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

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论文共 17 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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Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing Comment

Mallory J. Owen,Meredith S. Wright,Sergey Batalov,Yonghyun Kwon,Yan Ding,Kevin K. Chau,Shimul Chowdhury,Nathaly M. Sweeney,Elizabeth Kiernan,Andrew Richardson,Emily Batton,Rebecca J. Baer,Gretchen Bandoli,Joseph G. Gleeson,Matthew Bainbridge,Christina D. Chambers,Stephen F. Kingsmore

OBSTETRICAL & GYNECOLOGICAL SURVEYno. 8 (2023): 462-464

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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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Reclassification of the Etiology of Infant Mortality with Whole-Genome Sequencing

Mallory Owen,Meredith S. Wright,Sergey Batalov,Yong-Hyun Kwon,Yan Ding,Kevin Chau,Shimul Chowdhury,Nathaly M. Sweeney,Elizabeth Kiernan,Andrew Richardson,Emily Batton,Rebecca J. Baer,Gretchen Bandoli,Joseph G. Gleeson,Matthew N. Bainbridge,Christina Chambers,Stephen F. Kingsmore

Obstetrical & gynecological surveyno. 8 (2023): 462-464

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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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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）

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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）

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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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