Margit Burmeister - Publications

University of Michigan, Ann Arbor, Ann Arbor, MI 
genetics, behavioral, psychiatric, neurological

131 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 Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, ... ... Burmeister M, et al. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry. PMID 33674754 DOI: 10.1038/s41380-021-01063-8  0.52
2021 Jia X, Goes FS, Locke AE, Palmer D, Wang W, Cohen-Woods S, Genovese G, Jackson AU, Jiang C, Kvale M, Mullins N, Nguyen H, Pirooznia M, Rivera M, Ruderfer DM, ... ... Burmeister M, et al. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry. PMID 33483695 DOI: 10.1038/s41380-020-01006-9  0.52
2020 Li W, Frank E, Zhao Z, Chen L, Wang Z, Burmeister M, Sen S. Mental Health of Young Physicians in China During the Novel Coronavirus Disease 2019 Outbreak. Jama Network Open. 3: e2010705. PMID 32478846 DOI: 10.1001/jamanetworkopen.2020.10705  0.92
2019 Fang Y, Scott L, Song P, Burmeister M, Sen S. Genomic prediction of depression risk and resilience under stress. Nature Human Behaviour. PMID 31659322 DOI: 10.1038/S41562-019-0759-3  0.92
2019 Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, ... ... Burmeister M, et al. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. PMID 31043756 DOI: 10.1038/S41588-019-0397-8  0.52
2019 Langenecker SA, Mickey BJ, Eichhammer P, Sen S, Elverman KH, Kennedy SE, Heitzeg MM, Ribeiro SM, Love TM, Hsu DT, Koeppe RA, Watson SJ, Akil H, Goldman D, Burmeister M, et al. Cognitive Control as a 5-HT-Based Domain That Is Disrupted in Major Depressive Disorder. Frontiers in Psychology. 10: 691. PMID 30984083 DOI: 10.3389/Fpsyg.2019.00691  0.92
2018 Warthen KG, Sanford B, Walker K, Jones KG, Angstadt M, Sripada C, Goldman D, Zubieta JK, Welsh RC, Burmeister M, Mickey BJ. Neuropeptide Y and representation of salience in human nucleus accumbens. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 30337638 DOI: 10.1038/S41386-018-0230-6  0.4
2018 Seong E, Insolera R, Dulovic M, Kamsteeg EJ, Trinh J, Brüggemann N, Sandford E, Li S, Ozel AB, Li JZ, Jewett T, Kievit AJA, Münchau A, Shakkottai V, Klein C, ... ... Burmeister M, et al. Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects. Annals of Neurology. PMID 29604224 DOI: 10.1002/Ana.25220  0.64
2018 Trucco EM, Cope LM, Burmeister M, Zucker RA, Heitzeg MM. Pathways to Youth Behavior: The Role of Genetic, Neural, and Behavioral Markers. Journal of Research On Adolescence : the Official Journal of the Society For Research On Adolescence. 28: 26-39. PMID 29460350 DOI: 10.1111/Jora.12341  0.36
2017 Trucco EM, Villafuerte S, Hussong A, Burmeister M, Zucker RA. Biological Underpinnings of an Internalizing Pathway to Alcohol, Cigarette, and Marijuana Use. Journal of Abnormal Psychology. PMID 29172598 DOI: 10.1037/Abn0000310  0.44
2017 Love TM, Cranford JA, Burmeister M, Wojnar M, Zucker RA, J Brower K. Oxytocin Genotype Moderates the Impact of Social Support on Psychiatric Distress in Alcohol-Dependent Patients. Alcohol and Alcoholism (Oxford, Oxfordshire). 1-7. PMID 29040351 DOI: 10.1093/Alcalc/Agx077  0.36
2017 Cope LM, Munier EC, Trucco EM, Hardee JE, Burmeister M, Zucker RA, Heitzeg MM. Effects of the serotonin transporter gene, sensitivity of response to alcohol, and parental monitoring on risk for problem alcohol use. Alcohol (Fayetteville, N.Y.). 59: 7-16. PMID 28262188 DOI: 10.1016/J.Alcohol.2016.12.001  0.36
2016 Cope LM, Hardee JE, Soules ME, Burmeister M, Zucker RA, Heitzeg MM. Reduced brain activation during inhibitory control in children with COMT Val/Val genotype. Brain and Behavior. 6: e00577. PMID 28032000 DOI: 10.1002/Brb3.577  0.36
2016 Trucco EM, Villafuerte S, Burmeister M, Zucker RA. Beyond risk: Prospective effects of GABA Receptor Subunit Alpha-2 (GABRA2) × Positive Peer Involvement on adolescent behavior. Development and Psychopathology. 1-14. PMID 27581089 DOI: 10.1017/S0954579416000419  0.44
2016 Trucco EM, Hicks BM, Villafuerte S, Nigg JT, Burmeister M, Zucker RA. Temperament and Externalizing Behavior as Mediators of Genetic Risk on Adolescent Substance Use. Journal of Abnormal Psychology. PMID 26845260 DOI: 10.1037/Abn0000143  0.92
2016 Kim M, Sandford E, Gatica D, Qiu Y, Liu X, Zheng Y, Schulman BA, Xu J, Semple I, Ro SH, Kim B, Mavioglu RN, Tolun A, Jipa A, Takats S, ... ... Burmeister M, et al. Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay. Elife. 5. PMID 26812546 DOI: 10.7554/Elife.12245  0.92
2015 Cai L, Chen T, Yang J, Zhou K, Yan X, Chen W, Sun L, Li L, Qin S, Wang P, Yang P, Cui D, Burmeister M, He L, Jia W, et al. Serum trace element differences between Schizophrenia patients and controls in the Han Chinese population. Scientific Reports. 5: 15013. PMID 26456296 DOI: 10.1038/srep15013  0.92
2015 Sun J, Pan CQ, Chew TW, Liang F, Burmeister M, Low BC. BNIP-H Recruits the Cholinergic Machinery to Neurite Terminals to Promote Acetylcholine Signaling and Neuritogenesis. Developmental Cell. 34: 555-68. PMID 26343454 DOI: 10.1016/j.devcel.2015.08.006  0.92
2015 Sandford E, Li JZ, Burmeister M. Evaluation of exome sequencing variation in undiagnosed ataxias. Brain : a Journal of Neurology. PMID 25842391 DOI: 10.1093/brain/awv087  0.92
2015 Trucco EM, Villafuerte S, Heitzeg MM, Burmeister M, Zucker RA. Susceptibility effects of GABA receptor subunit alpha-2 (GABRA2) variants and parental monitoring on externalizing behavior trajectories: Risk and protection conveyed by the minor allele. Development and Psychopathology. 1-12. PMID 25797587 DOI: 10.1017/S0954579415000255  0.44
2014 Villafuerte S, Trucco EM, Heitzeg MM, Burmeister M, Zucker RA. Genetic variation in GABRA2 moderates peer influence on externalizing behavior in adolescents. Brain and Behavior. 4: 833-40. PMID 25365806 DOI: 10.1002/Brb3.291  0.92
2014 Burns R, Majczenko K, Xu J, Peng W, Yapici Z, Dowling JJ, Li JZ, Burmeister M. Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome. Neurology. 83: 2175-82. PMID 25361784 DOI: 10.1212/Wnl.0000000000001053  0.92
2014 Sandford E, Burmeister M. Genes and genetic testing in hereditary ataxias. Genes. 5: 586-603. PMID 25055202 DOI: 10.3390/genes5030586  0.92
2014 Heitzeg MM, Villafuerte S, Weiland BJ, Enoch MA, Burmeister M, Zubieta JK, Zucker RA. Effect of GABRA2 genotype on development of incentive-motivation circuitry in a sample enriched for alcoholism risk. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 39: 3077-86. PMID 24975023 DOI: 10.1038/npp.2014.161  0.92
2014 Trucco EM, Villafuerte S, Heitzeg MM, Burmeister M, Zucker RA. Rule breaking mediates the developmental association between GABRA2 and adolescent substance abuse. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 55: 1372-9. PMID 24811113 DOI: 10.1111/Jcpp.12244  0.92
2014 Luna-Cancalon K, Sikora KM, Pappas SS, Singh V, Wulff H, Paulson HL, Burmeister M, Shakkottai VG. Alterations in cerebellar physiology are associated with a stiff-legged gait in Atcay(ji-hes) mice. Neurobiology of Disease. 67: 140-8. PMID 24727095 DOI: 10.1016/J.Nbd.2014.03.020  0.92
2014 Glaser YG, Zubieta JK, Hsu DT, Villafuerte S, Mickey BJ, Trucco EM, Burmeister M, Zucker RA, Heitzeg MM. Indirect effect of corticotropin-releasing hormone receptor 1 gene variation on negative emotionality and alcohol use via right ventrolateral prefrontal cortex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 4099-107. PMID 24623788 DOI: 10.1523/Jneurosci.3672-13.2014  0.92
2013 Culverhouse RC, Bowes L, Breslau N, Nurnberger JI, Burmeister M, Fergusson DM, Munafò M, Saccone NL, Bierut LJ. Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression. Bmc Psychiatry. 13: 304. PMID 24219410 DOI: 10.1186/1471-244X-13-304  0.92
2013 Villafuerte S, Strumba V, Stoltenberg SF, Zucker RA, Burmeister M. Impulsiveness mediates the association between GABRA2 SNPs and lifetime alcohol problems. Genes, Brain, and Behavior. 12: 525-31. PMID 23566244 DOI: 10.1111/Gbb.12039  0.92
2013 Schoen CJ, Burmeister M, Lesperance MM. Diaphanous homolog 3 (Diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness. Plos One. 8: e56520. PMID 23441200 DOI: 10.1371/Journal.Pone.0056520  0.92
2013 Jakubczyk A, Klimkiewicz A, Kopera M, Krasowska A, Wrzosek M, Matsumoto H, Burmeister M, Brower KJ, Wojnar M. The CC genotype in the T102C HTR2A polymorphism predicts relapse in individuals after alcohol treatment. Journal of Psychiatric Research. 47: 527-33. PMID 23321485 DOI: 10.1016/j.jpsychires.2012.12.004  0.92
2013 Greenwald MK, Steinmiller CL, Sliwerska E, Lundahl L, Burmeister M. BDNF Val(66)Met genotype is associated with drug-seeking phenotypes in heroin-dependent individuals: a pilot study. Addiction Biology. 18: 836-45. PMID 22339949 DOI: 10.1111/J.1369-1600.2011.00431.X  0.92
2012 Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, ... ... Burmeister M, et al. Mutations in KCND3 cause spinocerebellar ataxia type 22. Annals of Neurology. 72: 859-69. PMID 23280837 DOI: 10.1002/Ana.23701  0.92
2012 Sikora KM, Nosavanh LM, Kantheti P, Burmeister M, Hortsch M. Expression of Caytaxin protein in Cayman Ataxia mouse models correlates with phenotype severity. Plos One. 7: e50570. PMID 23226316 DOI: 10.1371/journal.pone.0050570  0.92
2012 Zhang Y, Li J, Tardif T, Burmeister M, Villafuerte SM, McBride-Chang C, Li H, Shi B, Liang W, Zhang Z, Shu H. Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population. Plos One. 7: e42969. PMID 23028439 DOI: 10.1371/Journal.Pone.0042969  0.92
2012 Guan Y, Gorenshteyn D, Burmeister M, Wong AK, Schimenti JC, Handel MA, Bult CJ, Hibbs MA, Troyanskaya OG. Tissue-specific functional networks for prioritizing phenotype and disease genes. Plos Computational Biology. 8: e1002694. PMID 23028291 DOI: 10.1371/Journal.Pcbi.1002694  0.92
2012 Jasinska AJ, Lowry CA, Burmeister M. Corrigendum: Serotonin transporter gene, stress, and raphe–raphe interactions: a molecular mechanism of depression. Trends in Neurosciences. 35: 454-5. PMID 22919705 DOI: 10.1016/J.Tins.2012.03.002  0.92
2012 Majczenko K, Davidson AE, Camelo-Piragua S, Agrawal PB, Manfready RA, Li X, Joshi S, Xu J, Peng W, Beggs AH, Li JZ, Burmeister M, Dowling JJ. Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical cores. American Journal of Human Genetics. 91: 365-71. PMID 22818856 DOI: 10.1016/J.Ajhg.2012.06.012  0.92
2012 Jasinska AJ, Ho SS, Taylor SF, Burmeister M, Villafuerte S, Polk TA. Influence of threat and serotonin transporter genotype on interference effects. Frontiers in Psychology. 3: 139. PMID 22590463 DOI: 10.3389/Fpsyg.2012.00139  0.92
2012 Brower KJ, Wojnar M, Sliwerska E, Armitage R, Burmeister M. PER3 polymorphism and insomnia severity in alcohol dependence. Sleep. 35: 571-7. PMID 22467995 DOI: 10.5665/sleep.1748  0.92
2012 Jasinska AJ, Lowry CA, Burmeister M. Serotonin transporter gene, stress and raphe-raphe interactions: a molecular mechanism of depression. Trends in Neurosciences. 35: 395-402. PMID 22301434 DOI: 10.1016/J.Tins.2012.01.001  0.92
2012 Jakubczyk A, Wrzosek M, Lukaszkiewicz J, Sadowska-Mazuryk J, Matsumoto H, Sliwerska E, Glass J, Burmeister M, Brower KJ, Wojnar M. The CC genotype in HTR2A T102C polymorphism is associated with behavioral impulsivity in alcohol-dependent patients. Journal of Psychiatric Research. 46: 44-9. PMID 21930285 DOI: 10.1016/j.jpsychires.2011.09.001  0.92
2012 Villafuerte S, Heitzeg MM, Foley S, Yau WY, Majczenko K, Zubieta JK, Zucker RA, Burmeister M. Impulsiveness and insula activation during reward anticipation are associated with genetic variants in GABRA2 in a family sample enriched for alcoholism. Molecular Psychiatry. 17: 511-9. PMID 21483437 DOI: 10.1038/Mp.2011.33  0.92
2011 Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, Edenberg HJ, Nurnberger JI, Rietschel M, Blackwood D, Corvin A, Flickinger M, Guan W, Mattingsdal M, McQuillin A, ... ... Burmeister M, et al. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Nature Genetics. 43: 977-985. PMID 21926972 DOI: 10.1038/Ng.943  0.92
2011 Karg K, Burmeister M, Shedden K, Sen S. The serotonin transporter promoter variant (5-HTTLPR), stress, and depression meta-analysis revisited: evidence of genetic moderation. Archives of General Psychiatry. 68: 444-54. PMID 21199959 DOI: 10.1001/Archgenpsychiatry.2010.189  0.92
2010 Singer E, Couper MP, Raghunathan TE, Antonucci TC, Burmeister M, Van Hoewyk J. The Effect of Question Framing and Response Options on the Relationship between Racial Attitudes and Beliefs about Genes as Causes of Behavior. Public Opinion Quarterly. 74: 460-476. PMID 22476404 DOI: 10.1093/Poq/Nfq009  0.92
2010 Zhang P, Xiang N, Chen Y, Sliwerska E, McInnis MG, Burmeister M, Zöllner S. Family-based association analysis to finemap bipolar linkage peak on chromosome 8q24 using 2,500 genotyped SNPs and 15,000 imputed SNPs. Bipolar Disorders. 12: 786-92. PMID 21176025 DOI: 10.1111/j.1399-5618.2010.00883.x  0.92
2010 Schoen CJ, Emery SB, Thorne MC, Ammana HR, Sliwerska E, Arnett J, Hortsch M, Hannan F, Burmeister M, Lesperance MM. Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila. Proceedings of the National Academy of Sciences of the United States of America. 107: 13396-401. PMID 20624953 DOI: 10.1073/Pnas.1003027107  0.92
2010 Terracciano A, Sanna S, Uda M, Deiana B, Usala G, Busonero F, Maschio A, Scally M, Patriciu N, Chen WM, Distel MA, Slagboom EP, Boomsma DI, Villafuerte S, Sliwerska E, ... Burmeister M, et al. Genome-wide association scan for five major dimensions of personality. Molecular Psychiatry. 15: 647-56. PMID 18957941 DOI: 10.1038/Mp.2008.113  0.92
2009 Villafuerte SM, Vallabhaneni K, Sliwerska E, McMahon FJ, Young EA, Burmeister M. SSRI response in depression may be influenced by SNPs in HTR1B and HTR1A. Psychiatric Genetics. 19: 281-91. PMID 19829169 DOI: 10.1097/YPG.0b013e32832a506e  0.92
2009 Scott LJ, Muglia P, Kong XQ, Guan W, Flickinger M, Upmanyu R, Tozzi F, Li JZ, Burmeister M, Absher D, Thompson RC, Francks C, Meng F, Antoniades A, Southwick AM, et al. Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. Proceedings of the National Academy of Sciences of the United States of America. 106: 7501-6. PMID 19416921 DOI: 10.1073/Pnas.0813386106  0.92
2009 Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF. Genomewide association studies: history, rationale, and prospects for psychiatric disorders. The American Journal of Psychiatry. 166: 540-56. PMID 19339359 DOI: 10.1176/Appi.Ajp.2008.08091354  0.92
2009 Chen H, Wang N, Burmeister M, McInnis MG. MicroRNA expression changes in lymphoblastoid cell lines in response to lithium treatment. The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (Cinp). 12: 975-81. PMID 19254429 DOI: 10.1017/S1461145709000029  0.92
2009 Li MD, Burmeister M. New insights into the genetics of addiction. Nature Reviews. Genetics. 10: 225-31. PMID 19238175 DOI: 10.1038/nrg2536  0.92
2009 Wojnar M, Brower KJ, Strobbe S, Ilgen M, Matsumoto H, Nowosad I, Sliwerska E, Burmeister M. Association between Val66Met brain-derived neurotrophic factor (BDNF) gene polymorphism and post-treatment relapse in alcohol dependence. Alcoholism, Clinical and Experimental Research. 33: 693-702. PMID 19170664 DOI: 10.1111/j.1530-0277.2008.00886.x  0.92
2009 Zöllner S, Su G, Stewart WC, Chen Y, McInnis MG, Burmeister M. Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24. Genetic Epidemiology. 33: 357-68. PMID 19085946 DOI: 10.1002/gepi.20391  0.92
2008 Sen S, Burmeister M. Hardy-Weinberg analysis of a large set of published association studies reveals genotyping error and a deficit of heterozygotes across multiple loci. Human Genomics. 3: 36-52. PMID 19129089 DOI: 10.1186/1479-7364-3-1-36  0.92
2008 Burmeister M, McInnis MG, Zöllner S. Psychiatric genetics: progress amid controversy. Nature Reviews. Genetics. 9: 527-40. PMID 18560438 DOI: 10.1038/nrg2381  0.92
2008 Zandi PP, Zöllner S, Avramopoulos D, Willour VL, Chen Y, Qin ZS, Burmeister M, Miao K, Gopalakrishnan S, McEachin R, Potash JB, Depaulo JR, McInnis MG. Family-based SNP association study on 8q24 in bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 612-8. PMID 18163389 DOI: 10.1002/Ajmg.B.30651  0.92
2008 Saunders EH, Scott LJ, McInnis MG, Burmeister M. Familiality and diagnostic patterns of subphenotypes in the National Institutes of Mental Health bipolar sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 18-26. PMID 17525972 DOI: 10.1002/ajmg.b.30558  0.92
2008 Lesperance MM, Burmeister M. Commentary on "occupational noise, smoking and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: A European population-based multicentre study" by Fransen et al., J. Assoc. Res. Otolaryngol. DOI 10.1007/s10162-008-0123-1 Jaro - Journal of the Association For Research in Otolaryngology. 9: 261-263. DOI: 10.1007/s10162-008-0128-9  0.92
2007 Pomerleau OF, Burmeister M, Madden P, Long JC, Swan GE, Kardia SL. Genetic research on complex behaviors: an examination of attempts to identify genes for smoking. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. 9: 883-901. PMID 17654301 DOI: 10.1080/14622200701485125  0.92
2007 Newell-Litwa K, Seong E, Burmeister M, Faundez V. Neuronal and non-neuronal functions of the AP-3 sorting machinery. Journal of Cell Science. 120: 531-41. PMID 17287392 DOI: 10.1242/Jcs.03365  0.92
2007 Sliwerska E, Meng F, Speed TP, Jones EG, Bunney WE, Akil H, Watson SJ, Burmeister M. SNPs on chips: the hidden genetic code in expression arrays. Biological Psychiatry. 61: 13-6. PMID 16690034 DOI: 10.1016/j.biopsych.2006.01.023  0.92
2007 Singer E, Antonucci TC, Burmeister M, Couper MP, Raghunathan TE, Van Hoewyk J. Beliefs about genes and environment as determinants of behavioral characteristics International Journal of Public Opinion Research. 19: 331-353. DOI: 10.1093/Ijpor/Edm016  0.92
2007 Wojnar M, Brower KJ, Jakubczyk A, Zmigrodzka I, Burmeister M, Matsumoto H, Woźny E, Śliwerska E, Hegedus AM, Klimkiewicz A, Ślufarska A, Lipiński M, Zucker RA. Influence of impulsiveness, suicidality, and serotonin genes on treatment outcomes in alcohol dependence - A preliminary report Archives of Psychiatry and Psychotherapy. 9: 13-18.  0.92
2006 Wojnar M, Brower KJ, Jakubczyk A, Zmigrodzka I, Burmeister M, Matsumoto H, Woźny E, Sliwerska E, Hegedus AM, Husar A, Slufarska A, LipiÅ„ski M, Zucker RA. [Influence of impulsivity, suicidality and serotonin genes on treatment outcomes in alcohol dependence]. Psychiatria Polska. 40: 985-94. PMID 17217240  0.92
2006 Wong G, Conger SB, Burmeister M. Mapping of genetic modifiers affecting the eye phenotype of ocular retardation (Chx10or-J) mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 518-25. PMID 16783634 DOI: 10.1007/s00335-005-0159-z  0.92
2006 Vawter MP, Tomita H, Meng F, Bolstad B, Li J, Evans S, Choudary P, Atz M, Shao L, Neal C, Walsh DM, Burmeister M, Speed T, Myers R, Jones EG, et al. Mitochondrial-related gene expression changes are sensitive to agonal-pH state: implications for brain disorders. Molecular Psychiatry. 11: 615, 663-79. PMID 16636682 DOI: 10.1038/Sj.Mp.4001830  0.92
2006 Bueller JA, Aftab M, Sen S, Gomez-Hassan D, Burmeister M, Zubieta JK. BDNF Val66Met allele is associated with reduced hippocampal volume in healthy subjects. Biological Psychiatry. 59: 812-5. PMID 16442082 DOI: 10.1016/J.Biopsych.2005.09.022  0.92
2006 Stoltenberg SF, Glass JM, Chermack ST, Flynn HA, Li S, Weston ME, Burmeister M. Possible association between response inhibition and a variant in the brain-expressed tryptophan hydroxylase-2 gene. Psychiatric Genetics. 16: 35-8. PMID 16395128 DOI: 10.1097/01.Ypg.0000176528.30362.34  0.92
2005 Li J, Burmeister M. Genetical genomics: combining genetics with gene expression analysis. Human Molecular Genetics. 14: R163-9. PMID 16244315 DOI: 10.1093/hmg/ddi267  0.92
2005 Sen S, Nesse R, Sheng L, Stoltenberg SF, Gleiberman L, Burmeister M, Weder AB. Association between a dopamine-4 receptor polymorphism and blood pressure. American Journal of Hypertension. 18: 1206-10. PMID 16182111 DOI: 10.1016/J.Amjhyper.2005.04.010  0.92
2005 Schinka JA, Sen S, Burmeister M, Ghosh D, Munafò MR, Clark T, Flint J. Measurement scale does moderate the association between the serotonin transporter gene and trait anxiety: Comments on Munafo et al [1] (multiple letters) Molecular Psychiatry. 10: 892-897. PMID 15983622 DOI: 10.1038/  0.92
2005 Seong E, Wainer BH, Hughes ED, Saunders TL, Burmeister M, Faundez V. Genetic analysis of the neuronal and ubiquitous AP-3 adaptor complexes reveals divergent functions in brain. Molecular Biology of the Cell. 16: 128-40. PMID 15537701 DOI: 10.1091/Mbc.E04-10-0892  0.92
2004 Gilbert N, Bomar JM, Burmeister M, Moran JV. Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse. Human Mutation. 24: 9-13. PMID 15221784 DOI: 10.1002/humu.20060  0.92
2004 Sen S, Burmeister M, Ghosh D. Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 127: 85-9. PMID 15108187 DOI: 10.1002/Ajmg.B.20158  0.92
2004 Seong E, Saunders TL, Stewart CL, Burmeister M. To knockout in 129 or in C57BL/6: that is the question. Trends in Genetics : Tig. 20: 59-62. PMID 14746984 DOI: 10.1016/J.Tig.2003.12.006  0.92
2004 Sen S, Villafuerte S, Nesse R, Stoltenberg SF, Hopcian J, Gleiberman L, Weder A, Burmeister M. Serotonin transporter and GABAA alpha 6 receptor variants are associated with neuroticism. Biological Psychiatry. 55: 244-9. PMID 14744464 DOI: 10.1016/J.Biopsych.2003.08.006  0.92
2003 Swartz BE, Li S, Bespalova I, Burmeister M, Dulaney E, Robinson FR, Leigh RJ. Pathogenesis of clinical signs in recessive ataxia with saccadic intrusions. Annals of Neurology. 54: 824-8. PMID 14681893 DOI: 10.1002/Ana.10758  0.92
2003 Bomar JM, Benke PJ, Slattery EL, Puttagunta R, Taylor LP, Seong E, Nystuen A, Chen W, Albin RL, Patel PD, Kittles RA, Sheffield VC, Burmeister M. Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse. Nature Genetics. 35: 264-9. PMID 14556008 DOI: 10.1038/Ng1255  0.92
2003 Villafuerte S, Burmeister M. Untangling genetic networks of panic, phobia, fear and anxiety. Genome Biology. 4: 224. PMID 12914652 DOI: 10.1186/gb-2003-4-8-224  0.92
2003 Qiao X, Pennesi M, Seong E, Gao H, Burmeister M, Wu SM. Photoreceptor degeneration and rd1 mutation in the grizzled/mocha mouse strain. Vision Research. 43: 859-65. PMID 12668055 DOI: 10.1016/S0042-6989(02)00393-0  0.92
2003 Kantheti P, Diaz ME, Peden AE, Seong EE, Dolan DF, Robinson MS, Noebels JL, Burmeister ML. Genetic and phenotypic analysis of the mouse mutant mh2J, an Ap3d allele caused by IAP element insertion. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 157-67. PMID 12647238 DOI: 10.1007/s00335-002-2238-8  0.92
2003 Sen S, Nesse RM, Stoltenberg SF, Li S, Gleiberman L, Chakravarti A, Weder AB, Burmeister M. A BDNF coding variant is associated with the NEO personality inventory domain neuroticism, a risk factor for depression. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 28: 397-401. PMID 12589394 DOI: 10.1038/Sj.Npp.1300053  0.92
2002 Seong E, Seasholtz AF, Burmeister M. Mouse models for psychiatric disorders. Trends in Genetics : Tig. 18: 643-50. PMID 12446150 DOI: 10.1016/S0168-9525(02)02807-X  0.92
2002 Merikangas KR, Chakravarti A, Moldin SO, Araj H, Blangero JC, Burmeister M, Crabbe J, Depaulo JR, Foulks E, Freimer NB, Koretz DS, Lichtenstein W, Mignot E, Reiss AL, Risch NJ, et al. Future of genetics of mood disorders research. Biological Psychiatry. 52: 457-77. PMID 12361664 DOI: 10.1016/S0006-3223(02)01471-3  0.92
2002 Hill EM, Stoltenberg SF, Bullard KH, Li S, Zucker RA, Burmeister M. Antisocial alcoholism and serotonin-related polymorphisms: association tests. Psychiatric Genetics. 12: 143-53. PMID 12218658 DOI: 10.1097/00041444-200209000-00005  0.92
2002 Swartz BE, Burmeister M, Somers JT, Rottach KG, Bespalova IN, Leigh RJ. A form of inherited cerebellar ataxia with saccadic intrusions, increased saccadic speed, sensory neuropathy, and myoclonus. Annals of the New York Academy of Sciences. 956: 441-4. PMID 11960835 DOI: 10.1111/J.1749-6632.2002.Tb02850.X  0.92
2001 Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Human Molecular Genetics. 10: 2501-8. PMID 11709537 DOI: 10.1093/Hmg/10.22.2501  0.92
2001 Raphael Y, Kobayashi KN, Dootz GA, Beyer LA, Dolan DF, Burmeister M. Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice. Hearing Research. 151: 237-249. PMID 11124469 DOI: 10.1016/S0378-5955(00)00233-1  0.92
2001 Greene CC, McMillan PM, Barker SE, Kurnool P, Lomax MI, Burmeister M, Lesperance MM. DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24. American Journal of Human Genetics. 68: 254-60. PMID 11115382 DOI: 10.1086/316925  0.92
2001 Li S, Stoltenberg SF, Bullard KR, Zucker RA, Hill EM, Burmeister M. Transmission disequilibrium and quantitative analysis of multiloci polymorphisms within the MAOA gene using family trios with antisocial alcoholism American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 628.  0.92
2000 Puttagunta R, Gordon LA, Meyer GE, Kapfhamer D, Lamerdin JE, Kantheti P, Portman KM, Chung WK, Jenne DE, Olsen AS, Burmeister M. Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints. Genome Research. 10: 1369-80. PMID 10984455 DOI: 10.1101/gr.145200  0.92
2000 Smith B, Shatz R, Elisevich K, Bespalova IN, Burmeister M. Effects of vagus nerve stimulation on progressive myoclonus epilepsy of Unverricht-Lundborg type. Epilepsia. 41: 1046-8. PMID 10961635 DOI: 10.1111/J.1528-1157.2000.Tb00293.X  0.92
2000 Lesperance MM, Burmeister M. Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3. American Journal of Human Genetics. 67: 262-3. PMID 10848501 DOI: 10.1086/302975  0.92
2000 Stoltenberg SF, Burmeister M. Recent progress in psychiatric genetics-some hope but no hype. Human Molecular Genetics. 9: 927-35. PMID 10767316 DOI: 10.1093/Hmg/9.6.927  0.92
2000 Bespalova IN, Burmeister M. Identification of a novel LIM domain gene, LMCD1, and chromosomal localization in human and mouse. Genomics. 63: 69-74. PMID 10662546 DOI: 10.1006/geno.1999.6049  0.92
2000 Bone-Larson C, Basu S, Radel JD, Liang M, Perozek T, Kapousta-Bruneau N, Green DG, Burmeister M, Hankin MH. Partial rescue of the ocular retardation phenotype by genetic modifiers. Journal of Neurobiology. 42: 232-47. PMID 10640330 DOI: 10.1002/(SICI)1097-4695(20000205)42:2<232::AID-NEU7>3.0.CO;2-4  0.92
1999 Miller CL, Burmeister M, Stevens KE. Hippocampal auditory gating in the hyperactive mocha mouse. Neuroscience Letters. 276: 57-60. PMID 10586974 DOI: 10.1016/S0304-3940(99)00784-3  0.92
1999 Burmeister M, Bryda EC, Bureau JF, Noben-Trauth K. Mouse chromosome 10. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 950-1. PMID 10501952 DOI: 10.1007/s003359901129  0.92
1999 Bespalova IN, Burmeister M, Lesperance MM. No association between DFNA6 and Pro250Arg mutation in FGFR3. American Journal of Medical Genetics. 88: 451. PMID 10490695 DOI: 10.1002/(SICI)1096-8628(19991015)88:5<451::AID-AJMG1>3.0.CO;2-4  0.92
1999 Ghaziuddin M, Burmeister M. Deletion of chromosome 2q37 and autism: a distinct subtype? Journal of Autism and Developmental Disorders. 29: 259-63. PMID 10425588 DOI: 10.1023/A:1023088207468  0.92
1999 Van Camp G, Kunst H, Flothmann K, McGuirt W, Wauters J, Marres H, Verstreken M, Bespalova IN, Burmeister M, Van de Heyning PH, Smith RJ, Willems PJ, Cremers CW, Lesperance MM. A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus. Journal of Medical Genetics. 36: 532-6. PMID 10424813 DOI: 10.1136/Jmg.36.7.532  0.92
1999 Hill EM, Stoltenberg SF, Burmeister M, Closser M, Zucker RA. Potential associations among genetic markers in the serotonergic system and the antisocial alcoholism subtype. Experimental and Clinical Psychopharmacology. 7: 103-21. PMID 10340151 DOI: 10.1037/1064-1297.7.2.103  0.92
1999 Burmeister M. Basic concepts in the study of diseases with complex genetics. Biological Psychiatry. 45: 522-32. PMID 10088042 DOI: 10.1016/S0006-3223(98)00316-3  0.92
1998 Miller CL, Burmeister M, Thompson RC. Antisense expression of the human pro-melanin-concentrating hormone genes. Brain Research. 803: 86-94. PMID 9729295 DOI: 10.1016/S0006-8993(98)00626-X  0.92
1998 Kantheti P, Qiao X, Diaz ME, Peden AA, Meyer GE, Carskadon SL, Kapfhamer D, Sufalko D, Robinson MS, Noebels JL, Burmeister M. Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles. Neuron. 21: 111-22. PMID 9697856 DOI: 10.1016/S0896-6273(00)80519-X  0.92
1998 Miller CL, Thompson RC, Burmeister M. Radiation hybrid mapping of the two highly homologous human-variant pMCHL genes by PCR-SSCP. Genome Research. 8: 737-40. PMID 9685321 DOI: 10.1101/Gr.8.7.737  0.92
1998 Burmeister M, Bryda EC, Bureau JF, Noben-Trauth K. Encyclopedia of the mouse genome VII. Mouse chromosome 10. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: S200-14. PMID 9662627  0.92
1998 Zobeley E, Sufalko DK, Adkins S, Burmeister M. Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10. Genomics. 50: 260-6. PMID 9653653 DOI: 10.1006/geno.1998.5298  0.92
1997 Gong TW, Shin JJ, Burmeister M, Lomax MI. Complete cDNAs for CDC42 from chicken cochlea and mouse liver. Biochimica Et Biophysica Acta. 1352: 282-92. PMID 9224952 DOI: 10.1016/S0167-4781(97)00027-4  0.92
1997 Burmeister M, Meyer GE. The trefoil gene maps to mouse chromosome 17. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 223-4. PMID 9072957 DOI: 10.1007/S003359900637  0.92
1996 Mohrenweiser H, Olsen A, Archibald A, Beattie C, Burmeister M, Lamerdin J, Lennon G, Stewart E, Stubbs L, Weber JL, Johnson K. Report an abstracts of the third international workshop on human chromosome 19 mapping 1996. Cytogenetics and Cell Genetics. 74: 161-86. PMID 8941368 DOI: 10.1159/000134408  0.92
1996 Ziegler SF, Mortrud MT, Swartz AR, Baker E, Sutherland GR, Burmeister M, Mulligan JT. Molecular characterization of a nonneuronal human UNC18 homolog. Genomics. 37: 19-23. PMID 8921365 DOI: 10.1006/geno.1996.0515  0.92
1996 Gong TL, Burmeister M, Lomax MI. The novel gene D4Mil1e maps to mouse chromosome 4 and human chromosome 1p36. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 790-1. PMID 8854876 DOI: 10.1007/S003359900237  0.92
1996 Bryda EC, Ling H, Rathbun DE, Burmeister M, Flaherty L. Fine genetic map of mouse chromosome 10 around the polycystic kidney disease gene, jcpk, and ankyrin 3. Genomics. 35: 425-30. PMID 8812475 DOI: 10.1006/geno.1996.0381  0.92
1996 Burmeister M, Ren Q, Makris GJ, Samson D, Bennett V. Genes for the neuronal immunoglobulin domain cell adhesion molecules neurofascin and Nr-CAM map to mouse chromosomes 1 and 12 and homologous human chromosomes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 558-9. PMID 8672144 DOI: 10.1007/S003359900168  0.92
1996 Sapru MK, Gao JP, Walke W, Burmeister M, Goldman D. Cloning and characterization of a novel transcriptional repressor of the nicotinic acetylcholine receptor delta-subunit gene. The Journal of Biological Chemistry. 271: 7203-11. PMID 8636158 DOI: 10.1074/jbc.271.12.7203  0.92
1996 Burmeister M, Novak J, Liang MY, Basu S, Ploder L, Hawes NL, Vidgen D, Hoover F, Goldman D, Kalnins VI, Roderick TH, Taylor BA, Hankin MH, McInnes RR. Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. Nature Genetics. 12: 376-84. PMID 8630490 DOI: 10.1038/Ng0496-376  0.92
1993 Delabar JM, Créau N, Sinet PM, Ritter O, Antonarakis SE, Burmeister M, Chakravarti A, Nizetic D, Ohki M, Patterson D. Report of the Fourth International Workshop on Human Chromosome 21. Genomics. 18: 735-45. PMID 8307590 DOI: 10.1016/S0888-7543(05)80390-8  0.92
1993 Taylor BA, Frankel WN, Burmeister M, Bryda E. Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 10. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: S154-63. PMID 8268670  0.92
1993 Bespalova IN, Farjo Q, Mortlock DP, Jackson AU, Meisler MH, Swaroop A, Burmeister M. Mapping of the neural retina leucine zipper gene, Nrl, to mouse chromosome 14. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4: 618-20. PMID 8268663 DOI: 10.1007/BF00361397  0.92
1993 Taylor BA, Frankel WN, Burmeister M, Bryda E. Mouse chromosome 10 Mammalian Genome. 4. DOI: 10.1007/BF00360836  0.92
1992 Trask BJ, Massa HF, Burmeister M. Fluorescence in situ hybridization establishes the order cen-DXS28(C7)-DXS67(B24)-DXS68(L1)-tel in human chromosome Xp21.3. Genomics. 13: 455-7. PMID 1612605 DOI: 10.1016/0888-7543(92)90271-S  0.92
1991 Burmeister M, Kim S, Price ER, de Lange T, Tantravahi U, Myers RM, Cox DR. A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis. Genomics. 9: 19-30. PMID 2004760 DOI: 10.1016/0888-7543(91)90216-2  0.52
1991 Gaensler KM, Burmeister M, Brownstein BH, Taillon-Miller P, Myers RM. Physical mapping of yeast artificial chromosomes containing sequences from the human beta-globin gene region. Genomics. 10: 976-84. PMID 1916829 DOI: 10.1016/0888-7543(91)90188-K  0.52
1991 Burmeister M, Cox DR, Myers RM. TaqI RFLP at D21S137. Nucleic Acids Research. 19: 4020. PMID 1677761 DOI: 10.1093/Nar/19.14.4020  0.52
1991 Burmeister M, diSibio G, Cox DR, Myers RM. Identification of polymorphisms by genomic denaturing gradient gel electrophoresis: application to the proximal region of human chromosome 21. Nucleic Acids Research. 19: 1475-81. PMID 1674130 DOI: 10.1093/Nar/19.7.1475  0.52
1990 Cox DR, Burmeister M, Price ER, Kim S, Myers RM. Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. Science (New York, N.Y.). 250: 245-50. PMID 2218528 DOI: 10.1126/SCIENCE.2218528  0.52
1987 Westphal EM, Burmeister M, Wienker TF, Lehrach H, Bender K, Scherer G. Tyrosine aminotransferase and chymotrypsinogen B are linked to haptoglobin on human chromosome 16q: comparison of genetic and physical distances. Genomics. 1: 313-9. PMID 2896626 DOI: 10.1016/0888-7543(87)90030-9  0.92
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