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

Evaluating the Utility of RNAseq in Prenatal Diagnostics: Expression Profiles of Cultured Chorionic Villus and Amniotic Fluid Samples

评估RNA测序在产前诊断中的应用:培养绒毛膜绒毛和羊水样本的表达谱

Vladoiu, Maria C; Zhao, Sen; Zemet, Roni; Parobek, Christian M; Sinson, Jefferson Cruz; Tankersley, Stacy; Van den Veyver, Ignatia B; Liu, Pengfei

The effect of uterine entry technique on chorioamniotic membrane separation in fetoscopic laser photocoagulation for twin-to-twin transfusion syndrome: protocol for a randomized controlled trial

子宫入路技术对胎儿镜激光光凝治疗双胎输血综合征中绒毛膜羊膜分离的影响:一项随机对照试验方案

Burnett, Brian A; Munoz, Jessian L; Johnson, Rebecca M; Parobek, Christian M; Delgadillo Chabolla, Luis E; Buskmiller, Cara; Donepudi, Roopali V; Sanz Cortes, Magdalena; Belfort, Michael A; Nassr, Ahmed A

Diagnostic Value of Cell-Free DNA Fetal Fraction in Patients With Prenatally Suspected Placenta Accreta Spectrum Disorder

无细胞DNA胎儿片段在产前疑似胎盘植入谱系障碍患者中的诊断价值

Chirumbole, Danielle; Parobek, Christian M; Tai, Alex; Sangi-Haghpeykar, Haleh; Mendez, Yamely H; Kamepalli, Spoorthi; Reed, Christina C; Ladron de Guevara, Arthur; Lane, Keneshia; Hoppenot, Claire; Shamshirsaz, Amir A; Belfort, Michael A; Munoz, Jessian L; Lombaard, Hendrik A

A Qualitative Study of Pregnant Patient Perspectives on Genetic Privacy of Cell-Free DNA and Optimal Design of a Prenatal Genetics Video-Based Educational Intervention

一项关于孕妇对游离DNA遗传隐私的看法以及基于视频的产前遗传学教育干预最佳设计的定性研究

Thorsen, Margaret M; Mahoney, Rose C; Parobek, Christian; Jiménez Muñoz, Paola C; Nunez, Stephanie; Lewkowitz, Adam K; Slack, Carolyn; Russo, Melissa L

Family Lore, a Variant of Uncertain Significance, and CADASIL

《家族传说》、《意义不明的变体》和 CADASIL

Duarte, Rhys; Vossaert, Liesbeth; Darilek, Sandra A; Rose, Chelsi; Schauer, Evan; Parobek, Christian; Bland, Emily; Machol, Keren; Mizerik, Elizabeth; Murali, Chaya N

Limited Role of MSAFP Screening for Prenatal Omphalocele Detection

MSAFP筛查在产前脐膨出检测中的作用有限

Parobek, Christian M; Shanahan, Matthew A; Burnett, Brian A; Dadoun, Simon E; Adams, April D

Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis

临床外显子组测序揭示疑似缺氧缺血性脑病新生儿的遗传疾病:一项回顾性分析

Parobek, Christian M; Zemet, Roni; Shanahan, Matthew A; Burnett, Brian A; Mizerik, Elizabeth; Rosenfeld, Jill A; Vossaert, Liesbeth; Clark, Steven L; Hunter, Jill V; Lalani, Seema R

Video education about genetic privacy and patient perspectives about sharing prenatal genetic data: a randomized trial

关于基因隐私和患者对共享产前基因数据的看法的视频教育:一项随机试验

Parobek, Christian M; Thorsen, Margaret M; Has, Phinnara; Lorenzi, Paula; Clark, Melissa A; Russo, Melissa L; Lewkowitz, Adam K

Deep Sequencing to Detect Diversity of Trypanosoma cruzi Infection in Patients Coinfected With Human Immunodeficiency Virus and Chagas Disease

利用深度测序检测合并感染人类免疫缺陷病毒和恰加斯病患者体内克氏锥虫感染的多样性

Bowman, Natalie M; Balasubramanian, Sujata; Gilman, Robert H; Parobek, Christian; Calderon, Maritza; Waltmann, Andreea; Messenger, Louisa A; Sanchez, Leny; Bern, Caryn; Juliano, Jonathan J

Hypnozoite depletion in successive Plasmodium vivax relapses

间日疟原虫连续复发中的休眠子耗竭

Noviyanti, Rintis; Carey-Ewend, Kelly; Trianty, Leily; Parobek, Christian; Puspitasari, Agatha Mia; Balasubramanian, Sujata; Park, Zackary; Hathaway, Nicholas; Utami, Retno A S; Soebianto, Saraswati; Jeny, Jeny; Yudhaputri, Frilasita; Perkasa, Aditya; Coutrier, Farah N; Tirta, Yusrifar K; Ekawati, Lenny; Tjahyono, Bagus; Sutanto, Inge; Nelwan, Erni J; Sudoyo, Herawati; Baird, J Kevin; Lin, Jessica T