I. Hansmann

4.0k total citations
129 papers, 2.7k citations indexed

About

I. Hansmann is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, I. Hansmann has authored 129 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Genetics, 53 papers in Molecular Biology and 34 papers in Public Health, Environmental and Occupational Health. Recurrent topics in I. Hansmann's work include Reproductive Biology and Fertility (30 papers), Chromosomal and Genetic Variations (28 papers) and Genomic variations and chromosomal abnormalities (23 papers). I. Hansmann is often cited by papers focused on Reproductive Biology and Fertility (30 papers), Chromosomal and Genetic Variations (28 papers) and Genomic variations and chromosomal abnormalities (23 papers). I. Hansmann collaborates with scholars based in Germany, United States and Poland. I. Hansmann's co-authors include V.V.N. Gopal Rao, H. -D. Probeck, Susanne Schnittger, Edith Hümmler, Friedrich Beermann, G. Röhrborn, Iris Bartels, J. Jenderny, B. Eiben and B. Hinney and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

I. Hansmann

127 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
I. Hansmann Germany 30 1.2k 1.0k 628 528 497 129 2.7k
Dorothy Warburton United States 30 1.2k 1.1× 1.2k 1.2× 930 1.5× 414 0.8× 340 0.7× 73 3.1k
M Prieur France 26 1.5k 1.3× 1.4k 1.4× 449 0.7× 445 0.8× 455 0.9× 75 2.6k
J. de Grouchy France 35 2.0k 1.7× 1.6k 1.6× 908 1.4× 661 1.3× 394 0.8× 135 3.4k
Catherine G. Palmer United States 34 2.2k 1.9× 1.7k 1.6× 1.1k 1.7× 596 1.1× 274 0.6× 103 3.7k
Giandomenico Palka Italy 31 1.5k 1.3× 1.5k 1.5× 515 0.8× 284 0.5× 330 0.7× 145 3.3k
E. Niebuhr Denmark 29 1.5k 1.2× 1.3k 1.2× 476 0.8× 610 1.2× 195 0.4× 105 3.1k
Howard R. Slater Australia 32 1.8k 1.5× 1.3k 1.3× 795 1.3× 490 0.9× 263 0.5× 99 3.0k
Cédric Le Caignec France 29 1.5k 1.3× 1.7k 1.7× 770 1.2× 298 0.6× 237 0.5× 76 3.1k
Joy Delhanty United Kingdom 36 1.7k 1.4× 1.6k 1.5× 2.2k 3.5× 475 0.9× 889 1.8× 104 4.1k
Irene A. Uchida Canada 30 1.2k 1.0× 861 0.8× 717 1.1× 368 0.7× 273 0.5× 65 2.8k

Countries citing papers authored by I. Hansmann

Since Specialization
Citations

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

Fields of papers citing papers by I. Hansmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. Hansmann

This figure shows the co-authorship network connecting the top 25 collaborators of I. Hansmann. A scholar is included among the top collaborators of I. Hansmann 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 I. Hansmann. I. Hansmann 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.
Harendza, Sigrid, Christian A. Hübner, Christiane Gläser, et al.. (2005). Renal failure and hypertension in Alagille syndrome with a novel JAG1 mutation. Journal of Nephrology. 18(3). 312–317. 15 indexed citations
2.
Fischer, Andreas, et al.. (2004). Phenotypic variability in Hey2 ?/? mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome. Mammalian Genome. 15(9). 711–716. 28 indexed citations
3.
Thiele, Hannelore, et al.. (2001). Phenotypic findings due to trisomy 7p15.3-pter including theTWIST locus. American Journal of Medical Genetics. 103(1). 56–62. 33 indexed citations
4.
Nimmakayalu, Manjunath, et al.. (2001). Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting theJAG1 gene. American Journal of Medical Genetics. 103(2). 166–171. 18 indexed citations
5.
Schubert, Stephanie, Franco Laccone, & I. Hansmann. (1994). Towards positional cloning of the locus for benign neonatal epilepsy (EBN1) on chromosome 20. The American Journal of Human Genetics. 55. 1 indexed citations
6.
Rothschild, Cynthia, Gita Akots, Mark J. Pettenati, et al.. (1993). A genetic map of chromosome 20q12-q13.1: multiple highly polymorphic microsatellite and RFLP markers linked to the maturity-onset diabetes of the young (MODY) locus.. PubMed. 52(1). 110–23. 26 indexed citations
7.
8.
Hansmann, I. & Brigitte Pabst. (1992). Nondisjunction by failures in the molecular control of oocyte maturation. Annals of Anatomy - Anatomischer Anzeiger. 174(6). 485–490. 13 indexed citations
9.
10.
Bartels, Iris, I. Hansmann, & B. Eiben. (1990). Excess of females in chromosomally normal spontaneous abortuses. American Journal of Medical Genetics. 35(2). 297–298. 20 indexed citations
11.
Hansmann, I., et al.. (1983). X-ray Induced Reciprocal Translocations and Dicentrics in Human G 0 Lymphocytes. International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine. 43(1). 91–93. 13 indexed citations
12.
Hansmann, I., J. Jenderny, & H. -D. Probeck. (1983). Low doses of X-rays decrease the risk of diploidy in mouse oocytes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 109(1). 99–110. 15 indexed citations
13.
Hansmann, I. & H. -D. Probeck. (1979). The induction of non-disjunction by irradiation in mammalian oogenesis and spermatogenesis. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 61(1). 69–76. 13 indexed citations
14.
Hansmann, I., et al.. (1975). Chromosome aberrations in metaphase II oocytes of Chinese hamsters (Cricetulus griseus). Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 29(2). 218–219. 2 indexed citations
15.
Hansmann, I., et al.. (1975). Elimination of induced chromosome aberrations in embryogenesis of mice. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 29(2). 215–216. 1 indexed citations
16.
Hansmann, I., W. Reichert, & G. Röhrborn. (1975). X-ray-induced chromosome aberrations in oocytes of mice. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 29(2). 218–218. 2 indexed citations
17.
Hansmann, I., et al.. (1974). Chromosome aberrations in metaphase II oocytes of Chinese hamster (Cricetulus griseus) I. The sensitivity of the pre-ovulatory phase to triaziquone. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 25(3). 347–359. 15 indexed citations
18.
Hansmann, I.. (1974). Chromosome aberrations in metaphase II-oocytes stage sensitivity in the mouse oogenesis to amethopterin and cyclophosphamide. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 22(2). 175–191. 65 indexed citations
19.
Röhrborn, G. & I. Hansmann. (1974). Oral contraceptives and chromosome segregation in oocytes of mice. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 26(6). 535–544. 21 indexed citations
20.
Hansmann, I.. (1973). Induced chromosomal aberrations in pronuclei, 2-cell stages and morulae of mice. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 20(3). 353–367. 29 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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