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

Distinctive genomic features of hydroa vacciniforme lymphoproliferative disorder in Latin American patients: A multicenter multi-omics study

拉丁美洲患者水痘样淋巴增生性疾病的独特基因组特征:一项多中心多组学研究

Luniewski, Aleksander; Moore, Margaret; Williams, Eli S; Xi, Liqiang; Barrionuevo, Carlos; Konduru, Guruprasad Varma; Kumar, Pankaj; Kundu, Debamita; Patel, Nihir; Duenas-Hancco, Daniela; Cervantes, Elizabeth; Bacchi, Carlos E; da Silva, Tiago Vencato; Valencia, Adriana; Toledo Bahena, Mirna Eréndira; Ochoa Drucker, Ana Cecilia; Martínez Callado, Irma Jimena; Plaza, Jose A; Caire, Sonia Toussaint; Sangueza, Julio-Martin; Gru, Alejandro A; Obiorah, Ifeyinwa E

A process optimization and release modeling of coaxial electrospun aligned core-shell poly (ethylene oxide-poly(l-lactide-co-glycolide)) nanofibers encapsulating nerve growth factor.

对封装神经生长因子的同轴静电纺丝取向核壳聚(环氧乙烷-聚(L-乳酸-共-乙醇酸))纳米纤维进行工艺优化和释放建模

Hariprasad Bhoomija, Eslamian Mohammadjavad, Patel Nihir, Abidian Mohammad Reza

HRAS-Mutant Cardiomyocyte Model of Multifocal Atrial Tachycardia.

HRAS突变心肌细胞多灶性房性心动过速模型

Rodríguez Nelson A, Patel Nihir, Dariolli Rafael, Ng Simon, Aleman Angelika G, Gong Jingqi Q X, Lin Hung-Mo, Rodríguez Matthew, Josowitz Rebecca, Sol-Church Katia, Gripp Karen W, Lin Xianming, Song Soomin C, Fishman Glenn I, Sobie Eric A, Gelb Bruce D

Goliath clades and in vivo tracking of clonal dynamics show three phases of UV-induced skin carcinogenesis

巨型细胞系和体内克隆动态追踪显示紫外线诱导的皮肤癌变分为三个阶段

Avdieiev, Stanislav; Tordesillas, Leticia; Prieto, Karol; Chavez Chiang, Omar; Chen, Zhihua; Patel, Nihir; Cordero, Sofia; Simoes, Luiza Silva; Chen, Y Ann; Andor, Noemi; Gatenby, Robert A; Flores, Elsa R; Whelan, Christopher J; Brown, Joel S; Tsai, Kenneth Y

Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study

基于证据的先天性心脏病基因评估,以便在基因组研究中获得结果

Griffin, Emily L; Nees, Shannon N; Morton, Sarah U; Wynn, Julia; Patel, Nihir; Jobanputra, Vaidehi; Robinson, Scott; Kochav, Stephanie M; Tao, Alice; Andrews, Carli; Cross, Nancy; Geva, Judith; Lanzilotta, Kristen; Ritter, Alyssa; Taillie, Eileen; Thompson, Alexandra; Meyer, Chris; Akers, Rachel; King, Eileen C; Cnota, James F; Kim, Richard W; Porter, George A Jr; Brueckner, Martina; Seidman, Christine E; Shen, Yufeng; Gelb, Bruce D; Goldmuntz, Elizabeth; Newburger, Jane W; Roberts, Amy E; Chung, Wendy K

Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylation

全基因组评估短串联重复序列变异对局部DNA甲基化的影响

Martin-Trujillo, Alejandro; Garg, Paras; Patel, Nihir; Jadhav, Bharati; Sharp, Andrew J

Myopathic Cardiac Genotypes Increase Risk for Myocarditis

肌病性心脏基因型增加心肌炎风险

Kontorovich, Amy R; Patel, Nihir; Moscati, Arden; Richter, Felix; Peter, Inga; Purevjav, Enkhsaikhan; Selejan, Simina Ramona; Kindermann, Ingrid; Towbin, Jeffrey A; Bohm, Michael; Klingel, Karin; Gelb, Bruce D

A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations

采用基因型优先的方法探索具有明显外部表现的孟德尔心血管性状

Wenger, Brittany M; Patel, Nihir; Lui, Madeline; Moscati, Arden; Do, Ron; Stewart, Douglas R; Tartaglia, Marco; Muiño-Mosquera, Laura; De Backer, Julie; Kontorovich, Amy R; Gelb, Bruce D

Genomic analyses implicate noncoding de novo variants in congenital heart disease

基因组分析表明,非编码新生变异与先天性心脏病有关。

Richter, Felix; Morton, Sarah U; Kim, Seong Won; Kitaygorodsky, Alexander; Wasson, Lauren K; Chen, Kathleen M; Zhou, Jian; Qi, Hongjian; Patel, Nihir; DePalma, Steven R; Parfenov, Michael; Homsy, Jason; Gorham, Joshua M; Manheimer, Kathryn B; Velinder, Matthew; Farrell, Andrew; Marth, Gabor; Schadt, Eric E; Kaltman, Jonathan R; Newburger, Jane W; Giardini, Alessandro; Goldmuntz, Elizabeth; Brueckner, Martina; Kim, Richard; Porter, George A Jr; Bernstein, Daniel; Chung, Wendy K; Srivastava, Deepak; Tristani-Firouzi, Martin; Troyanskaya, Olga G; Dickel, Diane E; Shen, Yufeng; Seidman, Jonathan G; Seidman, Christine E; Gelb, Bruce D

A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions

一项对23116个人类基因组中罕见表观遗传变异的调查发现了与疾病相关的表观遗传变异和CGG扩增

Garg, Paras; Jadhav, Bharati; Rodriguez, Oscar L; Patel, Nihir; Martin-Trujillo, Alejandro; Jain, Miten; Metsu, Sofie; Olsen, Hugh; Paten, Benedict; Ritz, Beate; Kooy, R Frank; Gecz, Jozef; Sharp, Andrew J