mediates L1 elements transcriptional repression and their association with the nuclear lamina. Nucleic Acids Research. PMID 31226208 DOI: 10.1093/Nar/Gkz519  0.44
2019 Woodard LE, Welch RC, Veach RA, Beckermann TM, Sha F, Weinman EJ, Ikizler TA, Tischfield JA, Sahota A, Wilson MH. Metabolic consequences of cystinuria. Bmc Nephrology. 20: 227. PMID 31221135 DOI: 10.1186/s12882-019-1417-8  0.52
2019 Wetherill L, Lai D, Johnson EC, Anokhin A, Bauer L, Bucholz KK, Dick DM, Hariri AR, Hesselbrock V, Kamarajan C, Kramer J, Kuperman S, Meyers JL, Nurnberger JI, Schuckit M, ... ... Tischfield J, et al. Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans. Genes, Brain, and Behavior. e12580. PMID 31099175 DOI: 10.1111/Gbb.12580  0.48
2019 Lai D, Wetherill L, Bertelsen S, Carey CE, Kamarajan C, Kapoor M, Meyers JL, Anokhin AP, Bennett DA, Bucholz KK, Chang KK, De Jager PL, Dick DM, Hesselbrock V, Kramer J, ... ... Tischfield J, et al. Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Genes, Brain, and Behavior. PMID 31090166 DOI: 10.1111/Gbb.12579  0.48
2019 Kapoor M, Wang JC, Farris SP, Liu Y, McClintick J, Gupta I, Meyers JL, Bertelsen S, Chao M, Nurnberger J, Tischfield J, Harari O, Zeran L, Hesselbrock V, Bauer L, et al. Analysis of whole genome-transcriptomic organization in brain to identify genes associated with alcoholism. Translational Psychiatry. 9: 89. PMID 30765688 DOI: 10.1038/S41398-019-0384-Y  0.48
2019 McClintick JN, Tischfield JA, Deng L, Kapoor M, Xuei X, Edenberg HJ. Ethanol Activates Immune Response In Lymphoblastoid Cells. Alcohol (Fayetteville, N.Y.). PMID 30639126 DOI: 10.1016/J.Alcohol.2019.01.001  0.6
2018 Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... Tischfield JA, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544. PMID 30566877 DOI: 10.1016/j.celrep.2018.12.024  0.6
2018 Sahota A, Tischfield JA, Goldfarb DS, Ward MD, Hu L. Cystinuria: genetic aspects, mouse models, and a new approach to therapy. Urolithiasis. PMID 30515543 DOI: 10.1007/S00240-018-1101-7  0.52
2018 Johnson EC, Tillman R, Aliev F, Meyers JL, Salvatore JE, Anokhin AP, Dick DM, Edenberg HJ, Kramer J, Kuperman S, McCutcheon VV, Nurnberger JI, Porjesz B, Schuckit M, Tischfield J, et al. Exploring the relationship between polygenic risk for cannabis use, peer cannabis use, and the longitudinal course of cannabis involvement. Addiction (Abingdon, England). PMID 30474892 DOI: 10.1111/Add.14512  0.48
2018 Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... Tischfield JA, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 24: 3441-3454.e12. PMID 30257206 DOI: 10.1016/J.Celrep.2018.08.082  0.6
2017 Agrawal A, Chou YL, Carey CE, Baranger DAA, Zhang B, Sherva R, Wetherill L, Kapoor M, Wang JC, Bertelsen S, Anokhin AP, Hesselbrock V, Kramer J, Lynskey MT, Meyers JL, ... ... Tischfield J, et al. Genome-wide association study identifies a novel locus for cannabis dependence. Molecular Psychiatry. PMID 29112194 DOI: 10.1038/Mp.2017.200  0.48
2017 Sun N, Nasello C, Deng L, Wang N, Zhang Y, Xu Z, Song Z, Kwan K, King RA, Pang ZP, Xing J, Heiman GA, Tischfield JA. The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. Molecular Psychiatry. PMID 28894297 DOI: 10.1038/Mp.2017.179  0.6
2017 Kuperman S, Chan G, Kramer J, Wetherill L, Acion L, Edenberg HJ, Foroud TM, Nurnberger J, Agrawal A, Anokhin A, Brooks A, Hesselbrock V, Hesselbrock M, Schuckit M, Tischfield J, et al. A GABRA2 polymorphism improves a model for prediction of drinking initiation. Alcohol (Fayetteville, N.Y.). 63: 1-8. PMID 28847377 DOI: 10.1016/J.Alcohol.2017.03.003  0.48
2017 Andersen AM, Pietrzak RH, Kranzler HR, Ma L, Zhou H, Liu X, Kramer J, Kuperman S, Edenberg HJ, Nurnberger JI, Rice JP, Tischfield JA, Goate A, Foroud TM, Meyers JL, et al. Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence. Jama Psychiatry. PMID 28813562 DOI: 10.1001/Jamapsychiatry.2017.2269  0.48
2017 Zee T, Bose N, Zee J, Beck JN, Yang S, Parihar J, Yang M, Damodar S, Hall D, O'Leary MN, Ramanathan A, Gerona RR, Killilea DW, Chi T, Tischfield J, et al. α-Lipoic acid treatment prevents cystine urolithiasis in a mouse model of cystinuria. Nature Medicine. PMID 28165480 DOI: 10.1038/Nm.4280  0.52
2016 Meyers JL, Zhang J, Manz N, Rangaswamy M, Kamarajan C, Wetherill L, Chorlian DB, Kang SJ, Bauer L, Hesselbrock V, Kramer J, Kuperman S, Nurnberger JI, Tischfield J, Wang JC, et al. A Genome Wide Association Study of Fast Beta EEG in Families of European Ancestry. International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology. PMID 28040410 DOI: 10.1016/J.Ijpsycho.2016.12.008  0.48
2016 Olfson E, Bloom J, Bertelsen S, Budde JP, Breslau N, Brooks A, Culverhouse R, Chan G, Chen LS, Chorlian D, Dick DM, Edenberg HJ, Hartz S, Hatsukami D, Hesselbrock VM, ... ... Tischfield JA, et al. CYP2A6 metabolism in the development of smoking behaviors in young adults. Addiction Biology. PMID 28032407 DOI: 10.1111/Adb.12477  0.48
2016 Kamarajan C, Pandey AK, Chorlian DB, Manz N, Stimus AT, Edenberg HJ, Wetherill L, Schuckit M, Wang JC, Kuperman S, Kramer J, Tischfield JA, Porjesz B. A KCNJ6 gene polymorphism modulates theta oscillations during reward processing. International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology. PMID 27993610 DOI: 10.1016/J.Ijpsycho.2016.12.007  0.48
2016 Alexander J, Potamianou H, Xing J, Deng L, Karagiannidis I, Tsetsos F, Drineas P, Tarnok Z, Rizzo R, Wolanczyk T, Farkas L, Nagy P, Szymanska U, Androutsos C, Tsironi V, ... ... Tischfield J, et al. Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Frontiers in Neuroscience. 10: 428. PMID 27708560 DOI: 10.3389/Fnins.2016.00428  0.6
2016 Oni EN, Halikere A, Li G, Toro-Ramos AJ, Swerdel MR, Verpeut JL, Moore JC, Bello NT, Bierut LJ, Goate A, Tischfield JA, Pang ZP, Hart RP. Increased nicotine response in iPSC-derived human neurons carrying the CHRNA5 N398 allele. Scientific Reports. 6: 34341. PMID 27698409 DOI: 10.1038/Srep34341  0.72
2016 Abdulkadir M, Tischfield JA, King RA, Fernandez TV, Brown LW, Cheon KA, Coffey BJ, de Bruijn SF, Elzerman L, Garcia-Delgar B, Gilbert DL, Grice DE, Hagstrøm J, Hedderly T, Heyman I, et al. Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder. Journal of Psychiatric Research. 82: 126-135. PMID 27494079 DOI: 10.1016/J.Jpsychires.2016.07.017  0.72
2016 Hu L, Yang Y, Aloysius H, Albanyan H, Yang M, Liang JJ, Yu AC, Shtukenberg AG, Poloni LN, Kholodovych V, Tischfield JA, Goldfarb DS, Ward MD, Sahota A. L-CYSTINE DIAMIDES AS L-CYSTINE CRYSTALLIZATION INHIBITORS FOR CYSTINURIA. Journal of Medicinal Chemistry. PMID 27409142 DOI: 10.1021/Acs.Jmedchem.6B00647  0.52
2016 Vazquez BN, Thackray JK, Simonet NG, Kane-Goldsmith N, Martinez-Redondo P, Nguyen T, Bunting S, Vaquero A, Tischfield JA, Serrano L. SIRT7 promotes genome integrity and modulates non-homologous end joining DNA repair. The Embo Journal. PMID 27225932 DOI: 10.15252/embj.201593499  0.72
2016 De Filippis L, Halikere A, McGowan H, Moore JC, Tischfield JA, Hart RP, Pang ZP. Ethanol-mediated activation of the NLRP3 inflammasome in iPS cells and iPS cells-derived neural progenitor cells. Molecular Brain. 9: 51. PMID 27160314 DOI: 10.1186/S13041-016-0221-7  0.72
2016 Kapoor M, Chou YL, Edenberg HJ, Foroud T, Martin NG, Madden PA, Wang JC, Bertelsen S, Wetherill L, Brooks A, Chan G, Hesselbrock V, Kuperman S, Medland SE, Montgomery G, ... Tischfield J, et al. Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures. Translational Psychiatry. 6: e761. PMID 27003187 DOI: 10.1038/Tp.2016.27  0.48
2016 Sun N, Tischfield JA, King RA, Heiman GA. Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder. Frontiers in Psychiatry. 7: 11. PMID 26903887 DOI: 10.3389/fpsyt.2016.00011  0.72
2015 Jansen R, Penninx BW, Madar V, Xia K, Milaneschi Y, Hottenga JJ, Hammerschlag AR, Beekman A, van der Wee N, Smit JH, Brooks AI, Tischfield J, Posthuma D, Schoevers R, van Grootheest G, et al. Gene expression in major depressive disorder. Molecular Psychiatry. PMID 26100536 DOI: 10.1038/Mp.2015.94  0.72
2015 Huertas-Fernández I, Gómez-Garre P, Madruga-Garrido M, Bernal-Bernal I, Bonilla-Toribio M, Martín-Rodríguez JF, Cáceres-Redondo MT, Vargas-González L, Carrillo F, Pascual A, Tischfield JA, King RA, Heiman GA, Mir P. GDNF gene is associated with tourette syndrome in a family study. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 1115-20. PMID 26096985 DOI: 10.1002/mds.26279  0.72
2015 Jansen R, Penninx BW, Madar V, Xia K, Milaneschi Y, Hottenga JJ, Hammerschlag AR, Beekman A, van der Wee N, Smit JH, Brooks AI, Tischfield J, Posthuma D, Schoevers R, van Grootheest G, et al. Gene expression in major depressive disorder. Molecular Psychiatry. PMID 26008736 DOI: 10.1038/Mp.2015.57  0.72
2015 Salvatore JE, Edwards AC, McClintick JN, Bigdeli TB, Adkins A, Aliev F, Edenberg HJ, Foroud T, Hesselbrock V, Kramer J, Nurnberger JI, Schuckit M, Tischfield JA, Xuei X, Dick DM. Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. Translational Psychiatry. 5: e558. PMID 25918995 DOI: 10.1038/Tp.2015.36  0.72
2015 Agrawal A, Lynskey MT, Kapoor M, Bucholz KK, Edenberg HJ, Schuckit M, Brooks A, Hesselbrock V, Kramer J, Saccone N, Tischfield J, Bierut LJ. Are genetic variants for tobacco smoking associated with cannabis involvement? Drug and Alcohol Dependence. 150: 183-7. PMID 25770649 DOI: 10.1016/J.Drugalcdep.2015.02.029  0.72
2015 Wetherill L, Agrawal A, Kapoor M, Bertelsen S, Bierut LJ, Brooks A, Dick D, Hesselbrock M, Hesselbrock V, Koller DL, Le N, Nurnberger JI, Salvatore JE, Schuckit M, Tischfield JA, et al. Association of substance dependence phenotypes in the COGA sample. Addiction Biology. 20: 617-27. PMID 24832863 DOI: 10.1111/Adb.12153  0.72
2015 Dietrich A, Fernandez TV, King RA, State MW, Tischfield JA, Hoekstra PJ, Heiman GA. The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods. European Child & Adolescent Psychiatry. 24: 141-51. PMID 24771252 DOI: 10.1007/S00787-014-0543-X  0.72
2015 D'Aiuto L, Prasad KM, Upton CH, Viggiano L, Milosevic J, Raimondi G, McClain L, Chowdari K, Tischfield J, Sheldon M, Moore JC, Yolken RH, Kinchington PR, Nimgaonkar VL. Persistent infection by HSV-1 is associated with changes in functional architecture of iPSC-derived neurons and brain activation patterns underlying working memory performance. Schizophrenia Bulletin. 41: 123-32. PMID 24622295 DOI: 10.1093/Schbul/Sbu032  0.72
2014 Sahota A, Parihar JS, Capaccione KM, Yang M, Noll K, Gordon D, Reimer D, Yang I, Buckley BT, Polunas M, Reuhl KR, Lewis MR, Ward MD, Goldfarb DS, Tischfield JA. Novel cystine ester mimics for the treatment of cystinuria-induced urolithiasis in a knockout mouse model. Urology. 84: 1249.e9-15. PMID 25443947 DOI: 10.1016/J.Urology.2014.07.043  0.52
2014 Xu B, Wang W, Guo H, Sun Z, Wei Z, Zhang X, Liu Z, Tischfield JA, Gong Y, Shao C. Oxidative stress preferentially induces a subtype of micronuclei and mediates the genomic instability caused by p53 dysfunction. Mutation Research. 770: 1-8. PMID 25302047 DOI: 10.1016/j.mrfmmm.2014.08.004  0.72
2014 Olfson E, Edenberg HJ, Nurnberger J, Agrawal A, Bucholz KK, Almasy LA, Chorlian D, Dick DM, Hesselbrock VM, Kramer JR, Kuperman S, Porjesz B, Schuckit MA, Tischfield JA, Wang JC, et al. An ADH1B variant and peer drinking in progression to adolescent drinking milestones: evidence of a gene-by-environment interaction. Alcoholism, Clinical and Experimental Research. 38: 2541-9. PMID 25257461 DOI: 10.1111/Acer.12524  0.72
2014 Tereshchenko IV, Zhong H, Chekmareva MA, Kane-Goldsmith N, Santanam U, Petrosky W, Stein MN, Ganesan S, Singer EA, Moore D, Tischfield JA, DiPaola RS. ERG and CHD1 heterogeneity in prostate cancer: use of confocal microscopy in assessment of microscopic foci. The Prostate. 74: 1551-9. PMID 25175909 DOI: 10.1002/pros.22873  0.72
2014 McClintick JN, Brooks AI, Deng L, Liang L, Wang JC, Kapoor M, Xuei X, Foroud T, Tischfield JA, Edenberg HJ. Ethanol treatment of lymphoblastoid cell lines from alcoholics and non-alcoholics causes many subtle changes in gene expression. Alcohol (Fayetteville, N.Y.). 48: 603-10. PMID 25129674 DOI: 10.1016/J.Alcohol.2014.07.004  0.72
2014 Kapoor M, Wang JC, Wetherill L, Le N, Bertelsen S, Hinrichs AL, Budde J, Agrawal A, Almasy L, Bucholz K, Dick DM, Harari O, Xiaoling X, Hesselbrock V, Kramer J, ... ... Tischfield J, et al. Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families. Drug and Alcohol Dependence. 142: 56-62. PMID 24962325 DOI: 10.1016/J.Drugalcdep.2014.05.023  0.72
2014 Wright FA, Sullivan PF, Brooks AI, Zou F, Sun W, Xia K, Madar V, Jansen R, Chung W, Zhou YH, Abdellaoui A, Batista S, Butler C, Chen G, Chen TH, ... ... Tischfield J, et al. Heritability and genomics of gene expression in peripheral blood. Nature Genetics. 46: 430-7. PMID 24728292 DOI: 10.1038/Ng.2951  0.72
2014 Sadler B, Haller G, Agrawal A, Culverhouse R, Bucholz K, Brooks A, Tischfield J, Johnson EO, Edenberg H, Schuckit M, Saccone N, Bierut L, Goate A. Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. Scientific Reports. 4: 4497. PMID 24675634 DOI: 10.1038/Srep04497  0.72
2014 Jansen R, Batista S, Brooks AI, Tischfield JA, Willemsen G, van Grootheest G, Hottenga JJ, Milaneschi Y, Mbarek H, Madar V, Peyrot W, Vink JM, Verweij CL, de Geus EJ, Smit JH, et al. Sex differences in the human peripheral blood transcriptome. Bmc Genomics. 15: 33. PMID 24438232 DOI: 10.1186/1471-2164-15-33  0.72
2014 Culverhouse RC, Johnson EO, Breslau N, Hatsukami DK, Sadler B, Brooks AI, Hesselbrock VM, Schuckit MA, Tischfield JA, Goate AM, Saccone NL, Bierut LJ. Multiple distinct CHRNB3-CHRNA6 variants are genetic risk factors for nicotine dependence in African Americans and European Americans. Addiction (Abingdon, England). 109: 814-22. PMID 24401102 DOI: 10.1111/Add.12478  0.72
2014 Ren G, Liu Y, Zhao X, Zhang J, Zheng B, Yuan ZR, Zhang L, Qu X, Tischfield JA, Shao C, Shi Y. Tumor resident mesenchymal stromal cells endow naïve stromal cells with tumor-promoting properties. Oncogene. 33: 4016-20. PMID 24077286 DOI: 10.1038/onc.2013.387  0.72
2014 Haller G, Kapoor M, Budde J, Xuei X, Edenberg H, Nurnberger J, Kramer J, Brooks A, Tischfield J, Almasy L, Agrawal A, Bucholz K, Rice J, Saccone N, Bierut L, et al. Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence. Human Molecular Genetics. 23: 810-9. PMID 24057674 DOI: 10.1093/Hmg/Ddt463  0.72
2014 Wetherill L, Kapoor M, Agrawal A, Bucholz K, Koller D, Bertelsen SE, Le N, Wang JC, Almasy L, Hesselbrock V, Kramer J, Nurnberger JI, Schuckit M, Tischfield JA, Xuei X, et al. Family-based association analysis of alcohol dependence criteria and severity. Alcoholism, Clinical and Experimental Research. 38: 354-66. PMID 24015780 DOI: 10.1111/Acer.12251  0.72
2014 Yan J, Aliev F, Webb BT, Kendler KS, Williamson VS, Edenberg HJ, Agrawal A, Kos MZ, Almasy L, Nurnberger JI, Schuckit MA, Kramer JR, Rice JP, Kuperman S, Goate AM, ... Tischfield JA, et al. Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. Addiction Biology. 19: 708-21. PMID 23362995 DOI: 10.1111/Adb.12035  0.72
2013 Wang JC, Spiegel N, Bertelsen S, Le N, McKenna N, Budde JP, Harari O, Kapoor M, Brooks A, Hancock D, Tischfield J, Foroud T, Bierut LJ, Steinbach JH, Edenberg HJ, et al. Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry. Plos One. 8: e80204. PMID 24303001 DOI: 10.1371/Journal.Pone.0080204  0.72
2013 McClintick JN, Xuei X, Tischfield JA, Goate A, Foroud T, Wetherill L, Ehringer MA, Edenberg HJ. Stress-response pathways are altered in the hippocampus of chronic alcoholics. Alcohol (Fayetteville, N.Y.). 47: 505-15. PMID 23981442 DOI: 10.1016/J.Alcohol.2013.07.002  0.72
2013 Chorlian DB, Rangaswamy M, Manz N, Wang JC, Dick D, Almasy L, Bauer L, Bucholz K, Foroud T, Hesselbrock V, Kang SJ, Kramer J, Kuperman S, Nurnberger J, Rice J, ... ... Tischfield J, et al. Genetic and neurophysiological correlates of the age of onset of alcohol use disorders in adolescents and young adults. Behavior Genetics. 43: 386-401. PMID 23963516 DOI: 10.1007/S10519-013-9604-Z  0.72
2013 Kapoor M, Wang JC, Wetherill L, Le N, Bertelsen S, Hinrichs AL, Budde J, Agrawal A, Bucholz K, Dick D, Harari O, Hesselbrock V, Kramer J, Nurnberger JI, Rice J, ... ... Tischfield J, et al. A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. Human Genetics. 132: 1141-51. PMID 23743675 DOI: 10.1007/S00439-013-1318-Z  0.72
2013 Zhang Z, Wang JC, Howells W, Lin P, Agrawal A, Edenberg HJ, Tischfield JA, Schuckit MA, Bierut LJ, Goate A, Rice JP. Dosage transmission disequilibrium test (dTDT) for linkage and association detection. Plos One. 8: e63526. PMID 23691058 DOI: 10.1371/Journal.Pone.0063526  0.72
2013 Moya PR, Wendland JR, Rubenstein LM, Timpano KR, Heiman GA, Tischfield JA, King RA, Andrews AM, Ramamoorthy S, McMahon FJ, Murphy DL. Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette's disorder. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1263-70. PMID 23630162 DOI: 10.1002/Mds.25460  0.72
2013 Kos MZ, Yan J, Dick DM, Agrawal A, Bucholz KK, Rice JP, Johnson EO, Schuckit M, Kuperman S, Kramer J, Goate AM, Tischfield JA, Foroud T, Nurnberger J, Hesselbrock V, et al. Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. Genes, Brain, and Behavior. 12: 532-42. PMID 23607416 DOI: 10.1111/Gbb.12043  0.72
2013 Serrano L, Vazquez BN, Tischfield J. Chromatin structure, pluripotency and differentiation. Experimental Biology and Medicine (Maywood, N.J.). 238: 259-70. PMID 23598971 DOI: 10.1177/1535370213480718  0.44
2013 Serrano L, Martínez-Redondo P, Marazuela-Duque A, Vazquez BN, Dooley SJ, Voigt P, Beck DB, Kane-Goldsmith N, Tong Q, Rabanal RM, Fondevila D, Muñoz P, Krüger M, Tischfield JA, Vaquero A. The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylation. Genes & Development. 27: 639-53. PMID 23468428 DOI: 10.1101/gad.211342.112  0.44
2013 Moya PR, Dodman NH, Timpano KR, Rubenstein LM, Rana Z, Fried RL, Reichardt LF, Heiman GA, Tischfield JA, King RA, Galdzicka M, Ginns EI, Wendland JR. Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes. European Journal of Human Genetics : Ejhg. 21: 850-4. PMID 23321619 DOI: 10.1038/Ejhg.2012.245  0.72
2013 Wang JC, Foroud T, Hinrichs AL, Le NX, Bertelsen S, Budde JP, Harari O, Koller DL, Wetherill L, Agrawal A, Almasy L, Brooks AI, Bucholz K, Dick D, Hesselbrock V, ... ... Tischfield JA, et al. A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Molecular Psychiatry. 18: 1218-24. PMID 23089632 DOI: 10.1038/Mp.2012.143  0.72
2013 Agrawal A, Wetherill L, Bucholz KK, Kramer J, Kuperman S, Lynskey MT, Nurnberger JI, Schuckit M, Tischfield JA, Edenberg HJ, Foroud T, Bierut LJ. Genetic influences on craving for alcohol Addictive Behaviors. 38: 1501-1508. PMID 22481050 DOI: 10.1016/J.Addbeh.2012.03.021  0.72
2012 Ren G, Zhao X, Wang Y, Zhang X, Chen X, Xu C, Yuan ZR, Roberts AI, Zhang L, Zheng B, Wen T, Han Y, Rabson AB, Tischfield JA, Shao C, et al. CCR2-dependent recruitment of macrophages by tumor-educated mesenchymal stromal cells promotes tumor development and is mimicked by TNFα. Cell Stem Cell. 11: 812-24. PMID 23168163 DOI: 10.1016/J.Stem.2012.08.013  0.72
2012 Smelson D, Yu L, Buyske S, Gonzalez G, Tischfield J, Deutsch CK, Ziedonis D. Genetic association of GABA-A receptor alpha-2 and mu opioid receptor with cocaine cue-reactivity: evidence for inhibitory synaptic neurotransmission involvement in cocaine dependence. The American Journal On Addictions / American Academy of Psychiatrists in Alcoholism and Addictions. 21: 411-5. PMID 22882391 DOI: 10.1111/J.1521-0391.2012.00253.X  0.72
2012 Tichy ED, Pillai R, Deng L, Tischfield JA, Hexley P, Babcock GF, Stambrook PJ. The abundance of Rad51 protein in mouse embryonic stem cells is regulated at multiple levels. Stem Cell Research. 9: 124-34. PMID 22705496 DOI: 10.1016/J.Scr.2012.05.004  0.72
2012 Lin P, Hartz SM, Wang JC, Agrawal A, Zhang TX, McKenna N, Bucholz K, Brooks AI, Tischfield JA, Edenberg HJ, Hesselbrock VM, Kramer JR, Kuperman S, Schuckit MA, Goate AM, et al. Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. Alcoholism, Clinical and Experimental Research. 36: 1512-8. PMID 22702843 DOI: 10.1111/J.1530-0277.2012.01758.X  0.72
2012 Rani V, Neumann CA, Shao C, Tischfield JA. Prdx1 deficiency in mice promotes tissue specific loss of heterozygosity mediated by deficiency in DNA repair and increased oxidative stress. Mutation Research. 735: 39-45. PMID 22583657 DOI: 10.1016/J.Mrfmmm.2012.04.004  0.72
2012 Kang SJ, Rangaswamy M, Manz N, Wang JC, Wetherill L, Hinrichs T, Almasy L, Brooks A, Chorlian DB, Dick D, Hesselbrock V, Kramer J, Kuperman S, Nurnberger J, Rice J, ... ... Tischfield J, et al. Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6. Genes, Brain, and Behavior. 11: 712-9. PMID 22554406 DOI: 10.1111/J.1601-183X.2012.00803.X  0.72
2012 Kapoor M, Wang JC, Bertelsen S, Bucholz K, Budde JP, Hinrichs A, Agrawal A, Brooks A, Chorlian D, Dick D, Hesselbrock V, Foroud T, Kramer J, Kuperman S, Manz N, ... ... Tischfield J, et al. Variants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking. Plos One. 7: e33513. PMID 22438940 DOI: 10.1371/Journal.Pone.0033513  0.72
2012 Derringer J, Krueger RF, Dick DM, Aliev F, Grucza RA, Saccone S, Agrawal A, Edenberg HJ, Goate AM, Hesselbrock VM, Kramer JR, Lin P, Neuman RJ, Nurnberger JI, Rice JP, ... Tischfield JA, et al. The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. Behavior Genetics. 42: 626-35. PMID 22358648 DOI: 10.1007/S10519-012-9531-4  0.72
2012 Liu Y, Deng L, Nguyen SC, Au CL, Shao C, Tischfield JA, Liang L. A human cell-based reporter detects microhomology-mediated end joining. Mutation Research. 731: 140-4. PMID 22197482 DOI: 10.1016/J.Mrfmmm.2011.12.003  0.72
2012 Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO, Raubeson MJ, Song Y, Yasuno K, Ho WS, Bilguvar K, Glessner J, Chu SH, Leckman JF, King RA, ... ... Tischfield JA, et al. Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biological Psychiatry. 71: 392-402. PMID 22169095 DOI: 10.1016/J.Biopsych.2011.09.034  0.72
2012 Denissova NG, Nasello CM, Yeung PL, Tischfield JA, Brenneman MA. Resveratrol protects mouse embryonic stem cells from ionizing radiation by accelerating recovery from DNA strand breakage. Carcinogenesis. 33: 149-55. PMID 22049530 DOI: 10.1093/carcin/bgr236  0.32
2012 Bierut LJ, Goate AM, Breslau N, Johnson EO, Bertelsen S, Fox L, Agrawal A, Bucholz KK, Grucza R, Hesselbrock V, Kramer J, Kuperman S, Nurnberger J, Porjesz B, Saccone NL, ... ... Tischfield J, et al. ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry. Molecular Psychiatry. 17: 445-50. PMID 21968928 DOI: 10.1038/Mp.2011.124  0.72
2011 Denissova NG, Tereshchenko IV, Cui E, Stambrook PJ, Shao C, Tischfield JA. Ionizing radiation is a potent inducer of mitotic recombination in mouse embryonic stem cells. Mutation Research. 715: 1-6. PMID 21802432 DOI: 10.1016/j.mrfmmm.2011.06.017  0.72
2011 Lin P, Hartz SM, Wang JC, Krueger RF, Foroud TM, Edenberg HJ, Nurnberger JI, Brooks AI, Tischfield JA, Almasy L, Webb BT, Hesselbrock VM, Porjesz B, Goate AM, Bierut LJ, et al. Copy number variation accuracy in genome-wide association studies. Human Heredity. 71: 141-7. PMID 21778733 DOI: 10.1159/000324683  0.72
2011 Agrawal A, Lynskey MT, Hinrichs A, Grucza R, Saccone SF, Krueger R, Neuman R, Howells W, Fisher S, Fox L, Cloninger R, Dick DM, Doheny KF, Edenberg HJ, Goate AM, ... ... Tischfield J, et al. A genome-wide association study of DSM-IV cannabis dependence. Addiction Biology. 16: 514-8. PMID 21668797 DOI: 10.1111/J.1369-1600.2010.00255.X  0.72
2011 Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, ... ... Tischfield JA, et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85. PMID 21658581 DOI: 10.1016/J.Neuron.2011.05.002  0.72
2011 Xu B, Sun Z, Liu Z, Guo H, Liu Q, Jiang H, Zou Y, Gong Y, Tischfield JA, Shao C. Replication stress induces micronuclei comprising of aggregated DNA double-strand breaks. Plos One. 6: e18618. PMID 21525980 DOI: 10.1371/journal.pone.0018618  0.72
2011 Maher BS, Vladimirov VI, Latendresse SJ, Thiselton DL, McNamee R, Kang M, Bigdeli TB, Chen X, Riley BP, Hettema JM, Chilcoat H, Heidbreder C, Muglia P, Murrelle EL, Dick DM, ... ... Tischfield JA, et al. The AVPR1A gene and substance use disorders: association, replication, and functional evidence. Biological Psychiatry. 70: 519-27. PMID 21514569 DOI: 10.1016/J.Biopsych.2011.02.023  0.72
2011 Derringer J, Krueger RF, Manz N, Porjesz B, Almasy L, Bookman E, Edenberg HJ, Kramer JR, Tischfield JA, Bierut LJ. Nonreplication of an association of SGIP1 SNPs with alcohol dependence and resting theta EEG power. Psychiatric Genetics. 21: 265-6. PMID 21317682 DOI: 10.1097/Ypg.0B013E32834371Fd  0.72
2011 Tichy ED, Liang L, Deng L, Tischfield J, Schwemberger S, Babcock G, Stambrook PJ. Mismatch and base excision repair proficiency in murine embryonic stem cells. Dna Repair. 10: 445-51. PMID 21315663 DOI: 10.1016/J.Dnarep.2011.01.008  0.72
2011 Saccone SF, Quan J, Mehta G, Bolze R, Thomas P, Deelman E, Tischfield JA, Rice JP. New tools and methods for direct programmatic access to the dbSNP relational database. Nucleic Acids Research. 39: D901-7. PMID 21037260 DOI: 10.1093/Nar/Gkq1054  0.72
2011 Serrano L, Liang L, Chang Y, Deng L, Maulion C, Nguyen S, Tischfield JA. Homologous recombination conserves DNA sequence integrity throughout the cell cycle in embryonic stem cells. Stem Cells and Development. 20: 363-74. PMID 20491544 DOI: 10.1089/Scd.2010.0159  0.6
2010 Bauer L, Dick D, Bierut L, Bucholz K, Edenberg H, Kuperman S, Kramer J, Nurnberger J, O'Connor S, Rice J, Rohrbaugh J, Schuckit M, Tischfield J, Porjesz B, Hesselbrock V. Obesity, smoking, and frontal brain dysfunction. The American Journal On Addictions / American Academy of Psychiatrists in Alcoholism and Addictions. 19: 391-400. PMID 20716301 DOI: 10.1111/J.1521-0391.2010.00069.X  0.72
2010 Saccone SF, Bolze R, Thomas P, Quan J, Mehta G, Deelman E, Tischfield JA, Rice JP. SPOT: a web-based tool for using biological databases to prioritize SNPs after a genome-wide association study. Nucleic Acids Research. 38: W201-9. PMID 20529875 DOI: 10.1093/Nar/Gkq513  0.72
2010 Willemsen G, de Geus EJ, Bartels M, van Beijsterveldt CE, Brooks AI, Estourgie-van Burk GF, Fugman DA, Hoekstra C, Hottenga JJ, Kluft K, Meijer P, Montgomery GW, Rizzu P, Sondervan D, Smit AB, ... ... Tischfield JA, et al. The Netherlands Twin Register biobank: a resource for genetic epidemiological studies. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 13: 231-45. PMID 20477721 DOI: 10.1375/twin.13.3.231  0.48
2010 Dick DM, Meyers J, Aliev F, Nurnberger J, Kramer J, Kuperman S, Porjesz B, Tischfield J, Edenberg HJ, Foroud T, Schuckit M, Goate A, Hesselbrock V, Bierut L. Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 1179-1188. PMID 20468071 DOI: 10.1002/Ajmg.B.31089  0.72
2010 Tichy ED, Pillai R, Deng L, Liang L, Tischfield J, Schwemberger SJ, Babcock GF, Stambrook PJ. Mouse embryonic stem cells, but not somatic cells, predominantly use homologous recombination to repair double-strand DNA breaks. Stem Cells and Development. 19: 1699-711. PMID 20446816 DOI: 10.1089/Scd.2010.0058  0.72
2010 Ercan-Sencicek AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE, Abbott T, Gupta A, King RA, Pauls DL, Tischfield JA, Heiman GA, Singer HS, Gilbert DL, Hoekstra PJ, et al. L-histidine decarboxylase and Tourette's syndrome. The New England Journal of Medicine. 362: 1901-8. PMID 20445167 DOI: 10.1056/Nejmoa0907006  0.72
2010 Chen AC, Manz N, Tang Y, Rangaswamy M, Almasy L, Kuperman S, Nurnberger J, O'Connor SJ, Edenberg HJ, Schuckit MA, Tischfield J, Foroud T, Bierut LJ, Rohrbaugh J, Rice JP, et al. Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence. Alcoholism, Clinical and Experimental Research. 34: 988-96. PMID 20374216 DOI: 10.1111/J.1530-0277.2010.01173.X  0.72
2010 Lin P, Hartz SM, Zhang Z, Saccone SF, Wang J, Tischfield JA, Edenberg HJ, Kramer JR, M Goate A, Bierut LJ, Rice JP. A new statistic to evaluate imputation reliability. Plos One. 5: e9697. PMID 20300623 DOI: 10.1371/Journal.Pone.0009697  0.72
2010 Tereshchenko IV, Chen Y, McDaniel LD, Schultz RA, Tischfield JA, Shao C. Small scale genetic alterations contribute to increased mutability at the X-linked Hprt locus in vivo in Blm hypomorphic mice. Dna Repair. 9: 551-7. PMID 20299287 DOI: 10.1016/j.dnarep.2010.02.005  0.72
2010 Bierut LJ, Agrawal A, Bucholz KK, Doheny KF, Laurie C, Pugh E, Fisher S, Fox L, Howells W, Bertelsen S, Hinrichs AL, Almasy L, Breslau N, Culverhouse RC, Dick DM, ... ... Tischfield JA, et al. A genome-wide association study of alcohol dependence. Proceedings of the National Academy of Sciences of the United States of America. 107: 5082-7. PMID 20202923 DOI: 10.1073/Pnas.0911109107  0.72
2010 Edenberg HJ, Koller DL, Xuei X, Wetherill L, McClintick JN, Almasy L, Bierut LJ, Bucholz KK, Goate A, Aliev F, Dick D, Hesselbrock V, Hinrichs A, Kramer J, Kuperman S, ... ... Tischfield JA, et al. Genome-wide association study of alcohol dependence implicates a region on chromosome 11. Alcoholism, Clinical and Experimental Research. 34: 840-52. PMID 20201924 DOI: 10.1111/J.1530-0277.2010.01156.X  0.72
2010 Andrysik Z, Bernstein WZ, Deng L, Myer DL, Li YQ, Tischfield JA, Stambrook PJ, Bahassi el M. The novel mouse Polo-like kinase 5 responds to DNA damage and localizes in the nucleolus. Nucleic Acids Research. 38: 2931-43. PMID 20100802 DOI: 10.1093/nar/gkq011  0.72
2010 Chen J, Chen Y, Capizzi S, Yang M, Deng L, Bledsoe SB, Evan AP, Tischfield JA, Sahota A. 2,8-dihydroxyadenine nephrolithiasis induces developmental stage-specific alterations in gene expression in mouse kidney. Urology. 75: 914-22. PMID 20035974 DOI: 10.1016/J.Urology.2009.10.031  0.6
2010 Zhao X, Ren G, Liang L, Ai PZ, Zheng B, Tischfield JA, Shi Y, Shao C. Brief report: interferon-gamma induces expansion of Lin(-)Sca-1(+)C-Kit(+) Cells. Stem Cells (Dayton, Ohio). 28: 122-6. PMID 19890981 DOI: 10.1002/Stem.252  0.72
2010 Xuei X, Flury-Wetherill L, Dick D, Goate A, Tischfield J, Nurnberger J, Schuckit M, Kramer J, Kuperman S, Hesselbrock V, Porjesz B, Foroud T, Edenberg HJ. GABRR1 and GABRR2, encoding the GABA-A receptor subunits ρ1 and ρ2, are associated with alcohol dependence American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 418-427. PMID 19536785 DOI: 10.1002/Ajmg.B.30995  0.72
2010 Ercolani M, Sahota A, Schuler C, Yang M, Evan AP, Reimer D, Barone JG, Tischfield JA, Levin RM. Bladder outlet obstruction in male cystinuria mice. International Urology and Nephrology. 42: 57-63. PMID 19484501 DOI: 10.1007/s11255-009-9597-y  0.52
2010 Rani V, Shao C, Tischfield J. Age Dependent Effect on Cellular Phenotype with Loss of Prdx1 Free Radical Biology and Medicine. 49. DOI: 10.1016/J.Freeradbiomed.2010.10.212  0.72
2009 Shao C, Liang L, Zhao X, Chen Y, Zheng B, Chen J, Luo M, Tischfield JA. Mutagenesis in vivo in T cells of p21-deficient mice. Mutation Research. 670: 103-6. PMID 19744501 DOI: 10.1016/J.Mrfmmm.2009.09.001  0.72
2009 Chen AC, Tang Y, Rangaswamy M, Wang JC, Almasy L, Foroud T, Edenberg HJ, Hesselbrock V, Nurnberger J, Kuperman S, O'Connor SJ, Schuckit MA, Bauer LO, Tischfield J, Rice JP, et al. Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 359-68. PMID 18618593 DOI: 10.1002/Ajmg.B.30818  0.72
2009 Wang JC, Grucza R, Cruchaga C, Hinrichs AL, Bertelsen S, Budde JP, Fox L, Goldstein E, Reyes O, Saccone N, Saccone S, Xuei X, Bucholz K, Kuperman S, Nurnberger J, ... ... Tischfield J, et al. Genetic variation in the CHRNA5 gene affects mRNA levels and is associated with risk for alcohol dependence. Molecular Psychiatry. 14: 501-10. PMID 18414406 DOI: 10.1038/Mp.2008.42  0.72
2008 Wetherill L, Schuckit MA, Hesselbrock V, Xuei X, Liang T, Dick DM, Kramer J, Nurnberger JI, Tischfield JA, Porjesz B, Edenberg HJ, Foroud T. Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence. Alcoholism, Clinical and Experimental Research. 32: 2031-40. PMID 18828811 DOI: 10.1111/J.1530-0277.2008.00790.X  0.72
2008 Barrera-Oro J, Liu TY, Gorden E, Kucherlapati R, Shao C, Tischfield JA. Role of the mismatch repair gene, Msh6, in suppressing genome instability and radiation-induced mutations. Mutation Research. 642: 74-9. PMID 18538799 DOI: 10.1016/J.Mrfmmm.2008.04.006  0.72
2008 Bierut LJ, Stitzel JA, Wang JC, Hinrichs AL, Grucza RA, Xuei X, Saccone NL, Saccone SF, Bertelsen S, Fox L, Horton WJ, Breslau N, Budde J, Cloninger CR, Dick DM, ... ... Tischfield JA, et al. Variants in nicotinic receptors and risk for nicotine dependence. The American Journal of Psychiatry. 165: 1163-71. PMID 18519524 DOI: 10.1176/Appi.Ajp.2008.07111711  0.72
2008 Grucza RA, Wang JC, Stitzel JA, Hinrichs AL, Saccone SF, Saccone NL, Bucholz KK, Cloninger CR, Neuman RJ, Budde JP, Fox L, Bertelsen S, Kramer J, Hesselbrock V, Tischfield J, et al. A risk allele for nicotine dependence in CHRNA5 is a protective allele for cocaine dependence. Biological Psychiatry. 64: 922-9. PMID 18519132 DOI: 10.1016/J.Biopsych.2008.04.018  0.72
2008 Liang L, Deng L, Nguyen SC, Zhao X, Maulion CD, Shao C, Tischfield JA. Human DNA ligases I and III, but not ligase IV, are required for microhomology-mediated end joining of DNA double-strand breaks. Nucleic Acids Research. 36: 3297-310. PMID 18440984 DOI: 10.1093/Nar/Gkn184  0.72
2008 Foroud T, Wetherill LF, Kramer J, Tischfield JA, Nurnberger JI, Schuckit MA, Xuei X, Edenberg HJ. The tachykinin receptor 3 is associated with alcohol and cocaine dependence. Alcoholism, Clinical and Experimental Research. 32: 1023-30. PMID 18422838 DOI: 10.1111/J.1530-0277.2008.00663.X  0.72
2008 Edenberg HJ, Wang J, Tian H, Pochareddy S, Xuei X, Wetherill L, Goate A, Hinrichs T, Kuperman S, Nurnberger JI, Schuckit M, Tischfield JA, Foroud T. A regulatory variation in OPRK1, the gene encoding the kappa-opioid receptor, is associated with alcohol dependence. Human Molecular Genetics. 17: 1783-9. PMID 18319328 DOI: 10.1093/Hmg/Ddn068  0.72
2008 Dick DM, Aliev F, Wang JC, Saccone S, Hinrichs A, Bertelsen S, Budde J, Saccone N, Foroud T, Nurnberger J, Xuei X, Conneally PM, Schuckit M, Almasy L, Crowe R, ... ... Tischfield JA, et al. A Systematic single nucleotide polymorphism screen to fine-map alcohol dependence genes on chromosome 7 identifies association with a novel susceptibility gene ACN9. Biological Psychiatry. 63: 1047-53. PMID 18163977 DOI: 10.1016/J.Biopsych.2007.11.005  0.72
2008 Edenberg HJ, Xuei X, Wetherill LF, Bierut L, Bucholz K, Dick DM, Hesselbrock V, Kuperman S, Porjesz B, Schuckit MA, Tischfield JA, Almasy LA, Nurnberger JI, Foroud T. Association of NFKB1, which encodes a subunit of the transcription factor NF-kappaB, with alcohol dependence. Human Molecular Genetics. 17: 963-70. PMID 18079108 DOI: 10.1093/Hmg/Ddm368  0.72
2008 Xuei X, Flury-Wetherill L, Almasy L, Bierut L, Tischfield J, Schuckit M, Nurnberger JI, Foroud T, Edenberg HJ. Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence. Addiction Biology. 13: 80-7. PMID 17910740 DOI: 10.1111/J.1369-1600.2007.00082.X  0.72
2007 Sahota A, Brooks AI, Tischfield JA. Preparing DNA from Mammalian sources for genotyping. Csh Protocols. 2007: pdb.top19. PMID 21357154  0.52
2007 Sahota A, Brooks AI, Tischfield JA. Preparing DNA from saliva for genotyping. Csh Protocols. 2007: pdb.prot4831. PMID 21357152  0.52
2007 Sahota A, Brooks AI, Tischfield JA, King IB. Preparing DNA from blood for genotyping. Csh Protocols. 2007: pdb.prot4830. PMID 21357151  0.52
2007 Sahota A, Brooks AI, Tischfield JA. Preparing DNA from cell pellets for genotyping. Csh Protocols. 2007: pdb.prot4829. PMID 21357150  0.52
2007 Dick DM, Wang JC, Plunkett J, Aliev F, Hinrichs A, Bertelsen S, Budde JP, Goldstein EL, Kaplan D, Edenberg HJ, Nurnberger J, Hesselbrock V, Schuckit M, Kuperman S, Tischfield J, et al. Family-based association analyses of alcohol dependence phenotypes across DRD2 and neighboring gene ANKK1. Alcoholism, Clinical and Experimental Research. 31: 1645-53. PMID 17850642 DOI: 10.1111/J.1530-0277.2007.00470.X  0.72
2007 Foroud T, Wetherill LF, Dick DM, Hesselbrock V, Nurnberger JI, Kramer J, Tischfield J, Schuckit M, Bierut LJ, Xuei X, Edenberg HJ. Lack of association of alcohol dependence and habitual smoking with catechol-O-methyltransferase. Alcoholism, Clinical and Experimental Research. 31: 1773-9. PMID 17850222 DOI: 10.1111/J.1530-0277.2007.00505.X  0.48
2007 Dick DM, Agrawal A, Wang JC, Hinrichs A, Bertelsen S, Bucholz KK, Schuckit M, Kramer J, Nurnberger J, Tischfield J, Edenberg HJ, Goate A, Bierut LJ. Alcohol dependence with comorbid drug dependence: genetic and phenotypic associations suggest a more severe form of the disorder with stronger genetic contribution to risk. Addiction (Abingdon, England). 102: 1131-9. PMID 17567401 DOI: 10.1111/J.1360-0443.2007.01871.X  0.48
2007 Liang L, Deng L, Mendonca MS, Chen Y, Zheng B, Stambrook PJ, Shao C, Tischfield JA. X-rays induce distinct patterns of somatic mutation in fetal versus adult hematopoietic cells. Dna Repair. 6: 1380-5. PMID 17553756 DOI: 10.1016/j.dnarep.2007.04.005  0.72
2007 Liang L, Mendonca MS, Deng L, Nguyen SC, Shao C, Tischfield JA. Reduced apoptosis and increased deletion mutations at Aprt locus in vivo in mice exposed to repeated ionizing radiation. Cancer Research. 67: 1910-7. PMID 17332317 DOI: 10.1158/0008-5472.Can-06-1476  0.72
2007 Bahassi el M, Penner CG, Robbins SB, Tichy E, Feliciano E, Yin M, Liang L, Deng L, Tischfield JA, Stambrook PJ. The breast cancer susceptibility allele CHEK2*1100delC promotes genomic instability in a knock-in mouse model. Mutation Research. 616: 201-9. PMID 17174984 DOI: 10.1016/J.Mrfmmm.2006.11.025  0.72
2007 Hong Y, Cervantes RB, Tichy E, Tischfield JA, Stambrook PJ. Protecting genomic integrity in somatic cells and embryonic stem cells. Mutation Research. 614: 48-55. PMID 16914171 DOI: 10.1016/J.Mrfmmm.2006.06.006  0.72
2006 Jones KA, Porjesz B, Almasy L, Bierut L, Dick D, Goate A, Hinrichs A, Rice JP, Wang JC, Bauer LO, Crowe R, Foroud T, Hesselbrock V, Kuperman S, Nurnberger J, ... ... Tischfield J, et al. A cholinergic receptor gene (CHRM2) affects event-related oscillations. Behavior Genetics. 36: 627-39. PMID 16823639 DOI: 10.1007/S10519-006-9075-6  0.72
2006 Edenberg HJ, Xuei X, Chen HJ, Tian H, Wetherill LF, Dick DM, Almasy L, Bierut L, Bucholz KK, Goate A, Hesselbrock V, Kuperman S, Nurnberger J, Porjesz B, Rice J, ... ... Tischfield J, et al. Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis. Human Molecular Genetics. 15: 1539-49. PMID 16571603 DOI: 10.1093/Hmg/Ddl073  0.48
2006 Dick DM, Bierut L, Hinrichs A, Fox L, Bucholz KK, Kramer J, Kuperman S, Hesselbrock V, Schuckit M, Almasy L, Tischfield J, Porjesz B, Begleiter H, Nurnberger J, Xuei X, et al. The role of GABRA2 in risk for conduct disorder and alcohol and drug dependence across developmental stages. Behavior Genetics. 36: 577-90. PMID 16557364 DOI: 10.1007/S10519-005-9041-8  0.48
2006 Hinrichs AL, Wang JC, Bufe B, Kwon JM, Budde J, Allen R, Bertelsen S, Evans W, Dick D, Rice J, Foroud T, Nurnberger J, Tischfield JA, Kuperman S, Crowe R, et al. Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence. American Journal of Human Genetics. 78: 103-11. PMID 16385453 DOI: 10.1086/499253  0.72
2006 Liang L, Chen J, Vittal R, Selvanayagam ZE, McAteer JA, Deng L, Tischfield J, Chin KV, Sahota A. Expression profiling of crystal-induced injury in human kidney epithelial cells. Nephron. Physiology. 103: p53-62. PMID 16374038 DOI: 10.1159/000090503  0.6
2006 Dick DM, Jones K, Saccone N, Hinrichs A, Wang JC, Goate A, Bierut L, Almasy L, Schuckit M, Hesselbrock V, Tischfield J, Foroud T, Edenberg H, Porjesz B, Begleiter H. Endophenotypes successfully lead to gene identification: results from the collaborative study on the genetics of alcoholism. Behavior Genetics. 36: 112-26. PMID 16341909 DOI: 10.1007/S10519-005-9001-3  0.48
2005 Edenberg HJ, Bierut LJ, Boyce P, Cao M, Cawley S, Chiles R, Doheny KF, Hansen M, Hinrichs T, Jones K, Kelleher M, Kennedy GC, Liu G, Marcus G, McBride C, ... ... Tischfield JA, et al. Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14. Bmc Genetics. 6: S2. PMID 16451628 DOI: 10.1186/1471-2156-6-S1-S2  0.72
2005 Vernon HJ, Osborne C, Tzortzaki EG, Yang M, Chen J, Rittling SR, Denhardt DT, Buyske S, Bledsoe SB, Evan AP, Fairbanks L, Simmonds HA, Tischfield JA, Sahota A. Aprt/Opn double knockout mice: osteopontin is a modifier of kidney stone disease severity. Kidney International. 68: 938-47. PMID 16105024 DOI: 10.1111/J.1523-1755.2005.00487.X  0.6
2005 Liang L, Deng L, Chen Y, Li GC, Shao C, Tischfield JA. Modulation of DNA end joining by nuclear proteins. The Journal of Biological Chemistry. 280: 31442-9. PMID 16012167 DOI: 10.1074/jbc.M503776200  0.72
2004 Shao C, Deng L, Chen Y, Kucherlapati R, Stambrook PJ, Tischfield JA. Mlh1 mediates tissue-specific regulation of mitotic recombination. Oncogene. 23: 9017-24. PMID 15480418 DOI: 10.1038/Sj.Onc.1208148  0.72
2004 Wang JC, Hinrichs AL, Stock H, Budde J, Allen R, Bertelsen S, Kwon JM, Wu W, Dick DM, Rice J, Jones K, Nurnberger JI, Tischfield J, Porjesz B, Edenberg HJ, et al. Evidence of common and specific genetic effects: association of the muscarinic acetylcholine receptor M2 (CHRM2) gene with alcohol dependence and major depressive syndrome. Human Molecular Genetics. 13: 1903-11. PMID 15229186 DOI: 10.1093/Hmg/Ddh194  0.72
2004 Jones KA, Porjesz B, Almasy L, Bierut L, Goate A, Wang JC, Dick DM, Hinrichs A, Kwon J, Rice JP, Rohrbaugh J, Stock H, Wu W, Bauer LO, Chorlian DB, ... ... Tischfield JA, et al. Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition. International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology. 53: 75-90. PMID 15210286 DOI: 10.1016/J.Ijpsycho.2004.02.004  0.72
2004 Berrettini W, Bierut L, Crowley TJ, Cubells JF, Frascella J, Gelernter J, Hewitt JK, Kreek MJ, Lachman H, Leppert M, Li MD, Madden P, Miner C, Pollock JD, Pomerleau O, ... ... Tischfield JA, et al. Setting priorities for genomic research. Science (New York, N.Y.). 304: 1445-7; author reply. PMID 15178784 DOI: 10.1126/Science.304.5676.1445C  0.72
2003 Tzortzaki EG, Tischfield JA, Sahota A, Siafakas NM, Gordon MK, Gerecke DR. Expression of FACIT collagens XII and XIV during bleomycin-induced pulmonary fibrosis in mice. The Anatomical Record. Part a, Discoveries in Molecular, Cellular, and Evolutionary Biology. 275: 1073-80. PMID 14613307 DOI: 10.1002/ar.a.10120  0.52
2003 Tzortzaki EG, Yang M, Glass D, Deng L, Evan AP, Bledsoe SB, Stambrook PJ, Sahota A, Tischfield JA. Impaired expression of an organic cation transporter, IMPT1, in a knockout mouse model for kidney stone disease. Urological Research. 31: 257-61. PMID 12856169 DOI: 10.1007/s00240-003-0318-1  0.72
2002 Tzortzaki EG, Glass D, Yang M, Evan AP, Bledsoe SB, Stambrook PJ, Sahota A, Tischfield JA. Gender- and age-dependent changes in kidney androgen protein mRNA expression in a knockout mouse model for nephrolithiasis. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 50: 1663-9. PMID 12486089  0.72
2002 Wang L, Raikwar N, Yang M, Deng L, McAteer JA, Stambrook PJ, Sahota A, Tischfield JA. Induction of alpha-catenin, integrin alpha3, integrin beta6, and PDGF-B by 2,8-dihydroxyadenine crystals in cultured kidney epithelial cells. Experimental Nephrology. 10: 365-73. PMID 12381921 DOI: 10.1159/000065301  0.72
2002 Liang L, Shao C, Deng L, Mendonca MS, Stambrook PJ, Tischfield JA. Radiation-induced genetic instability in vivo depends on p53 status. Mutation Research. 502: 69-80. PMID 11996974 DOI: 10.1016/S0027-5107(02)00029-5  0.72
2002 Shao C, Yin M, Deng L, Stambrook PJ, Doetschman T, Tischfield JA. Loss of heterozygosity and point mutation at Aprt locus in T cells and fibroblasts of Pms2-/- mice. Oncogene. 21: 2840-5. PMID 11973643 DOI: 10.1038/Sj.Onc.1205358  0.72
2002 Cervantes RB, Stringer JR, Shao C, Tischfield JA, Stambrook PJ. Embryonic stem cells and somatic cells differ in mutation frequency and type. Proceedings of the National Academy of Sciences of the United States of America. 99: 3586-90. PMID 11891338 DOI: 10.1073/Pnas.062527199  0.72
2002 Porjesz B, Almasy L, Edenberg HJ, Wang K, Chorlian DB, Foroud T, Goate A, Rice JP, O'Connor SJ, Rohrbaugh J, Kuperman S, Bauer LO, Crowe RR, Schuckit MA, Hesselbrock V, ... ... Tischfield JA, et al. Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus. Proceedings of the National Academy of Sciences of the United States of America. 99: 3729-33. PMID 11891318 DOI: 10.1073/Pnas.052716399  0.72
2002 Degousee N, Ghomashchi F, Stefanski E, Singer A, Smart BP, Borregaard N, Reithmeier R, Lindsay TF, Lichtenberger C, Reinisch W, Lambeau G, Arm J, Tischfield J, Gelb MH, Rubin BB. Groups IV, V, and X phospholipases A2s in human neutrophils: role in eicosanoid production and gram-negative bacterial phospholipid hydrolysis. The Journal of Biological Chemistry. 277: 5061-73. PMID 11741884 DOI: 10.1074/Jbc.M109083200  0.72
2001 Degousee N, Stefanski E, Lindsay TF, Ford DA, Shahani R, Andrews CA, Thuerauf DJ, Glembotski CC, Nevalainen TJ, Tischfield J, Rubin BB. p38 MAPK regulates group IIa phospholipase A2 expression in interleukin-1beta -stimulated rat neonatal cardiomyocytes. The Journal of Biological Chemistry. 276: 43842-9. PMID 11571275 DOI: 10.1074/Jbc.M101516200  0.72
2001 Evan AP, Bledsoe SB, Connors BA, Deng L, Liang L, Shao C, Fineberg NS, Grynpas MD, Stambrook PJ, Youzhi S, Sahota A, Tischfield JA. Sequential analysis of kidney stone formation in the Aprt knockout mouse Kidney International. 60: 910-923. PMID 11532086 DOI: 10.1046/J.1523-1755.2001.060003910.X  0.72
2001 Shao C, Stambrook PJ, Tischfield JA. Mitotic recombination is suppressed by chromosomal divergence in hybrids of distantly related mouse strains Nature Genetics. 28: 169-172. PMID 11381266 DOI: 10.1038/88897  0.72
2000 Wang L, Raikwar N, Deng L, Yang M, Liang L, Shao C, Evan AP, Stambrook PJ, Sahota A, Tischfield JA. Altered gene expression in kidneys of mice with 2,8-dihydroxyadenine nephrolithiasis Kidney International. 58: 528-536. PMID 10916076 DOI: 10.1046/j.1523-1755.2000.00199.x  0.72
2000 Shao C, Deng L, Henegariu O, Liang L, Stambrook PJ, Tischfield JA. Chromosome instability contributes to loss of heterozygosity in mice lacking p53 Proceedings of the National Academy of Sciences of the United States of America. 97: 7405-7410. PMID 10861008 DOI: 10.1073/pnas.97.13.7405  0.72
2000 Liang L, Deng L, Shao C, Stambrook PJ, Tischfield JA. In vivo loss of heterozygosity in T-cells of B6C3F1 Aprt(+/-) mice Environmental and Molecular Mutagenesis. 35: 150-157. PMID 10712749 DOI: 10.1002/(SICI)1098-2280(2000)35:2<150::AID-EM10>3.0.CO;2-0  0.72
1999 Shao C, Deng L, Henegariu O, Liang L, Raikwar N, Sahota A, Stambrook PJ, Tischfield JA. Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous mice Proceedings of the National Academy of Sciences of the United States of America. 96: 9230-9235. PMID 10430925 DOI: 10.1073/pnas.96.16.9230  0.72
1999 Bolante-Cervantes R, Li S, Sahota A, Tischfield JA, Zwerdling T, Stambrook PJ. Pattern of localization of primitive hematopoietic cells in vivo using a novel mouse model Experimental Hematology. 27: 1346-1352. PMID 10428512 DOI: 10.1016/S0301-472X(99)00064-8  0.72
1998 Stockelman MG, Lorenz JN, Smith FN, Boivin GP, Sahota A, Tischfield JA, Stambrook PJ. Chronic renal failure in a mouse model of human adenine phosphoribosyltransferase deficiency. American Journal of Physiology. Renal Physiology. 275: F154-F163. PMID 29591671 DOI: 10.1152/ajprenal.1998.275.1.F154  0.6
1998 Bond C, LaForge KS, Tian M, Melia D, Zhang S, Borg L, Gong J, Schluger J, Strong JA, Leal SM, Tischfield JA, Kreek MJ, Yu L. Single-nucleotide polymorphism in the human mu opioid receptor gene alters beta-endorphin binding and activity: possible implications for opiate addiction. Proceedings of the National Academy of Sciences of the United States of America. 95: 9608-13. PMID 9689128 DOI: 10.1073/Pnas.95.16.9608  0.72
1998 Cloninger CR, Van Eerdewegh P, Goate A, Edenberg HJ, Blangero J, Hesselbrock V, Reich T, Nurnberger J, Schuckit M, Porjesz B, Crowe R, Rice JP, Foroud T, Przybeck TR, Almasy L, ... ... Tischfield JA, et al. Anxiety proneness linked to epistatic loci in genome scan of human personality traits. American Journal of Medical Genetics. 81: 313-7. PMID 9674977 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<313::Aid-Ajmg7>3.0.Co;2-U  0.72
1998 Reich T, Edenberg HJ, Goate A, Williams JT, Rice JP, Van Eerdewegh P, Foroud T, Hesselbrock V, Schuckit MA, Bucholz K, Porjesz B, Li TK, Conneally PM, Nurnberger JI, Tischfield JA, et al. Genome-wide search for genes affecting the risk for alcohol dependence. American Journal of Medical Genetics. 81: 207-15. PMID 9603606 DOI: 10.1002/(Sici)1096-8628(19980508)81:3<207::Aid-Ajmg1>3.0.Co;2-T  0.72
1997 Reddy ST, Winstead MV, Tischfield JA, Herschman HR. Analysis of the secretory phospholipase A2 that mediates prostaglandin production in mast cells. The Journal of Biological Chemistry. 272: 13591-6. PMID 9153207 DOI: 10.1074/Jbc.272.21.13591  0.72
1997 Chen J, Shao C, Lazar V, Srivastava CH, Lee WH, Tischfield JA. Localization of group IIc low molecular weight phospholipase A2 mRNA to meiotic cells in the mouse. Journal of Cellular Biochemistry. 64: 369-75. PMID 9057094 DOI: 10.1002/(SICI)1097-4644(19970301)64:3<369::AID-JCB3>3.0.CO;2-T  0.72
1996 Stambrook PJ, Shao C, Stockelman M, Boivin G, Engle SJ, Tischfield JA. APRT: a versatile in vivo resident reporter of local mutation and loss of heterozygosity. Environmental and Molecular Mutagenesis. 28: 471-82. PMID 8991080 DOI: 10.1002/(SICI)1098-2280(1996)28:4<471::AID-EM25>3.0.CO;2-B  0.72
1996 Engle SJ, Womer DE, Davies PM, Boivin G, Sahota A, Simmonds HA, Stambrook PJ, Tischfield JA. HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome. Human Molecular Genetics. 5: 1607-10. PMID 8894695  0.72
1996 Boyadjiev SA, Sahota A, Tischfield JA. Identification and application of polymorphisms flanking the human adenine phosphoribosyltransferase gene. Human Mutation. 8: 214-5. PMID 8889579 DOI: 10.1002/(SICI)1098-1004(1996)8:3<214::AID-HUMU3>3.0.CO;2-9  0.52
1996 Tischfield JA, Xia YR, Shih DM, Klisak I, Chen J, Engle SJ, Siakotos AN, Winstead MV, Seilhamer JJ, Allamand V, Gyapay G, Lusis AJ. Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and human. Genomics. 32: 328-33. PMID 8838795 DOI: 10.1006/Geno.1996.0126  0.72
1996 Engle SJ, Stockelman MG, Chen J, Boivin G, Yum MN, Davies PM, Ying MY, Sahota A, Simmonds HA, Stambrook PJ, Tischfield JA. Adenine phosphoribosyltransferase-deficient mice develop 2,8-dihydroxyadenine nephrolithiasis. Proceedings of the National Academy of Sciences of the United States of America. 93: 5307-12. PMID 8643571 DOI: 10.1073/Pnas.93.11.5307  0.72
1995 Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS. Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus. Human Molecular Genetics. 4: 459-63. PMID 7795603 DOI: 10.1093/Hmg/4.3.459  0.72
1995 Zhu Y, Bye S, Stambrook PJ, Tischfield JA. Aflatoxin B1, 2-aminoanthracene, and 7,12-dimethylbenz[a]anthracene-induced frameshift mutations in human APRT Environmental and Molecular Mutagenesis. 26: 234-239. PMID 7588649 DOI: 10.1002/em.2850260308  0.72
1994 Chen J, Engle SJ, Seilhamer JJ, Tischfield JA. Cloning and recombinant expression of a novel human low molecular weight Ca(2+)-dependent phospholipase A2. The Journal of Biological Chemistry. 269: 2365-8. PMID 8300559  0.72
1994 Chen J, Engle SJ, Seilhamer JJ, Tischfield JA. Cloning and characterization of novel rat and mouse low molecular weight Ca(2+)-dependent phospholipase A2s containing 16 cysteines. The Journal of Biological Chemistry. 269: 23018-24. PMID 8083202  0.72
1994 Bye S, Mallmann R, Duley J, Simmonds HA, Chen J, Tischfield JA, Sahota A. Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasis. The Clinical Investigator. 72: 550-3. PMID 7981585 DOI: 10.1007/Bf00207486  0.6
1994 Chen J, Engle SJ, Seilhamer JJ, Tischfield JA. Cloning, expression and partial characterization of a novel rat phospholipase A2. Biochimica Et Biophysica Acta. 1215: 115-20. PMID 7947992 DOI: 10.1016/0005-2760(94)90099-X  0.72
1994 Sahota A, Chen J, Boyadjiev SA, Gault MH, Tischfield JA. Missense mutation in the adenine phosphoribosyltransferase gene causing 2,8-dihydroxyadenine urolithiasis. Human Molecular Genetics. 3: 817-8. PMID 7915931  0.6
1994 Sahota A, Chen J, Bye S, Jaing J, Berenyi M, Fekete G, Tischfield JA. Occurrence of a missense mutation in one allele and a seven basepair deletion in the other allele in a patient with adenine phosphoribosyltransferase deficiency. Human Mutation. 3: 315-7. PMID 7912608 DOI: 10.1002/Humu.1380030324  0.6
1994 Sahota A, Bye S, Chen J, Khattar NH, Turker MS, Moro F, Simmonds HA, Emmerson BT, Gordon RB, Tischfield JA. Molecular characterization of a novel mutation in APRT heterozygotes. Advances in Experimental Medicine and Biology. 370: 675-8. PMID 7660994  0.72
1994 Bye S, Sahota A, Chen J, Tischfield JA. Analysis of APRT mutations by reverse-transcription PCR. Advances in Experimental Medicine and Biology. 370: 671-4. PMID 7660993  0.6
1994 Tischfield JA, Engle SJ, Gupta PK, Bye S, Boyadjiev S, Shao C, O'Neill P, Albertini RJ, Stambrook PJ, Sahota AS. Germline and somatic mutation at the APRT locus of mice and man. Advances in Experimental Medicine and Biology. 370: 661-4. PMID 7660991 DOI: 10.1007/978-1-4615-2584-4_137  0.72
1994 Boyadjiev SA, Sahota A, Tischfield JA. Identification of polymorphic markers flanking the human APRT gene. Advances in Experimental Medicine and Biology. 370: 657-60. PMID 7660990 DOI: 10.1007/978-1-4615-2584-4_136  0.52
1994 Gupta PK, Sahota A, Boyadjiev SA, Bye S, O'Neill JP, Hunter TC, Albertini RJ, Tischfield JA. Analysis of in vivo somatic mutations at the APRT locus. Advances in Experimental Medicine and Biology. 370: 653-6. PMID 7660989 DOI: 10.1007/978-1-4615-2584-4_135  0.52
1994 Zhu Y, Bye S, Stambrook PJ, Tischfield JA. Single-base deletion induced by benzo[a]pyrene diol epoxide at the adenine phosphoribosyltransferase locus in human fibrosarcoma cell lines Mutation Research/Genetic Toxicology. 321: 73-79. PMID 7510848 DOI: 10.1016/0165-1218(94)90122-8  0.72
1993 Fye KH, Sahota A, Hancock DC, Gelb AB, Chen J, Sparks JW, Sibley RK, Tischfield JA. Adenine phosphoribosyltransferase deficiency with renal deposition of 2,8-dihydroxyadenine leading to nephrolithiasis and chronic renal failure. Archives of Internal Medicine. 153: 767-70. PMID 8447714  0.6
1993 Zhu Y, Stambrook PJ, Tischfield JA. Loss of heterozygosity: The most frequent cause of recessive phenotype expression at the heterozygous human adenine phosphoribosyltransferase locus Molecular Carcinogenesis. 8: 138-144. PMID 8216732 DOI: 10.1002/mc.2940080304  0.72
1993 Chen J, Sahota A, Martin GF, Hakoda M, Kamatani N, Stambrook PJ, Tischfield JA. Analysis of germline and in vivo somatic mutations in the human adenine phosphoribosyltransferase gene: mutational hot spots at the intron 4 splice donor site and at codon 87. Mutation Research. 287: 217-25. PMID 7685481 DOI: 10.1016/0027-5107(93)90014-7  0.72
1992 Young K, Foroud T, Williams P, Jackson CE, Beckmann JS, Cohen D, Conneally PM, Tischfield J, Hodes ME. Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15. Genomics. 13: 1370-1. PMID 1505977 DOI: 10.1016/0888-7543(92)90074-3  0.72
1992 Bertino AM, Tischfield JA, Stambrook PJ. Reconstitution of an episomal mouse aprt gene as a consequence of recombination Mgg Molecular &Amp; General Genetics. 232: 24-32. PMID 1313148 DOI: 10.1007/BF00299133  0.72
1991 Chen J, Sahota A, Stambrook PJ, Tischfield JA. Polymerase chain reaction amplification and sequence analysis of human mutant adenine phosphoribosyltransferase genes: the nature and frequency of errors caused by Taq DNA polymerase. Mutation Research. 249: 169-76. PMID 2067530 DOI: 10.1016/0027-5107(91)90143-C  0.72
1991 Sahota A, Chen J, Stambrook PJ, Tischfield JA. Mutational basis of adenine phosphoribosyltransferase deficiency. Advances in Experimental Medicine and Biology. 309: 73-6. PMID 1781410  0.72
1991 Chen J, Sahota A, Laxdal T, Scrine M, Bowman S, Cui C, Stambrook PJ, Tischfield JA. Identification of a single missense mutation in the adenine phosphoribosyltransferase (APRT) gene from five Icelandic patients and a British patient. American Journal of Human Genetics. 49: 1306-11. PMID 1746557  0.72
1991 Gathof BS, Sahota A, Gresser U, Chen J, Stambrook PS, Tischfield JA, Zöllner N. A splice mutation at the adenine phosphoribosyltransferase locus detected in a German family. Advances in Experimental Medicine and Biology. 309: 83-6. PMID 1685862  0.72
1991 Sahota A, Chen J, Behzadian MA, Ravindra R, Takeuchi H, Stambrook PJ, Tischfield JA. 2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locus. American Journal of Human Genetics. 48: 983-9. PMID 1673292  0.72
1990 Schaff DA, Jarrett RA, Dlouhy SR, Ponniah S, Stockelman M, Stambrook PJ, Tischfield JA. Mouse transgenes in human cells detect specific base substitutions Proceedings of the National Academy of Sciences of the United States of America. 87: 8675-8679. PMID 2236079  0.72
1990 Gathof BS, Sahota A, Gresser U, Chen J, Stambrook PJ, Tischfield JA, Zöllner N. Identification of a splice mutation at the adenine phosphoribosyltransferase locus in a German family. Klinische Wochenschrift. 69: 1152-5. PMID 2135300 DOI: 10.1007/BF01815434  0.72
1990 Sahota A, Chen J, Asaki K, Takeuchi H, Stambrook PJ, Tischfield JA. Identification of a common nonsense mutation in Japanese patients with type I adenine phosphoribosyltransferase deficiency. Nucleic Acids Research. 18: 5915-6. PMID 1977137 DOI: 10.1093/nar/18.19.5915  0.72
1989 Turker MS, Stambrook PJ, Tischfield JA, Smith AC, Martin GM. Allelic variation linked to adenine phosphoribosyltransferase locus in mouse teratocarcinoma cell line and feral-derived mouse strains Somatic Cell and Molecular Genetics. 15: 159-166. PMID 2928841 DOI: 10.1007/Bf01535077  0.72
1989 Dlouhy SR, Schaff DA, Trofatter JA, Liu HS, Stambrook PJ, Tischfield JA. Denaturing gradient gel analysis of single-base substitutions at a mouse adenine phosphoribosyltransferase splice acceptor site Molecular Carcinogenesis. 2: 217-225. PMID 2803521 DOI: 10.1002/Mc.2940020408  0.72
1988 Dush MK, Briggs MR, Royce ME, Schaff DA, Khan SA, Tischfield JA, Stambrook PJ. Identification of DNA sequences required for mouse APRT gene expression Nucleic Acids Research. 16: 8509-8524. PMID 2901725 DOI: 10.1093/nar/16.17.8509  0.72
1987 Broderick TP, Schaff DA, Bertino AM, Dush MK, Tischfield JA, Stambrook PJ. Comparative anatomy of the human APRT gene and enzyme: Nucleotide sequence divergence and conservation of a nonrandom CpG dinucleotide arrangement Proceedings of the National Academy of Sciences of the United States of America. 84: 3349-3353. PMID 3554238 DOI: 10.1073/pnas.84.10.3349  0.72
1986 Fratini A, Simmers RN, Callen DF, Hyland VJ, Tischfield JA, Stambrook PJ, Sutherland GR. A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23) (FRA16D) loci Cytogenetic and Genome Research. 43: 10-13. PMID 3780312 DOI: 10.1159/000132291  0.72
1986 Dush MK, Tischfield JA, Khan SA, Feliciano E, Sikela JM, Kozak CA, Stambrook PJ. An unusual adenine phosphoribosyltransferase pseudogene is syntenic with its functional gene and is flanked by highly polymorphic DNAs. Molecular and Cellular Biology. 6: 4161-7. PMID 3025640  0.72
1986 Rashidbaigi A, Langer JA, Jung V, Jones C, Morse HG, Tischfield JA, Trill JJ, Kung HF, Pestka S. The gene for the human immune interferon receptor is located on chromosome 6. Proceedings of the National Academy of Sciences of the United States of America. 83: 384-8. PMID 2934742 DOI: 10.1073/Pnas.83.2.384  0.72
1985 Dush MK, Sikela JM, Khan SA, Tischfield JA, Stambrook PJ. Nucleotide sequence and organization of the mouse adenine phosphoribosyltransferase gene: presence of a coding region common to animal and bacterial phosphoribosyltransferases that has a variable intron/exon arrangement. Proceedings of the National Academy of Sciences of the United States of America. 82: 2731-5. PMID 3921964 DOI: 10.1073/pnas.82.9.2731  0.72
1984 Srivatsan ES, Stanbridge EJ, Saxon PJ, Stambrook PJ, Trill JJ, Tischfield JA. Plasmid, phage, and genomic DNA-mediated transfer and expression of prokaryotic and eukaryotic genes in cultured human cells Cytogenetic and Genome Research. 38: 227-234. PMID 6237889 DOI: 10.1159/000132065  0.72
1984 Stambrook PJ, Dush MK, Trill JJ, Tischfield JA. Cloning of a functional human adenine phosphoribosyltransferase (APRT) gene: Identification of a restriction fragment length polymorphism and preliminary analysis of DNAs from APRT-deficient families and cell mutants Somatic Cell and Molecular Genetics. 10: 359-367. PMID 6087472 DOI: 10.1007/BF01535631  0.72
1983 Sikela JM, Khan SA, Feliciano E, Trill J, Tischfield JA, Stambrook PJ. Cloning and expression of a mouse adenine phosphoribosyltransferase gene. Gene. 22: 219-28. PMID 6307822 DOI: 10.1016/0378-1119(83)90106-3  0.72
1981 Golden NL, Bilenker R, Johnson WE, Tischfield JA. Abnormality of chromosome 16 and its phenotypic expression Clinical Genetics. 19: 41-45. PMID 7460380 DOI: 10.1111/j.1399-0004.1981.tb00665.x  0.72
1974 Creagan RP, Carritt B, Chen S, Kucherlapati R, McMorris FA, Ricciuti F, Tan YH, Tischfield JA, Ruddle FH. Proceedings: Confirmation of the synteny of the human genes for cytoplasmic isocitrate dehydrogenase and cytoplasmic malate dehydrogenase and assignment to chromosome 2. Cytogenetics and Cell Genetics. 13: 79-82. PMID 4827500 DOI: 10.1159/000130239  0.72
1974 Tischfield JA, Creagan RP, Nichols EA, Ruddle FH. Assignment of a gene for adenosine deaminase to human chromosome 20. Human Heredity. 24: 1-11. PMID 4136545 DOI: 10.1159/000152631  0.72
1973 McMorris FA, Chen TR, Ricciuti F, Tischfield J, Creagan R, Ruddle F. Chromosome assignments in man of the genes for two hexosephosphate isomerases. Science (New York, N.Y.). 179: 1129-31. PMID 4120258 DOI: 10.1126/Science.179.4078.1129  0.72
1972 Ruddle F, Ricciuti F, McMorris FA, Darlington G, Chen T. Somatic cell genetic assignment of peptidase C and the Rh linkage group to chromosome A-1 in man. Science (New York, N.Y.). 176: 1429-31. PMID 4113665 DOI: 10.1126/Science.176.4042.1429  0.72
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