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

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

Eleanor C Broeren, Vanessa N Gitau,Alicia B Byrne, Pamela Ajuyah,Marie B Balzotti,Jonathan S Berg,Krista Bluske, B Monica Bowen, Matthew P Brown, Amanda Buchanan, Brendan T Burns,Nicole J Burns,Anjana Chandrasekhar,Aditi Chawla,Jessica X Chong,Maya Chopra,Amanda R Clause,Marina T DiStefano,Stephanie DiTroia,Marwa A Elnagheeb, Amanda N Girod,Himanshu Goel,Katie L Golden-Grant,Thuong Ha,Ada Hamosh, Jennifer M Huang, Madeline Y Hughes,Saumya S Jamuar,Sylvia Kam,Akanchha Kesari,Ai Ling Koh, Rhonda N T Lassiter,Sarah E Leigh,Gabrielle Lemire,Jiin Ying Lim,Alka Malhotra,Hannah R McCurry,Becky Milewski,Shahida Moosa, Stephen A Murray,Emma H Owens,Elizabeth E Palmer, Brooke C Palus,Mayher J Patel,Revathi Rajkumar, Julie C Ratliff,F Lucy Raymond, Bruno Della Ripa Rodrigues Assis, Samin A Sajan,Zinayida Schlachetzki,Sarah A Schmidt,Zornitza Stark,Samuel P Strom,Julie P Taylor,Courtney Thaxton,Devon L Thrush,Sabrina Toro, Kezang C Tshering,Nicole A Vasilevsky,Bess Wayburn, Ryan F Webb,Anne O'Donnell-Luria,Alison J Coffey

Genetics in medicine open (2025): 103429-103429

Cited0Views0WOSBibtex

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）

Cited2Views0WOSBibtex

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

Cited0Views0Bibtex

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

Cited0Views0Bibtex

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

Cited0Views0Bibtex

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

Cited0Views0Bibtex

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

Cited0Views0Bibtex

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）

Cited0Views0WOSBibtex

Author Statistics

Co-Author

Co-Institution

D-Core

合作者
学生
导师

No result temporarily, you can search similar Scholar with the same research interest

Data Disclaimer

The page data are from open Internet sources, cooperative publishers and automatic analysis results through AI technology. We do not make any commitments and guarantees for the validity, accuracy, correctness, reliability, completeness and timeliness of the page data. If you have any questions, please contact us by email: report@aminer.cn

Director

Papers共 48 篇Author StatisticsCo-AuthorSimilar Experts