Laura Planas‐Serra

Author

Laura Planas‐Serra

Institut d'Investigació Biomédica de Bellvitge ORCID

Also Known As

Agatha Schlüter, César O. Enciso-Olivera, Francesc Pla-Juncà, Francesc Pla-Juncà, Germán Peces-Barba, Isabelle Pellier, Laura Planas-Serra, Laura Planas‐Serra, Philippe Parola, Planas-Serra, Laura

Publications

7.2K

Citations

H-Index

Concepts

All Affiliations

Institut d'Investigació Biomédica de Bellvitge Centre for Biomedical Network Research on Rare Diseases Institució Catalana de Recerca i Estudis Avançats Instituto de Salud Carlos III Vall d'Hebron Institut de Recerca

About

Laura Planas‐Serra is an author at Institut d'Investigació Biomédica de Bellvitge specializing in medicine, mitochondrial function, and epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	285
2	Public Health	2	2	209
3	Health Sciences	1	1	44
4	Natural Sciences	1	1	32
5	Biochemistry	1	1	32

Laura Planas‐Serra

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19 Takaki Asano, Bertrand Boisson, Fanny Onodi, Science Immunology	2021	410
Accelerated biological aging in COVID-19 patients Xue Cao, Wenjuan Li, Ting Wang, Nature Communications	2022	214
Epigenome-wide association study of COVID-19 severity with respiratory failure Manuel Castro de Moura, Verónica Dávalos, Laura Planas‐Serra, EBioMedicine Respiratory DiseasesCovid-19 PandemicInfectious Respiratory DiseasePulmonary MedicineCovid-19 Epidemiology	2021	146
Neutralizing Autoantibodies to Type I IFNs in >10% of Patients with Severe COVID-19 Pneumonia Hospitalized in Madrid, Spain Jesús Troya, Paul Bastard, Laura Planas‐Serra, Journal of Clinical Immunology	2021	132
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Genome Medicine	2023	76
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males Margherita Baldassarri, Nicola Picchiotti, Francesca Fava, EBioMedicine Disease SusceptibilityEuropean MalesImmunologyGenetic EpidemiologyHuman Polymorphism	2021	63
Biallelic<i>PI4KA</i>variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophy Edgard Verdura, Agustí Rodríguez‐Palmero, Valentina Vélez-Santamaría, Brain	2021	47
Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome Àngels García‐Cazorla, Edgard Verdura, Natalia Juliá‐Palacios, Acta Neuropathologica Developmental BiologyMitochondrial FunctionBrain DevelopmentGenetic DisorderGenetics	2020	44
<scp> <i>HNRNPH1</i> </scp> ‐related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome Sara L. Reichert, Rachel Li, Scott A. Turner, Clinical Genetics	2020	43
Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity Laura Planas‐Serra, Nathalie Launay, Leire Goicoechea, Journal of Clinical Investigation Sphingolipid Desaturase Degs1Ceramide BiosynthesisMitochondrial BiogenesisAutophagyMetabolic Signaling	2023	32

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