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

Integrated digital pathology at scale: A solution for clinical diagnostics and cancer research at a large academic medical center

大规模整合数字病理学：大型学术医疗中心临床诊断和癌症研究的解决方案

期刊:Journal of the American Medical Informatics Association
影响因子:
doi:10.1093/jamia/ocab085
Schüffler, Peter J; Geneslaw, Luke; Yarlagadda, D Vijay K; Hanna, Matthew G; Samboy, Jennifer; Stamelos, Evangelos; Vanderbilt, Chad; Philip, John; Jean, Marc-Henri; Corsale, Lorraine; Manzo, Allyne; Paramasivam, Neeraj H G; Ziegler, John S; Gao, Jianjiong; Perin, Juan C; Kim, Young Suk; Bhanot, Umeshkumar K; Roehrl, Michael H A; Ardon, Orly; Chiang, Sarah; Giri, Dilip D; Sigel, Carlie S; Tan, Lee K; Murray, Melissa; Virgo, Christina; England, Christine; Yagi, Yukako; Sirintrapun, S Joseph; Klimstra, David; Hameed, Meera; Reuter, Victor E; Fuchs, Thomas J
肿瘤
肿瘤免疫
发表日期：2021
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Sulforaphane Modulates Cytokine Levels in Cell Culture Media of Triple-Negative Breast Cancer Cells Grown with Macrophages

萝卜硫素调节与巨噬细胞共培养的三阴性乳腺癌细胞培养基中的细胞因子水平

期刊:
影响因子:
doi:10.1155/2010/507475
Zhang, Zhe; Maurer, Kelly; Perin, Juan C; Song, Li; Sullivan, Kathleen E; Merrick, Courtney; Housley, Lauren
巨噬细胞
肿瘤
肿瘤免疫
巨噬细胞
乳腺癌
Cell Culture
细胞生物学
免疫/内分泌
发表日期：2020
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Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes

对骨髓衰竭患者进行单核苷酸多态性芯片分析，揭示了其特征性的基因改变模式。

期刊:British Journal of Haematology
影响因子:3.8
doi:10.1111/bjh.12603
Babushok, Daria V; Xie, Hongbo M; Roth, Jacquelyn J; Perdigones, Nieves; Olson, Timothy S; Cockroft, Joshua D; Gai, Xiaowu; Perin, Juan C; Li, Yimei; Paessler, Michele E; Hakonarson, Hakon; Podsakoff, Gregory M; Mason, Philip J; Biegel, Jaclyn A; Bessler, Monica
发表日期：2014
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Efficient digest of high-throughput sequencing data in a reproducible report

高效地对高通量测序数据进行摘要，并生成可重复的报告

期刊:BMC Bioinformatics
影响因子:3.3
doi:10.1186/1471-2105-14-S11-S3
Zhang, Zhe; Leipzig, Jeremy; Sasson, Ariella; Yu, Angela M; Perin, Juan C; Xie, Hongbo M; Sarmady, Mahdi; Warren, Patrick V; White, Peter S
发表日期：2013
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NMNAT1 mutations cause Leber congenital amaurosis.

NMNAT1基因突变会导致莱伯氏先天性黑蒙症

期刊:Nature Genetics
影响因子:29
doi:10.1038/ng.2361
Falk Marni J, Zhang Qi, Nakamaru-Ogiso Eiko, Kannabiran Chitra, Fonseca-Kelly Zoe, Chakarova Christina, Audo Isabelle, Mackay Donna S, Zeitz Christina, Borman Arundhati Dev, Staniszewska Magdalena, Shukla Rachna, Palavalli Lakshmi, Mohand-Said Saddek, Waseem Naushin H, Jalali Subhadra, Perin Juan C, Place Emily, Ostrovsky Julian, Xiao Rui, Bhattacharya Shomi S, Consugar Mark, Webster Andrew R, Sahel José-Alain, Moore Anthony T, Berson Eliot L, Liu Qin, Gai Xiaowu, Pierce Eric A
发表日期：2012
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Mitochondrial genome sequence analysis: a custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracy

线粒体基因组序列分析：定制的生物信息学流程显著提高了 Affymetrix MitoChip v2.0 的检出率和准确性

期刊:BMC Bioinformatics
影响因子:3.3
doi:10.1186/1471-2105-12-402
Xie, Hongbo M; Perin, Juan C; Schurr, Theodore G; Dulik, Matthew C; Zhadanov, Sergey I; Baur, Joseph A; King, Michael P; Place, Emily; Clarke, Colleen; Grauer, Michael; Schug, Jonathan; Santani, Avni; Albano, Anthony; Kim, Cecilia; Procaccio, Vincent; Hakonarson, Hakon; Gai, Xiaowu; Falk, Marni J
线粒体
发表日期：2011
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Genome-wide analysis of interferon regulatory factor I binding in primary human monocytes

人类原代单核细胞中干扰素调节因子I结合的全基因组分析

期刊:Gene
影响因子:2.4
doi:10.1016/j.gene.2011.07.004
Shi, Lihua; Perin, Juan C; Leipzig, Jeremy; Zhang, Zhe; Sullivan, Kathleen E
细胞生物学
单核细胞
发表日期：2011
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CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

CNV Workshop：一个用于高通量拷贝数变异发现和临床诊断的集成平台

期刊:BMC Bioinformatics
影响因子:3.3
doi:10.1186/1471-2105-11-74
Gai, Xiaowu; Perin, Juan C; Murphy, Kevin; O'Hara, Ryan; D'arcy, Monica; Wenocur, Adam; Xie, Hongbo M; Rappaport, Eric F; Shaikh, Tamim H; White, Peter S
发表日期：2010
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