J
Jeanne Carroll
Researcher at University of California, San Diego
Publications - 16
Citations - 662
Jeanne Carroll is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 6, co-authored 8 publications receiving 252 citations. Previous affiliations of Jeanne Carroll include University of California, Los Angeles & Children's Institute Inc..
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Journal ArticleDOI
A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.
Stephen F. Kingsmore,Julie A. Cakici,Julie A. Cakici,Michelle M. Clark,Mary Gaughran,Michele Feddock,Sergey Batalov,Matthew N. Bainbridge,Jeanne Carroll,Jeanne Carroll,Sara A. Caylor,Christina Clarke,Yan Ding,Katarzyna A. Ellsworth,Lauge Farnaes,Lauge Farnaes,Amber Hildreth,Amber Hildreth,Amber Hildreth,Charlotte A. Hobbs,Kiely N. James,Cyrielle Kint,Jerica Lenberg,Shareef Nahas,Lance Prince,Iris Reyes,Lisa Salz,Erica Sanford,Erica Sanford,Peter Schols,Nathaly M. Sweeney,Nathaly M. Sweeney,Mari Tokita,Narayanan Veeraraghavan,Kelly Watkins,Kristen Wigby,Kristen Wigby,Terence C. Wong,Shimul Chowdhury,Meredith S. Wright,David Dimmock,Zaira Bezares,Cinnamon S. Bloss,Joshua J.A. Braun,Carlos Diaz,Dana Mashburn,Dorjee Tamang,Daniken Orendain,Jenni Friedman,Joe Gleeson,Jaime Barea,George Chiang,Casey Cohenmeyer,Nicole G. Coufal,Marva Evans,Jose Honold,Raymond Hovey,Amy S. Kimball,Brian Lane,Crystal Le,Jennie Le,Sandra Leibel,Laurel Moyer,Patrick Mulrooney,Daeheon Oh,Paulina Ordonez,Albert Oriol,Maria Ortiz-Arechiga,Laura Puckett,Mark Speziale,Denise Suttner,Lucitia Van Der Kraan,Gail Knight,Charles Sauer,Richard S. Song,Sarah White,Audra Wise,Catherine Yamada +77 more
TL;DR: In conclusion, rapid genomic sequencing can be performed as a first-tier diagnostic test in inpatient infants and urWGS had the shortest time to result, which was important in unstable infants, and those in whom a genetic diagnosis was likely to impact immediate management.
Journal ArticleDOI
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation
Michelle M. Clark,Amber Hildreth,Amber Hildreth,Amber Hildreth,Sergey Batalov,Yan Ding,Shimul Chowdhury,Kelly Watkins,Katarzyna A. Ellsworth,Brandon Camp,Cyrielle Kint,Calum Yacoubian,Lauge Farnaes,Lauge Farnaes,Matthew N. Bainbridge,Curtis Beebe,Joshua J.A. Braun,Margaret Bray,Jeanne Carroll,Jeanne Carroll,Julie A. Cakici,Sara A. Caylor,Christina Clarke,Mitchell Creed,Jennifer Friedman,Jennifer Friedman,Alison Frith,Richard Gain,Mary Gaughran,Shauna George,Sheldon Gilmer,Joseph G. Gleeson,Joseph G. Gleeson,Jeremy Gore,Haiying Li Grunenwald,Raymond Hovey,Marie L. Janes,Kejia Lin,Paul D. McDonagh,Kyle McBride,Patrick Mulrooney,Shareef Nahas,Daeheon Oh,Albert Oriol,Laura Puckett,Zia Rady,Martin G. Reese,Julie Ryu,Julie Ryu,Lisa Salz,Erica Sanford,Erica Sanford,Lawrence Stewart,Nathaly M. Sweeney,Nathaly M. Sweeney,Mari Tokita,Luca Van Der Kraan,Sarah White,Kristen Wigby,Kristen Wigby,Brett Williams,Terence C. Wong,Meredith S. Wright,Catherine Yamada,Peter Schols,John Reynders,Kevin Hall,David Dimmock,Narayanan Veeraraghavan,Thomas Defay,Stephen F. Kingsmore +70 more
TL;DR: A platform for population-scale, provisional diagnosis of genetic diseases with automated phenotyping and interpretation and could aid clinicians to expedite an accurate genetic disease diagnosis, potentially hastening lifesaving changes to patient care.
Journal ArticleDOI
Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of care.
David Dimmock,Sara A. Caylor,Bryce Waldman,Wendy Benson,Christina Ashburner,Jason Carmichael,Jeanne Carroll,Elaine Cham,Shimul Chowdhury,John P. Cleary,Arthur D’Harlingue,Ami Doshi,Ami Doshi,Katarzyna A. Ellsworth,Carolina I. Galarreta,Charlotte A. Hobbs,Kathleen Houtchens,Juliette Hunt,Priscilla Joe,Maries Joseph,Robert H. Kaplan,Stephen F. Kingsmore,Jason Knight,Aaina Kochhar,Richard Kronick,Jolie Limon,Madelena Martin,Katherine A. Rauen,Adam Schwarz,Suma P. Shankar,Rosanna Spicer,Mario Augusto Rojas,Ofelia Vargas-Shiraishi,Kristen Wigby,Kristen Wigby,Neda Zadeh,Lauge Farnaes +36 more
TL;DR: In this paper, the authors evaluated the clinical and economic impact of using Rapid Whole-Genome Sequencing (rWGS)-based Rapid Precision Medicine (RPM) as a diagnostic test in the California Medicaid (Medi-Cal) program.
Journal ArticleDOI
An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm.
David Dimmock,David Dimmock,Michelle M. Clark,Michelle M. Clark,Mary Gaughran,Mary Gaughran,Julie A. Cakici,Julie A. Cakici,Julie A. Cakici,Sara A. Caylor,Sara A. Caylor,Christina Clarke,Christina Clarke,Michele Feddock,Michele Feddock,Shimul Chowdhury,Shimul Chowdhury,Lisa Salz,Lisa Salz,Cynthia Cheung,Lynne M. Bird,Lynne M. Bird,Charlotte A. Hobbs,Charlotte A. Hobbs,Kristen Wigby,Kristen Wigby,Kristen Wigby,Lauge Farnaes,Lauge Farnaes,Cinnamon S. Bloss,Stephen F. Kingsmore,Stephen F. Kingsmore,Matthew N. Bainbridge,Jaime Barea,Sergey Batalov,Zaira Bezares,Joshua J.A. Braun,Miguel Del Campo,Jeanne Carroll,Casey Cohenmeyer,Nicole G. Coufal,Carlos Diaz,Yan Ding,Katarzyna A. Ellsworth,Marva Evans,Annette Feigenbaum,Jennifer Friedman,Joe Gleeson,Christian Hansen,Jose Honold,Kiely N. James,Marilyn C. Jones,Amy S. Kimball,Gail Knight,Lucitia Van Der Kraan,Brian Lane,Jennie Le,Sandra Leibel,Jerica Lenberg,Dana Mashburn,Laurel Moyer,Patrick Mulrooney,Shareef Nahas,Daeheon Oh,Daniken Orendain,Albert Oriol,Maria Ortiz-Arechiga,Lance Prince,Seema Rego,Iris Reyes,Erica Sanford,Charles Sauer,Leila Schwanemann,Mark Speziale,Denise Suttner,Nathaly M. Sweeney,Richard S. Song,Mari Tokita,Narayanan Veeraraghavan,Kelly Watkins,Terence C. Wong,Meredith S. Wright,Catherine Yamada +82 more
TL;DR: Clinicians perceived high clinical utility and low likelihood of harm with first-tier RGS of infants in ICUs with diseases of unknown etiology, and RGS was perceived as beneficial irrespective of whether results were positive or negative.
Journal ArticleDOI
An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases
Mallory J Owen,Sébastien Lefebvre,Christian Hansen,Chris M Kunard,David Dimmock,Laurie D. Smith,Gunter Scharer,Rebecca Mardach,Mary Jo Willis,Annette Feigenbaum,Anna-Kaisa Niemi,Yan-li Ding,Luca Van Der Kraan,Katarzyna A. Ellsworth,Lucia Guidugli,Bryan R. Lajoie,Tim K McPhail,Shyamal S Mehtalia,Kevin Chau,Yong-Hyun Kwon,Zhanyang Zhu,Serge Batalov,Shimul Chowdhury,Seema Rego,James Perry,Mark Speziale,Mark Nespeca,Meredith S. Wright,Martin G. Reese,Francisco M. De La Vega,Joe Azure,Erwin Frise,Charlene Son Rigby,Sandy White,Charlotte A. Hobbs,Sheldon Gilmer,Gail Knight,Albert Oriol,Jerica Lenberg,Shareef A. Nahas,Katherine Perofsky,Kyu Kim,Jeanne Carroll,Nicole G. Coufal,Erica Sanford,Kristen Wigby,Jacqueline Weir,Vicki S Thomson,Louise Fraser,Seka Lazare,Yoon H Shin,Haiying Li Grunenwald,Richard Lee,David Jones,Du Tran,Andrew M. Gross,Patrick Daigle,Anne Renio Case,Marisa Lue,James A. Richardson,John Reynders,Thomas Defay,Kevin Hall,Narayanan Veeraraghavan,Stephen F. Kingsmore +64 more
TL;DR: Genome-to-Treatment as mentioned in this paper is an automated, virtual system for genetic disease diagnosis and acute management guidance, which can be used to facilitate optimal outcomes in children with rapidly progressive genetic diseases.