日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Germline mutations in PPP2R1B in patients with a personal and family history of cancer.

具有个人和家族癌症史的患者中 PPP2R1B 的种系突变

Mazhar Sahar, O'Connor Caitlin M, Harold Alexis, Dowdican Amanda C, Ulintz Peter J, Hanson Erika N, Zhang Yuping, Jacobs Michelle F, Merajver Sofia D, Jackson Mark W, Scott Anthony, Sieuwerts Anieta M, Chinnaiyan Arul M, Narla Goutham

Pediatric Oncology Patients With Germline Pathogenic Variants in Adult-Onset Cancer Predisposition Genes

携带成人发病癌症易感基因种系致病变异的儿科肿瘤患者

Jacobs, Michelle F; Austin, Sarah; Murad, Andrea M; Koeppe, Erika; Kumar-Sinha, Chandan; Robinson, Dan R; Wu, Yi-Mi; Vo, Josh N; Koschmann, Carl; Robertson, Patricia; Franson, Andrea; Leung, Denise; Chinnaiyan, Arul M; Mody, Rajen J

A Review of Genomic Testing and SDH- Deficiency in Gastrointestinal Stromal Tumors: Getting to the GIST

胃肠道间质瘤基因组检测和SDH缺陷综述:如何诊断GIST

Florou, Vaia; Jacobs, Michelle F; Casey, Ruth; Evans, Denisse; Owens, Becky; Raygada, Margarita; Rothschild, Sara; Greenberg, Samantha E

Use of NCCN distress thermometer in cancer genetics patients

在癌症遗传学患者中使用NCCN痛苦温度计

Kennedy, Aidan M; Murad, Andrea M; Koeppe, Erika S; Riba, Michelle B; Stoffel, Elena M; Jacobs, Michelle F

Detection of Germline Variants in Patients With Localized and Metastatic Prostate Cancer Through Guideline-Based Testing

通过基于指南的检测方法检测局限性和转移性前列腺癌患者的种系变异

Abusamra, Sophia M; Solorzano, Marissa A; Quarles, Jake; Luke, Mallory; Patel, Milan; Vince, Randy Jr; Jiang, Ralph; Volin, Joshua; Jacobs, Michelle F; Kaffenberger, Samuel D; Salami, Simpa S; Palmbos, Phillip; Caram, Megan E V; Hollenbeck, Brent K; Palapattu, Ganesh S; Merajver, Sofia D; Stoffel, Elena M; Hafron, Jason; Morgan, Todd M; Reichert, Zachery R

QLTI-01. ASSESSING THE EFFECTIVENESS OF SUPPORT FROM ST. JUDE CHILDREN’S RESEARCH HOSPITAL TO VIETNAMESE TEAM IN TREATMENT FOR CHILDREN WITH BRAIN TUMORS

QLTI-01. 评估圣裘德儿童研究医院对越南团队在治疗脑瘤患儿方面提供的支持的有效性

Jacobs, Michelle F; Goldman, Joshua W; Austin, Sarah; Koeppe, Erika S; Murad, Andrea M; Koschmann, Carl J; Chinnaiyan, Arul M; Mody, Rajen J; Nguyen, Hoa Thi Kim; Bui, Lan Ngoc; Phan, Duy Canh; Dao, An Thi Thanh; Nguyen, Anh Hoang Mai; Hoang, Thach Ngoc; Do, Thanh Cam; Van Nguyen, Dinh; Handayani, Andini; Blair, Sally; Lam, Catherine G; Qaddoumi, Ibrahim

Promoting international, locally focused, and patient-oriented genetic counseling

推广国际化、本地化、以患者为中心的遗传咨询

Weil, Jon; Alaeddin, Dina; Awwad, Rawan; Chanouha, Nour; Elbassiouny, Batoul; Furqan, Aisha; Jacobs, Michelle F; Kavanaugh, Grace; Neogi, Arpita; Rao, Smita K; Sebastin, Monisha

Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants

罕见的临床表现可能提示不止一种罕见疾病:例如,一位同时携带 CDKN2A 和 BRCA1 致病性变异的患者,其个人和家族癌症史都非常引人注目。

Trupiano, Nicole; Koeppe, Erika; Jacobs, Michelle F; Else, Tobias; Cha, Kelly B

Satisfaction With Clinician-Led Germline Genetic Counseling in Patients With Prostate Cancer

前列腺癌患者对临床医生主导的生殖系遗传咨询的满意度

Abusamra, Sophia M; Solorzano, Marissa A; Luke, Mallory; Quarles, Jake; Jacobs, Michelle F; Das, Sanjay; Kasputis, Amy; Okoth, Linda A; Patel, Milan; Seymore, Mariana; Caram, Megan E V; Dunn, Rodney L; Merajver, Sofia D; Stoffel, Elena M; Reichert, Zachery R; Morgan, Todd M

Outcomes of retesting in patients with previously uninformative cancer genetics evaluations

对先前癌症遗传学评估结果不明确的患者进行复检的结果

Sanoba, Shenin A; Koeppe, Erika S; Jacobs, Michelle F; Stoffel, Elena M