P Goetz

1.3k citations
30 papers · 518 · h-index 13

Impact in

    • Sperm and Testicular Function
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • DNA Repair Mechanisms 4
    • Epigenetics and DNA Methylation 3
    • Mitochondrial Function and Pathology 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3

P Goetz

28 papers receiving 499 citations

Peers

P Goetz
Comparison fields: 5 of 63
  • Reproductive Medicine 46
  • Genetics 144
  • Cancer Research 72
  • Molecular Biology 296
  • Cellular and Molecular Neuroscience 50
Replace Mohamed-Amin Choukrallah with:
Mohamed-Amin Choukrallah Switzerland
Hsueh‐Ping Chu Taiwan
Sophie Tourpin France
Michela Bossolasco Canada
G. K. Brown United Kingdom
Isabelle Tratner France
Jack J. Huizenga Canada
A. Misra-Press United States
Haiping Liu China
Sandrine Thénot France
P Goetz relative to Mohamed-Amin Choukrallah Switzerland Mohamed-Amin Choukrallah's profile →
Citations per field
00.5×1.5×1.8×
Mohamed-Amin Choukrallah · 1×
Citations per year

Countries citing papers authored by P Goetz

Since Specialization
Citations

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

Fields of papers citing papers by P Goetz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1984125
2 198148
3 200342
4 199835
5 200233
6 197932
7
Polymorphisms and low plasma activity of dopamine-beta-hydroxylase in ADHD children.
200620
8 200819
9 201318
10 197916
11 200116
12 200516
13 200815
14 197410
15 200510
16 19749
17 20049
18 20068
19
Cyclophosphamide-induced chromosomal aberrations in meiotic cells of male mice.
19808
20
Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion.
20057

About P Goetz

P Goetz is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Cancer Research and Neurology, having authored 30 papers that have together received 518 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (4 papers), Genetic Neurodegenerative Diseases (4 papers), Sperm and Testicular Function (3 papers), Carcinogens and Genotoxicity Assessment (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Epigenetics and DNA Methylation (3 papers), Chromosomal and Genetic Variations (3 papers) and Mitochondrial Function and Pathology (3 papers). The work is most often cited by research in Reproductive Medicine (46 citations), Genetics (144 citations), Cancer Research (72 citations), Molecular Biology (296 citations) and Cellular and Molecular Neuroscience (50 citations). P Goetz has collaborated with scholars based in Czechia, Japan and Russia. Frequent co-authors include R.M. Speed, Ann C. Chandley, Jiřı́ Forejt, Zdeněk Sedláček, Božena Novotná, Radim J. Šrám, Ivo Paclt, Václav Maťoška, Marie Trková and Z. Zudová. Their work appears in journals such as Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Chromosoma, Cancer Letters, European Journal of Medical Genetics and Prenatal Diagnosis.

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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