Mallory J Owen - Department of Pediatrics, University of California, San Diego

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论文共 15 篇作者统计合作学者相似作者

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Whole Exome and Whole Genome Sequencing for the Diagnosis of Mitochondrial Diseases in Critically Ill Children (S8.002)

Mallory Owen,Stephen Kingsmore,Richard Haas,Jennifer Yang

Neurology（2024）

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P156: Genomic Disease Contribution for Unknown Causes of Infant Mortality Via Genome Sequencing of Newborn Dried Blood Spots and Semiautomated Interpretation*

Eric Ontiveros, Liana Protopsaltis,Rebecca Baer,Matthew Bainbridge, Bryant Cao,Yan Ding,Katarzyna (Kasia) Ellsworth, Laura Forero,Erwin Frise,Lucia Guidugli,YongHyun Kwon,Jennie Le,Scott Oltman,Mallory Owen,Erica Sanford Kobayashi, Lucita Van Der Kraan,Meredith Wright, Mark Yandell,Laura Jelliffe-Pawlowski,Gretchen Bandoli

Genetics in Medicine Open (2024): 101053

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Scalable, High Quality, Whole Genome Sequencing from Archived, Newborn, Dried Blood Spots

Yan Ding,Mallory Owen,Jennie Le,Sergey Batalov,Kevin Chau,Yong Hyun Kwon, Lucita Van Der Kraan, Zaira Bezares-Orin,Zhanyang Zhu,Narayanan Veeraraghavan,Shareef Nahas,Matthew Bainbridge, Joe Gleeson,Rebecca J. Baer,Gretchen Bandoli,Christina Chambers,Stephen F. Kingsmore

npj Genomic Medicine（2023）

引用5浏览0WOSNATURE引用

Rapid Whole Genome Sequencing for Diagnosis of Single Locus Genetic Diseases in Critically Ill Children

Mallory Owen,Sergey Batalov,Katarzyna A. Ellsworth,Meredith S. Wright, Sylvia Breeding, Kwon Hugh,Stephen F. Kingsmore,Yan Ding

Methods in molecular biologypp.217-239, (2023)

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Response to Grosse Et Al

Stephen F Kingsmore,Laurie D Smith,Chris M Kunard,Matthew Bainbridge,Sergey Batalov,Wendy Benson, Eric Blincow,Sara Caylor,Christina Chambers,Guillermo Del Angel,David P Dimmock,Yan Ding,Katarzyna Ellsworth,Annette Feigenbaum,Erwin Frise,Robert C Green,Lucia Guidugli,Kevin P Hall,Christian Hansen,Charlotte A Hobbs, Scott D Kahn,Mark Kiel, Lucita Van Der Kraan, Chad Krilow,Yong H Kwon, Lakshminarasimha Madhavrao,Jennie Le,Sebastien Lefebvre,Rebecca Mardach, William R Mowrey, Danny Oh,Mallory J Owen, George Powley,Gunter Scharer, Seth Shelnutt,Mari Tokita, Shyamal S Mehtalia,Albert Oriol,Stavros Papadopoulos, James Perry,Edwin Rosales,Erica Sanford,Steve Schwartz, Duke Tran,Martin G Reese,Meredith Wright,Narayanan Veeraraghavan,Kristen Wigby,Mary J Willis,Aaron R Wolen,Thomas Defay

American journal of human geneticsno. 6 (2023): 1017-1017

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A Genome Sequencing System for Universal Newborn Screening, Diagnosis, and Precision Medicine for Severe Genetic Diseases

Stephen F. Kingsmore,Laurie D. Smith,Chris M. Kunard,Matthew Bainbridge,Sergey Batalov,Wendy Benson, Eric Blincow,Sara Caylor,Christina Chambers,Guillermo Del Angel,David P. Dimmock,Yan Ding,Katarzyna Ellsworth,Annette Feigenbaum,Erwin Frise,Robert C. Green,Lucia Guidugli,Kevin P. Hall,Christian Hansen,Charlotte A. Hobbs, Scott D. Kahn,Mark Kiel, Lucita Van Der Kraan, Chad Krilow,Yong H. Kwon, Lakshminarasimha Madhavrao,Jennie Le,Sebastien Lefebvre,Rebecca Mardach, William R. Mowrey, Danny Oh,Mallory J. Owen, George Powley,Gunter Scharer, Seth Shelnutt,Mari Tokita, Shyamal S. Mehtalia,Albert Oriol,Stavros Papadopoulos,James Perry,Edwin Rosales,Erica Sanford,Steve Schwartz, Duke Tran,Martin G. Reese,Meredith Wright,Narayanan Veeraraghavan,Kristen Wigby,Mary J. Willis,Aaron R. Wolen,Thomas Defay

American journal of human genetics（2022）

引用39浏览0WOS引用

Retrospective Identification of Prenatal Fetal Anomalies Associated with Diagnostic Neonatal Genomic Sequencing Results

Kathy Zhang-Rutledge,Mallory Owen,Nathaly M. Sweeney,David Dimmock,Stephen F. Kingsmore,Louise C. Laurent

Prenatal diagnosis（2022）

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An Automated 13.5 Hour System for Scalable Diagnosis and Acute Management Guidance for Genetic Diseases

Mallory J. Owen,Sebastien Lefebvre,Christian Hansen,Chris M. Kunard,David P. Dimmock,Laurie D. Smith,Gunter Scharer,Rebecca Mardach,Mary J. Willis,Annette Feigenbaum,Anna-Kaisa Niemi,Yan Ding,Luca Van Der Kraan,Katarzyna Ellsworth,Lucia Guidugli,Bryan R. Lajoie, Timothy K. McPhail, Shyamal S. Mehtalia,Kevin K. Chau,Yong H. Kwon,Zhanyang Zhu,Sergey 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, Kate Perofsky, Kyu Kim,Jeanne Carroll,Nicole G. Coufal,Erica Sanford,Kristen Wigby, Jacqueline Weir,Vicki S. Thomson,Louise Fraser,Seka S. Lazare, Yoon H. Shin,Haiying Grunenwald,Richard Lee,David Jones, Duke Tran,Andrew Gross, Patrick Daigle, Anne Case, Marisa Lue,James A. Richardson,John Reynders,Thomas Defay,Kevin P. Hall,Narayanan Veeraraghavan,Stephen F. Kingsmore

Nature Communications（2022）

引用23浏览0WOSNATURE引用

Ep286: Genome-to-treatment: A System to Guide the Acute Management of Genetic Disorders in Children

Mary Willis,Mallory Owen,Sebastien Lefebvre,Christian Hanson,David Dimmock,Gunter Scharer,Rebecca Mardach,Annette Feigenbaum,Laurie Smith,Stephen Kingsmore

Genetics in Medicine（2022）

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