| 35100349 | Ankfn1-mutant vestibular defects require loss of both ancestral and derived paralogs for penetrance in zebrafish. | G3 (Bethesda) | 2022 |
| 32967895 | Strain-Dependent Modifier Genes Determine Survival in Mice. | G3: Genes, Genomes, Genetics | 2020 |
| 31943697 | The lipid elongation enzyme ELOVL2 is a molecular regulator of aging in the retina. | Aging Cell | 2020 |
| 32925911 | ZNF423 patient variants, truncations, and in-frame deletions in mice define an allele-dependent range of midline brain abnormalities. | PLoS Genetics | 2020 |
| 29305158 | TBR2 antagonizes retinoic acid dependent neuronal differentiation by repressing Zfp423 during corticogenesis. | Developmental Biology | 2018 |
| 28059714 | Regeneration of fat cells from myofibroblasts during wound healing. | Science | 2017 |
| 28011710 | Identification of novel loci affecting circulating chromogranins and related peptides. | Hum Mol Genet | 2017 |
| 27814941 | Deleting an Nr4a1 Super-Enhancer Subdomain Ablates Ly6C<sup>low</sup> Monocytes while Preserving Macrophage Gene Function. | Immunity | 2016 |
| 27977693 | Deep Reads: Favorites from a Few Different Shelves. | PLoS Genetics | 2016 |
| 27727273 | Zfp423 Regulates Sonic Hedgehog Signaling via Primary Cilium Function. | PLoS Genetics | 2016 |
| 26131556 | Nmf9 Encodes a Highly Conserved Protein Important to Neurological Function in Mice and Flies. | PLoS Genetics | 2015 |
| 25835743 | Nxf1 natural variant E610G is a semi-dominant suppressor of IAP-induced RNA processing defects. | PLoS Genet | 2015 |
| 23468657 | Retrotransposon activates ectopic Ptf1 expression: a short tail. | PLoS Genetics | 2013 |
| 23762491 | Zfp423 binds autoregulatory sites in p19 cell culture model. | PLoS ONE | 2013 |
| 21918574 | Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twins. | Am J Hypertens | 2012 |
| 22511884 | Modifier genes and the plasticity of genetic networks in mice. | PLoS Genetics | 2012 |
| 22863007 | Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. | Cell | 2012 |
| 22172665 | Tracking intron removal in real time. | Developmental Cell | 2011 |
| 21104344 | Catecholamine storage vesicles: role of core protein genetic polymorphisms in hypertension. | Curr Hypertens Rep | 2011 |
| 21321132 | Modifier genes for mouse phosphatidylinositol transfer protein α (vibrator) that bypass juvenile lethality. | Genetics | 2011 |
| 20814407 | Human dopamine β-hydroxylase promoter variant alters transcription in chromaffin cells, enzyme secretion, and blood pressure. | Am J Hypertens | 2011 |
| 21729880 | Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice. | Human Molecular Genetics | 2011 |
| 20204374 | Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach. | Mamm Genome | 2010 |
| 21061160 | Naturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease. | Cell Mol Neurobiol | 2010 |
| 20861615 | Common charge-shift mutation Glu65Lys in K+ channel βâ¿-Subunit KCNMB1: pleiotropic consequences for glomerular filtration rate and progressive renal disease. | Am J Nephrol | 2010 |
| 19903454 | Letter to the editor on "Threonine 53 in alpha-synuclein is conserved in long-living non-primate animals". | Biochemical and Biophysical Research Communications | 2010 |
| 20009769 | Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure. | J Hypertens | 2010 |
| 19820027 | 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. | J Clin Endocrinol Metab | 2009 |
| 28199513 | Peptide YY (PYY) Gene Polymorphisms in the 3'-Untranslated Region and Proximal Promoter Regions Regulate Cellular Gene Expression and PYY Secretion and Metabolic Syndrome Traits in Vivo. | Endocr Rev | 2009 |
| 19436707 | Multipotent genetic suppression of retrotransposon-induced mutations by Nxf1 through fine-tuning of alternative splicing. | PLoS Genetics | 2009 |
| 19712806 | 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. | J Am Coll Cardiol | 2009 |
| 19520754 | Chromogranin A regulates renal function by triggering Weibel-Palade body exocytosis. | J Am Soc Nephrol | 2009 |
| 18235090 | Chromogranin A polymorphisms are associated with hypertensive renal disease. | J Am Soc Nephrol | 2008 |
| 19017515 | 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. | J Am Coll Cardiol | 2008 |
| 18432188 | Common genetic variants in the chromogranin A promoter alter autonomic activity and blood pressure. | Kidney Int | 2008 |
| 16427031 | ROR alpha in genetic control of cerebellum development: 50 staggering years. | Brain Research | 2007 |
| 17211240 | 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. | J Hypertens | 2007 |
| 17584765 | An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension. | Hum Mol Genet | 2007 |
| 17353515 | Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism. | Hypertension | 2007 |
| 17440933 | Interaction between the ADAM12 and SH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease. | Am J Med Genet B Neuropsychiatr Genet | 2007 |
| 17438154 | 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 | 2007 |
| 16648942 | Analyses of 5' regulatory region polymorphisms in human SLC22A6 (OAT1) and SLC22A8 (OAT3). | J Hum Genet | 2006 |
| 17151198 | 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 | 2006 |
| 17026486 | Catecholamine storage vesicles and the metabolic syndrome: The role of the chromogranin A fragment pancreastatin. | Diabetes Obes Metab | 2006 |
| 16164626 | Analyses of coding region polymorphisms in apical and basolateral human organic anion transporter (OAT) genes [OAT1 (NKT), OAT2, OAT3, OAT4, URAT (RST)]. | Kidney Int | 2005 |
| 14740315 | Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology. | Am J Hum Genet | 2004 |
| 15326220 | The catecholamine release-inhibitory "catestatin" fragment of chromogranin a: naturally occurring human variants with different potencies for multiple chromaffin cell nicotinic cholinergic responses. | Mol Pharmacol | 2004 |
| 15514066 | Mutation rate and predicted phenotypic target sizes in ethylnitrosourea-treated mice. | Genetics | 2004 |
| 15028296 | alpha-Synuclein A53T substitution associated with Parkinson disease also marks the divergence of Old World and New World primates. | Genomics | 2004 |
| 14687547 | RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathways. | Neuron | 2003 |