Primo Baybayan

10.2k citations
27 papers · 1.6k · 2 hit papers · h-index 15

Impact in

Papers in

    • Genomics and Phylogenetic Studies 8
    • Molecular Biology Techniques and Applications 2
    • RNA and protein synthesis mechanisms 2
    • Genomics and Rare Diseases 5
    • Genomic variations and chromosomal abnormalities 3

Primo Baybayan

25 papers receiving 1.6k citations

Primo Baybayan's Hit Papers

X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein 1996 · 557 citations
5570+10+20Years since publication100200300400500

Peers

Primo Baybayan
Comparison fields: 5 of 107
  • Oral Surgery 152
  • Cell Biology 277
  • Molecular Biology 1.1k
  • Genetics 430
  • Urology 79
Replace E. van Garderen with:
E. van Garderen Netherlands
Renée Laufer Amorim Brazil
Christa Freudenstein Germany
Robert B. Rebhun United States
Clyde J. Dawe United States
Laura Bongiovanni Italy
J. Merregaert Belgium
Kazuto Yamada Japan
Ken Fukuda Japan
R Paasivuo Finland
Primo Baybayan relative to E. van Garderen Netherlands E. van Garderen's profile →
Citations per field
00.5×4.8×
E. van Garderen · 1×
Citations per year

Countries citing papers authored by Primo Baybayan

Since Specialization
Citations

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

Fields of papers citing papers by Primo Baybayan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Primo Baybayan, 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 Primo Baybayan Line = papers co-authored together Primo Baybayan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
Hit paper breakdown →
1996593
2
X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
Hit paper breakdown →
1996557
3 201990
4 201539
5 201636
6
Fine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribed.
199633
7 201932
8 202230
9 202025
10 201824
11 202023
12 201819
13 202019
14 202318
15 201916
16 201312
17 201912
18 201311
19 201510
20 20227

About Primo Baybayan

Primo Baybayan is a scholar working on Molecular Biology, Genetics, Cancer Research, Plant Science and Surgery, having authored 27 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (8 papers), Genomics and Rare Diseases (5 papers), Cancer Genomics and Diagnostics (4 papers), Helicobacter pylori-related gastroenterology studies (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (3 papers), Molecular Biology Techniques and Applications (2 papers) and RNA and protein synthesis mechanisms (2 papers). The work is most often cited by research in Oral Surgery (152 citations), Cell Biology (277 citations), Molecular Biology (1.1k citations), Genetics (430 citations) and Urology (79 citations). Primo Baybayan has collaborated with scholars based in United States, Malaysia and Australia. Frequent co-authors include Ellson Y. Chen, David Schlessinger, Reid Huber, Alex MacKenzie, Giovanni Neri, Giuseppe Pilia, Antonino Forabosco, Antonio Cao, Ulpu Saarialho‐Kere and Anand Srivastava. Their work appears in journals such as Cancer Research, Genes, European Journal of Human Genetics, Nature Genetics and Gut Pathogens.

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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