P. W. Jungblut

3.1k total citations · 1 hit paper
66 papers, 2.3k citations indexed

About

P. W. Jungblut is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, P. W. Jungblut has authored 66 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 20 papers in Molecular Biology and 15 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in P. W. Jungblut's work include Estrogen and related hormone effects (35 papers), Hormonal and reproductive studies (12 papers) and Reproductive Physiology in Livestock (7 papers). P. W. Jungblut is often cited by papers focused on Estrogen and related hormone effects (35 papers), Hormonal and reproductive studies (12 papers) and Reproductive Physiology in Livestock (7 papers). P. W. Jungblut collaborates with scholars based in Germany, France and Australia. P. W. Jungblut's co-authors include Eugene R. DeSombre, T. Kawashima, E. V. Jensen, Walter E. Stumpf, Tetsuro Suzuki, Jerzy Adamski, R. K. Wagner, Walter Sierralta, Bettina Husen and Frauke Leenders and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Cancer.

In The Last Decade

P. W. Jungblut

63 papers receiving 2.1k citations

Hit Papers

A two-step mechanism for ... 1968 2026 1987 2006 1968 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. W. Jungblut Germany 23 1.2k 987 599 219 198 66 2.3k
Ján Mešter France 32 1.5k 1.3× 2.1k 2.1× 537 0.9× 298 1.4× 366 1.8× 93 3.8k
J A Wells United States 9 487 0.4× 1.0k 1.1× 623 1.0× 270 1.2× 197 1.0× 10 1.9k
Stephen J. Higgins United Kingdom 27 721 0.6× 1.4k 1.4× 693 1.2× 462 2.1× 160 0.8× 48 2.7k
Christine Radanyi France 33 796 0.7× 2.1k 2.1× 420 0.7× 149 0.7× 619 3.1× 48 2.9k
Paul R. Housley United States 20 839 0.7× 1.4k 1.4× 470 0.8× 41 0.2× 253 1.3× 31 2.0k
M. Atger France 32 2.1k 1.7× 1.8k 1.8× 1.0k 1.7× 908 4.1× 748 3.8× 55 4.1k
A. Chapdelaine Canada 24 392 0.3× 624 0.6× 419 0.7× 468 2.1× 99 0.5× 60 1.7k
H.M. Westphal Germany 19 1.1k 0.9× 1.4k 1.4× 544 0.9× 66 0.3× 357 1.8× 24 2.6k
Bonnie A. Maler United States 12 1.4k 1.2× 1.4k 1.4× 620 1.0× 55 0.3× 365 1.8× 12 2.4k
Ulrich Gehring Germany 32 1.0k 0.9× 2.0k 2.1× 526 0.9× 97 0.4× 412 2.1× 76 2.8k

Countries citing papers authored by P. W. Jungblut

Since Specialization
Citations

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

Fields of papers citing papers by P. W. Jungblut

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. W. Jungblut

This figure shows the co-authorship network connecting the top 25 collaborators of P. W. Jungblut. A scholar is included among the top collaborators of P. W. Jungblut 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. W. Jungblut. P. W. Jungblut 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
1.
Waberski, Dagmar, et al.. (1999). Studies on a Local Effect of Boar Seminal Plasma on Ovulation Time in Gilts. Journal of Veterinary Medicine Series A. 46(7). 431–438. 16 indexed citations
2.
Waberski, Dagmar, Thomas P. Hahn, P. W. Jungblut, et al.. (1997). LH profile and advancement of ovulation after transcervical infusion of seminal plasma at different stages of oestrus in gilts. Reproduction. 109(1). 29–34. 39 indexed citations
3.
Qualmann, Britta, Michael M. Kessels, Hans‐Jürgen Musiol, et al.. (1996). Synthesis of Boron‐Rich Lysine Dendrimers as Protein Labels in Electron Microscopy. Angewandte Chemie International Edition in English. 35(8). 909–911. 60 indexed citations
4.
Qualmann, Britta, Michael M. Kessels, Hans‐Jürgen Musiol, et al.. (1996). Synthese Bor‐reicher Lysindendrimere zur Proteinmarkierung in der Elektronenmikroskopie. Angewandte Chemie. 108(8). 970–973. 15 indexed citations
5.
Adamski, Jerzy, Thierry Normand, Frauke Leenders, et al.. (1995). Molecular cloning of a novel widely expressed human 80 kDa 17β-hydroxysteroid dehydrogenase IV. Biochemical Journal. 311(2). 437–443. 193 indexed citations
6.
Thole, Hubert, Itzhak Maschler, & P. W. Jungblut. (1995). Surface Mapping of the Ligand-Filled C-Terminal Half of the Porcine Estradiol Receptor by Restricted Proteolysis. European Journal of Biochemistry. 231(2). 510–516. 9 indexed citations
7.
Waberski, Dagmar, Holger Sudhoff, Thomas P. Hahn, et al.. (1995). Advanced ovulation in gilts by the intrauterine application of a low molecular mass pronase-sensitive fraction of boar seminal plasma. Reproduction. 105(2). 247–252. 54 indexed citations
8.
Leenders, Frauke, Jerzy Adamski, Bettina Husen, H. H. Thole, & P. W. Jungblut. (1994). Molecular cloning and amino acid sequence of the porcine 17β‐estradiol dehydrogenase. European Journal of Biochemistry. 222(1). 221–227. 86 indexed citations
9.
Thole, H. H. & P. W. Jungblut. (1994). The Ligand-Binding Site of the Estradiol-Receptor Resides in a Noncovalent Complex of Two Consecutive Peptides of 17 and 7 kDa. Biochemical and Biophysical Research Communications. 199(2). 826–833. 12 indexed citations
10.
Husen, Bettina, et al.. (1994). Alterations in the subcellular distribution of 17?-estradiol dehydrogenase in porcine endometrial cells over the course of the estrous cycle. Cell and Tissue Research. 278(2). 227–233. 12 indexed citations
11.
Jungblut, P. W., et al.. (1994). The C-terminal half of the porcine estradiol receptor contains no post-translational modification: determination of the primary structure. Molecular and Cellular Endocrinology. 104(2). 163–172. 22 indexed citations
12.
Adamski, Jerzy, et al.. (1992). The membrane-bound 17β-estradiol dehydrogenase of porcine endometrial cells: Purification, characterization and subcellular localization. The Journal of Steroid Biochemistry and Molecular Biology. 43(8). 1089–1093. 6 indexed citations
13.
Jungblut, P. W., et al.. (1989). Receptor deprivation with unimpaired edema formation in porcine uteri by "dissociated estrogens". European Journal of Endocrinology. 120(3_Suppl). S160–S161. 1 indexed citations
14.
Adamski, Jerzy, Walter Sierralta, & P. W. Jungblut. (1989). Assignment of estradiol-17β dehydrogenase and of estrone reductase to cytoplasmic structures of porcine endometrium cells. European Journal of Endocrinology. 121(2). 161–167. 15 indexed citations
15.
Kallweit, Erhard, et al.. (1987). Biosynthesis and posttranslational finishing of the estradiol receptor. Journal of Steroid Biochemistry. 27(1-3). 109–113. 4 indexed citations
16.
Jungblut, P. W., et al.. (1985). Exhaustive solubilization of microsomal estrogen receptor with polyanions. European Journal of Endocrinology. 110(1_Suppla). S122–S123. 1 indexed citations
17.
Jungblut, P. W., et al.. (1983). Subcellular Distribution, Properties and Interrelationship of Oestrogen Receptors in Endometrium and Other Target Tissues. Clinical Chemistry and Laboratory Medicine (CCLM). 21(8). 473–80. 6 indexed citations
18.
Sierralta, Walter, et al.. (1980). Studies on the Involvement of Lysosomes in Estrogen Action, III. The Dehydrogenation of Estradiol to Estrone by Porcine Endometrial Lysosomes. Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 361(1). 959–968. 18 indexed citations
19.
Wagner, R. K. & P. W. Jungblut. (1976). Differentiation between steroid hormone receptors CBG and shbg in human target organ extracts by a single-step assay. Molecular and Cellular Endocrinology. 4(1). 13–24. 13 indexed citations
20.
Little, Melvyn, et al.. (1973). INTERRELATIONSHIP OF TWO MICROSOMAL ESTROGEN RECEPTOR MOLECULES. European Journal of Endocrinology. 71(4_Suppl). S67–S67. 2 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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