Bettina A. Hamilton, Ph.D. - Publications

2006 University of Miami, Coral Gables, FL 
Management Business Administration, Industrial Psychology

58 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
2015 Zhang S, Ross KD, Seidner GA, Gorman MR, Poon TH, Wang X, Keithley EM, Lee PN, Martindale MQ, Joiner WJ, Hamilton BA. Nmf9 Encodes a Highly Conserved Protein Important to Neurological Function in Mice and Flies. Plos Genetics. 11: e1005344. PMID 26131556 DOI: 10.1371/Journal.Pgen.1005344  0.01
2015 Concepcion D, Ross KD, Hutt KR, Yeo GW, Hamilton BA. Nxf1 natural variant E610G is a semi-dominant suppressor of IAP-induced RNA processing defects. Plos Genetics. 11: e1005123. PMID 25835743 DOI: 10.1371/Journal.Pgen.1005123  0.01
2015 Martindale VE, Hamilton BA. Bringing evidence to the practice of human performance. Aerospace Medicine and Human Performance. 86: 64-6. PMID 25565539 DOI: 10.3357/AMHP.4194.2015  0.01
2014 Hilliard N, Fassett WE, Hamilton BA. Report of the Academy Presidents: Leading key initiatives as part of APhA's strategic plan. Journal of the American Pharmacists Association : Japha. 54: 102-20. PMID 24632926 DOI: 10.1331/JAPhA.2014.14510  0.01
2013 Radley JJ, Anderson RM, Hamilton BA, Alcock JA, Romig-Martin SA. Chronic stress-induced alterations of dendritic spine subtypes predict functional decrements in an hypothalamo-pituitary-adrenal-inhibitory prefrontal circuit. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 14379-91. PMID 24005291 DOI: 10.1523/Jneurosci.0287-13.2013  0.01
2013 Cho YW, Hong CJ, Hou A, Gent PM, Zhang K, Won KJ, Hamilton BA. Zfp423 binds autoregulatory sites in p19 cell culture model. Plos One. 8: e66514. PMID 23762491 DOI: 10.1371/journal.pone.0066514  0.01
2013 Hamilton BA. Retrotransposon activates ectopic Ptf1 expression: a short tail. Plos Genetics. 9: e1003331. PMID 23468657 DOI: 10.1371/journal.pgen.1003331  0.01
2012 Chaki M, Airik R, Ghosh AK, Giles RH, Chen R, Slaats GG, Wang H, Hurd TW, Zhou W, Cluckey A, Gee HY, Ramaswami G, Hong CJ, Hamilton BA, Cervenka I, et al. Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Cell. 150: 533-48. PMID 22863007 DOI: 10.1016/J.Cell.2012.06.028  0.01
2012 Hamilton BA, Yu BD. Modifier genes and the plasticity of genetic networks in mice. Plos Genetics. 8: e1002644. PMID 22511884 DOI: 10.1371/journal.pgen.1002644  0.01
2012 Rao F, Chiron S, Wei Z, Fung MM, Chen Y, Wen G, Khandrika S, Ziegler MG, Benyamin B, Montgomery G, Whitfield JB, Martin NG, Waalen J, Hamilton BA, Mahata SK, et al. Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins. American Journal of Hypertension. 25: 29-40. PMID 21918574 DOI: 10.1038/Ajh.2011.163  0.01
2011 Hamilton BA, Fu XD. Tracking intron removal in real time. Developmental Cell. 21: 979-80. PMID 22172665 DOI: 10.1016/J.Devcel.2011.11.010  0.01
2011 Alcaraz WA, Chen E, Valdes P, Kim E, Lo YH, Vo J, Hamilton BA. Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice. Human Molecular Genetics. 20: 3822-30. PMID 21729880 DOI: 10.1093/Hmg/Ddr300  0.01
2011 Concepcion D, Johannes F, Lo YH, Yao J, Fong J, Hamilton BA. Modifier genes for mouse phosphatidylinositol transfer protein α (vibrator) that bypass juvenile lethality. Genetics. 187: 1185-91. PMID 21321132 DOI: 10.1534/Genetics.110.125906  0.01
2011 Hamilton BA, Naismith SL, Scott EM, Purcell S, Hickie IB. Disability is already pronounced in young people with early stages of affective disorders: data from an early intervention service. Journal of Affective Disorders. 131: 84-91. PMID 21112640 DOI: 10.1016/j.jad.2010.10.052  0.01
2011 Zhang K, Chen Y, Wen G, Mahata M, Rao F, Fung MM, Vaingankar S, Biswas N, Gayen JR, Friese RS, Mahata SK, Hamilton BA, O'Connor DT. Catecholamine storage vesicles: role of core protein genetic polymorphisms in hypertension. Current Hypertension Reports. 13: 36-45. PMID 21104344 DOI: 10.1007/S11906-010-0170-Y  0.01
2011 Chen Y, Zhang K, Wen G, Rao F, Sanchez AP, Wang L, Rodriguez-Flores JL, Mahata M, Mahata SK, Waalen J, Ziegler MG, Hamilton BA, O'Connor DT. Human dopamine β-hydroxylase promoter variant alters transcription in chromaffin cells, enzyme secretion, and blood pressure. American Journal of Hypertension. 24: 24-32. PMID 20814407 DOI: 10.1038/Ajh.2010.186  0.01
2010 Chen Y, Rao F, Wen G, Gayen JR, Zhang K, Vaingankar SM, Biswas N, Mahata M, Friese RS, Fung MM, Salem RM, Nievergelt C, Bhatnagar V, Hook VY, Ziegler MG, ... Hamilton BA, et al. Naturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease. Cellular and Molecular Neurobiology. 30: 1395-400. PMID 21061160 DOI: 10.1007/S10571-010-9600-2  0.01
2010 Chen Y, Salem RM, Rao F, Fung MM, Bhatnagar V, Pandey B, Mahata M, Waalen J, Nievergelt CM, Lipkowitz MS, Hamilton BA, Mahata SK, O'Connor DT. Common charge-shift mutation Glu65Lys in K+ channel β₁-Subunit KCNMB1: pleiotropic consequences for glomerular filtration rate and progressive renal disease. American Journal of Nephrology. 32: 414-24. PMID 20861615 DOI: 10.1159/000320131  0.01
2010 Rodríguez-Flores JL, Zhang K, Kang SW, Wen G, Ghosh S, Friese RS, Mahata SK, Subramaniam S, Hamilton BA, O'Connor DT. Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 195-204. PMID 20204374 DOI: 10.1007/S00335-010-9253-Y  0.01
2010 Chen Y, Wen G, Rao F, Zhang K, Wang L, Rodriguez-Flores JL, Sanchez AP, Mahata M, Taupenot L, Sun P, Mahata SK, Tayo B, Schork NJ, Ziegler MG, Hamilton BA, et al. Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure. Journal of Hypertension. 28: 76-86. PMID 20009769 DOI: 10.1097/Hjh.0B013E328332Bc87  0.01
2010 Hamilton BA. Letter to the editor on "Threonine 53 in alpha-synuclein is conserved in long-living non-primate animals". Biochemical and Biophysical Research Communications. 391: 1154. PMID 19903454 DOI: 10.1016/j.bbrc.2009.11.042  0.01
2009 Shih PA, Wang L, Chiron S, Wen G, Nievergelt C, Mahata M, Khandrika S, Rao F, Fung MM, Mahata SK, Hamilton BA, O'Connor DT. Peptide YY (PYY) gene polymorphisms in the 3'-untranslated and proximal promoter regions regulate cellular gene expression and PYY secretion and metabolic syndrome traits in vivo. The Journal of Clinical Endocrinology and Metabolism. 94: 4557-66. PMID 19820027 DOI: 10.1210/Jc.2009-0465  0.01
2009 Wang L, Rao F, Zhang K, Mahata M, Rodriguez-Flores JL, Fung MM, Waalen J, Cockburn MG, Hamilton BA, Mahata SK, O'Connor DT. Neuropeptide Y(1) Receptor NPY1R discovery of naturally occurring human genetic variants governing gene expression in cella as well as pleiotropic effects on autonomic activity and blood pressure in vivo. Journal of the American College of Cardiology. 54: 944-54. PMID 19712806 DOI: 10.1016/J.Jacc.2009.05.035  0.01
2009 Chen Y, Mahata M, Rao F, Khandrika S, Courel M, Fung MM, Zhang K, Stridsberg M, Ziegler MG, Hamilton BA, Lipkowitz MS, Taupenot L, Nievergelt C, Mahata SK, O'Connor DT. Chromogranin A regulates renal function by triggering Weibel-Palade body exocytosis. Journal of the American Society of Nephrology : Jasn. 20: 1623-32. PMID 19520754 DOI: 10.1681/ASN.2008111148  0.01
2009 Concepcion D, Flores-García L, Hamilton BA. Multipotent genetic suppression of retrotransposon-induced mutations by Nxf1 through fine-tuning of alternative splicing. Plos Genetics. 5: e1000484. PMID 19436707 DOI: 10.1371/journal.pgen.1000484  0.01
2008 Chen Y, Rao F, Rodriguez-Flores JL, Mahata M, Fung MM, Stridsberg M, Vaingankar SM, Wen G, Salem RM, Das M, Cockburn MG, Schork NJ, Ziegler MG, Hamilton BA, Mahata SK, et al. Naturally occurring human genetic variation in the 3'-untranslated region of the secretory protein chromogranin A is associated with autonomic blood pressure regulation and hypertension in a sex-dependent fashion. Journal of the American College of Cardiology. 52: 1468-81. PMID 19017515 DOI: 10.1016/j.jacc.2008.07.047  0.01
2008 Chen Y, Rao F, Rodriguez-Flores JL, Mahapatra NR, Mahata M, Wen G, Salem RM, Shih PA, Das M, Schork NJ, Ziegler MG, Hamilton BA, Mahata SK, O'Connor DT. Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure. Kidney International. 74: 115-25. PMID 18432188 DOI: 10.1038/Ki.2008.113  0.01
2008 Salem RM, Cadman PE, Chen Y, Rao F, Wen G, Hamilton BA, Rana BK, Smith DW, Stridsberg M, Ward HJ, Mahata M, Mahata SK, Bowden DW, Hicks PJ, Freedman BI, et al. Chromogranin A polymorphisms are associated with hypertensive renal disease. Journal of the American Society of Nephrology : Jasn. 19: 600-14. PMID 18235090 DOI: 10.1681/Asn.2007070754  0.01
2007 Wen G, Wessel J, Zhou W, Ehret GB, Rao F, Stridsberg M, Mahata SK, Gent PM, Das M, Cooper RS, Chakravarti A, Zhou H, Schork NJ, O'connor DT, Hamilton BA. An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension. Human Molecular Genetics. 16: 1752-64. PMID 17584765 DOI: 10.1093/Hmg/Ddm123  0.01
2007 Harold D, Jehu L, Turic D, Hollingworth P, Moore P, Summerhayes P, Moskvina V, Foy C, Archer N, Hamilton BA, Lovestone S, Powell J, Brayne C, Rubinsztein DC, Jones L, et al. Interaction between the ADAM12 and SH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 448-52. PMID 17440933 DOI: 10.1002/Ajmg.B.30456  0.01
2007 Rao F, Wen G, Gayen JR, Das M, Vaingankar SM, Rana BK, Mahata M, Kennedy BP, Salem RM, Stridsberg M, Abel K, Smith DW, Eskin E, Schork NJ, Hamilton BA, et al. Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension. Circulation. 115: 2271-81. PMID 17438154 DOI: 10.1161/Circulationaha.106.628859  0.01
2007 Rao F, Wessel J, Wen G, Zhang L, Rana BK, Kennedy BP, Greenwood TA, Salem RM, Chen Y, Khandrika S, Hamilton BA, Smith DW, Holstein-Rathlou NH, Ziegler MG, Schork NJ, et al. Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism. Hypertension. 49: 1015-31. PMID 17353515 DOI: 10.1161/Hypertensionaha.106.081679  0.01
2007 Wessel J, Moratorio G, Rao F, Mahata M, Zhang L, Greene W, Rana BK, Kennedy BP, Khandrika S, Huang P, Lillie EO, Shih PA, Smith DW, Wen G, Hamilton BA, et al. C-reactive protein, an 'intermediate phenotype' for inflammation: human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/beta-adrenergic pathway loci. Journal of Hypertension. 25: 329-43. PMID 17211240 DOI: 10.1097/Hjh.0B013E328011753E  0.01
2007 Gold DA, Gent PM, Hamilton BA. ROR alpha in genetic control of cerebellum development: 50 staggering years. Brain Research. 1140: 19-25. PMID 16427031 DOI: 10.1016/J.Brainres.2005.11.080  0.01
2006 Alcaraz WA, Gold DA, Raponi E, Gent PM, Concepcion D, Hamilton BA. Zfp423 controls proliferation and differentiation of neural precursors in cerebellar vermis formation. Proceedings of the National Academy of Sciences of the United States of America. 103: 19424-9. PMID 17151198 DOI: 10.1073/Pnas.0609184103  0.01
2006 Zhang K, Rao F, Wen G, Salem RM, Vaingankar S, Mahata M, Mahapatra NR, Lillie EO, Cadman PE, Friese RS, Hamilton BA, Hook VY, Mahata SK, Taupenot L, O'Connor DT. Catecholamine storage vesicles and the metabolic syndrome: The role of the chromogranin A fragment pancreastatin. Diabetes, Obesity & Metabolism. 8: 621-33. PMID 17026486 DOI: 10.1111/J.1463-1326.2006.00575.X  0.01
2006 Bhatnagar V, Xu G, Hamilton BA, Truong DM, Eraly SA, Wu W, Nigam SK. Analyses of 5' regulatory region polymorphisms in human SLC22A6 (OAT1) and SLC22A8 (OAT3). Journal of Human Genetics. 51: 575-80. PMID 16648942 DOI: 10.1007/S10038-006-0398-1  0.01
2005 Xu G, Bhatnagar V, Wen G, Hamilton BA, Eraly SA, Nigam SK. Analyses of coding region polymorphisms in apical and basolateral human organic anion transporter (OAT) genes [OAT1 (NKT), OAT2, OAT3, OAT4, URAT (RST)]. Kidney International. 68: 1491-9. PMID 16164626 DOI: 10.1111/J.1523-1755.2005.00612.X  0.01
2004 Concepcion D, Seburn KL, Wen G, Frankel WN, Hamilton BA. Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated mice. Genetics. 168: 953-9. PMID 15514066 DOI: 10.1534/genetics.104.029843  0.01
2004 Mahata SK, Mahata M, Wen G, Wong WB, Mahapatra NR, Hamilton BA, O'Connor DT. The catecholamine release-inhibitory "catestatin" fragment of chromogranin a: naturally occurring human variants with different potencies for multiple chromaffin cell nicotinic cholinergic responses. Molecular Pharmacology. 66: 1180-91. PMID 15326220 DOI: 10.1124/Mol.104.002139  0.01
2004 Hamilton BA. alpha-Synuclein A53T substitution associated with Parkinson disease also marks the divergence of Old World and New World primates. Genomics. 83: 739-42. PMID 15028296 DOI: 10.1016/j.ygeno.2003.09.016  0.01
2004 Wen G, Mahata SK, Cadman P, Mahata M, Ghosh S, Mahapatra NR, Rao F, Stridsberg M, Smith DW, Mahboubi P, Schork NJ, O'Connor DT, Hamilton BA. Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology. American Journal of Human Genetics. 74: 197-207. PMID 14740315 DOI: 10.1086/381399  0.01
2003 Gold DA, Baek SH, Schork NJ, Rose DW, Larsen DD, Sachs BD, Rosenfeld MG, Hamilton BA. RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathways. Neuron. 40: 1119-31. PMID 14687547 DOI: 10.1016/S0896-6273(03)00769-4  0.01
2003 Floyd JA, Gold DA, Concepcion D, Poon TH, Wang X, Keithley E, Chen D, Ward EJ, Chinn SB, Friedman RA, Yu HT, Moriwaki K, Shiroishi T, Hamilton BA. A natural allele of Nxf1 suppresses retrovirus insertional mutations. Nature Genetics. 35: 221-8. PMID 14517553 DOI: 10.1038/Ng1247  0.01
2003 Alb JG, Cortese JD, Phillips SE, Albin RL, Nagy TR, Hamilton BA, Bankaitis VA. Mice lacking phosphatidylinositol transfer protein-alpha exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemia. The Journal of Biological Chemistry. 278: 33501-18. PMID 12788952 DOI: 10.1074/Jbc.M303591200  0.01
2003 Eraly SA, Hamilton BA, Nigam SK. Organic anion and cation transporters occur in pairs of similar and similarly expressed genes. Biochemical and Biophysical Research Communications. 300: 333-42. PMID 12504088 DOI: 10.1016/S0006-291X(02)02853-X  0.01
2002 Hamilton BA. Variations in abundance: genome-wide responses to genetic variation and vice versa. Genome Biology. 3: reviews1029. PMID 12372150  0.01
2001 Hamilton BA, Frankel WN. Of mice and genome sequence. Cell. 107: 13-6. PMID 11595181 DOI: 10.1016/S0092-8674(01)00514-1  0.01
2000 O'Connor DT, Insel PA, Ziegler MG, Hook VY, Smith DW, Hamilton BA, Taylor PW, Parmer RJ. Heredity and the autonomic nervous system in human hypertension. Current Hypertension Reports. 2: 16-22. PMID 10982526 DOI: 10.1007/S11906-000-0053-8  0.01
2000 Jones JM, Huang JD, Mermall V, Hamilton BA, Mooseker MS, Escayg A, Copeland NG, Jenkins NA, Meisler MH. The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a. Human Molecular Genetics. 9: 821-8. PMID 10749990 DOI: 10.1093/Hmg/9.5.821  0.01
1999 Floyd JA, Hamilton BA. Intranuclear inclusions and the ubiquitin-proteasome pathway: Digestion of a red herring? Neuron. 24: 765-766. PMID 10624938 DOI: 10.1016/S0896-6273(00)81022-3  0.01
1997 Hamilton BA, Smith DJ, Mueller KL, Kerrebrock AW, Bronson RT, van Berkel V, Daly MJ, Kruglyak L, Reeve MP, Nemhauser JL, Hawkins TL, Rubin EM, Lander ES. The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression. Neuron. 18: 711-22. PMID 9182797 DOI: 10.1016/S0896-6273(00)80312-8  0.01
1996 Hamilton BA, Frankel WN, Kerrebrock AW, Hawkins TL, FitzHugh W, Kusumi K, Russell LB, Mueller KL, van Berkel V, Birren BW, Kruglyak L, Lander ES. Disruption of the nuclear hormone receptor RORalpha in staggerer mice. Nature. 379: 736-9. PMID 8602221 DOI: 10.1038/379736A0  0.01
1994 Hamilton BA, Zinn K. From clone to mutant gene. Methods in Cell Biology. 44: 81-94. PMID 7707978 DOI: 10.1016/S0091-679X(08)60907-3  0.01
1991 Hamilton BA, Palazzolo MJ, Meyerowitz EM. Rapid isolation of long cDNA clones from existing libraries. Nucleic Acids Research. 19: 1951-2. PMID 1903205 DOI: 10.1093/Nar/19.8.1951  0.01
1991 Hamilton BA, Palazzolo MJ, Chang JH, VijayRaghavan K, Mayeda CA, Whitney MA, Meyerowitz EM. Large scale screen for transposon insertions into cloned genes. Proceedings of the National Academy of Sciences of the United States of America. 88: 2731-5. PMID 1849274 DOI: 10.1073/pnas.88.7.2731  0.01
1991 Strathmann M, Hamilton BA, Mayeda CA, Simon MI, Meyerowitz EM, Palazzolo MJ. Transposon-facilitated DNA sequencing. Proceedings of the National Academy of Sciences of the United States of America. 88: 1247-50. PMID 1847513 DOI: 10.1073/Pnas.88.4.1247  0.01
1990 Palazzolo MJ, Hamilton BA, Ding DL, Martin CH, Mead DA, Mierendorf RC, Raghavan KV, Meyerowitz EM, Lipshitz HD. Phage lambda cDNA cloning vectors for subtractive hybridization, fusion-protein synthesis and Cre-loxP automatic plasmid subcloning. Gene. 88: 25-36. PMID 2140336 DOI: 10.1016/0378-1119(90)90056-W  0.01
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