| Year |
Citation |
Score |
| 2024 |
Ha HT, Liu S, Nguyen XT, Vo LK, Leong NC, Nguyen DT, Balamurugan S, Lim PY, Wu Y, Seong E, Nguyen TQ, Oh J, Wenk MR, Cazenave-Gassiot A, Yapici Z, ... ... Burmeister M, et al. Lack of SPNS1 results in accumulation of lysolipids and lysosomal storage disease in mouse models. Jci Insight. PMID 38451736 DOI: 10.1172/jci.insight.175462 |
0.552 |
|
| 2024 |
Meng X, Navoly G, Giannakopoulou O, Levey DF, Koller D, Pathak GA, Koen N, Lin K, Adams MJ, Rentería ME, Feng Y, Gaziano JM, Stein DJ, Zar HJ, Campbell ML, ... ... Burmeister M, et al. Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nature Genetics. PMID 38177345 DOI: 10.1038/s41588-023-01596-4 |
0.49 |
|
| 2023 |
Wang J, Fang Y, Frank E, Walton MA, Burmeister M, Tewari A, Dempsey W, NeCamp T, Sen S, Wu Z. Effectiveness of gamified team competition as mHealth intervention for medical interns: a cluster micro-randomized trial. Npj Digital Medicine. 6: 4. PMID 36631665 DOI: 10.1038/s41746-022-00746-y |
0.394 |
|
| 2023 |
Cleary JL, Fang Y, Zahodne LB, Bohnert ASB, Burmeister M, Sen S. Polygenic Risk and Social Support in Predicting Depression Under Stress. The American Journal of Psychiatry. appiajp21111100. PMID 36628515 DOI: 10.1176/appi.ajp.21111100 |
0.434 |
|
| 2022 |
Chen L, Zhao Z, Wang Z, Zhou Y, Zhou X, Pan H, Shen F, Zeng S, Shao X, Frank E, Sen S, Li W, Burmeister M. Prevalence and risk factors for depression among training physicians in China and the United States. Scientific Reports. 12: 8170. PMID 35581251 DOI: 10.1038/s41598-022-12066-y |
0.413 |
|
| 2021 |
Burmeister M, Sen S. Genetic interactions with stressful environments in depression and addiction. Bjpsych Advances. 27: 153-157. PMID 35529524 DOI: 10.1192/bja.2021.21 |
0.457 |
|
| 2021 |
Giannakopoulou O, Lin K, Meng X, Su MH, Kuo PH, Peterson RE, Awasthi S, Moscati A, Coleman JRI, Bass N, Millwood IY, Chen Y, Chen Z, Chen HC, Lu ML, ... ... Burmeister M, et al. The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. Jama Psychiatry. PMID 34586374 DOI: 10.1001/jamapsychiatry.2021.2099 |
0.445 |
|
| 2021 |
Tyler J, Fang Y, Goldstein C, Forger D, Sen S, Burmeister M. Genomic heterogeneity affects the response to Daylight Saving Time. Scientific Reports. 11: 14792. PMID 34285349 DOI: 10.1038/s41598-021-94459-z |
0.439 |
|
| 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 |
0.422 |
|
| 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 |
0.493 |
|
| 2020 |
Bilal M, Hayat A, Umair M, Ullah A, Khawaja S, Malik E, Burmeister M, Bibi N, Umm-E-Kalsoom, Memon MI, Basit S, Ahmad W, Khan B. Sequence Variants in the and Genes Underlying Isolated Split-Hand/Split-Foot Malformation. Genetic Testing and Molecular Biomarkers. PMID 32762550 DOI: 10.1089/gtmb.2020.0024 |
0.346 |
|
| 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 |
0.375 |
|
| 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 |
0.495 |
|
| 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 |
0.533 |
|
| 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 |
0.614 |
|
| 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 |
0.508 |
|
| 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 |
0.59 |
|
| 2018 |
Duda M, Zhang H, Li HD, Wall DP, Burmeister M, Guan Y. Brain-specific functional relationship networks inform autism spectrum disorder gene prediction. Translational Psychiatry. 8: 56. PMID 29507298 DOI: 10.1038/S41398-018-0098-6 |
0.33 |
|
| 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 |
0.357 |
|
| 2017 |
Palencia-Campos A, Ullah A, Nevado J, Yildirim R, Unal E, Ciorraga M, Barruz P, Chico L, Piceci-Sparascio F, Guida V, De Luca A, Kayserili H, Ullah I, Burmeister M, Lapunzina P, et al. GLI1 Inactivation is associated with Developmental Phenotypes Overlapping with Ellis-Van Creveld Syndrome. Human Molecular Genetics. PMID 28973407 DOI: 10.1093/hmg/ddx335 |
0.335 |
|
| 2017 |
Culverhouse RC, Saccone NL, Horton AC, Ma Y, Anstey KJ, Banaschewski T, Burmeister M, Cohen-Woods S, Etain B, Fisher HL, Goldman N, Guillaume S, Horwood J, Juhasz G, Lester KJ, et al. Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Molecular Psychiatry. PMID 28373689 DOI: 10.1038/Mp.2017.44 |
0.315 |
|
| 2017 |
Burmeister M, Trucco E, Ramdas S, Parker S, Heitzeg M, Villafuerte S, Zucker R. GABRA2 Association With Addiction-Related Endophenotypes Is Environmentally Influenced European Neuropsychopharmacology. 27: S410-S411. DOI: 10.1016/J.Euroneuro.2016.09.453 |
0.36 |
|
| 2017 |
Burmeister M, Zhao Z, Sen S. Replicating Internship Stress-Induced Depression In China European Neuropsychopharmacology. 27: S363. DOI: 10.1016/J.Euroneuro.2016.09.386 |
0.504 |
|
| 2017 |
Burmeister M, Liu C, Schulze TG. Progress In Psychiatric Genetics In China European Neuropsychopharmacology. 27: S361. DOI: 10.1016/j.euroneuro.2016.09.382 |
0.369 |
|
| 2017 |
Warthen K, Sanford B, Walker K, Black S, Angstadt M, Sripada C, Welsh R, Zubieta J, Burmeister M, Mickey B. 817. Neuropeptide Y Genetic Risk Affects Striatal Response to Potential Loss Biological Psychiatry. 81: S331-S332. DOI: 10.1016/J.Biopsych.2017.02.884 |
0.504 |
|
| 2016 |
Klimkiewicz A, Mach A, Jakubczyk A, Klimkiewicz J, Wnorowska A, Kopera M, Fudalej S, Burmeister M, Brower K, Wojnar M. COMT and BDNF Gene Variants Help to Predict Alcohol Consumption in Alcohol-dependent Patients. Journal of Addiction Medicine. PMID 27898499 DOI: 10.1097/ADM.0000000000000277 |
0.301 |
|
| 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 |
0.307 |
|
| 2016 |
Zhang Y, Li J, Song S, Tardif T, Burmeister M, Villafuerte SM, Su M, McBride C, Shu H. Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population. Plos One. 11: e0153603. PMID 27100778 DOI: 10.1371/Journal.Pone.0153603 |
0.377 |
|
| 2016 |
Sandford E, Bird TD, Li JZ, Burmeister M. PRICKLE2 Mutations Might Not Be Involved in Epilepsy. American Journal of Human Genetics. 98: 588-9. PMID 26942291 DOI: 10.1016/J.Ajhg.2016.01.009 |
0.337 |
|
| 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 |
0.319 |
|
| 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 |
0.359 |
|
| 2016 |
Klionsky DJ, Abdelmohsen K, Abe A, Abedin MJ, Abeliovich H, Acevedo Arozena A, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G, Agarwal R, Aghi MK, ... ... Burmeister M, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy. 12: 1-222. PMID 26799652 DOI: 10.1080/15548627.2015.1100356 |
0.306 |
|
| 2015 |
Woodcock EA, Lundahl LH, Burmeister M, Greenwald MK. Functional mu opioid receptor polymorphism (OPRM1 A(118) G) associated with heroin use outcomes in Caucasian males: A pilot study. The American Journal On Addictions / American Academy of Psychiatrists in Alcoholism and Addictions. 24: 329-35. PMID 25911999 DOI: 10.1111/ajad.12187 |
0.318 |
|
| 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 |
0.329 |
|
| 2014 |
Sandford E, Burmeister M. Genes and genetic testing in hereditary ataxias. Genes. 5: 586-603. PMID 25055202 DOI: 10.3390/genes5030586 |
0.359 |
|
| 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 |
0.535 |
|
| 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 |
0.533 |
|
| 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 |
0.724 |
|
| 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 |
0.743 |
|
| 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 |
0.359 |
|
| 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 |
0.362 |
|
| 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 |
0.301 |
|
| 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 |
0.364 |
|
| 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 |
0.638 |
|
| 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 |
0.36 |
|
| 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 |
0.731 |
|
| 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 |
0.312 |
|
| 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 |
0.661 |
|
| 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 |
0.339 |
|
| 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 |
0.551 |
|
| 2012 |
Davidson A, Majczenko K, Camelo-Piragua S, Li X, Joshi S, Xu J, Peng W, Li J, Burmeister M, Dowling J. C.O.4 Dominant mutation in CCDC78 in a unique congenital myopathy with central nuclei and atypical cores Neuromuscular Disorders. 22: 840. DOI: 10.1016/J.Nmd.2012.06.126 |
0.34 |
|
| 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 |
0.36 |
|
| 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 |
0.523 |
|
| 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 |
0.369 |
|
| 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 |
0.767 |
|
| 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 |
0.351 |
|
| 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 |
0.36 |
|
| 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 |
0.562 |
|
| 2009 |
Li MD, Burmeister M. New insights into the genetics of addiction. Nature Reviews. Genetics. 10: 225-31. PMID 19238175 DOI: 10.1038/nrg2536 |
0.371 |
|
| 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 |
0.359 |
|
| 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 |
0.321 |
|
| 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 |
0.53 |
|
| 2008 |
Burmeister M, McInnis MG, Zöllner S. Psychiatric genetics: progress amid controversy. Nature Reviews. Genetics. 9: 527-40. PMID 18560438 DOI: 10.1038/Nrg2381 |
0.33 |
|
| 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 |
0.372 |
|
| 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 |
0.58 |
|
| 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 |
0.339 |
|
| 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 |
0.36 |
|
| 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 |
0.508 |
|
| 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 |
0.626 |
|
| 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 |
0.355 |
|
| 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 Molecular Psychiatry. 11: 615-615. DOI: 10.1038/Sj.Mp.4001850 |
0.443 |
|
| 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 |
0.397 |
|
| 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 |
0.506 |
|
| 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 |
0.581 |
|
| 2005 |
Sen S, Burmeister M, Ghosh D. 5-HTTLPR and anxiety-related personality traits meta-analysis revisited: response to Munafo and colleagues Molecular Psychiatry. 10: 893-895. DOI: 10.1038/Sj.Mp.4001705 |
0.492 |
|
| 2005 |
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. Erratum: Corrigendum: Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse Nature Genetics. 37: 555-555. DOI: 10.1038/Ng0505-555B |
0.586 |
|
| 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 |
0.497 |
|
| 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 |
0.56 |
|
| 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 |
0.561 |
|
| 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 |
0.618 |
|
| 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 |
0.595 |
|
| 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 |
0.576 |
|
| 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 |
0.543 |
|
| 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 |
0.622 |
|
| 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 |
0.346 |
|
| 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 |
0.341 |
|
| 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 |
0.332 |
|
| 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 |
0.326 |
|
| 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 |
0.317 |
|
| 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 |
0.335 |
|
| 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 |
0.381 |
|
| 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 |
0.303 |
|
| 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 |
0.336 |
|
| 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 |
0.355 |
|
| 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 |
0.32 |
|
| 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 |
0.33 |
|
| 1996 |
Kapfhamer D, Sweet HO, Sufalko D, Warren S, Johnson KR, Burmeister M. The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3. Genomics. 35: 533-8. PMID 8812488 DOI: 10.1006/Geno.1996.0394 |
0.339 |
|
| 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 |
0.331 |
|
| 1996 |
Chu FF, Esworthy RS, Burmeister M. The mouse glutathione peroxidase Gpx2 gene maps to chromosome 12; its pseudogene Gpx2-ps maps to chromosome 7. Genomics. 33: 516-8. PMID 8661011 DOI: 10.1006/geno.1996.0227 |
0.325 |
|
| 1995 |
Kapfhamer D, Miller DE, Lambert S, Bennett V, Glover TW, Burmeister M. Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10. Genomics. 27: 189-91. PMID 7665168 DOI: 10.1006/Geno.1995.1023 |
0.314 |
|
| 1992 |
Burmeister M. Strategies for mapping large regions of Mammalian genomes. Methods in Molecular Biology (Clifton, N.J.). 12: 259-84. PMID 21409639 DOI: 10.1385/0-89603-229-9:259 |
0.314 |
|
| 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 |
0.472 |
|
| 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 |
0.489 |
|
| 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 |
0.454 |
|
| 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 |
0.308 |
|
| 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 |
0.467 |
|
| 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 |
0.303 |
|
| 1986 |
Burmeister M, Lehrach H. Long-range restriction map around the Duchenne muscular dystrophy gene. Nature. 324: 582-5. PMID 3024018 DOI: 10.1038/324582a0 |
0.323 |
|
| 1986 |
Hofker MH, van Ommen GJ, Bakker E, Burmeister M, Pearson PL. Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus. Human Genetics. 74: 270-4. PMID 2877935 DOI: 10.1007/Bf00282547 |
0.316 |
|
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