Jay Tischfield - Publications

Graduate School - New Brunswick Rutgers University, New Brunswick, United States 
Microbiology Biology

117 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
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 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  0.4
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
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 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  0.4
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.56
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.56
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  0.64
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  0.64
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  0.64
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  0.56
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.56
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  0.64
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  0.64
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  0.64
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  0.64
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  0.4
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.56
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  0.64
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
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.56
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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  0.64
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