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Featured researches published by Stephanie M. Gogarten.


Astrophysical Journal Supplement Series | 2009

The ACS Nearby Galaxy Survey Treasury

Julianne J. Dalcanton; Benjamin F. Williams; Anil C. Seth; Andrew E. Dolphin; Jon A. Holtzman; Keith Rosema; Evan D. Skillman; Andrew A. Cole; Léo Girardi; Stephanie M. Gogarten; I. D. Karachentsev; Knut Olsen; Daniel R. Weisz; Charlotte R. Christensen; Kenneth C. Freeman; Karoline M. Gilbert; Carme Batlle i Gallart; Jason Harris; Paul W. Hodge; Roelof S. de Jong; V. E. Karachentseva; Mario Mateo; Peter B. Stetson; Maritza Tavarez; Dennis Zaritsky; Fabio Governato; Thomas P. Quinn

The ACS Nearby Galaxy Survey Treasury (ANGST) is a systematic survey to establish a legacy of uniform multi-color photometry of resolved stars for a volume-limited sample of nearby galaxies (D 14 million stars. In this paper we present the details of the sample selection, imaging, data reduction, and the resulting photometric catalogs, along with an analysis of the photometric uncertainties (systematic and random), for both ACS and WFPC2 imaging. We also present uniformly derived relative distances measured from the apparent magnitude of the TRGB.


Nature Genetics | 2012

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Cathy C. Laurie; Cecelia A. Laurie; Kenneth Rice; Kimberly F. Doheny; Leila R. Zelnick; Caitlin P. McHugh; Hua Ling; Kurt N. Hetrick; Elizabeth W. Pugh; Christopher I. Amos; Qingyi Wei; Li-E Wang; Jeffrey E. Lee; Kathleen C. Barnes; Nadia N. Hansel; Rasika A. Mathias; Denise Daley; Terri H. Beaty; Alan F. Scott; Ingo Ruczinski; Rob Scharpf; Laura J. Bierut; Sarah M. Hartz; Maria Teresa Landi; Neal D. Freedman; Lynn R. Goldin; David Ginsburg; Jun-Jun Li; Karl C. Desch; Sara S. Strom

We detected clonal mosaicism for large chromosomal anomalies (duplications, deletions and uniparental disomy) using SNP microarray data from over 50,000 subjects recruited for genome-wide association studies. This detection method requires a relatively high frequency of cells with the same abnormal karyotype (>5–10%; presumably of clonal origin) in the presence of normal cells. The frequency of detectable clonal mosaicism in peripheral blood is low (<0.5%) from birth until 50 years of age, after which it rapidly rises to 2–3% in the elderly. Many of the mosaic anomalies are characteristic of those found in hematological cancers and identify common deleted regions with genes previously associated with these cancers. Although only 3% of subjects with detectable clonal mosaicism had any record of hematological cancer before DNA sampling, those without a previous diagnosis have an estimated tenfold higher risk of a subsequent hematological cancer (95% confidence interval = 6–18).


The Astronomical Journal | 2007

Stellar SEDs from 0.3 to 2.5 μm: Tracing the Stellar Locus and Searching for Color Outliers in the SDSS and 2MASS

Kevin R. Covey; Ž. Ivezić; David J. Schlegel; Douglas P. Finkbeiner; Nikhil Padmanabhan; Robert H. Lupton; Marcel A. Agüeros; John J. Bochanski; Suzanne L. Hawley; Andrew A. West; Anil C. Seth; Amy E. Kimball; Stephanie M. Gogarten; Mark W. Claire; Daryl Haggard; Nathan A. Kaib; D. P. Schneider; Branimir Sesar

The Sloan Digital Sky Survey (SDSS) and Two Micron All Sky Survey (2MASS) are rich resources for studying stellar astrophysics and the structure and formation history of the Galaxy. As new surveys and instruments adopt similar filter sets, it is increasingly important to understand the properties of the ugrizJHKs stellar locus, both to inform studies of ‘normal’ main sequence stars as well as for robust searches for point sources with unusual colors. Using a sample of � 600,000 point sources detected by SDSS and 2MASS, we tabulate the position and width of the ugrizJHKs stellar locus as a function of g i color, and provide accurate polynomial fits. We map the Morgan-Keenan spectral type sequence to the median stellar locus by using synthetic photometry of spectral standards and by analyzing 3000 SDSS stellar spectra with a custom spectral typing pipeline, described in full in an attached Appendix. Having characterized the properties of ‘normal’ main sequence stars, we develop an algorithm for identifying point sources whose colors differ significantly from those of normal stars. This algorithm calculates a point source’s minimum separation from the stellar locus in a seven-dimensional color space, and robustly identifies objects with unusual colors, as well as spurious SDSS/2MASS matches. Analysis of a final catalog of 2117 color outliers identifies 370 white-dwarf/M dwarf (WDMD) pairs, 93 QSOs, and 90 M giant/carbon star candidates, and demonstrates that WDMD pairs and QSOs can be distinguished on the basis of their J Ks and r z colors. We also identify a group of objects with correlated offsets in the u g vs. g r and g r vs. r i color-color spaces, but subsequent follow-up is required to reveal the nature of these objects. Future applications of this algorithm to a matched SDSS-UKIDSS catalog may well identify additional classes of objects with unusual colors by probing new areas of color-magnitude space. Subject headings: surveys — stars:late-type — stars:early-type — Galaxy:stellar content — infrared:stars


The Astrophysical Journal | 2011

THE ACS NEARBY GALAXY SURVEY TREASURY. VIII. THE GLOBAL STAR FORMATION HISTORIES OF 60 DWARF GALAXIES IN THE LOCAL VOLUME

Daniel R. Weisz; Julianne J. Dalcanton; Benjamin F. Williams; Karoline M. Gilbert; Evan D. Skillman; Anil C. Seth; Andrew E. Dolphin; Kristen B. W. McQuinn; Stephanie M. Gogarten; Jon A. Holtzman; Keith Rosema; Andrew A. Cole; I. D. Karachentsev; Dennis Zaritsky

We present uniformly measured star formation histories (SFHs) of 60 nearby (D less than or similar to 4 Mpc) dwarf galaxies based on color-magnitude diagrams of resolved stellar populations from images taken with the Hubble Space Telescope and analyzed as part of the ACS Nearby Galaxy Survey Treasury program (ANGST). This volume-limited sample contains 12 dwarf spheroidal (dSph)/dwarf elliptical (dE), 5 dwarf spiral, 28 dwarf irregular (dI), 12 dSph/dI (transition), and 3 tidal dwarf galaxies. The sample spans a range of similar to 10 mag in MB and covers a wide range of environments, from highly interacting to truly isolated. From the best-fit SFHs, we find three significant results for dwarf galaxies in the ANGST volume: (1) the majority of dwarf galaxies formed the bulk of their mass prior to z similar to 1, regardless of current morphological type; (2) the mean SFHs of dIs, transition dwarf galaxies (dTrans), and dSphs are similar over most of cosmic time, and only begin to diverge a few Gyr ago, with the clearest differences between the three appearing during the most recent 1 Gyr; and (3) the SFHs are complex and the mean values are inconsistent with simple SFH models, e. g., single bursts, constant star formation rates (SFRs), or smooth, exponentially declining SFRs. The mean SFHs show clear divergence from the cosmic SFH at z less than or similar to 0.7, which could be evidence that low-mass systems have experienced delayed star formation relative to more massive galaxies. The sample shows a strong density-morphology relationship, such that the dSphs in the sample are less isolated than the dIs. We find that the transition from a gas-rich to gas-poor galaxy cannot be solely due to internal mechanisms such as stellar feedback, and instead is likely the result of external mechanisms, e. g., ram pressure and tidal stripping and tidal forces. In terms of their environments, SFHs, and gas fractions, the majority of the dTrans appear to be low-mass dIs that simply lack Ha emission, similar to Local Group (LG) dTrans DDO 210. However, a handful of dTrans have remarkably low gas fractions, suggesting that they have nearly exhausted their gas supply, analogous to LG dTrans such as Phoenix. Finally, we have also included extensive exploration of uncertainties in the SFH recovery method, including the optimization of time resolution, the effects of photometric depth, and impact of systematic uncertainties due to the limitations in current stellar evolution models.


Gastroenterology | 2013

Identification of genetic susceptibility loci for colorectal tumors in a genome-wide meta-analysis

Ulrike Peters; Fredrick R. Schumacher; Carolyn M. Hutter; Aaron K. Aragaki; John A. Baron; Sonja I. Berndt; Stéphane Bézieau; Hermann Brenner; Katja Butterbach; Bette J. Caan; Peter T. Campbell; Christopher S. Carlson; Graham Casey; Andrew T. Chan; Jenny Chang-Claude; Stephen J. Chanock; Lin Chen; Gerhard A. Coetzee; Simon G. Coetzee; David V. Conti; Keith R. Curtis; David Duggan; Todd L. Edwards; Charles S. Fuchs; Steven Gallinger; Edward Giovannucci; Stephanie M. Gogarten; Stephen B. Gruber; Robert W. Haile; Tabitha A. Harrison

BACKGROUND & AIMS Heritable factors contribute to the development of colorectal cancer. Identifying the genetic loci associated with colorectal tumor formation could elucidate the mechanisms of pathogenesis. METHODS We conducted a genome-wide association study that included 14 studies, 12,696 cases of colorectal tumors (11,870 cancer, 826 adenoma), and 15,113 controls of European descent. The 10 most statistically significant, previously unreported findings were followed up in 6 studies; these included 3056 colorectal tumor cases (2098 cancer, 958 adenoma) and 6658 controls of European and Asian descent. RESULTS Based on the combined analysis, we identified a locus that reached the conventional genome-wide significance level at less than 5.0 × 10(-8): an intergenic region on chromosome 2q32.3, close to nucleic acid binding protein 1 (most significant single nucleotide polymorphism: rs11903757; odds ratio [OR], 1.15 per risk allele; P = 3.7 × 10(-8)). We also found evidence for 3 additional loci with P values less than 5.0 × 10(-7): a locus within the laminin gamma 1 gene on chromosome 1q25.3 (rs10911251; OR, 1.10 per risk allele; P = 9.5 × 10(-8)), a locus within the cyclin D2 gene on chromosome 12p13.32 (rs3217810 per risk allele; OR, 0.84; P = 5.9 × 10(-8)), and a locus in the T-box 3 gene on chromosome 12q24.21 (rs59336; OR, 0.91 per risk allele; P = 3.7 × 10(-7)). CONCLUSIONS In a large genome-wide association study, we associated polymorphisms close to nucleic acid binding protein 1 (which encodes a DNA-binding protein involved in DNA repair) with colorectal tumor risk. We also provided evidence for an association between colorectal tumor risk and polymorphisms in laminin gamma 1 (this is the second gene in the laminin family to be associated with colorectal cancers), cyclin D2 (which encodes for cyclin D2), and T-box 3 (which encodes a T-box transcription factor and is a target of Wnt signaling to β-catenin). The roles of these genes and their products in cancer pathogenesis warrant further investigation.


Astrophysical Journal Supplement Series | 2012

THE PANCHROMATIC HUBBLE ANDROMEDA TREASURY

Julianne J. Dalcanton; Benjamin F. Williams; Dustin Lang; Tod R. Lauer; Jason S. Kalirai; Anil C. Seth; Andrew E. Dolphin; Philip Rosenfield; Daniel R. Weisz; Eric F. Bell; Luciana Bianchi; Martha L. Boyer; Nelson Caldwell; Hui Dong; Claire E. Dorman; Karoline M. Gilbert; Léo Girardi; Stephanie M. Gogarten; Karl D. Gordon; Puragra Guhathakurta; Paul W. Hodge; Jon A. Holtzman; L. Clifton Johnson; Søren S. Larsen; Alexia R. Lewis; J. Melbourne; Knut Olsen; Hans-Walter Rix; Keith Rosema; Abhijit Saha

The Panchromatic Hubble Andromeda Treasury is an ongoing Hubble Space Telescope Multi-Cycle Treasury program to image ~1/3 of M31s star-forming disk in six filters, spanning from the ultraviolet (UV) to the near-infrared (NIR). We use the Wide Field Camera 3 (WFC3) and Advanced Camera for Surveys (ACS) to resolve the galaxy into millions of individual stars with projected radii from 0 to 20 kpc. The full survey will cover a contiguous 0.5 deg^(2)area in 828 orbits. Imaging is being obtained in the F275W and F336W filters on the WFC3/UVIS camera, F475W and F814W on ACS/WFC, and F110W and F160W on WFC3/IR. The resulting wavelength coverage gives excellent constraints on stellar temperature, bolometric luminosity, and extinction for most spectral types. The data produce photometry with a signal-to-noise ratio of 4 at m F_(275W) = 25.1, m_(F336W) = 24.9, m_(F475W) = 27.9, m_(F814W) = 27.1, m_(F110W) = 25.5, and m_(F160W) = 24.6 for single pointings in the uncrowded outer disk; in the inner disk, however, the optical and NIR data are crowding limited, and the deepest reliable magnitudes are up to 5 mag brighter. Observations are carried out in two orbits per pointing, split between WFC3/UVIS and WFC3/IR cameras in primary mode, with ACS/WFC run in parallel. All pointings are dithered to produce Nyquist-sampled images in F475W, F814W, and F160W. We describe the observing strategy, photometry, astrometry, and data products available for the survey, along with extensive testing of photometric stability, crowding errors, spatially dependent photometric biases, and telescope pointing control. We also report on initial fits to the structure of M31s disk, derived from the density of red giant branch stars, in a way that is independent of assumed mass-to-light ratios and is robust to variations in dust extinction. These fits also show that the 10 kpc ring is not just a region of enhanced recent star formation, but is instead a dynamical structure containing a significant overdensity of stars with ages >1 Gyr.


Human Molecular Genetics | 2011

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA

Janey L. Wiggs; Jae H. Kang; Brian L. Yaspan; Daniel B. Mirel; Cathy C. Laurie; Andrew Crenshaw; Wendy Brodeur; Stephanie M. Gogarten; Lana M. Olson; Wael Abdrabou; E. DelBono; Stephanie Loomis; Jonathan L. Haines; Louis R. Pasquale

Primary open-angle glaucoma (POAG) is a genetically complex common disease characterized by progressive optic nerve degeneration that results in irreversible blindness. Recently, a genome-wide association study (GWAS) for POAG in an Icelandic population identified significant associations with single nucleotide polymorphisms (SNPs) between the CAV1 and CAV2 genes on chromosome 7q31. In this study, we confirm that the identified SNPs are associated with POAG in our Caucasian US population and that specific haplotypes located in the CAV1/CAV2 intergenic region are associated with the disease. We also present data suggesting that associations with several CAV1/CAV2 SNPs are significant mostly in women.


The Astrophysical Journal | 2007

The Morphological Content of 10 EDisCS Clusters at 0.5 < z < 0.8

Vandana Desai; Julianne J. Dalcanton; Alfonso Aragon-Salamanca; Pascale Jablonka; Bianca M. Poggianti; Stephanie M. Gogarten; Luc Simard; B. Milvang-Jensen; Gregory Rudnick; Dennis Zaritsky; Douglas Clowe; C. Halliday; R. Pello; R. P. Saglia; Simon D. M. White

We describe Hubble Space Telescope (HST) imaging of 10 of the 20 ESO Distant Cluster Survey (EDisCS) fields. Each ~40 arcmin^2 field was imaged in the F814W filter with the Advanced Camera for Surveys Wide Field Camera. Based on these data, we present visual morphological classifications for the ~920 sources per field that are brighter than I_(auto) = 23 mag. We use these classifications to quantify the morphological content of 10 intermediate-redshift (0.5 < z < 0.8) galaxy clusters within the HST survey region. The EDisCS results, combined with previously published data from seven higher redshift clusters, show no statistically significant evidence for evolution in the mean fractions of elliptical, S0, and late-type (Sp+Irr) galaxies in clusters over the redshift range 0.5 < z < 1.2. In contrast, existing studies of lower redshift clusters have revealed a factor of ~2 increase in the typical S0 fraction between z = 0.4 and 0, accompanied by a commensurate decrease in the Sp+Irr fraction and no evolution in the elliptical fraction. The EDisCS clusters demonstrate that cluster morphological fractions plateau beyond z ≈ 0.4. They also exhibit a mild correlation between morphological content and cluster velocity dispersion, highlighting the importance of careful sample selection in evaluating evolution. We discuss these findings in the context of a recently proposed scenario in which the fractions of passive (E, S0) and star-forming (Sp, Irr) galaxies are determined primarily by the growth history of clusters.


Monthly Notices of the Royal Astronomical Society | 2009

Feedback and the formation of dwarf galaxy stellar haloes

Greg Stinson; Julianne J. Dalcanton; Thomas P. Quinn; Stephanie M. Gogarten; Tobias Kaufmann; James Wadsley

Stellar population studies show that low-mass galaxies in all environments exhibit stellar haloes that are older and more spherically distributed than the main body of the galaxy. In some cases, there is a significant intermediate age component that extends beyond the young disc. We examine a suite of Smoothed Particle Hydrodynamic simulations and find that elevated early star formation activity combined with supernova feedback can produce an extended stellar distribution that resembles these haloes for model galaxies ranging from ν 200 = 15 to 35 km s -1 , without the need for accretion of subhaloes.


The Astrophysical Journal | 2010

The advanced camera for surveys nearby galaxy survey treasury. V. Radial star formation history of NGC 300

Stephanie M. Gogarten; Julianne J. Dalcanton; Benjamin F. Williams; Rok Roskar; Jon A. Holtzman; Anil C. Seth; Andrew E. Dolphin; Daniel R. Weisz; Andrew A. Cole; Victor P. Debattista; Karoline M. Gilbert; Knut Olsen; Evan D. Skillman; Roelof S. de Jong; I. D. Karachentsev; Thomas R. Quinn

We present new Hubble Space Telescope (HST) observations of NGC 300 taken as part of the Advanced Camera for Surveys Nearby Galaxy Survey Treasury (ANGST). Individual stars are resolved in these images down to an absolute magnitude of M F814W = 1.0 (below the red clump). We determine the star formation history of the galaxy in six radial bins by comparing our observed color-magnitude diagrams (CMDs) with synthetic CMDs based on theoretical isochrones. We find that the stellar disk out to 5.4 kpc is primarily old, in contrast with the outwardly similar galaxy M33. We determine the scale length as a function of age and find evidence for inside-out growth of the stellar disk: the scale length has increased from 1.1 ± 0.1 kpc 10 Gyr ago to 1.3 ± 0.1 kpc at present, indicating a buildup in the fraction of young stars at larger radii. As the scale length of M33 has recently been shown to have increased much more dramatically with time, our results demonstrate that two galaxies with similar sizes and morphologies can have very different histories. With an N-body simulation of a galaxy designed to be similar to NGC 300, we determine that the effects of radial migration should be minimal. We trace the metallicity gradient as a function of time and find a present-day metallicity gradient consistent with that seen in previous studies. Consistent results are obtained from archival images covering the same radial extent but differing in placement and filter combination.

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Julianne J. Dalcanton

Carnegie Institution for Science

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Tamar Sofer

Brigham and Women's Hospital

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Jerome I. Rotter

Los Angeles Biomedical Research Institute

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Kent D. Taylor

Los Angeles Biomedical Research Institute

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