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

A Phase III Randomized Trial of Integrated Genomics and Avatar Models for Personalized Treatment of Pancreatic Cancer: The AVATAR Trial

一项整合基因组学和虚拟化身模型用于胰腺癌个性化治疗的III期随机试验:AVATAR试验

Sarno, Francesca; Tenorio, Jair; Perea, Sofia; Medina, Laura; Pazo-Cid, Roberto; Juez, Ignacio; Garcia-Carbonero, Rocío; Feliu, Jaime; Guillen-Ponce, Carmen; Lopez-Casas, Pedro P; Guerra, Carmen; Duran, Yolanda; López-Acosta, José Francisco; Alonso, Carolina; Esquivel, Estrella; Dopazo, Ana; Akshinthala, Dipikaa; Muthuswamy, Senthil K; Lapunzina, Pablo; Bockorny, Bruno; Hidalgo, Manuel

Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range

编码突触前蛋白 Bassoon 的 BSN 基因变异会导致一种独特的神经发育障碍,其表型范围很广。

Guzman, Stacy G; Ruggiero, Sarah M; Ganesan, Shiva; Ellis, Colin A; Harrison, Alicia G; Sullivan, Katie R; Stark, Zornitza; Brown, Natasha J; Kana, Sajel L; Tuttle, Anabelle; Tenorio, Jair; Lapunzina, Pablo; Nevado, Julián; McDonald, Marie T; Jensen, Courtney; Wheeler, Patricia G; Stange, Lila; Morrison, Jennifer; Keren, Boris; Heide, Solveig; Keating, Meg W; Butler, Kameryn M; Lyons, Mike A; Jain, Shailly; Yeganeh, Mehdi; Thompson, Michelle L; Schroeder, Molly; Nguyen, Hoanh; Granadillo, Jorge; Johnston, Kari M; Murali, Chaya N; Bosanko, Katie; Burrow, T Andrew; Morgan, Syreeta; Watson, Deborah J; Hakonarson, Hakon; Helbig, Ingo

Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances

贝克威思-威德曼综合征中高度可变的基因组甲基化与多位点印记紊乱相关

Cecere, Francesco; Pignata, Laura; D'Angelo, Emilia; Giaccari, Carlo; Saadat, Abu; Sparago, Angela; Angelini, Claudia; Hay Mele, Bruno; Mussa, Alessandro; Ferrero, Giovanni Battista; Scarano, Gioacchino; Gori, Giulia; Di Maria, Emilio; Romano, Corrado; Tarani, Luigi; Piscopo, Carmelo; Scala, Iris; Tenorio, Jair Antonio; Lapunzina, Pablo; Cerrato, Flavia; Riccio, Andrea

Pulmonary arterial hypertension associated with exposure to toxic rapeseed oil

接触有毒菜籽油引起的肺动脉高压

Cruz-Utrilla, Alejandro; Cantero-Acedo, Álvaro; Tenes, Andrés; Enguita, Ana Belén; Delgado-Jiménez, Juan Francisco; López-Meseguer, Manuel; Martínez-Meñaca, Amaya; Lázaro Salvador, María; Martín De Miguel, Irene; Gutiérrez-Ortiz, Eva; Tenorio, Jair Antonio; Segovia-Cubero, Javier; Blanco, Isabel; Escribano-Subias, Pilar

Variants in BSN, encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range

编码突触前蛋白 Bassoon 的 BSN 基因变异会导致一种新型神经发育障碍,其表型范围很广。

Guzman, Stacy G; Ruggiero, Sarah M; Ganesan, Shiva; Ellis, Colin A; Harrison, Alicia G; Sullivan, Katie R; Stark, Zornitza; Brown, Natasha J; Kana, Sajel L; Tuttle, Anabelle; Tenorio, Jair; Lapunzina, Pablo; Nevado, Julián; McDonald, Marie T; Jensen, Courtney; Wheeler, Patricia G; Stange, Lila; Morrison, Jennifer; Keren, Boris; Heide, Solveig; Keating, Meg W; Butler, Kameryn M; Lyons, Mike A; Jain, Shailly; Yeganeh, Mehdi; Thompson, Michelle L; Schroeder, Molly; Nguyen, Hoanh; Granadillo, Jorge; Johnston, Kari M; Murali, Chaya N; Bosanko, Katie; Burrow, T Andrew; Morgan, Syreeta; Watson, Deborah J; Hakonarson, Hakon; Helbig, Ingo

Comprehensive Screening of Genetic Variants in the Coding Region of F8 in Severe Hemophilia A Reveals a Relationship with Disease Severity in a Colombian Cohort

对哥伦比亚人群中重型血友病A患者F8编码区遗传变异的全面筛查揭示了其与疾病严重程度的关系

Sarmiento Doncel, Samuel; Peláez, Ronald Guillermo; Lapunzina, Pablo; Corrales-Medina, Fernando F; Díaz Mosquera, Gina Alejandra; Bonanad, Santiago; Cortes, Javier Mauricio; Cazalla, Mario; Gallego, Natalia; Querol-Giner, Felipe; Tenorio, Jair; López Guerrero, José A

Pain and health-related quality of life in patients with hypophosphatasemia with and without ALPL gene mutations

伴有和不伴有ALPL基因突变的低磷血症患者的疼痛和健康相关生活质量

Santurtún, Maite; Mediavilla-Martinez, Eva; Vega, Ana I; Gallego, Natalia; Heath, Karen E; Tenorio, Jair A; Lapunzina, Pablo; Riancho-Zarrabeitia, Leyre; Riancho, José A

Epigenome-wide association study of COVID-19 severity with respiratory failure

一项关于COVID-19严重程度与呼吸衰竭的全基因组表观关联研究

Castro de Moura, Manuel; Davalos, Veronica; Planas-Serra, Laura; Alvarez-Errico, Damiana; Arribas, Carles; Ruiz, Montserrat; Aguilera-Albesa, Sergio; Troya, Jesús; Valencia-Ramos, Juan; Vélez-Santamaria, Valentina; Rodríguez-Palmero, Agustí; Villar-Garcia, Judit; Horcajada, Juan P; Albu, Sergiu; Casasnovas, Carlos; Rull, Anna; Reverte, Laia; Dietl, Beatriz; Dalmau, David; Arranz, Maria J; Llucià-Carol, Laia; Planas, Anna M; Pérez-Tur, Jordi; Fernandez-Cadenas, Israel; Villares, Paula; Tenorio, Jair; Colobran, Roger; Martin-Nalda, Andrea; Soler-Palacin, Pere; Vidal, Francesc; Pujol, Aurora; Esteller, Manel

Radiological Findings in Multidetector Computed Tomography (MDCT) of Hereditary and Sporadic Pulmonary Veno-Occlusive Disease: Certainties and Uncertainties

遗传性和散发性肺静脉闭塞性疾病的多层螺旋CT(MDCT)放射学表现:确定性和不确定性

Pérez Núñez, Marta; Alonso Charterina, Sergio; Pérez-Olivares, Carmen; Revilla Ostolaza, Yolanda; Morales Ruiz, Rafael; Enguita Valls, Ana Belén; Tenorio, Jair Antonio; Gallego Zazo, Natalia; De Pablo Gafas, Alicia; Lapunzina, Pablo; Rodríguez Chaverri, Adriana; Escribano Subías, Pilar

Prenatal ultrasound findings in Koolen-de Vries foetuses: Central nervous system anomalies are frequent markers of this syndrome

库伦-德弗里斯综合征胎儿的产前超声检查结果:中枢神经系统异常是该综合征的常见标志。

García-Santiago, Fe Amalia; Martínez-Payo, Cristina; Mansilla, Elena; Santos-Simarro, Fernando; Ruiz de Azua Ballesteros, Miguel; Mori, María Ángeles; Antolín Alvarado, Eugenia; Nieto, Yolanda; Vallcorba, Isabel; Tenorio, Jair; Nevado, Julián; Lapunzina, Pablo