Ordóñez-Ugalde Andrés - Fundación Pública Galega de Medicina Xenómica-SERGAS, IDIS

基本信息

浏览量：8

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 13 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Tract-specific Damage at Spinal Cord Level in Pure Hereditary Spastic Paraplegia Type 4: a Diffusion Tensor Imaging Study

Navas-Sánchez Francisco J.,Marcos-Vidal Luis,de Blas Daniel Martín,Fernández-Pena Alberto,Alemán-Gómez Yasser,Guzmán-de-Villoria Juan A.,Romero Julia,Catalina Irene,Lillo Laura,Muñoz-Blanco José L.,Ordoñez-Ugalde Andrés,Quintáns Beatriz,Sobrido María-Jesús,Carmona Susanna,Grandas Francisco,Desco Manuel

Journal of Neurology（2022）

引用4浏览0WOS引用

Corticospinal Tract and Motor Cortex Degeneration in Pure Hereditary Spastic Paraparesis Type 4 (SPG4)

Francisco J. Navas-Sanchez,Daniel Martin De Blas,Alberto Fernandez-Pena,Yasser Aleman-Gomez,Agustin Lage-Castellanos,Luis Marcos-Vidal,Juan A. Guzman-De-Villoria,Irene Catalina,Laura Lillo,Jose L. Munoz-Blanco,Andres Ordonez -Ugalde,Beatriz Quintans,Maria-Jesus Sobrido,Susanna Carmona,Francisco Grandas,Manuel Desco

Amyotrophic lateral sclerosis and frontotemporal degeneration/Amyotrophic lateral sclerosis & fronto...（2021）

引用5浏览0WOS引用

A Novel ABCA12 Pathologic Variant Identified in an Ecuadorian Harlequin Ichthyosis Patient: A Step Forward in Genotype‐phenotype Correlations

Martha Montalvan-Suarez,Uxia Saraiva Esperon-Moldes,Laura Rodriguez-Pazos,Andres Ordonez-Ugalde, Fernanda Moscoso, Nora Ugalde-Noritz,Luis Santome,Laura Fachal, Daniel Tettamanti-Miranda,Juan Carlos Ruiz,Manuel Ginarte,Ana Vega

Molecular genetics & genomic medicine（2019）

引用3浏览0WOS引用

bdetection of gene dosage alterations in patients with spinocerebellar disease using an exon-dense snp array

B. Quintans,F. Barros,I. Quintela,A. Ordonez-Ugalde, C. Castro-Fernandez,P. Blanco-Arias,D. Garcia-Estevez,I. Sanz,M. Arias,M. Sobrido

EUROPEAN JOURNAL OF HUMAN GENETICS（2019）

引用0浏览0引用

Biogeographical Origin and Timing of the Founder Ichthyosis TGM1 C.1187g > A Mutation in an Isolated Ecuadorian Population

U. S. Esperón-Moldes,J. Pardo-Seco, M. Montalván-Suárez,L. Fachal,M. Ginarte,L. Rodríguez-Pazos,A. Gómez-Carballa, F. Moscoso, N. Ugalde-Noritz,A. Ordóñez-Ugalde, D. Tettamanti-Miranda, J. C. Ruiz,A. Salas,A. Vega

Scientific Reports（2019）

引用7浏览0WOSNATURE引用

The geographic mosaic of Ecuadorian Y-chromosome ancestry

U. Toscanini,A. Gaviria,J. Pardo-Seco,A. Gómez-Carballa, F. Moscoso,M. Vela,S. Cobos, A. Lupero,A.K. Zambrano,F. Martinón-Torres, A. Carabajo-Marcillo, R. Yunga-León, N. Ugalde-Noritz,A. Ordoñez-Ugalde,A. Salas

Forensic Science International: Genetics（2018）

引用22浏览0WOS引用

PLA2G6 Mutations Associated with a Continuous Clinical Spectrum from Neuroaxonal Dystrophy to Hereditary Spastic Paraplegia

B. Ozes, N. Karagoz,R. Schuele,A. Rebelo,M. -J. Sobrido,F. Harmuth,M. Synofzik,S. I. P. Pascual, M. Colak,B. Ciftci-Kavaklioglu,B. Kara,A. Ordonez-Ugalde,B. Quintans,M. A. Gonzalez,A. Soysal,S. Zuchner,E. Battaloglu

Clinical Genetics（2017）

引用32浏览0WOS引用

Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number Variants

P. Cacheiro,A. Ordóñez-Ugalde,B. Quintáns,S. Piñeiro-Hermida,J. Amigo,M. García-Murias,S. I. Pascual-Pascual,F. Grandas,J. Arpa,A. Carracedo,M. J. Sobrido

Molecular diagnosis & therapy（2017）

引用7浏览0WOS引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn