P Goetz

1.3k citations

30 papers · 629 indexed · h-index 13

Impact in

Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Reproductive Medicine top 10%
- Sperm and Testicular Function

Papers in

Genetics 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genomic variations and chromosomal abnormalities 3
Reproductive Medicine 3
- Sperm and Testicular Function 3

Co-authors: R.M. Speed Ann C. Chandley A.C. Chandley T. B. Hargreave Ann Mary Joseph Jiřı́ Forejt Zdeněk Sedláček Božena Novotná
Journals: Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (3 papers)Chromosoma (2 papers)British Journal of Cancer (1 paper)European Journal of Medical Genetics (1 paper)Human Genetics (1 paper)
Partner nations: Czechia Japan United Kingdom

In The Last Decade

P Goetz

28 papers receiving 606 citations

Peers

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

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20 of 20 papers shown

#	Work
1	The Bleeding Risk during Warfarin Therapy Is Associated with the Number of Variant Alleles of CYP2C9 and VKORC1 Genes Cardiology ·Aleš Tomek, Václav Maťoška, Tereza Kolářová, Jiří Neumann, Martin Šrámek, Ivana Šarbochová, L Táborský, Martin Bojar, P Goetz, Victor L. Serebruany	2013	18
2	OmniPlex—a new QF‐PCR assay for prenatal diagnosis of common aneuploidies based on evaluation of the heterozygosity of short tandem repeat loci in the Czech population Prenatal Diagnosis ·Martina Putzová, Ľubomíra Pecnová, Lucie Dvořáková, I. A. Soldatova, P Goetz, D. Stejskal	2008	6
3	QF-PCR-based prenatal detection of common aneuploidies in the Czech population: Five years of experience European Journal of Medical Genetics ·Martina Putzová, I. A. Soldatova, Ľubomíra Pecnová, Lucie Dvořáková, Nada Jencikova, P Goetz, D. Stejskal	2008	19
4	Polymorphisms of Dopamine-β-Hydroxylase in ADHD Children Folia Biologica ·Marta Kopečková, Ivo Paclt, P Goetz	2006	8
5	Polymorphisms and low plasma activity of dopamine-beta-hydroxylase in ADHD children. PubMed ·Marta Kopečková, Ivo Paclt, P Goetz	2006	20
6	Absence of spinocerebellar ataxia type 3/Machado–Joseph disease within ataxic patients in the Czech population European Journal of Neurology ·Peter Bauer, Alena Zumrová, Václav Maťoška, T Maríková, Stefanie Krilová, Arpád Bóday, Brijendra Singh, P Goetz	2005	16
7	Fluorescent Multiplex PCR: Fast Method for Autosomal Dominant Spinocerebellar Ataxias Screening Russian Journal of Genetics ·Peter Bauer, Svetlana Kotliarova, Václav Maťoška, Zuzana Mušová, Petra Hedvičáková, Arpád Bóday, Aleš Tomek, Nobuyuki Nukina, P Goetz	2005	10
8	Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients? Medical Hypotheses ·Peter Bauer, Alena Zumrová, Václav Maťoška, Kentaro Mitsui, P Goetz	2004	9
9	DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion American Journal of Medical Genetics Part A ·Oliver Bartsch, Michaela Nemecková, Eduard Kočárek, Annett Wagner, Alena Puchmajerová, Maja Poppe, Katrin Õunap, P Goetz	2003	42
10	Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome? Journal of Human Genetics ·Marie Trková, Marie Hladíková, P Kasal, P Goetz, Zdeněk Sedláček	2002	34
11	Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours British Journal of Cancer ·Zdeněk Sedláček, Roman Kodet, (unknown), E Seemanová, P Vodvářka, Petra Wilgenbus, J. Mareš, Albert J. Poustka, P Goetz	1998	35
12	[Amplification of oncogenes in solid tumors in children]. PubMed ·J. Mareš, Lesková, Zdeněk Sedláček, T Maríková, Petr Boček, Roman Kodet, P Goetz	1996	1
13	On the nature and extent of XY pairing at meiotic prophase in man Cytogenetic and Genome Research ·A.C. Chandley, P Goetz, T. B. Hargreave, Ann Mary Joseph, R.M. Speed	1984	124
14	XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus) Chromosoma ·Jiřı́ Forejt, So a Gregorov�, P Goetz	1981	48
15	Effects of alkylating agents on lymphocytes from controls and from patients with Fanconi's anemia Human Genetics ·Božena Novotná, P Goetz, N I Surkova	1979	32
16	Identification of human male meiotic chromosomes. PubMed ·P Goetz, J Knobloch	1975	0
17	The mutagenic effect of lysergic acid diethylamide I. Cytogenetic analysis Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·P Goetz, Radim J. Šrám, Z. Zudová	1974	10
18	The mutagenic effect of lysergic acid diethylamide III. Evaluation of the genetic risk of LSD in man Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Radim J. Šrám, P Goetz	1974	5
19	The mutagenic effect or lysergic acid diethylamide II. Dominant lethal test in mice Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·Radim J. Šrám, Z. Zudová, P Goetz	1974	10
20	[Cystinuria and lysinuria in Down's syndrome]. PubMed ·J Hyánek, P Goetz, J Hoza, M. Kubik, E Seemanová, M Sedlácková	1970	1

About P Goetz

P Goetz is a scholar working on Genetics, Reproductive Medicine, Cancer Research, Neurology and Cellular and Molecular Neuroscience, having authored 30 papers that have together received 629 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (4 papers), DNA Repair Mechanisms (4 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), Sperm and Testicular Function (3 papers), Mitochondrial Function and Pathology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (251 citations), Reproductive Medicine (64 citations), Molecular Biology (382 citations), Cancer Research (77 citations) and Plant Science (150 citations). P Goetz has collaborated with scholars based in Czechia, Japan and United Kingdom. Frequent co-authors include R.M. Speed, Ann C. Chandley, A.C. Chandley, T. B. Hargreave, Ann Mary Joseph, Jiřı́ Forejt, Zdeněk Sedláček, Božena Novotná, Radim J. Šrám and Ivo Paclt. Their work appears in journals such as Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Chromosoma, British Journal of Cancer, European Journal of Medical Genetics and Human Genetics.

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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