Alejandra Gámez

2.0k citations

38 papers · 1.5k indexed · h-index 23

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders 22
Biochemistry top 5%
- Amino Acid Enzymes and Metabolism 5
Molecular Biology top 10%
- Biochemical and Molecular Research 13
- Glycosylation and Glycoproteins Research 11
- Mitochondrial Function and Pathology 8
- Ubiquitin and proteasome pathways 5
Rheumatology top 5%
- Folate and B Vitamins Research 10
Physiology top 10%
- Diet and metabolism studies 3

Co-authors: Belén Pérez Magdalena Ugarte Lourdes R. Desviat Raymond C. Stevens Christineh N. Sarkissian Charles R. Scriver Ángel L. Pey Heidi Erlandsen
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: Proceedings of the National Academy of Sciences (2 papers)Journal of Biological Chemistry (1 paper)PLoS ONE (1 paper)
Partner nations: Spain United States Canada

In The Last Decade

Alejandra Gámez

38 papers receiving 1.5k citations

Peers

Countries citing papers authored by Alejandra Gámez

Since Specialization

Citations

This map shows the geographic impact of Alejandra Gámez's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Alejandra Gámez with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alejandra Gámez more than expected).

Fields of papers citing papers by Alejandra Gámez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alejandra Gámez. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Alejandra Gámez. The network helps show where Alejandra Gámez may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Alejandra Gámez, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Alejandra Gámez Line = papers co-authored together Alejandra Gámez links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Transcriptomic analysis identifies dysregulated pathways and therapeutic targets in PMM2-CDG Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Diana Gallego,Mercedes Serrano,J. Caballero,Alejandra Gámez,Pedro Seoane,James R. Perkins,Juan A. G. Ranea,Belén Pérez	2024	3
2	Myasthenia gravis concurrent with Parkinson’s disease in a Spanish cohort. Causation or correlation? Neurological Sciences ·Josep Gámez,Francesc Carmona,Carles Lorenzo‐Bosquet,Gemma Cuberas‐Borrós,Oriol de Fàbregues,Alejandra Gámez	2024	3
3	Proteostasis regulators as potential rescuers of PMM2 activity Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Alicia Vilas,Patricia Yuste‐Checa,Diana Gallego,Lourdes R. Desviat,Magdalena Ugarte,Celia Pérez‐Cerdá,Alejandra Gámez,Belén Pérez	2020	14
4	Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations Molecular Genetics and Metabolism ·Ana Rivera‐Barahona,Rosa Navarrete,Raquel García‐Rodríguez,Eva Richard,Magdalena Ugarte,Celia Pérez‐Cerdá,Belén Pérez,Alejandra Gámez,Lourdes R. Desviat	2018	16
5	DPAGT1-CDG: Functional analysis of disease-causing pathogenic mutations and role of endoplasmic reticulum stress PLoS ONE ·Patricia Yuste‐Checa,Ana Vega,Cristina Martín-Higueras,Celia Medrano,Alejandra Gámez,Lourdes R. Desviat,Magdalena Ugarte,Celia Pérez‐Cerdá,Belén Pérez	2017	19
6	Chaperone-Like Therapy with Tetrahydrobiopterin in Clinical Trials for Phenylketonuria: Is Genotype a Predictor of Response? JIMD Reports ·Christineh N. Sarkissian,Alejandra Gámez,Patrick Scott,Jérôme Dauvillier,Alejandro Dorenbaum,Charles R. Scriver,Raymond C. Stevens	2011	11
7	Evaluation of orally administered PEGylated phenylalanine ammonia lyase in mice for the treatment of Phenylketonuria Molecular Genetics and Metabolism ·Christineh N. Sarkissian,Tse Siang Kang,Alejandra Gámez,Charles R. Scriver,Raymond C. Stevens	2011	37
8	Different altered pattern expression of genes related to apoptosis in isolated methylmalonic aciduria cblB type and combined with homocystinuria cblC type Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Ana Jorge‐Finnigan,Alejandra Gámez,Belén Pérez,Magdalena Ugarte,Eva Richard	2010	13
9	Functional and structural analysis of five mutations identified in methylmalonic aciduria cbIB type Human Mutation ·Ana Jorge‐Finnigan,Cristina Aguado,Rocío Sánchez-Alcudia,David Abia,Eva Richard,B. Merinero,Alejandra Gámez,Ruma Banerjee,Lourdes R. Desviat,Magdalena Ugarte,Belén Pérez	2010	22
10	Converting an injectable protein therapeutic into an oral form: Phenylalanine ammonia lyase for phenylketonuria Molecular Genetics and Metabolism ·Tse Siang Kang,Wang Lin,Christineh N. Sarkissian,Alejandra Gámez,Charles R. Scriver,Raymond C. Stevens	2009	48
11	Structure-based chemical modification strategy for enzyme replacement treatment of phenylketonuria Molecular Genetics and Metabolism ·Wang Lin,Alejandra Gámez,Christineh N. Sarkissian,Mary Straub,Marianne G. Patch,Gye Won Han,Steve Striepeke,Paul Fitzpatrick,Charles R. Scriver,Raymond C. Stevens	2005	50
12	Development of Pegylated Forms of Recombinant Rhodosporidium toruloides Phenylalanine Ammonia-Lyase for the Treatment of Classical Phenylketonuria Molecular Therapy ·Alejandra Gámez,Christineh N. Sarkissian,Lin Wang,Woomi Kim,Mary Straub,Marianne G. Patch,Lin Chen,Steve Striepeke,Paul Fitzpatrick,Jeffrey F. Lemontt,Charles O’Neill,Charles R. Scriver,Raymond C. Stevens	2005	42
13	Trends in Enzyme Therapy for Phenylketonuria Molecular Therapy ·Woomi Kim,Heidi Erlandsen,Sankar Surendran,Raymond C. Stevens,Stephen K. Tyring,Reuben Matalon,Alejandra Gámez,Kimberlee Michols-Matalon	2004	51
14	Mechanisms underlying responsiveness to tetrahydrobiopterin in mild phenylketonuria mutations Human Mutation ·Ángel L. Pey,Belén Pérez,Lourdes R. Desviat,M. Ángeles Martínez‐García,Cristina Aguado,Heidi Erlandsen,Alejandra Gámez,Raymond C. Stevens,Matthı́as Thórólfsson,Magdalena Ugarte,Aurora Martı́nez	2004	103
15	Biopterin responsive phenylalanine hydroxylase deficiency Genetics in Medicine ·Reuben Matalon,Richard Koch,Kimberlee Michals‐Matalon,Kathryn Moseley,Sankar Surendran,Stephen K. Tyring,Heidi Erlandsen,Alejandra Gámez,Raymond C. Stevens,Anne Romstad,Lisbeth Birk Møller,Flemming Güttler	2004	50
16	A Mass Spectrometry Plate Reader: Monitoring Enzyme Activity and Inhibition with a Desorption/Ionization on Silicon (DIOS) Platform ChemBioChem ·Zhouxin Shen,Eden P. Go,Alejandra Gámez,Junefredo V. Apon,Valery V. Fokin,Mike Greig,Manuel Ventura,John E. Crowell,Ola Blixt,James C. Paulson,Raymond C. Stevens,M. G. Finn,Gary Siuzdak	2004	48
17	Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations Proceedings of the National Academy of Sciences ·Heidi Erlandsen,Ángel L. Pey,Alejandra Gámez,Belén Pérez,Lourdes R. Desviat,Cristina Aguado,Richard Koch,Sankar Surendran,Stephen K. Tyring,Reuben Matalon,Charles R. Scriver,Magdalena Ugarte,Aurora Martı́nez,Raymond C. Stevens	2004	138
18	Toward PKU Enzyme Replacement Therapy: PEGylation with Activity Retention for Three Forms of Recombinant Phenylalanine Hydroxylase Molecular Therapy ·Alejandra Gámez,Lin Wang,Mary Straub,Marianne G. Patch,Raymond C. Stevens	2003	38
19	Phenylketonuria: Genotype-phenotype correlations based on expression analysis of structural and functional mutations inPAH Human Mutation ·Ángel L. Pey,Lourdes R. Desviat,Alejandra Gámez,Magdalena Ugarte,Belén Pérez	2003	105
20	Expression Analysis of Phenylketonuria Mutations Journal of Biological Chemistry ·Alejandra Gámez,Belén Pérez,Magdalena Ugarte,Lourdes R. Desviat	2000	74

About Alejandra Gámez

Alejandra Gámez is a scholar working on Clinical Biochemistry, Biochemistry and Rheumatology, having authored 38 papers that have together received 1.5k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (22 papers), Biochemical and Molecular Research (13 papers), Glycosylation and Glycoproteins Research (11 papers), Folate and B Vitamins Research (10 papers), Mitochondrial Function and Pathology (8 papers), Amino Acid Enzymes and Metabolism (5 papers), Ubiquitin and proteasome pathways (5 papers) and Diet and metabolism studies (3 papers). The work is most often cited by research in Clinical Biochemistry (795 citations), Biochemistry (159 citations) and Molecular Biology (1.1k citations). Alejandra Gámez has collaborated with scholars based in Spain, United States and Canada. Frequent co-authors include Belén Pérez, Magdalena Ugarte, Lourdes R. Desviat, Raymond C. Stevens, Christineh N. Sarkissian, Charles R. Scriver, Ángel L. Pey, Heidi Erlandsen, Celia Pérez‐Cerdá and Paul Fitzpatrick. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

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