Samuel P. Strom

基本信息

Career Trajectory

Bio

I support all things genetics at Fulgent: single variant testing, whole genome sequencing, and everything in between. In this new role, I will be dedicating more of my efforts towards building and strengthening collaborations with hospitals, labs, biopharma, and anyone else who wants to sequence nucleic acids.

Research Interests

Papers共 48 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选

Expanded Newborn Screening Using Genome Sequencing for Early Actionable Conditions

Alban Ziegler, Carrie Koval-Burt,Denise M. Kay,Sharon F. Suchy,Amber Begtrup,Katherine G. Langley,Rebecca Hernan,Laura M. Amendola, Brenna M. Boyd, Jennifer Bradley,Tracy Brandt,Lilian L. Cohen,Alison J. Coffey, Joseph M. Devaney, Beata Dygulska,Bethany Friedman,Ramsay L. Fuleihan, Awura Gyimah,Sihoun Hahn, Sean Hofherr,Kathleen S. Hruska,Zhanzhi Hu,Mederic Jeanne, Guanjun Jin, D. Aaron Johnson,Haluk Kavus,Rudolph L. Leibel,Steven J. Lobritto,Stephen Mcgee,Joshua D. Milner,Kirsty Mcwalter,Kristin G. Monaghan,Jordan S. Orange, Nicole Pimentel Soler, Yeyson Quevedo, Samantha Ratner,Kyle Retterer, Ankur Shah, Natasha Shapiro,Robert J. Sicko,Eric S. Silver,Samuel Strom,Rebecca I. Torene,Olatundun Williams, Vincent D. Ustach,Julia Wynn,Ryan J. Taft,Paul Kruszka,Michele Caggana,Wendy K. Chung

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION（2025）

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P636: Lp(a) Genetic Risk Screening Using Genome Sequencing

Samuel Strom,Laura Amendola,Aditi Chawla, Vitor Onucic,Denise Perry,Akanchha Kesari,Ryan Taft

Genetics in Medicine Open (2024): 101542

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P368: Novel Mutation in ZIC3 in a Peruvian Family with Variable Phenotype VACTERL-H Association

Giulliana Chávez-Pasco,Jeny Bazalar-Montoya, Cecilia Bonilla Suarez,Krista Bluske,Samuel Strom,Alka Malhotra,Becky Milewski,Erin Thorpe,Ryan Taft,Gioconda Manassero-Morales

Genetics in Medicine Open (2024): 101262

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The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships

Eleanor Broeren, Vanessa Gitau,Alicia Byrne, Pamela Ajuyah,Marie Balzotti,Jonathan Berg,Krista Bluske, B Monica Bowen, Matthew P Brown, Amanda Buchanan, Brendan Burns,Nicole J Burns,Anjana Chandrasekhar,Aditi Chawla,Jessica Chong,Maya Chopra,Amanda Clause,Marina DiStefano,Stephanie DiTroia,Marwa Elnagheeb, Amanda Girod,Himanshu Goel,Katie Golden-Grant,Thuong Ha,Ada Hamosh, Jennifer Huang, Madeline Hughes,Saumya Jamuar,Sylvia Kam,Akanchha Kesari,Ai Ling Koh, Rhonda Lassiter,Sarah Leigh,Gabrielle Lemire,Jiin Ying Lim,Alka Malhotra,Hannah McCurry,Becky Milewski,Shahida Moosa, Stephen Murray,Emma Owens,Emma Palmer, Brooke Palus,Mayher Patel,Revathi Rajkumar, Julie Ratliff,F Lucy Raymond, Bruno Della Ripa Rodrigues Assis, Samin Sajan,Zinayida Schlachetzki,Sarah Schmidt,Zornitza Stark,Samuel Strom,Julie Taylor,Courtney Thaxton,Devon Thrush,Sabrina Toro, Kezang Tshering,Nicole Vasilevsky,Bess Wayburn, Ryan Webb,Anne O'Donnell-Luria,Alison J Coffey

medRxiv the preprint server for health sciences (2024)

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P507: Implementation of Automated Pharmacogenomics Reporting for a Clinically Validated Whole Genome Sequencing Test

Alka Malhotra,Rueben Hejja,James Avecilla, Andrew Walker,Phillip Medrano,Felipe Mullen,Anusha Balusu,Pratyusha Vankayala,Maren Bennett,Aditi Chawla,Subramanian Ajay,Samuel Strom,Akanchha Kesari,Denise Perry,Ryan Taft

Genetics in Medicine Openno. 1 (2023): 100554

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P565: Optimized Whole Genome Screening: the Impact of Variant Calling Accuracy Improvements on Curation Burden

Kristen Sund,Samuel Strom, Pauline Fujita,Batsal Devkota,Jennifer Shah,Nathan Berkowitz, LeAnne Lovato,Elliott Margulies, Mitch Bekritsky

Genetics in Medicine Openno. 1 (2023): 100612-100612

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P420: Development of a Comprehensive Cardiovascular Disease Whole Genome Sequencing Test

Laura Amendola,Alison Coffey,Samuel Strom,Akanchha Kesari,James Avecilla,Josh Lowry, Stetson Thacker,Julie Taylor, Kathryn Golden-Grant,Matt Brown,Becky Milewski,John Belmont,Denise Perry,Ryan Taft

Genetics in Medicine Openno. 1 (2023): 100467-100467

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Somatic Non-Cancerous Overgrowth Syndrome of Obscure Molecular Etiology: What Are the Causes and Options

Garneau, Alexandre P.,Haydock, Ludwig,Tremblay, Laurence E.,Harvey-Michaud, Pierre-Luc, Hsiao, Yun-Hua Esther,Strom, Samuel P.,Canaud, Guillaume,Isenring, Paul

Journal of molecular medicine (Berlin, Germany)（2022）

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Papers共 48 篇Author StatisticsCo-AuthorSimilar Experts