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S

Sara L. Bristow

natera
H指数:15
被引数:890

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Validation of a methylation-based, tissue-free MRD assay in colorectal cancer patients from the GALAXY study

来自GALAXY研究的结直肠癌患者中基于甲基化的无组织MRD测定的验证

npj Precision Oncology
IF8
2026-01-190
OAAI
Yoshiaki Nakamura; Johannes G. Reiter; Prashanthi Natarajan; Joshua Babiarz; Preethi Srinivasan; Jayashree Joshi; Yu Lin; Tzu-Chun Chen; Nathan Liang; Su Maw; Ehsan Haghshenas; Garima Kushwaha; Boris Gutman; Ilker Tunc; Wen-Ching Chan; Antony Tin; Yuefan Huang; Sara L. Bristow; Meenakshi Malhotra; Shruti Sharma; Stephanie A. Sanchez; Adham Jurdi; Minetta C. Liu; Trupti Kawli; Matthew Rabinowitz; Alexey Aleshin; Daisuke Kotani; Oki Eiji; Takayuki Yoshino
Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug-Gene, Drug-Drug-Gene, and Drug-Gene-Gene Interaction Risks in a Large Patient Population

药物基因组相互作用概率 (PIP) 评分在预测大量患者人群中药物-基因、药物-基因和药物-基因相互作用风险中的验证

JOURNAL OF PERSONALIZED MEDICINE
IF3
2022-11-293
OAAI
Ashcraft, Kristine; Grande, Kendra; Bristow, Sara L. L.; Moyer, Nicolas; Schmidlen, Tara; Moretz, Chad; Wick, Jennifer A. A.; Blaxall, Burns C. C.
Germline Pathogenic Variant Prevalence Among Latin American and US Hispanic Individuals Undergoing Testing for Hereditary Breast and Ovarian Cancer: A Cross-Sectional Study
JCO GLOBAL ONCOLOGY
IF3
2022-07-0113
OAAI
Ossa Gomez, Carlos Andres; Achatz, Maria Isabel; Hurtado, Mabel; Sanabria-Salas, Maria Carolina; Sullcahuaman, Yasser; Chavarri-Guerra, Yanin; Dutil, Julie; Nielsen, Sarah M.; Esplin, Edward D.; Michalski, Scott T.; Bristow, Sara L.; Hatchell, Kathryn E.; Nussbaum, Robert L.; Pineda-Alvarez, Daniel E.; Ashton-Prolla, Patricia
Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program

X连锁和其他遗传性低磷血症的分子诊断: 来自赞助的基因检测计划的结果

JOURNAL OF BONE AND MINERAL RESEARCH
IF5.9
2021-10-1125
OAAI
Rush, Eric T.; Johnson, Britt; Aradhya, Swaroop; Beltran, Daniel; Bristow, Sara L.; Eisenbeis, Scott; Guerra, Norma E.; Krolczyk, Stan; Miller, Nicole; Morales, Ana; Ramesan, Prameela; Sarafrazi, Soodabeh; Truty, Rebecca; Dahir, Kathryn
One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation
GENETICS IN MEDICINE
IF6.2
2021-09-0151
OAAI
Lincoln, Stephen E.; Hambuch, Tina; Zook, Justin M.; Bristow, Sara L.; Hatchell, Kathryn; Truty, Rebecca; Kennemer, Michael; Shirts, Brian H.; Fellowes, Andrew; Chowdhury, Shimul; Klee, Eric W.; Mahamdallie, Shazia; Cleveland, Megan H.; Vallone, Peter M.; Ding, Yan; Seal, Sheila; DeSilva, Wasanthi; Tomson, Farol L.; Huang, Catherine; Garlick, Russell K.; Rahman, Nazneen; Salit, Marc; Kingsmore, Stephen F.; Ferber, Matthew J.; Aradhya, Swaroop; Nussbaum, Robert L.

研究方向

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S
Swaroop Aradhya
H 指数:44论文数:182被引数:1.2万
R
Rebecca Truty
H 指数:27论文数:75被引数:1.8万
A
Ana Morales
H 指数:35论文数:122被引数:6,229
H 指数:0论文数:187被引数:2,182
D
Dianalee McKnight
H 指数:32论文数:81被引数:4,300
K
Kathryn E. Hatchell
H 指数:17论文数:83被引数:1,208
A
Alexandra Peyser
H 指数:11论文数:125被引数:470
A
Alexey Aleshin
H 指数:35论文数:224被引数:7,642
J
Johannes G. Reiter
H 指数:26论文数:98被引数:6,847
P
Preethi Srinivasan
H 指数:17论文数:93被引数:6,666