G Vaca

483 total citations
47 papers, 393 citations indexed

About

G Vaca is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Physiology. According to data from OpenAlex, G Vaca has authored 47 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Pediatrics, Perinatology and Child Health and 13 papers in Physiology. Recurrent topics in G Vaca's work include Neonatal Health and Biochemistry (11 papers), Metabolism and Genetic Disorders (11 papers) and Erythrocyte Function and Pathophysiology (9 papers). G Vaca is often cited by papers focused on Neonatal Health and Biochemistry (11 papers), Metabolism and Genetic Disorders (11 papers) and Erythrocyte Function and Pathophysiology (9 papers). G Vaca collaborates with scholars based in Mexico, United States and Ecuador. G Vaca's co-authors include B Ibarra, Jaime Font de Mora, J. M. Cantú, Beryl Westwood, JT Prchal, Luciano Baronciani, Ernest Beutler, Horacio Rivera, J. M. Cant� and Cantú Jm and has published in prestigious journals such as Blood, Journal of Bacteriology and Diabetologia.

In The Last Decade

G Vaca

44 papers receiving 365 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
G Vaca Mexico 11 177 135 126 68 58 47 393
D.A. Beckman United States 13 164 0.9× 114 0.8× 37 0.3× 36 0.5× 32 0.6× 20 407
Miguel Angel Alcántara‐Ortigoza Mexico 12 78 0.4× 163 1.2× 149 1.2× 71 1.0× 15 0.3× 57 386
F Pascu Germany 6 81 0.5× 213 1.6× 125 1.0× 51 0.8× 11 0.2× 7 412
J. Gehler Germany 12 67 0.4× 176 1.3× 71 0.6× 242 3.6× 69 1.2× 30 446
W. Hilscher Germany 16 60 0.3× 331 2.5× 234 1.9× 24 0.4× 33 0.6× 62 806
Ilkka Kouvonen Finland 12 38 0.2× 183 1.4× 47 0.4× 28 0.4× 53 0.9× 21 384
Ruth Cohen United States 8 65 0.4× 301 2.2× 27 0.2× 67 1.0× 34 0.6× 18 524
G Fioretti Italy 14 73 0.4× 131 1.0× 128 1.0× 43 0.6× 41 0.7× 28 402
Christine Hendrickson United States 10 54 0.3× 251 1.9× 99 0.8× 82 1.2× 38 0.7× 13 506
Stephanie Beall United States 11 77 0.4× 150 1.1× 53 0.4× 21 0.3× 26 0.4× 15 460

Countries citing papers authored by G Vaca

Since Specialization
Citations

This map shows the geographic impact of G Vaca'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 G Vaca with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G Vaca more than expected).

Fields of papers citing papers by G Vaca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G Vaca. 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 G Vaca. The network helps show where G Vaca may publish in the future.

Co-authorship network of co-authors of G Vaca

This figure shows the co-authorship network connecting the top 25 collaborators of G Vaca. A scholar is included among the top collaborators of G Vaca based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with G Vaca. G Vaca is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
2.
Vaca, G, et al.. (2010). MS70 STUDY ON THE MOLECULAR BASIS OF FAMILIAL HYPERCHOLESTEROLEMIA IN MEXICO. ADVANCES OF PROJECT. Atherosclerosis Supplements. 11(2). 124–124. 1 indexed citations
3.
Vaca, G, et al.. (1992). Effects of G-6-PD deficiency, experimentally induced or genetically transmitted, on the sorbitol pathway activity. In vitro and in vivo studies.. PubMed. 23(1). 25–32. 3 indexed citations
4.
Beutler, Elliot K., et al.. (1992). New glucose-6-phosphate dehydrogenase mutations from various ethnic groups. Blood. 80(1). 255–256. 40 indexed citations
5.
Beutler, Ernest, et al.. (1992). New glucose-6-phosphate dehydrogenase mutations from various ethnic groups. Blood. 80(1). 255–256. 39 indexed citations
6.
Vaca, G, et al.. (1991). Síndrome histiocito hemofagocitario asociado a una infección por leishmanía. Anales de Pediatría. 35(4). 273–275. 2 indexed citations
7.
Ibarra, B, et al.. (1989). Screening for thermostability and electrophoretic red blood cell sorbitol dehydrogenase (E.C.1.1.1.14) variants.. PubMed. 32(2). 102–5. 2 indexed citations
8.
Ibarra, B, et al.. (1988). Genetic Heterogeneity of Thalassemias in Mexican Mestizo Patients with Hemolytic Anemia. Human Heredity. 38(2). 95–100. 4 indexed citations
9.
Vaca, G, et al.. (1987). Screening for red blood cell sorbitol dehydrogenase deficiency in patients with diabetes or cataracts. Ophthalmic Paediatrics and Genetics. 8(3). 197–202. 2 indexed citations
10.
Rivera, Horacio, et al.. (1986). Bloom syndrome in a Mexican mestizo girl.. PubMed. 29(1). 39–41. 7 indexed citations
11.
García‐Cruz, Diana, et al.. (1985). Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.. PubMed. 28(3). 193–6. 2 indexed citations
12.
González, Alicia, et al.. (1983). Neurospora crassa mutant impaired in glutamine regulation. Journal of Bacteriology. 155(1). 1–7. 9 indexed citations
13.
Vaca, G, et al.. (1983). A fluorimetric method for red blood cell sorbitol dehydrogenase activity.. Journal of Clinical Pathology. 36(6). 697–700. 8 indexed citations
14.
Vaca, G, et al.. (1982). G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia. Human Genetics. 61(2). 175–176. 24 indexed citations
15.
Ibarra, B, G Vaca, J. M. Cantú, et al.. (1981). Heterozygosity and Homozygosity for the High Oxygen Affinity Hemoglobin Tarrant or α126 (H9) ASP→ASN in two Mexican Families. Hemoglobin. 5(4). 337–348. 8 indexed citations
16.
Díaz, M.E., et al.. (1981). α, 1–4 Glucosidase Activity in Human Seminal Plasma from Normal, Vasectomized, and Subfertile Men. Archives of Andrology. 7(4). 319–321. 8 indexed citations
17.
Cantú, J. M., et al.. (1980). Post-pubertal female psychosexual orientation in incomplete male pseudohermaphroditism type 2 (5α-reductase deficiency). European Journal of Endocrinology. 94(2). 273–279. 10 indexed citations
18.
Cantú, J. M., et al.. (1979). Partial mispairing and crossing-over between β0 and δ genes as the origin of the δ β0 thalassemia gene. Human Genetics. 49(2). 191–198. 1 indexed citations
19.
Vaca, G. (1978). Galactosemia as a result of galactose-1-phosphate uridyltransferase deficiency.. PubMed. 9(3). 22–24.
20.
Vaca, G & Jaime Font de Mora. (1977). Nitrogen regulation of arginase in Neurospora crassa. Journal of Bacteriology. 131(3). 719–725. 29 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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