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Sofía Garrido
ResearcherPublications, citations & collaboration network
Sofía Garrido is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 21 works, 483 citations, an h-index of 14 and an i10-index of 15.
21
Works
483
Citations
14
h-index
15
i10-index
IDs:OpenAlex
How has Sofía Garrido's publication output changed over time?
ScholarIQpublication output · 2004–2025
Output grew0% over the shown period — from 1 works in 2004 to 1 in 2025.
1
1
1
1
1
1
2
1
1
1
2004200920102011201220142015201620182025
What are the most-cited papers on Sofía Garrido?
ScholarIQmost cited works
Complement factor I deficiency: a not so rare immune defect. Characterization of new mutations and the first large gene deletion
María Alba‐Domínguez, Alberto López‐Lera, Sofía Garrido, Pilar Nozal, Luis Ignacio González‐Granado, Josefa Melero, Pere Soler‐Palacín, Carmen Cámara, Margarita López‐Trascasa
Orphanet Journal of Rare Diseases. 201259 CitationsOPEN ACCESS
SERPING1 mutations in 59 families with hereditary angioedema
Alberto López‐Lera, Sofía Garrido, O. Roche, Margarita López‐Trascasa
S92126311. 201157 Citations
Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome
María E Bernabeu-Herrero, Miguel Jiménez-Alcázar, Jaouad Anter, Sheila Pinto, Daniel Sánchez Chinchilla, Sofía Garrido, Margarita López‐Trascasa, Santiago Rodrı́guez de Córdoba, Pilar Sánchez‐Corral
S92126311. 201557 Citations
A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation
Alberto López‐Lera, Bertrand Favier, Rocío Mena, Sofía Garrido, Christian Drouet, Margarita López‐Trascasa
Journal of Allergy and Clinical Immunology. 201051 CitationsOPEN ACCESS
Autoantibodies Against Perilipin 1 as a Cause of Acquired Generalized Lipodystrophy
Fernando Corvillo, Verónica Aparicio, Alberto López‐Lera, Sofía Garrido, David Araújo‐Vilar, María P. De Miguel, Margarita López‐Trascasa
Frontiers in Immunology. 201843 CitationsOPEN ACCESS
Related on ScholarIQ
Hospital Universitario Puerta de Hierro Majadahonda
Institution
Complement factor I deficiency: a not so rare immune defect. Characterization of new mutations and the first large gene deletion
Paper
SERPING1 mutations in 59 families with hereditary angioedema
Paper
Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome
Paper
A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation
Paper
Autoantibodies Against Perilipin 1 as a Cause of Acquired Generalized Lipodystrophy
Paper