Concepedia

Author

Isabel Rivera

University of LisbonORCID

Also Known As

I Rivera, I. A. Rivera, I. Muñoz -Rivera, I. Rivera, I.A. Rivera, Isabel A. Rivera, Isabel Rivera, RIVERA, ISABEL, Rivera Isabel, Rivera, Isabel

100

Publications

2.5K

Citations

23

H-Index

86

Concepts

All Affiliations

University of LisbonHospital de Santa MariaAmsterdam UMC Location Vrije Universiteit AmsterdamRadboud University Medical CenterRadboud University Nijmegen
IR

About

Isabel Rivera is an author at University of Lisbon specializing in medicine, genetics, and natural sciences.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

14

21

465

2

Natural Sciences

10

11

315

3

Biochemistry

9

9

197

4

Public Health

2

2

31

5

Biology

1

1

16

Isabel Rivera

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39

Publications

1.6K

Citations

20

H-Index

YearCitations

Increased Homocysteine and S-Adenosylhomocysteine Concentrations and DNA Hypomethylation in Vascular Disease

Rita Castro, Isabel Rivera, Eduard A. Struys,

Clinical Chemistry

2003

406

The natural history of classic galactosemia: lessons from the GalNet registry

M. Estela Rubio‐Gozalbo, Minela Haskovic, Annet M. Bosch,

Orphanet Journal of Rare Diseases

2019

141

5,10‐Methylenetetrahydrofolate reductase 677C→T and 1298A→C mutations are genetic determinants of elevated homocysteine

Rita Castro, Isabel Rivera, Paula Ravasco,

QJM

2003

108

Intracellular S-adenosylhomocysteine increased levels are associated with DNA hypomethylation in HUVEC

Rita Castro, Isabel Rivera, Carla P. Martins,

Journal of Molecular Medicine

2005

100

Suppressing Aneuploidy-Associated Phenotypes Improves the Fitness of Trisomy 21 Cells

Sunyoung Hwang, Jessica F. Williams, Maja Kneissig,

Cell Reports

2019

57

Molecular evidence of type 2 mosaicism in Gorlin syndrome

Antonio Torrelo, Á. Hernández‐Martín, Isabel Colmenero,

British Journal of Dermatology

2013

48

Pyruvate dehydrogenase complex deficiency: updating the clinical, metabolic and mutational landscapes in a cohort of Portuguese patients

Hana Pavlú-Pereira, Maria João Silva, Cristina Florindo,

Orphanet Journal of Rare Diseases

2020

43

Functional and structural impact of the most prevalent missense mutations in classic galactosemia

Ana I. Coelho, Matilde Trabuco, Ruben Ramos,

Molecular Genetics & Genomic Medicine

2014

42

Modulation of Alzheimer's amyloid β peptide oligomerization and toxicity by extracellular Hsp70

Isabel Rivera, Ricardo Capone, David M. Cauvi,

Cell Stress and Chaperones

2017

41

The V388M Mutation Results in a Kinetic Variant Form of Phenylalanine Hydroxylase

Paula Leandro, Isabel Rivera, Maria Celeste Lechner,

Molecular Genetics and Metabolism

2000

39

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