P. H. Vogt

6.5k total citations · 2 hit papers
90 papers, 4.9k citations indexed

About

P. H. Vogt is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, P. H. Vogt has authored 90 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Genetics, 54 papers in Molecular Biology and 35 papers in Reproductive Medicine. Recurrent topics in P. H. Vogt's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (53 papers), Sperm and Testicular Function (30 papers) and Sexual Differentiation and Disorders (30 papers). P. H. Vogt is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (53 papers), Sperm and Testicular Function (30 papers) and Sexual Differentiation and Disorders (30 papers). P. H. Vogt collaborates with scholars based in Germany, United States and Netherlands. P. H. Vogt's co-authors include Octavian Henegariu, Gail H. Vance, Nyla A. Heerema, S. R. Dlouhy, Wolfgang Hennig, A. C. Chandley, R Keil, Andrew Sharkey, Keyi Ma and Susana Fernandes and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and Journal of Molecular Biology.

In The Last Decade

P. H. Vogt

88 papers receiving 4.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11

1996 997 citations P. H. Vogt Human Molecular Genetics profile →
Multiplex PCR: Critical Parameters and Step-by-Step Protocol

1997 743 citations Octavian Henegariu, Nyla A. Heerema et al. profile →

Peers

Countries citing papers authored by P. H. Vogt

Since Specialization

Citations

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

Fields of papers citing papers by P. H. Vogt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. H. Vogt

This figure shows the co-authorship network connecting the top 25 collaborators of P. H. Vogt. A scholar is included among the top collaborators of P. H. Vogt 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 P. H. Vogt. P. H. Vogt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	FMR1 and AKT/mTOR signalling pathways: potential functional interactions controlling folliculogenesis in human granulosa cells 2017 ·Reproductive BioMedicine Online ·(unknown), (unknown), Ilma Simoni Brum, Katrin Hinderhofer, (unknown), T. Strowitzki, P. H. Vogt	19
2	Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies 2014 ·Molecular Syndromology ·Alexander M. Zink, Eva Wohlleber, Hartmut Engels, Olaug K. Rødningen, Kirstine Ravn, Stefanie Heilmann‐Heimbach, (unknown), (unknown), Cornelia Kraus, Susanne Blichfeldt, Per Hoffmann, Heiko Reutter, F.F. Brockschmidt, Martina Kreiß‐Nachtsheim, P. H. Vogt, Trine Prescott, Zeynep Tümer, (unknown)	6
3	Das schilddrüsenähnliche follikuläre Nierenzellkarzinom 2013 ·Der Pathologe ·(unknown), P. H. Vogt, Hatem Alkadhi, Nicole Berger, Holger Moch	10
4	Variable expression of the Fragile X Mental Retardation 1 (FMR1) gene in patients with premature ovarian failure syndrome is not dependent on number of (CGG)n triplets in exon 1 2011 ·Human Reproduction ·(unknown), (unknown), J. Zimmer, Hans‐Peter Sinn, Cornelia von Hagens, T. Strowitzki, P. H. Vogt	32
5	Stammzellangereicherte Fetttransplantation - eine mögliche Therapieoption bei Strahlenulzera? 2011 ·Zentralblatt für Chirurgie - Zeitschrift für Allgemeine Viszeral- Thorax- und Gefäßchirurgie ·Christian Herold, Hans O. Rennekampff, (unknown), Axel M. Hillmer, Karsten Knobloch, P. H. Vogt	3
6	Translational control of the AZFa gene DDX3Y by 5′UTR exon-T extension 2010 ·International Journal of Andrology ·(unknown), J. Zimmer, Daniela Fietz, Michael Bergmann, Sabine Kliesch, P. H. Vogt	15
7	A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure 2009 ·Human Reproduction ·Tanguy Corre, J. Schuettler, Silvia Bione, Anna Marozzi, Luca Persani, Raffaella Rossetti, Federica Torricelli, (unknown), P. H. Vogt, Daniela Toniolo, (unknown)	28
8	Rapid screening of the Y chromosome in idiopathic sterile men, diagnostic for deletions in AZF, a genetic Y factor expressed during spermatogenesis 2009 ·Andrologia ·Octavian Henegariu, P.N. Hirschmann, K. Kilian, Stefan Kirsch, Christoph Lengauer, Robert Maiwald, (unknown), P. H. Vogt	12
9	Premature Ovarian Failure (POF) Syndrome: Towards the Molecular Clinical Analysis of its Genetic Complexity 2006 ·Current Medicinal Chemistry ·(unknown), (unknown), T. Strowitzki, P. H. Vogt	40
10	Polymorphisms associated with the DAZ genes on the human Y chromosome 2005 ·Genomics ·(unknown), (unknown), Pao‐Lin Kuo, Chao‐Chin Hsu, (unknown), (unknown), P. H. Vogt, Walter Krause, Alberto Ferlin, Carlo Foresta, Thierry Bienvenu, W. Schempp, Pauline H. Yen	34
11	Reply to Repping et al. 2004 ·The American Journal of Human Genetics ·Susana Fernandes, Silvia Paracchini, Lukas Meyer, Giovanna Floridia, Chris Tyler‐Smith, P. H. Vogt	1
12	Genomic heterogeneity and instability of the AZF locus on the human Y chromosome 2004 ·Molecular and Cellular Endocrinology ·P. H. Vogt	68
13	Polymorphic DAZ gene family in polymorphic structure of AZFc locus: Artwork or functional for human spermatogenesis? 2003 ·Apmis ·P. H. Vogt, Susana Fernandes	45
14	DAZ (Deleted In AZoospermia) genes encoie proteins located in human late spermatids and In sperm tails 1998 ·Human Reproduction ·Bianca Habermann, (unknown), Anke Edelmann, C. Bohring, Ingo Backert, Franklin Kiesewetter, (unknown), P. H. Vogt	99
15	Human chromosome deletions in Yq11, AZF candidate genes and male infertility: history and update 1998 ·Molecular Human Reproduction ·P. H. Vogt	156
16	Multiplex PCR: Critical Parameters and Step-by-Step Protocol 1997 ·IUScholarWorks (Indiana University) ·Octavian Henegariu, Nyla A. Heerema, S. R. Dlouhy, Gail H. Vance, P. H. Vogt	33
17	Chromatin condensation behaviour of the Y chromosomes in the human testis 1993 ·Chromosoma ·R.M. Speed, P. H. Vogt, (unknown), T. B. Hargreave, Ann C. Chandley	17
18	Code domains in tandem repetitive DNA sequence structures 1992 ·Chromosoma ·P. H. Vogt	43
19	Towards the molecular localisation of the AZF locus: mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome 1992 ·Human Molecular Genetics ·Keyi Ma, Andrew Sharkey, Stefan Kirsch, P. H. Vogt, R Keil, T. B. Hargreave, S. McBeath, A. C. Chandley	177
20	Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved ?chromatin folding code? 1990 ·Human Genetics ·P. H. Vogt	181

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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